EPA-600/9-78-012
May 1978
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ANALYTICAL
REFERENCE STANDARDS
AND SUPPLEMENTAL
DATA FOR PESTICIDES AND
OTHER ORGANIC COMPOUNDS
O
<^ "*" 6 y •
%,
Q
U.S. ENVIRONMENTAL PROTECTION AGENCY
Health Effects Research Laboratory
Environmental Toxicology Division
Research Triangle Park, N.C. 27711
-------
EPA-600/9-78-012
ANALYTICAL REFERENCE STANDARDS
AND
SUPPLEMENTAL DATA
FOR
PESTICIDES AND OTHER ORGANIC COMPOUNDS
Prepared by
Analytical Chemistry Branch
Environmental Toxicology Division
Editors: J.F. Thompson and R.R. Watts
Health Effects Research Laboratory
Office of Research and Development
U.S. Environmental Protection Agency
Research Triangle Park, N.C. 27711
May 1978
-------
DISCLAIMER
This report has been reviewed by the Health Effects Research
Laboratory, U.S. Environmental Protection Agency, and approved for
publication. Mention of trade names or commercial products does not
constitute endorsement or recommendation for use.
11
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CONTENTS
Page
Preface ......................... iv
Section I, a List of available pesticide standards ...... 1
Section I, b
A. List of compounds deleted from 1976 stock .... 95
B. List of approved common name changes ...... 95
C. List of compounds by chemical name ........ 96
List of organic pollutant standards ....... 108
Handling of primary standards .......... 130
Section II
Section III
Section IV
Preparation and storage of reference
standard solutions 131
Section V
Section VI
Decoding residue analytical method citations
139
List of contributing pesticide producing
companies 145
Section VII Index of pesticide equivalent names 146
Section VIII Mailinq list confirmation 186
Technical Reoort Data 187
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PREFACE
The reference standards repository of the Health Effects Research
Laboratory was originally established in 1965 at the Perrine, Florida facility
then known as the Pesticides Research Laboratory at the U.S. Public Health
Service. The repository was created as a central source of high purity pesti-
cide reference standards available only to in-house scientists and laboratories
in the field conducting area or "community" monitoring of pesticides in human
biota under contract with the Public Health Service.
During ensuing years at Perrine and more recently at Research Triangle
Park, N.C., the laboratory now known as the Environmental Toxicology Division
of the EPA Health Effects Research Laboratory, has extended its service to
other non-profit pesticide research and monitoring laboratories on a discre-
tionary basis as time and resources have permitted.
In Section I,a the current Index lists 438 pesticidal and related com-
pounds. Five compounds listed in the 1976 Index have been deleted because
(1) there has been no demand; (2) they are either no longer produced, or
(3) they have proved too difficult to obtain. On the other hand, 57 new
pesticidal compounds and/or derivatives have been added to the stock.
In this edition a new section (II) has been added concurrent to our
repository stock expansion to include 122 organic compounds other than pesti-
cides. The majority of these compounds are listed in the 1974 TOXIC SUBSTANCES
LIST published by the National Institute for Occupational Safety and Health,
and many of them have been detected in monitoring programs of the nation's
waterways. The decision to stock these compounds was based on the fact that
many monitoring laboratories are now interested in a wide spectrum of toxic
organic pollutants.
In this edition supplemental data has been expanded to include
(1) in Section l,b,C a full list of the 1978 repository compounds in alpha-
betical order by chemical name, and (2) opposite each chemical name, the
common name, if assigned, or the proprietary name if no common name has been
assigned.
Residue methodology citations have been updated, deleting some of the
older citations and incorporating newer publications. Following the format
started in the 1976 edition, references are given in code in the faceplate
for each compound in Section l,a, with decoding information provided in
Section V. The validity or integrity of the analytical data in the cited
publications is neither recommended nor endorsed. The data are provided
only for supplemental information.
A special note of appreciation is extended to those commercial
producers of pesticidal compounds who provide analytical grade reference
standard materials. Without their help, it would be next to impossible to
maintain the repository service. Contributing companies are shown in
Section VI.
-------
Continuing with the policy instituted in the 1973 edition of this Index,
supplemental data such as USE, CHEMICAL NAME, MOLECULAR WEIGHT, EMPIRICAL AND
STRUCTURAL FORMULAE and TOXICITY are given for each compound whenever data
were available. Unless otherwise stated, toxicity is expressed as the LD50
based on oral feeding of male rats. The figure given is the number of milli-
grams of the compounds required per kilogram of animal weight to produce
mortality in 50% of test animals. Thus the lower the figure, the higher the
toxicity. All users are strongly advised to exercise extreme care in the
handling of any compound with an LD50 of 50 or below. A number of these
highly toxic compounds are also dermally toxic, and scrupulous care must be
taken to avoid contact with the skin (see Section III).
In Section I,a each compound is listed in capital letters by its common
name, if one has been assigned. Also shown parenthetically is any other name
by which the compound is or has been widely known in the marketplace. In
cases where no common name has been assigned, a trade or proprietary name is
used. For the convenience of the reader, Section VII contains a list of over
pesticide names along with assigned common names where an assignment
has been made. If a common name has not been assigned, the most widely known
trade name is used. The omission of any proprietary name does not imply
endorsement of one product over another. The subject of compound names is
complex and subject to rapid change.
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Section I,a
LIST OF AVAILABLE PESTICIDE STANDARDS AND ORDERING INFORMATION
As this edition goes to press, each compound listed in the following
pages is commercially available and can be supplied in 100 mg portions.
However, during the two-year life of this edition it is more than likely
that the production of certain compounds will be discontinued and reference
standard materials will no longer be available. Those who request such
compounds will be notified of this on the bottom line of the mail-back
acknowledgment card which accompanies each shipment.
For the reader's convenience all compounds are listed alphabetically
by common name with code numbers on the next four pages so that the entire
stock may be scanned quickly. In ensuing pages each compound is listed and
data such as chemical name, formulae, toxicity, percent purity, etc. are
given.
The percentage purity given for many compounds should be regarded
as approximate. Assays on various lots by the producer may vary slightly.
In any case the value printed on the sample bottle will be the precise
assay value provided for the specific lot. A few compounds are available
only as a formulation, and expectedly the assay value will be relatively
low; in the order of 40-50% active ingredient. It will also be observed
that certain compounds have "adjusted" or "stabilized" purity values.
This means that because of the instability of the particular compound at
extremely high concentration levels, this level has been purposely reduced
to achieve a more stable standard.
Wherever the symbol = is used at the end of a line in the typing of
the chemical name, it means that the word in the first portion of the next
line is a continuing part of the word at the end of the line above. An
ordinary hyphen at the end of a line indicates that the hyphen is a normal
part of the chemical name.
Our service is intended solely to provide analytical reference
standards. Because of great demand and limited supplies, the amount of each
standard is restricted to no more than 100 milligrams. Researchers needing
larger quantities, such asTor animal feecHng studies, should contact the
manufacturer or purchase from a commercial supplier. We cannot supply large
quantities.
Most of the high-purity analytical standard compounds are difficult
to prepare and therefore in short supply. We suggest that not more than 20 mg
of primary standard be weighed out and diluted to 100 ml with an appropriate
solvent. This yields a concentration of 200 yg per ml and should provide a
sufficiently high concentration for just about any gas-liquid or thin layer
chromatographic method. In fact, a solution of this concentration should
require one or more serial dilutions to provide an appropriate concentration
for most electron-capture GC work.
-------
Occasionally we hear that bottles of standards are received empty.
There is a remote possibility that this may be the case, but generally the
bottle only appears to be empty from the outside. Some of the colorless,
highly viscous liquids may coat the interior of the bottle or collect inside
the bottle cap. When a bottle is received that appears empty, the cap should
be carefully removed and the interior of the bottle and cap examined.
In preparing requests for standards, each compound needed should be
listed by code number and common name to assist repository personnel in pro-
cessing requests. An Advice of Receipt card and a sample request form are
enclosed with each shipment. It is important that the card be mailed back
immediately. This provides our only verification that each shipment has
reached its destination. When these mail-back cards do not return within a
month, a tracer is mailed to the requester. No covering letter is required
with the request form, but a full address must be given along with requester's
name.
Requests are .occasionally received listing compounds which are not
given in the Index. They may have been stocked at the time of the previous
edition or the requester may be overly optimistic and assume they can be
caused to materialize. If any compound is not listed, it is not available
from the repository.
A final note is directed to all scientists associated with university
laboratories. Requests for standards must be made on stationery bearing the
letterhead of the institution and must be signed by a university official
such as a department head. Pesticides will not be mailed to individuals
submitting requests on personal stationery.
All requests for standards should be directed to:
Quality Assurance Section (Please use the
Analytical Chemistry Branch, ETD/HERL (MD-69) entire address)
U.S. Environmental Protection Agency
Research Triangle Park, N.C. 27711
Phone requests will be accepted if the list does not exceed five
compounds. The commercial number is 919-541-2564, or the Federal WATS line
number is 629-2564. We request that persons phoning do not attempt to reach
repository laboratory personnel; they have been instructed to refer all phone
requests to the above number. In any case the shipment is made within one
working day from the time the request is received irrespective of how or by
whom it is received.
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ALPHABETICAL LISTING AND CODE NUMBERS OF PESTICIDAL COMPOUNDS
COMMON NAME
ACEPHATE
ACROLEIN
ALACHLOR
ALDICARB
ALDRIN
ALLETHRIN
AMETRYN
2-AMINOBENZIMIDAZOL
AMINOCARB
4-AMINO-5-CHLOROPYRIDAZ-6-ONE
AMITROLE
AMOBAM
ANCYMIDOL
ANILAZINE
ANTHRAQUINONE
ANTU
ASPON
ASULAM
ATRATON
ATRAZINE
AZINPHOSETHYL
AZINPHOSMETHYL
AZOBENZENE
BARBAN
BENDIOCARB
BENEFIN
BENOMYL
BENSULIDE
BENTAZON
BENZADOX
BENZOYLPROP ETHYL
BENZYL BENZOATE
BHC, a-ISOMER
BHC, B-ISOMER
BHC, y-ISOMER
BHC, S-ISOMER
BIFENOX
BIPHENYL
BPMC
BROMACIL
4-BROMO-2.5-DICHLOROPHENOL
BROMOFENOXIM
BROMOPHOS
BROMOPHOS ETHYL
BROMOPROPYLATE
BROMOXYNIL
BUFENCARB
BUNEMA
BUTACHLOR
BUTHIDAZOLE
BUTRALIN
BUTYLATE
CACODYLIC ACID
CALCIUM ARSENATE
CAPTAFOL
CODE
NUMBER
0025
0027
4160
0060
0080
0100
0120
0171
0180
0186
0200
0220
0230
2920
0250
0260
0300
0310
0320
0420
3840
3820
0340
0400
0472
0480
0500
0520
0425
0577
0578
0580
0620
0640
0680
0660
0733
0740
0791
0800
0822
0832
0840
0860
0872
0820
0960
0916
0922
0926
0933
0940
0961
0980
1000
COMMON NAME
CAPTAN
CARBARYL
CARBENDAZIM
CARBETAMIDE
CARBOFURAN
3-HYDROXYCARBOFURAN
3-KETOCARBOFURAN PHENOL
CARBOFURAN PHENOL
CARBOPHENOTHION
CARBOPHENOTHION, OXYGEN ANALOG
CARBOXIN
CDAA
CDEC
CHLORAMBEN
CHLORANIL
CHLORBROMURON
CHLORDANE, TECH.
CHLORDANE-a
CHLORDANE-Y
CHLORDECONE
CHLORDENE
CHLORDENE-a
CHLORDENE-e
CHLORDENE-Y
CHLORDIMEFORM
CHLORFENVINPHOS
CHLORMEPHOS
CHLOROBENZILATE
CHLORONEB
CHLOROPHACINONE
CHLOROTHALONIL
CHLORPROPHAM
CHLORPYRIFOS
CHLORPYRIFOS, OXYGEN ANALOG
CHLORPYRIFOS METHYL
CHLORTHIOPHOS
CHLORTOLURON
CISANILIDE
CLONITRALID
COUMAFURYL
COUMAPHOS
CROTOXYPHOS
CRUFOMATE
CRYOLITE
CYANAZINE
CYANOFENPHOS
CYCLOATE
CYCLOHEXIMIDE
CYCLOPRATE
CYPERQUAT
CYPRAZINE
CYTHIOATE
DALAPON
DAMINOZIDE
DCPA
DDA-p.p'
CODE
NUMBER
1020
1060
1071
1074
1040
1041
1042
1043
1080
1081
1100
1140
1160
0140
1180
1188
1200
1220
1240
1280
1260
1261
1262
1263
1480
1300
1316
1360
1380
1425
1640
1420
2900
2901
2902
1491
1512
1523
0460
3720
1540
1500
6020
1546
1552
6360
1591
1600
1606
1611
1615
1621
1660
1681
1720
1740
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COMMON NAME
ODD, MIXED
DDD-M.P1
DDD-O.P1
DDD-P.P'
DDE-O.P1
DDE-P.P'
DDT-MIXED (TECH.)
DDT-O.P'
DDT-P.P1
DEF
DEMETON-0
DEMETON-S
DESMEDIPHAM
DIAL I FOR
DIALLATE
DIAPHENE
DIAZINON
DIBROMQCHLOROPROPANE
DIBUTYL.PHTHALATE
DICAMBA
DICHLOBENIL
DICHLOFENTHION
DICHLONE
DICHLORAN
DICHLOROBENZENE-0
DICHLOROBENZENE-P
ota-DICHLOROPROPENE
tiww-DICHLOROPROPENE
DICHLOROSALICYLIC ACID
DICHLORPROP
DICHLORVOS
DICOFOL
DICROTOPHOS
DIELDRIN
DI ETHYL PHOSPHATE
DIFENOXURON
DIFENZOQUAT
DIFLUBENZURON
DIMETHAMETRYN
DIMETHIRIMOL
DIMETHOATE
DIMETHOATE, OXYGEN ANALOG
DIMETHYL PHOSPHATE
DIMETHYL PHTHALATE
DINITRAMINE
DINOCAP
DINOSEB
DINOSEB ACETATE
OIOXACARB
DIOXATHION
DIPHACINONE
DIPHENAMID
DIPHENYL MERCURY
D1PROPETRYN
DIQUAT DIBROMIDE
DISULFOTON
DITHIANON
DIURON
CODE
NUMBER
1750
1820
1760
1780
1840
I860
1880
1900
1920
1940
1981
1982
2006
2035
2040
2060
2080
2090
2120
2140
2200
222D
2180
2260
2280
2300
2306
2307
2308
2309
2320
2340
0700
2380
2386
2391
2395
Z406
2411
2416
2420
2421
2458
2460
2551
2560
2760
2566
2573
2580
2600
2620
2640
2653
2660
2720
2721
2740
' COMMON NAME
DNOC
DODINE
DRAZOXOLON
DSMA
2,4-D, ACID
2,4-D, BOEE
2,4-D, BE
2,4-D, DEA SALT (FORMULATION)
2,4-D, DMA SALT (FORMULATION)
2,4-D, IBE
2,4-D, IOE
2,4-D, IPE
2,4-D, PGBEE
2,4-OB, ACID
2,4-DB, BE
2,4-DB, IBE
2,4-DB, IOE
ENDOSULFAN
ENDOSULFAN I
ENDOSULFAN II
ENDOSULFAN CYCLIC SULFATE
ENDOTHALL, ACID
ENDRIN
EPN
EPTC
ETHAZOL
ETHEPHON
ETHIOLATE
ETHION
ETHIRIMOL
ETHOFUMESATE
ETHOPROP
ETHYLAN
ETHYLHEXANEDIOL
ETHYLMERCURIC CHLORIDE
ETRIMFOS
EXD
FAMPHUR
FENAC
FENAMINOSULF
FENBUTATIN-OXIDE
FENITROTHION
FENSULFOTHION
FENTHION
FENTIN ACETATE
FENTIN HYDROXIDE
FERBAM
FLUCHLORALIN
FLUOMETURON
FLUORIDAMID
FLURECOL-N-BUTYLESTER
FOLEX
, FOLPET
FONOFOS
FONOFOS, OXYGEN ANALOG
FORMETANATE HCL
CODE
NUMBER
2770
2780
2792
2860
2940
2960
2980
2985
2990
3000
3020
3040
3060
3080
3100
3120
3140
31 EO
3200
3220
3232
3240
3260
3280
3300
6590
3330
3335 '
3340
3359
3373
5880
5380
3380
3400
3412
3420
3440
3460
2020
7013
3480
3500
3520
3527
3540
3600
0407
3620
3623
3630
3640
3660
2910
2911
3680
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COMMON NAME
FORMOTHION
GIBBERELLIC ACID
GLYOXIME
GLYPHOSATE
GLYPHOSINE
HEPTACHLOR
HEPTACHLOR EPOXIDE
HEXACHLOROBENZENE
HEXACHLOROPHENE
5-HYDROXY-2-BENZIMIDAZOLE CARBAMATE
1-HYDROXYCHLORDENE
IBP
IOXYNIL
ISOPROPALIN
JODFENPHOS
KARBUTILATE
KINOPRENE
KRENITE
LAMPRECIDE
LEAD ARSENATE
LENACIL
LEPTOPHOS
LEPTOPHOS, OXYGEN ANALOG
LETHANE 384
LINURON
MALATHION
MALATHION, OXYGEN ANALOG
MANEB
MCPA, ACID
MCPA, IOE
MCPB, ACID
MCPP, ACID
MCPP, IOE
MECARBAM
MENAZON
MEOBAL
MEPHOSFOLAN
METHAM
METHAMIDOPHOS
METHANEARSONIC ACID
METHAZOLE
METHIDATHION
METHIOCARB
METHOMYL
METHOMYL OXIME
METHOPRENE
METHOXYCHLOR (TECH)
METHOXYCHLOR-P.P1
METHYLMERCURIC CHLORIDE
METHYLMERCURIC IODIDE
CODE
NUMBER
3732
3790
3796
3801
3802
3860
3880
3920
3940
3949
3960
4011
4040
4070
4103
6420
4146
4156
4166
4180
4J85
4190
4191
4220
4240
4260
4261
4300
4340
4360
4380
4400
4420
4441
4453
4460
1630
6620
4750
4490
4496
6340
4500
4520
4521
4531
4540
4541
4560
4572
COMMON NAME
METIRAM
METOBROMURON
METOXURON
METRIBUZIN
MEVINPHOS
MEXACARBATE
MH
MIREX
MOLINATE
MONALIDE
MONOCROTOPHOS
MONOLINURON
MONURON
MONURON-TCA
MSMA
NALED
NAPHTHALENE ACETAMIDE
NAPHTHALENE ACETIC ACID
1-NAPHTHOL
NAPROPAMIDE
NAPTALAM-NA SALT
NEBURON
NITRALIN
NITRAPYRIN
NITROFEN
4-NITROPHENOL
ferems-NONACHLOR
NORFLURAZON
ORYZALIN
OXADIAZON
OXAMYL
OXAMYL OXIME
OXYCHLORDANE
OXYDEMETON-METHYL
OXYTHIOQUINOX
PARAQUAT DICHLORIDE
PARATHION ETHYL
PARATHION METHYL
PARINOL
PCNB
PCP
PEBULATE
PENOXALIN
PERFLUIDONE
PHENKAPTON NA
PHENMEDIPHAM
PHENOTHIAZINE
PHENYLMERCURIC ACETATE
PHENYLMERCURIC BORATE
PHENYLMERCURIC CHLORIDE
PHENYLMERCURIC HYDROXIDE
PHENYLMERCURIC IODIDE
PHENYLPHENOL
PHORATE
CODE
NUMBER
4583
4612
4631
4634
4640
7080
4280
4720
4740
4747
0360
4751
4760
4780
4820
4860
4880
4900
4925
2010
4920
4940
5020
5031
5040
5060
5080
5136
5148
5176
5186
5187
5200
5220
4800
5240
5245
4580
5251
5280
5260
5300
5331
5366
5400
5410
5420
5680
5460
5480
5485
5487
5490
5500
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COMMON NAME
PRORATE OXYGEN ANALOG
PHORATE SULFOXIDE
PHOSALONE
PHOSFOLAN
PHOSMET
PHOSMET OXYGEN ANALOG
PHOSPHAMIDON
PICLORAM
PIPERALIN
PIPERONYL BUTOXIDE
PIRIMICARB
PIRIMIPHOS ETHYL
PIRIMIPHOS METHYL
POLYCHLORINATED BIPHENYLS (PCB's):
AROCLOR 1016
AROCLOR 1221
AROCLOR 1232
AROCLOR 1242
AROCLOR 1248
AROCLOR 1254
AROCLOR 1260
AROCLOR 1262
POLYCHLORINATED NAPHTHALENES (PCN's):
HALOWAX 1000
HALOWAX 1001
HALOWAX 1013
HALOWAX 1014
HALOWAX 1051
HALOWAX 1099
POTASSIUM AZIDE
POTASSIUM DIETHYL DITHIOPHOSPHATE (KDEDTP)
POTASSIUM DIETHYL THIOPHOSPHATE (KDETP)
POTASSIUM DIMETHYL DITHIOPHOSPHATE (KDMDTP)
POTASSIUM DIMETHYL THIOPHOSPHATE (KDMTP)
PROCYAZINE
PROFLURALIN
PROMECARB
PROMETON
PROMETRYN
PRONAMIDE
PROPACHLOR
PROPANIL
PROPARGITE
PROPAZINE
PROPHAM
PROPOXUR
PROTECT
PYRACARBOLID
PYRAZON
PYRAZOPHOS
PYRETHRINS
QUINALPHOS
RELEASE
RESMETHRIN
RONNEL
ROTENONE
CODE
NUMBER
5501
5502
5520 .
1610
4000
4001
5580
5600
5640
5620
5632
5642
5643
5700
5701
5702
5703
5704
5705
5706
5707
5720
5721
5722
5723
5724
5725
5728
5731
5732
5733
5734
5739
5746
5752
5760
5780
4090
5820
5840
5160
5800
5860
0440
5882
5905
5925
5932
5940
5966
6022
6055
5980
6000
COMMON NAME
SALITHION
SI DURON
SILVEX, ACID
SILVEX, IDE
SILVEX, PGBEE
SIMAZINE
SODIUM AZIDE
SODIUM PENTACHLOROPHENATE
SODIUM PHENYLPHENATE
STREPTOMYCIN SULFATE
STROBANE T TOXAPHENE
SULFOXIDE
TECNAZENE
TEMEPHOS
TEPP
TERBACIL
TERBUFOS
TERBUTHIURON
TERBUTHYLAZINE
TERBUTRYN
TETRACHLORVINPHOS
TETRADIFON
TETRASUL
THANITE
THIABENDAZOLE
THIOBENCARB
THIOFANOX
THIOMETON
THIOPHANATE
THIOPHANATE METHYL
THIRAM
TOXAPHENE
TRIALLATE
TRIAZOPHOS
TRICHLORFON
2,4,5-TRICHLOROPHENOL
TRICLOPYR
TRIDEMORPH
TRIETAZINE
TRIFLURALIN
TRIFORINE
2,4,5-T, ACID
2,4, 5-T, BOEEE
2,4,5-T, BE
2,4,5-T, IDE
2,4,5-T, PGBEE
2,4,5-T, TEA SALT (FORMULATION)
4-(2,4,5-TB)
2,3,6-TBA
VELPAR
VERNOLATE
WARFARIN
ZINEB
ZIRAM
CODE
NUMBER
6050
6100
6120
6130
6140
6160
6172
2820
2800
6222
6240
6300
6435
0020
6540
6560
6573
6583
6589
3980
3740
6600
6630
6640
6660
0570
6663
6665
6670
6671
6680
6740
6770
6777
6780
6890
6786
6792
6796
6800
6822
6840
6860
6870
6880
6885
6895
6900
6920
7001
7020
7060
7120
7100
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Code Common Name Emp. Form.
Chemical Name
0025 ACEPHATE (Orthene)
Mol.Wt. 183
Us* Insectic.
L DM 945
Purity 99 X
0027
0,S-Dimethyl N-acetyl=
phosphoramidothioate
Ref
1
2
3
4
5
6
AL
21
AL
74
75
57/1
58
189
1015
3
9
2,4
a
a
e
ACROLEIN (Aqualin)
C,H,,0
2-Propenal
Mol.Wt. 56.06
A B C D E F
Use Herbic.
I.DSO 46
Purity 92-94 X „.,
1
2
3
4
5
6
7U
12
t
Structure
9
H H
I I
CH,= C — C—O
4160 ALACHLOR (Lasso) C14H2()C1N02
Mol.Wt. 270
A
Use Herbic.
L DSO 3,000
Purity 99.5+S R,f.
2-Chloro-2' ,6'-diethyl-N-
(methoxymethyl ) acetanilide
1
2
3
4
5
6
C
BH
KA
AJ
AL
WD
71
73
75
76
76
II
11/4
50/5
23/1
59
129
257
333
77
854
309
3
19
15,
11
3,8
2
2
:gh
xu
X
X
C
U
CH2CH3
CH2OCH3
— / C - CH2
CH2CH3'
0060 ALDICARB (Temik)
Mol.Wt. 190
Use Insectic.'
IDM 0.93
Purity 99+ X
C7H,.N,0,S 2-Methyl-2-(methylthio)propional=
,,.,o
R.f.
dehyde-0-(methylcarbomoyl)oxime
1
2
3
4
5
6
C
AL
AJ
AJ
AL
67
68
69
70
II
50
16
17/1
53
1242
549
70
1296
4,1!
12
10
6
4
g
e
aef
af
def
CH,
O
CH3S-C-C=N-O-C-N-CH,
CH
H
I
H
0080
ALDRIN (HHDN)
Mot.Wt. 365
Use Insectic.
I DM 55
Purity 99+ X
C12H8C16
R»f.
1,2,3,4,10,10-Hexachloro-l,4,4a,
5,8,8a-hexahydro-l,4-endo-
emj-STS-dimethanonaphthalene
1
2
3
4
5
6
L
A
A
A
AL
ZK
*
75
76
I
5
8B
IDA
58
12
1015
275
2,b
2
2
2
2,11
2
a
jl
V
t
e
k
-------
Code Common Name Emp. Form.
Chemical Name
Structure
0100 ALLETHRIN C19H26°3 dl-2-Allyl -4-hydroxy-3-methyl-
i» <:o j 2-cyclopenten-l-one ester of
dl -ois/trans-2 ,2-dimethyl -3-
( 2-methyl propenyl ) -cycl opropanecar=
Mol.Wt. 302 boxylic acid
A B C D E F
Use Insectic.
ID 50 680
Purity 92+ % Ref.
1
2
3
4
5
6
AJ
58
6
643
21
JO
(CH3)2C=CH-CH 0 CH3
NCH-C-O-jxWcH2-CH=CH1
(CH3)2'C o
0120 AMETRYN (Evik) CqH,7N,S 2-(Ethylamino)-4-(isopropylamino)-
70 6-(methylthio)-l,3,5-triazine
Mol.Wt. 227 SCH3
,,L. A B C D E F JL^
Use Heroic.
IDjo 1.110
Purity 99+ % Ref.
1
2
3
4
5
6
C
WD
73
II
80
137
6
11
2fio
u
N^ ^N H
I i '
i ^SVKJ*X'^
1 N
H
0171 2-AMINOBENZIMIDAZOLE C7H7N3 Do
Mol.Wt. 133 H
A B C D E F ^ J.
Use Deriv. of Benotnyl
IDjo
Purity — % R,f.
0180 AMINOCARB (Matacil) C,
1
2
3
4
5
6
\ WMU
k/S/
1H,,N,0, 4-Dimethylamino-m-tolyl
methyl carbamate
Mol.Wt. 208 H 0 / v
Ule Insectic.
L050 30
Purity 98+ % R.f.
A B C D E F
1
2
3
4
5
6
A
WD
ZD
WD
AJ
AL
77
69
70
70
72
72
IDA
45/(3.4)
50/1
50/1
20/2
55/6
362
92
92
443
1259
2
3
14
11
2,3
11
t
X
0
X
X
X
CH3-N-C-0-/ \-N(CH3)2
^==A
CH3
0186 4-AMINO-5-CHLORO- C.H.C1N-0 Do
PYRIDAZ-6-ONE H * J
NH2
Mol.Wt. 146 i
A B C D E F Clx^^\
Use Deriv. of Pyrazon
.
D50
Purity 99. 5* Ref.
1
2
3
4
5
6
!
k'
N
I
!
H
-------
Code Common Name Emp. Form.
Chemical Name
Structure
0220
0230
2920
0250
AMITROLE (Cytrol) C2H4N4 3-Am1no-l ,2,4-tr1azole
Mol.Wt. 84 , . .K.L . ...
y Herbic,
I Dw 24,600
Purity 99+ % R.f.
A B C D E F nV^ ^V'NH2
)
2
3
4
5
6
AL
AL
ZJ
b!
62
70
44
45
18
196
382
439
12
12
12
d,e
e
t
1 1
N N
H/
AMOBAM (Chem-0-Bam) C.H-.N.S. Dlammonium ethylene =
* '* * * b1sd1th1ocarbamate
Mol.Wt. 246
Ut. Funglc.
I DSO 450
Pwrlty 41-43** R.f.
A B C D E F
1
2
3
4
5
6
AL
BA
AL
AJ
67
68
69
74
50/5
93/11.05
52/6
22/5
1102
219
1226
886
18
15
10
10
a
a,c
del
a
CH2NHCS2NH4
1
CH2NHCS2NH4
ANCYMIDOL (A-Rest) C,,;H,,N,0, a-Cyclopropyl-a-(p-methoxyphenyl)-
10 '" ' ' 5-pyr1m1d1nemethanol
OH
Mel.Wt. 256
A B C Off F* — \ /==\
U<« Grwth. Regul .
ID jo 4,500
Purity 99+ % R.f.
1
2
3
4
i
6
AL
3E
75
58/4
850
3
3
w
u
(' \-C -4. /V- OCH
\=/ i VJ^
A
A
* -*
ANILAZINE (Dyrene) C0H,C1,N. 2,4-D1chloro-6-(2-chloroan1l-
9 b J * 1no)-l,3.5-tr1az1ne
u Cl
Mol.Wt. 275.5
UM Funglc.
ID 50 2,710
Purity 95* * % R.f.
AS C D E F
1
2
3
4
5
6
C
AJ
76
II
24
1236
12
1
ef
c
YVC5
^^^^^^ ^^^^
X
Cl
ANTHRAQUINONE (CorbH) C14H802 9,lO-Anthraqu1none
Mol.Wt. 208 ^
UM Bird Repel 1 ant
1.0 jo 5,000+
Purity 97+ % R.f.
A B C D E F
1
2
3
JA
AT
66
72
30/9
17/6
935
710
11
11
X
X
r^^V^N^^
LIT]
^tXx^/k^1
-------
Code Common Name Emp. Form.
Chemical Name
Structure
0260
ANTU
l(l-Naphthyl)-2-thiourea
Mol. Wl. 202
U»e Rodent!c.
ID*) 7
Purity 95-98 •{
Ref.
1
2
3
4
5
6
GG
WD
50
67
89
5/11
115
552
12
2
X
X
NH-CS-NH2
0300
ASPON
C,,H,00,-P,S,
\i ^8 b L i
Tetra-n-propyl dith1o=
pyrophosphate
Mol.Wt. 378
Use Insectic.
I DM 891
Purity 98+ X
Ref.
1
2
3
4
5
6
AL
70
53/3
499
4
X
t s
(C3H7O)2-P-O-f>-(OC3H7)2
0310
ASULAM (Asulox)
Methyl (4-amino ben=
zenesulfonyl) carbamate
Mol.Wt. 230
lUe Herbic.
I Oso 5,000+
Purity 99 S
Ref.
1
2
3
4
5
6
AC
71
73
7
497
12
3,4
i
u
H,N
SO2NHCOOCH3
0320
ATRATON (Gesatamin) CQH,,N,.0 2-(Ethylamino)-4-(isopropylamino)-
6-methoxy-l,3,5-triazine
Mol.Wt. 211
Uco Herbic.
LDso 1,465
Purity 88-89 %
Ref.
A B
€ F
1
2
3
4
5
6
BH
ZD
64
70
4
32
64
371
—
6
—
u
OCH3
0420 ATRAZINE (Aatrex)
Mol.Wt. 216
Use Herbic.
LDso 3'080
Purity 99+ S
Ref.
2-Chloro-4(ethylamino)-6-(1so=
propylaminoj-l,3,5-triazine
1
2
3
4
5
6
A
AL
RC
AJ
AJ
AJ
77
68
70
73
74
76
10A
51
35
21
22
24
682
64
93
137
122
2
3
11
1,2
2
3
t
ctu
a,j
ctu
f
t
C2H5N'
H
H
-N-C(CH3)2
H
10
-------
Code Common Name Emp. Form.
Chemical Name
Structure
3840
AZINPHOS ETHYL C,,H,,N,0,PS., 0,0-Diethyl phosphorodithioate
(Ethyl Guthion) ' S-ester with 3- (mercaptomethyl )-
l,2,3-benzotriazin-4(3H)-one
Mol.Wt. 345 O
A B C D E F if
U»e Insectic.
I.DSO 7-17
Purity --- % Ref.
1
2
3
AJ
WD
ZD
68
69
69
16/5
43/3
26
808
388
17
11
10
10
X
t
t
(C2H50)2 P- S -CH2-S) >^
•I i
s r^ L.
3820 AZINPHOS METHYL
(Guthion)
Mol.Wt. 317
Use Insectlc.
LOjo 16
Purity 98+ %
C10H12N303PS2
Ref.
0,0-Dimethyl phosphorodithioate
s-ester with 3-(mercaptomethyl)-
1 ,2,3-benzotriazin-4(3H)-one
1
2
3
4
5
6
C
A
WD
AD
AL
AD
77
69
74
74
74
II
IDA
43/3
11/3
57/5
11/6
388
224
1033
532
12,1'
4
10
4
4
4
deg
t
t
u
t
t
(CH3O)2 P-S-CH2 -
0340
AZOBENZENE
C12H10N2
Dlphenyl diimide
Mol.Wt. 182
U«e Acaric.
L DSO 1,000
Purity gg+ 1
Ref.
1
2
3
4
5
6
AV
73
01721
10, T
J
0400 BARBAN (Carbyne)
Mol.Wt. 258
u»» Herbic.
1 DS» 1,350
Purity gg+ %
C,,HQC1-NO.,
11 3 ' '
A B
Ref
4-Chlorobut-2-ynyl 3-
chlorophenyl carbamate
1
2
3
4
5
6
C
WD
BA
71
72
II
57
97/1153
303
294
12
11
2
a
t,u
a,c
0
H-N-C-0-CH2-CEC-CH2CI
0472
BENDIOCARB (Ficam)
C11H13N04
2 ,3-Isopropyl i denedioxy-
phenyl methyl carbamate
Mol.Wt. 223 (^ Y^
A B C O E F j
"te Insectic.
IDs,, 17g
Purity gg g S Ref.
1
2
3
4
5
6
3N
3N
v
3
2
w
r
I J^
^v^^^-^
O-C-NH-CH
O
-------
Code Common Name Emp. Form.
Chemical' Name
Structure
0480
BENEFIN (Balan)
Met.Wt. 335
UM Herblc.
IDM 10,000+
Purity 100 *
cnHlfiFlNi°4
IJ lb J J 4
*•'.
N-Butyl N-ethyl-2,6-d1n1tro-
4-(tr1fluoromethyl) benzeneamlne
1
2
3
4
5
6
u
WD
AN
AJ
AL
AJ
71
72
73
73
74
II
63/2
10/3
21
56/2
22/1
364
176
457
82
2
1.2
2
2
3
2
bdf
X
u
a
X
a
CH3CH2-MCH2)3CH3
0500 BENOMYL (Benlate)
Mel. Wt. 290
UM Funglc.
LDw 10,000+
Purity 99+ %
^.H-.N-O,
l» IB t a
R«f.
Methyl 1 -{butyl carbamoyl)-
benz1m1dazo1-2-ylcarbamate
A B C D E F
1
2
3
4
5
6
AJ
AL
AJ
AO
AJ
WD
69
71
72
73
73
74
17/2
54/6
20
21/3
21/2
101
267
1399
1230
368
171
33
1214
12J4
12
16
16
11]4
a,J
e.h
e
a,u
Jin,
no
e
9 V
C-N (CH2)3CH3
0520 BENSULIDE (Prefer) C,.H,.NO,PS,
- 14 u * 3
Mel.WI. 397.5
"«• Herblc.
I Du 770
Purity 99 % *•'•
0,0-D11sopropyl phosphorodl-
thloate S-ester with N-(2-
mercaptoethyl) benzenesul-
fonamlde
1
2
3
4
s
6
C
AC
AL
AL
67
75
75
II
5
58
58
483
1015
1020
J.4
11
2,11
9
afg
e
d
0 H
0-I-N(CH2)2S-f LOCH(CH3)J2
0425
BENTAZON (Basagran)
3-Isopropyl-lH-benzo-2,l ,3-
th1ad1az1n-4-one-2,2-d1ox1de
Mel. Wt. 240
UM Herblc.
LDso 1.100
Purity 99+ %
R*'.
AB
1
2
3
4
5
6
1Q
WD
73
76/1
272
1,4
11
igtu
X
0577
BENZADOX (Topdde)
CgHgN04
Benzamldo-oxyacetlc acid
Mel. Wt. 195
UM Herblc.
ID jo 5,600
Purity 99+ X
Rtfi
A B
1
2
3
4
S
6
C
32
II
3
3,11
af
f
\ II I I
V-C-N-0-CH,-C-
12
-------
Code Common Name Emp. Form.
Chemical Name
Structure
0578 BENZOYLPROP ETHYL C,RH17C1?NO, Ethyl N-benzoyl-N-(3,4-dichloro=
(Suffix) phenyl )-2-aminopropionate
Mol.Wt. 366 \ — ^ 9 /==
ABC 0 E F rj/ V_M rJ \
Uie Herbic.
IDso 1,555
Purity 99+ % Ref.
1
2
3
4
5
6
7U
WD
76
129
309
2
2
cu
u
\ / ^ ^
H3C— C-C-O-C2H5
H A
0580 BENZYL BENZOATE C,,H,,0, Benzole acid.benzyl ester
~" ' 1 4 1 L. L.
M.I.W1. 212 H2C-O-CO
U 'cable A B C D E F JL JL
lD,o 1,700
Purity 99+ % ,,„,
1
2
3
4
5
6
r^* ^i f^ ^i
1 HI y
^x^^
0620 BHC, ALPHA ISOMER C,H,C1, Hexachlorocyclohexane,
b b b alpha isomer
*
i
Mol.Wt. 291 * /r*
Use Compon. of
tech. BHC
L DSO 500
Purity 98+ % Ref.
1
2
3
4
5
6
A
A
B
A
WD
AL
B
77
77
67
68
C
10A
24,100-
105
5A.8B,
10A.11
27
51
D
250
45
E
2
12
2
2
2
F
t
de
jl
tuv
u
i
,v/
*"/ — ^ /
./ ^ . *ci
•f- — ' 1
r *' i
0640 BKC, BETA ISOMER C,H,C1,- Hexachlorocyclohexane,
~^^ 6 6 6 beta isomer
Mol. Wt. 291 //•--*
•• Compon. of
tech. BHC
L DM 6>°°°
Purity 99+ % »ef.
ABCDEF , ?//
1
2
3
4
5
6
See
0620
/ ' *
•L1 - Cl
r^i
0680 BHC, GAMMA ISOMER ZM^p, Hexachlorocyclohexane,
(Lindane) o c o gamma isomer
*
Mol.Wt. 291 1
ABCDEF , /t '*
U«e Insectic.
I Dso 125
Purity 99+ % Ref.
]
1
3
4
5
6
See
0620
1 -r K /
/ I /
/ / *CI
* / ' / -
V-^.'
I ' *
' *
13
-------
Code Common Name Emp. Form.
Chemical Name
Structure
0660
0733
0740
0791
BHC, DELTA ISOMER C,H<-C1, Hexachlorocyclohexane,
6 b b delta isomer
Mel. Wt. 291 [_
.. Compon. of
tech. BHC
I DIO 1 ,000
Purity 95+ % R.f.
A B C D E F
I
2
3
4
5
6
See
0620
..... Kf -
/ /
/ /
' *
BIFENOX (Modown) C,.H9C12N05 Methyl 5-(2,4-dichloro=
phenoxy) -2-ni trobenzoate
Mel.Wt. 342 ?
A B C D E F H3C-O-C Cl
Uie Herblc.
LDW 6,400+
Purity 99+ % Ref.
1
2
3
4
5
6
5M
6
eg
>~^\ /\
°2N \ / ° \ /Cl
BIPHENYL (Dlphenyl) C12H1Q Do
Mel.Wt. 154
A B C 0 E F f, \ f, \
Us* Funglc.
IDjo 3,280
Purity — % R.f.
1
2
3
4
5
6
AL
AL
C
AL
AL
57
67
75
75
40
50
II
58
58
249
934
1013
1015
12
11,12
12
12,16
2,11
e
X
e
e
e
v v-v N)
BPMC (Osbac) C,,H17N,0 2-sec-Butylphenyl N-methyl
>c " f carbamate
O
Mel.Wl. 207 O— C— NH-CH
ABC D E F V 3
U" Insecftc.
I Dso 623
Purity 99.5 % Ref.
1
2
3
4
5
6
AP
2
c
^x'^^xCH C2H6
CH3
^/^
BROHACIL (Hyvar) C0rL,BrN,0» 5-Bromo-3-eea-butyl-6-
3 l;> ' ^ methyl uradl
H
Mel.Wt. 261 1
* B C D E F H,C. ^N\ .0
Use Herblc.
LDM 5,200
Purity 99+ % Ref.
1
2
3
A
AJ
AJ
AC
A 1
66
67
67
CO
14
15
5
1C
94
174
335
Cyl
6
2
20
C
a
a,u
n4i
f
S. ^»LJ
14
-------
Code Common Name Emp. Form.
Chemical Name
Structure
0822 4-BROMO-2.5- C,H,BrCl,,0 Do
DICHLOROPHENOL
OH
Mol.Wt. 242 1
A B C D E F ^^\ ^Cl
Die Deriv. of Leptofos
IDso
Purity 100 X R«».
1
2
3
4
5
6
!j
4, J
G^^>/
i
Br
0832 BROMOFENOXIM 3,5-D1bromo-4-hydroxyben=
(Faneron) zaldehyde 0-(2,4-dinitrO=
phenyl) oxime
D,
Mol. Wl. 461
UM Herbic.
LD5o 1,217
Purity 99.5 X R,f
A B C D E F
1
2
3
4
5
6
AL
AB
73
75
56
47
387
2450
18
5
X
c
"k
HO-/ VcHTN-O-/ \-N02
\ - / \ /
Br NO2
0840 BROMOPHOS (Nexion) CnHHBrCl ,,0,PS 0-(4-Bromo-2,5-dichlorophenyl )
° B ' J 0,0-dimethyl phosphorothioate
c CL
Mol.Wt. 366 S > .
Utt Insectic.
ID jo 3,750-7,700
Purity 99 X R.f.
1
2
3
4
5
6
AJ
ZD
66
72
14
41
609
65
12
11,
12
17
m,u
d.j
u
(CH30)2P-0< >Br
V— /
Cl
0860 BROMOPHOS ETHYL C.nH., BrC1.0.PS 0-(4-Bromo-2,5-dichlorophenyl )=•
(Nexagan) ' 0,0-dlethyl phosphorothioate
c Cl
Mol.Wt. 394 5 K- \
, ., . ABC D E F , v I _ // \
UM Insectic. &
Acarlc.
LDM 52-170
Purity 99+ % R.f.
1
2
3
4
5
6
ZD
72
41
65
11,
]?'
d,
,u
u~2ry~"2r u~\ >-Br
Cl
0872 BROMOPROPYLATE C,,H,,Br,0, Isopropyl 4,4'-d1bromobenzilate
~^ (Acarol) 17 '* Z 3
, OH f/ .
Mol.Wt. 428 // \ | ff \
UM Acarlc.
L Dso 500
Purity 98.5 % R
-------
Code Common Name Emp. Form.
Chemical Name
Structure
0820 BROMOXYNIL C7H,Br2NO 3,5-Dibromo-4-hydroxybenzonitrile
(Brominal )
Mol.Wt. 277
Die Herbic.
L DSO 190
Purity 99 % Ref.
0960 BUFENCARB (Bux) C,
Mel. Wt. 205
U«e Insectic.
LD50 170
Purity 97.5-99 X Ref.
A B C D E F
1
2
3
4
5
6
AC
WD
67
71
5
57
347
20
11
—
tu
OH
^ /
CN
,H,QNO- Mixture of m- (1 -ethyl propyl )=
J phenyl methylcarbamate and m-
( 1 -methyl butyl ) phenyl methyl =
carbamate (ratio of 1:3)
A B C D E F
1
2
3
4
5
A
C
II
11,
17
c
/^OCONHCHj .x^OCONHCHj
LJ ** v
H3C-C-(CH2)2CH3 H-C(CH2CHji
H
0916 BUNEMA C,H,KNOS, Potassium N-hydroxymethyl-
3 6 ' N-methyldithiocarbamate
Mel. Wt. 175
„ Fungic., Bacteric,
"*• Nematoc.
I D50 1 ,032
Purity 40* X Ref
A B C D E F
1
2
3
AC
64
3
69
12
ade
h
II
K-S-C-N-CH2OH
CH3
*Formulation
0922
BUTACHLOR (Machete) C,7H,,C1NO, N-(Butoxymethyl )-2-chloro
17 ib i 2' ,6'-diethylacetanilide
C2H5
Mel.Wt. 312
Uie Herbic.
LDjo 3,300
Purity 99.5+ X Ref.
A B C Off
1
2
3
4
5
A
5Q
3
c
^\ / 2 4H'
^=\ rocH2ci
0926 BUTHIDAZOLE (Ravage) C,0H,6N.02S l-(5-Butyl-l ,3,4-thiadazol-2-yl )-
3-methyl-5-hydroxy-2-imidazolidinone
Mel.Wt. 256
Use Herbic.
LDso 1 ,581
Purity 100 X R.f.
A B C 0 E F
1
2
3
4
S
A
9A
V
16
4
OH
, /^ S~ N N — CH3
O
16
-------
Code Common Name Emp. Form.
Chemical Name
Structure
0933 BUTRALIN (Amex. 220) C14H91N,04 4-(l ,l-01methylethyl )-N-(l-
methyl propyl)-2,6-
-------
Code Common Name Emp. Form.
Chemical Name
Structure
1020
CAPTAN
Mol.Wl. 301
U» Fungic.
LDjo 9,000
Purity 98.5-99 %
C0HoCl,NO.,S N-(TrichlorometnyUhio)-3a,4,7,7a-
* B J i tetrahydrophthalimide
R,f.
1
2
3
4
5
A
ft
AJ
AL
AD
AL
77
67
68
69
70
II
10A
15
5/15
4
53
1035
1058
55
154
12 'ajlc
2
2
2,11
11
2
t
X
X
a
a
N-S-CCI,
1060 CARBARYL (Sevin)
Mol.Wl. 201
U» Insectic.
L DIO 560
Purily 99.5+%
1-Naphthyl N-methylcarbamate
R.f.
A B
1
1
3
4
5
6
C
A
AL
AJ
AL
AL
77
68
69
74
74
II
IDA
51
17 .
57
57
679
56
570
592
12
2
11
2
3
12
a
t
X
a
a,d
c,w
O H
Q-C-N-CH3
1071
CARBENDAZIM (Derosal) CqH,Ji,0.,
* * J '
Mol.Wl. 191
Uu Fungic.
LDso 15,000+
Purily 99+ %
*•*•
AB
*Methyl-2-benz1mida=
zole carbamate
1
2
3
4
5
A
BE
BE
74
76
5/4
7
465
193
20
12
--
e
I
H
*This is also a derivative compound
from benomyl (0500)
1074 CARBETAMIDE (Legurame) C12H16N2°3 D-N- Ethyl acetamide carbanilate
M.I. Wt. 236
U,e Herbic.
I0j0 11,000
Purily
99
R,f.
1
2
3
4
5
A
AC
71
73
7
509
12
2
ijou
ac
O HO
II I II
I-C-O-C-C-N-
I CH3 H
1040 CARBOFURAN (Furadan)
Mol.Wl. 221
Ute Insectic.
ID90 8-14
Purity 99.5+ * R»f.
C19H1I;NO,
'5
2,3-Dihydro-2,2-dimethylbenzo=
furan-7-yl methyl carbamate
1
2
3
4
5
A
C
A
AJ
AJ
AL
AJ
77
69
69
71
75
II
10A
17
17
54/6
23/2
56
277
1357
315
6,11
2
2
6
2
2
cfu
t
a
c
au
j
O-C-N-CH3
n i J
O H
18
-------
Code Common Name Emp. Form. Chemical Name
Structure
1041 3-HYDROXYCARBOFURAN C12H15N04 2,3-Dihydro-2,2-dimethyl-3-hydroxy-7-
benzofuranyl N-methylcarbamate
Mol.Wl. 237 ^
A B C D E F L
Use Carbofuran derivat.
Purity 99 % Ref.
2
3
4
5
6
OH
vir^0? 2,3-Ditiydro-2,2-dimethyl-7-hydroxy=
lu " benzofuran
Mol. Wt. 164 ^
ABC DEF Lv
Use Carbofuran derivat.
L Dso —
Purity 99.4 % jj,f.
1
2
3
4
5
6
T
Or
1080 CARBOPHENOTHION C^H^O-dPS,, S-[(p-Chlorophenylthio)methyl]
(Trithion) 0,0-diethyl phosphorodithioate
T-N CH3
II XCH
Ql ^n3
M,i.wi.343 S-CH2-S-P(OC2H<),
A B C DEF ^^
Use Insectic.
IDjo 10-30
Purity 98. 5-99 % Ref.
1
2
3
4
5
6
C
M
U
HL
\
67
74
74
77
II
50
57
57
10A
430
930
1034
17
2
3,4
4
4
a
a,e
a,d
t
t
\ 1
l
-------
Code Common flame Emp. Form.
Chemical Name
Structure
1100 CARBOXIN (Vltavax) C^H.-.NOjS 5,6-D1hydro-2-methyl-l ,4-
IJ oxath11n-3-carboxan1!1de
-O-w r*"u
Mel.Wt. 235 flf 3
U* Funa- A B C D E F | || ^~\
UfV ruiiy . \. .
LD50 3,200-3,820
Purity 98-99 % R,f.
1
2
3
4
6
AJ
AJ
70
71
18
19
409
738
12
6
a
c
\c-^C-N-\ >
&H \=/
1140 CDAA (Randox) CgH12ClNO 2-Chloro-N,N-d1allylacetam1de
Mel.Wt. 174
UM Herblc.
10 jo 700
Purity 99.5+ X Ref
ABC D E F
1
2
3
4
6
C
5Q
II
6
6
acd
acd
CI-CH2CN(CH2CH-CH2)2
U60 CDEC (Sulfallste) C8H14C1NS2 2-Chorosllyl d1ethyld1th1ocarbamate
Mel.Wt. 224
UM Herblc.
LDM 850
Purity 99.5+ % Ref.
A B C D E P
1
2
3
4
5
6
C
5Q
II
2,6
12
d
af
S Gl
(C2HS)2N-C-S-CH2C-CH2
QUO CHLORAMBEN (Amlben) C7H5C12N02 3-Am1no-2,5-d1chlorobenzo1c acid
Cl
Mel.Wt. 206 \
A B C DIP /===\
UM Herblc
LDw 3,500
Purity 97-97.5% Ref.
1
2
3
4
5
6
C
AC
67
II
5
321
b, 1
12
20
d
...
\\ //— COOH
v__y
NH2 Cl
1180 CHLORANIL (Spergon) CjCl^Oj 2,3,5,6-Tetrachloro-l ,4-benzoqulnone
Mel.Wt, 246 V
A B C D E F *..X\v
Ui« Fungi c 4
I DM 4.000
Purity 95 % Ref.
1
2
3
AJ
AL
AN
58
69
70
6
41/12
8/3
667
1662
166
12
12
2,3
c
c
X
X >*
w ^s^ _s^ *
JC *CI
-------
Code Common Name Emp. Form.
Chemical Name
Structure
1188
_1200
J220
1240
1280
CHLORBROMURON (Maloran) CaH, nBrCl N,0, 3-(4-Bromo-3-chlorophenyl )-
y ]v ' c 1-methoxy-l -methyl urea
Mol.Wt. 294
Use Herbic.
LD50 2,150
Purity 99.5 X Ref.
/ \
ABC D E F Rr-/ \-KIU ^_ K,--OCH:
1
2
3
4
5
6
GE
AL
AL
71
76
76
256
59
59
194
1066
1061
21
12
8
X
a
a
„ „.,.,. ,,^
\\ ft J
Cl
CHLORDANE (TECH.) C1QHSC1R 1 ,2,4, 5,6,7,8, 8-Octachloro-2,3,3a,4
7,7a-hexahydro-4,7-methanoindene
Mol.WI. 410 J.
* *r r*v
ABC D E F ^ \, f*
Use Insectic.
L Dso 457
Purity 100* * R,f.
*Active Ingredients
1
2
3
4
5
6
C
AK
AL
AD
AD
AL
67
69
69
72
75
II
59
52
4
7
58
752
1220
297
33
1015
2,12
2
2
2
2
2,11
a
t
b,c
j
X
e
J *-c-
* i^c.
CHLORDANE, ALPHA CinHKClR l-eao,2-ai:o,4,5,6,7,8,8-
(cis-chlordane) Octachloro-2,3,3a,4,7,7a-
hexahydro-4,7-methanoindene
*\s'
Mol.WI. 410 A
U,« Compon. of
tech. chlordane
ID» ca 500
Purity 100 % R,f,
A B C D E F
1
2
3
4
5
6
See
1200
* ^^f~-
V
CHLORDANE, GAMMA ClnH,Cl., l-ezo,2-e«do,4,5,6,7,8.8-
(trans-chlordane) B Octachloro-2,3,3a,4,7,7a-
hexahydro-4,7-methanoindene
Mel.Wt. 410 A *
Compon of A B C D E F \ /-<^
tech. chlordane
ll>30 ca 500
Purity 99.5 % „.,
1
2
3
4
5
6
See
1200
// J^ /vsx*
*-^^~~~\ ] *Q
*
CHLORDECONE (Kepone) C,nCl,nO* Decachloro-octahydro-1 ,3,4-
lu lu metheno-2H-cyclobuta[cd]=
pentalen-2-one
Mol.WI. 491* _*O
Use Insectic.
I DSO 132
Purity 86-87 % Ref.
*Bas1s anhydrous state
A B C D E F
'
2
3
4
S
AJ
AD
AJ
ZM
2
70
72
74
77
77
18/1
7/4
22/3
6-2/3
• c nf&l
159
207
442
221
5
3
2
1
a,e
X
X
ktu
nt
\ /
X.
/>. ^^^s,^.
^ ^-Mfl
-------
Code Common Name Emp. Form.
Chemical Name
Structure
1260 CHLORDENE ClnH,Cl, 4,5,6,7,8,8-Hexachloro-3a,
1U b b 4,7,7a-tetrahydro-4,7-
methanoindene
Mol.Wt. 339
U,e Compon. of
tech. chlordane
1 DSO 500+
Purity 99+ X Ref-
1261 CHLORDENE, ALPHA C-,
Mol.Wt. 339
Compon. of tech.
U» chlordane
*-D5o 10,200
Purity 96.5-97 * Hot.
A B C DEF '"Y'l^i ,
1
2
3
4
5
6
See
1200
-C-.
•N^^^-o
-H,C1, l,2,3,5,7,8-Hexachloro-l,3a,4,
066 5^6,6a-hexahydro-l,4-etheno-
pentalene /f- —
A B C DEF
1
2
3
4
5
6
See
1200
,>< :^
• Compon. of tech.
chlordane
LDso 4,600
Purity 99+ X Rot.
A B C DEF
1
2
3
4
5
6
See
1200
>i^-
•^-f"
\ > *CI
* *
1480 CHLORDIMEFORM CTnfin-ClN, N'-(4-Chloro-o-tolyl )-N,
(Chlorphenam1d1ne) N-dlmethylformamldlne
Mol.Wt. 196.5
Uio Acarlc.
IDso 178
Purity 99.5+ % Rol.
A B C DEF
1
2
3
;
AJ
AJ
71
72
II
19
20
360
565
2,11
1012
12
e
e
e
N=CH-N(,CH3)2
k^^J
n
22
-------
Code Common Name Emp. Form.
Chemical Name
Structure
1300 CHLORFENVINPHOS C^rL.Cl 0,1? 2-Chloro-l-(2,4-dichlorophenyl )
(Supona) vinyl dieth/1 phosphate
0
Mel.Wt. 359.5
UM Insectic.
1 DSO '2-30
Purity 98+ % R.I.
A B C D E F
1
2
3
4
5
6
ZL
PD
WD
PA
GE
PB
72
74
74
74
75
75
14
25
93
7
274
25
119
695
457
43
371
395
4
17
9
10
10
9
m
1
d
ajv
j
de
, 9 0-«OC2H5)2
C'\ / ^V-n
\=y i
1 1
1316 CHLORMEPHOS (MC2188) Cj-H.-ClPS,, S-Chloromethyl-0,0-diethyl
phosphorodithioate
Mel. Wt. 203 5 H
A B C D E F || 1
Use Insectic.
