EPA-600/9-76-012
May 1976
ANALYTICAL
REFERENCE STANDARDS
AND SUPPLEMENTAL DATA
FOR PESTICIDES
AND OTHER
SELECTED ORGANIC COMPOUNDS
w
k ^^^^^^^^^^^ A
U.S. ENVIRONMENTAL PROTECTION AGENCY
Health Effects Research Laboratory
Environmental Toxicology Division
Research Triangle Park, N.C. 27711
-------
EPA-600/9-76-012
ANALYTICAL REFERENCE STANDARDS
AND
SUPPLEMENTAL DATA
FOR
PESTICIDES AND OTHER ORGANIC COMPOUNDS
Prepared by
Analytical Chemistry Branch
Environmental Toxicology Division
Editor: J. F. Thompson
HEALTH EFFECTS RESEARCH LABORATORY
OFFICE OF RESEARCH AND DEVELOPMENT
U.S. ENVIRONMENTAL PROTECTION AGENCY
RESEARCH TRIANGLE PARK, N. C. 27711
May 1976
-------
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.
-------
CONTENTS
Preface
SECTION I, a
SECTION I, b
SECTION II
SECTION III
SECTION IV
SECTION V
List of available standards
List of compounds deleted from stock ....
The handling and storage of organophosphorous
pesticides
Preparation and storage of analytical
standards
Decoding residue method references
List of contributing pesticide producing
companies
Page
i v
1
84
86
87
94
100
SECTION VI
Index of pesticide equivalent names 101
m
-------
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 of 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 bona fide pesticide research and monitoring laboratories on a discretion-
ary basis as time and resources have permitted,, As this edition goes to press,
over 700 laboratories are on the mailing list, including 76 laboratories in 31
foreign countries which have cooperative relationships with the U.S. government.
In calendar year 1975, 7,228 subsamples were issued from the repository in
response to 849 requests.
In Section I,a the current Index lists 387 pesticidal and related com-
pounds. Eighty-eight compounds listed in the 1973 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, 84 new
compounds have been added to the stock.
In this edition, supplemental data has been expanded to include refer-
ences to residue analytical methodology for each pesticical compound listed if
any could be located. References are given in code on the faceplate for each
compound in Section I,a, with decoding information provided in Section IV. We
neither recommend nor endorse the validity or integrity of the analytical data
in the cited publications. They are provided only for supplemental information.
The editor wishes to extend a special word of appreciation and gratitude
to those commercial producers of pesticidal compounds who provide analytical
grade reference standard materials on a gratis basis. Without their help, it
would be next to impossible to maintain the repository service. Contributing
companies are shown in Section V.
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 LDso based on
oral feeding of male rats. The figure given is the number of milligrams of the
compound 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 LD5o 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.
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 widely known in the United States. In cases where no
iv
-------
common name has been assigned, a trade or proprietary name is used. For the
convenience of the reader, Section VI contains a list of over 2,400 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. For example, 28 compounds listed in 1973 under proprietary names have
since been assigned common names and are so listed in this edition.)
Because of great demand from many sources and limited supplies, the
amount of each standard issued is restricted to no more than 100 milligrams,
and the number of standards to only those necessary for limited immediate needs.
The short shelf life of many standards is one of the reasons for restricting
field inventories, and requesters are asked to order only those compounds which
will be needed for a six-month period.
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 6LC work. Researchers requiring larger quantities,
such as for animal feeding studies, should contact the manufacturer or purchase
from a commercial supplier. We cannot supply large quantities.
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 en-
closed with each shipment. It is important that the card be mailed back imme-
diately. 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
order form, but a full address must be given along with requester's name-
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, EPA entire address)
Health Effects Research Laboratory
Research Triangle Park, N0C. 27711, MD-69
-------
Section I,a
LIST OF AVAILABLE STANDARDS
As this edition goes to press, each compound listed in the following
pages is commercially available and can be supplied in the 100 mg portions
specified in the PREFACE. However, during the two-year life of this edition
it is more than likely that the production of certain compounds will be dis-
continued 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
with code numbers on the next three 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, etc. are given.
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 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.
-------
ALPHABETICAL LISTING AND CODE NUMBERS OF COMPOUNDS
COMMON NAME
ACEPHATE
ACROLEIN
ALACHLOR
ALDICARB
ALDRIN
ALLETHRIN
AMETRYN
AMINOCARB
AMITROLE
AMOBAM
ANCYMIDOL
ANILAZINE
ANTHRAQUINONE
ANTU
ASPON
ASULAM
ATRATON
ATRAZINE
AZINPHOS ETHYL
AZINPHOS METHYL
AZOBENZENE
BARBAN
BENEFIN
BENOMYL
BENSULIDE
BENTAZON
BENTHIOCARB
BENTRANIL
BENZADOX
BENZOYLPROP ETHYL
BENZYL BENZOATE
BHC, MIXED
BHC, a
BHC, B
BHC, y
BHC, 6
BIFENOX
BIPHENYL
BROMACIL
BROMOPHOS
BROMOPHOS ETHYL
BROMOXYNIL
BUNEMA
BUTACHLOR
BUTRALIN
BUTYLATE
CACODYLIC ACID
CALCIUM ARSENATE
CAPTAFOL
CAPTAN
CARBARYL
CARBENDAZIM
CARBETAMIDE
CARBOFURAN
CARBOPHENOTHION
CARBOXIN
CDAA
CDEC
CHLORAMBEN
CHLORANIL
CHLORBENSIDE
CHLORDANE, TECH.
CHLORDANE, a
CHLORDANE, Y
CHLORDECONE
CHLORDENE
CHLORDENE, a
CHLORDENE, B
CHLORDENE, y
CHLORDIMEFORM
CHLORFENVINPHOS
CHLORMEPHOS
CHLOROBENZILATE
CHLORONEB