LD«, 7
Purity 98-99* »•'•
1
2
3
4
5
6
(c2H5o;2 p— s— c-ci
f!,
1360 CHLOROBENZILATE C16H14C12°3 Ethyl 4'4'd;ichlorot)enz1late
(Acaraben)
OH
Mel. Wl. 325 f. \ f, \
ABC D E F -. // \ - fl \ -.
UM Mitic.
L 0,0 700
Purity 99.5+ % R«(.
1
1
3
4
5
6
C
AJ
ZD
64
71
II
12
39
183
40
6,12
6
6
e g
e g
X
\ / \ /
\ — / \ — /
COOC2H5
1380 CHLORONEB (Demosan) CgHgCl202 1 ,4-Dichloro-2,5-diaiethoxybenzene
Cl
Mel.Wt. 207 ^
UM Fungic.
I DSO 11,000+
Purity 99+ % R.I.
A B C D E F
1
2
3
4
5
6
C
AJ
AJ
67
71
II
15
19
917
750
6
6
3
ajgo
ajm
jmo
I T
J. M
Cl
Ji25_ CHLOROPHACINONE (Rozol) C23H15C10, 2-[(p-Chlorophenyl )phenyl=
acetyl]-l,3-1ndandione
M.I.WI. 375 J~\-C\
„„ r^r ,, A B C D 1 F V 0 /\ AU
US* KOQentlCi
ID j,, 20.5
Purity 100 % R.I.
1
2
3
AJ
2E
75
23/1
72
2
2
a j
x °
ML_TC"C\ /-^
o \— /
23
-------
Code Common Name Emp. Form. Chemical Name Structure
1640 CHLOROTHALONIL C8C14N2 2,4,5,6-Tetrachloroisophthaiorntrile
(Daconil)
CN
Mol.Wt. 266 > (
Ute Fungic.
LDso 10,000+
Purity 99.5+ % Ref.
A B C D E F
1
2
3
4
5
6
C
AD
GE
GE
70
70
73
II
5/6
250/2
265/1
565
125
4
2,6
14
11
10
f
X
a,j
V
" vv CN -c,
* *
147(1 CHLORPROPHAM (CIPC) C, nH,,, Cl NO, Isopropyl N-(3-chloro=
phenyl)carbamate
Moi.wt. 214 H-N-C-O-CHtohi^
A B C D E F ^A^
U«e Herbic.
IDso 5,000-7,500
Purity 99.5+% Ref.
1
2
3
4
5
6
C
AJ
AJ
AJ
AJ
63
64
72
76
II
11
12
20
24
234
46
344
1236
2,12
12
2
12
1
a
m,o
X
b
c
f n
2900 CHLORPYRIFOS (Dursban) C0H,,C1,NO,PS 0,0-Diethyl 0-(3,5,6-trichloro-
a M J j 2-pyridyl) phosphorothioate
Mol. Wt. 351
U»e Insectic.
LDM 135
Purity 99+ % Ref.
A B C D E F
1
2
3
4
5
6
AJ
AL
AJ
AJ
AJ
AJ
68
68
69
70
76
78
16
51
17
18
24
26
867
1243
1166
178
283
(In
iress
2
2
2
3,4
4
4,5
22
tu
jo
j
,jkt
j
j
C'OCI
I 5 2
s
2901 CHLORPYRIFOS CQHlnCl,NO,,P 0,0-Diethyl 3,5,6-trichloro-2-
OXYGEN ANALOG pyridyl phosphate
Mol. Wl. 335 CIY^ ^^Y'CI
A B C D E F !| 1
U» Deriv. of chlorpy=
rifos
ID,, 135
Purity — % Ref.
2
3
4
5
6
See
2900
II 1
II
0
2902 CHLORPYRIFOS METHYL C,H7CUNO,PS 0,0-Dimethyl 0-(3,5,6-trichloro-
(Reldan) 1133 2-pyridyl) phosphorothioate
Mol.WI. 323 Cly^^O
, .. ^, ' A B C D E F | 1
U$t insscti c •
LD,o 2140
Purity 99+ % R.f.
1
2
3
4
5
6
Kj O ""P\ OC Hg / 2
i
s
24
-------
Code Common Name Emp. Form.
Chemical Name
Structure
;
( CMS 2957)
C11H15C12°3PS2 0.0-Dlethyl 0-2.5-d1chlcro-4-
" 16 i 3 z methyl thlophenyf phosphoroth
phosphorothloate
Mol.Wt. 329
Ui* InsecUc.
10 jo 8-?3
Purity 79 X R.f.
1512 CHLORTOLURON (Dlcuran) C1
Mol.Wt. 213
U» Herblc.
ID jo 10,000
Purity 99.5+ % R,f.
A B C D E F
1
2
3
4
5
6
AX
71
4
271
10,
12
X
-H, ,C1 N,0 N ' - ( 3-Chl oro-4-methyl phenyl )
u IJ e N,N-d1methylurea
A B C D E F
1
2
3
4
5
6
BH
WD
AL
ZM
71
75
76
76
11
107
59
4
111
407
716
101
12
>
19
u
u
X
X
IB" CISANILIDE (Rowtate) C,,H,-N.O c1s-2,6-D1inethyl-l-
13 '8 ' pyrrol Idlne carboxanlUde
Mel. Wt. 218
Ote Herblc.
I0«o 4,100
Purity 99+ X R.(.
A B C DIP
1
2
3
4
5
6
ZU
2
be
0460 CLONITRALID C15H15C12N3°5 Z' .5-D1chloro-4'-n1tro-
— ~- (Baylusdde) sal1cylanH1de ethanolamlne
Mol. Wt. 388
Uie Mollusdc. ^ *
LDM 1,500 *°
Purity — X ••*•
^* A B C DIP
1
2
3
4
3
6
EA
AL
AI
70
72
73
13/3
55/6
3/1
369
1276
61
15
12
11.
14
X
t
X
3720 COUMAFURVL (Fumarln) C,7HU0S 3-« (Acetonylfur-
furyl )-4-hydroxycoumar1n
Mel.Wt. 298
U«» Rodentlc.
L 0K 400
Purity 99+ X R«f.
A B C D E F
1
2
3
4
5
s /
(C2H5Q)2-P-0~/~VsCH3
\ °
NXNHC-N(CH3)2
O-C
-------
Code Common Name Emp. Form.
Chemical Name
Structure-
1540 COUMAPHOS (Co-Ral) CUH16C105PS 0,0-Diethyl 0-(3-chloro-4-
it 10 j methyl -7-coumari nyl)phos=
phorothioate
c ,X\>XXjO
Mol.Wt. 363 5 0-C-C=C-0-P(CH30),
i n J 2
H 0
6020 CRUFOMATE (Ruelene) C,7H,<,C1NO,P H-tert -Butyl -2-chlorophenyl-
~~^ methyl phosphorami date
C(CH3)3
Mol.Wt. 292 /-W
A B C D E F f ^1
Use Insectic.
LDjo 770
Purity 99 % Ref.
1
2
3
4
5
6
AD
AL
72
74
7
57
237
1033
10
4
1
t
0
O-P-OCH3
1
NHCH3
1546 CRYOLITE (Kryocide) NaAlFg Sodium Fluoaluminate
Mol.Wt. 210 Na3AIF6
ABCDEF JO
Use Insectic.
I Dso 10,000+
Purity 98-99 % Ref.
1552 CYANAZINE (Bladex) C
•
1
2
3
4
5
6
B
11
6.019
79
18
w
H.-CIN, 2-[(4-Chloro-6-(ethylamino)-s
13 ° triazin-2-yl)amino]-2-methyl=
propionitrile H C=-N
1 i
Mol.Wt. 240 N— C(CH3)2
A B C DEF N (
Use Herbic.
L Djo 334
Purity 99 % Ref.
1
2
3
4
AD
BE
AJ
AJ
70
72
73
73
5/1
3/4
21/6
21/6
6
379
1091
1016
3
2
2
1
a
a u
atu
u
a// ^
\ /
N-CH3CH2
H
26
-------
Code Common Name Emp. Form.
Chemical Name
Structure
6360 CYANOFENPHOS (Sureclde) C.-H.-NO^PS 0-(p-Cyanophenyl )0-ethyl=
phenyl phosphonothi oate
o
Mol. Wt. 303
Die Insectic.
L D50 1 ,000
Purity 99.5+ X Ref.
A B C D E F
1
2
3
4
5
6
8A
4,9
ac
fg
C,H,O-P O
0^^
kvj
CN
1591 CYCLOATE (Ro-Neet) C,,H,,,NOS S-Ethyl ethylcyclo=
hexyl thlocarbamate
Mel. Wt. 215
U$e Herbic.
LD50 2,595
Purity 99+ S Ref
1600 CYCLOHEXIHIDE C,,
(Actldione) n
Mol.Wt. 281
Use Funglc.
LDjo 2-5
Purity 99.5+ % Rtf
1606 CYCLOPRATE (Zardex) C20
Mol.Wt. 311
U,e Acarlc.
lD,o 12.2°°
Purity 88 % „„,
1611 CYPERQUAT C^
Mol.Wt. 190
U
-------
Code Common Name Emp. Form.
Chemical Name
Structure
IKT: CYPRAZINE (Outfox) CQH,.ClHc 2-Chloro-4-(cyclopropylam1no)-
s IH 6-(1sopropylam1no)-i,3,B-tr1i2lne
Cl
Mol. Wt. 228 I
A B C D E F ^^
Uu Herblc.
10,0 1-200
Purity 99+% «•'•
1621 CYTHIOATE (Proban) CgH,
1
2
3
4
s
6
3Z
AJ
73
21/1
93
2
,2
a u
ctu
N N
CH32C-N N N <]
H H H
.NCVPS, 0,0-Dlmethyl 0-p-sulfamoyl-
phenyl phosphorothloate
s o
Mol.Wt. 297 II /==\ II
UM Insectlc.
IDM 2,500+
Purity 98 % R««.
*«C D E F (CH,OL P 0— d ,V-S NH,
1
2
3
4
5
6
AL
WD
WD
WO
69
70
71
71
52/2
48/3
59/1
60/2
286
478
135
213
16
11
11,14
11 ,U
X
X
X
t
* » • • O -"^ t £ " 'W ML It •— • ' - ' -f
O
1660 DALAPON (Dowpon) C^CljOj 2,2-D1chloroprop1on1c add
M.I.WI. us CH3CCI2COOH
H LI A » C D E F
UM Herblc.
I0,o 7-000
Purity 99 % R.f
1681 DAMINOZIDE (Alar) CgH
1
2
3
4
S
6
C
AL
A*
Af
A
11
63 46
63 55
69 3
. 69 52
269
639
69
824.
11
10
12
10
2
d e
e
t
t
aim
0
loNoO, Butaned1o1c add mono
(2,2-d1irethylhydraz1de)
O
Mol.Wt. 160
Uw Grth. Reg.
LDjo 8,400
Purity 99 % R.f.
A B C D E F
1
2
3
4
5
6
BE
71
2
176
12
a
CH2-C-NH-N (CH3)2
CH2-C-OH
o
J22D_ DCPA (Dacthal) C.-H-Cl-O,, Dimethyl 2.3,5,6-tetra-
chloroterephthalate
C02CH3
Mol.Wt. 332 ^^.
A B C 0 E F *>^ ^*
Ut« Heroic.
LDjo 3,000
Purity 99.5+ % R.I.
I
2
3
C
AY
AL
69
71
I!
5
54/6
345
1376
6,12
2
2,6
dg
f u
V
AS^* .
COCH Cl
28
-------
Code Common Name Emp. Form. Chemical Name
Structure
1740 DDA-D.c' C,,
Mol.Wt. 281
Use DDT metabol .
I D50 1 .900
Purity 98 % Re,
1750 ODD, MIXED, TECH. C,,,
(TOE, Rhothane)
Mol.Wt. 320
Use Insectic.
1 DJO 3,400
Purity 97 % Kef.
1820 DDD-m.o' C^H
Mol. Wt. 320
Ute DDT deHvat.
L DJO 3,400
Purity 98 X R»f.
1760 DDD-o.p' C14
Mol. Wt. 320
Ui« DDT derlvat.
I °30 ca 3,400
Purity 99+ % R.f.
1780 DDD-R.P' c,
H.-Cl-O,, Bis(p-chlorophen.yl /acetic acid
A B C D I f
2
3
4
5
6
A
77
5, A,
2
IT
^c-c^'
HlnCl. 2,2-Bi's(cblorophenyl)-l ,l-dichloro=
lu ethane and related compounds
A B C D E F
1
2
3
4
5
6
C
A
A
A
ZK
77
77
77
76
I
5, A
10, A
8,B
11, A
12
275
2,6
12
2
2,4
2,4
2,4
2
a
jllPO
t
V
u
k
See structures below for
1760 and 1780
,nCl. l-(m-Chlorophenyl)-l-(p-chloro=
phenyl)-2,2-dichloroethane
A B C D E F
1
2
3
4
5
6
See
17SO
Cl
H-CCI2
J,nCl. l-(o-Chlorophenyl}-l-(p-chloro=
lu phenyl)-2,2-d1chloroethane
A B C D E F
1
2
3
4
i
6
See
1750
CHCl)
!|H10C14 ',2-B1s(p-chlorophenyl)-l,
l-d1chloroethane
Mol.Wl. 320 ff~- ^ H f. 1,
U>* DDT derivative
LOso 2,500 - 3,400
Purity 99+ X R,f.
1
2
3
4
5
6
A B
C D E F
See
17EO
C~
-------
Code Common Name Emp. Form. Chemical Name
1840
Structure
IRfiri
iasn
lonn
1920
DDE-o_,£' C-.HgCl. l-(o-fhlorophenyl)-l-(p-chloro-
phenyl )-2,2-d1chlorcethylene
Mel.Wt. 318
Ut* DDT derivative
LDsQ 880
Purily 99+ X R,f.
DDE -£,£.' C]4
Mel.Wt. 318
U»e DDT derivative
I D50 750
Purity 99 % R.,
DDT, MIXED (TECH.) CH
Mel.Wt. 354.5
U«e Insectlc.
ID*, 113
Purity — X »•*•
DDT-o,£' C^
Mel.Wt. 354.5
Ui« DDT component
L DJO 100
Purity 99+ X Ref.
DDT-2..E.' C14
Mel.WI. 354.5
Die DDT component
LDso 113
Purity 99+ X R,f.
A B C D E F
1
2
3
4
5
6
See
1750
V
~ fei^
HRC1. 2,2-B1s-(p-chlorophenyl)-
1 ,1-dichloroethylene
A B C D E F
1
2
3
4
5
6
See
1750
ici2
H0C1 - Di chl orodiphenyl tri chl oroethane
y (mixt. of metabolites of ca
80% p,p' and 20« o,p')
A B C D E F
1
2
3
4
5
6
See
1750
HQClc l-(o-Chlorophenyl)-l-(p-chloro=
phenyl)-2,2,2-tr1chloroethane
A B C D E F
1
2
3
4
5
6
See
1750
ei
HnClc l,l-B1s-(p-chlorophenyl)-
2,2,2-trlchloroethane
A B C D E F
1
2
3
4
5
6
See
1750
CCI3
30
-------
Code Common Name Emp. Form.
Chemical Name
Structure
loan
DEF
C12H27OPS3 S,S,S-THbutyl phosphorotHthioate
Mol.Wt. 314.5
U« Defoliant
I D$0 350
Purity 99+ %
R.f.
A B
1
2
3
4
5
6
C
AJ
WD
A.L
66
69
75
-
II
14/2
40/2
58
143
289
1015
9
2
4
2,11
9 o
9
X
e
(CH3CH2CH2CH2S)3P=O
1981 DEMETON-0 (Systox-0)
\THIONO)
Mol.Wt. 258
U» Insectlc.
IDM 7.5
Purity 96 % Ref.
0,0-Diethyl 0-2[(ethylthio)=
ethylIphosphorothloate
1
2
3
4
5
6
ZO
WD
JI
69
70
70
26
48/3
22
17
468
13
10
10
3,4
t
d
c d
e
(C2H5O)2P-O-C2H4-S-C2H5 (Thiono)
2006 DESMEDIPHAM (Betanex) C]e
Mol. Wt. 300
UM Herbic.
LD50 10,250+
Purity 97+ % R.f.
3-Ethoxy carbonyl amino=
phenyl phenylcarbamate
1
2
3
4
5
6
BH
7Q
6A
70
10/4
340
10,12
10
24'
a
af
af
O H
25
N— C— O— C2H
H O
?na5 DIALIFOP (Torak)
Mol.Wt. 393.5
U» Insectlc.
1050 69
Purity 99 %
CUH17C1NO,PS. 0,0-D1ethyl S-(2-chloro-l-
phthalim1(Joethyl)phosphorod1thioate
Ref.
1
2
3
4
5
6
4A
AJ
AJ
71
71
19
19
SCO
1191
2,9
2,9
3,1<
e
mno
e
CH2C, S
N—C—S—P(OC2H5)2
H
2040_ DIALLATE (Avacex)
Mol.Wt. 270
Ut« Herbic.
L Dro 395
Purity 99 X
R.f.
S-(2,3-D1chloroallyl)
d1 Isopropyl tMocarbanate
1
2
3
4
5
6
AJ
FB
BH
AL
AJ
by
69
70
71
76
17/5
62/686
1C/4
54/6
24
10E2
214
331
1366
1236
'i
10
2
4,9
1
u
t
u
a g
c
r °
L(CH3)2CHJ N-(i!-s-CH2-CCI=CHCI
-------
Code Common Name Emp. Form.
Chemical Name
Structure
2060 DIAPHENE (Brcirisalans) C,-Or-NO, 3,4,5-Tribromosalicylanilide,
1;> 9 ' i 4,5-dibromosalicylanilide
and other bromlnated salicylanilides
Mol.Wt. 371
Use Funglc.
LD50 40'2
Purity 98+ X Ref
A B
D E F
2080
D1AZINOK
(Spectracide)
Mol.Wt. 304
Uio Insectic.
IDM 100-150
Purity 88-89* %
*Stabilizer added
Ref.
0,0-Oiethyl 0-(2-isopropyl-f-methyl-
4-pyrimidiryl phosphorothioate
t
2
3
4
5
6
C
PD
BA
AL
AJ
AL
68
69
69
72
74
II
3
94/1H6
52
20
57
247
221
1067
624
1033
12
2
3
3
2,4
4
a
acj
tu
j
a
a j
t
2090
DIBROMOCHLOROPROPANE C.H-Br.Cl 1,2-DibrO!no-3-chloropropane and
(DBCP) related haloqenated C, hydrocarbons
Mol.Wt. 236
Uso Soil Fumigant
IDjo 172
Purity 99+ % Ref.
A B
1
2
3
4
5
6
AJ
AM
RB
7U
AJ
63
68
70
77
11/6
6
35
25
479
124
59
681
—
2
12
2
2
—
u
t
atu
f
CH2Br-CHBr~CH2CI
2120 DIBUTVL PHTHALATE
(DBP)
Mol. Wt. 278
U»o Insect Repel 1 ant
IDjo 20,000
D1-n-butyl phthalJte
Purity
99 %
Rof.
1
2
3
4
5
6
BA
GD
AJ
AD
AE
WD
67
72
73
74
77
92/1068
68/6
21/6
12/6
71-1172738
132
575
ISO
1128
721
--
277
2
1C
3
2
10
2
t
J
k
t
t
t
COOCH2(CH2)2CH3
?un DICAMBA (Banvel D)
Mol.Wt. 221
Uu Herbic.
IDjo 1,040
Purity 100 %
C8H6C12°3
R.f.
2-Methoxy-3,6-di=
chlorobenzoic add
1
2
3
4
5
6
AJ
AL
AJ
C
AL
64
65
71
75
22
48
19
II
58
453
1161
1181
1020
2
2
11
2
9
tu
a
a
be
de
OH Q
x£_pa
32
-------
Code Common Name Emp. Form.
Chemical Name
Structure
??nr, DICHLOBENIL (Casoron) C,K,
2,6-D1chlorobenzonl tr1 le
Mel.Wl. 172
U» Herblc.
LDW 3,160
Purity 99+ %
Kef.
t
2
3
4
5
6
C
AL
AD
WD
AJ
AO
66
67
74
76
76
II
19
2
97
24
5
976
178
103
1236
315
2
2
6
2
1
2
e
ekti
a
u
c
t
CN
gggo
DICHLOFENTHION
(VC-13)
Mol. Wt.
Un
315
Nematoc.
& Insectlc.
L DSO 270
Purity
97+
C,nH,,Cl,0,PS
IU IJ i J
Kef.
0,0-Dlethyl 0-(2,4-d1ch!oro-
phosphorothloate
A B C D t f
1
2
3
4
5
6
AJ
AL
59
64
7
47
615
287
17
12
X
a
>ian DICHLONE (Phygon XL) C]c
Mel.Wt. 227
Uie Funglc.
lDso 1,300
Purity 98 X R.f.
2,3-D1chloro-l,4-naphthoqu1nore
A B
1
2
3
4
J
6
B
AJ
AJ
58
69
24.181-
.184
17
746
585
12
2
d e
i
DICHLORAN (Botran)
Mel.Wt. 207
Uie Funglc.
LDjo 10,000
Purity 100 %
2,6-D1chloro-4-n1troan111ne
R.f.
1
2
3
4
5
6
C
AJ
76
II
24
1236-
>,12
1
a
c
??BO DICHLOROBENZENE.ORTHO Cfi
Mel.Wt. 147
Uie Herblc, 8
Insectlc.
L DM
Purity
500
98 x
aCl,
R.f.
1,2-D1chlorobenzene
A B
1
2
3
4
5
6
WD
WD
AH
AN
67
70
72
73
30/1
53/2
3
11/11
77
143
281
580
2
8
3
V.
3
X
X
k,t
t
33
-------
Code Common Name Emo. Form. Chemical Name Structure
2300 DICHLOROBENZENE, PAPA C,H.C1. 1 ,4-Dichlorobenzene
(PDB) 64 '
Mol.Wt. 147
Ute Funilgant
ID50 2-560
Purity 99-5+X «•'•
2306 DICHLOROPROPENE-ois CjH
Mol.Wt. in
Use Nematoc.
L D50 375
Purity 96-97 X Ref.
?307 DICHLOROPROPENE-frcnc CjH
Mol.Wt. Ill
Ut« Nematoc.
1 Dso 375
Purity 96-97 X Ref.
2306 DICHLOROSALICYLIC C?H
1
2
3
4
5
6
WD
WD
AD
AN
67
70
70
71
30/1
53/2
5/4
9/8
77
K3
35'
497
2
8
2
10
X
X
X
.C"U r-?v-l ,3-Dichloropropene
A B C DEF
1
2
3
4
5
6
AP
AJ
AJ
AF
AW
68
70
71
74
75
61/5
18/6
19/6
31/7
0^53
1432
1124
1270
3C34B
-
2
10
6
10
2
u
tu
f
u
f
Cl
^r
Cl
Cl H H
i i
H-C-C-C
H Cl
Cl trana-l,3-D1chloropropene
Cl H Cl
i i i
ABC DEF u /- r /-
1
2
3
4
5
6
See
2306
II >*- V- — \»,
1 1
H H
fC^Oi 3,6-Dichlorosalicylic acid
ft
Mol.Wt. 207 C-OH
U» Dlcamba derivat.
Purity 99.5 % Ref.
?3(1<) DICHLOPPROP (2,4-DP) CgH
Mol.Wt. 235
Use Herbic.
LDjo 800
Purity 99 % Ref.
A B C DEF
1
2
3
4
5
6
RC1?0, 2-(2,4-Dichlorophe=
noxyj-propionic acid
H°Y^^N^ci
^\^
ABC DEF Cl-/ \-0-r rnr^H
i
2
3
AP
AD
AJ
68
69
71
61/5
4/4
19/6
1132
2^6
1270
2
16
6
u
a c
f
\ // 1
V S H
Cl
34
-------
Code Common Name Emp. Form.
Chemical Name
Structure
2320 DICHLORVOS (DDVP) C^Cl^P 2,2-Dichlorvinyl dimethyl phosphate
o
Mol.Wt. 221 ]-
Uto Insectic.
I Oso 56-8(1
Purity 98 % Ret.
A B C D E F
1
2
3
4
5
6
C
BD
AL
AJ
BA
69
69
71
73
II
5
52
19
98
417
1248
1238
176
6
10
4
10
9
d
c
jop
j
jl
CI2C=CH-O-P(OCH3)2
?3in DICOFOL (Kelthane) C,.HQClcO l,l-Bis(p-chlorophenyl)-
14 9 5 2,2,2-trichloroethanol
Mol.Wt. 370.5 ^ ^ 9^/£ ^\
'ABC D E F n_// VAj/ \\ ,-.
Use Mi tic.
I D50 600
Purity 97-99% R«*.
1
2
3
4
5
6
C
AL
AC
AJ
AL
60
69
69
73
II
53
4
17
56/6
127
297
1070
1335
12
2
2
2,11
2,3
bde
0
k
h
X
\ / ' \ /
CCIj^7
0700 DICROTOPHOS (Bidrin) CRH1(-NO,.P 3-(Dimethoxyphosph1nyloxy)-N,
H "> 5 N-dimethylisocrotonamide
Mol.Wt. 237 9 H
U»« Insectic.
ID*, 22
Purity 95 % Ro».
ABC D E F (CH-nl-D-0 r- A ,- .,^..N
1
2
3
4
5
6
AJ
AC
AJ
AN
67
67
69
71
15
5
17
9
465
213
56
44
4
20
4
3
c
—
a
C 0
0 < ^ ^ *-* *-^ iNVv^riT/
1 II J
CH3 0
2380 DIELDRIN (HEOD) C,,HCC1,0 1 ,2,3,4,10,10-Hexachloro-^o-6,7-epoxy-
i<; B o l,4,4a,5,6,7,8,8a-octahydro-l,4-en&>-
ea-o-5 , 8-dimethanonaphthal ene
Cl Cl
Mol. Wt. 381 X
, A B C D E F n^---/^
UM 11156011 C.
I Djo 46
Purity 99.5+ % Ref
1
2
3
4
5
6
C
A
AP
AL
AL
AD
65
69
69
76
I
58
52
52
16
266
1220
1280
98
2
2
2
2
10
Olt
uv
0
b c
bof
u
// / / — ~7 — "7f
J!—-~r-——J ///'
\1 0
V
22BL. DIETHYL PHOSPHATE C.H^O.P 0,0-Diethyl phosphate
(DEP) tut
Mol.Wt. 154 O
U«« Deri vat.
1 Djo
Purity 98* S R.f.
*Questionable
A B C D E F
1
2
3
4
5
6
A
77
6,A,(2),
4
m
1 "
(C2H5O)2 P— OH
35
-------
Code Common Name Emp. Form.
Chemical Name
Structure
2391 DIFENOXURON C,
(L1ron1on)
H N,0, 3-[4-(4-Methoxyphenoxy)-
6 18 Z 3 phenyl]-l,l-dimethylurea
Mot.Wt. 286 r-T. /-^ 0
UM Herblc.
LDM 7,750
Purity 99.5+ % R(f.
1
2
3
4
5
6
*-ry-r\ / \ /^i*>n i_ iN|<_rT,J2
2395 DIFENZOQUAT (Avenge) C, 0H,Ji,O.S 1 ,2-D1methyl-3,5-d1pheny1-lH-
IB <:u <: 4 pyrazollum methyl sulfate
M.I.Wt. 360 f^ V ff^*)
UM Herblc.
L DM 470
Purity 99+ X R,f.
A B C D E F
1
2
3
4
5
6
^T^ e
N — N CH3OS03
H3C CH3
2406 DIFLU8ENZURON (D1m1Hn) C,,HqClF2N202 N-{{(4-Chlorophenyl Jamlno)
carbonyl }-2,6-d1fluorobenzam1de
F
Mol.Wt. 311 , ( H H , ,
A B C D E F / \ _ 1. 1 /^\
UM Grth. Regul.
I DM 10,000+
Purity 99 X *•'•
1
2
3
4
5
6
AL
74
57/6
1269
16
0
V_/I V ''A /
\=={ 6 o X; — '
2411 DIMETHAMETRYN (C-18898) C,,H,..C1N,0 2-(l ,2-D1methylpropylam1no)-
11 '' * 4-ethylam1no-6-methylth1o-
L3.S-tr1.z1n. NHC^
Mol. Wl. 255 /N \
UM Herblc.
10,0 3,000
Purity 99+ X Rof.
ABC D E F
T"
2
3
4
5
,6
/' V
CH3S-/' N
\=(
NHCH -CH(CH3)2
CH3
2416 DIMETHIRIMOL (Hllcurb) C^H^N^O 5-?i-Butyl-2-d1methylam1no-
4-hydroxy-6-methylpyr1m1d1ne
r(CH2)3CH3
Mol.Wt. 209 | 2 3 J
UM Fungi c.
LDjo 2,350
Purity 99.5+ % R.f
A B C D E F
1
2
3
4
J
6
n
1,12
a
H3CxiiT
M 1
N N
NS(
N(CH3)2
36
-------
Code Common Name Emp. Form.
Chemical Name
?4?n
Structure
DIMETHOATE (Cygon) C5H12N03PS2 0,0-Dimethyl S-(N-methylcar=
bamoylmethyl } phosphorodithioate
Mol.Wt. 229 S ^
LDjo 215
Purity 99.5+ X Ref.
1
2
3
A
C
AJ
BA
B
66
68
C
II
14
93
D E F
371
756
4,12
12
2,11
JOl
ao
de
T V
v_n3u/;P S CH2 C N CH3
H
2421 DIMETHOATE, OXYGEN C5H,2NO.PS 0,0-Dimethyl S-(N-methyl=
ANALOG (Dimethoxon) carbamoylmethyljphosphorothioate
Mol.Wt. 181
Use Dimethoate derivat.
LDjo --
Purity X Ref.
A B C D E F
1
1
3
4
5
6
AL
AJ
72
75
55
23
1280
758
3,4
4
ajop
e
O
(CH30)2 P-S-CH2-C~NH-CH3
2458 DIMETHYL PHOSPHATE
(DMP)
Mol.Wl. 126
Use Derivat.
Purity 98* X
*Questionable
C-H0,P
AB
Ref.
0,0-Dimethyl phosphate
1
2
3
4
5
6
A
AJ
77
76
6,A,(2),
WZ4
1221
4
4
m
m
(CH3
P—(
2460
DIMETHYL PHTHALATE
cioH10°4
Do
Mol. Wt. 194
U«e Insect repel 1.
L D:0 8,200
Purily 99 X
Ref.
1
2
3
4
5
6
WD
GD
AN
70
72
74
46/2
68/6
12/3
137
180
149
3
10
10
X
j
X
COOCH,
2551 DINITRAMINE (Cobex)
Mol. Wl. 322
Use Herbic.
L 050 3,000
Purity 99.5+ X
Ref.
N3,N3-Diethyl-2,4-dinitro-
6-(trifluoromethyl)-l,3-
phenylenediamine
1
2
3
4
5
6
AJ
WD
72
7t
20/6
97
1222
103
2
2
a u
u
NO2
37
-------
Code Common Name Emp. Form.
Chemical Name
Structure
-2560.
DINOCAP (Karathane)
Mel. Wt. 364
Utc
IPso
Purity 99+
Fungic. &
Mitic.
980
ci8H;
Ref.
.N,0,
°
Hixt. of 2,6-D1nitro-4-octyl=
phenyl crotonates
and
2,4-Dinitro-6-octyl=
phenyl crotonates
C D E F
1
2
3
4
5
6
AL
RD
70
71
53
9
887
761
3
11
w
ef
o OH
V i 3
-C-CH=CH
NO2
2:1 ratio
?7fifl
D1NOSEB (DNBP)
Mal.Wt. 240
U«« Herblc.
IDso 37-50
Purity 99 S
Cl 0H1 2N2°5
2- (
R«f.
-4, 6-d1 n1 trophenol
1
2
3
4
5
6
At
6/
5
385
20
.-
O2N
NO;
C2H5
2566
DINOSEB ACETATE C,,,H, -N.O, 2-(sec-Butyl)-4,6-d1=
(AretU) nltrophenyl acetate
Mol.Wl. 282
A B C 0 E F
Ute Herblc.
LDM 65
Purity 99+ % Ref.
1
2
3
4
5
6
4E
12
w
O2N
C2H5
2573 DIOXACARB (Elocron)
Mel.Wt. 223
U» Insectic.
ID50 72-156
Purity 99+ *
R«f.
A B
2-(l,3-D1oxolan-2-yl) phenyl
N-methylcarbamate
)
2
3
4
5
6
GE
AJ
71
73
257
21
125
178
12,18
11,17
X
X
2580 DIOXATHION (Delnav)
Mol.Wl. 456.5
U» Insectic.
L DJO 23-43
Purity 74 %
C12H26°6P2S4
A B
ft.f.
S,S-l,4-D1oxan-2,3-yl1dene b1s-
0,0-d1ethyl phosphorothlolothlonate,
70%, and related compounds
1
2
3
4
5
6
C
AL
AL
69
71
II
52
54
522
513
12
3
3
ej
eh
eh
38
-------
Code Common Name Emp. Form.
Chemical Name
Structure
2600
2620
2640
2653
2660
DIPHACINONE C23H16°3 2-Diphenylacetyl-l ,3-indandione
Mol.Wt. 340 V u U J/ v\
ABC D E F ,^X ,L H n/\_/
Ute Podentlc.
LD50 3.2-5.1
Purity 99+ 1 Ref.
1
2
3
4
5
6
BF
WD
WD
AJ
67
71
73
75
14/1
57/2
79
23/1
103
319
217
72
14
11
11,14
2
1
x
X
jl
1 I ^C~C~C
\^ ^ II \fi~\
O \—/
OIPHENAMIO (Enide) C16H17ra N,N-01methyl-2,2-
diphenylacetamide
Mol.Wt. 239 // \^
Ute Herbic.
LDM 1,000
Purify 100 % Kef.
A B C D E F
1
2
3
4
5
6
C
AJ
AC
AJ
AJ
AL
66
67
69
74
75
II
14
5
17
22
58
312
375
56
79
1015
3
3
20
2
12
2,11
def
a
—
a
tu
e
\=A 9
C_/-v Kl/fU \
L. iNvV-rU^n
\ / ^
V — /
DIPHENYL MERCURY C12H10Hg D°
Mol.Wt. 355
Use Fungi c.
LDso 500
Purity 98 S Ref.
A B C D E F
1
2
3
4
5
6
AB
AI
71
71
43
1
950
85
7
10
k
k
\ 7Hg\ /
DIPROPETRYN (Sancap) C.-H.^pS 2-(Ethylthio)-4,6-bis-(1sopropyl =
11 atnino)-l,3,5-triazine
Mol.Wt. 255 S~C2HS
ABC D E F ^J^
U*e Herbi c .
1 D50 5,000
Purity 99+ % R.f.
,
1
3
4
5
6
H ¥ T H
(CH3)2-C— N^^^^N— C— (CH3)2
b H
DIOUAT DIBROMIDE Cn,H,,Br-,N,.H,0 6,7-Dihydrodipyrido[l ,
u 2-a:2',l'-c]pyrazid1nium
di bromide, monohydrate _
f ~| 2 Br~
Mol. Wf. 362 fi TV f. ?.
ABC D E F ff Vi // Vv
Ute Herbic. S Desiccant
L DM 400
Purity 100 % Re«.
1
2
3
4
C
AJ
BA
AC
66
66
67
II
14
91
5
377
625
397
12
15
12
20
i
f
at
\=t(+ +N=/ -H2°
\_v
39
-------
Code Common Name Emp. Form.
Chemical Name
Structure
2720
DISULFOTON (01-System) CgH^OjPSj
0,0-Diethyl S-[2-(ethy1th1o)=
ethyl] phosphorodithioate
Mol. Wt. 274
Ui« Insectlc.
tOjo 12.5
Purity 98-99 %
A B
Ref.
ff
1
1
3
4
5
6
C
AJ
AL
AL
AJ
AL
68
69
69
71
74
II
16/6
52/6
52/1
19/6
57/5
895
1231
157
1196
1033
9
9
4
4
3
4
bdeg
a
ano
a
f
t
2721 DITHIANON (Thynon) C^H.N.O-S. 2,3-Dicyano-l ,4-dithia-
'^ anthraquinone
Mol.Wt. 296
A B C D E F
Use Fungi c.
L D5o 638
Purity 95+ % Ref.
1
2
3
4
5
6
2A
12
X
DIURON CqH1(1Cl?N?0 3-(3,4-Dichlorophenyl)-
1-dlmethylurea
Mol.Wt. 233
A B C Off
Use Herbic.
LOso 3,400
Purity 99+ S Ref.
1
2
3
AL
76
59
1061
8
de
(
o
o
2770
DNOC
4,6-D1n1tro-o-cresol
Mol.Wt. 198
U«e Insectlc. & Funqic.
LDso 30
Purity 97-99 % Ref.
AB
D E F
1
2
3
4
5
6
AL
AJ
AJ
68
71
73
51
19
21
24
1181
295
2
11
2
a
a
m
2780 DODINE (Caroene) C15H33N302 n-Dodecylquanidine acetate
Mol. Wt. 287
U» Funqic.
LD90 1,000
Parity 100 %
A B
E F
R.f
J
2
3
4
5
6
B
C
AL
AJ
73
76
24.122-
.125
11
56
24
299
997
__
12
11
2
._
e
t
e
Q2H25-NH-C-NH2- CH3-COOH
40
-------
fifide. Common Name Emp. Form.
Chemical Name
Structure
2860
?oan
2960
?qsn
DRAZOXOLON (Ganodde) ClnHBClN,0, 4-(2-Chlorophenylhydrazono)-
108 i * 3-methyl-5-1soxazolone
Mol.Wt. 238 / \ J. M_r r CH
ABC 0 E F \ r-" " ;- \ ^
UM Funglc.
L DSO 126
Purity 100 X R»f.
1
2
3
4
5
6
41
12
a
( O=C .. N
\
DSMA CH,AsNa,,0,-6H,0 Olsodlum methane*
arsonate, hexahydrate
Mol.Wt. 29? Q
Uu Herbic.
I DSO 1,000
Purity 99+ % Rof.
1
2
3
4
5
6
AL
ZB
ZF
AJ
5
68
69
69
72
9E
51/6
22
33/2
20/2
1300
51
279
341
18
21
21
8
18
w
au
abu
w
X
CH3-As(ONa)2-6H20
2,4-0, ACID C0H,C1,0, 2,4-D1chloroohenoxyacet1c add
o 0 £. J
O-CH2COOH
Mol.Wt. 221 CIVXX\.
A B C D E F T 1
Uio Herbic.
L DSO 500
Purity 99.5+ % R.f.
1
2
3
4
5
6
C
A
A
AJ
AJ
AJ
77
77
71
71
74
II
5,A,(4),
CC)
10, B
19
19
22
73
186
453
2,6
2
2
2
2
2
:eou
mt
t
u
u
tu
^S-X
T
Cl
2,4-D, BUTOXYETHANOL C14H1PC1,0. 2,4-D1chlorophenoxyacet1c add,
ETHER ESTERS * 14 18 2 4 „ ethanol ether esters
O
Moi.wt. 321 0-CH2C-O(CH2)p(CHj)3CH3
U H II A B C D E F r.. J^
us* Heroic.
IDH 800
Purity 99+ * Rof.
* n-Butoxyethyl ester — 59.3%
Isobutoxyethyl ester - 39.6SS
Butinkweth»nnl 0 £¥
24-h ariiH n fit
2,4-D, BUTYL ESTERS C
1
2
3
4
6
See
2940
, -H, ,C1 .0, 2 ,4-01 chl orophenoxyac
r i
^^^x^
Cl
etlc add,
(MIXED) * " "* ' a mixed butyl esters
O
«"•»«• 2" A . c D E F OCH2C-0(CH2)3CH3
UM Herbic.
I DSO 500
Pvrlty 98-99 % R«f,
* n-Butu! alrnhnl -»»--n fifi<
Fr0fl A/*1H »•••••••••• fl 49%
1
2
3
4
5
AL
69
52
See also
2940
187
2
t
f TCI
^^^
T^
Cl
41
-------
Code Common Name Emp. Form.
Chemical' Name
Structure
29S5_ 2,4-D, DIETHANOL= C,,H,,C1,NO,. 2,4-Dichloroohenoxyacetic acid,
AHINE SALT (Weedar 64D) 5 diethanolamine salt Q
H
Mol.Wl. 326 i 2 2- J s
A B C D E F ^"^ ,-.
UM ncrulCi
I DSO
Purity 41* % R,f.
* Formulation
1
2
3
4
5
6
AJ
65
13
See also
2940
123
2
b
I
^S^Sk. ^r
;r
Cl
2990 2, 4-0, DIMETHYL* ClnH,,Cl;,NO, 2,4-Dichloroohenoxyacetic
AHINE SALT acid, dimethylamlne salt Q
O-CHjC-O-lWcHj),
Mol.Wl. 266 i
ABC D E F ^£\ _.
Use Herbic.
I Dso 50°
Purity 19* % Ref.
* Formulation
3000 2,4-D ISOBUTYL C
ESTERS (MIXED) *
1
2
3
4
5
6
AK
AY
AD
W
68
71
72
-
60/7
4/4
7/(2-3)
7 J-2382
See alsi
2940
827
199
115
-
2
2
2,16
10
t
ktu
ku
t
1 I
^^•X^
Cl
, ,H, .Cl 0, 2 ,4-Di chl orophenoxyacetic
'' '* ^ J acid, mixed isobutyl esters
o
Moi.wt. 277 O-CH2C-O-CH2CH(CH3),
.... ABC D E F ^A^
U$0 Herbi c .
I DSO 5M
Purity 98-99 % Ref.
* Other i somers 0 86%
Free acid -- - 0 13%
1
2
3
4
5
6
AL
b'J
52
See also
2940
187
2
t
r^ T~CI
vS. I
^V^
I
3020 2,4-D, ISOOCTYL C.-.H.-CI.O, 2,4-Dichloroohenoxyacetic
ESTERS (MIXED) * acid, isooctyl esters
II
M.I.WI. 333 O-CH2-C-CCH2)5CH(CH3)2
A B C D E F ^J\
U*e Herbic.
L DSO 500
Purity 98-99 % R«f.
* Ethyl hexyl alcohol - 1.6%
Other i somers 0 20 %
1
2
3
4
5
6
AL
69
52
See also
2940
187
2
t
\^ TCI
Lv. I
^v^
Cl
J3Mfl_ 2,4-D ISOPROPYL ^i^Cl^ 2,4-Dichlorophenoxyacetic
ltR ' acid, isooropyl ester
II
«<"•«'• 263 9-CH2-C-0-CH(CH3)2
U h'
er ic.
I DSO 700
Purity 98-99 % Ref.
* B C D E F ^-V
'
2
3
AL
AL
69
75
52
58
187
1015
2
2,11
t
e
r TCI
l^xxl
Cl
42
-------
Code Common Name Emp. Form.
Chemical Name
Structure
3nfi(l 2,4-D, PROPYLENE GLY= 1. C, ,-HonCl ,0. 2,4-Dichlorophenoxyacetic
COL BUTYL ETHER ESTERS, r u >, „ acid, propylene glycol butyl
'• U18M26U2U5 ether esters o
3. C,,H,,,C1,,0,- V 1 1
M.,W, 358 (Averse) * * ^ p £ p 9-CH2-C-OL(CH2)3oJx(CH,),CH1
Use Herbic.
LDso 500
Purity 100 % Rel.
3080 2,4-DB, ACID C
1
2
3
4
5
6
AL
69
52
See also
2940
187
2
t
Cl^>1
X = 1,2,3
W/1
T^
Cl
,,H. .,C1 ,0, 4- (2 ,4-Di chl oronhenoxy)
0 10 2 3 butyric acid
0(CH2)3CQOH
U>e Herbic.
L D50 400
Purify 99+ % Raf.
A B C D E F
1
2
3
4
5
6
AC
AJ
A
67
71
77
5
19
10, B
369
1181
20
11
2
—
a
t
r rcl
U^ J
^V^
Cl
3100 2,4-DB, BUTYL ESTER ClaH10Cl,0, 4-(2,4-Dichlorophenoxy)
IH IB ' 3 butyric add, butyl ester
O
Mo'-Wt. 305 A B C D E F O(CH2)3-C-O(CH2)3-CH3
(jtft neruic.
I DSO ca" 40°
Purity 99+ % R«*.
1
2
3
4
5
6
See
3080
r TC|
S^
Cl
3120 2,4-DB, ISOBUTYL ESTER C, ^,,,01,0, 4-(2,4-Dichlorophenoxy)
"* IB ' J butyric acid, isobutyl ester
O
MOI.WI. 305 O(CH2)3-C-O-CH2-CH(CH3),
A B C Off ^J^ '
se Heroic.
I DSO ca. 400
Purity 96-99 % Ref.
1
2
3
4
5
6
See
3080
r irc|
L^. 1 J
^v^
Cl
_21iC_ 2,4-DB, ISOOCTYL ESTER C1RH,,C1,0, 4-(2,4-Dichlorophenoxy)
' * butyric acid, isooctyl ester _
MOI.W,. 361 O(CH2)3-C-0(CH2)5CH(CH3)2
V,, 1,-,-tl- A B C D E F ^k
L Dso 500
Purity 98.99 X Re,
1
2
3
4
5
6
See
3080
r>" >-CI
IN^ j
^V^
Cl
43
-------
Code Common Name Emp. Form.
Chemical Name
Structure
vrnc
(MIXED ISOMERS)
C9H6C16°3S 6,7,8,9,10,10-Hexachloro-
1,5,5a,6,9,9a-hexahydro-6,9-
methano-2,4,3-benzodioxa-
thlepln 3-oxlde
Mel.Wt. 407
At C D E F
U»» Insectlc.
ID jo 18-43
Purity 96+ * R.f.
1
2
3
4
5
6
C
AP
AL
AD
AL
65
69
71
72
II
58
52
6
55
160
1240
40
1232
6
2
2
2
2
idef
cu
a
t
ktu
32°" ENDOSULFAN I C0H,C1,0,S The early elutlng, low melting
(Thlodan I) a b b J (106°C.) Isomer of endosulfan
Mel.Wt. 407
endosulfan
l"so 18-43
Purity 97+ ft R.f
1
2
3
4
5
6
See
3180
3MO ENDOSULFAN II C0H,C1.;0,S The late elutlng, high melting
(Thlodan II) 9 b b J (212°C.) Isomer of endosulfan
Mel.Wt. 407
.. Isomer of tech.
endosulfan
L DSO 240
Purity 97+ % Rof.
A B C D E F
1
2
3
4
5
6
See
3180
323? ENDOSULFAN CYCLIC C0H..C1,O.S 6,7.8,9,10,10-HeXachloro-l ,5,
SULFATE » t B 1 5a,6,9,9a-hexahydro-6,9-
CH20V
CH2O
S=O
Mel. Wt. 421
Uu Endosulfan derlvat.
10,0 —
Purity 100 % R«f.
methano-!.4,3-benzod1oxa*
th1ep1n-3,3-d1ox1de
1
2
3
4
5
6
HL
55
AL
73
75
76
56
117
59
and
See
3180
733
1
209
2
21
2
g
X
de
s«o
3?an
ENDOTHALL, ACID
Mol.Wt. 204
Uu Herblc.
IP*, 51
Purity 99.5+ X
C8H12°6
R>f.
A B
7-Oxab1cyclo(2.2.l)heptane-2.3-
dlcarboxyllc add monohydrate
1
2
3
4
S
6
C
AJ
73
II
21/5
842
6
1
g
tu
COOH
O I -H20
COOH
-------
Code Common Name Emp. Form.
Chemical Name
Structure
ipfin
ENDRIN
Mcl.Wl. 381
U»e Insectlc.
I DSO 10
Purity 99+ %
Ref.
1,2,3,4,10,10-Hexachloi"o-6,7-epoxy-l,
4,4a,5,6,7,8,8a-octahydro-l,1-endo,
endo-5,8-dimethanonaphthalene
1
2
3
4
5
6
c
A
AL
AL
AD
AL
77
69
69
72
74
I
4A
52
52
8
57
1220
1280
169
585
2
2
2
2
2
2
a
jltu
be
acj
ktu
ktu
3280 EPN
Mol.Wt. 323
Ui* Acaric. & Insectic.
42
L U5Q
Purity 99+
Ref.
0-Ethyl 0-p-nitrophenyl phenyl=
phosphonothioate
1
2
3
4
5
6
C
AJ
AL
AL
67
74
74
I
15
57
57
187
930
1288
2
3,4
12
a
de
j
3^nn
EPIC (Eptam)
CgH19NOS
S-Ethyl dipropylthiocarbamate
Mol.Wt. 189
U.e Herbic.
LDso 1,631
Purity 99.5+ %
Ref.
1
2
3
4
5
6
C
AJ
ftL
RC
WD
M
68
71
71
72
76
II
16/5
54/6
36,4
64/2
24
839
1366
84
383
1236
6
2,3
4,9
3
11,17
1
de
f
bde
f
X
c
O
II
C2H5-S-C-N(C3H,)2
6590 ETHAZOL (Terrazole) CgHjCl^OS
5-Ethoxy-3-trichloromethyl-
1,2,4-thiadlazol
Mol.Wt. 247.5
u» Funglc.
l°50 2,000 (mice)
Purity 96-98 % Ref.
A B C D E F
1
2
3
4
5
6
61
2
au
H5C,0
3330 ETHEPHON (CEPHA)
Mol.Wt. 144.5
U» Grth. Regul.
10,0 4,229
Purity 98+ %
C2H6C103P
R.f.
(2-Chloroethyl)phosphon1c acid
1
2
3
4
5
6
AL
WD
AJ
AJ
AL
70
71
73
75
76
53/4
60/2
21
23/2
59
730
219
742
290
617
9
11
3
9
4
ef
g
nno
e
e
O
CICH2CH2P(OH)2
45
-------
Code Common Name Emp. Form.
Chemical Name
Structure
3335 ETHIOLATE (Prefox) C?H15NOS S-Ethyl diethylthiocarbamate
Mol.Wt. 161
Uie Herbic.
1 DSO 40°
Purity 99.5+ % Ref.
A B C D E F
1
2
3
4
5
6
3Z
4
C
(C2H5)2N-C— S— C2H5
O
3340 ETHION CqH2?0,P2S. 0,0,0 ,0'-Tetraethyl S,S'-
methyl ene bisphosphoro=
dithioate
Mol.Wt. 384.5
Ut« Insectic. & Mi tic.
I DSO 27-65
Purity 95-96 % R.f.
3359 ETHIRIMOL (Milstem) C^
Mol.Wt. 209
Use Fungic.
LDso 4'000*
Purity 98.5+ S Ref.
* Basis female rats
3373 ETHOFUMESATE (Nortron) C}
Mol.Wt. 286
Use Herbic.
I Djo 5,650
Purity 99.5+ % Ref.
5RRQ ETHOPROP (Mocap) CB
Mol.Wt. 242
Ute Nematoc.
L DSO 30-56
Purity 98.5- % Ref
99
A B C D E F
1
2
3
4
5
6
C
C
AL
AL
AL
67
74
75
I
II
50
57
58
430
1033
1015
12
2,17
2
4
2,T
a
de
ae
t
e
S S
T T
(C2H50)2P-S-CH2-S-P(OC2H5)2
H-,gN30 5-Butyl-2-(ethylamino)-4-
hydroxy-6-methyl pyrimi di ne
A B C D E F
1
2
3
4
5
6
41
9
be
(CH2)3CH3
J J.
H-N-C2H5
,H1R05S 2-Ethoxy-2,3-dihydrc-3,3-di=
methyl -5-benzofuranyl methane-
sulfonate
/\ CH3
ABC D E F CH3SO2O^^' \^ CH
1
2
3
4
5
6
3N
3N
*,I6
3
adf
w
H1902PS, 0-Ethyl S,S,-dipropyl
phosphorodithioate
A B C D E F
1
2
3
4
5
6
C
II
6
cde
II
k |l
^^^° °C
O
C2H50-P-(SC3H7)2
2H5
46
-------
Code Common Name Emp. Form.
Chemical Name
Structure
5380
ETHYLAN (Perthane) C18H20C12
l,l-D1chloro-2,2-b1s(p-
ethylphenyllethane
Mel. Wl. 307
Uie Insecti c.
1050 8,170
Purity 99 % Kef.
1W1 ETHYLHEXANEDIOL C0H
o
Mel. Wt. 146
U«» Insect. Repel 1.
l-Dso 2,600
Purity 97 X R«f.
A B C D E F
1
2
3
4
5
6
C
AL
AL
AL
72
73
73
II
55
56
56
1042
721
10,12
2
2
2
ajo
a
0
deo
Ig02 2-Ethyl-l,3-hexanediol
A B C D E F
1
2
3
4
5
6
AJ
59
I
259
12
X
H5C2/~\C-^^C
~~ CHClT"
C2H5
HO-CH2-C-CH-C3H7
H OH
3400 ETHYLMERCURY CHLORIDE CjHgHgCl Do
(Ceresan)
Mel. Wt. 265
U«e Fungi c.
I D5o 30
Purity 96 % R.f.
3412 ETRIMFOS (Ekamet) C,
Mel.Wt. 292
Uie Insectic.
10 w 1,800
Purity 99 % R.f.
1
2
3
4
5
6
A
A
WA
AB
74
74
68
71
13A
13B
22
43
2277
950
2
13
2
2
klm
t
k
k
CH3CH2-Hg-CI
nH,,N,O.PS 0-(6-Ethoxy-2-ethyl-4-pyr1m=
Idlnyl) 0,0-d1methyl phosphorothioate
/— 1 J
A B C D E F
1
2
3
4
S
6
7M
3
au
f\ *
N VO-P (OCH3)2
OC2H5
•"'" EXD (Herbisan) C6H10°2S4 Dlethyl dithiobis (thlonoformate)
Mel.Wt. 242
Ute Herblc.
IDso 603
Purity 98+ % R.f.
A 8 C D E F
1
2
3
4
5
6
C2H5-OC-S-S-CO-C2HS
S S
C2H5
47
-------
Code Common Name Emp. Form.
Chemical Name
Structure
3440 FAMPHUR C,,
,H,,NOCPS, 0,0-Rimethyl o-p-(dimethyU
' lb b * sulfamoyl) phenyl phosphorothioate
S
M.I. Wt. 325 0-P(OCH3)2
A B C D E F ^iv^
U>9 IrlbeC 1 1 C .
I D,o 35
Purity 98.5+ % R.f
1
2
3
4
5
6
C
AJ
AL
67
76
II
15
59
920
261
3
3
4
j
jlo
j
fl 1
^
T^
O=S-N(CH3)2
6
3460 FENAC CgHjCl^ 2,3,6-TMchlorophenylacetic acid
ci n
Mol.Wt. 239.5 ^ y
Uio Herbic.
L DM 3,000
Purity 91 % Rof.
A B C D E F
1
2
3
4
5
6
AJ
A
67
77
15
10, B
208
2
2
U
t
-------
Code Common Name Emp. Form.
Chemical Name
Structure
3500 FENSULFOTHION (Dasanlt) C^rUJyS. 0,0-D1ethyl 0[p-(methyl =
' " " sulf1nyl)phenyl]phosphoroth1oate
Mel.Wt. 308 5 r-_ v O
UK Insectic.
LDM 2-11
Purity 94.5 % R.f.
A B C Off
1
2
3
4
5
6
C
AJ
AJ
AJ
AC
71
71
72
73
II
19/3
19/2
20/6
7
456
342
1219
253
9,1 1
4
4
3
20
a
af
aco
u
-
T / — \ T
(C2H5O)2P-O-(\ />-S-CH3
3S?0 FENTHION (Baytex) C, -H, C0,PS, 0,0-Dimethyl 0-[4-(methy1*h1o)-
lu ls J i m-tolyl] phosphorothloate
/ v S
Mel.Wt. 278 / A J
U» Insectic.
I DM 215
Purity 98+ % R,f.
3527 FENTIN ACETATE C,
(Brestan)
1
2
3
4
5
6
C
AJ
AG
AJ
AL
AD
66
67
68
69
71
II
14/6
1/8
16/3
52/6
6/1 .
619
639
399
1231
55
9,4
2
2,4
4
4
4
jo
aj
t
ao
aou
X
n3«w o->A // 'vJ^-r'3J2
X~/^
CM?
•W. IJ
•.H-igO-Sn Tr1phenylt1n acetate
/=\
Mel. Wt. 409 \_A
r i AI i- t * B c otf /=\ \
Ufte rungic., Higic., o
Mollusclc.
1 D50 140-491
Purity 99+ % Ref.
1
2
3
4
5
6
BF
we
WB
AE
4E
70
72
74
-
17/11
78/1
71/1
66-750032
1059
41
192
—
15
15
14
10
15
t
a
af
c
aef
^_J) — SnO —CO -CH3
/=v/
\-/
3540 FENTIN HYDROXIDE ClgH16OSn Tr1phenylt1n hydroxide
Mel.Wt. 367 f- \
U» Fungi c.
L DM 500
Purity 98+ % Ref.
A B C Off
1
2
3
4
5
6
C
81
II
12
12
hj
fghu
\J sn°H
*— —Is
3600 FERBAM CgH^FeNjSg Ferric dlmethyldUhlocarbamate
Mel.Wt. 416.5 5
Uie Funglc.
LOjo 4,000
Purity 99.5+ * R.f.
A B C D E F
1
2
3
C
WO
AL
64
69
II
14
52/1
348
249
12
10
12
a
X
X
(CH3)2-N-C-S- Fe
J3
49
-------
Code Common Name Emp. Form.
Chemical Name
Structure
3620
3623
FLUCHLORALIN (Basalln) C12H13C1F3N,0. N-(2-Chloroethyl )-tr1fluoro-Z,6-
dinltro N-propyl-p-toluldine
N02
Mol-Wl- 356 f/ ^ ru /-u ru
.... ABC DEF _ „ // >\ />~n2-(_n2-i_n3
USA Hsrbic.
10,0 1,550
Purity 99.5+ % R«f.
1
1
3
4
5
6
1Q
1,2
agtu
~y-~\ /~N
\=/ NCH2-CH2-CI
NO2
FLUOMETURON (Cotoran) ClnH11F,N?0 l,l-D1methyl-3-(3-tr1fluoro=
lu " J d methyl phenyl) urea
O
Mol.Wt. 232 H-N-C-N(CH3)2
A B C D 1 F ^^
U» Herbic.
LDM 11,100 '
Purity 99+ % Rgf.
1
2
3
4
5
6
C
WD
W
WD
BH
AL
68
69
69
71
76
II
36
17.
44
11
59
234
1409
419
111
1061
12
2
10
11
12
8
91
X
w
u
u
de
r 1
kJ^CF3
FLUORIDAMID (Sustar) C^H^FJU), N-4-Methyl-3-[[(l,l,l-tr1fluoromethyl)=
lu " J ' J sulfonyl]am1no]phenyl]acetamide .^
it
M.I.Wt. 264 NHCCH3
A B C D E F J_
Us« Plant Grth. Regulat.
L Djo 9,230
Purity 100 % R«f.
1
2
3
4
5
6
4Z
t
u
r ^
1
\^NHS02CF3
T
CH3
3630
FLURECOL-n BUTYL ESTER C1(,H1B0, n-Butyl 9-hydroxy=
(Florence!) fluorene-(9)-carboxylate
Mol.Wt. 282
Uu Herbic.
LDso 5,000
Purity 99+ %
A B
1
2
3
4
5
6
WD
AX
68
72
36/3
6
318
157
11
21
X
actu
HO^COOQH,
if,&n
FOLEX (Merphos)
Mol.Wt. 298.5
U>* Defoliant
ID,,, 1,270
Purity 96+ %
Ref.
Tributyl phosphorotrithloite
1
2
3
4
5
6
AL
AL
5M
70
71
53/3
54/2
499
359
4
2,9
6
X
X
g
(C4HoS)3P
50
-------
Code Common Name Emp. Form.
Chemical Name
Structure
3660 FOLPET(Phaltan) CgH.Cl,N02S N-(Trichloromethylthio)phthal1m1de
Mol.Wt. 297 ^\, P
Ute Funqic.
ID50 10,000
Purity 99.5+ % M
A B C DEF
1
2
3
4
5
6
C
AL
BA
70
72
II
53
97
154
713
12
2
2
de
a
e
N-S-CCI3
^" (,
19.10 FONOFOS (Dyfonate) C.-rL-OPS,, 0-Ethyl S-pheny! ethyl =
phosphonodithioate
Mol.Wl. 246
Us* Insectic.
10 so 8-16
Purify 99.5+ X Ref.
A B C DEF
1
2
3
4
5
6
C
AL
71
II
54
1086
9,11
4
a
0
r\ s>c2H5
\r=^/
291 1 FONOFOS, OXYGEN ANALOG C. H.,0,PS 0-Ethyl S-phenylethyl
(Fonofoxon) phosphonothioate
Mol.Wl. 230
Use Fonofos derivat.
LDjo
Purity % Ref.
A B C DEF
1
2
3
4
5
6
/~\*£«*
\__/
Jfian FORMETANATE HYDRO- C..H, ,N,0,-HC1 m[[ (Dimethyl ami no )methyl =
CHLORIDE (Carzol SP) " lo J ' ene]amino]phenyl methyl=
carbamate hydrochloride Q
Mol.Wl. 258 0-C-NH-CH3
ABC DEF JL.
Ufa Acaric. & Insectic.
L DSO 20
Purity 98-99 % R,l.
1
2
3
4
5
6
C
GA
II
2,11
2,12
e
a
f > -HCI
1 1 H
3722 FORMOTHION (Anthio) C H NO.PS. 0,0-Dimethyl S-(N-methyl-N-fo™yl*
carbamoylmethyl)phosphorod1th1oate
Mol. Wt. 257
Uso Insectic.
1 050 365
Purity 54 % R«f.
(Adjusted)
1
2
3
4
5
6
CH3x OH s
ABC DEF \ II 1 II ,
7M
3,9
aeu
.N — ^ — L — 5 — PILH
CH° H
30)2
-------
Code Common Name Emp. Form.
Chemical Name
Structure
3790
GIBBERELLIC ACID
C19H22°6
Mol. Wt. 346
Uu Plant Grth. Regulat.
I DJO (relatlv. non-toxic)
Purity 96-98 % R«f.
A 8
G1bb-3-ene-l ,!0-d1carboxyl1c add,
2,4a,7-trlhydroxy-1-methyl-8-methyl ene-
l,4a-lactone
1
2
3
4
5
6
C
AC
AF
67
71
II
5
32/4
413
2001 B
II.V
20
2
de
-
a
-OH
COOH
3796
GLYOX1ME (P1k-!)ff)
tthanedUl dloxlme
Mel. Wl. 88.1
HON=CHCH=NOH
Un Grth. Regulat.
L 0,o 99.5
Purity 99-5 % „.,.
3801 GLYPHOSATE (Roundup) C3
1
2
3
4
5
6
HgNO^P N-(Phosphonomethyl Jglyclne
Mol.Wt. 169
U» Herblc.
LD,o 4,320
Purity 99+ % R.f.
3802 GLYPHOSINE (Polaris) C^
Mol.Wt. 263
U» Rlpener
ID jo 3,925
Purity 99+ % R.f.
A B C D E F
1
2
3
4
3
6
5Q
4
be
H,,NOBP, N,N-B1s(phosphono-
" ° methyl )-g1yc1ne
ABC D E F
1
2
3
4
S
6
3860 HEPTACHLOR ClnH,C17 1.4,5,6,7.8,8-Heptachloro-
3a,4,7,7a-tetrahydro-4,7-
methanolndene
Mol.Wt. 373
UM Insectlc.
I D,o 90
Purity 99.5 % R,f.
A B C D E F
1
2
3
A
C
C
77
4A
I
II
2
2
12
jit
uv
aou
adf
HO —C — CHj— N —CH2-P—OH
H
I
OH
? o
(OH), P-CH2-N-CH2-P(OH)2
i
CH2COOH
52
-------
Code Common Name Emp. Form.
Chemical Name
Structure
3880 HEPTACHLOR EPOXIDE
Mol. Wt. 389
U>* Heptachlor derivat.
L DM 40-60
Purity 99+ % *«f.
C10H5C170
1,4,5,6,7,8,8-Heptachloro-2,
3-epoxy-2,3,3a,4,7,7a-tetra=
hydro-4,7-methanolndene
1
2
3
4
5
6
See
3860
*ci •
39?0 HEXACHLOROBENZENE (HCB) C(
Mel. Wt. 285
Uu Fungi c.
L Dj, 3,500
Purity 98+ % R*f.
Hexachlorobenzene
A B C D E F
1
2
3
4
5
6
A
C
AL
AL
AG
AD
77
72
74
74
75
5..J1).
II
55
57
8
14/3
806
580
584
273
2
6
2
2
2
2
j
a
op
j
V
j
3940 HEXACHLOROPHENE (Nabac)
C,,H,C1,0,
13 6 ° 2
Mel. Wt. 407
U>« Fungic. Bacterlc.,
Acarlc.
L DSO 300
Purity 99+ % Rt
2,2'-Methylene b1s(3,4,6-
trichlorophenol)
A B C D E F
1
1
3
4
5
6
AS
AL
AD
69
70
73
58
53
10
251
522
57
2
2
2
1
c
j
3949 5-HYDROXY-2-BENZIMIDAZOLE
CARBAMATE
Mol.Wt. 191
U«» Benomyl derivat.
Purity 99+ X
R.f.
5-Hydroxy-2-BenZ1m1d«ole Carbamate
D E F
_««! 1-HYDROXYCHLORDENE
Mel.Wt. 355
Uw Heptachlor derivat.
I DM 2,400
Purity 100 X R,f
1-eao, Hydroxy-4,5,6,7,8,8-hexachloro-
3a,4,7,7a-tetrahydro-4,7-methano1ndene
1
2
3
4
5
6
A
C
AJ
77
72
4.A
II
20
328
2
2
2
X
a
aku
*CI
53
-------
Code Common Name Emp. Form,
Chemical Name
Structure
4011 IBP (Kitazin) C,,H710,PS Phosphorothioic acid, 0,0-b1s(l-
methylethyl) S-(phenylmethyl Jester
Mol.Wt. 288
UM Fungic.
10 50 660 (mice)
Purity 99+ % R»f.
r i ?
ABC Off 1 ,_ . ... J 1
1
3
4
5
6
L\<_r-!3;2<-rlUJ2 Y —
4040 IOXYNIL (Actril) C7H3I2NO 4-Hydroxy-3,5-diiodobenzonitrile
SCH2--P(OCH3)2
1
O H
Mol.Wt. 279
Ui* Herbic.
1.0,0 3,000
Purity 97-98 % R,|.
A B C D E F
1
2
3
4
e
3Q
AJ
77
25
567
16
12, If
tu
atu
<.o-c-r
\ 7
^N-C-N
HO
M-C(CH3)3
54
-------
Code Common Name Emp. Form.
Chemical Name
Structure
4146 KINOPRENE (Enstar) C
0H,00, Prop-2-ynyl(+)-(E,E)-
8 '° ' 3,7,ll-trimethyldodeca-2,
4-dienoate
Mol.WI. 276 ,x n
A B C D E F ^/\/^ /\\ /\ /\ /\
Use Grth. Regul .
IDso 3,540
Purity 92 % R«f.
j
2
3
4
5
6
9M
3
X
|j ^Y \v Y V >
o
41Sfi KRENITE C3H11N2°4P Ammonium ethyl carbamoylphosphonate
Mol.WI. 170 ( Jj
U»« Brush Contr., Grth.
Regulat.
IDso 24,000
Purity 99+ % Ref
4166 LAMPRECIDE (TFN) C;
A B C D E F
1
2
3
4
5
6
3A
4
au
C2H50-P-C-NH2
ONH4
H.,F,NO,Na 3-Tri f 1 uoromethyl -4-ni tro=
Dhenol, sodium salt
O— Na
Mol.WI. 229 1
A B C D E F ,/^^
Use Lamprey Killer
L DJO 370-440
Purity 98+ X Kef.
1
2
3
4
5
6
AL
AL
74
76
57/2
59
387
862
2
2
k
t
L ..^
N02
4180 LEAD ARSENATE PbHAs04 Arsenic acid, lead salt
Mol. Wt. 347
ABC D E F
UIA InsGCti c .
I Oj,, 100
Purity 95-98 X R.f.
1
2
3
4
5
6
b
25,000-
.017
12
X
4185 LENACIL (Venzar) C13H18N2°2 3-Cyclohexyl-6,7-d1hydro-
lH-cyclopentapyr1midine-
2,4(3H,5H)-dione ^
M.I.WI. 234 ^^ ^ n
Ui* Herbic.
LDso 11,000
Purity 99+ S R.f
A B C D E F
1
2
3
BC
bb
17/3
121
J
at
\ ^ (s)
II
55
-------
Code Common Name Emp. Form.
Chemical Name
Structure
JiQ" LEPTOPHOS (Phosvel)
Mol.Wt. 412
U«e Insectic.
IDM 53
Purity 99+ % Ref.
0-(4-Brotno-2,5-dichlorophenyl)
0-methyl phenylphosphonothioate
1
2
3
4
5
6
AL
AL
AJ
AJ
74
74
75
74
57/5
57/1
23/1
22/4
1056
182
90
704
4
4
4
10,
11,
17
9
d
ad
d e
4191
LEPTOPHOS OXYGEN
ANALOG (Leptophoxon)
C,,HlnBrCl;,0,P 0-Methyl 0-(4-braro-2,5-
dichlorophenylJphenylphosphonate
Mol.Wt. 372
Use Leptophos derivat.
Purity 100 *
Ref.
A B
D E F
4220 LETHANE 384
Mel. Wt. 203
UM Insectic.
I Di0 90
Purity 50-55% *
'Formulation
CQH,,NO,S 2-(2-Butoxyethoxy)ethyl
a " ' thiocyanate
R.f.
1
1
3
4
5
6
AO
61
6
478
12
jo
C4H90(CH2)2-O-(CH2)j-S-CN
j?an
LINURON (Lorox)
Mol.WI. 249
U«« Herbic.
1050 1,500
Purity 99+X
CQH1nCl,N,0, 3-(3,4-01 chlorophenyD-1-
methoxy-1-methyl urea
*•'.
1
2
3
4
5
6
C
AD
AJ
MO
AJ
AL
67
69
71
76
76
II
2
17
57
24
59
75
1409
303
1236
1061
12
12
4
12
1
8
X
u
X
tu
C
de
Cl
=J fi S0-CH3
Jif-n MALATHION C
" Mol. Wt. 330
Uit Insectic.
lOso 1,000-1,375
Purity 99+ X R«f.
D1 ethyl mercaptosucdnate,
a-ester with 0,0-d1methyl
phosphorodlthloate
1
2
3
4
5
6
C
AL
AD
AJ
AL
AL
67
68
68
71
74
II
50
3
16
• 54
57
581
247
361
513
1033
12
3
2
4
4
4
de
0
acj
tu
ajo
a
t
S M
(CH30)2P-S-C-COOC2H5
CH2-COOC2HS
56
-------
Code Common Name Emp. Form.
Chemical Name
Structure
4261
MALATHION, OXYGEN
ANALOG (Malaoxon)
ClnH,.0,PS
lu la '
Mel.WI.
UM
Purity
314
Malathlon derlvat.
90
— *
R.f.
0,0-D1methyl S-[l,2-d1-(ethoxycarb=
onyl)ethyl]phosphoroth1oate
1
2
3
4
5
6
AJ
PD
AP
AL
AJ
72
72
73
74
76
20
23
66
57
24
624
23
332
1043
631
2,4
n
12
12
4
Jt
de
a
X
k
? V
(CH30)2P-S-C-COOC2H5
CH2-COOC2H5
4200-
MANEB
(C,,H,.MnN,S.) Manganous ethylene-1,2-
(PoySeHc) *" b1.fd1tMoc.rta.te)
434n
43fin
4380
Mol.Wt. *265
Ut« Fungi c.
ID so 6,750
Purity 98+ * ft«f.
*Un1t mol. wt.
ABC D E F
1
2
3
4
5
6
C
AL
AL
69
71
II
52
54/6
1226
1373
12
4
3
a
d e
a b
n H o
H-C-|W-S-
i
H-C-N-C-S-Mn-
H H S x
MCPA, ACID C9H9C103 (4-Chloro-2-methylphenoxy)-acet1c add
M.I.Wt. 201 _ £H3
UM Herblc.
LDM 700
Purity 99+ % g.f.
A B C D E F
1
2
3
4
5
6
A
AC
AL
WD
77
67
69
71
10, B
5
52
57
439
187
303
2
20
2
11
t
t
tu
Cl-/ \OCH2COOH
V /
MCPA, ISOOCTYL ESTER C.,H,,C10, (4-Chloro-2-methylphenoxy)-
" " J acetic add, Isooctyl ester
Mol.Wt. 313 , / 3
UM Herblc.
L DSO 700
Purity 98-98.5% „.,.
A B C D E F
1
2
3
4
5
6
See
4340
\ /"°CHj~
-------
Code Common Name Emp. Form.
44nn
Chemical Name
Structure
4420
44/11
1453
MCPP, ACID C-.H^CIO, 2-(4-Chloro-2-methyl=
11 phenoxy)propionic acid
CH3
/ ( H
Mol.Wt. 215 // \\ 1
Ut. Herbic.
L DJO 650
Purity 99+ % R.f.
A 8 C D E F
1
2
3
4
5
6
A
WD
AO
AL
77
71
71
75
10, B
57
19
58
303
1181
1027
'i
11
11
2
t
tu
abg
cu
ci-<^ y-oc -COOH
^=^ CH3
MCPP, ISOOCTYL ESTER C1SH,,C10, 2-{4-Chloro-2-methylphenoxy)
IB '' J propionic acid, isooctyl ester
Mol. Wl. 327 r. — r< ^ H O H
UM Herbic.
L DM ca 650
Purity 96-99% R.f.
A B C D E F
1
2
3
4
5
6
See
4400
Cl-/ \OC-C-0(CH2)5-C(CH3)2
\ / '
3
MECARBAM (MC-474) C10H2t)N06PS 0,0-Diethyl S-(N-ethoxycar=
bonyl N-methylcarbamoylmethyl)
phosphorodithioate
Mel.Wl. 297 ? 9
U». Insectic. &
Acaric.
L DM ^6
Purity 99+ % R.f.
* * C D E F (<-_u_nV D c ru. r M i-orvi- u
1
2
3
4
5
6
BA
69
94/1117
275
4,11
t
1 I ' '
CH3
MENAZON (Azidithion) C-H.^htOpPS, 0,0-Dimethyl S-(4,6-diamino-
u ° i ' l,3,5-triazin-2-ylniethyl)
phosphorodithioate
NH2
Mel.Wt. 281 KJ (
A B C D E F , , /, . \>
Us. Aphic.
IDso 1,950 (female rats)
Purity 99+ % R.f.
1
2
3
4
5
6
BA
AC
AD
69
73
73
94/1117
7
10/5
275
317
285
1,11
20
3
t
—
X
\(-n3(Ji2 Y— b— CH2— V N
II [vj — /
S hH2
MEOBAL CnnH,,NO, 3,4-Dimethylphenyl
lu IJ ^ N-methylcarbamate
0-CO-NH-CH3
Mol. Wt. 179 ^5^\
ABC D E F r 71
UM Insectic.
L DM 290-380
Purity 99+ % R.f.
1
2
3
JB
AJ
70
73
35
21
72
178
2
n, i;
C
X
oTCH3
58
-------
Code Common Name Emp. Form. Chemical Name
Structure
1630 MEPHOSFOLAN (Cytrolane)CBHlfiNO,PS., 2-(Diethoxyphosphinylimino)-
B '° •» i 4-methyl-l,3-dithiolane
Mol. Wt. 269
Use Insectic.
L DM 8.9
Purity 97.5-99% Ref.
A B C DEF
1
2
3
4
5
6
HjC-i^^N-rMoC^
1 s
6620 METHAM (SHDC) C,H,,NS.Na Sodium N-methvldithiocarbamate
s
Mol.WI. 129 ||
. ABC D E F CH3-NH-C-S-Na
USB oOi I rumig.
L DJO 820
Purity 33* X Ref.
*Formulat1on
1
2
3
4
5
6
7Z
18
w
4750 METHAMIDOPHOS C,ti,NO,PS 0,S-Dimethyl phosphoramidottifoate
(Monitor) i 8 i
Mol.Wt. 141 Q
Ti. ABC DEF CHiCLlI
U$9 Insscti c.
LD50 18.9-21
Purity 98-99 X Ref
1
2
3
4
5
6
AL
AJ
GH
AL
71
73
-
75
54/6
21/1
24/2
58
1396
143
252
1027
9
4
3
2
afd
d
a
cu
CH Sx 2
3
.4420. METHANEARSONIC ACID CH,AsO, Methyl arsonic acid
(MAA) 3 3
n
Mol.Wt. 140 n
Uie Herbic.
LDso 1,300
Purity 99.5 X Ref.
A B C DEF
1
2
3
4
5
6
B
25.011-
.017
12
g
CH3-As(OH;2
4496 METHAZOLE (Probe) CgH-rCl-N-O, 2-(3,4-Dichlorophenyl )-4-methyl-
'" J l,2,4-oxadiazolidine-3,5-dione
Mol.Wt. 261 \ — /
A B C DEF „',
U*e Herbic.
IDso 1,350
Purity 99+ % „„,.
1
2
3
4
5
6
9A
-,16
gu
>-i
•^ \ / \-
° N O
CH3
59
-------
Code Common Name Emp. Form.
Chemical Name
Structure
_6340
METHIDATHION
(Suoradde)
Mel. Wt. 302
Ute Insectlc.
I DSO 25-48
Purity 99.5+%
CcH^N-O.PS, 0,0-D1methyl S-(2,3-d1hydro-5-
ft I I <: » J methoxy-2-oxo-l ,3,4-thiad1azol-
3-ylmethyl )phosphorod1 th1 oate
Ref.
1
2
3
4
5
6
A
AJ
AJ
69
70
17
18
565
164
6
4
b
c P
N N-CH2-S-P(OCH3)j
4500
METHIOCARB (Mesurol) C,,H,
"
Mel. Wl. 225
Purity
Acarlc. &
Insectlc.
130-135
99 %
*•'•
,.NO,,S
i
4-(Methylth1o)-3,5-xylyl
N-methylcarbamate
1
2
3
4
5
6
AL
WD
A8
AJ
AL
AL
69
70
72
72
73
74
52/5
49/2
44/12
20/2
56/3
57/4
1054
215
2046
443
713.
570
4
2
11,14
2,3
2
3
ad
adet
tu
X
a
d
S-CH3
4520
METHOMYL (Lannate) C-H1nN,0,S
5 10 z z
Mel. Wt.
U»
LPM
Purity
162
Insectlc. &
Nematoc.
17-24
99+ %
Ref.
S-Methyl N-[( methyl carba-
moyljoxy] thloacetlmldate
1
2
3
4
5
6
C
AJ
JI
AJ
AJ
68
72
74
75
II
16
28
22
23
554
22
76
695
6
6
4
4
4
i d
a
f
itU
0
CH3-C-N-0-d-N-CH3
S-CH3
A
4521
METHOMYL OXIME
Methyl N-hydroxyth1oacet1m1date
M...W,. 105
A B
OIF
U>e Methomyl derivative
lD§o Toxic
Purity 99+ % »,(.
2
3
4
5
6
See
4520
CH3-C=N-OH
in
CH3
4531
METHOPRENE (AHosId) C,aH,,0,
ly J* J
Isopropyl (2E,4E)-ll-methoxy-
3.7,ll-tr1methyl-2>4-dodecad1enoate
Mel.Wt.
Ute
•urlty
310
Insect Grth.
Regulat.
L DJO 34,600+
96-97 X
,ff
A B
1
2
3
4
5
6
AP
AJ
AL
73
74
75
66/3
22/4
58/1
707
582
10
3
3
3,5
X
X
,1ko
tu
60
-------
Code Common Name Emp. Form.
Chemical Name
Structure
4540 METHOXYCHLOR (TECH.) C,
(Marlate) '
(-H-icClnO- di(p-methoxyphenyl)-trichloro=
J methyl methane, mixed p,p' and
o,p' isomers
Mol.Wt. 346
U«e Insectic.
ID jo 6,000
Purity 89-90* % Ref.
*Basis p,p' content
4541 METHOXYCHLOR-p,p' C}
Mol.Wt. 346
U»e Major Component of
Tech. Methoxychlor
IDjo 6,000
A B C D E F
1
2
3
4
5
6
See structure below for 4541
,H,,-C1,,0, l,l,l-Trichloro-2,2-bis(p-
013 J methoxyphenyl ) ethane
A B C D E F
1
2
B
BA
69
24.128-
.152
94
900
12
2
e
u
M
Purity
99+
„.,
4560 METHYLMERCURIC
CHLORIDE
CH3HgCl
Do
4572
KfU
Mol. Wf. 251
Uu Fungi c.
I DM 30-35
Purity 98 % R.f.
A B C D E F
1
2
3
4
5
6
A
A
CA
AB
WD
74
74
70
71
74
13, A
13, B
50
43
97
597
950
65
2
13
13
10
2
jklm
t
cu
k
1
CH3-Hg-CI
METHYLMERCURIC IODIDE CHjHgl Do
Mol.Wt. 342.5
ABC D E F CH3MgJ.
Uto Reagent i n
Hg Method
L DJO
Purity 98 % R«f.
1
2
3
4
5
6
4560
METIRAM (Polyram) Varies 83. 9% Ammoniates of [Etnylenebis- [~
(dithiocarbamate)] zinc with 16.14 s s _;
ethylenebis(dithiocarbamic acid)bi= (-S-C-NH-C,H,-NH-C-S-) Zn
molecular and trimolecular cyclic
Mol. Wl. Varies - polymeric anhydro sulfides and bisulfides p •> -|
U»« Fungi c.
LDjO 6,200
Purity 37.6*% Ref
*% cs2
A B C D E F
1
2
3
4
5
6
RD
73
11
840
21
q
CH,-NH-C'
1- s J«
r » i
CH,-NH-C-5
1 1
CH, NH-C-S
« y
nsl or2 / x t y M
-2of3
-------
Code Common Name Emp. Form.
Chemical Name
Structure
4612
J631
4M4
4640
7D8Q
METOBROMURON (Patoran) CgH^BrN-O,, 3-(p-Bromophenyl)-l-
1 methoxy-1-methylurea
Mol.Wi. 254 BrY^^^Xl
A B C D E F n
Us* Herbic.
ID 50 3,000
Purity 99+ S R«f.
1
2
3
4
5
6
BH
WD
RH
GB
WF
GK
71
72
72
73
74
74
4
65
31
9
11
7
111
533
89
261
54
245
12
4
16
11
11
6
u
d
dtv
u
X
a
\J f*\r*t I
^^ix^^NH-C— N
~"-CH3
METOXURON (Dosanex) CmH^ClN.O. .3-(3-Chloro-4-methoxy=
lu 1J ' ' phenyl)-l,l-dimethylurea
ri
Mel.Wt. 229
Uu Herbic.
IDjo 3,200
Purity 99+ % R«f.
A B C D E F
1
2
3
4
5
6
7M
12
abc
fu
\ H 0
CH30-/ \-N-C -N(CH3)
\ /
v^ ' J
METRIBUZIN (Lexone) CgHlivN4OS 4-Am1no-6-[l .l-dlmethyUethylJl-
tAHJ-one ' Q
Mel. Wt. 214
U<* Herbic.
LD90 1,937
Purity 99+ % R.f.
A B C D E F
1
2
3
4
5
6
3A
WD
BI
AO
AJ
71
75
76
77
56
28
24
25
345
96
122
380
2
4
19
3
2
X
u
u
t
Jeu
(H3C)3YVNH>
N J^
N 3
MEVINPHOS (Phosdrin) C-H,,0,P 2-Carbomethoxy-l -methyl =
' IJ ° vinyl dimethyl phosphate
Mel. Wt. 224
U§« Insectic.
ID50 ^
Purity 64-65* % R.f.
Alpha isomer
A B C D E F
1
2
3
4
5
6
B
BA
BA
AJ
AL
67
68
70
75
24.174-
92
93
18
58
578
691
401
1015
17
12
11
3
2,11
d e
V
a f
a
e
O HO
(CH30)/-0-C=C-£
CH3 bCH,
MEXACARBATE (Zectran) C.-HnaNoO, 4-DimethyUmino-3,5-xylyl
1 methyl carbamate
O H
Mel. Wt. 222 O~C-N-CH3
A B C D E F ^^
Us* Insectic.
IDjo 15-63
Purity 99 % R«f.
\
1
3
ID
AJ
AL
69
69
74
26
17
57/3
63
56
570
1,6
2
3
a
a
a
1 n
H r-^s /^rn
Mfr-U^
62
-------
Code Common Name Emp. Form.
Chemical Name
Structure
4280 MH (Haleic Hydrazide) C4H4N2
Mol.Wl. H2
UW Herbic. 5 Grth.
Regulat.
LDSO 2,340-6,950
Purity
99
6-Hydroxy-3-(2H)-pyridazinone
A B
]
2
3
4
5
6
B
AL
73
24.141-
.147
56
1164
\i
11
f
af
MIREX (Dechlorane) C-|oC112
Mol.Wt. 546
Ut« Insectic.
ID 50 306
Purity 98+ %
Ref.
Dodecachlorooctahydro-1,3,4-metheno-
2H-cyclobuta[cd]pentalene
1
2
3
4
5
6
C
A
AL
AJ
AL
AL
77
63
73
73
75
II
4,A;10,A
46
21/6
56/3
58/3
884
1099
721
557
6
2
10
1
2
2
ajo
t
a
X
a e
j
4740 HOLINATE (Ordram)
Mol.Wt. 187
Uw Herbic.
ID jo 660
Purity 99,5+ %
R.f.
S-Ethyl N,N-hexameth=
ylsne thlocarbamate
1
2
3
4
5
6
C
AC
AO
67
68
II
5
16
469
839
6
20
2
ct
—
t
0-C-S-C2H5
o
4747 MONALIDE (Potablan) C,,H1BC1NO N-{4-Chlorophenyl}-2,2-
'" I0 dimethyl valeramlde
Mol.Wl. 239-5
U<« Herbic.
LD,0 4,000
Purity 99+ %
„.,
AB
E F
1
2
3
4
s
6
7Q
2
a
V ?*
-N-C-C-CHj-C
O CH3
0360
HONOCROTOPHOS (Azodrln) C?H14N05P
Mol.Wl. 223
Uu Insecti c.
10M 21
Purity 98+ %
R.I.
Dimethyl phosphate of 3-
hydroxy-N-methyl -ois-cro=
tonamlde
1
2
3
4
5
6
AJ
AO
AC
AJ
BA
AD
66
67
67
68
73
74
14/2
15/3
5
16/6
98
11/5
145
465
193
899
194
434
16
4
12
3
21
4
a
a
X
a
a
a
(CH30)2p-(p H
CH3-C=C-C=O
63
-------
Code Common Name Emp. Form. Chemical Name
4751 MONOLINURON (Aresin) CgH^ClNO,
Mol.Wt. 201
U» Herbic.
ID50 2,250
Purity 99+ % Ref.
3-(p-Chlorophenyl)-l-methoxy-
1-methyl urea
1
2
3
4
5
6
WD
WD
GF
WD
67
69
71
71
27/1
44/2
256/3
63/2
296
419
194
364
11
10,
11
),15
l,28
au
X
X
X
Structure
N-C-N-CH3
4760
MONURON
Mol.Wt. 199
U» Herbic.
ID50 3,600
Purity 99+ %
3-(p-Chlorophenyl)-l,1-dimethylurea
R,f.
1
2
3
4
5
6
r
AL
AL
WD
WD
AL
62
66
69
71
76
II
45/2
49
44
57
59
377
452
419
303
1061
11,
1212
11,
12
10,
j|
8
del
a
t
u
tu
de
o
H-N-(i-N(CH3)2
J78Q
MONURON-TCA (Urox)
3-(p-CM orophenyl )-l ,l-d1-
methylurea trlchloroacetate
Mol.Wt. 362 H-N-C.
.... ABC D E F ^#\
Uso Herbic.
LDso 2,300
Purity 97 % R.f.
1
2
3
4
5
6
See
4760
\
^v/
Cl
H-N-C-N+H(CH3)2-OCOCI3
4820
MSMA (Bueno)
Mol.Wt. 162
Uto Herbic.
IDso 700
Purity 51-52* %
'Formulation
R.f.
A B
Monosodium add methanearsonate
1
2
3
4
5
6
ZF
ZB
ZJ
AJ
69
69
71
71
33/2
22
19
19/4
279
51
412
412
21
21
12
12
abu
ag
a
a
9
4860
NALED (Dibrom)
Mol.Wt. 381
Us, Insectic.
L Dso 130
Purity 99* S
C,H7Br,Cl,0,,P
* ' ' * *
R.f.
1 ,2-Dibromo-2,2-dichloro=
ethyl dimethyl phosphate
1
2
3
4
5
6
C
AL
65
II
48
748
6
6
ade
de
(CH3O)2P-O-C-CCI2Br
Br
64
-------
Code Common Name Emp. Form.
Chemical Name
Structure
4880 NAPHTHALENE ACETAHIDE C^h^NO 1-Naphthalene acetamlde
Mel. Wl. 185
U«« Grth. Regul.
1050 i.ooo
Purity 98+ %
R.f.
1
2
3
4
5
6
AC
67
5
455
10,
12
a
4900 NAA (Naphthalene
Acetic Add)
Mel. Wl. 186
UK Grth. Regul.
L 0,0 1.000
Purity 97+ %
C12H10°2
R.f.
1-Naphthalene acetic add
\
2
3
4
5
6
C
AL
AJ
AC
AL
A
64
64
67
71
77
II
47
12
5
54
10, B
348
59
455
327
2,
212
12
20
14
2
e
e
9
—
e
t
CH2COOH
4925
1-NAPHTHOL
C10H8°
Mol.Wt. 144
UM Carbaryl Derlvat.
LDM 2,590
Purity 99+ * R.f
A (
DO
1
2
3
4
5
6
A
AL
AD
AL
74
70
71
76
7A
53
6
59
495
34
188
2
2
2
2
m
jo
m
tu
2010 NAPROPAMIDE (Devrlnol) C
Mol.Wt. 271
U» Herblc.
ID jo 5,000
Purity 99+ % R,f.
A S
2-(a-Naphthoxy)-N,N-
d1ethylprop1onam1de
1
2
3
4
5
6
7Z
AE
62-8452
3B
1
10
aju
au
0-CH-
O
CN(C2HS)2
4920 NAPTALAM, SODIUM SALT
Mel.Wt. 313
UM Herblc.
IPM ca 1770
Purity 94.95 % R.I.
C18H12NNao3
Sodium N-1-naphthylphthalamate
A t
1
2
3
4
3
6
AB
AJ
AC
53
58
64
25
6
4
1397
671
1
12
12
20
a
a
-
65
-------
Code Common Name Emp. Form.
Chemical Name
Structure
4940 NEBURON C,
.H^CKN.O l-(«-Butyl)-3-(3,4-di =
chl orophenyl ) -1 -methyl urea
o
,,, n
**"'*"' A B c D E F H-N-C-N-C4H9
UfA n6rblC.
LD50 11,000
Purity 99+ % Ref.
1
2
3
4
5
6
AL
WD
WD
WD
62
68
69
69
45/2
36
44
44
377
234
419
60
12
2
2,11
2
a
X
u
u
^^^3
1 )
Cl
5020 NITRALIN (Planavin) C, ,Hn qN,OfiS 4-(Methylsulfonyl )-2,6-
u la j D dinitro-N,N-dipropylaniline
0 ,N02
Mol.Wt. 345 -[ f—^
U,e Herbic.
L DM 2,000+
Purity 99. 5 g R.f.
A B C D E F
1
2
3
4
5
6
^
WD
AL
ZB
70
72
73
II
53/2
55/5
26
397
913
390
2,11
11
12
19
d,9
X
w
u
CH3-S-f >N(CH2CH2CH3)2
0 N02
5031 NITRAPYRIN (N-Serve TG) CgH-Cl.N 2-Chloro-6-trichloromethylpyridine
"" (and related chlorinated pyridines)
Mol.Wt. 231 f ^1
A B C D E F ||
Use nitrogen
Stabilizer
IDjo 1,230
Purity 99 % Ref.
1
2
3
4
5
6
2Z
2
acj
Cl C^^-N^^
3 C'
5040 NITROFEN (TDK) C-.-H-.Cl.NO, 2,4-Dichlorophenyl-
" p-nitrophenyl ether
Mol.Wt. 284 ff \ // \
A B C D E F CK V-O-C V-NO?
u«« Herbic.
1 °50 3,580
Purity 99 % „.,.
1
2
3
C
AL
WD
75
76
II
58
129
1015
309
2,12
2,11
2
af
e
u
\ / \ /
5060 4-NITROPHENOL
Mol.Wt. 139
Ui« Parathion Derivat.
10,0 75
Purity 97 % R.f.
C6H5N03
DO
i
2
3
4
5
6
A
AJ
AJ
AD
AL
74
71
73
73
74
6,A,(2K
19 M
21
9/3
57
758
295
134
1288
2
2
2
2
2
m
0
m
m
m
66
-------
Code Common Name Emp. Form. Chemical Name Structure
5080 Trana NONACHLOR C-inHi;c1Q l-eax>, 2-endo ,-3-axo
4,5,6,7,8,8-Nonachloro-
Sa^J^a-tetrahydro-A,?- (
roethanoindane y
Mol.Wt. 444
Uta Compon. of
tech. chlordane
LDjo 500
Purity 100 X gtf
5136 NORFLURAZON (Evital) C]
Mol.Wt. 304
Us* Herbic.
IDso 9,300
Purity 98.5+% R.f
5148 ORYZALIN (Surflan) C1
Mel. Wt. 346
Use Herbic.
LDjo 10,000+
Purity 99.5^ Ref
5176 OXADIAZON (Ronstar) C]
Mel. Wf. 345
Uie Herbic.
I.DSO 8,000+
Purity 99 % Ref.
5186 OXAHYL (Vydate) C7
Mol.Wt. 219
n Nematoc. &
Insectic.
L Djo 5.4
Purity 99+ % Ref
A B C D E F
1
2
3
4
5
6
C
I
2
X
v-A
*"^^Yy'
Li_( *a
*
?HqClF,N,0 4-Chloro-5-(methylamino -2-
(o,a,a-tr1f1uoro-m-tolyi)-3-
- (2H)-pyridazinone
CF3
A B C D E F
1
2
3
4
5
6
7M
2
egu
,H10N,0,S 3,5-Dinitro-N4,N4-
^ 1B * ° dipropylsulf anil amide
A B C D E F
1
2
3
4
5
6
3E
AJ
76
24
617
2
2
acu
au
o^ vci
o N°2
H2N S— b. /)— N(C3H7)2
A ^M^
NO2
,H,oClnN20, 2-tert-Butyl-4-(2,4-
dichloro-5-isopropoxyphenyl )-
4-1 ,3,4-oxadiazolin-5-one
LJ
A B C D E F
1
2
3
4
5
6
71
Z
ajo
P
(CH3)2C-O C'v^O^/CfCHjlj
Cl
H,,N,0,S Methyl N',N'-dimethyl-N-
• ' [(methylcarbamoyl)oxy]-l-thio-
oxamimidate
A B C D E F
1
2
3
3A
AJ
76
24
263
4
4
a
aju
0 OH
, . II II 1
(CH5)2N-C-C=N-0-C-N-CH3
SCH3
67
-------
Code Common Name Emp. Form. Chemical Name
5187 OXAMYL OXIME CKH1nN,0,S Methyl N'N'-dlmethyl-N-
0 u * l hydroxy-l-th1ooxam1m1date
Structure
Mol.Wl. 148
U»» Oxamyl Derlvat.
1050 Very toxic
Purity 99+ % R«f.
A B
E F
O
(CH3)2N-C-C-N-OH
1
2
3
4
5
6
See
5186
5200 OXYCHLORDANE
MoUWl. 424
UM Chlordane Metabol.
LDM 457
Purity 98+ % R.f.
C1QH4C180
l-eso,2-endo-4,5,6,7,8,8-Octa-
chloro-2,3-sco-epoxy-2,3,3a,4,
7,7a-hexahydro-4,7-methano1ndene
1
2
3
4
5
6
AD
AD
AJ
AD
AD
AJ
70
71
72
72
73
73
5
5/6
20/2
•7/1
lb/3
21/6
521
521
395
33
208
1099
20
2,3
6
2
2
2
1
jou
j
X
jo
X
5220 OXYDEMETON METHYL C6H15°4PS2
Mel. Wt. 246
Un Insectlc.
I DJO 70
Purity 96 % R.f.
S-[2-(ethylsulf1nyl)ethyl]-
0,0-d1methyl phosphorothioate
1
2
3
4
5
6
BA
AL
BA
WD
WD
AD
67
69
69
69
70
71
92/1092
52/1
94/1122
44/2
48/3
6/1
170
157
805
414
468
55
11
4
11,
17
11
7
4
a
a
X
X
a
a
4800 OXYTHIOQUINOX
(Morestan)
Mel.Wt. 234
Uu H1t1c.
LDM 3,000
Purity 98.5%
C,,,H,N,OS,
10 b ' i
6-Methyl -2-0X0-1 ,3-dUMolo
[4.5-b]qu1noxal1ne
1
2
3
4
5
6
AC
GH
JC
AL
AL
67
68
69
69
71
5
20/2
18/11
52/1
54/5
277
550
1344
151
1122
12
2
2
11
17
2
w
de
X
t
de
5240 PARAQUAT DICHLORIDE
(Gramoxone)
Mol.Wt. 257
Ui* Herblc.
LDW 150
Purity 100
R«f,
A B
1.1'-Dimethyl-4,4'-b1'
pyrldlHum dlchlorlde
1
2
3
4
5
6
L
AJ
AJ
AL
AD
WD
74
74
74
75
76
II
22
22
57
14
125
863
79
202
1015
439
12
3
12
12
Ml
2
tg
u
tu
tu
e
e
CH,-I
+-CH:
2CI"
68
-------
Code Common Name Emp. Form.
Chemical Name
524S PARATHION ETHYL
Mol.Wl. 291
Use Insectic.
L D50 3-30
Purity 99+ X
Ref.
0,0-Di ethyl-0-p-ni tro=
phenyl phosphorothioate
1
2
3
4
5
6
A
C
AJ
BA
AL
AL
77
69
72
74
74
»B,8A,10A
II
17
97
57
57
1066
378
930
1033
4
12,
15
3
2
3,4
4
tv
idej
b
ad
de
t
Structure
s
-P(OC2HS);
«80_ PARATHION METHYL CgH^NOjPS 0,0-Dimethyl 0-p-nitro-
phenyl phosphorothioate
Mol.Wl. 263
USA Inssctic.
I DSO 9-25
Purity 99+ % „„,.
A B C D £ F
1
2
3
4
5
6
See
5245
0-P(OCH3)2
.5251.
PARINOL (Parnon)
C18H13C12NO
Mol.Wt. 330
Use Fungic .
LDso 5,000
Purity 99.5+ % R»f.
A B C D E F
1
2
3
4
5
6
OH
Cl
Cl
5280_ PCNB (Ouintozene)
Mol.Wt. 295.5
U»e Fungic.
LD50 12,000
Purity 98+ %
Pentachl oroni trobenzene
R.f.
1
2
3
4
5
6
c
kj
BA
\l
HD
ID
67
72
72
74
74
II
15/4
97/1154
55/4
11/6
93/1
648
378
794
567
91
2,12
15
2
2
2
2
2
eg
aef
u
de
c
u
a
5260 PCP (Pentachlorophenol)
Mel. Wl. 266
Herbic S
Uu
Wood Preservat.
L Dso 125-210
Purity 99+ %
R.f.
2,3,4,5,6-Pentachlorophenol
1
2
3
4
5
6
\
AC
AJ
BG
AD
AL
77
67
69
70
73
74
5A(3b,4a
5
17
4
10
57
313
871
533
57
389
2
20
2
5
2
2
Imt
...
ktu
jt
j
t
69
-------
Code Common Name Emp. Form.
Chemical Name
Structure
5300 PEBULATE (Tlllara) C10H,.,NOS S-Propyl butylethylthiocarbamate
/-)
Mol.Wt. 203 V
Ut» Herbic.
10,0 1.10°
Purity 99+ * Ref.
5331 PENOXALIN (Prowl) C,
A B C D E F
1
2
3
4
5
6
C
II
6
adf
CH3(CH2)2S-C-N(CH2)3CH3
CH2CH3
,HnQN,0. N-(l-Ethylpropyl)-3,4-di=
methyl-2,6-dinitrobenzenam1ne
i"3
Mel.Wt. 268 ^\^CH3
ABCDEF r I
UM Herbic.
L Dso 1 ,250
Purity 99.5 % Ref
1
2
3
4
5
6
II
2
be
I. 1^
2 \^ NOj
NH-CH2-CH3
CjHj
5366 PERFLUIDONE (Destun) C14H1PF.,NO,S., 1 ,1 ,1-Trifluoro-N-
[2-methyl-4-(phenylsulfonyl )
phenyl ]methanesulfonamide
Mel.Wt. 379
U« Herbic.
LDso 920 (mouse)
Purify 100 " Ref.
5400 PHENKAPTON C,
A B C D E F
1
2
3
4
S
6
4Z
2
gu
aSO2— ^ V-NHSO2CF3
\=^
CH3
.H^Cl-O.PS, 0,0-D1ethyl S-(2,5-
di chl orophenyl thi omethyl )
phosphorodithloate
S-CH2-S-P(OC2H5)2
ABCDEF ri ^W S
Us* Acaric.
I DM 65-182
Purity 98+ % R.f.
1
2
3
4
5
6
BA
BA
67
69
92/1092
94/1117
170
275
11
4
a
t
1
L. ^^JL^-|
5410 PHENMEDIPHAM C1,H.,N,0. 3-Methoxycarbonylam1no=
(Betanal) 161624 phenyl N- (3 '-methyl phenyl)
carbamate _
Mol W, 300 rf~\ ° 1 XT-^
''..,. ABCDEF Q\ >-0-C-N-f \)
UM Heroic .
LDso 8,000+
Purity 99+ % R,f.
1
2
3
7Q
!H
70
10/4
340
10
10,
12
f
a
If r~^ \ /
CH3-0-C-N-H CH3
70
-------
Code Common Name Emp. Form.
Chemical Name
Structure
5420 PHENOTHIAZINE CpH^NS Dlbenzo-1 ,4-thiazlne
Mol.WI. 199 «##?XV^SX/^s
T .. ABCOEF 1 T T 1
Utt jnsectic.
L DSO 5,000
Purily 99.5+j Ref.
1
2
3
4
5
6
B
/U.
69
33.086-
.092
52
162
12
12
c
a
t^ ^^ JL *sj
^i/^N-^X^
H
5680 PHENYLMERCURIC ACETATE CqHRHgO, DO
(Common name PMA)
Mol. Wt. 337 f, :\ O
U» Fungic.
10,0 16-60
Purily 97 % Ral.
ABC 0 E F // ^ ,, ^ jl ^u
1
2
3
4
5
6
l\
AB
71
13B
43
950
13
t
k
v V^ng w \_ v_n3
\ /
5460 PHENYLMERCURIC BORATE C^BHgOj DO
Mol.WI. 339
Ut« Fungic.
I DSO <10°
Purily 97 % Ref.
5480 PHENYLMERCURIC C,
CHLORIDE '
1
2
3
4
5
6
A
JE
BA
74
68
69
13B
14
94
131
143
13
10
21
t
a
cfj
/ \-Hg-O-B(OH)2
\=/
HjClHg DO
Mol.Wt. 313 f/ ^
»«• Fungic.
LDjo 60
Purity 100 % R«f.
A B C D E F
1
2
3
4
5
6
See
5680
Hg-CI
5485 PHENYLMERCURIC CfiHsHgOH DO
HYDROXIDE
Mol.Wt. 295
"»• Fungic.
LDso <100
Purity 94 % R.f.
A B C D E F
1
2
3
4
5
6
•
See
5680
/ \HgOH
\=y
-------
Code Common Name Emp. Form.
Chemical Name
Structure
5487 PHENYLMERCURIC CfiH,-HgI DO
IODIDE
Mol.Wt. 405 // \
R,,n.nt ,„ |to A B C D E F (f \_Hn I
Ufa KeagenL in rig
method
L D5o -—Toxic
Purity 36 % Ref.
1
2
3
4
S
b
See
5680
\=/
5490 PHENYLPHENOL C1?H10° " 0-Phenyl phenol
(Dowicide 1)
OH
Mol.Wt. 170 ^x\ A.
ABC D E F f^>r^>l
Uie Acaric. S
Fungic.
LD50 2,480
Purity 98 % R«*.
5500 PHORATE (Thimet) C-
1
2
3
5
6
C
BA
AL
AL
AL
WD
70
71
73
75
76
II
95
54
56
58
125
490
975
299
1015
439
12
12
11
12
2,1'
2
def
i
de
b
e
e
MI y
H170,PS, 0,0-Diethyl S-[(ethylthio)=
methyl Jphosphorodithioate
Mol. Wt. 260 u
U«e Insectic.
I DSO 1-5
Purity 93-94* % R.f.
*Secondary Standard
A B C 0 E F
1
2
3
4
5
6
C
AJ
AL
AD
AP
AL
67
69
69
70
74
II
15
52
4
63
57
192
1231
224
52
1033
3,4
2
4
4
9
4
ajo
dc
bcon
j
u
t
(C2H50)2P-S-CH2-S-C2H5
5501 PHORATE, OXYGEN ANALOG C7H170?PS,, 0,0-Diethyl S-ethylthio=
(Phoratoxon) methyl phosphorothioate
o
M"'WI' 244 A B c D E F (C2H50)2P-S-CH2-S-C,H<
Use Prorate derivat.
LD50
Purity — % Ref.
5502 PHORATE SULFOXIDE
1
2
3
4
5
6
C7H170,PS,, 0,0-Diethyl S-ethylsulfinyl =
methyl phosphorodithioate
0
Mol.Wt. 260 • • "
u" Phorate derivat.
LDso
Purity ... % Ref.
A B C D E F
1
2
3
4
5
6
(C2H5q2 P-S-CH2— SO-C2H5
72
-------
Code Common Name Emo. Form. Chemical Name Structure
5520 PHOSALONE (Zolone) C, ..H, RC1 NO. PS., 0,0-D1ethyl S-(6-chloro-
•* l<: lb * l benzoxazolon-3-yl)methyl
phosphorodHMoate ^
Mel.Wt. 368
UM Insectlc.
ID jo 135
Purity 99.5+ * R.f.
ifiin PHOSFOLAN (Cyolane) C-,
Mel.Wt. 255
UM Insectlc.
I DM, 8.9
Purity 99.5+% R.f.
4000 PHOSMET (Imldan) C,
Mel.Wt. 317
UM Insectlc.
I DJO 147
Purity 99.5+ * R.f.
A B C D E F
1
2
3
4
5
6
C
AO
71
II
19
742
2,3
11
e
e
H,.NO,PS, 2-(D1ethoxyphosph1nyl*
14 3 * 1mfno)-1,3-d1th1olane
A B C 0 E F
2
3
4
S
6
L
0 N-CH2S-P(OCjHs)2
\J
Cl
|^Sx|=N-p'-(OC2H5)2
, H, jNO.PS, 0,0-D1methyl -S-phthal 1m1-
domethyl phosphorodlthloate
A B C D E F
1
2
3
A
C
AC
AJ
At
67
68
CO
II
5
16
C9
257
796
C99
M
4
9
bej
a
r^V^V *? T
I 1 N-CrS-P(OCH3)2
O
4001 PHOSMET OXYGEN C11H,,NO,PS N-(Mercaptomethyl)phtha!1m1de
ANALOG II u 5 S-(0,0-d1methyl phosphorothloate)
Mel.Wt. ""
U,t Phosmet derlvat.
I DM
Purity 92 % R.f.
A B C D E F
1
2
3
4
5
6
r^NA " °
1 1 N-CrS-P(OCH3)2
^I';i^'^vSf H
0
55BQ PHOSPHAHIDON ClnH10ClNO,;P 2-Chloro-2-d1ethylcarbamoyl-
"^^ (Dlmecron) ' 1 -methyl v1 nyl dimethyl phosphate
Mel. Wt. 300
UM Insectlc.
1 DJO 15-33
Purity 97+ * R.f.
A B C D E F
1
2
3
C
ZD
71
II
37
All
12,
207
deh
CHO ?0? ?
0- -C- -N(C2H5)2
73
-------
Code Common Name Emp. Form.
Chemical Name
Structure
5600 PICLORAM (Tordon)
Mol.Wt. 241.5
Use Herbic.
LDjo 8,200
Purity 99 %
Ref.
4-Amino-3,5,6-tri=
chloropicolinic acid
1
2
3
4
5
6
AJ
BA
AC
ZA
WD
67
67
67
70
70
15
92
5
23
53/2
469
371
507
323
367
2
2
20
2
2
c
au
—
tu
b
5640
PIPERALIN (Pipron)
C.-.rUCOO, 3-(2-Methylpiperidino)propyl-
'" "' 3,4-dichlorobenzoate
Mol.Wt. 330
U,e Fungi c.
LDM 2,500
Purity 98-99 % Ref
A B C Off
1
2
3
4
5
6
5620 PIPERONYL BUTOXIDE ClqH,nO,-
Mol. Wt. 338.5
Uio Synergist
lD5o 7,500
Purity 97.5-98 % Ref.
d-(2-(2-n-Butoxyethoxy)ethoxy)-
4,5-methylenedioxy-2-propyltoluene
1
2
3
4
5
6
1
ZG
AJ
ZC
AB
D
69
71
72
75
II
62
19/1
-
47/4
414
192
293
674
12
10
12
20
3
21
c
i
c
—
fo
ch
CH3(CH2)27=vCH2-O(CH2)2O(CH2)2O
\ / H9C4
O O
V
5632
PIRIMICARB (Pirimor) cnH18N4°2
2-(Dimethylamino)-5,6-dimethyl-
1 "t~yy\ Jiuiu \\\y \ u in it: LI 17 1 1,
Mol. Wt. 238
A B C D E F
Use Aphic.
ID,,, 147
Purity 99+ % Ref.
1
2
3
4
5
6
41
9
a
5642 PIRIHIPHOS ETHYL C11H-.N.,0,PS 0,0-Diethyl 0-(2-diethy
(Primicid) amino-6-methylpyrimidin
4-yl ) phosphorothioate
Mol.Wt. 333
ABC D E F
Use Insectic.
LDSO 140-200
Purity 100 % Ref.
1
2
3
4
5
6
41
4,y
au
N(CH3)2
74
-------
Code Common Name Emp. Form.
Chemical Name
Structure
5643 PIRIMIPHOS METHYL C
(Actellic)
,H,nN,0,PS 0,0-Dimethyl 0-(2-diethyl=
1 'u J J armno-6-methylpynmidin-
4-yl) phosphorothioate
L.n3
Mol.Wt. 305 /W
ABCDEF c [ ™
Use Ins6Ct"ic,
LDso 2,050
Purity 100 % Ref.
1
2
3
41
ARA
74
11/1
17
4,9
10
ajol
c
|| I I
CH3O)2P-Ox\Ni^N (C2H5
POLYCHLORI MATED BIPHENYLS
5700
AROCLOR 1016
Polychlorinated biohenyl with
41.5* Cl
Mol.Wt. 257.5
A B C D E F
Use Industrial
LDso 2,300
Purity 41.5* % Ref.
* °L n
h L, ]
5701 AROCLOR 1221 C
1
2
3
4
5
6
A
AB
AD
AO
AL
AL
77
70
71
73
73
74
9(A-F)
42
6
21
56
57
1483
377
87
188
576
2
2
2
2
5
2
jotu
V
t
.1
k
K
k
oHn ocli 9 Polychlorinated biphenyl with
2 8.8 1.2 2n C1
Mol.Wt. 196
A B C D E F
Use Industrial
LDjo 3,980 (undiluted)
Purity 21* % Ref.
* % Cl
1
2
3
4
5
6
See
5700
5702 AROCLOR 1232 C12H8 ^C}} g Polychlorinated biphenyl with
Mol.Wt. 219
ABC D E F
Use Indus tri a.1
I D;0 4, "70 (undiluted)
Purity 32* % Ref.
* ?! Cl
1
2
3
4
5
6
See
5700
75
-------
Code Common Name Emp. Form. Chemical Name
Structure
5703 AROCLOR 1242 C,,H, 0C1, . Polychlorlnated blphenyl with
•.•At Xfm \£ rj.y J. 1 Apae pi
Mol.Wt. 258 // \ // \
A B C D E F \ / \ \/
Ui« Industrial
1 DM e>650 (undiluted)
Purity 12* * «•'•
* * Cl
1
2
3
4
5
6
See
5700
\^—J V "'.V\
3.1
5704 AROCLOR 1248 C12H6 ^Ij g Polychlorlnated blphenyl with
Mol.Wt. 289 / \ // V>
A B C D E F \ ) \ \J
Uu Industrial
L DJO 11,000 (undiluted)
Purity 48* % R«f.
* % Cl
2
3
4
5
6
See
5700
CI3,
570£ AROCLOR 1254 C12H5C15 Polychlorlnated blphenyl with
Mel. Wl. 326 // ^. // ^.
U I 1 L M A B C D E F <( V (( 0>
U»« Industrial
I DJO 11,900 (undiluted)
Purity 54* * R.f.
* * Cl
2
3
4
5
6
See
5700
^^Clj
5706 AROCLOR 1260 C,,H- ,C1, , Polychlorlnated blphenyl with
••^•^^^ it j . / D . j cnt n
Mol.Wt. 371 /~\ /~~\
A B C D E F f V— " x^
U«» Industrial
lDso 10.000 (50* sol.
in corn oil)
Purity 60* % R.f.