CHLOROPHACINONE
CHLOROTHALONIL
CODE
NUMBER
0025
0027
4160
0060
0080
0100
0120
0180
0200
0220
0230
2920
0250
0260
0300
0310
0320
0420
3840
3820
0340
0400
0480
0500
0520
0425
0570
0574
0577
0578
0580
0600
0620
0640
0680
0660
0733
0740
0800
0840
0860
0820
0916
0922
0933
0940
0961
0980
1000
1020
1060
1071
1074
1040
1080
1100
1140
1160
0140
1180
1340
1200
1220
1240
1280
1260
1261
1262
1263
1480
1300
1316
1360
1380
1425
1640
COMMON NAME
CHLORPROPHAM
CHLORPYRIFOS
CHLORTHIOPHOS
CLONITRALID
COUMAFURYL
COUMAPHOS
CROTOXYPHOS
CRUFOMATE
CRYOLITE
CYANAZINE
CYCLOATE
CYCLOHEXIMIDE
CYPRAZINE
CYTHIOATE
DALAPON
DCPA
DDA-£,£'
ODD, MIXED
ODD, m,£'
DOO, o,£'
ODD, £,£'
DDD-£,£Y, olefin
DDE, o,£'
DDE, £,£'
DDT, MIXED
DDT, o,£'
DDT, D,D'
DEF
DEMETON-0
DEMETON-S
DESMEDIPHAM
DIAL I FOR
DIAL LATE
DIAPHENE
DIAZINON
DIBROMOCHLOROPROPANE
DIBUTYL PHTHALATE
DICAMBA
DICHLOBENIL
DICHLOFENTHION
DICHLONE
DICHLORAN
DICHLOROBENZENE, o
DICHLOROBENZENE, p
DICHLOROPROPENE
DICHLOROPROP
DICHLORVOS
DICOFOL
DICROTOPHOS
DIELDRIN
DIETHYL PHOSPHATE
DIFENZOQUAT
DIFLUBENZURON
DIMETHIRIMOL
DIMETHOATE
DIMETHYL PHOSPHATE
DIMETHYL PHTHALATE
DINITRAMINE
DINOCAP
DINOSEB
DINOSEB ACETATE
DIOXATHION
DIPHACINONE
DIPHENAMID
DIPHENYL MERCURY
DIQUAT DIBROMIDE
DISULFOTON
QITHIANON
DIURON
DNOC
DODINE
DRAZOXOLON
DSMA
2,4-D, ACID
2,4-D, BOEE
2,4-D, BE
2,4-D, DEA SALT
CODE
NUMBER
1420
2900
1491
0460
3720
1540
1500
6020
1546
1552
1591
1600
1615
1621
1660
1720
1740
1750
1820
1760
1780
1800
1840
1860
1880
1900
1920
1940
1981
1982
2006
2035
2040
2060
2080
2090
2120
2140
2200
2220
2180
2260
2280
2300
2306
2309
2320
2340
0700
2380
2386
2395
2406
2416
2420
2458
2460
2551
2560
2760
2566
2580
2600
2620
2640
2660
2720
2721
2740
2770
2780
2792
2860
2940
2960
2980
2985
-------
COMMON NAME
2,4-D, DMA SALT
2,4-D, IBE
2,4-D, IDE
2,4-D, IPE
2,4-D, PGBEE
2,4-DB, ACID
2,4-DB, BE
2,4-DB, IBE
2,4-DB, IDE
ENDOSULFAN
ENDOSULFAN I
ENDOSULFAN II
ENDOTHALL, ACID
ENDRIN
EPN
EPIC
ERBON
ETHEPHON
ETHIOLATE
ETHION
ETHIRIMOL
ETHOPROP
ETHYL HEXANEDIOL
ETHYL MERCURIC CHLORIDE
EXD
FAMPHUR
FENAC
FENAMINOSULF
FENITROTHION
FENSULFOTHION
FENTHION
FENTIN ACETATE
FENTIN HYDROXIDE
FERBAM
FLUCHLORALIN
FLUOMETURON
FLUORIDAMID
FLURECOL-n-BUTYLESTER
FOLEX
FOLPET
FONOFOS
FORMETANATE HYDROCHLORIDE
FORMOTHION
GIBBERELLIC ACID
GLYPHOSATE
HEPTACHLOR
HEPTACHLOR EPOXIDE
HEXACHLOROBENZENE
HEXACHLOROPHENE
1-HYDROXYCHLORDENE
IBP
IOXYNIL
ISOPROPALIN
KARBUTILATE
LAMPRECIDE
LEAD ARSENATE
LENACIL
LEPTOPHOS
LETHANE 384
LINURON
MALATHION
MANEB
MCPA
MCPA, IOE
MCPB
MCPP
MCPP, IOE
MECARBAM
MENAZON
CODE
NUMBER
2990
3000
3020
3040
3060
3080
3100
3120
3140
3180
3200
3220
3240
3260
3280
3300
3320
3330
3335
3340
3359
5880
3380
3400
3420
3440
3460
2020
3480
3500
3520
3527
3540
3600
0407
3620
3623
3630
3640
3660
2910
3680
3722
3790
3801
3860
3880
3920
3940
3960
4011
4040
4070
6420
4166
4180
4185
4190
4220
4240
4260
4300
4340
4360
4380
4400
4420
4441
4453
COMMON NAME
MEOBAL
MEPHOSFOLAN
METAL KAMATE
METHAM
METHAMIDOPHOS
METHANEARSONIC ACID
METHAZOLE
METHIDATHION
METHIOCARB
METHOMYL
METHOPRENE
METHOXYCHLOR
METHYLMERCURIC CHLORIDE
METHYLMERCURIC IODIDE
METOXURON
MEVINPHOS
MEXACARBATE
MH
MIREX
MOLINATE
MONALIDE
MONOCROTOPHOS
MONOLINURON
MONURON
MONURON-TCA
MORPHOTHION
MSMA
NABAM
NALED
NAPHTHALENE ACETAMIDE
NAPHTHALENE ACETIC ACID
1-NAPHTHOL
NAPROPAMIDE
NAPTALAM, SODIUM SALT
NEBURON
NITRALIN
NITRAPYRIN
NITROFEN
4-NITROPHENOL
NONACHLOR-T
NORFLURAZON
ORYZALIN
OXADIAZON
OXAMYL
OXAMYL OXIME
OXYCHLORDANE
OXYDEMETON METHYL
OXYTHIOQUINOX
PARAQUAT DICHLORIDE
PARATHION ETHYL
PARATHION METHYL
PARINOL
PCNB
PCP
PEBULATE
PERFLUIDONE
PERTHANE
PHENCAPTON
PHENMEDIPHAM
PHENOTHIAZINE
PHENYLMERCURIC
ACETATE (PMA)
PHENYLMERCURIC
BORATE
PHENYLMERCURIC
CHLORIDE
PHENYLMERCURIC
HYDROXIDE
PHENYLMERCURIC
IODIDE
PHENYLPHENOL
PHORATE
PHOSALONE
PHOSFOLAN
PHOSMET
CODE
NUMBER
4460
1630
0960
6220
4750
4490
4496
6340
4500
4520
4531
4540
4560
4572
4631
4640
7080
4280
4720
4740
4747
0360
4751
4760
4780
4803
4820
4840
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
5366
5380
5400
5410
5420
5680
5460
5480
5485
5487
5490
5500
5520
1610
4000
-------
COMMON NAME
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 ]000
HALOWAX 1001
HALOWAX 1013
HALOWAX 1014
HALOWAX 1051
HALOWAX 1099
POTASSIUM AZIDE
POTASSIUM DI ETHYL
DITHIOPHOSPHATE
POTASSIUM DIETHYL
THIOPHOSPHATE
POTASSIUM DIMETHYL
DITHIOPHOSPHATE
POTASSIUM DIMETHYL
THIOPHOSPHATE
PROMECARB
PROMETON
PROMETRYN
PRONAMIDE
PROPACHLOR
PROPANIL
PROPAGITE
PROPAZINE
PROPHAM
PROPOXUR
PROTECT
PYRACARBOLID
PYRAZON
PYRAZOPHOS
PYRETHRINS
QUINALPHOS
RESMETHRIN
RONNEL
ROTENONE
SALITHION
SIDURON
SILVEX, ACID
SILVEX, IDE
SILVEX, PGBEE
SIMAZINE
SODIUM AZIDE
SODIUM PENTA-
CHLOROPHENATE
SODIUM PHENYLPHENATE
STIROFOS
STREPTOMYCIN SULFATE
STROBANE
SULFOXIDE
SURECIDE
TECNAZENE
TEMEPHOS
CODE
NUMBER
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
5752
5760
5780
4090
5820
5840
5160
5800
5860
0440
5882
5905
5925
5932
5940
5966
6055
5980
6000
6050
6100
6120
6130
6140
6160
6172
2820
2800
3740
6222
6240
6300
6360
6435
0020
COMMON NAME
TEPP
TERBACIL
TERBUTRYN
TERRAZOLE
TETRAD I FON
TETRASUL
THANITE
THIABENDAZOLE
THIOFANOX
THIOMETON
THIOPHANATE
THIOPHANATE METHYL
THIRAM
TOXAPHENE
TRIALLATE
TRIAZOPHOS
TRICHLORFON
2,4,5-TRICHLOROPHENOL
TRIDEMORPH
TRIFLURALIN
TRIFORINE
2,4, 5-T, ACID
2,4,5-T, BOEE
2, 4, 5-T, BE
2,4,5-T, IOE
2,4,5-T, PGBEE
2,4,5-T, TEA SALT
4-(2,4,5-TB)
2,3,6-TBA
VENDEX
VERNOLATE
WARFARIN
ZINEB
ZIRAM
CODE
NUMBER
6540
6560
3980
6590
6600
6630
6640
6660
6663
6665
6670
6671
6680
6740
6770
6777
6780
6890
6792
6800
6822
6840
6860
6870
6880
6885
6895
6900
6920
7013
7020
7060
7120
7100
-------
Code Common Name Emp. Form.
Chemical Name
Structure
0025 ACEPHATE (Orthene)
0, S-Dimethyl acetyl=
phosphorami dothi oate
Mol.Wt. 183
Ute Insectic.
ID 50 945
Ref.
1
2
3
4
5
6
AL
21
74
57/1
189
3
9
a
a
0027 ACROLEIN (Aqualin)
C3H40 2-Propenal
Mol.Wt. 56.06
Ute Herbic.
Ll>50 46
Ref.
A B C D E F
1
2
3
4
5
6
7U
12
t
H H
1 1
CH2=C — C=O
ALACHLOR (Lasso) C, .H.-C1NO. 2-Chloro-2' ,6'-d1ethyl-N-(methoxy=
U mothvl^ afoi-aFll 1 i Aa
Mol. Wl. 270
Ute Herbic.
L D50 3,000
Ref.