* % Cl
2
4
i
6
See
5700
\ / \ Y
'' " "^ *•— ' X^ti
'4-3
.'J7n7 AROCLOR 1262 C,,H, ,C1. „ Polychlorlnated blphenyl with
l£ J.£ O.o rna »,
D£% U 1
Mol.Wt. 388 f. — ^ f. \
A B C D E F // \s II VV
Ui. Industrial
,_ 11,300 (50% sol.
lBio 1n corn oil)
Purity 62* % R.f
* * Cl
1
2
3
4
5
6
See
5700
\ / \ v
76
-------
Code Common Name Em p. Form. Chemical Name
Structure
POLYCH LORI MATED NAPHTHALENES
"i7?n HALOWAX 1000 C,,,H, -rCl, i * Polychlorinated naphthalene
I U o . / 1 . J . .i *u
-------
Code Common Name Emp. Form. Chemical Name
Structure
5724 HALOWAX 1051 ClflHn ,C17 Q Pol /chlorinated naphthalene
IU "•' '-3 with 70% Cl
Mol.Wt. 400
Us* Industrial
IDjo
Purity 70* % R.f
* % Cl
A B C 0 E F
1
2
3
4
5
6
CO0-
5725 HALOWAX 1099 C,.H. -Cl- „ Polychlorlnated naphthalene
-"**- IU n.t J.8 Wlth 52% C1
Mol.Wl. 258 f| if— l—ri
ABC 0 E F || J -T-UM
Uft industna I
IDjo
Purity 52* % R,f.
* « Cl
1
2
3
4
5
6
\^\$5^
5728 POTASSIUM AZIDE (Kazoe) KM, Potassium azide
(See 6172-NaN3)
MOI.WI. si.i _ K— N=N=N
Heroic., Funqic. ,
UM Nematoc., Insectic.
I Dso 60-80
Purity 94-99% „.,.
5731 POTASSIUM DIETHYL DI=
THIOPHOSPHATE (KDEDTP)
A B C Off
1
2
3
4
5
6
7A
12
au
C4H1002PS2K Do
S
Mol.Wl. 224 I
UM Orqanoohosphorous
derivative
ID*, ...
Purity % ••*•
1
2
3
4
S
6
A
77
6.A,(2),
(a)
4
m
K;2ns
-------
Code Common Name Emp. Form.
_5733
Chemical Name
Structure
POTASSIUM DIMETHYL DI» C,H,PS,,K Do
TH10PHOSPHATE (KDMDTP)
Mol.WI. 196 §
Orqanophosphorous
u" derivative
1 DJO
Purity * R.f
ABC DEF , ,11
1
2
3
4
5
6
See
5731
ICH3U;2 P — 5— K
5734 POTASSIUM DIMETHYL C,HC0,PSK
THIOPHOSPHATE (KDMTP)
2n6"3r
DO
Mel.Wl. 180
ABC DEF
5739
•J7afi
5752
Use urganupnuspnorous
derivative
Purify % R.f.
PROCYAZINE (Cycle) C]
Mol.Wt. 252
Uu Herblc
1 DJO 362
Purity 98+ * R.f.
1
2
3
4
5
6
See 5731
i,t_n3(j/2 r — u — K
nH. ,C1 N, 2- ( (4-Chl oro-6- (cycl opropyl=
am1no)-l,3,5-tr1a2in-2-yl)am1no)-
2-methyl propionitrlle
A
A B C DEF krx^ "^^K,
1
2
3
4
5
6
1 I
r\>_NHji J-NH-C (CH3)2
^^^ ^ CN
PROFLURALIN (Tolban) C. .H...F-N-0. N-(Cyclopropyl methyl )-o,o,a-
14 15 3 3 4 tr1fluoro-2,6-d1n1tro-M- .
propyl-p-toluid1ne P\^
I ^\. ^11 1 1 f~ t i
Mai. Wl. 346
Ui. Herblc.
LD50 2,200
Purity 99 % R.f.
PROMECARB C
(Carbamult)
Mol.Wt. 207
Use Insectlc.
L DJO 78-90
Purity 98 % Re«.
A B C DEF
1
2
3
4
5
6
^N^^NO,
T"^
CF3
,H,,NO, 3-Isopropyl-5-methylphenyl
L " ^ methyl carbamate
CH(CH3)2
V— A ° H
ABC DEF r^\ II 1
1
2
3
^
BE
AL
AL
?n
70
73
74
I
56/3
57/3
197
713
570
12
2
3
1
J
a
ad
a
^ /)-O-C— N— CH3
CH3
79
-------
Code Common Name Emp. Form. Chemical Name Structure
5760 PROMETON (Pramltol) C,nH10N,0 2,4-B1s(isopropylamino)-
lu ls b 6-methoxy-l,3,5-trtazine
OCH3
Mel.Wl. 225 t.ii^^
ABC D E F ,, V W ...
Use Herbic.
L DM 2,980
Purity 99+ % R«f.
1
2
3
4
5
6
ZJ
zo
AJ
69
70
74
17
32
22
309
371
139
19
20
2
d
-.
f
V L II 7
(CH3)2C-NA^Nx^AN-C(CH3)
H H
5780 PROMETRYN (Caparol ) ClnH1QN,S 2,4-B1s(1sopropylam1no)-
-*"**• r 10195 6-(methyltMo)-l,3,5-tr1az1ne
SCH3
Mel. Wt. 241 H^^t4
UM Herbic.
I DM 3,800
Purity 99+ * R.f.
A B C D E F
1
2
S
6
C
AJ
65
II
13/2
120
6,12
10
ijot
X
Hi II H
(CH } C— Kl'^. .xNsI— rfru
^ ^z Y N i ~^t-l"|3
H H
4090 PRONAHIDE (Kerb) C,2H,,C12NO N-(l ,1 -Dimethyl propynyl )-
3 , 5-di chl orobenzaml de
CL v _ u _.
Mel.Wl. 256 ff Yv T Y T 3
„ , . A B c D f f (/ \VC-N-C-C=CH
Us* Heroic,
LDso 8,350
Purity 96-99 % R.f.
1
2
3
4
5
6
AL
AJ
72
72
55
20
802
1233
2
2
jmn
op
W in3
***l
5820 PROPACHLOR C^H-.CINO 2l-Chloro-N-1sopropylacetan1Hde
(Ramrod) " 14
Mel.Wl. 212
Use Herbic.
IDjo 1,580
Purity 99.5+ * R.f.
A B C D E F
1
2
3
4
5
6
C
II
3
a
QCH(CH3)2
N-C-CH2CI
5840 PROPANIL (Roque) CjHgCljNO 3' ,4'-D1chloroprop1onan1l1de
Cl
Mel. Wt. 218
UM Herbic.
LDso 1,384
Purity 96-9* R.f.
A B C D E F
1
2
3
C
AI
Z>
65
70
II
3
18
7
464
2,1
2
2
cjop
0
cu
OO
(v|-C-C2H5
H
80
-------
Code Common Name Emp. Form.
Chemical Name
Structure
PROPARGITE (Omlte)
2-(p-tert-Butylphenoxy)cyclohexyl•
2-propynyl sulflte
Mel.Wt. 350.5
ABC D E F ^
Use Acarlc.
I DJO 2,200
Purity 92 % Ref.
1
2
3
4
5
6
C
AJ
AJ
AC
AD
71
72
73
73
II
19/5
20/1
7
12/6
894
59
355
641
6
4
4
20
16
eh
e
aeh
e
^
5800 PROPAZINE (Milogard) CoH.-ClN,. 2-Chloro-4,6-bU(1sopropyU Ino)
1.3.5-trlMlne
Mel. Wt. 230
ABC D E F
Use Herblc.
L 050 5,000
Purity 99 + % Ref.
1
2
3
4
5
6
C
AJ
AJ
65
74
II ~"
13
22
120
139
12
21
2
be
be
f
5860 PROPHAH (IPC) C10H13N02 Isopropyl N-phenylcarbamate
Mel.Wt. 179
A B C D E F
Use Herbl c .
LPso 4,250
Purity 100 * Ref.
1
2
3
4
5
6
AJ
GB
AL
69
73
76
17
9
59
1062
261
1061
12
12
8
a
a
de
JMSL. PROPOXUR (Baygon) C^H^NO, o-Isopropoxyphenyl
N-methylcarbamate
Mel.Wt. 209
A B C D E F
Use Insectlc.
LDso 100
Purity 98-99 % Ref.
1
2
3
4
5
6
A
AJ
AC
AJ
AL
AL
77
72
73
73
73
75
10A
20/6
7
17
56/6
58/3
562
1265
163
56
1319
562
2
2
20
2
2
2
t
a
-
a
u
aef
5882 PROTECT C12H6°3 l,8-Naphthal1c anhydride
Mel.Wt. 198
ABC D I f
Use Seed Protectant
I DJO 12,300
Purity 95-96 % R.f.
1
2
3
4
5
6
3Z
2
a
-S-O-CH,-C»CH
Cl
N
0-CH(CH3)2
9 ^
0-C-N-CH3
81
-------
Code Common Name Emp. Form.
Chemical Name
Structure
5905 PYRACARBOLID (Slcarol) C,,Hlc.O,, 2-Methyl-5,6-d1hydro-4H-
IJ pyrane-3-carboxyl1c anlllde
0 H
M.I.WI. 203 || | ^— ^
Uie Fungi c.
LDso 15,000?
Purity 98-99 % R.f.
ABC DEF ^rN_Y/\\
1
2
3
4
5
6
— \ /
v^ CH3
5925 PYRAZON (Pyramln) ClnHBClN,0 5-Am1no-4-chloro-2-
lu ° J phenyl-3(2H)-pyradazinone
q p
Mol.Wf. 222 ) 9 . ,
ABC D E F ... //\. /H\
Ute Herblc.
LDso 2,500
Purity 99+% R*'.
1
2
3
4
5
6
AF
BH
68
71
29/3
11/4
8993
257
21
19
u
X
INH2-V IN-V y
\=.f/ \=/
5932 PYRAZOPHOS (Afugan) C,.,H,,nN,01.PS 0,0-Diethyl 0-6-ethoxycarbonyl-
'^ 5-methylpyrazolo-[l,5a]pyrimi=
din-2-yl phosphorothloate
Mol.Wt. 349 °
Ute Fungic.
LDjo 1*0-632
Purity 95-96 S Ref.
ABC DEF C.H.O-C ^
1
2
3
4
5
6
WD
GE
4E
70
73
49/2
267/3
325
173
11
2,3
.
X
a
\s?- ^N N 5
H3C^N'^/xo— P(OC H5}2
5940 PYRETMRINS MIXTURE Standardized mixture of
— — pyrethrins I and II (Mixed
esters of pyrethrolone) „„,.,. „, 4 ,ompounj,
ICH )
Mol.Wt. — °-| \ ? s-\
j L. A B C D E F | >-«-c-
-------
Code Common Name Emp. Form.
Chemical Name
Structure
6022 RELEASE C.rl.ClN,0, 5-Chloro-3-methyl-4-
* * J ' nltro-lH-pyrazole
u
Mol.Wt. 162
Uu Plant Growth
Regulat.
IDso 350
Purity 99+ % Rel.
A B C D E F
1
2
3
4
5
6
AZ
74
87
321
2
e
/N
°Y N
Kl *^*H
02"^ 3
<"""= RESMETHRIN (SBP-1382) C.,H,,0, (5-Benzyl-3-furyl Jmethyl 2,2-d1=
J methyl -3- (2-methyl propenyl)
cyclopropane-carboxylate (approx.
70X ti>OTB, 30% ais Isomers) Y*
Mol.Wt. 338 CH3-C=CH o
A B C D E F K A _ ...
U»e Insectic.
LOso ca. 1,500
Purify 89-90 * Ref.
1
2
3
4
5
6
3Q
AL
75
58
1032
8
3
w
C
L^^^ - 2~li — il
CH3 O i~\-
5980 RONNEL CgH.CU&yS 0,0-Dimethyl 0-(2,4,5-tr(=
chloroDhenyl) phosphorothloate
s
Mol.Wt. 321.5 O-rV>rH *
. .. A B C D E F T KtOCH3'2
Use InSftCtl C >
1050 1.740
Purify 99+ X R«f.
6000 ROTENONE C,,
1
2
3
4
5
6
C
C
A
AL
AJ
AJ
77
74
75
76
I
II
88 ,-10/1
57
23
24
1033
840
1044
11
12
4
4
4
4
H.,0. l,2,12,12a, Tetrah
enyl-8,9-d1methoxy
pyrano-[3,4-b]furo
a
e
tv
p
P
J
r^f°
0^^
T
Cl
ydro-2-1soprop=
- 11] benzo=
benzopyran-6(6aH)one ^ ^-Q ^^~n3
Mol. Wt. 394 3 "l/^l o
A B C D i F \#^^«^ ^^
U«« Insectic.
IDso 132
Purity 100 S Ref.
1
2
3
4
5
6
AL
AN
AL
WO
69
70
73
74
52/1
8/5
56/6
95/2
182
276
1343
243
II
10
3
11,14
a
a
aw
X
d I II 1
^^TD'y^p rH2
1 — £(*" 2
CH3
6050 SALITHION C8H9°3PS 2-Methoxy-4H-l ,3,2-benzo=
dioxaphosphorine-2-sulf1de
Mol.Wt. 216 r^r\Y/'OXJJ _
U Irrctl A B C D E F |[ r~O-CH3
USV lIlbcLL 1 L .
L D50 91 (mouse)
puri(V S R.f.
1
2
3
JG
72
21
9
10
1
L n i
^^x'^X^/O
83
-------
Code Common Name Emp. Form.
Chemical Name
Structure
SIOURON (Tupersan) C14H20N2°
Mel.Wt. 232
U>e Herblc.
LDH 7,500*
Purity 99+ % Ref.
A B
l-(2-Methylcyclohexyl)-
3-phenylurea
1
2
3
4
5
6
AM
AJ
ZJ
AL
66
69
69
74
4/11
17/5
17/1
57/1
424
1004
31
60
2
11
19
3
X
u
u
w
SILVEX, ACID
[2-U.4.5-TP)]
Mel.Wt. 269.5
Ute Herblc.
IDM 650
iPurlty 99 %
C0H7C1,0,
y / i 3
Ref.
A B
2-(2,4,5-Tr1chlorophenoxy)=
proplonlc add
1
2
3
4
5
6
A
IA
AJ
AX
AL
77
71
72
72
76
10B
15
20
5
59
485
963
72
617
2
2
2
2
4
t
C
0
C
e
6UP SILVEX, ISOOCTYL ESTERS C,,H,,C1,0, 2-(2,4,5-Tr1chlorophenoxy)-
" " J J proplonlc acid, Isooctyl
6140
es ters \mi xea ) _..
VH3
Mei.wt. 381.5 O-CH-rnnr w
A B C D E F i *-" <~UOC8H,7
UM Herblc.
I DM 400-800
Purity 98.5-99 % R«».
1
2
3
4
5
6
See 6120
r*^^
Ci^sx
£
Cl
SILVEX, PROPYLENE C.,H,,C1,0. 2-(2,4-5-Tr1chlorophenoxy)-
GuYCOL BUTYL t. proplonlc add, propylene
rci
)
ETHER ESTERS qlycol butyl ether esters ru
C..H,,C1,0, (C3HS0 to CgHle03) VM3
M... wt. 383.5-500 22 ^ 6 § ^ ^ ™ ^ 9-CH-COO-(C3H6O)x-QH,
Uie Herblc.
L Dw 650
Purity 95+ % Ref.
1
2
3
4
5
6
See
6170
x^^^s-'CI
T Mixed esters
Cl
6160 SIMAZINE (Prlncep)
Mel.Wt. 202
Uie Herblc.
I DM 5.000
Purity 99+ %
C7H,,C1N,.
' u 6
Ref.
2-Chloro-4,6-b1s(ethyl ami no)-
1,3,5-tHazlne
1
2
3
4
5
6
C
AL
AJ
WD
AJ
AL
68
68
71
74
75
II
51
16
57
22
58
682
284
303
137
1015
12
3
12
11
2
2,11
acet
ctu
atu
f
«
84
-------
£ode. Common Name Emp. Form.
Chemical Name
Structure
6172 SODIUM AZIDE (Smite), NaN, Sodium Azlde
(See 2728 - KNj)
Moi.wt. 65.02 Na— N=N=N
U>. Herbic., Fungic.,
Nematoc., Insectlc.
1 °30 60-80
Purity 97-99 % Ref
1
2
3
4
5
6
7A
12
au
2820 SODIUM PENTACHLOROPHENATE CgCl.NaO.H.O 2,3,4,5,6-Pentachlorophenol ,
(Dowlcide S) sodium salt, monohydrate
ONa-HjO
Mol.Wt. 306.5 1 '
Ui. Herbic.
IDX 210
Purity 92-96 % R.f.
1
2
3
4
5
6
AR
AL
AJ
BG
AJ
AL
66
69
69
70
73
74
31
52/2
17/4
4/8
21/2
56/2
742
294
871
533
295
389
21
2
2
2
2
2
e
Jim
ktu
kt
m
t
1 J
*'S^S» jS^ie
T *
Cl
2SOO SODIUM PHENVTPHENATE C-.-HoNaO.O o-Pheny? phenol , sodium salt,
(Dowldde A) monohydrate
Mol.Wt. 210 9^a'^2O
A B C D E F ^\ ^^
Us* Fungic.
LDjo 1,160
Purity 99 X R.f.
1
2
3
4
5
6
C
AL
71
II
54
See also
5490
975
12
11
def
de
I il~"r^ 1
L y 1 I
^/ ^s>-^
f,??t STREPTOMYCIN SULFATE C,,H,0N,0,,' D-Streptam1ne, 0-5-deoxy-2- (methyl ami no-a-
(Agr1-Strep) L-glucopyranosyl-(l*2)-0-5-deoxy-3-C-formyl-
,u ... a-L-lyxofuranosyl-(l*4)-N,N'-b1s(am1no=
3H25U4 imlnomethyl)-, sulfate(2:3)(salt)
Mol.Wt. 1457 I" i? VH "
A B C D E F HV H07 — ^N-c-NHj
Uc. Bacterloc.
LOw
Purity 75-78S R.f.
1
2
3
4
*
C
AL
JI
AL
70
71
72
II
53/1
11
55/4
54
133
714
19
19
3
17,1!
e
g
X
9
M'N-C-MNVOH
HjC-r-0-^ 3 H'sa
HOHjC 7-00
HO-( ) V
L HO-^ — — N-CHa
6240 STROBANE T TOXAPHENE
Mol.Wt. 379(average)
Ut» Insectlc.
L DSO 200
Purity 100*%
*Act1ve Ingredients
(average)
R.f.
Polychlorlnates of camphene,
plnene and related terpenes
1
2
3
4
5
6
C
AD
77
II
17/4
See 6740
456
12
2
g
X
85
-------
Code Common Name Emp. Form.
Chemical Name
Structure
6300 SULFOXIDE
Mol.Wt. 324.5
Use Synergist
L Dso 2,000-2,500
Purity 92-99 *
C10H,00,S
l8 /8 J
Rof.
l-Methyl-2-(3,4-methylened1oxy=
phenyDethyl octyl sulfoxide
1
2
3
4
5
6
GM
AL
64
47
264
11
21
cjop
X
6435 TECNAZENE (Fusarex)
Mol.Wt. 261
Uw Fungi c. &
Growth Regul.
100
Purity 99+ *
1 ,2,4,5-Tetrachloro-3-nitrobenzene
R«f.
NO2
1
2
3
4
5
6
41
2
at
'a
0020 TEMEPHOS (Abate)
Mol.Wt. 166
Uio Insectic.
LDjo 4,000
Purity 98.5+ %
C16H20°6P2S3
R,f.
O.O.O'.O'-Tetramethyl 0,0'(th1o-
d1-p-phenylene)d1phosphorothioate
1
2
3
4
S
6
AJ
AJ
AJ
wn
AB
66
67
69
71
71
14
15
17
59
43
152
1038
401
1053
12
3
11
3
16
aktu
t
t
t
tw
6540
TEPP
Mol.Wt. 290
JM Insectic.
Purity 42-44* %
'Formulation
C8H20°7P2 Tetraethyl pyrophosnhate
R.f.
A B
E F
1
2
3
4
5
6
AL
70
53
1036
3
de
6560 TERBACIL (Sinbar)
Mel. Wt. 217
Uto Herbic.
LD50 5,000-7,500
Purity 99+ %
CQH,,C1N,0,
a M i l
„.,.
3-(tei-t-Butyl )-5-chloro-6-
methyl uradl
1
2
3
4
5
6
C
AJ
AJ
AJ
AJ
68
76
77
77
II
16
24
25
25
54
1236
373
432
6
6
1
6
2
be
•J
c
m
e
H
I
86
-------
Code Common Name Emp. Form.
Chemical Name
Structure
6573 TERBUFOS (Counter) CJL.OJ'S, S-(((l ,1-Dlmethylethyl )th1o)methyl )
0,0-dlethyl phosphorodlthloate
Mel. Wt. 288
UM Insectlc.
IDM 9.2
Purity 97.5+% R.f.
s
AB C DEF /,-ii^DC/~LJCr- 1<~U \
1
2
3
4
5
6
6583 TERBUTHIURON (Spike) CQH,,N.OS N-(5-(l, 1 -Dimethyl )-l ,3, 4-th1a=
y '" * d1azol-2-yl)-N,N'-d1methylurea
Mel. Wl. 228
UM Herblc.
I DM 644
Purity 99.5+ % Ref.
A B C DEF
1
2
3
4
5
6
11 °
(CH3)3 C S N-C-NH-CH3
CH3
6589 TERBUTHYLAZINE C.H..C1N. 2-(teJ.t-Butylam1no)-4-chloro-
(Gardoprlm) * IB * 6-(ethylam1no)-l,3,5-tMaz1ne
M
Mel. Wt. 215
UM Herblc.
LDso 2,160
Purity 99+ % Ref
3980 TERBUTRYN (Iqran) C
Mol.Wt. 241
"«• Herblc.
lDso 2,100-2,900
Purity 98+ % R.f.
A B C DEF
1
2
3
4
5
6
"5C'~f **\-™-C*">
^^\
a
0^1 9^5^ 2- (t««t-Butyl ami no )-4- (ethyl=
am1no)-6-(methylth1o -l,3,5-tr1az1ne
A B C DEF
1
2
3
4
s
6
3740 TETRACHLORVINPHOS C,nH0C1.0.P trnn8-2-Chloro-l-(2,4,
(Gardona) iu a t t phenyl)v1nyl dimethyl
Mol.Wt. 366
UM Insectlc.
IDgo 4,000
Purity 99+ % R.f.
A B C DEF
1
2
3
C
AP
70
II
63
1355
9
2
e
n
S-CH3
1 ' |!f ^ rl
5-tr1chloro=
phosphate
CIHC=C-0-P(OCH3)2
clr^S
I 1
Cl
87
-------
Code Common Name Emp. Form.
Chemical Name
Structure
fifinn TETRADIFON (Tedion)
Mol.Wt. 356
U»e Hitic.
LOso 5,000
Purity 99 %
Ref.
4-Chlorophenyl 2,4,5-tri=
chlorophenyl sulfone
1
2
3
4
5
6
C
Al
AL
AL
63
73
76
II
46
56
59
177
296
209
6,12
6
20
2
de
de
—
de
fifiin TETRASUL (Animert)
Mol. Wl. 324
Ut» Acarlc.
LDjo 12,600
Purity 98+ %
C12HgCl4S
Ref.
S-p-Chlorophenyl 2,4,5-
trichlorophenyl sulflde
1
2
3
4
5
6
C
FB
JC
AL
JA
69
69
73
74
II
62/685
18/11
56
38/2
75
1344
296
279
2
!,17
2
20
1,11
e
t
X
—
X
6640
THANITE
Mel. Wl. 253
U»« Insectlc.
L DM 1603
Purity 82-86 %
C13HlgN02S Isobornyl thlocyanoacetate
Rof.
A B
1
2
3
4
5
6
AL
70
53/3
499
4
X
•O-(!i-CH2-S-CN
6660
THIABENDAZOLE
(Mertect)
Mol.Wt. 201
UM
3,100
IDso
Funglc. &
Anthelm1nt1c.
Purity 99 5+
Ref.
2-(4'Th1azolyl) benz1m1dazole
1
2
3
4
5
6
C
AZ
AJ
AL
71
72
72
II
84
20
55
272
1227
1239
14
12
I2.K
11,14
ef
e
e
eg
0570
THIOBENCARB (Bolero) C12H16C1NOS
Mol.Wt. 258
U»o Herblc.
I DM 1,903
Purity 99.5+ %
Ref.
S-(4-Chlorobenzyl)N,N-d1ethyl=
thlolcarbamate
1
2
3
4
5
6
JA
AW
21
71
74
35/8
1586
1161
4
4
2,4
u
cu
actu
:N(C2H5)2
-------
Code Common Name Emp. Form.
Chemical Name
Structure
6663 THIOFANOX (DS-15647) C0HlaN,0,S 3,3-D1methyl-l-(methylth1o)-2-
9 butanone O-(methylamlno)-
carbamoyl oxlme
O H
Mel.Wt. 218 II 1
UM Insectlc.
LDM 8.5
Purity 99+ % R,f
ABC D E F ,_,.. ^XN-0-C-N-CH3
1
2
3
4
5
6
ZU
AJ
75
23
963
4
4
afq
tu
atu
\\-i 13/3 v. v, v
XCH2— S— CH3
6665 THIOMETON (Ekatln) C.rU-O.PS, 0,0-D1methyl S-[2-(ethylth1o)-
b l5 t J ethyl] phosphorodlthloate
Mel.Wt. 246 j>
,,,..,,. ABC D E F (CH,0). P-S-C,H.-S -C.H.
wtv insect i c .
LD50 107
Purity 97.5 % R.f.
1
2
3
4
S
6
7M
3
u
6670 THIOPHANATE C,.rl1aN,O.S, 1 ,2-D1-(3-ethoxycarbony1-
1* IB * »* 2-th1oure1do)faenzene
^ I ?
Mel. Wf. 370 I^^N-NH-C-NH-C-O-CjHj
Use Funglc.
L DM 15,000 (mice)
Purity 92.93% *•'.
1
2
3
4
5
6
5Z
11
ade
^^X^ P"""i Sr '^n V ^^ * *
s o
6671 THIOPHANATE METHYL C.-H. .N.O,S, 1 ,2-D1-(3-methoxycarbonyl-
-**"- 12 14 4 4 2 2-th1oure1do)benzene
M...W..342 B D ^^-iNH-to-CH,
Use Funglc.
LOjo 3,514 (mice)
Purity 97 % R.f.
1
2
3
4
5
6
5Z
12
ade
^!^X-NH-C-NH-C-O-CHj
S 0
6680 THIRAM (Arasan) C6H12N2S4 Tetramethylthluram dUulflde
S S
Mol'Wt- 2.4° . A B c D E F (CH3)2N-(!:-S-S-£-N(CH3)2
Ute Funglc.
L DJO 780
Purity 99+ % „.,,
1
2
3
C
B
AL
69
11
I2:§ot
52
1226
12
12
4
cde
8
-------
Code Common Name Emp. Form.
Chemical Name
Structure
6740
TOXAPHENE
A mixture of chlorinated camphenes
of uncertain identity
Mol.Wt. Uncertain
Ute Insectic.
ID jo 90
Purity 67-69* %
* % Cl: total active
ingredients 100X
Ref.
1
2
3
4
5
6
A
C
AD
AL
BG
AL
AD
68
70
70
75
77
II
3
53
4
58
17/4
71
524
547
1015
456
12
2
2,1!
10
2,11
2
e
a
b
ktu
e
X
6770 TRIALLATE C10H16C13NOS
Mol.Wt. 305
A B
Use Herbic.
LDM 1,675-2,165
Purity 99.5+ % Ref.
S-(2,3,3-Tr1chloroallyl)di=
i sopropylthi ocarbamate
1
2
3
4
5
6
AJ
FB
WD
67
69
74
15
62
97
935
214
103
2
2
2
cu
t
u
o
|(CH3)2CH]2N-C-S-CH2CCI-CCI2
6777
TRIAZOPHOS (Hostathion) C1(]H16N303PS
Mol. Kit.
Uta
LDjo
Purity
313
Insectic.,
Nematoc .
82
94 %
Mitic.,
R<
0,0-Diethyl 0-(l-phenyl-lH-
l,2,4-triazol-3-yl)phos=
phorothioate
1
2
3
4
5
6
GE
4E
73
267/3
173
2,3
4
a
a
N — N
6780
TRICHLORFON (Dylox)
C4H8C13P04
Dimethvl (2,2,2-trichloro-l-
hydroxyethylJphosphonate
Mol.Wt. 257
Uu Insectic.
I DM 45°
Purity 98-99 %
Raf.
1
2
3
4
5
6
C
AJ
AO
AD
AO
AD
66
68
71
73
74
II
14/5
16/5
6/1
21/6
11/1
508
808
55
1095
78
2,6
2
11,17
4
4
4
ajo
adj
X
X
atu
j
(CH3O)2P-CH-CCI3
OH
6890 2,4,5-TRICHLOROPHENOL C,H,C1,0
(Dowicide 2) b * i
Mol.Wt. 197.5
Uia Funqic.
L DJO ca. 800
Purity 98 % Ref.
2,4,5-Trichlorophenol
1
2
3
4
5
6
AJ
72
20
963
2,6
0
90
-------
Code Common Name Emp. Form.
Chemical Name
Structure
6786 TRICLOPYR (DOWCO 233) C7H,C1,NO, 3,5,6-Trichloro-2-pyrid=
yloxyacetic acid
, ^-\
Mol. Wt. 256.5
Die Herbic.
L Dso 713
Purity 99.5 % R»f.
A B C Off
1
2
3
4
5
6
I 1 ?
CI"\N^^0-CH2-C -OH
6792 TRIDEMORPH (Calixfn) C19H3gNO 2,6-Dimethyl-4-tri=
decylraorpholine
Mol.Wt. 297.5 H3C^^O\^,CH3
U(« Funqic.
IDso 650
Purity 99+ X R,f.
6796 TRIETAZINE CQ
(Gesafloc)
A B C D £ f
1
2
3
4
5
6
U
H.,C1N, 2-Chloro-4-(diethylamino)-6-
10 5 (ethylamino)-l,3,5-triazine
ci
Mol.Wt. 230 ^
Use Herbic.
LDjo 2,830-4,000
Purity 99.5+ X R,f
6800 TRIFLURALIN (Treflan) C,
A 8 C Off
1
2
3
4
5
3N
3N
3
3
d
w
i 1
A /-i
C-THtNIH ^\ k , "^-' KI//^ LJ i
IN '^lV— Ofle Jo
,H1,F,N,0, tr,
-------
Code Common Name Emo. Form.
Chemical Name
Structure
6840 2,4,5-T, ACID C8H5C13°3 2,4,5-Tr1chlorophenoxyacet1c add
0-CH2COOH
Mol.WI. 255.5 _. J^
A B C 0 E F Cl^^^^
U» Herblc.
L DM 500
Purity 99+ % R.f.
1
2
3
4
5
6
WO
AI
BE
WO
M
A
71
71
72
72
74
77
57
1
3/4
69
22
10.B
303
23
371
204
453
11
2
6
2
2
2
tu
m
d
u
tu
t
^s/"CI
ir
Cl
6860 2,4,5-T BUTOXYETHANOL C14H,7C1,,04 2,4,5-Tr1chlorophenoxyacet1c add,
ETHER ESTERS mixed ether esters of butoxyethanol
and Isobutoxyethanol
f-\
Q
Mel. Wt. 355.5 OCH,CO(CH,),O(CH,lrH.
UM Herblc.
I DSO ca. 500
Purity 96-100 % R.f
A B C D E F
1
2
3
4
5
6
See
6840
r**S"a 9
JLjsni PCHjCOfCHjjOCHCHjCH,
a riTa 3
a^s
a
6670 2,4,5-T, BUTYL ESTERS C^rU-CUO, 2,4,5-Tr1chlorophenoxyacet1c
u 3 * add, butyl esters (mixed)
O-CH2-COO-C4H9
Mel.Wl. 312 ±.
.... ABC D I F Clvf^^ >,
Use Herblc.
LDM «. 50°
Purity 95-100 K R.f.
1
2
3
4
5
6
See
6840
^^^0
^T u
a
6880 2,4,5-T, ISOOCTYL C.-H-nCl-O, 2,4,5-THchlorophenoxyacetlc
ESTERS I0 " * * add, Isooctyl esters (mixed)
M.I.WI. 368 0-CH2-COO-C8H,7
H*v.H, ABC OIF r^^?^
Uit Herbl c .
1 DM ca. 500
Purity 98.5 % R.f,
1
2
3
4
5
6
See
6840
1
LJia
Cl
6886 2,4,5-T, PROPYLENE 1, C,«H,.C1,04 2,4,5-THchloroDhenoxy
GLYCOL BUTYL ETHER , r u n n ««t1c add, propylene
ESTERS k'18rl26LI3u5 olycol butyl ether esters n
Mol. Wt. 3925 (average) OCHjCO |(CH2)3OL'CH2)3(
.. u, ABC D 1 F ^^^. ft
Ux Herbi c.
1 DSO ca. 500
Purity 95-98 % R.f.
1
2
3
M
69
17
See also
6840
1168
6
In
|V >p-' X-l.2,3
CI'^vX
Cl
92
-------
Code Common Name Emp. Form.
Chemical Name
Structure
6895. 2,4,5-T-TRIETHYL- C,,H,nCl,0,N 2,4,5-Trichlorophenoxyacetic
AMINE SALT acid, triethylamine salt
Mol. Wt. 357
Use Herbic
L D50 50° (acid basis)
Purity 56-58U Kef.
*Formulation
A B
1
2
3
4
5
6
See
6840
OCH2COOH-N(C2H5)3
Cl
6900
4-(2,4,5-TB)
Mol. Wt. 284
Use Herbic.
L DJO 650
Purity 99+ %
C10H9C13°3 4-(2,4,5-TrichloroDhenoxy)=
A B
Re».
1
2
3
4
5
6
A
77
10, B
2
t
O(CH2)3CCOH
6920
2,3,6-TBA
2,3,6-Trichlorobenzolc acid
and related compounds:
2,3,6-TBA 60.65?, 2,4,6-TBA 2.6
C,H,C1302
2,4,5-TBA 26.3 Tetra and dichloro
Mol. Wt. 225 2,3,4-TBA 9.35 benzoic acids 1.
U» llerbl- ABC D E F
Uf0 nerDl c .
LDso ca. 750
Purity 90 % Ref
1
2
3
AJ
AL
WO
68
71
71
16/6
54/4
57/2
908
966
303
2
2.6
11
ac
efo
u
COOH
7001 .. VELPAR
3-Cyclohexyl -6-(d1methyl =
am1no)-l-methyl-l,3,5-
tr1az1ne-2,4-(lH, 3H)-dione
Mol.Wt. 252 1 1 A
Us* Herbic.
LDso 1,690
Purity 99 % R*f.
A B C D I f
1
2
3
4
5
6
3A
3
itu
f 7
0^\N^N(CH,i2
CH3
7020 VERNOLATE (Vernam) ClnH,,NOS S-Prdpyl N,N-dipropyl=
lUtl j_[_J L,_«4--
^-^-^~ tmocarDoina te
n
Mol.Wt. 203 H
Us* Herbic.
IDso 1,800
Purity 99+ % R*f.
A B C D E F
1
2
3
C
AJ
71
60
£t
ii
8
c
214
C-ST
b
12
4
tn
tg
a
cf
CH3(CH2)2-S-C-N(C3H7)2
-------
Code Common Name Emp. Form.
Chemical Name
Structure
7060
WARFARIN
Mel. Wt. 308
UH Rodentic.
L D50 323
Purity 98+ %
C19H16°4
Ref.
3-(a-Acetonylbenzyl)-
4-liydroxycoumarin
A B
1
2
3
4
5
6
BA
JC
67
69
92
18
192
943
12
15
X
X
7120
ZINEB
Mel. Wt. 276
Use Fungic.
I DM 5,200+
Purity 8°-87%
(polymeric)
Ref.
Zinc ethylenebisdithio=
carbamate
1
2
3
4
5
6
C
Al
At
AJ
67
71
72
II
50
54
20
1102
1120
967
12
12
12
2
X
a
ct
e
tj
-S-C-NH-CH,
CH2-NH-C-S-Zn-
S
7100
ZIRAM
Zinc dimethyldithiocarbamate
Mel. Wt. 306
Die Fungic.
LDjo 1,400
Purity 98+ %
Ref.
1
2
3
4
5
6
C
AL
AL
69
70
II
52
53
1226
1043
12
4
12
X
a
c
[(CH3)2N-C-s]2Zn
94
-------
Section I, b, A & B
COMPOUNDS DELETED FROM STOCK AND NAME CHANGES
All compounds in the repository stock are reviewed biennially to deter-
mine if they should be continued. Compounds are deleted if manufacturing is
discontinued or if, during a two-year period, we receive no requests for a
given compound.
A. The following 5 compounds listed in our 1976 Index have been deleted
in this edition for one of the above reasons:
BHC, Mixed Isomers
Chlorbenside
p,p'-DDD, olefin
Erbon
Nabam
B. The following compounds are listed by a different name than the one
given in our 1976 edition. This may be due to a common name being
assigned or to withdrawal of the old name to be replaced by another:
Benthiocarb to Thiobencarb
Metalkamate to Bufencarb
Perthane to Ethyl an
Stirofos to Tetrachlorvinphos
Strobane to Strobane T Toxaphene
Surecide to Cyanofenphos
Terrazole to Ethazol
Vendex to Fenbutatin-oxide
-95-
-------
Section I, b, C
LIST OF PESTICIDAL COMPOUNDS BY CHEMICAL NAME
We are presenting for the first time in the following pages an alpha-
betical list of the compounds described in Section I, a. The pesticide
chemist is often confronted with only a chemical name. It is sometimes
time-consuming to track down the common name from the chemical name because
of the structural similarities between many compounds, particularly those
in the organophosphorous class. As an example, formothion (3722) and
dimethoate (2420).
Formothion: 0,0-dimethyl S-(N-methyl-N-formylcarbamoylmethyl
phosphorodithioate
S 0 CH~
H II I 3
(CH30)2-P-S-CH2-C-N
CHO
Dimethoate: 0,0-dimethyl S-(N-methylcarbamoylmethyl) phosphorodithioate
S 0 CH0
il II i 3
(CH30)2-P-S-CH2-C-N
fl
-96-
-------
LIST OF PESTICIDAL COMPOUNDS BY CHEMICAL NAME
Code
No.
7060
3720
0100
0171
5925
0186
0140
4634
0200
5600
4156
0250
4180
0577
0580
6055
0740
1740
1780
1750
1860
5251
1920
2340
5760
5780
3802
0800
1188
0822
0860
0840
4190
4612
1681
5620
4220
0922
6589
3980
6560
6020
Chemical Name
3-(a-Acetonyl benzyl )-4-hydroxycoumar1n
3-(o-Acetonylfurfuryl)-4-hydroxycoumar1n
dl-2-Allyl-4-hydroxy-3-methyl-2-cyclopenten-l-one ester of dl -aia/trane-
2,2-d1methyl-3-(2-methylpropenyl)cyclopropanecarboxyl1c
2-Ami nobenzlmldazol e
5-Aro1no-4-chloro-2-pnenyl-3(2H)-pyr1daz1none
4-Am1no-5-chloropyr1daz-6-one
3-Am1no-2,5-d1chlorobenzo1c add
4-Am1no-6- [1,1 -dimethyl (ethyl )]-3-(methylth1o)-l ,2,4-tr1az1n-5(4H)one
3-Am1no-l ,2,4-tr1azole
4-Am1no-3,5,6-tr1chlorop1col1n1c acid
AimDnlum ethyl carbamoyl phosphonate
9,lO-Anthraqu1none
Arsenic add, lead salt
Benzam1do-oxyacet1c add
Benzole add, benzyl ester
(5-Benzyl-3-furyl )methyl 2,2-d1methyl-3-(2-methylpropenyl )
cyclopropane-carboxylate (approx. 70% trans, 30/6 oie Isomers)
Blphenyl
Bls(p-chlorophenyl) acetic add
2,2-B1s(p-chlorophenyl )-l ,l-d1chloroethane
2,2-B1s(chloropnenyl)-l,l-d1chloroethane and related compounds
2,2-B1s-(p-chlorophenyl)-l,l-d1chloroithylene
o,o-B1s(p-chlorophenyI )-3-pyr1d1ne methanol
1 ,l-B1s(p-chlorophenyl )-2,2,2-tr1chloroethane
1 ,l-B1s(p-chlorophenyl )-2,2,2-tr1chloroethanol
2,4-B1s(1sopropylam1no)-6-methoxy-e-tr1az1ne
2,4-B1s(1sopropyUm1no)-6-(methylth1o)-«-tr1az1ne
N,N-Bfs(pnospnonometnyl )glyc(ne
5-Bromo-3-««o-butyl -6 -methyl uradl
3- (4-Bromo-3-chlorophenyl ) -1 -methoxy-1 -methyl urea
4-Bromo-2,5-d1chlorophenol
0-(4-Bromo-2,5-d1cnlorophenyl) 0,0-d1ethyl phosphorothloate
0-(4-Bromo-2,5-d1cnloropbenyl) 0,0-d1n»thyl phosphorothloate
0,(4-Bromo-2,5-d1chlorophenyl) 0-methyl phenylphosphonothloate
3- ( p-Bromophenyl ) -1 -methoxy-1 -methyl urea
Butanedlolc add mono (2,2-d1methylhydraz1de)
d-(2-(2ra-Butoxyethoxy)ethoxy)-4,5-methylened1oxy-2-propyl toluene
2-{2-Butoxyethoxy) ethyl thlocyanate
N-tButoxymathylJ^-chloro-Z'.e'-dlethylocetanlllde
2- ( tert-Butyl ami no ) -4-chl oro-6- ( ethyl ami no ) -1 . 3 , 5-tr1 az 1 ne
2-(t«-t-Butylam1no-4-(ethylam1no-6-(methylth1o-l,3,5-tr1az1ne
3-ttrt- Butyl -5-chloro-6-methyl uradl
i-t«rt-Butyi-2-chlorophenyl methyl methyl phosphoroanldate
Coranon Name*
WARFARIN
COUMAFURYL
ALLETHRIN
BENOMYL OERIVAT.
PYRAZON
PYRAZON DERIVAT.
CHLORAMBEN
METRIBUZIN
AMITROLE
PICLORAM
KRENITE
ANTHRAQUINONE
LEAD ARSENATE
BENZADOX
BENZYL BENZOATE
RESMETHRIN
B1PHENYL
DDA-p.p1
ODD. p.p'
ODD. MIXED, TECH.
DDE, D.D'
PARINOL
DDT, p,p'
DICOFOL
PROMETON
PROMETRYN
SLYPHOSINE
BROMACIL
CHLORBROMURON
LEPTOPHOS DERIVATIVE
BROMOPHOS ETHYL
BRONOPHOS
LEPTOPHOS
METOBROMURON
DAMINOZIDE
PIPERONYL BUTOXIDE
LETHANE 384
BUTACHLOR
TERBUTHYLAZINE
TERBUTRYN
TERBACIL
CRUFOMATE
*The proprietary name will be used when there 1s no assigned common name.
-97-
-------
Code
No.
5176
4940
2416
2760
2566
3359
0480
3630
5160
0791
0926
6573
0980
6740
4640
1160
0570
6160
5800
0400
1615
5739
1140
1300
6796
5580
4160
0420
1552
3330
0407
5820
4631
5136
1316
6022
4340
4360
4380
4400
4420
Chemical Name
2-tert-Butyl-4-(2,4-dichloro-5-isopropoxyphenyl )-A -1 ,3,4-oxadiazolin-
5-one
1 - (rc-Butyl ) -3- ( 3 ,4-di chl orophenyl ) -1 -methyl urea
5-n-Butyl-2-dimethy1amino-4-hydn>xy-6-methylpyrimidine
2- (see-Butyl )-4,6-dinitro phenol
2-(se
-------
Code
No.
1512
2406
1820
1760
1840
1900
4760
4780
4747
2792
4751
1081
1425
1080
6630
6600
1480
5031
3740
6360
4185
7001
0230
5746
1280
0220
5420
2090
4860
0906
0820
2120
2040
2280
2300
2200
5380
2920
1380
1880
2180
2260
0460
Chemical Name
N ' - (3-Chl oro-4-roethyl phenyl )N ,N-dimethyl urea
N- ( (4-Chl orophenyl ) ami nocarbonyl ) -2 ,6-dl f 1 uorobenzami de
1 - (m-Chl orophenyl )-l - (p-chl orophenyl )-2 ,2-dichl oroethane
1 - (o-Chl orophenyl )-l - {p-chl orophenyl ) -2 ,2-di chl oroethane
1 -(o-Chlorophenyl )-l - (p-chlorophenyl )-2 ,2-dichl oroethylene
1 - (o-Chl orophenyl )-l - (p-chl orophenyl )-2 ,2 ,2-tri chl oroethane
3-(p-Chlorophenyl)-l,l -dimethyl urea
3- (p-Chl orophenyl ) -1 ,1 -dimethyl urea tri chl oroacetate
N-(4-Chlorophenyl)-2,2-dimethylvaleramide
4- (2-Chl orophenyl hydrazono)-3-methyl-5-isoxazo1 one
3- ( p-Chl orophenyl ) -1 -methoxy-1 -methyl urea
S-(p-Chlorophenylmethylthio) 0,0-d1ethyl phosphorothioate
2- [(p-Chl orophenyl )phenylacetyl]-l ,3-indandione
S-[(p-Chlorophenylthio)methyl] 0,0-diethyl phosphorodithioate
S-(p-Chlorophenyl)2,4,5-trichlorophenyl sulfide
4-Chl orophenyl 2,4,5-trichlorophenyl sulfone
N'-(4-Chloro-o-tolyl)-N, N-dimethylformamidine
2-Chloro-6-tr1chloromethyl pyridine (and related chlorinated pyridines)
Trans 2-Chloro-l -(2,4,5-trichlorophenyl )vinyl dimethyl phosphate
0-(4-Cyanophenyl) 0-ethyl phenylphosphonothioate
3-Cyclohexyl-6,7-dihydro-lH-cyclopentapyrimidine-2,4(3H,5H)-dione
3-Cyclohexyl -6- (dimethyl ami no )-l -methyl -1,3, 5- triazine 2,4(lH,3H)-dione
a-Cyclopropyl-a-(p-methoxyphenyl)-5-pyrimidinemethanol
N-(Cyclopropyl methyl )-a,a,ci-trifluoro-2,6-dinitro-N-propyl-p-toluidine
Decachl orooctahydro-1 ,3 ,4-metheno-2H-cycl obuta [cd] pental en-2-one
Diammonium ethyl enebisdithiocarbamate
Dibenzo-1 ,4-thiazine
1 ,2-Dibromo-3-chloropropane and related halogenated Cj hydrocarbons
l,2-Dibromo-2,2-dichloroethyl dimethyl phosphate
3,5-Dibromo-4-hydroxybenzaldehyde 0-(2,4-dinitrophenyl) oxime
3 ,5-Di bromo-4-hydroxybenzoni tri 1 e
Di-n-butyl phthalate'
S-(2,3-Dichloroallyl ) diisopropylthiocarbamate
1 ,2-Dichlorobenzene
1 ,4-Dichlorobenzene
2 ,6-Dichl orobenzoni tri 1 e
1 ,l-Dichloro-2,2-bis(p-ethylphenyl Jethane
2,4-Dichloro-6-(2-chloroani1ino)-l ,3,5-triazine
1 ,4-Dichloro-2,5-dimethoxybenzene
Dichloro diphenyl trichloroethane (mixt. of metabolites of ca.
80% p,p' and 20% o,p')
2,3-Dichloro-l ,4-naphthoquinone
2 ,6-Dichloro-4-nitroanil ine
2 ' ,5-Dichloro-4 ' -nitrosal icyl ani 1 ide ethanol amine
Common Name*
CHLORTOLURON
DIFLUBENZURON
ODD, m,p'
ODD, o,p'
DDE, o,p'
DDT, o,p'
HONURON
MONURON-TCA
MONALIDE
DRAZOXOLON
MONOLINURON
CARBOPHENOTHION OXYGEN ANALOG
CHLOROPHACINONE
CARBOPHENOTHION
TETRASUL
TETRAD I FON
CHLORDIMEFORH
NITRAPYRIN
TETRACHLORVINPHOS
CYANOFENPHOS
LENACIL
VELPAR
ANCYMIDOL
PROFLURALIN
CHLORDECONE
AMOBAM
PHENOTHIAZINE
DIBROMOCHLOROPROPANE
NALED
BROMOFENOXIM
BROMOXYNIL
DIBUTYL PHTHALATE
DIALLATE
DICHLOROBENZENE, ORTHO
DICHLOROBENZENE, PARA
DICHLOBENIL
ETHYLAN
ANILAZINE
CHLORONEB
DDT, MIXED (TECH.)
DICHLONE
DICHLORAN
CLONITRALID
-99-
-------
Code
No.
2940
3960
2980
2985
2990
3000
3020
3040
3060
3080
3100
3120
3140
2309
2740
4240
4496
5040
2306
2307
5840
1660
2308
2320
2721
6670
1610
1630
5520
1540
2035
1491
2220
5400
5642
2551
3420
4441
5932
5502
2720
1981
Chemical Name
2,4-D1chlorophenoxy»cet1c add
2,4-D1chlorophenoxyacet1c add, butoxy ethanol ether esters
2,4-D1chlorophenoxyacet1c add, butyl esters
2,4-D1chlorophenoxyacet1c add, ,d1ethanolam1ne salt
2,4-D1chlorophenoxyacet1c add, dlmethylamlne salt
2,4-D1chlorophenoxyacet1c add, Isobutyl esters
2,4-D1chlorophenoxyacet1c add, Isooctyl esters
2,4-D1chlorophenoxyacet1c add, Isopropyl ester
2,4-D1chlorophenoxyacet1c add, propylene glycol butyl ether esters
4-(2,4-D1chlorophenoxy) butyric add
4-(2,4-D1chlorophenoxy) butyric add, butyl ester
4-(2,4-D1chlorophenoxy) butyric add, Isobutyl ester
4-(2,4-D1chlorophenoxy) butyric add, Isooctyl ester
2-(2,4-D1chlorophenoxy)-prop1on1c add
3-(3,4-D1chlorophenyl)-l-d1methylurea
3-(3,4-D1chlorophenyl)-l-methoxy-l-methylurea
2-(3,4-D1chlorophenyl)-4-methyl-l,2,4-oxad1azol1d1ne-3,5-d1one
2 ,4-D1 chl orophenyl -p-n 1 trophenyl ether
aie-1 ,3-D1chloropropene
trana-1 ,3-D1chloropropene
3 ' ,4 ' -D1chl oroproplonani 1 1de
2,2-D1chloroprop1on1c add
3,6-D1chlorosal1cyl1c add
2,2-D1chlorov1nyl dimethyl phosphate
2,3-D1cyano-l ,4-d1th1aanthraqu1none
1,2-01 (3-ethoxycarbonyl-2-th1oure1do)benzene
2-(D1ethoxyphosph1nyl1m1no)-l,3-d1th1olane
2-(D1ethoxyphosph1nyl1m1no)-4-methyl-l,3-d1th1olane
0,0-D1ethyl S-(6-chlorobenzoxazolon-3-yl Jmethyl phosphorodlthloate
0,0-D1ethyl 0-(3-chloro-4-methyl-7-coumar1nyl )phosphoroth1oate
0.0-D1ethyl S-(2-chloro-l-phthal1m1doethyl)phosphorod1th1oate
0,0-D1ethyl 0-2,5-d1chloro-4-methylth1ophenyl phosphorothloate
0,0-D1ethyl 0-(2,4-d1chlorophenyl)phosphoroth1oate
0.0-D1 ethyl -S-(2,5-d1chlorophenylth1omethyl)phosphorod1th1oate
0,0-D1ethyl 0-(2-d1ethylam1no-6-methyl pyr1m1d1n-4-yl) phosphcrothloate
H3, N3-D1ethyl-2,4-d1n1tro-6-(tr1fluoromethyl)-l,3-phenylened1amfne
Dlethyl dlthlobls (thlonoformate)
0,0-D1ethyl S-(N-ethoxycarbonyl-N-methylcarbamoyl methyl )phosphorod1th1oate
0,0-D1ethyl 0-6-ethoxycarbonyl-5-methylpyra2olo-[l ,5a]pyr1m1d1n-2-yl phos»
phorothloate
0,0-D1ethyl S-ethylsulf1nyl methyl phosphorodlthloate
0,0-D1ethyl S-[2-(ethylth1o)ethyl]phosphorod1th1oate
0,0-Dlethyl 0-2- [(ethyl th1o)ethyl]phosphoroth1oate
Common Name*
2,4-D, ACID
2,4-D, BUTOXYETHANOL ETHER ESTERS
2,4-D BUTYL ESTERS (MIXED)*
2,4-D, DIETHANOLAMINE SALT
2,4-D, DIMETHYLAMINE SALT
2,4-D, ISOBUTYL ESTERS (MIXED)*
2,4-D, ISOOCTYL ESTERS (MIXED)*
2,4-D, ISOPROPYL ESTER
2,4-D, PROPYLENE GLYCOL BUTYL ETHER
ESTERS
2,4-DB, ACID
2,4-DB, BUTYL ESTER
2,4-DB, ISOBUTYL ESTER
2,4-DB, ISOOCTYL ESTER
DICHLORPROP
DIURON
LINURON
METHAZOLE
NITROFEN
OS-DICHLOROPROPENE
ra«S-DICHLOROPROPENE
PROPANIL
DALAPON
DICHLOROSALICYCLIC ACID
DICHLORVOS
DITHIANON
THIOPHANATE
PHOSFOLAN
MEPHOSFOLAN
PHOSALONE
COUMAPHOS
DIALIFOR
CHLORTHIOPHOS
DICHLOFENTHION
PHENKAPTON
PIRIMIPHOS ETHYL
DINITRAMINE
EXD
MECARBAM
PYRAZOPHOS
PHORATE SULFOXIDE
DISULFOTON
DEMETON-0
-100-
-------
Code
Jto.
5500
5501
2080
4260
3500
5345
6777
2386
3840
5966
2901
2900
1040
1043
1041
1042
2660
1100
0520
6571
0700
0025
2020
5632
3680
0180
7080
0961
5240
4453
4103
4261
5643
6340
3440
2520
2395
0933
6665
2420
2421
3722
Chemical Name
0,0-Diethyl S-[(ethylthio)methyl] phosphorodithioate
0,0-Diethyl S-ethylthlomethyl phosphorothioate
0,0-Diethyl 0-(2-isopropyl-6-methyl-4-pyr1midinyl) phosphorothioate
Diethyl mercaptosuccinate, s-ester with 0,0-dimethyl phosphorodithioate
0,0-Diethyl 0-[p- (methyl sulfiny} Jphenyl] phosphorothioate
0,0-Diethyl -0-p-nitrophenyl phosphorothioate
0,0-Diethyl 0-(l-phenyl-lH-l , 2 ,4-triazol -3-yl ) phosphorothioate
0,0-Diethyl phosphate
0,0-Diethyl phosphorodithioate S-ester with 3-(mercaptomethyl)-l ,2,3-
benzotriazin-4(3H)-one
0,0-Diethyl 0-2-quinoxalinyl phosphorothioate
0,0-Diethyl 3,5,6-trichloro-2-pyridyl phosphate
0,0-Diethyl 0-(3,5,6-trichloro-2-pyridyl)phosphorothioate
2,3-Dihydro-2,2-dimethylbenzofuran-7-yI methyl carbamate
2,3-Dihydro-2,2-dimethyl-7-hydroxybenzofuran
2, 3-Dihydro-2,2-dimethyl-3-hydroxy-7-benzofuranyl-N-methyl carbamate
2,3-Dihydro-2,2-dimethyl-3-Keto-7-hydroxybenzofuran
6,7-Dihydrodipyrido[l ,2-a:2',l '-c]pyrazidiin1um dibromide, monohydrate
5,6-Dihydro-2-methyl-l ,4-oxathiin-3-carboxanilide
0,0-Diisopropyl phosphorodithioate S-ester with N-(2-mercaptoethyl)
benzenesul fonamide
1 ,2-Di(3-methoxycarbonyl-2-thioureido) benzene
3-(Dimethoxy phosphinyloxy)N,N-dimethyIisocrotonamide
0,S-Dimethyl N-acetylphosphoramidothioate
p-(Dimethylamino)benzenediazo sodium sulfonate
2-(Dimethylamino)-5,6-dimethyl-4-pyrimidinyl dimethyl carbamate
m [ [ ( Dimethyl ami no )methyl ene] ami no] phenyl methyl carbamate hydrochl or i de
4-Dimethylamino-m-tolyl methyicarbamate
4-Dimethylamino-3,5-xylyl methyicarbamate
Dimethyl arsinic acid
1 ,1 '-Dimethyl-4,4'-bipyridilium dichloride
0,0-Dimethyl S-(4,6-diamino-l ,3,5-triazin-2-ylmethyl Jphosphorodithioate
0,0-Dimethyl 0-(2,5-dichloro-4-iodophenyl )thiophosphate
0,0-Dimethyl S-[l,2-di (ethoxycarbonyl )ethyl] phosphorothioate
0,0-Dimethyl 0-(2-diethylamino-6-methylpyridinin-4-yl)phosphorothioate
0,0-Diemthyl S-(2,3-dihydro-5-methoxy-2-oxo-l ,3,4-thiadiazol-3-ylmethyl)
phosphorodithioate
0,0-Dimethyl 0-p-(dimethylsulfamoyl Jphenyl phosphorothioate
N,N-Dimethyl-2,2-diphenylacetamide
1 ,2-Dimethyl-3,5-diphenyl-lH-pyrazolium methyl sulfate
4-(l ,1-Dimethylethyl )-N-(l-methyl propyl)-2,6-dinitrobenzenamine
0,0-Dimethyl S-[2-(ethylthio)ethyl Jphosphorodithioate
0,0-Dimethyl S-(N-methylcarbamoylmethyl) phosphorodithioate
0,0-Dimethyl S-(N-methylcarbamoylmethyl Jphosphorothioate
0,0-Dimethyl S-(N-methyl-N-formylcarbamoylmethyl Jphosphorodithioate
Common Name*
PHORATE
PHORATE OXYGEN ANALOG
DIAZINON
MALATHION
FENSULFOTHION
PARATHION ETHYL
TRIAZOPHOS
DIETHYL PHOSPHATE
AZINPHOS ETHYL
QUINALPHOS
CHLORPYRIFOS OXYGEN ANALOG
CHLORPYRIFOS
CARBOFURAN
CARBOFURAN PHENOL
3-HYDROXYCARBOFURAN
3-KETOCARBOFURAN PHENOL
DIQUAT DIBROMIDE
CARBOXIN
BENSULIDE
THIOPHANATE METHYL
DICROTOPHOS
ACEPHATE
FENAMINOSULF
PIRIMICARB
FORMETANATE HYDROCHLORIDE
AMINOCARB
HEXACARBATE
CACODYLIC ACID
PARAQUAT DICHLORIDE
MENAZON
JODFENPHOS
MALATHION OXYGEN ANALOG
PIRIMIPHOS METHYL
METHIDATHION
FAHPHUR
DIPHENAMID
DIFENZOQUAT
BUTRALIN
THIOHETON
DIMETHOATE
DIMETHOATE OXYGEN ANALOG
FORMOTHION
-------
Code
No.