1
2
3
4
5
6
C
AJ
BH
KA
75
71
73
II
23/1
11/4
50/5
77
257
333
3
3,8
19
15,
11
cgh
jo
X
X
X
CH2CH3
CH2CH3
° Cl
0060 ALDICARB (Temik)
C7H14N2°2S
2-Methyl-2-(methylthio)propional=
dehyde-0-(methylcarbomoyl)oxiroe
Mol. Wt. 190
Ute Insectic.
L Deo 0-93
Ref.
1
2
3
4
5
6
C
AL
AJ
AJ
AL
67
69
68
70
II
50
17/1
16
53
1242
70
549
1296
4,12
12
6
10
4
9
e
af
aef
def
CH3 O
I II
CH3S -C -C =N-O-C-N-CH,
W *
0080 ALDRIN
Mol.Wt. 365
Ute Insectic.
I DM 55
C12H8C16 l,2,3,4,10,10-Hexachloro-l,4,4a,
5,8,8a-hexahydro-l A-endo-
ezc-STB-dimethanonaphtnaiene
1
2
3
4
5
6
C
A
A
A
I
5
8B
IDA
2,6
2
2
2
a
jl
V
t
-------
Code Common Name Emp. Form.
Chemical Name
Structure
0100 ALLETHRIN
Cl 9H26°3 2"A1 'y1 -4-hydroxy-3-methyl -
2-cyclopenten-l-one ester of
2,2-dimetnyl-3-(2-methylpropenyl)-
cyclopropanecarboxylic acid
Mol.Wt. 302
U*» Insectic.
I DM 680
.Ref.
A B C D E F
1
2
3
4
5
6
AJ
58
6
643
21
:,o
(CH3)2C=CH-CH O CH3
\
CH-C-0-i^VCH2-CH=CH2
(CH3)2-C
1—lv
0120 AMETRYN (Evik)
Mol. Wl. 227
Ut» Herbic.
L DSO 1,110
Ref.
2-(Ethylamino)-4-(isopropylamino)-
6-(methyl thio)-s-triazine
1
2
3
4
5
6
C
14D
73
II
80
137
6
11
efio
u
H
SCH,
N H
I
-N-CH(CH3)2
0180 AMINOCARB (Matacil)
Mol.Wt. 208
Use Insectic.
I.DSO 30
CHH16N2°2
Ref.
4-Dimethylamino-m-tolyl
methylcarbamate
1
2
3
4
5
6
AJ
ZD
AJ
MD
WO
AL
69
70
72
69
70
72
17/1
50/1
20/2
L5/(3.4)
50/1
55/6 .
56
92
443
362
92
1259
2
14
2,3
3
11
11
ade
0
X
X
X
X
H O
CH3-N-C-
N(CH3)
3'2
CH,
0200
AMITROLE (Cytrol)
3-Amlno-l,2,4-triazole
Mol.Wt. 84
Use Herbic.
I.DSO 24,600
Ref.
1
2
3
4
5
6
AL
AL
ZJ
61
62
70
44
45
18
196
382
439
12
12
12
d,e
e
t
N N
AMOBAM (Chemo-0-Bam)
Mol. Wt. 246
U» Fungic.
I D50 450
Ref.
Diamronjum ethylene=
bisdithiocarbamate
A B
1
2
3
4
5
6
AJ
BA
AL
AL
74
68
69
67
22/5
93/11.05
52/6
50/5
886
219
1226
1102
10
15
10
18
a
a,d
def
a
CH2NHCS2NH4
CHjNHCSjNK,
-------
Code Common Name Emp. Form.
Chemical Name
Structure
0230 ANCYMIDOL (A-Rest) C.-H-.N-O,, o-Cyclopropyl-a-(p-methoxyphenyl)-
is m 5-pyrimidinemethanol
Mol. Wt. 256
U» Grth. Inhibit.
I DSO 4,500
A B
Off
Ref.
1
2
3
4
5
6
AL
3E
75
58/4
850
3
3
w
u
2920 ANILAZINE (Dyrene)
. 2,4-Dichloro-6-(o-chloro=
anilincO-a-triazine
Mol.Wt. 275.5
Use Fungic.
IDso 2,710
Ref.
A B C D E F
1
2
3
4
5
6
C
II
12
ef
02SQ ANTHRAQUINONE (Corbit) C14Hg02 9,10-Anthraquinone
Mol.Wt. 208
Uia Bird Repel 1 ant
IDso 5000+
A B C D E F
Ref.
1
2
3
5
6
AT
JA
72
66
17/6
30/9
710
935
11
11
X
X
0260 ANTU
l(l-Naphthyl)-2-thiourea
Mol. Wt. 202
UM Rodentic.
ID50 7
A B
ff
1
2
3
4
5
6
WD
GG
67
50
5/11
89
552
115
2
12
X
X
NH-CS-NH,
0300 ASPON
Mol. Wt. 378
U«e Insectic.
L D,0 891
0,0,0,0-Tetrapropyl dithio=
Pyrophosphate
A B
E F
Ref.
1
2
3
4
5
6
AL
70
53/3
499
4
X
s s
(C3H7O)2-P-O-f-(OC3H7)2
-------
Code Common Name Emp. Form.
Chemical Name
Structure
0310 ASULAM (Asulox)
CRHlnN?0,.S Methyl (4-amino benzene=
01 sulfonyDcarbamate
Mol.Wt. 230
Use Herbic.
1050 5,000+
Ref.
0320 ATRATON (Gesatamin) C.H,,
A B C D E F
1
2
3
4
5
6
AC
71
73
7
497
12
3,4
i
u
H2N-/ \-SO2NHCOOC
*LO 2-(Ethylamino)-4-{isopropylamino)-
6-methoxy-s-triazine
OCH3
Mol.Wt. 211 JL
Use Herbic.
ID50 1,465
Ref.
A B C D E F
1
2
3
4
5
6
BH
ZD
64
70
4
32
64
371
.-
6
--
u
0420 ATRAZINE (Aatrex) CoHj.ClNj 2-Chloro-4-(ethylamino)-6-
' (isopropylamino)-s-triazine
Mol.Wt. 216
U»e Herbic.
LDso 3,080
Ref.
3840 AZINPHOS ETHVL (Ethyl Guthion
Mol. Wt. 345
Use Insectic.
I D50 7-17
Ref.
A B C D E F
1
2
3
4
5
6
C
AL
RC
AJ
AJ
68
70
73
74
II
51
35
21
22
682
64
93
137
12
3
11
1,2
2
bee
ct
ct
f
^ f V
C2H5-^-N N-C(CH32
Cl
f^lf H
C2H5N^N/^N-C(CH3)2
H H
C12H16N303PS2 0,0-Diethyl S-[4-oxo-l ,2 ,
3-benzotriazin-3(4H)-yl methyl]
phosphorodithioate
A B C D E F
1
2
3
4
5
6
AL
ZD
WD
AD
AJ
WD
74
69
69
70
68
71
57/5
26
43/3
5/1
16/5
59/1
1033
17
388
42
808
135
4
10
10
10
11
11
t
t
t
0
X
X
O
u
(C2H50)2 P- S -CHi-rf^Y^
1 %x
3820 AZINPHOS METHYL (Guthion) CinH-,.,N.,0,PS;, 0,0-Dimethyl S-[4-oxo-l ,2,
' 3-benzotriazin-3(4H)-ylmethyl]
phosphorodithioate
Mol.Wt. 317
Use Insectic.
ID» 16
A B C D E F
1
2
C
AD
74
II
11/3
224
12,1'
4
deg
u
O
(CH3O)2 P-S-CH2 -N'X^sY^rX'
Ref.
-------
Code Common Name Etnp. Form.
Chemical Name
Structure
0340 AZOBENZENE
C12H10N2
Diphenyl diimide
Mol.Wi. 182
Uw Acari'c.
11>50 1,000
Ref.
1
1
3
4
5
6
AV
73
01721
-
10J1
j
0400 BARBAN (Carbyne)
Mol. Wl. 258
U«e Herbic.
1.050 1,350
C,,H.,C1,NO, 4-Cnloro-2-Butynyl-m-chloro=
M9^^ carbanilate
Ref.
1
2
3
4
5
A
C
WD
BA
71
72
II
57
97/1153
303
294
12
11
2
a
t.u
a,c
O
II
H-N-C-OCH2-C5C-CH2CI
0480 BENEFIN (Balan)
Mol.Wi. 335
Use Herbic.
ID 50 10,000+
,H1,F,N,0;i
10 i
Ref.