1500
6663
3520
4580
3480
1600
4460
2458
0360
4750
3820
2460
4000
2411
4090
1523
1621
1720
6583
6780
5980
2902
6792
3620
6420
2770
4070
5148
2560
2573
2580
2600
0340
2640
2860
4720
2780
3796
2006
3373
3412
Chemical Name
Dimethyl cis-l-methyl-2-(l-phenylethoxycarbonyl)vinyl phosphate
3, 3-D1methyl-l- (methyl th1o)-2-butamone 0-[ (methyl ami no )]carbamoyl oxlme
0,0-Dimethyl 0-[4-(methylthio)-m-tolyl] phosphorothioate
0,0-D1methyl O-p-rn'trophenyl phosphorothioate
0,0-Dimethyl 0-(4-nitro-m-tolyl) phosphorothioate
3-[2-(3,5-Dimethyl-2-oxo-cyclohexyl)-2-hydroxyethyl]glutarim1de
3,4-Dimethylphenyl N-methylcarbamate
0,0-Dimethyl phosphate
Dimethyl phosphate of 3-hydroxy-N-methyl-ffis-crotonamide
0,S-Dimethyl phosphoramidothioate
0,0-Dimethyl phosphorodithioate S-ester with 3-(mercaptomethyl)-l ,2,3-
benzotriazin-4(3H)-one
Dimethyl phthalate
0,0-Dimethyl -S-phthalimidomethyl phosphorodithioate
4-(l,2-Dimethylpropylamino)-4-ethylamino-6-methylthio-l,3,5-triazine
N-(l,l-Dimethylpropynl)-3,5-dichlorobenzamide
ais-2 ,5-Dimethyl -1 -pyrrol idlnecarboxanil ide
0,0-Dimethyl 0-p-sulfamoylphenyl phosphorothioate
Dimethyl 2 ,3 ,5 ,6-tetrachl oroterephthal ate
N-^-O.l-DimethyD-l.S^-thiadiazol^-yD-N.N'-dimethylurea
Dimethyl (2,2,2-trichloro-l-hydroxyethyl)phosphonate
0,0-Oimethyl Q-(2,4,5-trichlorophenyl)phosphoroth1oate
0,0-Dimethyl 0-(3,5,6-tr1chloro-2-pyridyl Jphosphorothioate
2,6-Dimethyl-4-tridecylmorpholine
1 ,l-Dimethyl-3-(3-trifluoro-m-tolyl Jurea
m-(3,3-dimethylure1do)phenyl iert-butyl carbamate
4,6-Dinitro-o-cresol
2,6-Dinitro-N,N-dipropylcumidine
3,5-Dinitro-N4,N4-dipropylsulfanilamide
2,6-Dinitro-4-and-2,4-Dinitro-6-octylphenyl crotonates
2-(l ,3-dioxolan-2-yl )phenyl methyl carbamate
S,S l,4-Dioxan-2,3-ylidene bis-0,0-diethyl phosphorothiolothionate
{ate and trans isomers)
2-Diphenylacetyl -1 ,3-indandione
Diphenyl diimide
Diphenyl mercury
Dlsodium methanearsonate, hexahydrate
Dodecachlorooctahydro-1 ,3 ,4-metheno-2H-cycl obuta [cd] pental ene
M-Dodecylguanidine acetate
Ethanedial dioxime
3-Ethoxycarbonyl aminophenyl phenyl carbamate
2-Ethoxy-2,3-dihydro-3,3-dimethyl-S-benzofuranyl methanesulfonate
0-(6-Ethoxy-2-ethyl -4-pyrimidinyl )0,0-dimethyl phosphorothioate
Common Name*
CROTOXYPHOS
THIOFANOX
FENTHION
PARATHION METHYL
FENITROTHION
CYCLOHEXIHIDE
MEOBAL
DIMETHYL PHOSPHATE
MONOCROTOPHOS
METHAHIDOPHOS
AZINPHOS METHYL
DIMETHYL PHTHALATE
PHOSMET
DIMETHAMETRYN
PRONAMIDE
CISANILIDE
CYTHIOATE
DCPA
TERBUTHIURON
TRICHLORFON
RONNEL
CHLORPYRIFOS METHYL
TRIDEMORPH
FLUOMETURON
KARBUTILATE
DNOC
ISOPROPALIN
ORYZALIN
DINOCAP
DIOXACARB
DIOXATHION
DIPHACINONE
AZOBENZENE
DIPHENYL MERCURY
DSMA
MIREX
DODINE
GLYOXIME
DESMEDIPHAM
ETHOFUMESATE
ETRIMFOS
-102-
-------
Code
No.
6590
1074
0320
0120
0578
1360
3335
0940
5880
3300
4583
1591
4740
3380
3400
3280
2910
3673
5331
0960
5220
2653
Chemfcal Name
5-Ethoxy-3-trichloromethyl-l,2,4-thiadiazol
D-N- Ethyl acetamide carbanilate
2-(Ethylaniino)-4-(isopropylamino)-6-methoxy-l,3,5-triazine
2-(Ethylamino)-4-(1sopropylamino)-6-(methyHhio)-l,3,5-triazine
Ethyl N-benzoyl-N-(3,4-d1chlorophenyl )-2-am1nopropionate
Ethyl 4,4'-dichlorobenzilate
S-Ethyl diethylthiocarbamate
S-Ethyl N ,N-di i sobutyl thiocarbamate
0-Ethyl S,S,-dipropyl phosphorodlthioate
S-Ethyl dipropylthiocarbamate
(Ethylenebis-(dithiocarbamate))zinc ammoniates with Ethylenebis
(dithiocarbamic acidjbimolecular and triroolecular cyclic an-
hydrosulfides and disulfides
S-Ethyl ethyl cyclohexylthiocarbamate
S-Ethyl N,N-hexamethylene thiocarbamate
2-Ethyl-l,3-hexanediol
Ethylmercury chloride
0-Ethyl 0-p-nitrophenyl phenylphosphonothioate
0-Ethyl S-phenyl ethyl phosphonodithioate
0-Ethyl S-phenyl ethyl phosphoncthioate
N-(]-Ethylpropyl)-3,4-dimethy]-2,6-d7nitrobenzenanrine
Mixture of m-0 -ethyl propyl)pheny1 methyl carbamate and m-(l -methyl butyl )=
phenylmethyl carbamate (ratio of 1:3)
S- [2- ( ethyl sul f i nyl )ethyl ] -0 ,0-dimethyl phosphorothioate
2-(Ethylthio)-4,6-bis-(isopropylamino)-1,3,5-triazine
Coirroon Name*
ETHAZOL
CARBETAMIDE
ATRATON
AMETRYN
BENZOYLPROP ETHYL
CHLOROBENZILATE
ETHIOLATE
BUTYLATE
ETHOPROP
EPTC
METIRAM
CYCLOATE
MOLINATE
ETHVLHEXANEDIOL
ETHYLMERCURY CHLORIDE
EPN
FONOFOS
FONOFOS OXYGEN ANALOG
PENOXALIN
BUFENCARB
OXYDEMETON METHYL
DIPROPETRYN
3600
Ferric dimethyldithiocarbamate
FERBAM
3790
Gibb-3-ene-l,10-dicarboxylic acid, 2,4a,7-trihydroxy-l-methyl-8-
methylene-1,4a-lactone
GIBBERELLIC ACID
3880 l,4,5,6,7,8,8-Heptachloro-2,3-epoxy-3a,4,7,7a-hydro-4,7-methanoindene HEPTACHLOR EPOXIDE
3860 1,4,5,6,7,8,8-Heptachloro-3a,4,7,7a-tetrahydro-4,7-methano1ndene HEPTACHLOR
3920 Hexachlorobenzene HEXACHLOROBENZENE
0620 Hexachlorocyclohexane-alpha isomer BHC, ALPHA ISOMER
0640 Hexachlorocyclohexane-beta isomer BHC, BETA ISOMER
0680 Hexachlorocyclohexane-gamma isomer BHC, GAMMA ISOMER
0660 Hexachlorocyclohexane-delta isomer BHC, DELTA ISOMER
3260 l,2,3,4,10,10-Hexachloro-6,7-epoxy-l,4,4a,5,6,7,8,8a-octahydro-l,4,e!Kfc,
endo-5,8-dimethanonaphthalene ENDRIN
2380 1,2,3,4,10,10-Hexachloro-ezo-6,7-epoxy-l,4,4a,5,6,7,8,8a-octahydro-l ,4-
eHdc-,
-------
Code
No.
3232
3180
3200
3220
1260
1263
1262
1606
7013
3949
4040
3960
4280
Chemical Name
Common Name*
6,7,8,9,10,10-Hexachloro-l,5,5a,6,9,9a-hexahy
-------
Code
No.
4521
4560
4572
4520
6300
0060
4800
1611
5640
5020
4500
3623
4820
4880
4900
5882
4925
2010
1060
0260
5060
5080
1200
1240
1220
5200
3240
5280
5260
2820
5680
5460
5480
5485
5487
5490
2800
Chemical Name
Methyl -N-hydroxyth1oacet1m1 date
Methylmercury chloride
Methylmercury Iodide
S-Methyl N-[(methylcar6amoyl)oxyJ thloacetlnrfdate
l-Methyl-2-(3,4-methylened1oxyphenyl)ethyl octyl sulfoxlde
2-Methy1-2-(methylth1o)prop1onaldehyde-0-(methylcarbomoyl ) oxlme
6-Methyl -2-oxo-l ,3-d1th1olo- [4, 5-blqu1noxal1ne
1 -Methyl -4-phenylpyr1d1n1um chloride
3-(2-Methylp1perid(no)propyl-3,4-d1ch1orobenzoate
4-(Methylsulfonyl)-2,6-din1tro-N,N-d1propylan1l1ne
4- (Methyl thlo )-3 ,5-xylyl N-methyl carbamate
N-4-Methyl-3-[[t(l,l,l-tr1fluoromethy1)sulfonyl)am1no]phenyl]acetam1de
Monosodlum add methanearsonate
1 -Naphthal ene-acetam1de
1-Naphthalene acetic add
1,8-Naphthallc anhydride
1-Naphthol
2-(a-Naphthoxy)-N,N-diethylprop1onam1de
1-Naphthyl N-methyl carbamate
l(l-Naphthyl)-2-th1ourea
4-N1trophenol
\-exo, Z-endo, -3-exo 4,5,6,7,8,8-Nonachloro-3a,4,7,7a-tetrahydro-4,7-
methanolndane
1 ,2 ,4 ,5,6 ,7 ,8,8-Octachl oro-2 ,3 ,3a ,4 ,7 ,7a-hexahydro-4 ,7-methano1ndene
l-eao,2-etKZo,4,5,6,7,8,8-Octachloro-2,3,3a,4,7,7a-hexahydro-4,7-
methanolndene
methanolndene
\-exo, 2-endc, 4,5,6,7,8,8-Octachloro-2,3-e*c-epoxy-2,3,3a,4,7,7a-
hexahydro-4 ,7-methano1ndene
7-Oxab1cyclo(2.2.l)heptane-2,3-d1carboxyl1c add monohydrate
Pentachl oronl tro benzene
2 ,3 ,4 ,5 ,6-Pentachl orophenol
2,3,4,5,6-Pentachlorophenol , sodium salt, monohydrate
Phenylmercury acetate
Phenylmercury borate
Phenylmercury chloride
Phenylmercury hydroxide
Phenylmercury Iodide
o-Phenyl phenol
o-Phenyl phenol , sodium salt, monohydrate
Common Name*
METHOMYL OXIME
METHYLMERCURIC CHLORIDE
METHYLMERCURIC IODIDE
METHOMYL
SULFOXIDE
ALDICARB
OXYTHIOQUINOX
CYPERQUAT
PIPERALIN (Plpron)
NITRALIN
METHIOCARB
FLUORIDAMID
MSMA
NAPHTHALENE ACETAMIDE
NAA (Naphthalene Acetic Add)
PROTECT
1-NAPHTHOL
NAPROPAMIDE
CARBARYL
ANTU
4-NITROPHENOL
BMAS-NONACHLOR
CHLORDANE
CHLORDANE, GAMMA (trans-chlordane)
CHLORDANE, ALPHA (ds-chlordane)
OXYCHLORDANE
ENDOTHALL, ACID
PCNB
PCP
SODIUM PENTACHLOROPHENATE
PHENYLMERCURIC ACETATE
(Coiunon Name PMA)
PHENYLMERCURIC BORATE
PHENYLMERCURIC CHLORIDE
PHENYLMERCURIC HYDROXIDE
PHENYLMERCURIC IODIDE
PHENYLPHENOL
SODIUM PHENYLPHENATE
-105-
-------
Code
No.
3801
4011
6822
5700
5701
5702
5703
5704
5705
5706
5707
6240
5720
5721
5722
5723
5724
5725
5728
5731
Chemical Name
N-(Phosphonomethyl Jglycine
Phosphorothioic acid, 0,0-bis(l-methylethyl)S-(phenylmethyl Jester
Piperazin-l,4-diyl-bis-(l-(2,2,2-trichloroethyl)forroanride)
Polychlorinated blphenyl with 41.5% Cl
Polychlorinated biphenyl with 21% Cl
Polychlorinated biphenyl with 32% Cl
Polychlorinated biphenyl with 42% Cl
Polychlorinated biphenyl with 48% Cl
Polychlorinated biphenyl with 54% Cl
Polychlorinated biphenyl with 60% Cl
Polychlorinated biphenyl with 62% Cl
Polychlorinates of camphene, pinene and related terpenes
Polychlorinated naphthalene with 26% Cl
Polychlorinated naphthalene with 50% Cl
Polychlorinated naphthalene with 56% Cl
Polychlorinated naphthalene with 62% Cl
Polychlorinated naphthalene with 70% Cl
Polychlorinated naphthalene with 52% Cl
Potassium azide
Potassium Diethyl Dithiophosphate (Kdedtp)
Common Name*
GLYPHOSATE
IBP
TRIFORINE
AROCLOR 1016
AROCLOR 1221
AROCLOR 1232
AROCLOR 1242
AROCLOR 1248
AROCLOR 1254
AROCLOR 1260
AROCLOR 1262
STROBANE T TOXAPHENE
HALOWAX 1000
HALOWAX 1001
HALOWAX 1013
HALOWAX 1014
HALOWAX 1051
HALOWAX 1099
POTASSIUM AZIDE
POTASSIUM DIETHYL DIT
5732 Potassium Diethyl Thiophosphate (Kdetp)
5733 Potassium Dimethyl Dithiophosphate (Kdmdtp)
5734 Potassium Dimethyl Thiophosphate (Kdmtp)
0916 Potassium N-hydroxyTCthyl-N_-methyldithiocarbamate
0027 2-Propenal
5300 S-Propyl butylethylthiocarbamate
7020 S-Propyl N,N-dipropylthiocarbamate
4146 Prop-2-ynyl(+)-(£,E)-3,7,11-trimethyl dodeca-2,4-dienoate
5940 Standardized mixture of pyrethrins I and II (Mixed esters of pyrethrolone)
(KDEDTP)
POTASSIUM DIETHYL THIOPHOSPHATE
(KDETP)
POTASSIUM DIMETHYL DITHIOPHOSPHAT!
(KDMDTP)
POTASSIUM DIMETHYL THIOPHOSPHATE
(KDMTP)
BUNEMA
ACROLEIN
PEBULATE
VERNOLATE
KINOPRENE
PYRETHRINS
6172 Sodium azide
1546 Sodium Fluoaluminate
6220 Sodium N-methyldithiocarbamate
4920 Sodium N-1-naphthylphthalamate
6222 D-Streptamine, 0-2-deoxy-2-(methylaminoJ-a-L-glucopyranos-yl-(l->2)-0-5-
deoxy-3-C-formyl-d-l.-lyxofuranosyl-(l->4)-N,N'bis(aminoiminomethyl)-,
sulfate (2:3) (salt)
SODIUM AZIDE
CRYOLITE
METHAM
NAPTALAM, SODIUM SALT
STREPTOMYCIN SULFATE
-106-
-------
Code
No.
1180
1000
1640
6435
3340
6540
6000
0020
6680
0300
6660
2060
3640
1940
6770
6920
4540
3660
1020
6890
6840
6860
6870
6880
688
6895
6900
6120
6130
6140
3460
6786
6800
4166
5366
3527
3540
7100
7120
Chemical Name
2,3,5,6-Tetrachloro-l ,4-benzoquinone
cis-N-(l ,1 ,2,2-Tetrachloroethylthio)tetrahydrophthalimide
2,4,5,6-Tetrachloroisophthalonitrile
1 , 2,4,5-Tetrachloro-3-nitrobenzene
0,0,0' ,0'-Tetraethyl S,S' -methyl ene blsphosphorodithioate
Tetraethyl pyrophosphate
1 ,2 ,12 ,12a , Tetrahydro-2-isopropenyl -8,9-dimethoxy- [1 ] benzo=
pyrano-[3,4-b]furo[2,3-b][l]benzopyran-6(6aH)one
O.O.O'.O'-Tetramethyl 0,0'-(th1o-di-p-phenylene)d1phosphorothioate
Tetramethylthiuram disulfide
Tetra-n-propyl dithiopyrophosphate
2-(4'-Thiazolyl) benzimidazole
3,4,5-Tribromosalicylanilide, 4,5-dibromosalicylanilide and other
brominated salicylanllides
Trlbutyl Phosphorotrithiolte
S,S,S-Tributyl phosphorotrithioate
S-(2,3,3-Tr1chloroallyl)diisopropylth1ocarbamate
2,3,6-Trichlorobenzoic acid and related compounds
1 ,1 ,l-Trichloro-2,2-b1s (p-methoxyphenyl ) ethane
N-(Tr1chloromethylthio)phthalim1de
N-(TricMoromethylthio)-3a,4,7,7a-tetrahydrophthalimide
2 ,4 , 5-Tri chl orophenol
2,4,5-Trichlorophenoxyacetic acid
2,4,5-Trichlorophenoxyacetic acid, mixed ether esters of butoxyethanol
and isobutoxyethanol
2,4,5-Trichlorophenoxyacetic acid, butyl esters (mixed)
2,4,5-Trichlorophenoxyacetic acid, isooctyl esters (mixed)
2,4,5-Trichlorophenoxyacetic acid, propylene glycol butyl ether esters
(mixed)
2,4,5-Trichlorophenoxyacetic acid, trlethylamine salt
4-(2,4,5-Trichlorophenoxy)butyric acid
2-(2,4,5-Trichlorophenoxy)propionic acid
2-(2,4,5-Trichlorophenoxy)propionic acid, isooctyl esters (mixed)
2-(2,4,5-Trichlorophenoxy)propionic acid, propylene glycol butyl ether
esters (CjHgO to CgH^Oj)
2,3,6-Trichlorophenylacetic acid
3,5,6-Trichloro-2-pyridyloxyacetic acid
o,o,a-Trifluoro-2 ,6-dinitro-N,N-dipropyl-p-toluidine
3-Trifl uoromethyl-4-nitrophenol , sodium salt
1 ,1 ,l-Trifluoro-N-[2-methyl-4-(phenylsulfonyl )phenyl Jmethanesulfonamide
Triphenyltin acetate
Triphenyltin hydroxide
Zinc dimethyldithiocarbamate
Zinc ethyl enebisdithiocarbamate
Conroon Name*
CHLORANIL
CAPTAFOL
CHLOROTHALONIL
TECNAZENE
ETHION
TEPP
ROTENONE
TEHEPHOS
THIRAM
ASPON
THIABENDAZOLE
DIAPHENE
FOLEX
DEF
TRIALLATE
2,3,6-TBA
HETHOXYCHLOR, p,p'
FOLPET
CAPTAN
2,4,5-TRICHLOROPHENOL
2,4,5-T. ACID
2,4, 5-T BUTOXYETHANOL ETHER ESTERS
2,4,5-T, BUTYL ESTERS
2,4,5-T, ISOOCTYL ESTERS
2,4,5-T, PROPYLENE GLYCOL BUTYL
ETHER ESTERS
2,4,5-T, TRIETHYLAMINE SALT
4-(2,4,5-TB)
SILVEX, ACID
SILVEX, ISOOCTYL ESTERS
SILVEX, PROPYLENE GLYCOL BUTYL
ETHER ESTERS
FENAC
TRICLOPYR
TRIFLURALIN
LAMPRECIDE
PERFLUIDONE
FENTIN ACETATE
FENTIN HYDROXIDE
ZIRAM
ZINEB
-107-
-------
Section II
LIST OF AVAILABLE ADDITIONAL ORGANIC COMPOUNDS
At the time of this edition, the repository stock is being expanded
to include additional non-pesticidal organic compounds. These will be
provided on request to qualified laboratories only on the North American
Continent and in samples of no more than 200 milligrams.
The majority of these compounds are designated as toxic and are
included in the TOXIC SUBSTANCES LIST published by NIOSH in 1974. Many
of them were also included in the list of 113 chemicals, the "Consent
Decree Compounds," specified by the U. S. EPA in 1977 as compounds which
constitute an appreciable health hazard to man and animals and which are
to be monitored in industrial effluents.
Soecial safety precautions should be taken in handling and analysis
of these compounds. A number of them are known or suspected carcinogens
and, therefore, must be handled accordingly.
In the supplemental data supplied for each compound, the terms
"Industry Source" and "Hazard" require some brief explanation: "Industry
Source" refers to the type of industry whose effluent has been monitored
by EPA and a specific compound has been identified by analysis. "Hazard"
provides information to the analyst concerning the potential danger in the
handling of the compound. Where these spaces show "No Data," it is meant
that none could be located in our search. Toxicity data were available
for many compounds but were unavailable for some.
Because of shipping restrictions, this group of compounds is available
only to laboratories on the North American continent where surface carriers
may be utilized.
108
-------
Code Common Name Emp. Form. Chemical Name
Structure
P011 ACENAPHTHENE C19H]n 1 ,2-Dihydroacenaphthylene
Mol.Wi. 154.2
. Petrochem. , pes-
indust. Srce. t-jc_( woo(j pre_
serve
LDso No data
Hazard No data p,f
Purity 99%
A B C D E F ^^\ ^^^
1
2
3
4
5
6
\
^ /^\ xi^
^r^^ ^^^^
\ 1
P018 ACENAPHTHYLENE C,2Hg Acenaphthylene
Mol.Wi. 152.2 X^^^^
luJu 1 5 Mo data
LDso No data
Hazard No data R<>f
Purity 95%
1
2
3
4
5
6
L 1
L^_l
P024 ACETOPHENONE CnHR0 1-Phenylethanone
(Hypnone)
Mol.Wt. 120'2 ^^\
i j i Chloroaraffin' A B C D E F f ^^
Indus!. Srce. **>"*" KQI ul
IDso 3,000
Hazard Flammable Ref>
Purity 99%
1
2
3
4
5
6
o
L ^J\ II
\^^C-CH3
P033 ADIPIC ACID tf.^nQi Hexanedioic acid
Mol.Wl. I"6-1 O O
Indusl. Srce. Synth. Fibers
IDjo 3,600
Hazard No data R,(
Purity 98%
A B C 0 E F ,^.._li lm\ r nu
1
2
3
4
S
6
nv-' >- \>-i >2 14 ^- ^^' '
P042 ANETHOLE ClnH,,,0 l-Hethoxy-4-(l-propenyl ) benzene
(Anise camphor)
Mol. Wt. 148-2 °CH3
Indusl. Srce. paPer mf9-
10SO 2'090
' Hazard Flammable ...
'
Purity
A B C D E F
1
2
3
4
5
6
r i
;r
tH=CH-CH3
109
-------
Code Common Name Emp. Form. Chemical Name
Structure
P051 ANTHRACENE
Anthracene
Mel. Wt. I'8-2
Induit. Srce. No data
t Djo No data
Hazard No data R,(.
Purity 97+%
A B C DEF
1
2
3
4
5
6
P065 BENZALDEHYDE
C7HgO
Benzaldehyde
Mol.Wt. 106.1
Induit. Srce. Paper mfg.
1,300
Hazard Flammable, Ref.
sKin irrit.
Purity 99%
AB
DEF
P074 BENZYL ALCOHOL
C?HgO
Benzenemethanol
Mol.Wt. 108.1
Indus). Srce. Petrocnem.
IDM 1,230
Haiard Flammable Ref
Purity 99+%
AB
DEF
P086 Bis-(2-CHLOROETHOXY)
METHANE
Mol.Wt. 173
Indus!. Srce. No data
ID
50
Purity
65
absorpt, toxic
vapor
99%
Bis-(2-Chloroethoxy)methane
ABC DEF
(CICH2CH2O)2CH2
P091 Bis-(2-CHLOROETHYL)
ETHER
Mol.Wt. 143
Indus!.
LD»
Hazard
Puritv
Bis-(2-Chloroethyl ) ether
A B C DEF
KuDoer niTy.
75
Carcinog. sus-
pect, extremeUef.
ly toxic, skin
absorpt, toxic
vapor
1
2
3
4
5
6
(CICH2CH2J20
no
-------
Code Common Name Emp. Form.
Chemical Name
Structure
PI 04 BROMOCHLOROMETHANE CH2BrCl Bromochloromethane
M.I.W.. 129'4
Indmt. Srce. No data
LD5o 4'300 (mse'
Hazard Toxic Vapor Ref
Purity 98%
P116 2-BUTOXYETHANOL Cg
Mol.Wt. 118-2
Indmt. Srce. No data
ID, '.«»
Hazard Flammable, Ref.
vapor toxic,
skin absorpt.
Purity 99%
P122 2-(2-n-BUTOXYETHOXY)- Cp
ETHANOL °
Mol.Wt. 162.3
Induir. Srce. Rubber mfg.
IDj,, 2,000 (g.p.)
Hazard Flammable R,f
Purity
PI 31 BUTYL BENZYL C,c
PHTHALATE
Mol.Wt. 312
Induil. Srco. No data
IDjo 18.000
Hazard No data R.f
Purity 95%
A B C D E F
1
2
3
4
5
6
rU.O- 2-Butoxyethanol
A B C D E F
1
2
3
4
5
6
CH2CIBr
HO(CH2 )2OC4H9
41803 2,(2->j-Butoxyethoxy)-ethanol
A B C D E F
1
2
3
4
5
6
H20°4 BUtyl benzyl Phthalate
A B C D E F
1
2
3
4
5
6
HO(CH2)20(CH2)-,OC4H9
p
r^^yC-OQH,
k.^-OCH,-^)
\.T-^/
P140 d-CAMPHOR CinH160 1 ,7,7-Trimethylbicyclo[2.2.1]
lu ld heptari-2-one
CH3
Mol.Wt. 152'2
lndu»t. Srce. paPer mf9-
lDjo No data
Hazard Toxic „.,
Purity
A B C D E F
1
2
3
4
5
6
r/V
^
111
-------
Code Common Name Emp. Form. Chemical Name
Structure
PH8 CARBAZOLE C12HgN 9H-Carbazole
H
Mel.Wl. 167-2 ^X^ -Ak ^>~^
Indutt. Sr«. Wood Pi-eserv.
LDjo 5,000+
Hazard No data Ref
Purity 99+«
A B C D E F
1
2
3
4
5
6
^ ^X"-x^ \
^x^^ <555;:^X
PI 56 CHLOROBENZENE CgHjCl Chlorobenzene
Cl
Moi.wi. n2-6 JL
lndu$t. Srce. N° data
IDso 2'910
Hazard Very flanrnablgef
Purity 99%
A B C D E F
1
2
3
4
5
6
I 1
L J
\^x
P164 2-CHLOROETHYL VINYL C^CIO (2-Chloroethoxy)ethene
ETHER
Mol.Wt. 106.6
Indus*. Srte. No data
I Dso 250
Hazard Flammable, p.f.
toxic
Purity 99%
PUS 4-CHLORO-3-METHYLPHENOL C,
(4-chloro-m-cresol )
A B C D E F
1
2
3
4
5
6
CI(CH2)2OCH=CH2
H7C10 4-Chloro-3-Methyl phenol
Mol.Wt. 142-6 5^H
Induct SFCQ No d3t3
10 50 N° data
Hazard Irritant g.f
Purity 98X
A B C D t F ^^ \,
1
2
3
4
5
6
\|x^^ 3
Cl
PI 82 e-CHLORONAPHTHALENE C^HyCl 2-Chloronaphthalene
Mol.Wl. 162.6 ^, .^^
IJII Hoteto ABC D E F (^ ^^ ^^°
IDjo 2,078
Hazard No data R.f
Purity 99%
1
2
3
4
5
6
1
112
-------
Code Common Name Emp. Form.
Chemical Name
P192 2-CHLOROPHENOL CgHjCIO 2-Chlorophenol
OH
Mol.Wt. 128.6 1
Induit. Srco No data
1050 670
Hazard Irritant, Rof.
f 1 anmabl e ,
toxic
Purity 98+*
A B C Off
1
2
3
4
5
6
r^V
\. j^^1^
^^^^^^
PI 93 3-CHLOROPHENOL C6H5C1° 3-Chlorophenol
OH
i
Mol.Wt. 128.6 /^^x,
Induit Sr«. No data A B C 0 E F f 1
L0jo 570
Hazard Toxic, skin g,f
absorpt.,
Irritant
Purity 99%
!
2
3
4
5
6
^\ ssZ/^Q
^^v^
P208 0-CRESOL C?HgO 2 -Methyl phenol
OH
Moi.wt. 108-1 ^^ ru
Induit S . Wood preserv. A B C D E F ^ ^^<-H3
I fit* us f. 5rc ••«*"* r - • •
LDso 121
Hazard Very toxic, , «
skin absorpt..
Irritant, flam-
mable
Purity 99+*
1
2
3
4
5
6
1 1 "
1 J
P209 m-CRESOL C^O 3-Methyl phenol
OH
Mol.Wt. 108.1 1
Indust. Srt». Wood preserv.
10,0 ««
Hazard Toxic, skin R.f.
absorpt., Irri-
tant, flammable
Purity 99+X
A B C D E F
1
2
3
4
5
6
r^^i
\ /^ru
^^^ CH3
P210 p-CRESOL C?H80 4-Methyl phenol
9"
Mol.Wt. 108.1 /^^x
Induit. Src*. Wood preserv.
ID jo 207
Hazard Toxic, skin Ref.
absorpt . , 1 rr* -
tant, flammable,
toxic vapor
Purity 99+X
1
2
3
4
5
6
A B C D E F
^^^
^>
^^Y^
CH3
113
-------
Chemical Name
Structure
P222 CUMENE CgH^ (1 -Methyl ethyl Jbenzene
Mol.Wl. 120-2
Indus!. Srce. No data
ID*, 1 -400
Hazard Very flaranabl|ef
Purity 99%
P232 CYCLOHEXANOL C£H
Mol.Wt. 100'2
Indust. Srce. ^nlh- f1bers
lDso 2,060
"— asr- «•«•
Purity 98%
P243 p-CYMENE Cn
Mol.Wl. 134-2
Indutl. Srce. PaPer mf9-
IDso 4,750
Hazard Very flanrnabljj,,
Purity 98%
P254 2 ,3-DIBROMOPROPANOL C3r
Mol.Wl. 218
Indutt. Srce. Synthet. fibers
L D5O No data
Hazard Toxic „„,
Purity 96%
P265 Di-n-BUTYLAMINE C8
Mol. Wt. 129.3
Induii. Srce. Rubber mfg.
1 0M 550
Hazard Fl amiable, R«f.
irritant
Purity 99%
A B C D E F
1
2
3
4
5
6
-20 Cyclohexanol
A B C D E F
1
2
3
4
5
6
)HH
1
2
3
4
5
6
A B
p-Isopropyl tol uene
C D E F
t,Br,0 2,3-Dibromopropanol
D C.
A B C D E F
1
2
3
4
5
6
,
H,0N Di-n-Butylamine
1 y
A B C D E F
1
2
3
4
5
6
H-C-(CH3)2
r*i
U
,
I ,J
CH(CH3}2
CH2BrCHBrCH2OH
[CH3(CH2)3]2NH
1U
-------
Code Common Name Emp. Form. Chemical Name
P275 m-DICHLOROBENZENE CKHAC1,, 1,3-Dichlorobenzene
Mol.Wt. 147
Indust. Srce. No data
10 No data
Hazard Very flammab^,
Purity 98%
A B
D E F
P285 1,1-DICHLOROETHANE C2H4C12 1 ,l-D1chloroethane
P286 1 ,2-DICHLOROETHANE C2H4C12 1 ,2-Dichloroethane
Structure
Moi.wt. 99 wr-rw
ABC DEF <~l2nl_ LH3
fndusf. Srce. No data
IDso 725
Hazard Very flam- nef.
mable
Purity 98*:
1
2
3
4
5
6
Mol.Wt. 99
Indust. Srce. No data
L DSO 680
Hazard Flammable Ref
Purity 99
A B
D E F
CIH2C-CH2CI
P292 1,1-DICHLOROETHYLENE CjHjClj 1,1-Dichloroethylene
Mol.Wt. 97
Indust. Srce. No data
I DM 40°
Hazard Very flam- - ,
mable, quite™ '
toxic
Purity 95X
A B
D E F
CI2C =CH2
P296 Tromr-1,2-
DICHLOROETHYLENE
Mol.Wt. 97
Indust. Srce. No data
A B
LDso
Hazard
Purity
770
Flammable, R>f
toxic
98+%
Trons-l ,2-Dichloroethylene
D E F
Ck H
115
-------
Code Common Name Emu. Form.
Chemical Name
Structure
P306 2,4-DICHLOROPHENOL C6H4C12° 2,4-D1chlorophenol
9H
Mol.Wt. 163
Indutt. Srce. No data
1050 580
Hazard Irritant, R.I.
Flammable,
toxic
Purity 99*
P314 1 ,2-DICHLOROPROPANE C
Mol.Wt. 113
Indutt. Src*. No data
LDjo 1,900
Irritant, very
Hazard flammable, R,f.
toxic vapor
Purity —
P322 1,3-DICHLOROPROPYLENE C
(Mixed Isomers)
Mol.Wt. Ill
Indutt. Sret. No data
LDM 250
Hazard Irritant, varju.f
tox
-------
Code Common Name Emp. Form.
Chemical Name
P358 3,4-DIMETHOXYBENZALDEHYDE
(Veratraldehyde)
Mai. Wl. 166.2
Indust. Srce. Paper mfg.
L DSO Mo data
Hazard No data Ref.
Purity
P370 2,4-DIMETHYLANILINE C
Mol.Wl. 121.2
Indust. Sree. No data
I DJO 467
Hazard Irritant, Her1.
flammable
Purity —
P380 2,5-DIMETHYLFUfWN C(
CgHlp03 3,4-Dimethoxybenzaldehyde
A B C D E F
1
2
3
4
5
6
gH^N 2,4-Dimethylaniline
A B C D E F
2
3
4
5
6
HgO 2,5-Dimethylfuran
Mol.Wl. 96-]
Indust. Srce. Petrochem.
LDW 300
Hazard Very flam- R.f
mable, toxic
Purity 99%
A B C D E F
1
2
3
4
5
6
P389 2.6-DIMETHYL-4- CqH1R0 2,6-D1methyl-4-Heptanone
HEPTANONE (Tech.)
Mol.Wt. 142.1
Indust. Srce. No data
I DJO 1,416 (iuse)
Hazard Flammable R|(
Purity 80%
P403 2,3-DIMETHYLPHENOL C,
(2,3-Xylenol)
A B C D E F
1
2
3
4
5
6
H1Q0 2 ,3-Dlmethyl phenol
Mel.Wt. 1^2.2
Indust. Srce. Mood preserv.
LDM ca 400
Hazard Irritant, Ref.
Toxic
Purity 97%
AS C D E F
1
2
3
4
5
6
Structure
((CH3)2CH-CH2)2C-0
117
-------
Code Common Name Emp. Form.
Chemical Name
Structure
P404 2,4-DIHETHYLPHENOL Cg
Moi.Wt. 122.2
Induil. Srce. Wood Preserv.
IDso ca 400
Hazard Irritant, R«f.
toxic
Purity 99%
P405 2,5-DIHETHYLPHENOL Cg
(2,5-Xylenol)
H.0o 2,4-Dimethylphenol
OH
j
A B C D E F
2
3
4
5
6
H,Q0 2, 5-Dimethyl phenol
'
CH3
OH
Mol.Wt. 122.2 ^l^
Indus!. Srce. Wood Preserv.
L Dso 444
Haiard Irritant, n,f
toxic
Purity 96+%
A B C D E F
1
2
3
4
5
6
r T*
CH,-k^
P415 2,4-DINITROPHENOL C6H4N2°5 2,4-Dinitrophenol
Mol.Wt. 184.1
Induit. Srce. No data
I DSO 30
Hazard Severly toxifo,
SKin absorpt., '
toxic vapor
Purity 85+
P424 2,4-DINITROTOLUENE C
Mol.Wl. 182.1
Indust. Srce. No data
LD,o 268
Hazard Toxic R*f.
Purity 85+%
A B C D E F
1
2
3
4
5
6
pHjjNjO^ 2,4-Dinitrotoluene
A B C D E F
1
2
3
4
5
'b
^NO,
1 ,.
NO2
0^ 2
NO2
P434 DIOCTYL PHTHALATE C,.H,flO. Bis-(2-ethylhexyl )
(DEHP) phthalate
Mol.Wl. 390.6
Indutt. Srce. Synthet. fibers
LDn 43,000
Hazard No data R«|.
Purity 98%
A B C D E F
1
2
3
4
5
6
Q?-o-c,-«4'::
o 2 Q '
118
-------
Code Common Name Emp. Form. Chemical Name
Structure
P443 p-DIOXANE C4
Mol.Wf. 88.1
Induit. Srce. No data
LDso 3,150 (g.p.)
Hazard Flammable, „ ,
carcinogen
suspect
Purity 99+%
P453 1 ,2-DIPHENYLHYDMZINE C,
(Hydrazobenzene)
Mol.Wt. 184.2
Induit. Srce. No data
IDjo 301
Hozord Toxic R,f.
Purity 97%
P462 D:PHENYL SULFIDE c.
Mol.Wt. 186.3
Induit. Srce. Wood preserv.
I Dso 490
Hazard Quite Toxic Ref.
Purity 99%
H000 1,4-Diethylene dioxide
O C
A B C D E F
1
2
3
4
5
6
2H12N2 1,2-Diphenylhydrazine
A B C D E F
1
2
3
4
5
2H1()S l,l-Thiobis[benzene
A B C D E F
1
2
3
4
5
6
n
L J
O/~f \
UN HN-/^
QS \ /
\ /
P475 ETHYLBENZENE CgH1Q Ethyl benzene
Mol.Wt. 106.1
Induit. Srce. No data
I DJO 3,500
Hazard Irritant, Rel.
very flammable
Purity 99%
P485 2-ETHYL-l-HEXANOL C
Mol.Wt. 130.2
Induit. Srce. paper Mfg.
ID jo 800
Hazard Flammable Rof.
Purity 99%
A B C D E F
1
2
3
4
5
6
!H18°
A
1
2
3
4
5
6
B
2-Ethyl-l-Hexanol
C D E F
^^ClHi
k^
CH,(CH2)3CH-CH2OH
119
-------
Code Common Name Emp. Form. Chemical Name
P495 N-ETHYLHORPHOLINE C6H13NO N-Ethylmorpholine
Mol.WI. 115.2
... Nc Jita ABC D E F
Indus!. Sree. no oata
IDso 1 >480
Hazard Very flaranab^j
Purity 995!
1
1
3
4
5
6
P505 2-ETHYLPHENOL C8H10° 2-Ethyl phenol
Mol.WI. 122'2
A B C D E F
LD No data
Hazard Irritant, Ref
flanmable
Purity 99X
1
2
3
4
5
6
P506 3-ETHYLPHENOL C8H10° 3-Ethyl phenol
Mol.WI. 122-2
* ABC D E F
Indus!. Sree. PaPer mt9'
ID jo No data
Hazard Irritant, «,f
somewhat
flammable
Purity 99%
1
2
3
4
5
6
P507 4-ETHYLPHENOL C8H10° 4-Ethyl phenol
Mol.WI. 122.2
Induct. Sree. roper miy.
I DSO No data
Hazard Irritant Ref
Purity 97X
1
2
3
4
5
6
P525 EUGENOL C10H12°2 4-Allyl-2-methoxyphenol
Mol.WI. 164.2
AS C Off
Inducl. Sree. Paper mfg.
LDjo 2,680
Hozord Flanmable *e».
Purity 99X
1
2
3
4
S
6
Structure
C2H5
CH2CH=CH,
120
-------
Code Common Name Emo. Form.
Chemical Name
Structure
P536 d-FENCHONE C10H16° d.l ,3,3-Tr1inethyl-2-
norbornanone
CH3
Mol.Wl. 152.2 J^
tndust. Sr«. Paper mfg.
IDjO 4,400
Hazard No data R«f.
Purity 95*
A B C Off
1
2
3
4
5
6
r/ i^°
\
\\ /T^
^•^CHu
P547 FLUORANTHENE ClgH10 Fluoranthene
M.I.WI. 202.3 ^^ ff-^
Indu.i. Src«. Wood preserv.
LDjo 2,000
Hazard Skin absorpt^j
Purity 98*
ABC D E F
1
2
3
4
5
6
%^X \-/
P555 FLUORENE C13H1Q o-B1phenylenemethane
Mel.Wl. 166.2 ^f^^^ /^5^
Indutt. Sr«. No data
LDM 15. 000
Hazard No data R»f.
Purity 98*
A B C D 1 F
1
2
3
4
5
6
kJdJ
P565 6UA1ACOL C7Hfl02 o-MethoxyphenoI
Mol.Wl. 124.1 f ^^S^OH
A B C D 1 F | |
Induit. fret. Paper mfg.
IDN 72S
H«"rd Flanmable, R(|.
somewhat toxic
Purity 98*
1
2
3
4
t
a
\^x^sOCH
P575 n-HEPTADECANOIC ACID C17H,,CL n-Heptad«eano1c Add
(NargaHc add) " * c
•>tn i O
Mol. Wr. 270-5 jf
, j ( $ p.p.. m,a ABC D i F CH,(CH,LC -nu
i DM No dat8
Hazard Toxic Rtf_
Purity 97*
1
2
3
4
3
6
121
-------
Chemical Name
Structure
P586 HEXACHLORO-1 ,3- C^6 Hexachloro-1 ,3-8utadiene
BUTADIENE
Mol.Wt. 260'8
Indust. Srce. Pestic. mfg.
LD50 300
Hazard Toxic, Ref
irritant
Purity 953!
A B C D E F
1
2
3
4
5
6
CI2C-CCI-CCI=CCI2
P595 HEXACHLOROCYCLO- CeCl- Hexachlorocyclopentadiene
PENTADIENE ° °
Mol.Wt. 272.8
Indust. Sree. Pestic. mfg.
IDso 505
Hazard Moderate toxjtef.
Purity 983!
A B C Off
1
2
3
4
5
6
q a
u I
Cl Cl
P605 HEXACHLOROETHANE C2C16 Hexachloroethane
Mol.Wt. 236.7
Indust. Srce. No data
1050 No data
Hazard Toxic, skin Ref
absorpt., toxic
vapor
Purity 98%
P615 2,4-HEXADIENAL Cg
(Sorbaldehyde)
Mol.Wl. 96.1
Indust. Stce. Pestic. mfg.
I DM 730
Hazard Flammable, Ref
toxic, skin
absorpt.
Purity
P624 HEXANOIC ACID C
(Caproic acid)
Mol.Wt. 116.2
Indust. Srce. Synthet. fibers
I DM 3,000
Hazard Fl amiable, _ .
skin absorpt.
Purity 99.5+5;
D E F
1
2
3
4
5
6
HR0 2,4-Hexadienal
A B C D E F
1
2
3
4
5
6
,H,,0, Hexanoic Acid
3 1 C f.
ABC D E
1
2
3
4
5
6
F
CI3C-CCI3
CH3-CH-CH-CH=CH-C-H
CH3(CH2)4COOH
122
-------
Code Common Name Emp. Form. Chemical Name
Structure
P633 HEXYL ALCOHOL Cfi
Mol.Wl. 102.2
Indmt. Sree. Petrochem.
ID jo 1,590
Hazard Skin absorpt.g.f.
f 1 amnabl e
P645 o-HYDROXYACETOPHENONE Cg
H140 1-Hexanol
A B C D E F
1
2
3
4
5
6
Hg02 o-Hydroxyacetophenone
CH3(CH2)4CH2OH
O
Mol.Wt. 136.2
lndu*t. Sree. No data
I DJJJ No data
Hazard Toxic Ref.
Purity 973
A B C Off
1
2
3
4
5
6
C-CH,
rS
k^OH
Pfi4fi ra-HYDROXYACETOPHENONE CDH00, m-Hydroxyacetophenone
(Tech.) 8 8 2
Mol.Wl. 136.2
Indutt. Sree. No data
LDjo No data
Hazard Toxic Ref.
Purity 952
P647 p-HYDROXYACETOPHENONE C
Mol.Wl. 136-2
Indmt. Sree. No data
Hazard Toxic Ref
Purity 98%
P660 P-HYDROXYBENZALOEHYDE C
(4-Formylphenol)
Mol.Wt. I22'1
Indusl. Sree. Paper mfg.
LDso N° data
Hazard Toxic R.f.
Purity
A B C D E F
1
2
3
4
5
6
O
j>CH3
XS^°H
k^
0H00. p-Hydroxyacetophenone
3 0 C
A B C D E F
1
2
3
4
5
6
O
ii
C-CH3
0
\^
OH
H.O. p-Hydroxybenzaldehyde
/ b 2
?..
A B C 0 E F
\
2
3
4
5
6
i--rl
[ I
OH
123
-------
Code Common Name Emp. Form.
Chemical Name
Structure
P672
P685
P695
P704
P705
4-HYDROXY-4-METHYL-2- C,H1?0? 4-Hvdroxy-4-methyl-2-pentanone
PENTANONE (Oiacetone
alcohol)
Mel.Wl. 116-2
lndu.1. Sree. Petrochem.
10,0 4,000
Hazard Flammable, j,,f
toxic vapor
Purity
ABC D E F w r r rw r ru
i
2
3
4
5
6
OH
INDENE (Tech.) C-H. Indene
(Indonaphthene)
Mel.Wl. I16-2
lndu.1. Srce, Petrochem.
L D50 No data
Haiotd Fl amiable R>(
Purity 90+*
A B C D E F
1
2
3
4
5
6
o^
ISOPHORONE CaH1A0 2-Cyclohexen-l-one-
a " 3,5,5-trlmethyl
Mel.Wl. 138.1
Induit. Srce. No data
I D» 2-330
Hazard Flammable, R.t.
toxic vapor
Purity 98)1
A B C D E F
1
2
3
4
5
6
Hf£ 1
3*** 1 1
f*LJ
v-n3
2-ISOPROPYLPHENOL C,H120 2-Isopropylphenol
Mel.Wl. 136.2
Indutl. Srce. No data
LDM No data
Hazard Toxic, Irrl- Rif.
tant, flammable
Purity 97%
3-ISOPROPYLPHENOL(tech. )
A B C D E F
1
2
3
4
5
6
CgHjjO 3-Isopropylphenol
OH
aCH(CH3)2
OH
Mot.Wt. 136.2 1
Induit. Sm. No data
I DM No data
Hazard Toxic, 1rr1- R,f.
tant, flammable
Purity 60X
ABC D E F
1
2
3
4
5
6
/-v
k>CH(CH3)2
124
-------
Code Common Name Emp Form. Chemical Name
Structure
_P716
P717
P726
P735
4-ISOPROPYLPHENOL CgH120 4-Isopropylphenol
OH
Mol.Wt. 136.2
Indust. Srce. No data
LDso No data
Hazard Toxic, irri- R«f
tant
Purity 98S
2,4-LUTIDINE C
Mol.Wt. 107.2
Indutf. Srce. No data
LDso 200-800
Hazard Irritant, R,f
very flammable,
skin absorpt.
Purity 96+%
2,6-LUTIDINE C
Mol.Wi. 107.2
Induit. Srce. No data
L Dso 200-800
Hazard Irritant, ver)fc,f
flammable, skin
absorpt.
Purity 96«
DL-MANOELIC ACID C
Mel.Wt. 152.1
Induit. Srce. Paper mfq.
LDro 3'000
Hazard No data Ref.
Purity 98?
A B C D E F
1
2
3
4
5
6
7HgN 2,4-Dimethylpyridine
A B C D E F
1
2
3
4
5
6
HgN 2,6-Dimethylpyridine
ABC D E F
1
2
3
4
5
6
.H.O, a-Hydroxybenzene=
acetic add
A B C D E F
1
2
3
4
5
6
fl
CH(CH3)2
,A
r^i
HsC^^/x^CH
ao
CH-C-OH
OH
1-METHYLNAPHTHALENE C]JH10 1 -Methyl naphthalene
Mol.Wi. 1«.2 /^\ ^\^
lndu»t. Sree. Petrochem.
Hazard Flammable R,f
Purity 97?
A B C D E F
1
2
3
4
5
6
^ \ M
^/•^
125
-------
Chemical Name
Structure
P736 2-METHYLNAPHTHALENE C^H^ 2-Methylnaphthalene
M.I.WI. i«-z r ^^r^T0
P I tern A B C D E F | | |
Induil. Sree. Petrocnem.
IDso *'360
Hazard No data R.f.
Purity 99+!8
1
2
3
4
5
6
^^\^
P745 4-METHYL-2-NITROPHENOL C?H7N03 4-Methyl-Z-nitrophenol
(2-nitro-p-cresol)
OH
I
Mol.Wl. 153-! ,/X^-NO
A B C D E F f, T
Indutt. Sree. Chemical mfg.
lDjo 3,360
Hazard Irritant R.f.
Purity —
1
2
3
4
5
6
CHj
P754 MYRISTIC ACID C14H28°2 Tetradecanoic acid
Mol.Wl. 228.4 Q
Indutt. Sree. Paper mfg.
LDjo No data
Hazard No data R,f
Purity 99.5+*
A B C Off
1
2
3
4
5
6
CH3(CH2),2C-OH
P763 NAPHTHALENE C1QHg Naphthalene
Mo, wt 128.2
Synth, fibers,
lndu.1. Sree. petro-chem., wall-
board mfq.
LDjo L780
Hazard Flammable Ref.
Puri ty 99+*
ABC D E
1
2
3
4
5
6
F
r^i^i
^x^^X^V^/^^
\X^ \/
P771 1-NAPHTHOIC ACID C^HgOj l-Naphtho1c Acid
9
Mol.Wl. 172.1 9^H
ABC D E F ^^ /^
Induil. Sree. Wood preserv.
IDjo 1,620 (mse)
Hazard Irritant Ref
Purity 98%
1
2
3
4
5
6
r T i
k^ ^-^ ^v
^5^/^^x^-x
-------
Code Common Name Emp. Form.
Chemical Name
Structure
2-NAPHTHOIC ACID
C11H8°2
2-Naphthoic Add
E F
inouti. sree. wooa nreserv.
LDso No data
Hazard Moderate R,f
Irritant
Purity 99X
1
2
3
4
5
6
P780
NITROBENZENE
W°2
Nitrobenzene
Mol.Wr.
123.1
Induit. Sree. Chemical mfg,
IDW 640
Very flammable,
Hazard skin absorpt.Ref
somewhat toxic
Purity 99%
A B
P7sq
N-NITROSODIPHENYLAHINE
N-Ni trosod! phenyl ami ne
Mol.Wt. 198.2
Induil. Sree. No data
LOjo 1,650
Hazard Card nog. R«f.
suspect
Purity 93%
A B C D E F
1
2
3
4
5
6
P796
N-NITROSODIPROPYLAMINE
N-N1trosodlpropylami ne
Mol.Wt. 130.2
Induit. Srct. No data
LDjo No data
Hazard Card nog. R.f.
suspect
Purity 95*
A B C D E F
1
2
3
4
5
6
(C3H7)2N-N=O
P803 NONYL PHENOL
Mol.Wt. 196.4
Indust. Sr». Synthet. fibers
IDso 1.620
Skin absorpt.,
Hazard Somewhat flam-R,
mable
Purity 9U
Nonyl Phenol
C9H,9
127
-------
Code Common Name Emp. Form. Chemical Name
Structure
PB12 OLEIC ACID C18H34°2 9-Octadecanolc acid
o
Mol.Wt. 282.5
i j . . Tall oil refin.,
ln"««. Src.. paper mfg.
L DSQ No data
Hazard Quite toxic Kef.
Purity 73%
A B C D E F
1
2
3
4
5
6
CH3(CH2)7CH=CH(CH2)7C-C
P821 PALMITIC ACID C16H32°2 n-Hexadecanoic add
Mol.Wt. 256.4 O
lndu.t. Sr«. Tal1 o" refin. .
paper mfg. , syntl
i n fibers
LD» No data
Hazard Toxic Kef.
Purity 9058
A B C D E F
.1
2
3
4
5
6
CH3(CH2)14C-OH
P830 n-PENTADECANOIC ACID C^H-^Oj n-Pentadecanoic acid
O
Mol.Wt. 242.5 M
Indutt. Srn. Paper mfg.
IDM No data
Hazard Toxic R.f
Purity
A B C D E F
1
2
3
4
5
6
CH3ICH2),3C-OH
P838 PHENANTHRENE CUH10 Phenanthrene
Mol.Wt. 178.2 x^X.-^^s
... A B C D E F | II |
ID jo 700 (mse)
Hazard Toxi c , Rcf.
irritant
Purity 98+*
1
2
3
4
5
6
,1 J!. /i)
r^r^x^
\^y
P845 PHENOL C,-H,0 Phenol
(Carbolic add)
OH
Mol.WI. 94.1 ^4\
Induit. Srce. Petrochem, wood
preserv., paper
IDjo 414 mfg.
U.T..J Corros., flatn-
Ha""1 mable, toxic «•«.
Purity 99+U
A B C D E F
1
2
3
4
5
6
1 ff ^1
1 I
^SN,X^
128
-------
Code Common Name Emp. Form.
Chemical Name
P853 PHENYL ETHER C12H10° Phenyl Ether
Mel.Wl. 170.2
Indml. Src*. Synthet. fibers
I D,o 4,000 '
Hazard Toxic vapor, ncf.
f 1 ammabl e
Purity 98%
A B C D E F
1
2
3
4
5
6
P860 PHTHALIC ANHYDRIDE CgH^ 1 ,3-Isobenzofurand1one
Mel.Wl. 148.1
A B C D E F
Indait. Srce. No data
LDw 4,020
Hazard No data *,f.
Purity 99.7+X
1
2
3
4
5
6
P866 2-PICOLINE C6H7N 2-Methylpyr1d1ne
Mel.Wl. 93.1
Indmr. $ree. No dst«
I DM 790
Hoiord Flammable,
absorpt.
Purity 98X
ABC D 1 F
1
2
3
4
5
6
P867 3-PICOLINE C6H?N 3-Hethylpyr1d1ne
Mel.Wt. 93.1
Induil. Sru. No data
I DM No data
Hazard No data R*f.
Purity 99*
A B C D E F
1
2
3
4
5
6
P868 4-PICOLINE C6H?N 4-Methylpyr1d1ne
Mel.Wl. 93.1
, , . ABC D 1 F
Induil. Srce. No data
LDM 1.290
*— Mr**-
Purity 98X
1
2
3
4
5
6
Structure
129
-------
Code Common Name Emp. Form. Chemical Name
P875
Benzo[def]phenanthrene
Mo,.Wl. 202.3
Indutt. Sree. Wood preserv.
LDso No data
Carcinogen
Hazard Suspect Ret.
Purity 99+*
ABC D
1
2
3
4
5
6
E
f
Structure
P882 QUINOLINE
CgH?N
1-Benzazine
Mol.Wt. 129.2
Indust. Srce. Wood preserv.
L Djo 460
Purity 99+*
ABC D
1
2
3
4
5
6
E
F
P889 SALICYLIC ACID
C?H503
Mol.Wt. 138.1
Indus!. Srce. Paper mfg.
L DM 891
Hazard Toxic Ref.
Purity 99+*
o-Hydroxybenzoic acid
o
11
C-OH
A B C D E F
1
2
3
4
5
6
^x^^O\
r ^Y
^^
OH
P896 STEARIC ACID
Mol.Wt. 284.5
Indust. Srce. Paper mfg.
ID 50 No data
Hazard Toxic Raf
Purity 97+*
O
ABC 0 E F CH,(CHJ,AC-
1
2
3
4
5
6
O £. •
P902
STYRENE
CH
Styrene
Mol.Wt. 104.1
Indust. Srce. Petrochem.
LDso 4-920
Hazard Very flamnabl,^^
toxic vapor
Purity 99*
A B C D E F
1
2
3
4
5
6
u
-CH=CH2
130
-------
Chemical Name
Structure
P909 1.1.1.2-TETRA. C2H2C14 1 ,1 ,1 ,2-Tetrachloroethane
CHLOROETHANE
Mol.Wt. 167.8
Indust. Sree. No data
ID 50 No data
«— WE& ""•
Purity 98. 5%
P910 1,1,2,2-TETRA= C2
CHLOROETHANE
Mol.Wt. 167.8
Chlor. solvents
Indvtt. Sree. mfg
LDso No data
H"ord T°oxiCc'vapor *•<
Purity 98%
A B C D E F
1
2
3
4
5
6
CI3C-CH2CI
H Ci 1,1,2,2-Tetrachloroethane
ABC D E F
1
2
3
4
5
6
CI2HC -CHCI2
P913 TETRACHLOROETHYLENE C2C14
Tetrachloroethylene
Mol.Wt. 165.8
Indus!. Sree. No data
I Dso No data
Hazard Toxic vapor Ref |
Purity 99+%
A B
D E F
CI2C=CCI2
CCH0C1.0 Tetrachlorophenol
6 f- "
CHLUKUPHtNUL
Mol.Wt. 231.9
A B C D E F
Indutt. Sree. Mo data
105, HO
Hazard Irritant, R.f.
very toxic
Purity 98%
1
2
3
4
5
6
CI
P924 TETRAHYDROFURAN
Mol.Wt. 72.1
Induit. Sree.
LDso
Hazard
Purity
C4H80
Tetrahydrofuran
A B
D E F
3,000
Extremely
flammable, "•*•
irritant, toxic
vapor
99.9%
1
2
3
4
5
6
131
-------
Code Common Name Emp. Form. Chemical Name
Structure
P927 1,2,3,4-TETRA* cinHi? 1 ,2,3,4-Tetrahydronaphthalene
HYDRONAPHTHALENE lu '
(Tetralln)
j^^ jXX.
Mol.Wt, 132.1 ^ ^^T^^^^N
A B C D E F
indusi. A re 8 , no Qata
I DM 2 ,860
u A Flammable,
nazara -irritant ••'•
Purity 99%
1
2
3
4
5
6
L ,^1
^\^x"/^ ^^^ ,^^
P934 2,2'-TH10DlETHANOL C4Hio02S 2,2'-Thiodiethanol
Mol.Wt. 122.2 Hf~)l(~U \ dlfU \ /~\u
ABC D E F HU(CH2J2S(CH2)2OH
Induit. Src*. Rubber mfg.
1 DSO 3,960 (g.p.)
Hazard No data R.f.
Purity 98+*
I
2
3
4
S
6
P941 m-TOLUIC ACID C8Hg02 m-Tolufc Acid
9
M.LWI. 136'2 f'0"
Chlor. paraff.
Indust. Srce. mfg.
ID jo ca 400
Hazard Toxic R,f.
Purity W%
A B C D E F
1
2
3
4
s
6
II
\^^CH3
P942 p-TOLUIC ACID C8H8°2 p-Toluic Add
9
C-OH
Mol.WI. "6.2 J^
Chlor. paraff.
Induit. Src*. mfg.
L DSO 400
Hazard Toxic R0f
Purity 98%
A B C D E F
1
2
3
4
5
6
r n
^Y^
CM3
P949 1,2,4-TRICHLORO' C,H,C1, 1,2,4-Trlchlorobenzene
BENZENE 6 i
Cl
M.I.WI. «!•» J, -.
Synthet.
Indoit. Src*. fibers
I DSO 756
Hazard Irritant, ^*^'
somevrhtt toxic
Purity 99X
A B C D E F
1
2
3
4
5
6
11
k^1
T^
Cl
132
-------
Code Common Name Emp. Form. Chemical Name
Structure
P956 1,1,1-TRICHLOROETHANE C2H3C13 1 ,1 ,1-Trichloroethane
Mol.Wi. 133.4 CI3C-CH3
LDso 5,660 (rbbt)
Hazard No data Ref
Purity 97%
P957 1,1,2-TRICHLOROETHANE C2
1
2
3
4
5
6
H,Cl 3 1,1 ,2-Trichl oroethane
MOI.W.. 133.4 CI2HC-CH2CI
.... Chlor. solvts. A B C D E F
Indust. Srcc . mf ~
LDso 580
Hazard T°*ic, toxic
vapor, skin •
absorpt.
Purity 97%
1
2
3
4
5
6
P964 TRICHLOROETHYLENE C2HC13 Trichloroethylene
Mol.Wi. 131.4 CICH=CCI2
A B C D E F
Indus!. Srce. No data
10,0 4'920
.. . Carcinog. sus-
Haiard pect, toxic *•«•
vapor
Purity 98%
1
2
3
4
5
6
P974 2,4,6-TRICHLOROPHENOL C6H3C130 2,4,6-Trichlorophenol
OH
Mol.Wi. 197.5 ,_, ^
. . . Chlor. solv.
Indust. Srce. mfg
LDso 82°
Hazard Irritant R)(f
Purity 98%
A B C D E F
1
2
3
4
5
6
11
^ J
^r
Cl
P985 URETHANE C3H7N02 Ethyl carbamate
o
Mol.Wi. 89.1 II
„ ABC D E F NH2-C-OC2H5
Indutl. Srce. Paper mTg.
LDso 1^0 (mse)
Hazard Carcinogen
susp., toxic
Purity 995;
1
2
3
4
5
6
133
-------
fiodj. Common Name Emp. Form. Chemical Name
Structure
P995 VANILLIN
Mol.Wl. 152.1
Indutt. 5rc». Paper mfg.
I DJO 1,580
Hazard No data
Purity 993!
A B
4-Hydroxy-3-methoxy=
benzaldehyde
E F
134
-------
Section III
SAFE HANDLING OF PRIMARY REFERENCE STANDARDS
Personnel handling pesticide and other highly toxic organic standards
should be well trained so as to be fully aware of the health hazards involved.
Many pesticides are extremely toxic and some are suspected as being
carcinogenic as well.
Extreme caution must be exercised while handling many organophosphorous
pesticides. They are highly toxic, not only by oral ingestion, but dermally
and by inhalation. Disposable plastic gloves should be worn at all times
during the handling of the primary standard. Except for the time required for
weighing at the analytical balance, all handling of the standard should be
carried out in an exhaust hood to minimize inhalation of vapor. If, in spite
of all precautions, a drop of the primary standard should get on the skin,
thorough washing with copious amounts of soap and water should be carried out
immediately. In case of heavier spillage on the skin or any other accidental
exposure, the soap and water treatment should be applied and a physician
should be consulted AT ONCE.
135
-------
Section IV
PREPARATION AND STORAGE OF REFERENCE STANDARD SOLUTIONS
A. STORAGE OF PRIMARY STANDARDS:
Primary standards are the pure compounds you receive. The manner
of their storage is of considerable importance and should not be treated
as a haphazard thing. The majority of standards in the organochlorine
class may be safely stored at ambient temperature, whereas the latter,
should most emphatically be refrigerated (2-4°C). Since no harm should
result from the storage of the organochlorine compounds under refriger-
ation as well, the average laboratory would probably find it advisable
to store all primary standards under refrigeration.
Another bonus of refrigerated storage is that the lower temperature
reduces the odor problem in the laboratory by (1) a decrease in the
volatility and (2) odor confinement within the refrigerator.
When using refrigerated storage for primary pesticidal compounds,
it is advised that the small sample bottles be stored within some
type of larger air-tight container. If refrigerator space can be
spared, a cabinet type desiccator with about an inch of indicating
silica gel at the bottom works very satisfactorily, providing both
isolation and an anhydrous atmosphere. Laboratories with limited
refrigerator space may substitute large, wide mouth glass jars (such
as wholesalepack mayonnaise jars) with hand fashioned 1/4 inch mesh
wire platforms at the bottom. The silica gel may be placed in the
bottom and the bottles of standards can be held on the wire platform.
No organophosphorous compound should be held under any conditions
longer than six months. This factor should be borne in mind when requesting
compounds.
When a bottle is removed from the refrigerator for use, the
temperature should be f u 11 y equ i 1 i bra ted wi th that of the room _b_efor_e
opening bottle. Weighing should be done rapidly and bottle cap
should be left off only long enough to withdraw sample. After weighing,
the bottle should be returned to storage immediately.
136
-------
B. EQUIPMENT AND SOLVENTS:
1. Analytical balance capable of an accuracy of ±0.05 mg.
2. Flasks, volumetric - 25, 50, and 100 ml.
3. Spatula, stainless steel.
4. Stirring rods, glass, ca. 100 x 6 mm.
5. Bottles, prescription type, 1/2 or l~ounce with foil-lined plastic
screw caps Sizes 15 and 18 (available from many wholesale drug
firms).
6. Refrigerator, explosion-proof, with freezer across top, capable of
maintaining +4°C in refrigerator section and -15°C in freezer.
NOTE: Chemical and sample materials should preferably be stored in
separate refrigerators; however, if a laboratory has only one
refrigerator, sample materials should be stored in air-tight glass
containers to prevent contamination by spillage or airborne vapors
from pesticides.
7. Vials, screw cap, 15 x 45 mm, 1 dram, Kimble number 60910, without
caps.
8. Screw caps, plastic, with foil liners, Size 13, Arthur H. Thomas,
Cat. #2386-L22.
9. Microflex tube screw cap with Teflon-faced rubber liners, Size #13,
Kontes K-749003, size code 0001.
10. Primary pesticide standards. Available to qualified laboratories
from the Repository at Research Triangle Park, North Carolina.
NOTE: The organophosphorous compounds are subject to a wide
variety of oxidations, rearrangements, and hydrolytic reactions.
These should be stored in the refrigerator in a large air-tight
container (such as a wide-mouth mayonnaise jar), or in a desiccator,
to minimize moisture absorption, release of toxic vapors, or cross-
contamination. ALL HANDLING OF THESE STANDARDS SHOULD BE DONE UITH
RUBBER OR DISPOSABLE~PLASTIC GLOVES. SKIN CONTACT WITH HIGH
CONCENTRATES CAN RESULT IH_ ILLNESS OR DEATH.
11. Isooctane (2,2,4-trimethylpentane) or hexane, pesticide quality,
distilled in glass.
NOTES: (1) A 10 yl injection of the solvent to be used should
result in a chromatogram with zero background.
(2) Isooctane or hexane are both suitable for standard dilutions.
Isooctane, while more expensive, offers the advantage of a 100°C
137
-------
boiling point and is therefore less subject to evaporation from
repeated opening of bottles, particularly of working standard
mixtures.
12. Benzene or toluene pesticide quality, distilled in glass.
NOTE: Benzene is a suspected carcinogen and should be carefully
handled, avoiding inhalation of vapor and skin contact.
C. PROCEDURES:
1. Preparation of concentrated stock standard solutions.
Except for concentrates for special purposes, a concentration of
200 micrograms per milliliter is suitable for most common pesticides.
This concentration can be prepared by diluting 20 mg of the 100%
primary standard to 100 ml.
Either benzene or toluene are suitable solvents for most of the
primary standards. Benzene has the slight disadvantage of solidifying
at freezer temperatures, but the expansion has never proved sufficient
to cause bottle breakage in this laboratory.
The concentrated standards of chlorinated compounds should maintain
uniform strength for a 6-month period at -15 to -20°C. The organo-
phosphate standards are far less stable than the organochlorines.
It is recommended that the concentrated stock be held no longer
than 4 months at -15°C.
NOTE: Extreme care must be used in the formulation of this
standard. If an error is made here, all subsequent dilutions
for the life of the standard will be inaccurate. Obviously,
all quantisations of samples will be similarly incorrect.
2. Preparation of standard solutions of intermediate concentration.
These will be the standard solutions from which the final working
mixtures will be prepared. The decrease in strength from the
concentrated stock to the final working standard is generally too
great to achieve in one dilution step. Except for a few of the less
responsive compounds, it is generally preferable to prepare a solution
of an intermediate concentration. This solution, in turn, is further
diluted volumetrically to obtain the final working standard. Con-
venient intermediate concentrations of a number of the more common
pesticides are given in Table 1.
NOTE: Under no circumstances should a micro!Her syringe be
used to make the transfer from concentrated solution to the
flask of the final working standard. The chance for error is
greatly increased by this technique.
138
-------
The Intermediate concentration standards of the chlorinated compounds,
if stored in the freezer at -10 to -15°C, should be stable for a
6-month period. Except for the fact of repeated warming and opening
for making working standards, these standards could be held much
longer. However, considering this factor, a safer time limit is
6 months.
The organophosphorous intermediate standards should be similarly
stored in the freezer. The time limit on these standards should
not exceed 4 months.
3. Working Standard Mixtures.
a. Preparation and storage.
Isooctane is favored as the solvent for the working standard
mixtures because the many repeated bottle openings greatly
increase the possibility of evaporation and subsequent concen-
tration of standards if a lower boiling point solvent is used.
Table 2 is useful in rapid determination of the aliquot volumes
of the stronger concentrates required for given concentrations
of the diluted standards.
The use of standard mixtures of varying concentrations is a
necessity for reliable quantification of unknowns. The degree
of peak height variation between sample and standard should
ideally not exceed 10% although variations up to 25% should
not result in appreciable error. A simple means of achieving
this is to have available working standard mixtures of three
concentrations. The suggested mixtures given in Table 3 have
proved very useful in the analysis of tissues. Those labora-
tories conducting analysis on environmental samples may wish
to make alterations in the compound content, but the 3-
concentration concept should be applicable for any media.
D. CONTAINERS FOR STANDARD SOLUTIONS:
Volumetric flasks are, of course, the recommended glassware for prepa-
ration of all standard solutions. However, these containers are not
advised for storage primarily for the following reasons:
1. An inordinate amount of valuable refrigerator space is required
for the storage of any significant number of flasks.
2. A large quantity of expensive volumetric glassware is tied up
and therefore not available for other uses.
A most suitable container for the concentrated stock that will be
stored from 4 to 6 months is the bottle described in Item 5 under
EQUIPMENT AND SOLVENTS. These bottles are inexpensive, store well,
139
-------
and the recommended foil-lined caps present an inert surface in
case of contact by solvent. If desired, this type bottle may be
used for storing the standards of intermediate concentration.
When the foil liners are used, these provide a wholly suitable
container and store well.
The selection of working standard containers and manner of
handling and storage are, to some extent, a matter of local
preference. Following are two procedures, either of which has
proved satisfactory:
Method A
After the working standard mixtures are formulated in
volumetric flasks, they are transferred to 1/2-oz. pre-
scription bottles fitted with foil-lined screw caps.
These should be stored in the refrigerator at all times
when not in use. Organochlorine (OC) working standards
should be renewed monthly and the organophosphorous (OP)
compounds semimonthly.
Method B
The working standard mixtures are transferred from the
volumetric flasks into 1-dram vials (Item 7) fitted with
No. 13 foil-lined screw caps (Item 8). The set of standards
needed for immediate use may be conveniently fitted in a
small block of one inch polystyrene into which holes have
been cut with a rattail file to a size that will snugly
accommodate the vials. After drilling holes this block
can be laminated to another solid block of equal dimensions
with Elmers glue. The remainder of the filled vials will be
stored continuously at -10 to -15°C.
The OC standard solutions in the block are held continuously
at room temperature and are discarded at the end of 1 week;
fresh vials from the freezer should then be substituted
for the discarded solutions. Vials of OP solutions, however,
should be kept in the refrigerator at all times when not in
use. Vials of OC compounds that are kept frozen can be held
in the freezer for up to 6 months, whereas frozen OP compounds
should be discarded after 4 months. A sketch of the block
follows:
140
-------
Polystyrene block device as a holder for vials
141
-------
Table 1
SUGGESTED CONCENTRATIONS OF STANDARD SOLUTIONS
OF INTERMEDIATE CONCENTRATION
CHLORINATED
ng/yl
ORGANOPHOSPHOROUS
ng/yl
a-BHC
6-BHC
Lindane
Heptachlor
Aldrin
Heptachlor epoxide
o,p'-DDE
p,p'-DDE
Endosulfan
DDA (methyl ester)
Dieldrin
o,p'-DDD
Endrin
Perthane
p,p'-DDD
o,p'-DDT
p,p'-DDT
Oil an
Methoxychlor
Tetradifon
Mi rex
Chlordane
Toxaphene
1
2
1
1
1
1
1
2
4
*
2
2
4
*
4
4
4
10
10
20
10
10
*
Mevinphos
Phorate
Dimethoate
Diazinon
Methyl parathion
Ethyl parathion
Malathion
Ethion
Carbophenothion
Azinphos (methyl or ethyl)
Dichlorvos
Dioxathion
Ronnel
Fenthion
Phosphamidon
Folex
DEF
Phencapton
Monocrotophos
EPN
Phosmet
Coumaphos
Disulfoton
50
50
40
20
10
10
20
20
10
*
2
20
10
4
50
30
10
50
*
*
*
50
2
*Final working standard made up directly from the 200 ng/yl concentrate.
The solvent for the intermediate standards may be isooctane or hexane
(pesticide quality). Isooctane should be considered because of its
higher boiling point, hence reduced possibility of evaporation of solvent
when container is repeatedly opened.
142
-------
e
a M
j3 o
4J CO
C
H 01 to
B >
•H a)
01 OCX
.c -u
4J 10
a) >H
01 3 O
M rH
B CO C
> 0
trt
BO«
3 B M
rH O 4J
O O C
O 01
m o
*J J= C
«H U O
01
rH *J
« 01
e x
•H 01 4J
>
CO -H 01
01 *-4
3 H
rH [0 C
a E
> o 3
4-1 rH
O
01 rH O
se,=
rH O C.
to O rd
> rH 01
C h <(-(
O 01 0
•H O.
•U -O
3 T3 n
rH 01 01
•H l-i 43
•a -H
3 U
•a cr m
01 01
o) n 01
3 3
• rH
X C it)
rH rH >
C O
O CO
§ °>
6 T3 "
O 01
O U
n
• n o
rM u u
c
01 01 U
rH O j;
-a C 6C
H! O -H^
EH O )-.
*^ ^ ~~ ~ — —
Ovovoiriinu-imsj--3--»
-------
Section V
DECODING RESIDUE ANALYTICAL METHOD REFERENCES
Six residue method references for each compound are cited if this number
could be located. Those cited do not necessarily represent the complete bibliog-
raphy for any given compound. Where there were ample bibliography, methods
for various types of media are cited. With a few exceptions, references are
restricted to publications within the past ten years. There is no intention
to endorse or recommend any cited methodology. They are represented purely as
an aid to the analyst in the search for candidate methodology to resolve an
analytical task.
To conserve space, the references are presented in code, each citation
in a series of six blanks under capital letter headings of A through F in Sec-
tion II wherein all available reference standard compounds are listed. The
decoding key is given in the following:
A B C D E F
Source Year Volume Page Instrumentation Media
Name of Journal or Other Source
(Languages; B = Bulgarian, E = English, F = French, G = German, I = Italian,
P = Polish, A = Arabic, J = Japanese, R = Russian, S = Spanish)
A Analysis of Pesticide Residues in Human and Environmental Samples.
Ed. Thompson, JF. Environmental Protection Agency, Research
Triangle Park, N.C. 1975
B Official Methods of Analysis of the Association of Official
Analytical Chemists, llth Ed. (with supplements), 1970
C Pesticide Analytical Manual. Ed. John R. Wessel. Food and
Drug Administration, Washington, D.C.
Volume I, 1972 (MuHi residue)
Volume II, 1973 (Individual Residues)
D Standard Methods of the Stored Products Insects Branch.
Agricultural Research Service, U.S. Dept. of Agriculture
American (A...; Z...) (All E)
AA American Laboratory
AB Analytical Chemistry
AC Analytical Methods for Pesticides, Plant Growth Regulators, and
•Food Additives. Ed. Zweig, G. Academic (New York)
AD Bulletin of Environmental Contamination and Toxicology
AE Chemical Abstracts (Number in Column "C" represents the volume
number (hyphen) abstract number)
144
-------
AF Dissertation Abstracts International (Section B: Sciences and
Engineering)
AG Environmental Science and Technology
AH Food and Drugs from the Sea, Proceedings of the Conference on
Drugs from the Sea, 3rd Ed. Worthen, LR. Washington, D.C.
Marine Technological Society
AI International Journal of Environmental Analytical Chemistry
AJ Journal of Agricultural and Food Chemistry
AK Journal of the American Water Works Association
AL Journal of the Association of Official Analytical Chemists
AM Journal of Gas Chromatography (Ending December, 1968, name
changed to following title)
AN Journal of Chromatographic Science
AO Journal of Dairy Science
AP Journal of Economic Entomology
AQ Journal of Environmental Quality
AR Journal of Food Science
ARA Journal of Food Science Technology
AS Journal of Pharmaceutical Sciences
AT Microchemical Journal
AU Mississippi Farm Research
AV Health Aspects of Pesticides Abstracts Bulletin (Ending December,
1973, name changed to the following title)
(Column "C" is Abstract number)
AW Pesticides Abstracts (Column "C" is Abstract number)
AX Pesticide Chemistry, Proceedings of the International Congress of
Pesticide Chemistry, 2nd, Tel-Aviv, Israel. Ed. Tahori, AS.
Six volumes. Gordon and Breach
AY Pesticide Monitoring Journal
AZ Proceedings of the Florida State Horticultural Society
ZA Proceedings of the Southern Weed Conference (name changed to
the following title)
ZB Proceedings of the Southern Weed Science Society
ZC Pyrethrum: Natural Insecticide. Pap. Int. Symp., 1972
Ed. Casida, JE. Academic (New York)
ZD Residue Reviews. Ed. Gunther, FA. Springer-Verlag (New York
ZE Science of the Total Environment
ZF Soil Science of America, Proceedings
ZG Tappi
ZH Trace Substances in Environmental Health, Proceedings of the
University of Missouri's Annual Conference. Ed. Hemphill, DD.
University of Missouri (Columbia)
ZI Weeds (Ending October 1974, name changed to the following title)
ZJ Weed Science
ZK Environmental Research
ZL Journal of Occupational Medicine
ZM Archives Environmental Contamination and Toxicology
145
-------
British (B...)
BA Analyst - E
BB Chemistry and Industry - E
BC Journal of the Science of Food and Agriculture - E
BD Journal of Stored Prpducts Research - E
BE Pesticide Science - E
BF Talanta - E,F,6
BG Water Research - E
BH Weed Research - E,F,G
BI Proceedings of the New Zealand Weed Pest Control Conference - E
Canadian (C...)
CA Canadian Journal of Plant Science
Egyptian (E...)
EA Journal of Chemistry of the United Arab Republic - E,A
French (F...)
FA Annales de Biologie Clinique
FB Annales des Falsifications et de 1'Experise Chimique
German (G...)
GA Archiv fuer Pflanzenschutz - G,E
GB Arch. Phytopath. Pflanz.
GC Archiv fuer Toxikologie - G,E
GD Deutsche Lebensmittel-Rundschau - G
GE Fresenius1 Zeitschrift fuer Analytische Chemie - G
GF Nahrung - G
GG Pharmazeutische Zentralhalle - G
GH Pflanzenschutz-Nachrichten (American Edition) - E
GI Pflanzenschutz-Nachrichten Bayer - G
GJ Vitis - G,E
GK Beitraege zur Tabakforschung - E,F,G
GL Vom Wasser - G
Italian (I...)
IA Agrochemia - E,F,G,I.S
IB Industrie Conserve - I,E,F,G ("Canning Industry")
146
-------
Indian (K...)
KA Journal of the Indian Chemical Society - E
Japanese (J...)
JA Agricultural and Biological Chemistry - E
JB Bochu-Kagaku - E,J ("Scientific Pest Control")
JC Bunseki Kagaku - E,J ("Japan Analyst")
JD Igaku To Seibutsugaku - J ("Medidine and Biology")
JE Kobe Journal of the Medical Sciences - E
JF Nippon Dojo-Hiryogaku Zasshi - J ("Journal of the Science
of Soil and Animal Fertilizers")
JG Nippon Noson Igakki Zasshi
JH Noyaku Kensasho Hokoku - J ("Bulletin of the Agricultural
Chemistry Inspection Station")
JI Noyaku Seisan Gijutsu - J ("Pesticides and Technique")
JJ Nippon Sembai Kosha Chuo Kenkyusho Kenkyu Hokoku - J
Polish (P...)
PA Bromatologia i chemia Toksykologiczna - E,P,R
PB Prace Instytatow i Laboratoriow Badawczych Przemyslu
Spozywcego - E,F,P.R
PC Prace Instytutu Przemyslu Organicznego - E,P,R
PD Roczniki Panstwowego Zakladu Higieny - E,R
Russian (R...)
RA Gazovaya Khromatografiya - R
RB Gigiena i Sanitariya - R
RC Hygiene and Sanitation - E (English version of the above title)
RD Khimiya v Sel'skom Khozyaistve - R
RE Voprosy Pitaniya - R
RF Zavodskaya Laboratoriya - R
RG Metody Opredeleniya Fitogormonov, Ingibitorov Rosta,
Defoliantov i Gerbitsidov - R
RH Voprosy Pitaniya - R
South African (S...)
SA South African Journal of Science - E
147
-------
A West European—Miscellaneous (W...)
WA Acta Chemica Scandanavica - E
WB Analytica Cbimica Acta - E
WC Annales de Gembloux - F
WD Journal of Chromatography - E,F,G
WE Journal of Radioanalytical Chemistry -
WF Veterinaro-Meditinski Nauki - B,E,R
E Type of Instrumentation or Determinative Procedure Used
1 Gas-liquid Chromatography, Electrolytic Conductivity Detector
2 Electron Capture
3 Flame lonization
4 Flame Photometric
5 Mass Spectrometer
6 Microcoulometric
7 Inert Gas Plasma Emission
8 Thermal Conductivity
9 Thermionic
10 Other or Unspecified (in abstract)
11 Thin Layer or Paper Chromatography (All methods of detection)
12 Spectrophotometry or Colorimetry
13 Atomic Absorption Spectrometry
14 Fluorimetry or Phosphorimetry
15 Electrochemical (All methods)
16 High Pressure Liquid Chromatography, Column Chromatography, or
article dealing primarily with extractive methodology
17 Enzymatic
18 Titrimetric (All methods)
19 Bioassay
20 Review article
21 Exact Method Uncertain (in abstract)
22 Nuclear Magnetic Resonance
F Sample Materials
Plant
a Foliage, general or unspecified plant tissues
b Forage/Fodder Crop
c Cereal/Grain Crop
d Vegetable Crop
e Fruit Crop
f Root Crop
g Oil-bearing Seeds (Cotton, Soybeans, etc.) or Vegetable Oils
h Nuts
i Trunk, Stalk (e.g. sugarcane), or Paper
148
-------
F Animal
j Animal, Insect, or Human Tissue (including fats)
k Fish, or Aquatic Species Tissue or Fats
1 Blood
m Urine
n Feces
Food
o Dairy Products
P Eggs
q Honey
r Bread
s Beer or Wine
Environmental
t Water
u Soil
v Air
Other
w Pesticides Formulations
x Working Solutions or Unspecified
ILLUSTRATION OF USE OF THE KEY
Referring to the compound, Acephate, we note a total of three references.
Taking the first reference for illustration, we see
A B C D E F
AL 74 57 189 3 a
Reference to the journal list shows that the AL under A refers to the
Journal of the Association of Official Analytical Chemists; the number 74 under
_B_ shows the publication year to be 1974; the 57 under C is the volume num-
ber of the journal; the 189 under D is the starting page of the journal publi-
cation; the digit 3 under E indicates that the determinative instrumentation
was gas-liquid chromatography with a flame ionization detector; and the lower
case a under F indicates that the author conducted his research on plant
tissues.
Published residue methodology could not be located for a number of the
compounds listed, but in many instances the producing companies have developed
methodology which are available by writing the companies. These company-
developed methods are referenced in the coding under the A heading by a
single digit and a capital letter. This symbol refers to the symbol opposite
some company listed in Section VI. For example, the symbol IE appearing under
the heading A identifies Amchem Products, Inc. as the method source; the
symbol 3Z refers to Gulf Oil Chemical, and so on. In these company method
citations, data under B , C , and D headings are omitted as they are
inapplicable.
149
-------
Section VI
LIST OF CONTRIBUTING PESTICIDE PRODUCING COMPANIES
Cotte Company Code
1A Allied Chemical Corporation 51
IB Abbott Laboratories 5K
IE Amchem Products, Inc. 5M
II American Cyanamid Company, Inc. 5Q
1Q BASF Wyandotte Corporation 6A
1Z Buckman Laboratories, Inc. 61
2A Celamerck GMBH & Co. KG (W. Germ.) 6M
2C Cheminova (Denmark) 6Q
2E Chempar Chemical Company, Inc. 6S
21 Chevron Chemical 6U
2M Ciba-Geigy Corporation 7A
2U Diamond Shamrock Corporation 7E
22 Dow Chemical U.S.A. 71
3A I.E. DuPont de Nemours & Co. 7J
3E E.M. Laboratories 7M
3M Fike Chemicals, Inc. 7Q
3N Fisons, Ltd. (England) 7U
3Q FMC Corporation 7Z
3Z Gulf Oil Chemical Company 8A
4A Hercules, Inc. 8E
4E Hoechst, AG (West Germany) 81
46 Hooker Chemicals & Plastics 8M
4H Hopkins Ag. Chem. Co. 8Q
41 ICI United States, Inc. 8U
4J ICI (Great Britain) 8Z
4P Kumiai Chemical (Japan) 9A
4Z 3M Company 9E
5E McLaughlin Gormley King Co. 91
Addendum: 9M
3C Eastern Chemical
Company
Merck, Sharpe, & Dohme
Miller Chemical & Fertilizer
Mobil Chemical Company
Monsanto Commercial Products Co.
NOR-AM Agricultural Products Co.
01 in Corporation
S.B. Penick & Company
Penny/alt Corporation
Philagro S.A. (France)
Pfister Chemical, Inc.
PPG Industries, Inc.
Plant Protection, Ltd. (England)
Rhodia, Inc., Chipman Division
Rohm & Haas Company
Sandoz, Inc.
Schering (West Germany)
Shell Chemical Company
Stauffer Chemical Company
Sumitomo Chemical Co., Ltd. (Japan)
Tenneco Chemicals
Thompson-Hayward Chemical Co.
Union Carbide Corporation
Uniroyal, Inc.
The Upjohn Company
U.S. Borax Research Corporation
Velsicol Chemical Corporation
Vineland Chemical Co., Inc.
West Agro-Chemical, Inc.
Zoecon Corporation
150
-------
Section VII
INDEX OF PESTICIDE EQUIVALENT NAMES
The list of over 3,500 pesticide names in the following pages will
assist the reader in tracking down the official or common names of a wide
variety of pesticides when the only names available are of proprietary or
trade origin.
Each page of the compendium consists of two columns of pesticidal com-
pounds with each column showing on the left, in alphabetical order, a pesticide
name including "common" as well as proprietary or trade names. In the center
the common name is given if any has been assigned at the time of this edition.
On the right a stock code number appears if the compound is one which is
available from our repository stock.
The common or generic name is one confirmed for ordinary use by the
United States Standards Organization (USSO). The common names are proposed
by such organizations as the Weed Science Society of America (WSSA) or the
Entomological Society of America (ESA). In many cases the name appearing
under COMMON NAME is the name in most common use at the time of this edition
and may well be a proprietary name for lack of an accepted common name. The
reader should be aware, however, that during the life of this edition many
compounds known currently only by trade names will be assigned common names.
The subject of pesticide nomenclature is constantly changing. Many
people in the pesticide field have questioned the need to change relatively
short, simple and long-duration names such as Trithion, Guthion, and Bux
to such tongue-twisters as carbophenothion, azinphos methyl and bufencarb.
151
-------
PESTICIDE EQUIVALENT NAMES
NAME
Aa terra
Aatrex
Abar
Abate
Abathlon
Abletiz anhydride
Abstensil
Abstlnyl
AC 528
AC-4124
AC-12880
AC- 18682
AC-26691
AC-47031
AC- 52 160
AC-84777
AC-92553
Acarben
Acaralate
Acarin
Acarol
Acaron
Accelarate
Accothlon
Acephate
Acetaphos
Acethlon
Acetochlor
Acetophos
Acetoxon
Acrldd
Acrldol
Acrlzane
Acroleln
Acronlze
Acrylaldehyde
Actaroer
ActelHc
Act1-A1d
Act1d1one
Act1 spray
Actlvol
Actrll
Adamslte
Aerotheme TT
Afalon
Aresln
AFL-1082
AfHx
Afnor
Afos
Afugan
COMMON NAME
Ethazol
Atrazine
Leptophos
Temephos
Temephos
Rosin
Disulflram
Disulfiram
Dloxathion
Dlcapthon
Dimethoate
Prothoate
Cythloate
Phosfolan
Temephos
Difenzoquat
Penoxalin
Chi orobenzi late
Chloropropylate
Dlcofol
Bromopropylate
Chlordimeform
Endothall
Fenitrothlon
Acephate
Acetophos
Acethlon
Acetochlor
Acetophos
Acetoxon
Binapacryl
Binapacryl
Phenacrldane chloride
Acroleln
Chlortetracycllne
Acroleln
BltMonol
Pirimiphos-methyl
Cyclohex1m1de
Cyclohexlmide
Cycloheximlde
GibberelUc add
loxynil
Phenarsazone chloride
Trichloroethane
Llnuron
Monollnuron
Fluoroacetonlllde
Formothlon
Chi orophad none
Mecarbam
Pyrazophos
CODE
NUMBER
6590
0420
4190
0020
0020
2580
2420
1621
1610
0020
2395
1360
2340
1480
3240
3480
0025
0027
5643
1600
1600
1600
3790
4040
4240
4751
3722
1425
4441
5932
NAME
Agallol
Agrimycin
Agrisil
Agri strep
Agritol
Agritox
Agrosan
Agrotec
Agrothion
Agrox
Agroxon
AguaHne
Akar
Akton
Alachlor
Alamos
Alanap
Alar
Albamycin
Aldlcarb
Aldrin
Aldrite 4
Aldrosol
Alfacron
Alfa-tox
AH pur
Alipur-0
Alkron
Allantoln
Aileron
Allethrln
AlUdochlor
AlHsan
Alltox
Allyveratrole
Allyxycarb
Alon
Alodan
Alorac
Altoric
Altos 1d
Altozar
Ambox
Ambush
Amcide
Amerol
Amethopterln
Ametrex
Ametryn
Amex 820
Ami ben
Am1d1thion
COMMON NAME
MEMC
Streptomycin
Trichloronate
Streptomycin
Bacillus Thuringiensis
Trichloronate
PMA
2,4-D
Fenitrothlon
Phenylmercury urea
MCPA
Acrolein
Chlorobenzilate
Akton
Alachlor
Azothoate
Naptalam
Daminozlde
Novobiocin
Aldlcarb
Aldrln
Aldrln
Aldrln
lodofenphos
Methoxychlor & D1az1non
Cycloron & Chlorbufam
Cycluron
Parathlon ethyl
Allantoln
Parathlon ethyl
Allethrln
CDAA
Dlchloran
Toxaphene
Methyl eugenol
Allyxycarb
Isoproturon
Alodan
Alorac
THprene
Methoprene
Hydroprene
Blnapacryl
Aldlcarb
AMS
Atnitrole
Methotrexate
Ametryn
Ametryn
Butralln
Chloramben
Am1d1th1on
CODE
NUMBER
6222
6222
5680
2940
3480
0027
1360
4160
4920
0060
0080
0080
0080
4540, 2080
5245
5245
0100
1140
2260
6740
4531
0060
0200
0120
0120
0933
0140
152
-------
PESTICIDE EQUIVALENT NAMES
NAME
Anrtd-tMn W
Ami nocarb
Amlnoform
Amlnopterln
Amlnotrlazole
Am1noz1de
Amlphos
Amlton oxalak
Amltrole
Am1z1ne
Amlzol
Ammate
Ammoform
Amobam
Amoxone
Amrol
Ancymldol
Anllazlne
Aniline Green
Anlsuron
Anlten
Anofex
Ansar 8100
Ansar 157
Ansar 170
Antabuse
Antadlx
Antak
Anthlo
Anthon
Antletanol
Anthrazulnone
Ant1 carle
Ant1-K
Antlmllace
Antlphen
ANTU
ARC
APGA
Aphamlde
Aphldan
Apholate
Aphoxlde
Apl-Luster
APO
Appex
Aquaclde
Aqua-Kleen
COMMON NAME
Naphthalene acetamlde
Ami nocarb
Methenamlne
Amlnopterin
Amltrole
Dam1noz1de
DAEP
Tetram
Amltrole
S1maz1ne
Amltrole
AMS
Methenamlne
Amobam
2,4-D, trlethanoUmlne salt
Amltrole
Ancymldol
An1laz1ne
Maladrlte green
Anlsuron
F1 urecol -n-butyl ester
DDT
DSMA
KAMA
MSMA
Olsulflram
D1sulf1ram
Antak
Formothlon
Trlchlorfon
D1sulf1ram
Anthraqulnone
Hexachlorobenzene
Sulfa-qu1noxal1ne
Metal dehyde
Dlchlorophen
ANTU
Allyxycarb
Amlnopterin
Aphamlde
Aphldan
Apholate
Tepa
Thlabendazole
Tepa
Tetrachlor»1nphos
Dlquat
2,4-D
CODE
NUMBER
4880
0180
0200
0200
6160
0200
0220
0200
0230
0920
3630
1880
2860
4820
3722
6780
0250
3920
6660
3740
2660
2940
NAME
Aqualin
Aquathol
Aqua-Vex
Aqu1n1te
Aramlte
Arasan
Arathane
Aresln
A-Rest
Aretan
Aretlt
Ardall
Arlsan
Aroclors
Arprocarb
Arrhenal
Arsan
Arslnyl
Asar1n1n
Asazol
ASP-51
Aspon
Aspor
Asterol
Asulam
Asulox
Asuntol
AT-F
ATA
Atelor
Atgard
Athldathlon
Atlasclox
Atladde
Atlas 'A'
Atra-Bor
Atranex
Atratol
Atraton
Atraz^ne
Aureomydn
Avadex
Avadex BW
Avenge
Avlcol
Avlcol
Avltrol
Avlothane
Ax1om-n
Azacosterol
COMMON NAME
Acrolefn
Endothall
Sllvex
Chlorop1cr1n
Araml te
Thlram
Dlnocap
Monllnuron
Ancymldol
MEMC
Dlnoseb-acetate
Salicylic acid
Buturon
Polychlorlnated
blphenyls
Propoxur
DNSA
Cacodyllc add
DSMA
Sesamln
Aspon
Aspon
Z1neb
Dlamazole
Asulam
Asulam
Coumaphos
Hexachlorophene
AmUrole
Dlamazole
Dlchlorvos
Ath1dath1on
Demephlon
Sodium Chlorate
Sodium arsenlte
Atrazlne & Borate
Atrazlne
Atrazlne
Atraton
Atrazlne
Chlortetracycllne
Dlallate
Trlallate
Dlfenzoquat
PCNB
PCNB
4-AP
Hexachloroethane
Akton
Azacosterol
CODE
NUMBER
0027
3240
6120
6680
2560
4751
0230
2566
P889
5700-5707
0440
2S60
0961
2860
0300
0300
7120
0310
0310
1540
3940
0200
2320
0420
0420
0320
0420
2040
6770
2395
5280
5280
153
-------
PESTICIDE EQUIVALENT NAMES
NAME
Azak
Azidithion
Azlnphos-ethyl
ftzinphos-methyl
Aziprotryn
Azithiran
Azobenzene
Azobenzide
Azodrin
Azofume
Azolan
Azosam
Azothoate
B-995
B-900?
B-18510
B-31686
B-32394
B-33172
B-37289
B-40577
B-60618
B-78182
B-92114
Bacid
Bacteriostat-CS-1
Bactospeine
Bakthane
Balan
Balfin
Banafine
Bandane
Banex
Ban-Hoe
Banol
Bantex
Bantrol
Bantu
Banvel C
Banvel D
Banvel M
Banvel T
Barbara te
Barban
Barbasco
Baron
Barthrin
BAS 235-1
BAS 290-H
BAS 327-F
BAS 2903-H
BAS 3191
BAS 3460
COMMON NAME
Terbutol
Menazon
Azlnphos-ethyl
Azinphos-methyl
Azlprotryr
Azithirani
Azobenzene
Azobenzene
Monocrotophos
Azobenzene
teitrole
Tecordin
Azothoate
Daminozide
Naphtalophos
Phenthoate
Thioquinox
Fungi Ion
Fuberidazole
Trichloronate
Trimeturon
Fenzthiazuron
Chlorphoxim
Isofenphos
Fenthlon
Bithionol
Bacillus Thuringiensis
Bacillus Thuringiensis
Benefin
Benefin
Benefin
Bandane
Di camba
Lenacil 8 Propham 4185
Carbanolate
MBT, ZKC, Salt
loxynil
ANTU
Tri camba
DI camba
MCPA S Di camba 4340
Tri camba
Barban
Barban
P.otenone-containing plants
Erbon
Barthrin
Prynachlor
Fenethacarb
Prynachlor
Furcarbanil
Carbendazim
CODE
NUMBER
4453
3840
3820
0340
0340
0360
0340
0200
1681
3520
0480
0480
0480
2140
, 5860
4040
0260
2140
, 2140
0400
0400
1071
NAME
Basagran
Basalin
Basamaize
Basfapon
Basfungin
Basinite
Basudin
Batasan
Bavistin
Bay 13/59
Bay 21/199
Bay 2352
Bay 5212
Bay 6072
Bay 9010
Bay 10756
Bay 15080
Bay 15203
Bay 16259
Bay 17147
Bay 18510
Bay 19639
Bay 21097
Bay 22555
Bay 23323
Bay 23655
Bay 25141
Bay 23634
Bay 25648
Bay 29493
Bay 30130
Bay 30686
Bay 32394
Bay 33051
Bay 33172
Bay 36205
Bay 37289
Bay 37344
Bay 38819
Bay 39007
Bay 41831
Bay 44646
Bay 45432
Bay 46131
Bay 47531
Bay 49854
Bay 50282
Bay 60618
Bay 68138
Bay 70143
Bay 70533
Bay 71628
Bay 74283
Bay 77049
COMMON NAME
Bentazon
Fluchloralin
Prynachlor
Dalapon-NA
Methylmetiram
Dinoseb
Diazinon
Fentin acetate
Carbendazim
Trichlorphon
Coumaphos
Niclosamide
Tolyfluanid
Fenaminosulf
Propoxur
Demeton
Benquinox
Demeton -methyl
Azinphos-ethyl
Azinphos-methyl
Phenthoate
Disulfoton
Oxydeme ton-methyl
Fenaminosulf
Oxydisulfoton
Metasystox S
Fensulfothion
Coumatetralyl
Clonitralid
Fenthion
Propanil
Thioquinox
Fungi Ion
Phenthoate
Fuberidazole
Oxythioquinox
Trichloronate
Methiocarb
Gophacide
Propoxur
Fenitrothion
Aminocarb
Omethoate
Propineb
Dichlofluanid
Tolyfluanid
Allyxycarb
Benzthiazuron
Phenamiphos
Carbofuran
Methachlorphenprop
Methami dophos
Methabenzthiazuron
Quinalphos
CODE
NUMBER
0425
0407
1660
2760
2080
3527
1071
6780
1540
2020
0440
1981
3840
3820
2720
5220
2020
3500
0460
3520
5840
4800
4500
0440
3480
0180
1040
4750
5966
154
-------
PESTICIDE EQUIVALENT NAMES
NAME
Bay 77488
Bay 78418
Eay "9770
Bay 94337
Bay 1C5807
Baygcn
Bayluscide
Baymlx
Bayrusil
Baytan
Baytex
Baythion
Bazamid
BCM
BCP
BCPE
Belt
Benalan
Benazolin
Bencornox
Bendiocarb
Bendioxide
Benfluralin
Benlate
Benodanil
Benomyl
Benphos
Benquinox
Bensofume
Bensulide
Bentazon
Benthiocarb
Benthiocerb
Bentranil
Bentrazone
Benzabar
Benzac 354
Benzac 1281
Benzadox
Benzahex
Benzal Green
Benzamorf
Benzene hexachloride
Benzex
Benzilan
Benzomare
Benzomate
Benzoxymate
Benzoylprop ethyl
Benzthiazuron
Benzyl Benzoate
Beosit
Berelex
COMMON NAME
Phoxim
Edifenphos
Chi cran1" formethan
Metribuzin
Isoprocarb
Propoxur
Clonitralid
Coumaphos
Quinalphos
MEMC
Fenthion
Phoxim
Dazomet
Carbendazim
BCP
Dinite
Chlordane
Benefin
Benazolin
Berazolin
Bendiocarb
Bentazon
Benefin
Benomyl
Benodanil
Benomyl
Phosalone
Benquinox
Azobenzene
Bensulide
Bentazon
Thiobencarb
Thiobencarb
Bentranil
Bentazon
2,3,6-TBA
PBA
2,3,6-TBA
Benzadox
BHC
Malachite Green
Benzamorf
BHC
BHC
Chlorobenzilate
Phenobenzuron
Benzomate
Benzomate
Benzoylprop ethyl
Benzthiazuron
Benzyl Benzoate
Endosulfan
Gibberellic acid
CODE
NUMBER
4634
0440
0460
1540
5966
3520
1071
1200
0480
0472
0425
0480
0500
0500
5520
0340
0520
0425
0570
0570
0425
6920
6920
0577
0600
0600
0600
1360
0578
0580
3180
3790
NAME
Berkmyan
Betanal
Retanal AM
Beta-naphthol
Betanex
Betasan
Bexane
BFPO
BFV
BHC
BHC, gamma
Bidisin
Bidrin
Bifenox
Big Dipper
Bilevon
Bilobran
Binapacryl
Bine-Trol
Binnell
Bioallethrin
Biocide
Bioquin
Bioresmethrin
Biostat PA
Biotexin
Biothion
Biotrol BTV
Biotrol-Plus
BIPC
Biphenyl
Birlane
Bis-ethyl xanthogen
Bitemol
Bithin
Bithionol
Black Leaf 40
Bladafume
Bladan
Bladan-M
Bladex
Blastin
Blattanex
Blue Vitriol
Blulan
BMC
B-nine
Bo-Ana
Bolero
Bolls-Eye
Bomyl
Bonala
COMMON NAME
Oxytetrocydine
Phenmedipham
Desmedipham
2-NaphthoI
Desmedipham
Bensulide
MCPB
Dimefox
Formaldehyde
BHC
Lindane
Methachlorphenprop
Dicrotophos
Bifenox
Diphenylamine
Hexachlorophene
Monocrotophos , Dodine &
Dinocap
Binapacryl
MCPA
Benefin
Bioallethrin
Acrolein
Copper 8-Quinolate
Resmethrin
Oxytetracycline
Novobiocin
Temephos
Bacillus Thuringiensis
Bacillus Thuringiensis &
Pyrethrins
Chlorbutam
Biphenyl
Chlorfenvinphos
EXD
Simazine
Bithionol
Bithionol
Nicotine
Sulfotep
Parathion ethyl
Parathion methyl
Cyanazine
Pentachlorobenzol alcohol
Propoxur
Copper sulfate
Benefin
Methoquin-butyl
Daminozide
Famphur
Benthiocarb
Cacodylic acid
Bomyl
Benefin
CODE
NUMBER
5410
2006
4920
2006
0520
4380
0600
0680
0700
0733
3940
0360,
2780, 2560
4340
0480
0027
0027
6055
0020
0740
1300
3420
6160
5245
4580
1552
0440
0480
1681
3440
0570
0961
0480
155
-------
PESTICIDE EQUIVALENT NAMES
NAME
Border-master
Borolin
Botran
Botrilex
Bovinex
BPBSMC
BPMC
Brasoran
Brassical
Bravo
Brellin
Erestan
Broadside
Brofene
Bromacil
Bromax
Bromochlorphos
Bromeflor
Bromex
Brominal
Bromobonil
Bromocyclen
Bromodan
Bromofume
Bron)-0-Gas
Bromophenoxime
Bromophos
Bromophos-ethyl
Bromopropylate
Bromoxynil
Broropyrazone
Bromsalans
Bronate
Brophene
Brozone
Brulan
Brush-Rhap
BTB
BTV
Bucarpolate
Buctril
Bueno
Bufencarb
Bulan
Bulbosan
Bunema
Bunt-Mo-More
Bupirimate
Burex
Busan 72
Busan 77
Busulfan
COMMON NAME
MCFA
Picloram
Dlchloran
PCNB
Trichlorfon
BPBSMC
BPMC
Aziprotryn
PCNB
Chlorothalonil
Gibberellic acid
Fentin acetate
MSMA 8 Sodium Cacodylate
Bromophos
Bromacil
Chlorbromuron
Naled
Ethephon
Naled or Chlorbromuron
Bromoxynil Octanoate
Bromobonil
Bromocyclen
Bromocyclen
Ethyl ene di bromide
Methyl bromide
Bromophenoxime
Bromophos
Bromophos-ethyl
Bromopropylate
Bromoxynil
Bronnyrazone
Biaphene
MCPA & Bromoxynil
Bromophos
Methyl bromide &
Chloropicrin
Tebuthiuron
2,4,5-T
Bacillus Thuringiensis
Bacillus Thuringiensis
BCP
Bromoxynil Octanoate
MSMA
Bufencarb
Bui an
Bulbosan
Bunema
Hexachlorobenzene
Bupirimate
Pyrazon
TCMTB
PBED
Busulfan
CODE
NUMBER
4340
5600
2260
5280
6780
0791
5280
1640
3790
3527
0840
0800
1188
4860
3330
486C, 1188
0840
0860
0872
0820
2060
4340, 0820
0840
6840
4820
0960
0916
3920
5925
NAME
Butacarb
Butachlor
Butacide
Butban prynachlor
Buthidiazole
Butopyronoxyl
Butoxone
Butralin
Buturon
Butyl ate
Butyrac
Butyron
Bux
C-709
C-1414
C-1983
C-2059
C-2446
C-3126
C-3470
C-6313
C-6989
C-7019
C-7744
C-8353
C-8514
C-9122
C-9491
C-18898
C -19490
Cabblemone
Cacodylic acid
CAID
Calar
Caldium acid
methanearsonate
Calcium arsenate
Caldron
Calixin
Camphechlor
Cantrol
Caparol
Caprane
Capryl
Captafol
Captan
Captax
Caragard
Carbamorph
Carbamult
Carbanolate
Carbaryl
COMMON NAME
Butacarb
Butachlor
Piperonyl Butoxide
Buthidiazole
Indalone
2,4-DB
Butralin
Buturon
Butyl ate
2,4-DB
Buturon
Bufencarb
Dicrotophos
Monocrotophos
Chloroxuron
Fluometuron
Amidithion
Metobromuron
Dibenoxuron
Chlorbromuron
Fluorodifen
Aziprotryn
Carbaryl
Dioxacarb
Chlordimeform
Bromofenoxim
lodofenphos
Oimethametryn
Piperophos
Looplure
Cacodylic acid
Chi orophaci none
Calar
CAMA
Calcium arsenate
Di noseb
Tridemorph
Toxaphene
MCPB
Prometryn
Dinocap
Dinocap
Captafol
Captan
MBT
Terbumeton
Carbamorph
Promecarb
Carbanolate
Carbaryl
CODE
NUMBER
0922
5620
0920
3080
0933
0940
3080
0960
0700
0360
3620
4612
2391
1188
1060
2573
1480
0832
2411
0961
1425
0980
2760
6792
6740
4380
5780
2560
2560
1000
1020
1020
5752
1060
156
-------
'PESTICIDE EQUIVALENT NAMES
NAME
Carbasulam
Carbatene
Carbendazim
Carbetamlde
Carblcron
Carbofos
Carbofuran
Carbophenothlon
Carboxin
Carbyne
Cardelmycin
Carfene
Carmazlne
Carpene
Carpidor
Cartap
Carzol
Casoron
Castrix
Cathocin
Cathomycin
Caustic Barley
CBBP
CCC
CDAA
CDEA
CDEC
COT
Cekufon
Cedusan
Cela A-36
Cela S-1942
Cela S-2225
Cela S-2957
Cela S-4084
Cela S-4087
Cela S-6000
Cela S-6315
Cela W-B24
Celathlon
Celdion
Celfume
Celmer
Celmide
Celmone
Celphos
CEPHA
Cercobin
Cercobln K
Ceredon
Ceregam
Cereline
COMMON NAME
Carbasulam
Met 1 ram
Carbendazim
Carbetaml de
Dlcrotophos
Malathlon
Carbofuran
Carbophenothion
Carboxin
Barban
Novobiocin
Azinphos-methyl
Mancozeb
Dodlne
Benefln
Cartap
Formetanate hydrochlorlde
Dlchlobenil
Crlmidlne
Novobiocin
Novobiocin
Sabadilla
Chlorphonium
Chlormequat Chloride
CDAA
CDEA
CDEC
Simazine
Trfchlorfon
Dlchlorvos
Decafentln
Bromophos
Bromophos ethyl
Chlorthiophos
Cyanos
Cyanofenphos
Cypromid
Cyprazlne
Trl ferine
Chlorthiophos
Fentlazon
Methyl bromide
MEMC
Ethyl dlbromlde
Naphthalene
acetic acid
Aluminum phosphide
Ethephon
Thiophanate
Thiophanate-methyl
Benquinox
Methoxyethylroercury
silicate
Benquinox
CODE
NUMBER
4583
1071
1074
0700
4260
1040
1080
1100
0400
3820
2780
0480
3680
2200
1140
1160
6T60
6780
2320
0840
0860
1491
6360
1615
6822
1491
4900
3330
6670
6671
NAME
Ceresan
Certox
Certrol
CET
Cevadine
Cevadilla
CF-125
CGA 10832
CGA 18762
Chemathion
Chem 8am
Chemform
Chem-Hoe
Chem Neb
Chem-0-Bam
Chemocide PK
Chemox General
Chemrat
Chem R1ce
Chem Zineb
China Green
Chinomethionate
Chinosol
Chinothionat
Chip-Cal
Chipco Buctril
Chipco Crab Kleen
Chipco Spot Kleen
Chipcote
Chipco Turf
Herbicide "D"
Chipco Turf
Herbicide MCPP
Chipco Turf Kleen
Chiptox
Chloramben
Chlorambucil
Chlorammophene
Chloranil
Chloranocryl
Chlorasol
Chlorazine
Chlorbenside
Chlorbicyden
Chlorbromuron
Chlorbufam
Chi or Chem T-590
Chlordane
Chlordecone
Chlordene
Chlordimeform
Chloreal
Chlorex
Chlorfenac
COMMON NAME
Ethyl mercury chloride
Strychnine
loxynil
Simazine
Sabadilla
Sabadilla
Chlorflurenol
Prof 1 ural 1n
Procyazlne
Kalathion
Nabam
Streptomycin
Propham
Maneb
Amobam
Propyl Parabein
Dinoseb
Plndone
Propanll
Zineb
Malachite Green
Oxythloquinox
8-nuinolinol sulfate
Thioqulnox
Calcium arsenate
Bromoxynil
DSMA
Thiophanate
Methylmercury nitrite
2,4-D
MCPP
MCPP 8 2,4-D 4400
NCPA
Chloramben
Chlorambucil
Chlorambucil
Chloranil
Dicryl
Ethyl ene dichloride
Chlorazine
Chlorbenside
Chlorbicyden
Chlorbromuron
Chlorbufam
Toxaohene
Chlordane
Chlordecone
Chlordene
Chlordimeform
Trichloroisocyanuric acid
Dichlorethyl etrer
Fenac
CODE
NUMBER
3400
4040
6160
5746
5739
4260
6222
5860
4300
0220
2760
5840
7120
4800
0980
0820
2860
6670
2940
4400
, 2940
4340
0140
1180
674C
120C
1280
126C
1480
3460
157
-------
PESTICIDE EQUIVALENT NAMES
NAME
Chlorfenethol
Chlorfen1d1m
Chlorfenson
Chlorfenvlnphos
Chlorflurazole
Chlorflureeol
Chlorhexldlne
Chlorlnat
Chlorinated
Camphene
Chlor K11
Chlormephos
Chlormequat Chloride
Chlornltrofen
Chloroben
Chi orbenzl late
Chloroble Forte
Chloroble M
Chloroclde
Chlorofenlzon
Chlorofos
Chloro !PC
Chloromebuform
Chloromelamlne
Chloroneb
Chi orophad none
Chlorophos
Chloromethane
Chlorophenothane
Chlor-)-P1c
ChloroplcHn
Chloropon
Chloropropylate
Chi ore thai
Chlorothalonll
Chlorothene Nu
ChlorotMophene
Chlorox1fen1d1m
Chloroxone
Chloroxuron
Chloroxynll
Chlorparadde
Chlorphenamldlne
Chlorphonlum
Chlorphos
Chlorphoxlm
Chlorprazophos
Chlorprocarb
Chlorpropham
Chlorpyrlfos
Chlorpyrlfos methyl
Chlorqulnox
Chlorsulphaclde
COMMON NAME
D1m1te
Monuron
Ovex or Chlorfenson
Chlorfenvlnphos
Chlorflurazole
Chlorflurenal
Chlorhexldlne
Barban
Toxaphene
Chlordane
Chlormephos
Chlormequat chloride
Chlornltrofen
D1chlorobenzene-0
Chlorobenzllate
Llndane, endosulfan.