N-Butyl-N-ethyl-a,a,o-tr1fluoro-
2,6-dinitro-p-toluldine
1
2
3
4
5
6
C
AJ
AJ
AN
AL
WD
73
74
72
73
71
II
21
22/1
10/3
56/2
63/2
82
176
457
364
2
2
2
2
3
1,2
bdf
a
a
u
X
X
0500 BENOMYL (Benlate)
Mol.Wi. 290
U«» Fungic.
IDso 10,000+
Ref.
l-(butylcarbamoyl)-
2-benzimfdazolecarbamate
1
2
3
4
5
6
AJ
AL
AJ
WD
AJ
AJ
69
71
72
74
73
73
17/2
54/6
20
101
21/3
21/2
267
1399
1230
33
368
171
12J4
12J4
12
11,14
16
16
a,j
e.h
e
e
a,u
jlm
no
O H
C-N (CH2)3CH3
N H O
0520 BENSULIDE (Prefar)
Mol.Wi. 397.5
U«« Herbic.
I D;o 770
C H NO
" '* '
Ref.
PS S-(0,0-Oiisopropyl phosphorodithict
J ate) ester of N-(2-mercaptoethyl)
benzenesulfonamide
1
2
3
4
5
6
C
AC
67
II
5
483
3,4,
12
20
afg
_
O H
O=S-N(CH2)2S-
-OCH(CH3)J2
-------
Code Common Name Emp. Form. Chemical Name Structure
0570 BENTHIOCARB (Bolero) CI,HI
,C1NOS 5-(4-Chlorobenzyl)N,N-diethyl=
thiolcarbamate
Mol.Wt. 258 . . n
ABCDEF // \\ Y
Use Herbic.
LDjo 1,903
Ref.
0574 BENTRANIL C .H
1
2
3
4
5
6
JA
AM
21
71
74
35/8
1586
1161
-
4
4
2,4
u
c,u
actu
Cl-v V~t,n25CNlC2H5)2
\ — j
NO 2-Phenyl-3,l-benzoxa=
zinone-(4)
Mel.Wl. 223 {^ ^f ^1 \ ?
ABCDEF | | \=/
Use Herbic.
IDso ca. 1,600
Ref.
1
2
3
4
5
6
^^ s^*^ /
O
0577 BENZADOX (Topcide) CQHQNO/) (Benzamidooxy)acetic acid
Mol. Wl. 195 n H O
ABCDEF /; ^ V , V
use Herbic0
lDf0 5,600
Ref.
0578 BENZOYLPROP ETHYL (Suffix) C
1
2
3
4
5
6
C
3Z
II
3
3,11
af
f
// \\ ' "
// \\ (;_N— O— CH2 — C— O
\ ~^ — •^^ J
laH,7Cl2NO, Ethyl N-benzoyl-N-(3,4-
dichlorophenyl)-2-aminopropionate
c\ o
Mol. Wl. 366 >, :\ Y / .
Use Herbic.
L DJO 1,555
Ref.
ABC D E F _. // \\ .. i / \
1
2
3
4
5
6
7U
2
c,u
"~\ /-" <~~\ //
\=/ ^ /
H3C— C— C— O— C2H5
H 0
0580 BENZYL BENZOATE C^H-,,0, Benzyl benzoate
MOI.WI. 212 n n r^i rr\
ABC D E F H2C-O-CO
Use Scabicide
IDso 1,700
Ref.
1
2
3
4
5
6
r^N r^>
^xN. ^ ^^ s>
^^ \_/
-------
Code Common Name Emp. Form. Chemical Name
Structure
0600 BHC, MIXED ISOMERS
Mol.Wt. 291
Use Insectic.
LDso 200
6Clg Several isomers of 1,2,3,4,5,6-
hexachlorocyclohexane
D E F
Ref.
1
2
3
4
5
6
C
B
A
AL
WD
68
67
II
24.100-
.105
5A, 8B,
10A, 11
51
27
45
250
2,12
12
2
2
2
de
de
jl
tuv
j
u
*ci
0620 BHC, ALPHA ISOMER
gClg Alpha isomer of hexachloro-
cyclohexane
Mol. Wt. 291
A B
Off
u*« Compon. of
tech. BHC
1- O'O 500
Ref.
|
2
T
4
5
6
See
0600
*CI
0640 BHC, BETA ISOMER
CCHCC1C Beta isomer of hexachloro-
o b o ,
cyclohexane
Mol. Wt. 291
D E F
Use Compon. of
tech. BHC
1 Dso 6,000
Ref.
1
2
3
4
5
6
See
0600
Gamma isomer of hexachloro-
000 cyclohexane
Mol.Wt. 291
A B C Off
Use Insectic.
1.050 125
Ref.
.
2
3
4
5
6
See
0600
0660 BHC, DELTA ISOMER
C6H6C16
Delta isomer of hexachloro-
cyclohexane
Mol.Wt. 291
Use Lumpun. UT
tech. BHC
lt>50 1,000
Ref.
1
2
3
4
5
6
See
0600
-------
Code Common Name Emp. Form.
Chemical Name
Structure
0733 BIFENOX (Modown)
C14H9C12MO
5 Methyl 5-(2,4-dichloro=
phenoxy)-2-nitrobenzoate
O
Mol.Wt. 342 H C-Q-C
ABC D E F \
U$e Herbic.
L D50 6,400+
Ref.
1
2
3
4
5
6
5M
6
c,9
OW VO
\ /
\=/
0740 BIPHENYL (Diphenyl)
Biphenyl
Mol. Wt. 154
Use Fungic.
L D
50
3,280
Ref.
1
2
3
4
5
6
AL
AL
C
57
67
40
50
II
249
934
12
11J2
12
e
X
e
0800 BROMACIL (Hyvar)
Mol.Wt. 261
Use Herbic.
5,200
5-Bromo-3-sec-butyl -6-methyl uracll
Ref.
1
2
3
4
5
6
AJ
AJ
AJ
WD
AC
66
67
68
70
67
14
15
16
46
5
94
174
54
110
335
6
2
5
2
20
a
a,u
1JU
itu
...
N-CHCH2CH3
0840 BROMOPHOS (Brofene)
Mol. Wt. 366
U«e Insectic.
10.0 3,750-6,100
CgHgBrCljOjPS 0-(4-Bromo-2,5-dichlorophenyl)
0,0-dimethyl phosphorothioate
Ref.
1
2
3
4
5
6
AJ
ZD
66
72
14
41
609
65
12
11,12
17
m,u
u
CL
Br
Cl
0860
BROMOPHOS ETHYL (Nexagan) C H BrCl 0 PS 0-(4-Bromo-2,5-dichlorophenyl)
lu " ' J 0,0-idethyl phosphorot
Mol. Wt. 394
y%e Insectic. &
Acaric.
LD50 52-170
Ref.
A B C 0 E F
1
2
3
4
5
6
ZD
72
41
65
11,1
17
d,
j > LI
. T / \
!H'°)'P-°\=h
Cl
-------
Code Common Name Emp. Form. Chemical Name
Structure
0820 BROMOXYNIL (Brominal)
Mol.Wl. 277
Use Herbic.
I.DSO 190
3,5-Dibromo-4-hydroxybenzonitrile
D E F
Ret.
1
2
3
4
5
6
WD
AC
71
67
57
5
347
11
20
tu
—
0916 BUNEMA
C-,H,NOS~K Potassium ^-hydroxymethyl-
N-methyldithiocarbamate
Mel. Wi. 175
Use Fungic., Bacteric.
Nematoc.
LD50 1,032
A B
D E F
Ref.
1
2
3
4
5
6
AC
64
3
69
12
ade
h
K-S-C-N-CH2OH
CH3
0922 BUTACHLOR (Machete)
Mol. Wl. 312
Use Herbic.
I DH, 3,300
C,7H.,C1N0? 2-Chloro-2',6'-diethyl-N-
(butoxymethylJacetanilide
A B
D E F
Ref.
1
2
3
4
5
6
5Q
3
c
C2H5
C2H5
CH2OC4H9
COCH2CI
0933 BUTRALIN (Amex 820)
Mol.Wl. 295
Ute Herbic.
1,000
4-(l,l-Dimethylethyl)-N-(l-
methyl propyl)-2,6-dinitro=
benzeneamine
A B
D E F
Ref.