copper oxide
Maneb
Chlorbenslde
Ovex or Chlorfenson
Trlchlorfon
Chlorpropham
Chloromebuform
Tr1chloromelam1ne
Chloroneb
Chlorophaclnone
Trlchlorfon
Methyl chloride
DDT
Chlorop1cr1n
Chlorop1cr1n
Chloropon
Chloropropylate
DCPA
Chlorothalonll
Trlchloroethane
Chlorothlophene
Chloroxuron
2.4-D
Chloroxuron
Chloroxynll
Chlorbenslde
Chlordlmeform
Chlorphonlum
Trlchlorfon
Chlorphoxlm
Chlorprazophos
Chlorprocarb
Chlorpropham
Chlorpyrlfos
Chlorpyrlfos methyl
Chlorqulnox
Chlorbenslde
CODE
NUMBER
4760
1300
0400
6740
1200
1316
2280
1360
4300
6780
1420
1380
1425
6780
1880
1720
1640
2940
1480
6780
1420
2900
2902
NAME
Chi orthal -methyl
Chlorth1am1d
Chlorth1ep1n
Chlorthlophos
Chlortoluron
Chromaphon
Chryson
CIBA 709
CIBA 1414
CIBA 8353
CIBA 8514
C1d1al
dluan
C1ner1n I,
allyl homolog
C1odr1n
dovap
CIPC
C1san1Hde
CHram
dtrazon
Clarosan
CUn
Clobber
Cloflucarban
ClonHralld
Cloprop
Clorophene
Clout
CMA
CMDP
CMPP
CHU
CO-11
Cobex
COBH
Colloldex
Col ophony
Comlte
Compound 448
Compound 1080
Compound 1081
Compound 4072
Compound 7744
Compound C
Copper oxlnate
Coprantol
Copro
Co-Ral
CorbH
Cord1an1ne
Cornox CWK
Cornox M
COMMON NAME
DCPA
Chlorth1am1d
Endosulfan
Chlorthlophos
Chlortoluron
01t1on
Resmethrln
Olcrotophos
Monocrotophos
Dloxacarb
Chlordlmeform
Phenthoate
Pyr1d1n1tr1l
AllethHn
Crotoxyphos
Crotoxyphos & Dlchlorvos 1500
Chlorpropham
C1san111de
Tetram
Benzomate
Terbutryn
Salicylic Add
Cypromld
Cloflucarban
Clon1tral1d
Cloprop
Clorophene
DSMA
Calar
Mevlnphos
HCPP
Monuron
CO-11
D1n1tram1ne
Benqulnox
Copper oxychlorlde
ROSM
Proparglte
2-Phenylcyclohexanol
Sodium fluoroacetate
Fluoroacetamlde
Chlorfenvlnphos
Carbaryl
Trlcamba
Copper 8-Qu1nolate
Copper oxychlorlde
Copper oxychlorlde sulfate
Coumaphos
Anthrazulnone
Allantoln
Benazolln
MCPA
CODE
NUMBER
1720
3180
1491
1512
6055
0700
0360
2573
1480
0100
1500
, 2320
1420
1523
3980
P889
0460
2860
4640
4400
4760
2551
5160
1300
1060
1540
0250
4340
158
-------
PESTICIDE EQUIVALENT NAMES
NAME
Cornox RK
Corodane
Coromerc
Corothlon
Coroxon
Corozate
Cotnlon-ethyl
Cotnlon-roethyl
Cotofor
Cotoran
Coumachlor
Coumafene
Coumafuryl
Coumaphos
Coumatetralyl
Coumlthoate
Counter
Coxysan
CP C
3-CP
4-CP
CP 4742
CP 6343
CP 15336
CP 31393
CP 50144
CP 53619
3 CPA
4-CPA
CPA
CPBS
CPCBS
CPMC
CPMF
4-CPP
Crab-E-Rad 100
Crab Kleen
Crag Fly Repel 1 ant
Crag Fruit
Fungicide 341
Crag Fungicide 974
Crag Herbicide 1
Crag Herbicide 2
Crag Nemaclde
Credazine
Cr1m1d1ne
Croneton
Crop Rider
Crotamitop
Crotoxyphos
Crufomate
Cryolite
COMMON NAME
Pfchlorprop
Chlordane
Phenylmercury ethylenediamlne
Parathion ethyl
Coroxon
Z1ram
Azlnphos ethyl
Azlnphos methyl
Olpropetryn
Fluometuron
Coumachlor
Warfarin
Coumafuryl
Coumaphos
Coumatetralyl
Dltlon
Terbufos
Copper oxychloride
Cloprop
Cloprop
4-CPA
CDEC
DCAA
Dial! ate
Propachlor
Alachlor
Butachlor, Delachlor
CPA
4-CPA
CPA
Fenson
Ovex or Chlorfenson
CPMC
CPMF
4-CPP
DSMA
DSMA
Butoxy polypropylene glycol
Glyodln
Dazomet
Sesone
Dlchloralurea
Dazomet
Credazine
Crlmldine
Ethlophencarb
2,4-D
Crotamiton
Crotoxyphos
Crufomate
Cryolite
UMBER
2309
1200
5245
7100
3840
J820
2663
3620
7060
3720
1540
6573
1160
1140
2040
5820
4160
0922
2860
2860
2940
1500
6020
1546
NAME
60-CS-16
Cube
Cubor
Cue-lure
Cufram Z
CuJTiari
Cunllate
Cupramar
Cupravlt
Cuprinol
CuproKylt
Cuprox
Curamil
Curaterr
Curitan
Cu-Sprex
Cyalane
Cyanazine
Cyanofenphos
Cyanogas
Cyanophos
Cyanox
Cyanthoate
Cycle
Cycloate
Cyclodan
Cyclohexlmlde
Cyclon
Cycloprate
Cyclouron
Cycluron
Cycocel
Cycogan
Cyfen
Cyflee
Cygon
Cyhexatln
Cylan
Cymag
Cywetox
Cynem
Cyolane
Cyperquat
Cyprazine
Cyprex
Cypromid
Cystamin
Cystogen
Cytel
Cythioate
Cythion
Cytox 3711
COMMON NAME
Disugron
Rotenone
Rotenone
Cue-lure
Cufraneb
Z1ram
Copper 8-Quinolate
Copper oxychloride
Copper oxychloride
Copper naphthenates
Copper oxychloride
Copper oxychloride
Pyrazophos
Carbofuran
Dodine
Dichlobenil
Phosfolan
Cyanazine
Cyanofenphos
Calcium cyanide
Cyanophos
Cyanophos
Cyanthoate
Procyazine
Cycloate
Endosulfan
Cycloheximide
Hydrocyanic acid
Cycloprate
Cycluron
Cycluron
Chlormequat chloride
Chlormequat chloride
Fenltrothion
Cythloate
Dimethoate
Cyhexatin
Phosfolan
Sodium cyanide
Demephion
Thionazin
Phosfolan
Cyperquat
Cyprazine
Dodine
Cypromid
Metnenamine
Methenamine
Fenitrothion
Cythloate
Malathion
VBT
CODE
NUMBER
1
6000
6000
7100
5932
1040
2780
2200
1610
1552
6360
5739
1591
3180
1600
1606
3480
1621
2420
1610
1610
1611
1615
2780
3480
1621
4260
159
-------
PESTICIDE EQUIVALENT NAMES
NAME
Cytrol
Cytrolane
2,4-D
D-735
D-1221
DAC 893
Dacamine
Dacamine 4T
Dacamox
Daconate
Daconil 2787
Dacthal
Dacthalore
Dactin
DAEP
Dagadlp
Dalapon
Dal-E-Rad 100
Dal-E-Rad 120
Dalf
Danex
Danifos
DAPA
Daphene
Dasanit
DATC
Daxtron
Dazomet
Dazzel
2,4-D
2,4-OB
2,4-D Butyric
DBCP
2,6-DBN
DBP
DCMA
DCMO
DCMOD
DCMU
DCNA
d-Con
DCPA
DCPC
DCPH
DCU
D-D
DDA
DDC
DDD
DOOM
COMMON NAME
Amitrole
Mephosfolan
2,4-D
Carboxin
Carbofuran
DCPA
Salts of 2,4-D &
2,4,5-T
2,4.5-T
Thlofanox
MSMA
Chlorothalonil
DCPA
DCPA
Halane
DAEP
Carbophenothion
Dalapon
DSMA
MSMA
Parathion methyl
Trichlorfon
Danifos
Fenaminosulf
Dimethoate
Fensulfothlon
Dial late
Pyrlclor
Dazomet
Diazlnon
2,4-D
2,4-DB
2,4-DB
D1 bromochl oropropane
Dichlobenll
Dibutyl Phthalate
Dicryl
Carboxin
Oxycarboxln
Dluron
Dichloran
Warfarin
DCPA
Dimlte
Neotran
D1 chloral urea
D-D
DDA
DDC
DDD
Dlchlorophen
CODE
NUMBER
0200
1630
2940
1100
1040
1720
6840
6663
4820
1640
1720
1720
1080
1660
2860
4820
4580
6780
2020
2420
3500
2040
2080
3080
3080
2090
2200
2120
1100
2740
2260
7060
1720
1740
1750
NAME
DDDS
DDE
DDM
DDMU
DDPP
DDT
DDVE
DDVP
2,4-DEB
Decco Salt No. 5
Dechl orane
De-Cut
Dedelo
Dedevap
Ded-Weed
Deet
DEF
De-Fend
De-Fol-Ate
De-Green
Dei qua t
Delachlor
Del an
Del an-Col
Deleaf Defoliant
Del Ida
Delnav
Delphene
Del san
Demephlon
Demeton
Demeton-0
Demeton-S
Demo san
Demos-L40
Demox
Derma ton
Derosal
Derrln
Derrl s
Des-I-Cate
Desmedlpham
Desmetryn
2,4-DES-Na
De-Sprout
Dessin
Destun
DET
Detamide
Dethdlet
Dethmore
COMMON NAME
DDDS
DDE
Dlchlorophen
p,p'-DDD, olefln
Pyrldlnltrll
DOT
Dichlorvos
Dichlorvos
2,4-DEB
Trlchloromelamlne
Ml rex
MH
DDT
Dichlorvos
2,4-D, Dalapon-Na
4 2,4,5-T
Deet
DEF
Dimethoate
Magnesium Chlorate
DEF
Dlquat
Delachlor
Dithlanon
Dithianon
Folex
Aluminum phosphide
Dioxathlon
Deet
Thlram
Demephlon
Demeton
Demeton-0
Demeton-S
Chloroneb
Dimethoate
Demeton
Dichlorvos
Carbendazlm
Rotenone
Rotenone
Endothall
Desmedlpham
Desmetryn
Sesone
MH
Dinobuton
Perfluidone
Deet
Deet
Red Squill
Warfarin
CODE
NUMBER
1840, 1860
1880
2320
2320
4720
4280
1880
2320
2940,
1660, 6840
1940
2420
1940
2660
2721
2721
3640
2580
6680
1981
1982
1380
2420
1981, 1982
2320
1071
6000
6000
3240
2006
4280
5366
7060
160
-------
PESTICIDE EQUIVALENT NAMES
NAME
Dethnel
Devrinol
DEX
Dexon
Dextone X
Dextrone
DHA
Dialide
Dialifor
Dial late
Diamazole
Diametan
Diamond Green
Diamthazole
Dianat
Diaparene Chloride
Diaphene
Diazajet
Diazel
Diazide
Diazinon
Diazitol
! Diazoben
iDiazol
Diazoxon
Dibam
Dibrom
Dibromoethane
Dibutalin
Dibutyl phthalate
Dibutyl succlnate
Dicamba
Di-Captan
Di-Capthon
Dicarbam
Dicarzol
Dicestal
Dichlobenil
Dichlor
Dichlorfenidln
nichlof«nthion
Dichlorflurecol
Dichlont
Di chlorinate
Dichlorobenzene-o
Dichlorobenzene-p
Dichloroethane
Di chl oron i troethane
Dichlorophen
COMMON NAME
Warfarin
Napropamide
EXD
Fenaminosulf
Paraquat dichloride
Diquat
Dihydroacetic acid
Dialide
Dialifor
Diallate
Diamazole
Fulfogen
Malachite Green
Diamazole
Dicamba
Methylbenzethonium Chloride
Diaphene
Diazinon
Diazinon
Diazinon
Diazinon
Diazinon
Fenaminosulf
Diazinon
Diazoxon
Sodium dimethyl
dithiocarbamate
Naled
Ethyl ene di bromide
Butralln
Dibutyl phthalate
Tabutrex
Dicamba
Dicapthon
Di-Capthon
Carbaryl
Forme tana te
Hydrochloride dichlorophenol
Dichlobenil
Dichlobenil
Diuron
Dlchlofenthion
Dichlorflurecol
Dichlofluanid
Dichlone
Dichloraate
Dichlorobenzene-o
Dichlorobenzene-p
Ethylene dichloride
Ethlde
Dichlorophen
CODE
NUMBER
7060
2010
3420
2020
5240
2660
2035
2040
2140
2060
2080
2080
2080
2080
2080
2020
2080
4860
0933
2120
2140
1060
3680
2200
2200
2740
2220
2180
2280
2300
NAME
Dichlorophenoxy-
acetic acid
Dichloropropane
Dichloropropene
Dichloropropionic
acid
Dichlorphenidim
Dichlorphos
Dichlorprop
Dichlorvos
Dicloran
Diclotron
Dicofol
Dicoumarin
Dicoumarol
Dicrotrophos
Dicryl
Dicumarol
Dicumol
Dicurane
Didioxane
Dieldrin
Dienochlor
Diethchinalphion
Diethion
Diethquinalphione
Diethyl phosphate
Diethyl toluamide
Difenoxuron
Difenson
Difenthos
Difenzoquat
Diflubenzuron
DIFO
Difolatan
Difosan
Dihydropyrone
Dikar
Dikotex
Dilan
Dilan I
Dilan II
Dimaz
Dimecron
Dimefox
Dimelone
Dimephenthoate
Dimet
Dimethametryn
Dime than
Dimethirimol
COMMON NAME
2,4-D
Propylene dichloride
Dichloropropene
Dalapon
Diuron
Dichlorvos
Dichlorprop
Dichlorvos
Dicloran
Dichlobenil &
Fluometuron
Dicofol
Melitoxin
Melitoxin
Dicrotophos
Dicryl, chloranocryl
Melitoxin
Melitoxin
Chlortoluron
Dichlorophen
Dieldrin
Dienochlor
Quinalphos
Ethion
Quinalphos
Diethyl phosphate
Deet
Difenoxuron
Ovex or Chlorfenson
Temephos
Difenzoquat
Diflubenzuron
Dimefox
Captafol
Captafol
Indalone
Mancozeb & Dinocap
MCPA
Dilan
Prolan
Bulan
Disulfoton
Phosphamidon
Dimefox
Dimethyl carbate
Phenthoate
DSMA
Dimethametryn
Dimetan
Dimethirimol
CODE
NUMBER
2940
2306, 2307
1660
2740
2320
2309
2320
2260
2200, 3620
2340
0700
1512
2380
5966
3340
5966
2386
2391
0020
2395
2406
1000
1000
4340
2720
5580
2860
2411
2416
161
-------
PESTICIDE EQUIVALENT NAMES
NAME
Dimethoate
Dlmethogen
Dimethoxane
D1methylars1n1c
acid
Dimethyl phosphate
Dimethyl phthalate
D1met1lan
Dimeton
Dimexan
Dimilin
Dinex
Dinitramine
Dinitro
Dlnitrobutylphenol
Dinitrocreson
Dinitrocyclohexyl-
phenol
Dinitro-o-sec-
amyl phenol
Dinobuton
Dinocap
Dinocton
Dinofen
Dinoprop
Dinosam
Dinoseb
Dinoseb acetate
Dinoseb methacrylate
Dinoterb acetate
Di-on
Dioxacarb
Dioxathion
Dioxin
Dipan
Dipel
Diphacin
Diphacinone
Diphenadione
Diphenamid
Diphenatrile
Diphenyl
Diphenyl mercury
Dipram
Dipropetryn
Dipterex
Diquat dibromide
Direz
Dirimal
Disan
Di sodium methane-
arsonate
COMMON NAME
Dimethoate
Dimethoate
Dimethoxane
Cacodylic acid
Dimethyl phosphate
Dimethyl phthalate
Dimetilan
Dimeton
Dimexan
Diflubenzuron
Dinex
Dinitramine
Dinoseb
Dinoseb
DNOC
Dinex
Dinosam
Dinobuton
Dinocap
Dinocton
Dinobuton
Dinoprop
Dinosam
Dinoseb
Dinoseb acetate
Binapacryl
Dinoterb acetate
Diuron
Dioxacarb
Dioxathion
Dimethoxane
Diphenatrile
Bacillus Thur1ng1ens1s
Diphacinone
Diphacinone
Diphacinone
Diphenamid
Diphenatrile
Biphenyl
Diphenyl mercury
Propanil
Dipropetryn
Trichlorfon
Diquat
Anilazine
Oryzalin
Bensulide
DSMA
CODE
NUMBER
2420
2420
0961
2458
2460
24Q6
2651
2760
2760
2770
2560
2760
2566
2740
2573
2580
2600
2600
2600
2620
0740
2640
5840
2653
6780
2660
2920
5148
0520
2860
NAME
Disomar
Dlsparlure
Disparmone
Dlsugran
Disulfiram
Dlsulfoton
D1sul-Na
D1-Syston
Disyston S
Disyston sulphoxlde
D1-Tac
Ditalimfos
D1 thane A-40
Di thane D-14
Dithane M-22
Dithane M-45
Dithane Z-78
Dithianon
Dithio
Dlthiodemeton
Dithiomethon
Dithione
Dithiosystox
D1tran1l
Di-trapex
Diurex
Dlurol
Diuron
Divipan
DM
DMA
DMAA
DMC
DMDT
DMP
DMSP
OMPA
DMU
DMXD
DN-111
DN-289
DNAP
DNBP
DNC
DNOC
DNOCHP
DNOCP
DNOIPP
DNOSAP
DNOSPB
COMMON NAME
DSMA
Disparlure
Dlsparlure
Dlsugran
Disulfiram
Disulfoton
Sesone
Disulfoton
Oxydisulfoton
Oxydlsulfoton
DSMA
Ditalimfos
Nabam
Nabam
Maneb
Mancozeb
Zineb
Dithianon
Sulfotep
Disulfoton
Thiometon
Sulfotep
Disulfoton
Dichloran
Trapex
Diuron
Diuron & Amltrole
Diuron
Dichlorvos
Phenarsazine chloride
DSMA
Cacodylic acid
Dlmite
Methoxychlor
Dimethyl phthalate
Fensulfothion
Zytron
Diuron
Dimexan
Dinex
Dinoseb
Dinosam
Dinoseb
CNOC
DNOC
Dinex
Dinocap
Dinoprop
DNAP
Dinoseb
CODE
NUMBER
2860
2720
2720
2860
1
7120
2761
2720
6665
2720
2260
2740
2740, 0200
2740
2320
2860
0961
4540
2460
3500
2740
2760
2760
2770
2770
2560
2760
162
-------
PESTICIDE EQUIVALENT NAMES
NAME
DNSAP
DO 14
Dodemorph
Dodlne
Doquadlne
Ool Granule
Doom
OOP
Doquadlne
Dor lone
Dormone
Dosanex
Double-Noctln
Dovlp
Doweo 109
Dowco 118
Dowco 132
Dowco 169
Dowco 179
Dowco 189
Dowco 199
Dowco 213
Dowco 214
Dowco 233
Dowco 269
Dowco 290
Dowfume W-85
Dow General
Dowldde A
Dowldde B
Dowklde F
Dowldde G
Dow1c1de Q
Dowldde 1
Dowldde 2
Dowldde 2S
Dowldde 4
Dowldde 6
Dowldde 7
Dowldl 100
Dowlap
Dowpon
Dow S-192S
Dow Selective
Dowspray 9
DP-35
2,4-DP
DPA
DPA
Drat
Drawtnol
Draza
COMMON NAME
Dlnosan
Propaglte
Dodemorph
Dodlne
Dodlne
Llndane
Milky disease spores
Dloctyl phthalate
Oodlne
Dlchloropropene 2306
2.4-D
Metoxuron
Captan & N-f1x1ng bacteria
Famphur
Narlene
Zytron
Crufomate
NelUte
Chlorpyrlfos
Dowldde Q
D1tal1mfos
Cyhexatln
Chlorpyrlfos methyl
Trlclopyr
Pyroxychlor
3,6-D1chlorop1eol1n1c add
Ethyl d1 bromide
Dlnoseb
Sodium phenylphenate
Sodium trlchlorophenate
Sodium tetrachlorophenate
Sodium pentachlorophenate
Dowldde Q
0-Phenyl phenol
2 , 4 , 5-Tr1 chlorophenol
2,4,6-Trlchlorophenol
2-Ch 1 oro-4-phenyl phenol
2,3.4,6-Tetrachlorophenol
PCP 7 other chlorophenols
Dowldde Q
Tr1 chl oronl trophenol
Dalapon-Na
Propargyl Bromide
Dlnoseb
Styrene d1 bromide
Propanll
Dlchlorprop
Propanll
D1phenylam1ne
Chlorophadnone
Dlnobuton
Methlocarb
CODE
NUMBER
5160
2780
2780
0680
P434
2780
,2307
2940
4631
3440
6020
2900
2902
6786
2760
2800
2820
5490
6890
1660
2760
5840
2309
5840
1425
4500
NAME
Drazoxolon
ORB
DRC-1339
Drlnox
OHnox H-34
Drop Leaf
DSE
DSMA
DTPA
DTT
Du 112307
DuBay 115HH
Duf alone
Duphar
DuPont
Insecticide 1179
Duraset
Dursban
Du-Sprex
Du-Ter
Dyanadde
Dyanap
Dybar
Dyfonate
Dykon
Dylox
Dymld
Dynanap
Dynoram
Dyrene
Dyrez
E-6
E-500
E-600
E-605
E-838
E-1059
Easy Off-D
EC
ECTMCB
Ectoral
EDDP
EDE
EDC
Edlfenphos
Edolan
Ekalux
Ekamet
Ekatln
Ekatln M
Ekatox
Ektafos
El -103
COMMON NAME
Drazoxolon
N1r1t
Starladde
Aldrln
Heptachlor
Sodium chlorate
Nabam
DSMA
DTPA
DTT
Dlfluron
Ethyl mercury Iodide
Mel 1 toxin
Tetradlfon
Methomyl
N-m-t
Chlorpyrlfos
D1chloben1l
Fentln hydroxide
PMA
Naptalam
Fenuron
Fonofos
Dykon
Trlchlorfon
D1phenam1d
Dlnoseb & Naptalam
Chloramben & Dlnoseb
An11az1ne
An1laz1ne
Zanthone
Amb1th1on
Paraoxon
Parathlon
Potasan
Demeton
Folex
EC
Ethazol
Ronnel
Edlfenphos
Ethyl ene d1 bromide
Ethyl ene d1 chloride
Edlfenphos
Edolan
Qufnalphos
EtHmfos
Thlometon
Morphothlon
Parsthlon ethyl
Dlcrotophos
Tebuthluron
CODE
NUMBER
2792
0080
3860
2860
6600
4520
2900
2200
3540
5680
4920
2910
6780
2620
2760, 4920
0140, 2760
2920
2920
5245
1981
3640
6590
5980
5966
3412
6665
5245
0700
6583
163
-------
PESTICIDE EQUIVALENT NAMES
NAME
El-119
El-131
El-161
El -179
El-241
El -273
El -291
El-531
Elancolan
Elbanll
Elclde
Elgetol 30
Elgetol 318
El ocron
Elsan
Elvaron
EM-923
Embafume
Embathion
Embl em
Embutox
EMC
Emfac 1202
Emmatas
Endaven
Endocide
Endosan
Endosulfan
Endothall
Endothlon
Endox
Endrln
Endrodd
Enlde
Enovit Super
Enstar
Enterosalll
Entex
Envert T
EP-166
EP-161-E
EP-332
EP-333
EP-452
EP-475
Ephlrsulphonate
EPN
Epoxyethane
Epoxypropane
Eptam
Eptapur
EPTC
Equlgard
COMMON NAME
Oryzalln
Prosulfalln
Ethalfluralin
Isopropalln
Parlnol
Triarlmol
Tricyclazole
Ancymidol
Tr1flural1n
Chlorpropham
Thomerosal
DNOC
Dinoseb
Dloxacarb
Phenthoate
Dichlofluanid
Genite
Methyl Bromide
Ethion
Benefln
2,4-DB
Ethylmercury chloride
Pelargonlc add
Malathlon
Benzoylprop ethyl
Endothlon
Blnapacryl
Endosulfan
Endothall
Endothlon
Coumatetralyl
Endrin
Coumatetralyl
Dlphenamid
Thlophanate methyl
Kinoprene
Salicylic add
Fenthlon
2,4, 5-T
PhenacHdane chloride
Trapex
Formetanate hydrochlorlde
Chlordlmeform
Phenmedlpham
Desmedipham
Ovex or Chlorfenson
EPN
Ethylene oxide
Propylene oxide
EPTC
Buturon
EPTC
Dichlorvos
CODE
NUMBER
5148
4070
5251
0230
6800
1420
2770
2760
2573
3340
0480
3080
3400
4260
0578
3180
3240
3260
2620
6671
4146
P889
3520
6840
3680
3680
5410
2006
3280
3300
3300
2320
NAME
Equ1no-A1d
Erade
Eradex
Eradlcane
Erazldon
Erbon
Erbotan
ESP
Esteron
Esteron 245
Estone
Estonmlte
Estox
Etazine
Etem
Ethalfluralin
Ethazol
Ethephon
Ethoate methyl
Ethlofencarb
Ethiolate
Ethion
Ethirimol
Ethlrlnol
Ethodan
Ethofumesate
Ethohexadiol
Ethoprop
Ethoxyquln
Ethrel
Ethyl an
Ethyl Guthlon
Ethylhexanedlol
Ethylmercury chloride
Ethyl parathlon
Ethyl pyrophosphate
Ethyl xanthogen
disulflde
Etllon
Etlnofen
ETO
Etoxlnol
Etr1d1azol
Etrlmfos
F.trofol
Etrofolan
Etrolene
Eugenol
Eulan
Eulava SM
Euparen
Euparen
Euparen M
Eurax
COMMON NAME
Trlchlorfon
OxytMoqulnox
Thioqulnox
Eradlcane
Thioqulnox
Erbon
TMazfluron
ESP, Metasystox S
2,4-D
2, 4, 5-T
2,4-D
Ovex or Chlorfenson
Metasystox-S
Secbumeton
Etem
Ethalfluralin
Ethazol
Ethephon
Ethoate methyl
Ethlofencarb
Ethiolate
Ethion
Ethirimol
Ethlrlnol
Ethion
Ethofumesate
Ethylhexanedlol
Ethoprop
Ethoxyquln
Ethephon
Ethyl an
Azlnphos ethyl
Ethylhexanedlol
Ethylmercury chloride
Parathlon
TEPP
EXD
Parathlon
Etlnofen
Ethylene oxide
Etoxlnol
Thazol
Etrlmfos
CPMC
Isoprocarb
Ronnel
Eugenol
Eulan
Magnesium fluoslHcate
Dichlofluanid
Dichlofluanid
Tolyfluanid
Crotamlton
CODE
NUMBER
6780
4800
2940
6840
2940
6590
3330
3335
3340
3359
3359
3340
3373
3380
5880
3330
5380
3840
3380
3400
5245
6540
3420
6245
g
6590
3412
5980
P525
164
-------
PESTICIDE EQUIVALENT NAMES
NAME
Euraxll
Eurex
Ev1k
Evital
EXD
Exophene
Exotherm
Exothion
Exporsan
Extrax
E-Z-Off
E-Z-Off D
F-319
F-461
F-849
Fac
Fac-S
Fac Super
Fair-Tac
Fall
Faladln
Falone
Famid
Famofos
Famphur
Far-Go
Farmante
Fast Green
Fatal
FBHC
Fen-all
Fenac
Fenamln
Fenamlnosulf
Fenamiphos
Fenatrol
Fenazaflor
Fenbutatln oxide
Fence Rider
Fenchlorfos
Fenethacarb
Fenidin
Fenitrothlon
Fenlzon
Fenoflurazole
Fenolovo acetate
Fenophosphon
Fenoprop
Fenson
Fensulfothfon
Fenthlon
Fentlazon
COMMON NAME
Crotamlton
Cycloate
Ametryn
Norflurazor
EXD
Hexachlorophene
Chlorothalonll
Endothlon
Bensullde
Rotenone
Magnesium chlorate
DEF
Hymexazol
Oxycarboxin
Seedvax
Prothoate
Ferbam cyclohexylamlne
Prothoate & Ovex
n-Decanol
Sodium chlorate
2,4-DEP
2,4-DEP
Dloxacarb
Famphur
Famphur
Trlallate
Mancozeb
Malachite Green
DCPA
BHC
2,3,6-TBA
Fenac
Atrazlne
Fenamlnosulf
Phenamlphos
Atrazine, Amltrole, S
Fenac
Fenazaflor
Fenbutatln oxide
2,4,5-T
Ronnel
Fenethacarb
Fenuron
Fenitrothlon
Fenson
Fenazaflor
Fentln acetate
Trlchloronate
Sllvex
Fenson
Fensulfothlon
Fenthlon
Fentlazon
CODE
NUMBER
1591
0120
5136
3420
3940
1640
0520
6000
1940
5670
2573
3440
3440
1720
0600
6920
3460
0420
2020
0420, 0200,
3460
7013
6840
5980
3480
3527
6120
3500
3520
NAME
Fentichlor
Fentln acetate
Fentln hydroxide
Fentln nonylphenoxide
Fentrlcol
Fenulon
Fenuron
Fenuron TCA
Ferbam
Ferbam cyclo-
hexylamlne
Ferberk
Fermate
Fermi de 850
Fernacol
Fernasan
Fernesta
Fernlmlne
Fernoxone
Ferxone
Fleam
Field Kleen Meed
Killer
Filarlol
Finidim
Fltios B/77
Floraltone
Florel
Florencol
Florocid
Fluchloralln
Fluenetil
Fluenyl
Flumezin
Fl uometuron
Fluorakil
Fluorbenslde
Fluoridamld
Fluoroacetamlde
Fluoroacetanillde
Flurordlfen
Fluorogesarol
Flurorparacide
Flurorphene
Fluorosalan
Flurecol-n-butylester
FMC 9260
FMC 10242
FMC 17370
Focusan
Folbex
Folcid
Folex
Folldol E-605
COMMON NAME
Fentichlor
Fentln acetate
Fentln hydroxide
Fentln nonylphenoxide
Fentrlcol phenoxide
Fenuron
Fenuron
Fenuron TCA
Ferbam
Ferbam cyclohexylamine
Ferbam
Ferbam
Thiram
Thlram
Thiram
2,4-D
2,4-D
2,4-D
2,4-D
Bendlocarb
2,4-D
Bromophos ethyl
Fenuron
Ethoate-methyl
TIBA
Ethephon
Fl urecol -n-butylester
Sodium fluoride
Fluchloralin
Fluenetil
Fluenyl
Flumezin
Flumeturon
Fluoroacetamlde
Fluorbenside
Fluoridamid
Fluoroacetamlde
FluoroacetanlUde
Fluorodifen
DFDT
Fluorobenslde
Fluorophene
Fluorophene
Flurecol -n-butyl ester
Tetramethri n
Carbofuran
Resmethrin
Tolnafrate
Chlorobenzilate
Captafol
Folex
Parathion ethyl
CODE
NUMBER
3527
3540
3600
3600
3600
6680
6680
6680
2940
2940
2940
2940
0472
2940
0860
3330
3630
0407
3620
3623
3630
1040
6055
1360
1000
3640
5245
165
-------
PESTICIDE EQUIVALENT NAMES
NAME
Folldol M
FoHmat
Fol1th1on
Folosan
Folpan
Folpet
Fonofos
Fore
Forestan
Forlln
Formagenen
For-Mal 50
Formaldehyde
Formalon
Formetanate
hydrochlorlde
Formln
Formothlon
Formparanate
Forron
Forstan
Forstenon
For-Syn
Fortrol
Forturf
Fos-Fall "A"
Fosfamld
Fosferno 50
Fosferno M50
Fosplrate
Fostlon
Fostlon MM
Foxlene
Frescon
Frucote HC1 salt
Frultone A
Frultone CPA
Frultone H
Frultone T
Frumln Al
Fuberldatol
Fuber'dazol
Fuklasln
Fulcon
Fumarln
Fumasol
Fumazone
Fumette
Fundal EC
Fundex
Fungicide 328
Fungicide 1763
Funglclor
COMMON NAME
Parathlon methyl
Omethoate
Fen1troth1on
Tecnazene
Folpet
Fol pet
Fonofos
Mancozeb
Oxythloqulnox
Linda ne
Paraformaldehyde
Malathlon
Formaldehyde
Formaldehyde
Formetanate hydrochlorlde
Methenamlne
Formothlon
Form paranate
2.4,5-T
Oxyth1oqu1nox
Forstenon
Resmethrln
Cyanazlne
Chlorothalonll
DEF
Dlmethoate
Parathlon ethyl
Parathlon methyl
Chlorpyrlfos methyl
Prothoate
Dlmethoate
Plnolene
Trlfenmorph
sec-Butylamlne
2,4,5-T
3-CPA
Naphthaleneacetlc add
Sllvex
Dlsulfoton
FubeHdazole
Fuberldazole
Zlram
Sr1seofulv1n
Coumafuryl
Coumefuryl
Dlbromochloropropane
MSF
Chlordlmeform
Chlordlmeform
Mllneb
Fungicide 1763
PCNB
CODE
NUMBER
4580
3480
6435
3660
3660
2910
4800
0680
4260
3680
3722
6840
4800
6055
1552
1640
1940
2420
5245
4580
2902
2420
6840
4900
6120
2720
7100
3720
3720
2090
1480
1480
5280
NAME
Fungi Ion
Funglnex
Fungo 50
Furadan
Furcarbanll
Furethvln
Furfural
Furloe
Fusarex
FW-293
FW-734
FW-925
Fyfanon
G-4
G-ll
6-696
G-18359
G-19258
G-22008
G-22870
G-23330
G-23611
G-23645
G-2402F
G-24163
G-24438
G-24480
G-24622
G-25804
G-27901
G-28029
G-3004
G-30026
G-30027
G-30028
G-30031
G-30044
G-30130
G-30344
G-30494
G-31435
G-31717
G-32292
G-32911
G-34161
6-34162
G-34690
6-36393
G.A.
Galecron
Gallotox
COMMON NAME
Fung! Ion
THforlne
Thlophanate methyl
Carbofuran
Furcarbanll
Furethvln
Furfural
Chlorpropham
Tecnazene
Dicofol
Propanfl
Nitrofen
Malathion
Dlchlorophen
Hexachlorophene
G-696
KIK
Dlmetan
Pyrolan
D1met1lan
Pyramat
I solan
Etoxlnol
Pyrazothlon
Chloropropylate
Pyrazoxon
D1az1non
Pyrazlnon
Chlorazlne
Tr1etaz1ne
Phencapton
Slmetone
Norazlne
Atrazlne
Propazlne
Ipozln
Slmetone
Propanll
S1maz1ne
Methyl phencapton
Prometon
Ipatone
Atraton
Slmetryn
Prometryn
Ametryn
Methometon
Hethroprotryn
GlbberelUc add
Chlordlmeform
PMA
CODE
NUMBER
6822
6671 i
1040
I
1420
6435
2340
5840
5040
4260
3940
2080
6796
5400
0420
5800
5840
6160
5780
0320
5780
0120
3790
1480
5680
166
-------
PESTICIDE EQUIVALENT NAMES
NAME
Gamaphex
Gaimil 1 n
Gamma BHC
Gammagof
Gamrnex
Gammexane
Gamopten
Ganocide
Garddde
Gardentox
Gardona
Gardoprlm
Garlon
Garrathlon
Gatnon
GC-1124
GC-1283
GC-2466
GC-3707
GCP-1634
Gebutox
Benicide
Genlte
Genitol
Gerox
Gesabal
Gesadural
Gesafloc
Gesafram
Gesagard
Gesakur
Gesamil
Gesapax
Gesapon
Gesaprim
Gesapun
Gesaran
Gesavex
Gesarol
Gesatamin
Gesatop
Gesoran
Gibberellic acid
Gibrel
Gib-Tabs
Gib-sol
GIX
Glyodex
Glyodin
Glyoxaline
Glyoxime
Glyphosate
Glyphosine
COMMON NAME
Lindane
Lindane
Lindane
Lindane
Lindane
Lindane
Hexachlorophene
Drazoxolon
Tetrachlorvinphos
Diazinon
Tetrachlorvinphos
Terbuthylazine
Si 1 vex
Carbophenothion
Benzthiazuron
Nirit
Mi rex
Mucochloric anhydride
Bomyl
Cyperquat
Dinoseb
Xanthone
Genite
Genite
Streptomycin
-Ipazin
Sine tone
Trietazine
Prometon
Pronetryn
Chloropropylate
Propazine
Ametryn
DDT
Atrazine
Simazine
Methoproptryn
DDT
DDT
Atraton
Simazine
Simazine
Gibberellic acid
Gibberellic acid
Gibberellic acid
Gibberellic acid
DFDT
Glyodin
Glyodin
Imadazole
Glyoxime
Glyphosate
Glyphosine
CODE
NUMBER
0680
0680
0680
0680
0680
0680
3940
2792
3740
2080
3740
6589
6120
1080
4720
1611
2760
6222
6796
5760
5780
5800
0120
1880
0420
6100
I860
1880
0320
6160
6160
3790
3790
3790
3790
3796
3801
3802
___„ i
NAME
Glytac
Golden Decoy
Gophacide
Gotnion
Gralit 85
Gramevin
Gramonol
Gramoxone
Granol NM
Granosan
Granox NM
Granox PFM
Grascide
Grex
Grifulvin
Griseofulvin
Grisovin
Grocel
GS- 13005
GS-13006
GS-13528
GS-13529
GS-14254
GS-14259
GS-14260
GS-16068
GS-19851
GS-29696
Guanoctine
Guazatine
Gusathion M
Gusathion A
Guthion
Gyplure
Gypsine
Gyotol
Gyron
H-82
H-321
H-8043
H-1313
Halane
Hal izan
Halowaxes
Haloxydine
Halts
Hanane
Harvcn
HC-1281
HCA
HCB
COMMON NAME
Glytac
Dichlorvos & Ronnel 2320
Phosaretlm
Azinphos methyl
Chloral chloroamide
Dalapon-Na
Paraquat S Monolinuron 5240
Paraquat dichloride
Maneb & Lindane 4300
Ethylmercury chloride
Maneb & HCB 4300
Maneb & Captan 4300
Propanil
Benomyl
Grisactin
Griseofulvin
Griseofulvin
Gibberellic acid
Methidathion
Athidathion
Sebuthylazine
Terbuthylazine
sec-Bumeton
Terbumeton
Terbutryn
Dipropetryn
Bromopropylate
Thiazfluron
Guazatine
Guazatine
Azinphos methyl
Azinphos ethyl
Azinphos methyl
Gyplure
Lead arsenate
Gyptol
DDT
Isocil
Methiocarb
Dialide
Dichlobenil
Halane
Metaldehyde
Polychlorinated naphthalenes
Haloxydine
Bandane
Dimefox
Dihydroacetic acid
(Ha salt)
2,3,5-TBA
Hexachloroacetone
Hexachlorcbenzene
CODE
NUMBER
, 5980
3820
1660
, 4751
5240
, 0680
3400
, 3920
, 1020
5840
0500
3790
6340
6589
3980
2653
0872
3820
3840
3820
4180
1880
4500
220C
5720-
5725
6920
392C
167
-------
PESTICIDE EQUIVALENT NAMES
NAME
HCCH
HCH
HCN
Hedonal
Hedonal DP
Hellotox
Hemel
Hempd
HEOD
Heptachlor
Heptachlor epoxlde
Heptamul
Heptenophos
Herban
Herbatlm
Herbazim
Herbicide 44E
Herbicide 273
Herbicide 685
Herblsan
Herblzol
Hercules AC 528
Hercules AC5727
Hercules 7531
Hercules 9573
Hercules 14503
Herkol
Heteroauxln
HETP
Hexa C.S.
Hexachlor
Hexachloran
Hexachl orobenzene
Hexachlorophene
Hexachlorosan
Hexaferb
Hexafor
Hexalure
Hexamone
Hexanema
Hexasul
Hexa thane
HexatMr
Hexavln
Hexazlr
Hexosan
Hexyclan
HHDN
H1-Alaz1n
H1b1tane
Hlbrom
Hlnosan
COMMON NAME
BHC
BHC
Hydrocyanic add
Various formulations of
2,4-D, MCPA, MCPP,
2,4-DP » 2,4,5-T
Dlchlorprop
Toxaphene & DDT 6740
Hemel
Hexamethyl phosphoramlde
DleldHn
Heptachlor
Heptachlor epoxlde
Heptachlor
Heptenophos
Norea
Metham
S1maz1ne
Chlorazlne
Endothall
CPMF
EXD
Amltrole
Dloxathlon
UC 10854
Norea
Terbutol
D1 all for
Dlchlorvos
3-Indoleacet1c add
TEPP
Hexachlorobenzene
BHC
BHC
Hexachlorobenzene
Hexachlorophene
Hexachlorophene
Ferbam
BHC
Hexalure
Hexalure
D1chlofenth1on
Sulfur
Z1neb
Thlram
Carbaryl
Z1ram
Hexachlorophene
BHC
AldHn
Tolnaftate
Chlorhex1d1ne
Naled
Edlfenphos
CODE
NUMBER
0600
0600
2309
, 1880
2380
3860
3880
3860
5120
6220
6160
3240
3420
0200
2580
2035
2320
6540
3920
0600
0600
3970
3940
3940
3600
0600
2220
7120
6680
1060
7100
3940
0600
0080
4860
NAME
H1zaroc1n
HMM
HMPA
Hoe 2671
Hoe 2747
Hoe 2784
Hoe 2810
Hoe 2873
Hoe 2904
Hoe 2960
Hoe 2989, 6052,
6053, 13764
Hoe 16410
Hokmate
Homal
Hong N1em
Hopdde
Hormodln
Hormotuho
Hormotuho Special
Hostathlon
HPMTS
HPTMS
HRS-16
HRS-587
Hyumlne 10X
Hydout
Hydram
Hydrogen phosphide
Hydrol
Hydroprene
Hydro thol
1 -Hydroxychl ordene
2-Hydroxyd1 phenyl
Hyosan
Hyvar Bro
Hyvar X
IAA
IBA
IBP
ICI-24223
Idocyll Novum
IFC
Igran
Imldan
Imldazole
Imugan
Inacor
Inamydn
INPC
Insectophene
Inverton 245
COMMON NAME N|
Cycloheximlde
Hemel
Hexamethyl phosphoramlde
Endosulfan
Monolinuron
Blnapacryl
Llnuron
Pyrazophos
Dinoseb
Trlazophos
Pyracarbolld
Isoproturon
Ferbam
Thlram & Thiophanate
methyl 6680,
PMA
CMPC
Indolebutyric add
MCPA
MCPA & Dlcamba 4340,
Triazophos
HPMTS
Dlenochlor
Methyl benzethonium chloride
Methyl benzethonlum chloride
Trltac
Endothall
Mollnate
Phostoxln
Allyxycarb
Hydroprene
Endothall
1 -Hydroxychl ordene
Phenyl phenol
Dlchlorophen
Bromaci 1
Terbadl
3-Indoleacet1c add
Indolebutyric add
IBP
Moludd
Salicylic Add
Propham
Terbutryn
Phosmet
Imldazole
Chloranlformethan
Atrazlne
Novablodn
Propham
Endosulfan
2,4,5-T
ODE
MBER
1600
3180
4751
4240
5932
2760
6777
5905
3600
6671
5680
4340
2140
6777
3240
4740
3240
3960
5490
0800
6560
4011
5860
P889
5860
3980
4000
0420
5860
3180
6840
168
-------
PESTICIDE EQUIVALENT NAMES
NAME
Idobonll
lodofenphos
lotox
loxynil
Ipatone
Ipazlne
I PC
IPPC
IPX
Irgosan CF3
Irgosan CF3
Iscothane
Isobac
Isobenzan
Isocarb
Isochlorthion
Isocll
Iso-Cornox
Isodrln
Isofenphos
Isolan
Isopestox
Isoprodl
Isopropalln
Isoproturon
Isotox
Isoxathlon
IT-3233
IT-3456
I topaz
Ivoset
Jap1dem1c
Jasmolln
JH
Jiffy Grow
Jodfenphos
Jolt
Jon-Trol
Juvenile Hormone
Karbaspray
Karbation
Karbofos
Karbutllate
Karmex
Karphos
Karsll
Kartrll T
Kasumln
Kasugamydn
Kauri til
COMMON NAME
Idobonll
Jodfenphos
loxynil
loxynll
Ipatone
Ipazlne
Propham
Propham
Proxan
Clofucarban
Clofucarban
Dlnocap
Isobac 20
Telodrln
Isocarb
Phosnlchlor
Isocll
MCPP
Isodrln
Isofenphos
Isolan
Mi paf ox
Isocll
Isopropalin
Isoproturon
BHC
Isoxathion
Flurecol-n-butyl ester
Chi orflurecol -methyl ester
Ethion
Dinoseb acetate
Milky disease spores
Jasmolin
Juvenile Hormone
Indolebutyric acid
Jodfenphos
Ethoprop
DSMA
Juvenile Hormone
Carbaryl
Metham
Malathion
Karbutilate
Diuron
Isoxathion
Karsil
Diuron, aminotriazole J
sodium thiocyanate
KSM
KSM
Copper oxychloride
CODE
NUMBER
4103
4040
4040
5860
5860
2560
4400
4070
0600
3630
3340
2566
4103
5880
2860
1060
6220
4260
6420
2740
NAME
Kaybam
Kazpe
Kelevan
Kel thane
Kemate
Kenapon
Kepone
Kerb
Ketothlon
Kildip
Kill-All
Kill ex
Killkantz
Kilmlte 40
Kiloseb
Kiloprop
Kilsem
Kllsem
Kllval
Kinetin
Kinoprene
Kitazln
Kleer-Lot
Kloben
Klorex
KMH
Knoxweek
Koban
Kobutol
Koclde
Kop-Fume
Kop-M1te
Kopsol
Kop-Th1odar,
Kop-Thion
Korax
Korlane
K-Othr1ne
Kroma-Chlor
Krovar
Krumkil
Krysld
KSM
KUE 13032C
KUE 13183b
Kuron
Kurosal
Kusaklra
Kw1k-K1ll
Knit
Kylar
COMMON NAME
Kaybam
Azlde
Kelevan
Dicofol
Anilazine
Dalapon
Chlordecone
Pronamide
Ketothion
Dichlorprop
Sodium arsenlte
Trimec
ANTU
TEPP
Dinoseb
MCPP
MCPA
MCPA
Vamidothion
Kinetin
Kinoprene
IBP
Amitrole & Linuron
Neburon
Sodium chlorate
MH
EPTC & 2,4-D
Isooctyl ester
Ethazol
PCNB
Copper hydroxide
Ethyl ene dl bromide
Chi orobenzi late
DDT
Endosulfan
Malathion
Chi oronl tropropane
Ronnel
K-Othrlne
Cadmium succlnate S
potassium chromate
Diuron & Bromacil
Coumafuryl
ANTU
KSM
Dlchlofluanid
Tolyfluanid
Silvex, PGBE esters
Sllvex
Credazlne
Strychnine
Ethion
Daminozide
CODE
NUMBER
5728, 6172
2340
2920
1660
1280
4090
2309
0260
6540
2760
4400
4340
4340
4146
4011
0200, 4240
4940
2280
3300, 3020
6590
5280
5230
1360
1880
3180
4260
5980
2740, 0800
3720
0260
6140
6120
3340
1681
169
-------
PESTICIDE EQUIVALENT NAMES
NAME
Kypchlor
Kypfarin
Kypfos
Kypman 80
Kypzine
Lambast
Lambrol
Lamoryl
Lampreci'de
Landrin
Lanex
Lannate
Lanoc CN
Lanslide
Lanstan
Larvacide
Larvatrol
Lasso
Lauryl thiocyanate
Lauxtol A
Lazo
Lead Arsenate
Lebaycld
Legumex
Legumez Extra
Legurame
Lemonene
Lenacil
Lepton
Leptophos
Lethalaire G-54
Lethane 60
Lethane A-70
Lethane 384
Lexone
LeyCornox
Leytosan
LH 3012
Light Green N
Lignasan
Limit
Lindafor
Lindagram
Lindamul
Lindane
Line Rider
Linormone
Lintox
Linurex
Linuron
Liphadione
Liquiphene
COMMON NAME
Chlordane
Warfarin
Ma lath ion
Maneb
Zineb
MPMT
Fluenetyl
Griseofulvin
Lamprecide
Landrin
Fluometuron
Methomyl
Eulan
Lenacil & Linuron
Chi oroni tropropane
Chloropicrin
Bacillus Thuringiensis
Alachlor
Lauryl thiocyanate
PCP
Alachlor
Lead Arsenate
Fenthion
MCPB
Benazolin
Carbetami de
Biphenyl
Lenacil
Leptophos
Leptophos
Parathion ethyl
Lethane 60
Lethane A-70
Lethane 384
Metribuzin
Benazolin
Phenylmercury urea
Propineb
Malachite Green
Ethylmercury phosphate
CDAA 8 2,4-D
Lindane
Lindane
Lindane
Lindane or gamma BHC
2,4,5-T
MCPA
Lindane
Linuron
Linuron
Chi orophaci rone
PMA
CODE
NUMBER
1200
7C60
4260
4000
7120
4166
3620
4520
4185, 4240
4160
5260
4160
4180
3520
4380
1074
0740
4185
4190
'4190
5345
4220
4634
1140, 2940
0680
0680
0680
0680
6840
4340
0680
4240
4240
1425
5680
NAME
Liranox
Lironion
LM-91
Lonacol
Londax
Lonocolm
Looplure
Loro
Lorox
Lorsban
Lorvec (K)
Lousewort
Lovozal
Lucel
Lumeton
Luprisol
Lurat
Lutrol
Lythidathion
M-74
M-81
MAA
Mablin
Machete
Mad
Mafu
Magnetic 70
Magron
Maintain
Maintain 3
Maintain CF 125
Malachite Green
Malamar
Malaspray
Malathion
Malazide
Maleic hydrazide
Malix
Maloran
MAMA
Mancofol
Mancozeb
Maneb
Maneba
Manebgan
Manesan
Manzate
Manzate 200
MAPO
Maposol
MAPS
Mareton
COMMON NAME
MCPP
Difenoxuron
Chi orophaci none
Zineb
Linuron 8 Propachlor
Maneb
Looplure
Lauryl thiocyanate
Linuron
Chlorpyrifos
Pyroxychlor
Stavesacre
Fenozaflor
Chlorquinox
Methoprotryn
Propionic acid
Coumafuryl
Edifenphos
Lythidathion
Disulfoton
Thiometon
Methanearsonic acid
Busulfan
Butachlor
MSMA 7 2,4-D
Dichlorvos
Sulfur
Magnesium chlorate
Bromacil
MH
Chi orf 1 urenol -methyl
Malachite Green
Malathion
Malathion
Malathion -
MH
MH
Endosulfan
Chlorbromuron
MAMA
Mancozeb
Mancozeb
Maneb
Maneb
Maneb
Maneb
Maneb
Mancozeb
Metapa
Metham
Methiotepa
Naphthalaphos
CODE
NUMBER
4400
2391
1425
7120
4240, 5820
4300
4240
2900
3720
2720
6665
4490
0922
4820, 2940
2320
0800
4280
ester
4260
4260
4260
4280
4280
3180
1188
4300
4300
4300
4300
4300
6620
170
-------
PESTICIDE EQUIVALENT NAMES
NAME
Mar-Fr1n
Marl ate
Manner
Marpelon
Marvex
MAS
Matadl
Kataven
Mazldox
MB 9057
MB 10064
MBC
MBR-6033
MBR-8251
MBT
MC 25
MC 474
MC 833
MC 1053
MC 1108
MC 1488
MC 1947
MC 2188
MC 2420
MCA 600
MC Defoliant
MCN-1025
MCP
MCPA
MCPB
MCP-Butyr1c
MCPES
MCPP
MEA
Mebenll
MeBr
Mecarbam
Mecarblnazld
Mecarphon
Mecopar
Mecoper
Mecopex
Mecoprop
Medlben
Medlnoterb acetate
Medlure
Meldane
Mel 1 toxin
Melprex
Meltatox
MEMA
Menazon
COMMON NAME
Warfarin
Methoxychlor
Dluron
Unadl & Benzthlazuron
Dlchlorvos
Rhlzoctol
Amlnocarb
Dlfenzoquat
Mazldox
Asulam
Bromoxynll
Sodium chlorate
Fluoridamld
Perfluldone
MBT
Guazatlne
Mecarbam
Carbamorph
Dinobuton
Dlnoterb acetate
Medlnoterb acetate
D1nocton-4
Chlormephos
Mecarphon
Mobam
Magnesium chlorate
Norbormlde
MCPA
MCPA
MCPB
MCPB
MetMn
MCPP
Methoxyethylmercury
acetate
Methylmetlram
Methyl bromide
Mecarbam
Mecarblnazld
Mecarphon
The diet Hanoi ami ne salts
of MCPP S 2,4-D
MCPP
MCPP (K salt)
MCPP
Dlcamba
Medlnoterb acetate
Medlure
Counuphos
MelHoxIn
Dodlne
Dodemorph
Methoxyethylmercury acetate
Menazon
CODE
NUMBER
7060
4540
2740
2320
0180
2395
0310
0820
3623
5366
4441
1316
4340
4340
4340
4380
4400
4441
4400
4400
2140
1540
2780
4453
NAME
Her. ".
Mendrln
Kenlte
Meobal
MEP
Mephanac
Mephosfolan
Mepro
Merbac
Mercaptodlmethur
Mercaptofos
Mercaptothlon
Mercullne
Mercuram
Mercusol
Merfamon
Mergamma
Merkazin
Merpan
Merphos
Mersollte
Mertax
Mertect
Merthon
Mertorgan
Merzonln
Mesoranll
Mesurol
Metabrom
Metadde
Metadel phene
Metafos
Metafume
Metal dehyde
Metal kamate
Me tarn-sodium
Metaphos
Metaphoxlde
Metapslde
Metasystemox
Metasystox
Metasystox I
Metasystox II
Metasystox R
Metaxon
Metazoxolon
Metepa
Metflurazone
Methabenzthlazuron
Metham
Methamldophos
Methanearsonlc add
Methaphoxlde
COMMON NAME
Trapex
Endrln
Mevlnphos
Meobal
Fenltrothlon
MCPA
Mephosfolan
MCPP
Benzyl Bromoacetate
Methlocarb
Demeton-o
Malathlon
Phenylmercury sallcylate
Thlram
Phenylmercury sallcylate
Thlmerosol
BHC & organo Hg compound
Prometryn
Captan
Merphos
PMA
MBT
Thlabendazole
Polyethylmercury phosphate
Thlmerosal
Thlmerosal
Azlprotryn
Methlocarb
Methyl Bromide
Parathlon Methyl
Deet
Parathlon Methyl
Methyl Bromide
Metal dehyde
Bufencarb
Metham
Parathlon methyl
Metepa
Methlotepa
Oxydemeton methyl
Demeton methyl
Demeton-o-methyl
Demeton-s-methyl
Oxydemeton methyl
MCPA
Metazoxolon
Metepa
Metflurazone
Methabenzthlazuron
Metham
Methamldophos
Methanearsonlc add
Metepa
CODE
NUMBER
3260
4640
4460
3480
4340
1630
4400
4500
1981
4260
6680
5780
1020
3640
5680
6660
4500
4580
4580
0960
6620
4580
5220
5220
4340
6220 ,
4750
4490
i
171
-------
PESTICIDE EQUIVALENT NAMES
NAME
Methar
Methazole
Methenarane
Methldathion
Methlocarb
Methiotepa
Methiuron
Methocrotophos
Meth-0-Gas
Methometon
Me thorny!