)
2
3
4
5
6
ZB
73
26
390
79
u
CH3
H-N—CHCH2CH3
C(CH3)3
0940 BUTYLATE (Sutan) C^H^NOS S-Ethyl N,N-diisobutylthiocarbamate
Mol.Wt. 217
Uie Herbic.
ll>30 4,659
A B
0 E F
Ref.
1
2
3
4
5
6
C
AJ
60
II
8
214
6,12
12
c
a
O r -,
C2H5-S-C-NLCH2CH(CH3)J
'3'2->2
-------
Code Common Name Emp. Form.
Chemical Name
Structure
0961 CACODYIMC ACID C_H,0,,AS Dlmethvlarsinir arid
Mol. Wl. 138
U« ll-rbi- ABC D E F
L DSO 1 ,000
Ref.
1
2
3
4
5
6
B
70
25.016-
.399
399
12
de
u
II
(CH3)2As— OH
0980 CALCIUM ARSENATE - Ca,(AsOa), Calcium arsenate
Mol. Wl. 179
Use Insectic.
L DJO 35-100
Ref.
1000 CAPTAFOL (Difolatan) ClnH0
i u y
A
1
2
3
4
5
6
B
B C 0 E F
25.006-
.017
Cl.NOjS ffis-N-[(l, ,2,2-Tetrachloro=
4 ^ ethyl }thio]-4-cyclohexene-
1 ,2-dicarboximide
Mol.Wt. 349
ABC D E
Use Fungic.
I.DSO 4,600-6,700
Ref.
1
2
3
4
5
6
BA
AL
AL
AJ
AC
72
70
68
67
67
97/1158
53
51
15
5
713
154
1058
1118
293
2
2
2,11
2
20
F
c
a
X
X
—
/^\ #°
1 1 ^
N-S-CCI2CHCI2
^^^ *
1020 CAPTAN CqHRCl,NO;>S N-[(Trichl oromethyl ) thio]-4-
cycl ohexene-1 ,2-dicarboximide
o
Mol.Wt. 301 II
ABC D E
Use Fungic.
I DM 9,000
Ref.
1
2
3
4
5
6
C
B
AL
AD
AJ
AL
70
69
67
68
II
24.111-
.115
53
4
15
5/15
154
55
1035
1058
12
12
2
11
2
2,11
F
jlo
de
a
a
X
X
r^^\-'-'V
11 1 N-S-CCI
I 1^^ o (~<_I3
^
\J
1060 CARBARYL (Sevin) C,nH,,NOn 1-Naphthyl N-methyl carbamate
^ ~* \ L 1 1 L
O H
Mol. Wt. 201 H 1
ABC D E F O-C-N-CHo
se Insectic.
L Dso 560
D.I
1
2
3
C
AL
AL
65
68
II
48
51
676
679
12
12
11
a
a
x
^X^^\ -/"i>v
f II 1
1 II I
-------
Code Common Name Emp. Form.
Chemical Name
Structure
1071 CARBENDAZIM (Derosal) CQHQN
-,0? 2-(Methoxycarbonylamino
benzimidazol
-
^\ N
Mol. Wt. 191 S ^v' \
Use Fungic.
L D50 15,000+
Ref.
1074 CARBETAMIDE (Lequrame) C,_H,
A B C D E F
1
1
3
4
5
6
BE
74
5/4
465
20
_
II ^NCOOCH3
\^^N H
H
-0,N2 N-Phenyl-l-(ethylcarbamoyl)
3 ethylcarbamate, D isomer
Mol.Wt. 236
ABCDEF n u 0
Use Herbic.
tOso 11,000
1
2
AC
71
73
7
509
12
2
jou
ac
II II
C6H5-N-C-0-C-C~N-
Ref.
1040 CARBOFURAN (Furadan) C H,,NO, 2,3-Dihydro-2,2-dimethyl-7-
Mol.Wt. 221
Use Insectic.
LDso 8-14
12"15"U3
benzofuranyl methyl carbamate
A B
E F
Ref.
1
2
3
4
5
6
C
AJ
AJ
AL
AL
AJ
69
69
71
67
68
II
17
17
54/6
50
16
277
56
1357
926
403
6,11
6
2
2
4
2
cfu
c
a
a,u
X
X
O-C-N-CH3
6 H
1080 CARBOPHENOTHION (Trithion) C.nH.-.ClO-.PS, S-[(p-Chlorophenylthiojmethyl]
0,0-diethyl phosphorodithioate
Mol. Wt. 343
Use Insectic. S
Mitic.
I °;o 10-30
EF
1
2
3
4
5
6
C
AL
AL
AL
67
74
74
II
50
57
57
430
930
1034
17
2
3,4
4
a
a,e
a,d
t
S-CH3-S-P(OC2H5
S
1100 CARBOXIN (Vitavax)
C H NO S 5,6-Dihydro-2-methyl-l,4-
12132
oxathiin-3-carboxanilide
Mol. Wt. 235
Ute Seed Protect.
Fungic.
I DSO 3,200-3,820
A B
Ref
E F
1
2
3
4
5
6
AJ
AJ
70
71
18
19
409
738
12
6
a
c
-------
Code. Common Name Emp. Form. Chemical Name
Structure
1140 COAA (Randox)
Mol.Wi. 174
Use Herbic.
700
Ref.
D E F
1
2
3
4
5
6
C
5Q
II
6
6
acd
acd
CI-CH2CN(CH2CH=CH2):
'2/2
1160 CDEC (Sulfallate) C H C1NS 2-Chloroallyl diethyldithio=
carbamate
Mol.WI. 224
Use Herbic.
IDjo 850
A B
D E F
Ref.
1
2
3
4
5
t>
C
5Q
II
2,6
12
d
a,f
Cl
(C2H5)2N-C-S-CH2C=CH2
0140 CHLORAMBEN (Aniiben) C?H C
Mol. Wf 206
Us« Herbic.
1 °fO 3,500
3-Amino-2,5-dichlorobenzoic acid
D E F
Ref.
1
2
3
4
5
6
C
AC
67
II
5
321
6,11
12
?<1
d
1180 CHLORANIL (Spergon) C6C14°2 2,3,5,6-Tetrachloro-l,4-benzoquinone
Mol. Wt. 246
Use Fungic.
L D50 4,000
A B
D E F
Ref.
1
2
3
4
5
6
AN
AL
AJ
70
69
58
8/3
41/12
6
166
1662
667
2,3
12
12
X
c
C
134Q CHLORBENSIDE (Chlorparacide) c13H1ncl2S p-Chlorobenzyl-p-chloro=
phenyl sulfide
Mol.Wt. 269
Use Mitic.
10,000
A B
D E F
Ref.
1
2
3
4
5
6
C
AL
WD
AL
69
68
66
II
52
35/1
49/2
162
119
407
12
12
12
2
e
a
X
e
-------
Code Common Name Emp. Form.
Chemical Name
Structure
1200 CHLORDANE (TECH.) C,.H,
Mol. Wt. 410
Use Insectic.
I Dso 457
Ref.
:i 1 ,2,4,5,6,7,8,8-Octachloro-2,3,3a,4,
8 7,7a-hexahydro-4,7-methano1ndene
A B C D i F
2
3
4
5
6
C
AK
AL
AD
AD
1220 CHLORDANE, ALPHA C,nH^Cl0
" " (cis-chlordane) lu b
Mol. Wt. 410
,, Compon. of tech.
chlordane
1 "50 ca. 500
Ref.
1240 CHLORDANE, GAMMA C.J-
(trans-en lordane)
Mol.Wt. 410
Compon. of tech.
u" chlordane
1050 ca. 500
Ref
1280 CHLORDECONE (Kepone) *C1QC
Mol Wt. *491
Use Insectic.
IDso 132
Ref.
*Basis anhydrous state
1260 CHLORDENE C,»H,
Mol. Wt. 339
U,e Compon. of tech.
chlordane
L DSO 500+
Ref.
1
2
3
4
5
6
6C1
1
2
3
4
5
6
A
67
69
69
72
II
59
52
4
7
752
1220
297
33
2,12
2
2
2
2
a
t
b,c
j
X
1-6X0,2-6X0,4,5,6,7,8,8-
Octachloro-2,3,3a,4,7,7a-
hexahydro-4,7-methanoindene
B C D E F
See
1200
*\/*
I J *C'
*
3 Octachloro-2,3,3a,4,7,7a-
hexahydro-4,7-methano1ndene *
*^v^
A B C D E F % -T*^
See
1200
llnO Decachloro-octahydro-1 ,3,4-
metheno-2H-cyclobuta[cd]=
pentalen-2-one
A B C Off
1
2
3
4
5
6
AJ
AD
AJ
74
72
70
22/3
7/4
18/1
442
207
159
3
5
1,2
X
X
a,e
Cl, 4,5,6,7,8,8-Hexachloro-3a,
4,7,7a-tetrahydro-4,7-
methanofndene
A B C 0 E F
1
2
3
4
5
6
See
1200
*
\ V
•^
/ \^^CI10
••"
-------
Code Common Name Emp. Form.
Chemical Name
Structure
1261 CHLOROENE, ALPHA
C10H6C16
1,2,3,5,7,8-Hexachloro-l ,3a,4,
5,6,6a-hexahydro-l,4-etheno«
pentalene
Mol. Wl. 339
u'e
Compon. of tech0
chlordane
A B
L Dso 10,200
E F
1
2
3
4
5
6
See
1200
1262 CHLORDENE, BETA
Mol.Wt. 339
Use
IDso 6,800
2,3,3a,4,5,7-Hexachloro-3a,6,7,
7a-tetrahydro-l,6-methano-
1H-indene
Compon. of tech*
chlordane
A B
E F
1
2
3
4
5
6
See
1200
*ci
1263 CHLORDENE, GAMMA
Mol.Wt. 339
Use
2,3,3a,4,5,8-Hexachloro-3a,6,7,
7a-tetrahydro-l ,6-met.hano-
IH-indene
Compon. of tech.
chlordane
4,600
AB
E F
I
2
3
4
5
6
See
1200
Cl
1480 CHLORDIMEFORM
(Chlorphenamidine)
C,gH,,C1N2 N'-(4-Chloro-o-tolyl)-N
N-dimethylformamidine
Mol. Wl. 196.5
Use Acaric.
L D;0 178
A B
Ref.
E F
1
2
3
4
5
6
C
AJ
AJ
71
72
II
19
20
360
565
2,11
10J2
12
e
e
e
N=CH-N(CH3)2
CH3
1300 CHLORFENVINPHOS (Supona) C^H, .Cl-AP 2-Chloro-l-(2,4-dichlorophenyl)
vinyl diethyl phosphate
Mol. Wl. 359.5
Use Insectic.
•"50
L D5
AB
Ref.
E F
1
2
3
4
5
6
BC
AJ
66
73
17
21
162
822
10J7
4
X
j.o,
p
o
Cl O-P(OC2H5)2
H
-------
Code Common Name Emp. Form. Chemical Name
Structure
1316 CHLORMEPHOS (MC 2188) CrH]2ClPS, S-Chloromethyl 0,0-diethyl
0 phosphorothiolothionate
Mol.Wt. 203
Use Insectic.
7
A B
Ref.
D E F
S H
(C2H50)2 P — S — C-CI
H
1360 CHLOROBENZILATE (Acaraben)
Ethyl 4,4"-dichlorobenzilate
Mol.WI. 325
Use Mi 11c.
LDM 700
A B
D E F
1
2
3
4
5
6
C
AJ
ZD
64
71
II
12
39
183
40
6,12
6
6
e.9
e,g
X
OH
COOC2H5
1380 CHLORONEB (Demosan) C8H8C12°2 1,4-Dichloro-2,5-dimethoxybenzene
Mol. Wl. 207
Use Fungic.
L D?0 11,000+
A B
D E F
Ref.
1
2
3
4
5
6
C
AJ
AJ
67
71
II
15
19
917
750
6
6
3
ijgo
ajm
jmo
CH3O
OCH3
1425 CHLOROPHACINONE (Rozol) C,,H.rC10, Z-[(p-Chlorophenyl)phenyl=
" J J acetyl]-l,3-indand1one
Mol. Wl. 375
Use Rodentlc.
I- DSO 20.5
Ref.
D E F
]
2
3
4
5
6
AJ
2E
75
23/1
72
2
2
a,j,
0
X
1640 CHLOROTHALONIL
(Daconil 2787)
Mol.WI. 266
U» Fungic.
l°50 10,000+
2,4,5,6-Tetrachloroisophthalonitrile
A B
Ref.
D E F
1
2
3
4
5
6
C
GE
AD
GE
73
70
70
II
265/1
5/6
250/2
4
565
125
2,6
10
14
11
f
V
X
a.j
-------
Code Common Name Emp. Form.
Chemical Name
Structure
1420 CHLORPROPHAM (CIPC) ClnH,?ClNO,, Isopropyl N-(3-chlorophenyl)
lu ' carbamate
Mol. Wt. 214
Use Herbic.
I 050 5.000-7,500
A B
Raf.
D E F
1
2
3
4
5
6
C
AJ
AJ
AJ
63
64
72
II
11
12
20
234
46
344
2,12
12
2
12
a
m,o
X
b
2900 CHLORPYRIFOS (Dursban) CgH,1Cl,N03PS 0,0-Diethyl 0-(3,5,6-trichloro-
2-pyridyl) phosphorothioate
Mol.Wt. 351
Use Insectic.
135
A B
D i F
Ref.
1
2
3
4
5
6
AJ
AJ
AJ
AJ
AL
70
67
68
69
68
18
15
16
17
51
178
651
867
1166
1243
3,4
4
2
2
2
aj
kfii
b,c
t,u
j
Ji0
1491 CHLORTHIOPHOS
(CMS 2957) n 10 j c (methyl thio)pheny1 thionophosphate
Mol.Wt. 329
Irrcctic ' A B C D E F
U" Acaric.
IDW 8-13
Ref.
1
3
3
4
5
6
AX
71
4
271
10,12
X
o
il
(C2H50)2=P-0-
Cl
-SCH,
0460 CLON1TRALID (Bayluscide)
Mol. Wl. 388
Use Molluscic.
L OfO 1,500
2'.S-Dichloro-l1-nitro=
salicylanilide ethanolamine
A B C D E F
Ref
1
2
3
4
5
6
EA
AL
AI
70
72
73
13/3
55/6
3/1
369
1276
61
15
12
11J4
X
t
X
0=C
NO2-NH2(CH2)2OH
4-hydroxycoumarin
.^^. /X xO
Mol.Wl. 298 KIT T^
ABC D E F L 1 -1 „..
Use Rodentlc.
L D so 4j)0
Ref.
1
2
3
4
5
6
OH CH2
c=o
CH3
-------
Code Common Name Emp. Form.
Chemical Name
Structure
1540 COUMAPHOS (Co-Ral) C, .H,
CIO PS 0-(3-Chloro-4-methyl -2-oxo-
° s 2H-l-b'enzopyran-7-yl)0,0-
diethyl phosphorothioate
Mol.WI. 363 S X^^X^N^0
A B C D E F t r T T
U»e Insectic.
I.DSO 56-230
Ref.
1
2
3
4
5
6
C
AL
ZD
AP
AL
AB
67
69
68
75
75
II
50/6
26
61/2
58/3
47/4
1228
17
358
554
674
12J4
4
10
4
11J4
4
j.O
c,o
t
n,o
P
0
(C H5O) P-O-V JL .Ari
^%x^ ^f ^-'
CH3
1500 CROTOXYPHOS (Ciodrin) ClaH1Q0KP a-Methyl benzyl 3-hydroxy=
crotonate dimethyl phosphate
Mol. Wt. 314
Use Insectic.
ID.o 125
Ref.
6020 CRUFOMATE (Ruelene) CI,HI
A B C D E F
1
2
3
4
5
6
AL
AJ
AL
AL
AC
70
69
69
68
67
53/5
17/6
52/3
51/6
5
1045
1160
522
1270
243
4
15
16
2,7
20
j.O
j.o
a
X
...
0 CH3
5H3)-0-C-C-C-0-P(CH30)0
1 H J 2
H 0
qClNO,P 0-(4-tert-Butyl-2-chlorophenyl )0-
methyl N-methyl phosphoroamidate
C(CH3)3
Mol. Wt. 292 rX^5=5:1
A B C D E F ||
Use Insectic.
L D50 770
Ref.
i
2
3
4
i
6
AD
AL
72
74
7
57
237
1033
10
4
1
t
cl^Y*o
O-p-OCH3
i
NHCH3
1546 CRYOLITE (Kryocide) NajAlF,; Sodium Fl uoaluminate
Mol.Wt. 210
A B C D E F
Use Insectic.
IDM 10,000+
Ref.