Methoprene
Methoprotryn
Kethoquln-butyl
Methotrexate
Methoxclde
Methoxo
Methoxone
Methoxychlor
Hethoxyethanol
Methoxy propazlne
Methyl apholate
Methyl aphoxlde
Methyl benzethonium
chloride
Methyl Bromide
Methyl Cellosolve
Methyl Chemosept
Methyl Guthion
Methyl isothlocyanate
Methyl mercury chloride
Methylmercury
Dicyanodi amide
Methylmercury iodide
Methyl Niran
Methyl Paraben
Methyl Parasept
Methyl Trithion
Methylthiotrazine
Meticide
Metilmerkapto-
fasocsid
Ketiltriazotion
Metiram
Metmercapturon
Metobromuron
Metoprotryn
Metoxuron
Metriben
Metribuzin
Metron
Mevinphos
Mexacarbate
Mezene
COMMON NAME
DSMA
Methazole
Methenamme
Methidathlon
Methiocarb
Methlotepa
Methiuron
Methocrotophos
Methyl bromide
Methometon
Methomyl
Methoprene
Methoprotryn
Methoquin-butyl
Methotrexate
Methoxychlor
Methoxychlor
MCPP
Methoxychlor
Methoxyethanol
Prometon
Methyl Apholate
Metepa
Methylbenzethonium chloride
Methyl Bromide
Methoxyethanol
Methyl Paraben
Azinphos methyl
Metham
Methylmercury chloride
Cyano (methyl mercuri)
guanidine
Methylmercury Iodide
Parathion Methyl
Methyl Paraben
Methyl Parasept
Methyl carbophenothion
Desmetryn
Parathion-methyl
Oxydemeton-methyl
Azinphos methyl
Metiram
Methiocarb
Metobromuron
Metoprotryn
Metoxuron
Tricamba
Metribuzin
Parathion methyl
Mevinphos
Mexacarbate
Ziram
CODE
NUMBER
2860
4496
6340
4500
4520
4531
4540
4540
4400
4540
5760
3820
6620
4560
4572
4580
4580
5220
382C
4E83
4500
4612
4631
4634
4580
4640
7080
71 CC
NAME
MF-344
MGK Dog & Cat
Repel 1 ant
MGK R 326
MGK Synergist
MH
MH-30
MH 090
MIC
Micofume
Micridium
Microzul
Midox
Mielncin
Mil bam
Mil -Col
Mllcurb
Mlldex
Mildothane
Milfaron
Mil go
Milky Disease
Miller 531
Miller 658
Mil neb
Milogard
Mil stem
Mintacol
Mipafox
MIPC
MIPCIN
Mi rex
Misulban
Mitigan
Kitin Ch-3374
Mi tin Ch-3667
Mi tin NWE
Mitosulfan
Mitox
2H-4Kh-M
MLT
MMA
MNSA
Mobil awn
Mocap
Modown
Mole Death
Molinate
Molucid
MON-097
Monalide
Monarr
Monex 3
COMMON NAME
Koban
Methyl nonyl ketone
MGK R 326
Octyl bi zydoheptene
MH
MH
Methiuron
Trapex
Dazomet
Phenacridane Chloride
Chlorophacinone
Chlorbenside
Busulfan
Ziram
Drazoxolon
Dimethirimol
Dlnocap
Thiophanate methyl
Chloraniformethan
Ethirimol
Milky Disease
Cd-Ca zinc chromate complex
Copper zinc chromate
CHlneb
Propazine
Ethirimol
Paraoxon
Mipafox
Isoprocar
Isoprocar
Ml rex
Busulfan
Dicofol
M1tin NWE
Ml tin NWE
Mi tin NWE
Busulfan
Chlorbenside
MCPB
Malathion
MSMA
Nissol
Dlchlofenthion
Ethoprop
Bifenox
Strychnine
Molinate
Molucid
Acetochlor
Monalide
Metham
CODE
NUMBER
4280
4280
1425
7100
2792
2416
2560
6671
3359
5800
3359
4720
2340
4380
4260
4820
2220
5880
0733
4740
4747
62?0
Diuron & MSKA 2740. 4820
172
-------
PESTICIDE EQUIVALENT NAMES
NAME
MON-097
Monalide
Monam
Monex 3
Monitor
Monoammonlum
methanearsonate
Monocalcium
methanearsonate
Monocron
Monocrotophos
Monollnuron
Monosodium
methanearsonate
Monozone
Monurex
Monuron-TCA
MOPA
Morcram
Mores tan
Morfamquat
Morfoxon
Morklt
Morodde
Moromale
Morphactln
Morphothlon
Morphotox
Morsodren
Morzid
Motox 6-3 Cotton Spray
Mouse- Nots
Mouse-Rid
Mouse-Tox
Moxle
MPDT
MSF
MSMA
MSPA
MTMC
Mucochlorlc Anhydride
Murbetex
Murfotox
Muriel
Hurl tan
Murotox
Murvesoo
Muscalure
Muscamone
Muscatox
Mycotox
Mycozol
COMMON NAME
Acetochlor
Monalide
Metham
Dluron & MSMA
Methamidophos
MAMA
Calcium arsenlte
Monocrotophos
Monocrotophos
Monollnuron
MSMA
SMA
Monuron
Monuron-TCA
MOPA
Naptalam
Oxyth1oqu1nox
Morfamquat
Morfamquat
Anthraqulnone
Blnapacryl
Mancozeb
Chlorflurenal
Morphothlon
Morphothlon
Cyano (methylmercurl )
guanldlne
Morzld
Toxaphene & Parathlon,
methyl
Strychnine
Strychnine
Strychnine
Methoxychlor
Methluron
MSF
MSMA
Morzld
Tsumaclde
Mucochlorlc Anhydride
Medlnoterb acetate
Mecarbam
Chi orophad none
Promuri t
Mecarbam
Fenson
Muscalure
Muscalure
Coumaphos
Mycotox
Thiabendazole
CODE
NUMBER
4747
5220
2740, 4820
4750
0360
0360
4751
4820
4760
4780
4920
4800
0250
6740, 4580
4540
4820
4441
1425
4441
1540
0660
NAME
Myeleukon
Myleran
Mylone
Myprozine
N-2790
NAA
Nabac
Nabam
Nabasan
NAD
Naftll
Naled
Nalkll
Nami 1 an
Nankor
Na NPA
Napthalene ace t amide
Naphthalophos
1-Naphthol
Naphthyl acetic acid
Naphthyl phthalamlc
acid
NaphthyltMourea
Napromide
Naptalam
Naramycin
Narlene
Na TA
Natal
NATCA
Navadel
Navon
NC-3363
NC-4780
NC-5016
NC-6897
NC-8438
NDA
Neburea
Neburex
Neburon
Nectryl
Nedddol
Neguvon
Nellite
Nemabrom
Nemacide
Nemacur
Nernafos
Nemafume
Nemagon
Nemex
COMMON NAME
Busulfan
Busulfan
Dazomet
Plmarldn
Fonofos
Naphthaleneacetic add
Hexachlorophene
Nabam
Nabam
Naphthalene acetamlde
Carbaryl & Ovex
Naled
Bromacil
Chlordane 8 Llndane
Ronnel
Naptalam
Naphthalene acetamlde
Naphthalophos
1-Naphthol
Naphthyl acetic add
Naptalam
ANTU
Napromide
Naptalam
Cycloheximide
Narlene
TCA-sod1um
TCA-sodium
TCA
Dioxathion
Chlorpropham
Chlorflurazole
Fluoromidine
Fenozaflor
Ficam W
Ethofumesate
NDA
Neburon
Neburon
Neburon
0-Phenyl phenol
Dlazinon
Trlchlorfon
Nellite
Dibromochloropropene
Dichlofenthion
Phenamiphos
Thionazln
Di bromochl oropropane
Di bromochl oropropane
D-D
CODE
NUMBER
2910
4900
3940
4880
1060, -
4860
0800
1200, 0680
5980
4920
4880
4925
4920
0260
2010
4920
1600
2580
1420
3373
4940
4940
4940
5490
2080
6780
2220
2090
2090
173
-------
PESTICIDE EQUIVALENT NAMES
NAME
Hendrln
Neocld
Neoddol
Neo-Fulc1n
Neo-Pynam1n
Neoron
Neotran
Nephls
Nephocarp
Nerkol
New Mel
Nexa Fly-trap
Nexagan
Nexlon
NexlOn 1378
Nexlt
Nexoval
NF 46
NIA 1137
NIA 1240
NIA 2995
NIA 4512
NIA 4556
NIA 4562
NIA 5488
NIA 5767
NIA 5961
NIA 5996
NIA 9044
NIA 91C2
NIA 10242
NIA 11092
NIA 17370
NIA 24110
Nlacfdes
N1agaram1te
Niagaratran
Nlagarathol
Nlalate
Nlclofen
Nicotine
N1cou11ne
NID
Nlklor
H1m1tox
Nlmrod
NIP
Nlpagenln
N1pag1n
Nlpasol
N1pa-Th1n
N1ran
COMMON NAME
Endrln
DDT
D1az1non
Gr1seofulv1n
Tetramethrln
Bromopropylate
Neotran
Ethylene dlbromlde
Carbophenothlon
Dlchlorvos
Ethylmercury sulfate
Nexlon 1378
Bromophos ethyl
Bromophos
Nexion 1378
Llndane
Chlorpropham
Thiophanates
Phostex
Ethlon
SWEP
Solan
Dlcryl
Karsll
Tetradlfon
Endothlon
Chloronltropropane
D1chloben1l
Blnapacryl
Metlram
Carbofuran
Karbutllate
Resmethrln
K-Othr1ne
Mercaptobenzothlazole
Aramlte
Ovex
Endothall
Ethlon
Nltrofen
Nicotine
Rotenone
Radlone
Chloroplcdn
Temephos
BuplMmate
Nltrofen
Methyl Paraben
Methyl Paraben
Propyl Paraben
Naptalam
Parathlon ethyl
CODE
NUMBER
3260
1880
2080
0872
1080
2320
0860
0840
0680
1420
6670, 6671
3340
6600
2200
4583
1040
6420
6055
3240
3340
5040
6000
0020
5040
4920
5245
NAME
N1r1t
Nlrosan
Nlssol
NHrador
N1tral1n
N1trapyr1n
Nltrofen
4-N1trophenol
Nltropone C
Nltrox 80
NIX
N1x-Scald
NMRI-201
No Bunt
No-Crab
Nogos
No1ta-Ko1sumu
Nolvasan
Nomersan
Nonachlor
No-Pest
Norax
Norbormlde
Norea
Norflurazon
Nortran
Nortron
Noruron
No Scald
NovatMon
Novex
Novlgam
Novlgam Super
Novob1oc1n
NPA
NPD
NRDC-104
NROC-143
NSC- 10429
NTM
Nucldol
Nudrln
Nu-FUm
Nu-Lawn Weeder
Nuodex 84
Nurelle
Nuvacron
Nuvan
Nuvanol
Nuvanol N
Nux Vomlca
Nu-Z
COMMON NAME
N1Ht
Nlrosan
Nlssol
DNOC
N1tral1n
Nltrapyrln
Nltrofen
4-N1trophenol
Dlnoseb
Parathlon methyl
Procan-sodfum
Ethoxyquln
Phenyl cycl ohexanol
Hexachlorobenzene
Calcium propanearsonate
Dlchlorvos
DDT & Llndane
Chlorhex1d1ne
Thlram
Nonachlor
Dlchlorvos
Chloroxuron
Norbormlde
Norea
Norflurazon
Ethofumesate
Fluorom1d1ne
Norea
D1pheny1am1ne
Fen1troth1on
Fentochlor
Llndane
Pyrethrlns & P1p.
Butoxlde
Novob1oc1n
Naptalam
Aspon
Resmethrln
Permethrln
Morzld
Dimethyl phthalate
D1az1non
Methomyl
Plnolene
Bromoxyml 1
Mercaptobenzothlazole
Pyroxychlor
Monocrotophos
Dlchlorvos
Fen1troth1on
Jodfenphos
Strychnine
Z1nc sulfate (basic)
CODE
NUMBER
2770
5020
5031
5040
5060
2760
4580
3920
2320
1880, 0680
6680
5080
2320
5136
3373
3480
0680
5940, 5620
4920
0300
6055
2460
2080
4520
0820
0360
2320
3480
4103
174
-------
PESTICIDE EQUIVALENT NAMES
NAME
Oatax
Qctacide
Octachlor
Detach! or epoxide
Octalene
Octal ox
Octylbicycloheptene
dicarboxamide
ODB
Off
Ohric
Oko
Oleoculvre
Oleoparaphene
OM-1763
OM-2174
Omadine
Omethoate
OMPA
OMU
Ontrack-WE-2
OPS PA
Ordram
Ornitrol
Orthene
Ortho 5353
Ortho 9006
Ortho 12420
Orthocide 406
Ortho-Klor
Ortho LM preparations
Ortho MC
Orthopos
Ortho Phosphate
Defoliant
Orthoxenol
Oryzalin
Oryzon
OS-2046
Osbac
Osmosal ts
Osmosar
Oust
Outfox
Ovex
Ovochlor
Ovotran
OW-9
Oxadlaron
Oxamyl
Oxamyl oxlme
Cxine
Oxlne-copper
Oxlrane
COMMON NAME
Barban
KGK 264
Chlordane
Oxychlordane
Aldrin
Dieldrin
Octylbicycloheptene
dicarboxamlde
Dichlorobenzene-o
Deet
Dlmethachlon
Dichlorvos
Copper oxides
Parathion
Fungicide 1763
Apholate
Omadlne
Omethoate
Schradan
Cycluron
Prometon
Morzld
Molinate
Azacosterol
Acephate
Bufencarb
Methamldophos
Acephate
Captan
Chlordane
Methylmercury qulnollnolate
Magnesium chlorate
Parathion ethyl
DEF
Phenyl phenol
Oryzalin
Pentachl oromandel oni tri 1 e
Mevinphos
BPMC
Fluor Chrom Arsenate
Phenols
DCPA
Cyprazine
Chlorfenson or Ovex
Chlorfenson or Ovex
Chlorfenson or Ovex
Azide 5728,
Oxadiazon
Oxamyl
Oxamyl oxime
8-Quinolinol sulfate
Copper 8-Quinolate
Ethylene oxide
CODE
NUMBER
0400
1200
5200
0080
2380
2280
2320
5245
5760
4740
0025
0960
4750
0025
1020
1200
5245
1940
5490
5148
4640
0791
1720
1615
6172
5176
5186
5187
NAME
Oxycarboxin
Oxychlordane
Oxycil
Oxydemeton methyl
Oxydisulfoton
Oxy-Dumocyclin
Oxymycin
Oxypan
Oxyquinoline
Oxytetracid
Oxytetracycline
Oxythioquinox
P-1504
Paarlan
PAC
Padan
Pallethrin
Pamosol 2 Forte
Panoctine
Panodrin A-13
Panogen
Panoram D-31
Panthion
Papthion
Parabis
Paracide
Paradow
Parafluron
Paraform
Paraformaldehyde
Paral
Paraldehyde
Paramar
Para-Ni trophenol
Paraoxon
Paraphos
Paraquat dichloride
Parathene
Parathion ethyl
Parathion methyl
Parawet
Parinol
Parnon
Parfox
Partron M
Parzate
Parzate C
Patoran
Paxilon
PBA
PBA dimethylamine salt
COMMON NAME
Oxycarboxin
Oxychlordane
Sodium chlorate
Oxydemeton methyl
Oxydisulfoton
Oxytetracycline
Oxytetracycline
Oxytetracycline
8-Quinolinol
Oxytetracycline
Oxytetracycline
Oxythioquinox
Phosmet
Isopropalin
Phenacridane chloride
Cartap hydrochloride
Allethrin
Zineb
Guazatine
Cyano (methylmercuri)
guanidine
MEMA
Dieldrin
Parathion ethyl
Phenthoate
Dichlorophen
p-Dichlorobenzene
p-Dichlorobenzene
Parafluron
Paraformaldehyde
Paraformaldehyde
Paraformaldehyde
Paraformaldehyde
Parathion ethyl
4-Ni trophenol
Paraoxon
Parathion
Paraquat dichloride
Parathion ethyl
Parathion ethyl
Parathion methyl
Parathion
Parinol
Parinol
Chlorophacinone
Parathion methyl
Nabam & Zineb
Zineb
Metobromuron
Methazole
PBA
PBA dimethylamine salt
CODE
NUMBER
5200
5220
4800
4000
4070
0100
7120
2380
5245
2300
2300
5245
5060
5245
5240
5245
5245
4580
5245
5251
5251
1425
4580
4840, 7120
7120
4496
175
-------
PESTICIDE EQUIVALENT NAMES
NAME
PBED
PBR
PCA
PCBA
PCI
PCNB
PCP
PCPBS
PDB
PDQ
PDU
Peach-Thin 3 CPA
PEBC
Pebulate
Pedinex
Pelargonic Acid
Pelt-44
Penar
Pencal
Penchlorol
Penite
Pennamine D
Penncap M
PenoxaHr
Penphene
Penta
Pentac
Pentachlorin
Pentachl oroman-
delonitrile
Pentachloronltro-
benzene
Pentachl orobenzyl
alcohol
Pentachlorophenol
Pentachl orophenol ,
Na salt
Pentacon
Penta-KII
Pentanochlor
Penthanll
Penwar
Peprothion
Perchlorobenzene
Perecot
Perenox
Perfekthion
Perfluidone
Perfmlde
Permethrin
Persistol Hoi/195
Perthane
Pescombi
'-
COMMON NAME
PBED Propargyl Salt
Bromide
PBR
Pyrazon
Pentachl orobenzyl alcohol
Perchl orocycl opentadi ene
PCNB
PCP
Fenson
Dichlorobenzene-p
MCPB
Fenuron
CPA
Pebulate
Pebulate
Dinex
Pelargonic Acid
Thiophanate methyl
Penar
Calcium arsenate
PCP
Sodium arsenite
2,4-D
Parathion methyl
Penoxalln
Chlorthiophene
PCP
Dieochlor
DDT
Pentachl oromandel onitri 1 e
PCNB
Pentachlorobenzyl alcohol
PCP
Sodium pentachloro-
phenate
PCP
PCP
Solan
DTPA
PCP
DDT, Endosulfan &
Parathion methyl 3180
Hexachlorobenzene
Copper oxfdes
Copper oxides
Dimethoate
Perfluidone
Tebuthluron
Permethrin
Tretamine
Ethyl an
Mecarbam
CODE
NUMBER
5925
5280
5260
2300
4380
5300
5300
6671
0980
5260
2940
4580
5331
5260
1880
5280
5260
2820
5260
5260
5260
1880,
, 4580
3920
2420
5366
6583
5380
4441
NAME
Pestan
Pestnaster EDB 85
Pestox III
Pestox IV
Pestox XIV
Pestox IV
Pest Strip
PETD
PH 6040
Phaltar
PHC
Phenacicie
Phenocridane
chloride
Phenador-X
Phenatox
Phenazin
Pherazine
Phencaptone
Phenkapton
Phenmad
Phenmedipham
Phenobenzuron
Phenotan
Phenothiazfre
Phenothioxin
Phenoxalin
Phenpiazine
Phenthazlne
Phenthoate
Phentin acetate
Phenyl benzene
Phenylcyclohexand
COMMON NAME
Mecarbam
Ethyl ditromide
Schradan
Dimefox
Dimefox
Mipafox
Dichlorvos
Metiram
Diflubenzuron
Folpet
Propoxur
Toxaphene
Phenacridare chloride
Biphenyl
Toxaphene
Phenazine
Phenazine
Phencapton
Phencapton
PtfA
Phenmedipham
Phenobenzuron
Dinoseb-acetate
Phenothiazine
Phenothioxin
Penoxalin
Quinoxallne
Phenothiazine
Phenthoate
Fentin acetate
Biphenyl
Phenyl eye 1 ohexanon
Phenylmercury acetate Phenylmercury acetate
Phenylmercury
ammonium acetate
Phenylmercury
borate
Phenylmercury
chloride
Phenylmercury
hydroxide
Phenylmercury
iodide
Phenylmercury-
8-oxyquinolate
Phenyl phenol
Phercon BW
Pherocon CL
Pherocon GM
Pherocon MFF
Pherocon QFF
Phisonex
Phix
Phorate
Setrete
Phenylmercury borate
Phenylmercury chloride
Phenylmercury hydroxide
Phenylmercury Iodide
Quinex
Phenyl phenol
Gvondlure mixture
Looplure
Dlsparlure
Trlmedlure
Cue-lure
Hexachlorophene
PMA
Phorate
CODE
NUMBER
4441
2320
4583
2406
3660
0440
6740
0740
6740
5400
5400
5680
5410
2566
5420
5331
5420
3527
0740
5680
5460
5480
5485
5487
5490
3940
5680
5500
176
-------
PESTICIDE EQUIVALENT NAMES
NAME
Phortox
Phosacetlm
Phosalone
Phosdrln
Phosfene
Phosfolan
Phosfon
Phoskll
Phosmet
Phosnichlor
Phosphacol
Phosphamldon
Phosphlne
Phosphlnon
Phosphopyron
Phostex
Phos toxin
Phosvel
Phosvlt
Phoxlme
Phthallc Add
Phthalophos
Phthalthrin
Phyban H.C.
Phygon
Phyomone
Physan-HC
Phystasol
Phytar 550
Phytoactfn
Phytomydn
Phytosol
Plcfume
Plcloram
Plk-Off
PIN
Plndone
Pinoran
Piperalln
Plperlne
Plperonyl Butoxlde
Pipron
Plprotol
P1r1m1carb
Plrinriphos ethyl
P1r1m1phos methyl
Pirimor
Plvadn
Pival
P1vald1one
Plvalyn
P Kh NB
COMMON NAME
2,4,5-T
Phosacetlm
Phosalone
Mevlnphos
Mevinphos
Phosfolan
Chlorphonlum
Parathlon ethyl
Phosmet
Phosnichlor
Paraoxon
Phosphamldon
Aluminum phosphide
Phosphlnon
Endothlon
Phostex
Phostoxln
Leptophos
Dlchlorvos
Phoxlm
DCPA
Phosmet
Tetramethrin
MSMA
Dlchlone
oc-Naphthylacet1c acid
MSMA
Trichloronate
Cacodyllc add
Phytoactln
Streptomycin nitrate
Tlrchloronate
Chlorop1cr1n
Plcloram
Glyoxlme
EPN
Plndone
Dlfenoxuron
P1peral1n
Plperlne
Piperonyl Butoxlde
P1peral1n
Plprotal
P1r1m1carl .
Plrimlphos ethyl
P1r1m1phos methyl
P1r1m1carb
Plndone
Plndone
Plndone
Plndone
PCNB
CODE
NUMBER
6840
5520
4640
4640
1610
5245
4000
5580
4190
2320
1720
4000
4820
2180
4820
0961
5600
3796
3280
2391
5640
5620
5640
5632
5642
5643
5632
5280
NAME
Planavin
Plantvax
Plath-Lyse
PHctran
Plondrel
Plus de R1tz
PMA
PMAC
PMAS
PMP
PHP
Polaris
Pollsln
PolychloMnated
biphenyls
Polychlorinated
naphthalenes
Polychlorocamphene
Polymone 60
Polyram-Combl
Polyram M
Polyram-Ultra
Polyram Z
Polysol Forte
Pomasol Z Forte
Pond!
Potablan
Potasan
Potassium azlde
Potassium dlethyl
dlthlophosphate
Potassium dlethyl
thlophosphate
Potassium dimethyl
dlthiophosphate
Potassium dimethyl
thlophosphate
PP-062
PP-148
PP-149
PP 175
PP-211
PP-511
PP-588
PP-675
PP-745
PP-781
Pramex
Pramitol
PRO
Prebane
Pre-Beta 1
Pre-Beta 2
Prefalon
COMMON NAME
NUralin
Oxycarboxin
Dichlorophene
Cyhexatln
Ditalimfos
Propanll
PMA
PMAC
PMA
Phosmet
4-Mitrophenol
Glyphoslne
Prometryn
Polychlorinated
biphenyls
Polychlorinated
naphthalenes
Toxaphene
MCPP & 2,4-0
Met i ram
Maneb
Thiram
Zineb
Thiram
Ziram
Griseofulvin
Monalide
Potasan
Potassium azide
Potassium dlethyl
dithiophosphate
Potassium diethyl
thlophosphate
Potassium dimethyl
dlthlophosphate
Potassium dimethyl
thlophosphate
Pir1m1carb
Paraquat
Ethirimol
Menazon
Pirimiphos etnyl
Pirinviphos methyl
Bupirimate
Dlmethirimol
Morfamquat
Drazoxolon
WARF AntiresisUnt
Prometon
Dichlorothlolane dioxide
Terbutryn
Pebulate & Dial late
Cycloate 8 Dial late
Linuron
CODE
NUMBER
5C20
2306, 2307 |
5840 |
5680
5680
4000
5060
3802
5780
5700 -5707
5720 - 5725
6740
4400 -2940 '
4583 !
4300 i
6680
7120
6680
7100
4747
5728 !
1
5731 ',
5732
5733
5734
5632 '
5240
3359
4453
56«
5643
2416
2792
576C |
3980
5300, 2040
1591, 2040
4240
177
-------
PESTICIDE EQUIVALENT NAMES
NAME
Prefar
Prefix
Preflan
Prefmid
Preforan
Prefox
Pregard
Premerge
Pre-San
Prevarol
Preventol
Preservit
Prevlcur
Primatol
Primatol-M80
Primatol 025
Primatol A
Primatol P
Primatol Q
Primatol S
Primaze
Primicid
Primiti
Princep
Printop
Proban
Probe
Profluralin
Profume
Prolan
Pro! in
Promar
Promecarb
Prometon
Prometryn
Prometrex
Promuri t
Pronami de
Propachlor
Propanid
Propanil
Propargite
Propargyl Bromide
Propazine
Propena 7
Propham
Prophos
Propineb
Propi-Rhap
Prop-Job
Propon
Proponex D
COMMON NAME
Eensulide
Chi orthi amid
Tebuthiuron
Tebuthiuron
Fluorodifen
Cyprazine & Ethiolate
Profluralin
Dinoseb
Bensullde
Chlorpropham
Dichlorophen
Dazomet
Prothiocarb
Atraton
Terbuthylazine
Prometon
Atrazine
Propazine
Prometryn
Simazine
Atrazine 4 Prometryn
Pirimiphos ethyl
Isolan
Simazine
Simazine
Cyanthoate
Methazole
Profluralin
Methyl bromide
Phosmet
Warfarin
Diphacinone
Promecarb
Prometon
Prometryn
Prometryn
Promurit
Pronami de
Propachlor
Propanil
Propanil
Propargite
Propargyl Bromide
Propazine
Acrolein
Propham
Ethoprop
Propineb
Dichlorprop
Propani 1
Si 1 vex
Amines of CHPP &
2.4-D
CODE
NUMBER
C520
6583
6583
1615, 3335
5746
2760
0520
1420
0320
6589
5760
0420
5800
5780
6660
0420, 5780
5642
6160
6160
4496
5746
4000
7060
2600
5752
5760
5780
5780
4090
5820
5840
5840
5160
5800
0027
5860
5880
2309
5840
6120
NAME
Propoxon
Propoxur
Propyl Chemosept
Propyl Paraben
Propyl Parasept
Propyl ure
Propyzamide
Prosulfalin
Protect
Protex
Prothiocarb
Prothoate
Prowl
Proxal
Proxan
Proxan-sodium
Prussic acid
Prynochlor
PSP-204
PTF
PTMB
PTO
Purasan
Puratized B-2
Puraturf
Pynami n
Pyracarbolid
Pyracide
Pyramat
Pyrami n
Pyramin Plus
Pyrazon
Pyrazophos
Pyrethrlns
Pyrazothion
Pyridinltril
Pyroxychlor
Q-lure
Quel
Queltox
Quicksan
Quilan
Ouinalphos
Qulnazamid
Qulnex
Quinomethionate
Quinothion
Quinophenol
Qulnoxaline
Quintiofos
COMMON NAME
Propoxon
Propoxur
Propyl paraben
Propyl Paraben
Propyl Paraben
Propyl ure
Pronami de
Prosulfalin
Protect
Rotenone
Prothiocarb
Prothoate
Penoxalin
Trichlorfon
Proxan
Proxan Sodium
Hydrocyanic add
Prynochlor
Aphidam
Meti ram
Danifos
Omadi ne
PMA
Mercuric lactate
PMA
Allethrin
Pyracarbolid
Demephion
Pyramat
Pyrazon
Pyrazon 4 Dalapon
Pyrazon
Pyrazophos
Pyrethrins
Pyrazothion
Pyridinitrll
Pyroxychlor
Cue-lure
Ancymidol
Fenthion
PMA
Benefin
Quinalphos
Quinazamid
Phenyl mercuric
oxyquinolate
Oxythioquinox
Quinothion
8-Quinol1nol
Quinoxallne
Quintiofos
CODE
NUMBER
0440
4090
5882
6000
5331
6780
4583
5680
5680
0100
5905
5925
5925, 1660
5925
5932
5940
0230
3520
5680
0480
5966
4800
178
-------
PESTICIDE EQUIVALENT NAMES
NAME
Qulntoxene
88 R
R-242
R-1303
R-1504
R-1513
R-1582
R-1607
R-2061
R-2063
R-2170
R-4461
R-4572
R-4574
R-6199
R-7465
Rabon
Rabond
Rack Granular
Racuml n
Radapon
Radazln
Rad-E-Cate 25
Rad-E-Cate 35
Radione
Radoxone TL
Rametln
Ramlk
Rampart
Ramrod
Ramudde
Randox
Raphone
Raslkal
Ratafln
Rat-A-Way
Ratlcate
Ratllan
Ratomet
Rat or ex
Rattunal
Ravage
Ravap
Ravlac
Ravlon
Ravyon
Rawetln
Rax Mater Soluble
RE 4355
RE 11775
Readex
COMMON NAME
PCNB
Araml te
Sul phenone
Carbophenothlon
Phosmet
Azlnphos ethyl
Azlnphos methyl
Vernolate
Pebulate
Cycloate
Oxydemeton methyl
Bensulide
Mollnate
Byram
Tetram
Napropamlde
Tetrachlorvlnphos
Tetrachlorvlnphos
Fenac & Atrazlne
Coumetetralyl
Oalapon Na
Atrazlne
Sodium Cacodylate
Sodium Cacodulate 8
Cacody11c acid
Radione
Ammonium thlocyanate
Naphthalaohos
Dlphadnone
Phorate
Propachlor
Chi orophad none
CDAA
MCPA
Sodium chlorate
Coumafuryl
Coumafuryl
Norbormlde
Coumachlor
Chi orophad none
Warfarin
Warfarin
Buthldazole
Olchlorvos &
Tetrachlorvlnphos
Chi orophad none
Carbaryl
Carbaryl
Naphthalaphos
Warfarin
Naled
BPBSMC
Thloqulnox
CODE
NUMBER
5280
1080
4000
3840
3820
7020
5300
1591
5220
0520
4740
2010
3740
3740
3460, 0420
1660
0420
2600
5500
5820
1425
1140
4340
3720
3720
1425
7060
7060
0926
2320. 3740
1425
1060
1060
7060
4860
NAME
Rebel ate
Reddon
Reducymol
Reglm 8
Region
Reglone
Regulox
Reldan
Remasan
Reslstox
Resmethrln
Res-Q
Retard
RH-315
Rhodanlc add
Rhodanlne
Rhodethanll
Rhodlatox
Rhomene
Rhonox
Rhothane
R1cetr1ne
R1lo
R1om1ts1n
Ro-22453
Roccal
Ro-Dex
Rodlne
Rogor
Rogue
Ro-Ko
Romate
Ro-Neet
Ronmate
Ronnel
Ronstar
Rootone
Rospan
Rospln
Roteflve
Rotenone
Rotersept
Rotessenol
Rotox
Roundup
Rowtate
Roxlon
Royal MH-30
Rozol
R.P. 11974
R.P. 17623
R.U. 11679
COMMON NAME
Dlmethoate
2,4,5-T
Ancymidol
T1BA
Dlquat
Dlquat
MH
Chlorpyrlfos methyl
Maneb
Coumaphos
Resmethri n
Maneb, HCB &
Cantan
MH
Pronamlde
Phodanlne
Rhodanlne
Rhodethanll
Parathlon
MCPA
MCPA
ODD
Copper trlethanol-
amlne complex
Plperophos
Oxytetrocydlne
Olamazole
Benzalkonlum chloride
Strychnine
Red Squill
Dlmethoate
Propanll
Rotenone
Dlchlormate
Cycloate
Dlchlormate
Ronnel
Oxadlazon
Naphthalene ace t amide
Chloropropylate
Chloropropylate
Rotenone
Rotenone
Chlorhex1d1ne
Rotenone
Methyl bromide
Glyphosate
C1san1l1de
Dlmethoate
MH
Chlorophadnone
Phosalone
Oxadlazon
K-Othrlne
CODE
NUMBER
2420
6840
0230
2660
2660
4280
2902
4300
1540
6055
4300
3920, 1020
4280
4090
5245
4340
4340
1750
2420
5840
6000
1591
5980
5176
4880
6000
6000
6000
3801
1523
2420
4280
1425
6520
6176
179
-------
PESTICIDE EQUIVALENT NAMES
NAME
Rubltox
Ruelene
Rukseam
Runcatex
Ruohos
Rutgers 612
Ryanex
Ryanexcel
Ryaniclde
Ryanodine
Rycelan
Ryomycin
Ryzelan
S-14
S-276
S-410
S-767
S-1752
S-2940
S-2957
S-4084
S-4087
S-4400
S-6000
S-6999
S-9115
S-10165
S-15076
S-22012
Sabadllla
SADH
Safroxan
Safroxane
Salicyanilide
Salicylic add
Salinidol
Salithion
Salvo
Samuron
SAN 244
SAN 6706
SAN 9789
Sanaseed
Sandoz 6626
Sanlpd
Sanoclde
Sanspor
Santar
Santhene
Santobrite
Santochlor
COMMON NAME
Phosalone
Crufomate
DDT
MCPP
Dioxathion
Ethyl hexanediol
Ryanadine
Ryanadine
Ryanadine
Ryanodine
Oryzalin
Oxytetracyclene
Orzyalin
Dimefox
Disulfoton
Metasystox S
Fensulfothion
Fenthion
Phenthoate
Chlorthiophos
Cyanophos
Cyanofonphos
Trichloronate
Cypromid
Norbormide
Cyprazine
Propanil
Ethiolate
Benzthiazuron
Sabadilla
Daminozide
Safroxan
Safroxane
Salicyanilide
Salicylic acid
Salicyanilide
Salithion
2,4-D
Desmetryn
Formothion
Metflurazone
Norflurazon
Strychnine
Ouinalphos
Mil neb
Hexachlorobenzene
Captafol
Mercuric oxide
Xanthone
Sodium pentachloro-
phenate
Dichlorobenzene-p
CODE
NUMBER
5520
6020
1880
4400
2580
3380
5148
5148
2720
3500
3520
1491
3722
6360
1615
5840
3335
1681
P889
6050
2940
3722
5136
5966
3920
1000
2820
2300
NAME
Santophen I
Santoquin
Sapecron
Saphi-Col
Saphizon
Saphos
Sappiran
Saprol
Sarclex
Sarolex
Saturn
Sayfor A
Sayfos
SBP-1382
Scabrin
Scaldip
Schering 4075
Schering 34615
Schering 35830
Schering 36056
Schering 36268
Schering 38107
Schradan
Sclex
Scogal
SD 3418
SD 3562
SO 4294
SD 7859
SD 7961
SD 8447
SD 8530
SD 8786
SD 9098
SD 9129
SD 11831
SD 14114
SD 15418
SD 17250
SD 30053
Sebuthylazine
Secbumeton
Seedrin
Seedox
Seedvax
Select
Selectin
Selinon
Semeron 25
Semperol
Sencor
Sencoral
Sencorex
COMMON NAME
Chlorophene
Ethoxyquin
Chlorfenvinphos
Menazon
Menazon
Menazon
Ovex or Chlorfenson
Triforine
Linuron
Diazinon
Thtobencarb
Menazon
Menazon
Resmethrin
Scabrin
Diphenylamine
Phenmedlpham
Promecarb
Monalide
Formetanate Hydrochloride
Chlordimeform
Desmedipham
Schradan
Dichlozoline
Cyanazine & MCPA 1552
Isodrin
Dicrotophos
Crotoxyphos
Chlorfenvinphos
Chlorfenvinphos
Tetrachl orvi nphos
Landrin-3,4,5 Isomer
Landrin-2,3,5 Isomer
Akton
Monocrotophos
Nitralin
Fenbutatin-oxide
Cyanazine
Thiocarboxime
Benzoylprop ethyl
Sebuthylazine
Secbumeton
Aldrin
Mycotox
Seedvax
Naptalam
Protnetryn
DNOC
Desmetryn
Atrazine
Metribuzin
Metribuzin
Metribuzin
CODE
NUMBER
1300
4453
4453
4453
6822
4240
2080
0570
4453
4453
6055
5410
5752
4747
3680
1480
2006
, 4340
0700
1500
1300
1300
3740
0360
5020
7013
1552
0578
0080
4920
5780
2770
0420
4634
4634
4634
180
-------
PESTICIDE EQUIVALENT NAMES
NAME
Sendran
Septene
Septlphene
Sequestrine 330
SES
Sesamex
Sesamin
Sesamolin
Sesoxane
Sevln
Sevithion
SF-6505
Shed-A-Leaf
Shinmerex
SMrlan
Shlrlan Extra
Short-stop E
Shoxin
SI-6505
Slcarol
Siduron
Siglure
Sllvanol
Silvex
S1lvi-Rhap
S1lv1sar 510
Silvisar 550
Simadex
Simanex
Simazine
Simetone
Simetryn
Slnbar
Slndone
Sinituho
S1nox
Sinox General
Sirmate
Slstan
SK 1133
SK Preparation
Slam
Slimicide
STo-Gro
SHA
Smite 86
SN-41703
Snip Fly Bands
SNP
Sodium Azide
Sodium Fluoroacetate
Sofrll
COMMON NAME
Propoxur
Carbaryl
Chlorophene
DTPA
Sesone
Sesamex
Sesamin
Sesamolin
Sesamex
Carbaryl
Carbaryl & Parathion
methyl 1060,
Hymexazol
Sodium chlorate
Phenylmercuric acetate
Salicyanilide sodium salt
Salicyanilide
Terbutryn
Norbormide
Hydroxyisoxazole
Pyracarbolid
Siduron
Siglure
Lindane
Silvex
Silvex
Cacodylic acid
MSMA
Simazine
Simazine
Simazine
Simetone
Simetryn
Terbacil
Sindone
PCP
DNOC
Dinoseb
Dichlormate
Metham
Tretamine
SK Preparation
Azothoate
Acrolein
MH
Sodium Monochloroacetate
Azide 5728,
Prothiocarb
Oimetilan
Parathion ethyl
Sodium Azide
Sodium Fluoroacetate
Sulfur
CODE
NUMBER
0440
1060
1060
4680
5680
3980
5905
6100
0680
6120
6120
0961
4820
6160
6160
6160
6560
5260
2770
2760
6620
0027
4280
6172
5245
6172
NAME
Soilbrom 85 S 86
SDK
Solabar
Solan
Solfarin
Solid Green 0
Solo
Sol vi rex
Somilan
Sonalan
Sonalen
SOPP
Soprabel
Sopracol 781
Sopraqam
Sopranebe
Soprathion
Soprocide
Sorbic acid
Sorgoprim
Soyex
SP-1103
Spectracide
Spergon
Spheromycin
Spike
Spirofulvin
Sporofulvin
Sporilene
Spotrete
Spra-Cal
Spring-Bak
Sprout Nip
Sprout-Stop
Spud-N1c
Squill
SR 73
SRA 5172
Thylate
Thynon
Tiazon
TIBA
Tiezene
Tiguvon
Tilarex
imam
Tillantox
Timbo
Timet
Tlnactin
Tinaderm
Tionel
COMMON NAME
Ethylene dibromide
Carbanolate
Barium polysul.fide
Solan
Warfarin
Malachite Green
Naptalam
Disulfoton
Ethalfluralin
Ethalfluralin
Ethalfluralin
Sodium Phenylphenate
Lead aresenate
Drazoxolon
Parathion 6 Lindane
Maneb
Parathion ethyl
BHC
Sorbic acid
Terbuthylazine
Fluorodifen
Tetramethrin
Ciazinon
Chloranil
Novobiocin
Tebuthiuron
Griseofulvin
Griseofulvin
Tolnaftate
Thi ram
Calcium arsenate
Nabam
Chlorpropham
MH
Chlorpropham
Red Squill
Clonitralid
Methamidophos
Thi ram
Dithianon
Dazomet
TIBA
Zineb
Fenthion
PCNB & Quintozene
Pebulate
Benquinox
Rotenone
Phorate
Tolnaftate
Tolnaftate
Endosulfan
CODE
NUMBER
7060
4920
2720
2800
4180
2792
5245, 0680
4300
5245
0600
6589
2080
1180
6583
6680
0980
1420
4280
1420
0460
4750
6680
2721
7120
3572
5300
6000
5500
3180
181
-------
PESTICIDE EQUIVALENT NAMES
NAME
Tlppon
Tlrampa
Tlrpate
TMTDS
Tobaz
TDK
Tolban
Tolnaftate
Tolyfluanld
Tomacon
TomaHn
Tomaset
Tomatotone
Tomorl n
Tonoftal
Topane
Topdde
Toplclor 20
Topltox
Topper
Topsln
Tops1n-M
Topusln
Torac
Tordon
Tormona
Totrll
Toxakll
Toxaphene
2,4,5-TP
TPTH
TPTOH
Tramat
Trametan
Tranld
Trapex
Trasan
Trefanodde
Treflcon
Treflan
Treflonodde
Trefmld
Tre-hold
Tretamlne
Trevln
Trey
Trlallate
TrUmelln
THamlphos
Tr1 Brflir
Tr1ar1ir.ol
Trlasyn
THazophos
COMMON NAME
2,4.5-T
Thlram
Tlrpate
Thlram
Thlabendazole
NUrofen
Profluralln
Tolnaftate
Tolyfluanld
Tomacon
Coumafuryl
N-m-t
4-CPA
Coumachlor
Tolnaftate
0-Phenyl phenol
Benzadox
Chlordane
Chi orophad none
NDA
Thlophanate
Thlophanate methyl
Oesmetryn
Dial 1 for
Plcloram
2,4,5-T
loxynll
Toxaphene
Toxaphene
Sllvex
Fentln hydroxide
Fentln hydroxide
Ethofumesate
Thlram
Tranld
Trapex
KCPA
Tr1flural1n
Tr1flural1n
Tr1flural1n
THfluralln
Tr1flural1n &
D1phenam1d
Naphthaleneacetlc add
Tretamlne
Thlophanate methyl
Slduron
Trlallate
Tretoralne
THamlphos
Atratn
Tr1ar1mol
AnlUzlne
Trlezophos
CODE
NUMBER
6840
6680
6680
6660
5040
5746
3720
2800
0577
1200
1425
6670
6671
2835
5600
6840
4040
6740
6740
6120
3540
3540
3373
6680
4340
6800
6800
6800
6800
6800, 2620
4900
6671
6100
6770
2920
6777
NAME
THazotlon
Trlbac
Trlbactur
Trlban
Tdbetol
Trlbromsalon
Tr1bun1l
Trlbuton
THcamba
Tr1carbam1x Z
Trlcarnam
THchlorfenson
Trkhlorfon
Tr1chlorobenzo1c add
Tr1chloro1socyanur1c
add
THchloromelamlne
Trlchloronate
2,4.5-Trlchloro-
phenol
Trlchlorpyrphos
Trlclocarban
Tr1-Clor
Trlcornox
Trlcyclazole
Trldemorph
Trldex
Tr1dod1ne
Tr1-Endothall
Tr1etaz1ne
2,4,5-T, Tr1 ethyl -
ami ne salt
Trlfan
Trlfene
Trlfenmorph
Trlfenson
Tr1flural1n
Trlflurex
Trlfodde
Tr1for1ne
Tr1for1nol
Trlfungol
Tr1herb1de
Tr1herb1de-CIPC
Tr1hydroxytr1az1ne
Tr1-1odcbenzo1c add
Trim
Trlmangol
Trlmanoc
Trlmaton
Trlmedlure
Tr1met1on
Trlmeturon
Trlnox
COMMON NAME
Azlnphos ehtyl
2,3,6-TBA
Bacillus Thur1ng1ens1s
Plndone
Endothall & Propham 3240
TBS
MehtabenztM azuron
2,4-D t 2,4,5-T 2940
Trlcamba
Z1ram
Carbaryl
Ovex or Chlorfenson
Trlchlorfon
2,3.6-TBA
Tr1chloro1socyanur1c add
Tr1chloromelam1ne
Trlchloronate
2,4,5-Trlchlorophenol
Chlorpyrlfos
Trlclocarban
Chlorop1or1n
BenazoHn
Trlcyclazole
Trldemorph
EXD
Dodlne
Endothall
Tr1etaz1ne
2,4,5-T, Trl ethyl
amlne salt
Trffan
Fenac
Trlfenmorph
Fenson
THfluralln
Trlfluralln
DNOC
Tr1for1ne
Poraformaldehyde
Ferbam
Porpham
Chlorpropham
Tr1 hydro xytrl az1 ne
TIBA
THfluralln
Maneb
Maneb
Hetham
Trlmedlure
Dlmethoate
Trlmeturon
Trlchlorfon
CODE
NUMBER
3840
6920
, 5860
, 6840
7100
1060
6780
6920
6890
2900
6792
3420
2780
3240
6796
6896
3460
6800
6800
2770
6822
3600
5860
1420
6800
4300
4300
6620
2420
6780
182
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PESTICIDE EQUIVALENT NAMES
NAME
Trlofterol
Trloneb
THnoxol
Trioxone
Trl-PCNB
Tri-P.E.
Trl-Penar
THphenmorph
Tr1phenylt1n acetate
Tr1phenylt1n
hydroxide
Trlpomol
Trlcabol
Tri prene
Tr1prop1ndan
Trlscabol
Trishydroxymethyl-
ni tromethane
Trltac
Tritox
Trithion
Tritisan
Tritoftorol
Tri-VC 13
Trlxabon
Trixan
Tr1z1noc
Trizone
Troclosene potassium
Trolene
Tronabor
Tropital
Tropotox
Trotox
Troysan
Truban
Truddor
Tryben 200
Trysban
Trysben
Tserenox
Tsltrex
Tsumaclde
Tuads
Tualsal 100
Tuberlte
Tube toxin
Tugon FHegen Kugel
Tumbleleaf
Tumex
Tunic
Tupersan
COMMON NAME
Z1neb
Metlram
2,4,5-T
2.4.5-T
PCNB
Dlmexan
Penar
Trlphenmorph
Fentln acetate
Fentin hydroxide
Thlram
Ziram
Tri prene
Tripropindan
Ziram
Trlshydroxymethyl-
ni tromethane
Tritac
Tritox
Carbophenothion
PCNB
Z1neb
Dichlofenthlon
Dimexan, Cycluron 8
Chlorbufam
PCNB, Quintozene S
Thlram
Z1noc
Methyl bromide, Chloroplcrin
& Propargyl bromide
Troclosene potassium
Ronnel
Borax
Plprotal
MCPB
MCPB
MET
Ethazol
Vam1d1th1on
2,3,6-TBA
2,3,6-TBA
2,3,6-TBA
Benqulnox
Dodine
Tsumaclde
Thlram
TBS
Propham
Rotenone
Propoxur
Sodium chlorate
8-Qu1nol1nol
Methazole
Slduron
CODE
NUMBER
7120
4583
6840
6840
5280
3527
3540
6680
7100
7100
2200
1080
5280
7120
2220
5980
4380
4380
6590
6920
6920
6920
2780
6680
5860
6000
0440
4496
6100
NAME
Turf Fungicide
Tutane
U-27415
UC 7744
UC 10854
UC 19786
UC 20047A
UC 20299
UC 21149
UCP-21
Ultracide
Ultra-Sofril
Unden
Unipon
Uniroyal D 014
Urab
Urbaslc
Urbazid
Urintone
Urotropin
Urox
lirox B
V-18
V-101
Valexon
Valldadn
Validamydn A
Valone
Vamidoate
Vamidothion
Vancide 26
Vancide BL
Vandde FE-95
Vandde MZ
Vandde MZ-96
Vancide TM-95
Vandde TM Flowable
Van Dyk 264
Vapam
Vapona
Vaponite
Vapor Gard
Vapotone
VBT
VC-13 Nemadde
VC-9-104
VCS-506
Vectal
Vegadex
Veglben
COMMON NAME
Cyano (methyl rcercuri)
guanldine
sec-Butylamine
Banair.lte.
Carbaryl
Hercules AC 5727
Dinobuton
Tranld
Prep
Aldicarb
Etem
Methidathion
Benomyl
Propoxur
Dalapon-Na
Propargite
Fenuron-TCA
Urbazid
Urbazid
Methenamine
Methenamine
Honuron
Bromaci 1
Tetradifon
Tetrasul
Phoxim
Valldamycin A
Validamydn A
Pindone
Vamidothion
Vamidothion
Vancide 26
Bithlonol
Ferbam
Ziram
Ziram
Thiram
Thlram
Octyl b1 cycl oheptene
d1carbox1m1de
Metham
Dichlorvos
Dichlorvos
Plnolene
TEPP
VBT
Dichlofenthlon
Ethoprop
Leptophos
Atrazlne
CDEC
Chloramben
CODE
NUMBER
1060
0060
6340
0500
0440
1660
5160
4760
0800
6600
6630
j
7100
7100
7100 i
6680
6680
6220
2320
2320
6540
2220
5880
4190
0420
1160
0140
183
-------
PESTICIDE EQUIVALENT NAMES
1
NAME
Velpar
Velsicol 58-CS-11
Velsicol 1068
Vendex
Vendracin
Venzar
Veon
Veratridene
Veratrin
Veratrum
Verdarcln
Vergemaster
Vernam
Vertron 20
Vertron 2T
Vertron T
Vi-Cad
Victoria Green
Vldden D
Viozene
V1Par
Vi-pex
Viricuivre
Vitavax
Volaton
Vondalhyde
Vondcaptan
Vondodine
Vondrax
Vonduci
Vonduron
Vorlex
Voronit
Vorox
VPH
Vulcamicina
Vulcamydn
Vulkamycin
Vydate L oxamyl
2317-W
Wallop G
Warbex
Warf
Warfarin
Watathion
Weed-Ag-Bar
Weedar
Weedar-AT
Weedazol
Weedbeads
Weed-E-Rad
COMMON NAME
(None)
Dicamba
Chlordane
Fenbutatin oxide
Oxytetracycline
Lenacil
2,4,5-T
Sabadilla
Sabadllla
Hellebore
Oxytetracycline
2,4-D
Vernolate
2,4-D
2,4,5-T
2,4,5-T
Cadmium chloride
Malachite Green
D-D
Ronnel
MCPP I, 2,4-D
MCPP (Potassium salt)
Copper oxychloride
Carboxin
Phoxim
KH
Captan
Dodine
MH
Diuron
Dluron
Trapex
Fuberidazole
Simazine
Metham
Novobiocin
Novobiocin
Novobiocin
Oxamyl
Dimefox
Propachlor & Parathion
Famphur
Warfarin
Warfarin
Cyanofenphos
2,4-D
2,4-D & 2,4,5-T
Amitrole
Amitrole
Sodium pentachloro-
phenate
DSMA J MSHA
CODE
NUMBER
2140
1200
7013
4185
6840
2940
7020
2940
6840
6840
5980
4400, 2940
1100
1280
1020
2780
4280
2740
2740
6160
6620
5186
5820, 5245
3440
7060
7060
6360
2940
2940, 6840
0200
0200
2820
2860, 4820
NAME
Weedex
Weedez Wonder Bar
Weed-Hoe
Weedol
Weedone
Weedozol
Weed-Rhap
Weedri te
Wepsin
Wepsyn
WL-8008
WL 17,731
WL 19,805
WP-155
WSCP
Wydac
X-52
X-52
Xonthone
3Y9
Yellow Resin
Yomesan
Zardex
Zassol
Z-C Spray
Zeapur
Zeazin
Zebtox
Zectran
Zelan
Zelio
Zenophos
Zephiran
Zerdane
Zerlate
Zetax
Zidan
Zimate
Zinc Metiram
Zinc Uversol
Zineb
Zinophos
Zinosan
Ziram
Zirberk
Ziride
Zithiol
Zitox
Zobar
Zolone
Zoocoumarin
COMMON NAME
Slmazine
2,4-D
DSMA & MSMA
Paraquat dichloride
PCP, 2,4-D &
2,4,5-T
Amitrole
2,4-D
Diquat
Trlamiphos
Triamiphos
Trifenmorph
Benzoylprop ethyl
Cyanazine
Triamiphos
PBEO
Propanil & Carbaryl
X-52
X-52
Xonthone
2,4-Dep
Rosin
Niclosamide
Cycloprate
Sodium cyanate
Ziram
Simazine
Atrazlne
Zineb
Mexacarbate
MCPA
Thallium sulfate
Thionazln
Benzalkonium chloride
DDT
Ziram
MET Zinc Salt
Zineb
Zineb
Metiram
Zinc naphthenate
Zineb
Thlonazin
Zineb
Ziram
Ziram
Ziram
Malathion
Ziram
PBA
Phosalone
Warfarin
CODE
NUMBER
6160
2940
2860, 4820
5240
5260,
2940, 6840
0200
2940
2660
0578
1552
5840, 1060
1606
7100
6160
0420
7120
7080
4340
1880
7100
7120
7120
4583
7120
7120
7100
7100
7100
4260
7100
5520
7060
184
-------
PESTICIDE EQUIVALENT NAMES
NAME
COMMON NAME
CODE
NUMBER
NAME
COMMON NAME
CODE
NUMBER
Zorlal
Zotox Crab Grass
Killer
ZR-512
ZR-515
ZR-619
Zytox
Zytron
Norflurazon
Arsenic acid
Hydroprene
Methoprene
ZR-619
Methyl bromide J
ethylene d1 bromide
Zytron
5136
4531
185
-------
Section VI11
MAILING LIST CONFIRMATION
This cooy of the 1978 revision of our reference standards index was mailed
to the address appearing on our mailing list and only to those facilities
who have either (1) requested standards within a 2-year period, or (2) sig-
nified by returning the form helow which accompanied our 1976 edition.
Undoubtedly some addresses or names of facilities have changed or in some
cases have ceased to exist.
If you wish to remain on our mailing list to receive future updates of this
publication, please complete the mailback below the dashed line in full, snip
the mailback off with a pair of scissors, and return it to us. STips reaching
us with a signature alone without full name and address of facility will be
discarded. If you have no present use for this publication but know of
some other individual within your organization who is concerned with pesti-
cides or environmental analysis, would you please relay this index to that
individual.
DO HOT RETURN THIS ENTIRE PAGE - ONLY THE PORTION BELOW THE DASHED LINE.
To: U. S. Environmental Protection Agency
Health Effects Research Laboratory (MD-69) Date
Environmental Toxicology Division
Research Triangle Park, NC, U.S.A. 27711
We wish to be retained on your mailing list to receive future updates
of the Pesticides Standards Index. The address shown on the envelope
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We have no interest in future updates of this publication. Please
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Recipient
-------
TECHNICAL REPORT DATA
(Please read Instructions on the reverse before completing)
1, REPORT NO.
EPA-600/9-78-012
3. RECIPIENT'S ACCESSION>NO.
. TITLE AND SUBTITLE
ANALYTICAL REFERENCE STANDARDS AND SUPPLEMENTAL DATA
for Pesticides and Other Organic Compounds
5. REPORT DATE
MAY 1978
6. PERFORMING ORGANIZATION CODE
7. AUTHOR(S)
8. PERFORMING ORGANIZATION REPORT NO
J. F. Thompson and R. R. Watts, Editors
10. PROGRAM ELEMENT NO.
1EA615
9. PERFORMING ORGANIZATION NAME AND ADDRESS
Analytical Chemistry Branch
Environmental Toxicology Division
Health Effects Research Laboratory
Research Triangle Park, NC 27711
11. CONTRACT/QRANTNO.
12. SI
PpNSPfllNG AGENCY NAME AND.AQDRESS
Health Effects Research laboratory
Office of Research and Development
U. S. Environmental Protection Agency
Research Triangle Park, NC 27711
RTP.NC
13. TYPE OF REPORT AND PERIOD COVERED
14. SPONSORING AGENCY CODE
EPA-finn/n
16. SUPPLEMENTARY NOTES
16. ABSTRACT
This material lists several hundred compounds of analytical reference standards
of Insecticides, herbicides, algicldes, nematocides, rodenticides, fungicides,
and miscellaneous organic compounds which are available mostly in purified form
1n subsamnles of 50-100 milligrams to any non-profit laboratory in the world
free of charge. Also Included in the manual are miscellaneous data pertinent
to nesticidal compounds such as orecautionary notes in the handling and storage
of highly toxic compounds, the preparation and storage of solutions of standards,
residue methodology references, and an Index of over 3,500 pesticide equiva-
lent names.
KEY WORDS AND DOCUMENT ANALYSIS
DESCRIPTORS
b.IDENTIFIERS/OPEN ENDED TERMS C. COSATI I'luld/Croup
standards
chemical analysis
pesticides and derivatives
organic water pollutants
07 C, D
3. DISTRIBUTION STATEMENT
RELEASE TO PUBLIC
19. SECURITY CLASS (ThisReport)
UNCLASSIFIED
21. NO. OF PAGES
187
20. SECURITY CLASS {This page I
UNCLASSIFIED
22. PRICE
EPA Form 2220-1 (9-73)
187
6U.S. GOVERNMENT PRINTING OFFICE: 1979-61+0-013' 'tl 72 REGION NO. 4
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