1552 CYANAZINE (Bladex) CnH,,
1
2
3
4
5
6
B
11
6.019
79
18
w
NgCl 2-[(4-Chloro-6-(etnylamino)-
triazin-2-yl )amino]-2-methy'
Na3AIF6
S~ . . f-~ — - KJ
H C ^N
propioni trite 1 1
N — C(CH3)2
Mol.Wt. 240 /
A B C D E F N ^
Use Herbic.
IDso 334
D.f
1
2
3
AJ
BE
AJ
74
72
73
22/6
3/4
21/6
1143
379
1016
3
2
1
u
a.u
u
a^f x^
\ /
N-W
— CH3CH2
-------
Code Common Name Emp. Form.
Chemical Name
Structure
1591 CYCLOATE (Ro-Neet)
C H NOS S-Ethyl ethylcyclohexyl=
11 21
thiocarbamate
Mol. Wt. 215
A
Use Herbic.
ID50 2,595
Ref.
1
2
3
4
5
6
C
n
AC
1600 CYCLOHEXIMIDe (Actidione) C^H^NO,,
Mol. Wt. 281
A
Use Fungic,
LD50 2.5
Ref.
1
2
3
4
5
6
GJ
AJ
8U
1615 CYPRAZINE (Outfox) CgH^ClNj
Mol.Wt. 228
A
Uie Herbic.
IDjo 1,200
Ref.
1
2
3
4
5
6
32
AJ
1621 CYTHIOATE (Proban) CnH,.0,PNS0
- 8 1 c. b c
Mol.Wt 297
A
Use Insectic.
I DM 2,500+
Ref.
2
3
4
5
6
AL
WD
WD
WO
1660 DALAPON (Dowpon) C^Cl^
Mol.WI. 143
A
Use Herbic.
L DSO 7,000
1
2
C
AL
1
2
3
4
5
6
C
n
AC
67
II
5
491
6,12
4
20
af
a
—
3-[2-(3,5-Dimethyl-2-
oxo-cydohexyl )-2-hyd=
roxyethyl]glutarimide
i
2
3
4
5
6
GJ
AJ
8U
69
73
8/3
21/1
211
83
11
10
19
s
w
e
2-Chloro~4-(cyclopropylamino)-
6-{isopropylamino)-s-triazine
1
2
3
4
5
6
32
AJ
73
21/1
93
2
1,2
a,u
ctu
0,0-Dimethyl 0-p-sulfamoyl=
phenyl phosphorothioate
1
2
3
4
5
6
AL
WD
WD
WO
69
71
71
70
52/2
60/2
59/1
48/3
286
213
135
478
16
11,14
11J4
11
X
t
X
X
2,2-Dichloropropionic acid
Ref.
1
2
3
4
5
6
C
AL
AK
AG
AL
63
63
69
69
II
46
55
3
52
269
639
69
824
11
10
12
10
2
d,e
e
t
t
llmo
C2H5—S—C—N
CH3
H
C
OH
(CH,)2C-N
H H
(CH3O)2P— O
o
O
CH3CCI2COOH
-------
Code Common Name Emp. Form.
Chemical Name
Structure
1720 DCPA (Dacthal) C,nH
-Cl.O. Dimethyl 2,3,5,6-
3 tetrachloroterephthalate
C02CH3
Mol. Wl. 332 ^Sf\ .
A B C D E F *^(^ ^y
U«e Herbic.
I D50 3,000
Ref.
1
2
3
4
5
6
C
AC
AL
AL
AY
AY
73
71
74
74
69
II
9/5
54/6
57/3
8/1
5
305
1376
595
53
345
6,12
2
2,6
6
2
2
d,g
e
V
1
ktu
f.u
A^A .
^L Cl
^Jy^nj
1740 DDA-p_,£' C14H10t'1202 Bis(p-chlorophenyl ) acetic acid
Mol.Wt. 281 r * H
ABC D E F „. // \ I // \ _.
Use DDT metabolite
LDM 1,900
Ref.
1750 ODD, MIXED, TECH. C, Hn
(TDE, Rhothane) H '
1
2
3
4
5
6
A
5, A,
(4),(b)
2
m
\ / 1 \ /
COOH
Cl 2,2-Bis(chlorophenyl )-l ,l-dichloro=
0 * ethane and related compounds
Mol. Wl. 320
Use Insectic.
IDso 3,400
Ref.
1820 ODD, m,p' C,.H.
A B C D E F
1
2
3
4
5
6
C
A
A
A
A
I
5,A(1,2,
3,4)
10,A
8,B
11, A
2,6
12
2
2,4
2,4
2,4
a
jlmo
t
V
u
See structures below
under 1820, 1760, and
1780.
nCl . 2-(m-Chlorophenyl )-2~(p-chloro=
phenyl )-l ,1-dichloroethane
Cl
Mol. Wl. 320 \
Use ODD metabolite
LDjo 3,400
Ref.
1760 ODD, o,j>' C H
A B C D E F
1
2
3
4
5
6
See
1750
f>K>'
M-c'cH/
Cl 2- o-Chlorophenyl)-2-(p-chloro=
^ ^ phenyl )-l ,1-dichloroethane
Mol. Wt. 320 r.
ABCDEF S H
Use Compon. of
tech. ODD
I DSO ca. 3,400
Ref.
1
2
3
4
5
6
See
1750
(Tr-O01
CHCI^
-------
Code Common Name Emp. Form. Chemical Name
Structure
1780 ODD, £,£' ciaHinc1a 2,2-Bis(p-chlorophenyl )-l ,
1-dichloroethane
Mol.Wl. 320
,. Compon. of
U" tech. ODD
LDjo 2,500-3,400
Ref.
1800 ODD, £,£', OLEFIN C,.HQ
(DDMU) lq
Mol.Wt. 284
Use ODD Metabolite
Ref.
1840 DDE, o,p' C^Hp
Mol.Wt. 318
Use DDT metabolite
1050 880
Rel.
1860 DDE, £,£' C^Hg
Mol. Wl. 318
Use DDT metabolite
L D50 750
Ref.
1880 DDT, MIXED (TECH.) C,,H,
Mol.Wl. 354.5
Use Insectic.
LDj,, 113
Ref.
A B C D E F
1
2
3
4
5
6
See
1750
Cl, l-Chloro-2,2-bis(p-chloro=
phenyl) ethyl ene
A B C D I f
1
2
3
4
5
6
See
1750
°o&>
' H-C-Cl
Cl^ 1 , l-Dichloro-2-(o-chloro phenyl )-
2-( p-chlorophenyl ) ethyl ene
A B C Off
1
2
3
4
5
6
See
1750
c!ci2
Cl 1 ,l-Dichloro-2,2-bis( p-chloro=
phenyl )ethyl ene
A B c D E F ^, // "\ / ^,
1
2
3
4
5
6
See
1750
X^^=/CI
Clr Dichloro diphenyl trichloroethane
J (mixt. of metabolites of ca.
80% £,p_' and 20S o,£' )
A B C D E F
1
2
3
4
5
6
See
1750
24
-------
Code Common Name Emp. Form.
Chemical Name
Structure
1900
1920
DDT,
Mol.Wt. 354.5
Un
LDso
Compon. of
tech DDT
100
DOT, £,£'
Mol.Wt. 354.5
Use
LD50 113
Compon. of
tech. DDT
C H Cl. l,l,l-Trichloro-2-(o-chloro=
phenyl )-2-(p-chlorophenyl Jethane
Cl
/ 1 1
R.f.
C14H9
R.f
A B C D E F
2
3
4
5
6
See
1750
C16 l,l,l-Trichloro-2,2-bis(p-
chlorophenyl ) ethane
A 8 C D E F
1
2
3
4
5
6
See
1750
O&>
°OtO
1940 DEF
S,S,S-Tributyl phosphorotrithioate
Mol.Wt. 314.5
U>* Defoliant
I DJO 350
R.f
1
2
3
4
5
6
C
WD
AJ
69
66
II
40/2
14/2
289
143
9
4
2
o,g
X
g
(CH3CH2CH2CH2S)3P=0
1981
DEMETON-0 (Systox-0)
(THIONO)
0,0-Diethyl 0-2-[(ethylthio)=
ethylIphosphorothioate
Mol.Wt. 258
Use Insect!c.
7.5
R.f.
i
2
3
4
5
6
WD
ZD
JI
70
69
70
48/3
26
22
468
17
13
10
10
3,4
d
t
c,d,
e
(C2H50)2P-0-C2H4-S-C2H5 (Thiono)
1982
DEMETON-S (Systox-S)
(THIOLO)
C8H1903PS2
0,0-Diethyl S-2-[(ethylthio)=
ethylIphosphorothioate
Mol.Wt. 258
U» Insectic.
ID*, 2.5
R.f.
1
2
3
4
5
6
ZD
AL
BA
69
69
69
26
52/1
94/1117
17
157
275
10
4
10,11
t
a
t
(C2H50)2P-S-C2H4-S-C2H5 (ThioloJ
-------
Code Common Name Emp. Form.
Chemical Name
Structure
2006 DESMEDIPHAM (Betanex) C.,H,
gN-jO^ Ethyl m-hydroxycarbam'late
carbanilate ester) ^
U H , .
II 1 / \
Mol.Wt. 300 O— C N ( )
A B C D E F ^4^ \=/
Use Herbic.
1 D50 10,250+
Ref.
2035 DIALIFOR (Torak) C,.H,
1
2
3
4
5
6
BH
7Q
6A
70
10/4
340
10,12
10
2,11
12
a
af
af
I 1
\#^.N— C — O— C2H5
1 II
H 0
704NS2PC1 S-(2-Chloro-l-phthalimido=
ethyl) 0,0-diethyl phos*
phorodithioate
Mol.Wt. 393.5 Q
Use Insectic. S
Mitic.
L DSQ 69
Ref.
2040 DIALLATE (Avadex) C^H,
A B C D E F
1
2
3
4
5
6
4A
AJ
AJ
71
71
19
19
900
1191
2,9
2,9
3,19
e
mno
e
^A CH'CI ?
r 11 N— C-S-P(OC2H5)2
^^\y
II H
II
O
7C12NOS S-(2,3-Dichloroallyl) diiso=
propyl thiocarbamate
Mel. Wt. 270 „
Use Herbic.
IDso 395
Ref.
A B C D E F
1
2
3
4
5
6
AJ
AL
FB
BH
69
71
69
70
17/5
54/6
62/686
10/4
1052
1366
214
331
2
4,9
10
2
u
a,q
t
u
[(CH3)2CH]2N-<>s-CH2-CC!=CHCI
2060 DIAPHENE (Bromsalans) C13HgBr2N02 3,4,5-Tribromosal icylanil ide
4,5-dibromosal icylanil ide
and other brominated sa icylanil ides
Mol.Wt. 371 OH n H
..... ABCDEF Rr^VV /T~\
Use rungic.
LD50 40.2
Ref.
2080 DIAZINON ( Spectracide) C-,,H,
1
2
3
4
5
6
r^ ipC-NK/ v
L Ij \ — _/
^'^N^^'^
T
Br
-NjO-jPS 0,0-Diethyl 0-(2-isopropyl-6-methyl-
4-pyrimidinyl ) phosphorothioate
Mol. Wl. 304 H
Use Insectic.
I D50 100-150
Ref.
A B C D E F
1
2
3
4
C
AD
BA
AL
68
69
69
II
3
94/1116
52
247
221
1067
12
2
3
3
a
acj
tu
j
a
S M=
-------
Code Common Name Emp. Form.
Chemical Name
Structure
2090 DIBROMOCHLOROPROPANE C H Br Cl 1,2-D1bromo-3-chloropropane and related
(DBCP) halogenated C3 hydrocarbons
Mol.Wl. 236
Use Soil Fumigant
ID 50 172
Ret.
1
2
3
4
5
6
RB
7U
AM
AJ
70
68
63
35
6
11/6
59
124
479
12
2
2
t
atu
u
CH2Br-CHBr-CH2CI
2120 DIBUTYL PHTHALATE (DBP)
C16H22°4
Di-rc-butyl phthalate
Mel.Wt. 278
Use Insect Repellant
LDjo 20,000
Ref.
1
2
3
4
5
6
AJ
AD
BA
AE
GD
73
74
67
72
21/6
12/6
92/1068
71-117273
68/6
1128
721
575
i -
180
3
2
2
10
10
fc
j
t
t
j
COOCH2(CH2)2CH3
COOCH2(CH2)2CH3
2140 DICAMBA (Banvel D)
Mol. Wl. 221
U»« Herbic.
LDso 1,040
C H Cl 0 2-Methoxy-3,6-dichloro=
8623 benzoic acid
Ref.
1
2
3
4
5
6
C
AL
AJ
AJ
65
64
71
II
48
22
19
1164
453
1181
2
2
2
11
be
a
tu
a
OH Q
S*
2200 OICHLOBENIL (Casoron)
2,6-Dichlorobenzonitrile
Mol. Wl. 172
Use Herbic.
10,0 3,160
1
2
3
4
5
6
C
AL
AD
WD
66
67
74
II
49
2
97
976
178
103
2
2
6
2
e
iktu
a
u
2220 DICHLOFENTHION (VC-13) C.-H-.-Cl.O^PS 0-2,4-Dichlorophenyl 0,0-
diethyl phosphorothioate
Mel.Wi.
Use
315
Nematoc &
Insectic.
270
Ref.
1
2
3
4
5
6
AJ
AL
59
64
7
47
615
287
17
12
X
a
(C2H50):P-0
27
-------
Code Common Name Emp. Form.
Chemical Name
Structure
2180 DICHLONE (Phygon XL) Ci0H4C12°2 2,3-Dichloro-l,4-naphthoquinone
Mol.Wt. 227
Use Funglc.
LDjo 1,300
t f
Ref.
1
2
3
4
5
6
B
AJ
AJ
58
69
24.181-
.184
6
17
746
585
12
2
d,e
a
O
2260 DICHLORAN (Botran)
2,6-Dichloro-4-ni troanil ine
Mol.Wt. 207
Use Fungic.
I D50 10,000
A B
Raf.
D E F
1
1
3
4
5
6
C
II
6,12
a
2280 DICHLOROBENZENE, ORTHO C,H.C1,
(ODB) b 4 i
Mol. Wl. 147
Use
L D50 500
1 ,2-D1chlorobenzene
Herbic. &
Insectic.
A B
E F
R«f.
1
2
3
4
5
6
AN
WD
WD
AH
73
70
67
72
11/11
53/2
30/1
3
580
143
77
281
1,2,
8
2
3
t
X
X
t,k
2300 DICHLOROBENZENE, PARA C,H.C1,
(PDB) b 4 i
Mol.Wt. 147
Use Fumigant
2,560
1 ,4-Oichlorobenzene
A B
E F
Ref.
1
2
3
4
5
6
AD
WD
AN
WD
70
70
71
67
5/4
53/2
9/8
30/1
354
143
497
77
2
8
10
2
l,m
X
X
X
2306 DICHLOROPROPENE (Telone)
1 ,3-Dichloropropene
Mol.Wt. Ill
Use Nematoc0
LOjo 375
A B
E F
Ref.
1
2
3
4
5
6
AJ
AP
AJ
AM
AF
71
68
70
75
74
19/6
61/5
18/6
0453
34/7
1270
1432
1124
-
3034B
6
2
10
2
10
f
u
tu
f
u
Cl H Cl
I I I
28
-------
Code Common Name Emp. Form.
Chemical Name
Structure
2309 DICHLORPROP (2,4-DP)
Mol. Wt. 235
Uie Herbic.
ID 50 800
C9H8C12°3
2-(2,4-Dichlorophenoxy)-
propionic acid
Ref.
1
2
3
4
5
6
AP
AM
AV
AJ
AD
68
75
72
71
69
6',/S
0453
1333
19/6
4/4
1432
-
-
1270
246
2
2
10J2
6
16
u
f
t
f
a,c
CH3
Q —C —COOH
2320 DICHLORVOS (DOVP)
C H.Cl-O.P
*
2,2-Dichlorovinyl dimethyl
phosphate
Mol. Wt. 221
Uie Insectic.
I D50 56-80
Ref.
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-0-P(OCH3)2
2340 DICOFOL (Kel thane)
Mol.Wt. 370.5
Use Mitic.
600
Ref
l,l-Eis(p-chlorophenyl)-
2,2,2-trichloroethanol
1
2
3
4
5
6
C
AL
AD
AJ
60
69
69
II
53
4
17
127
297
1070
12
2
2
!,11
bde
0
k
h
0700 DICROTOPHOS (Bidrin)
Mol.Wt. 237
Use Insectic.
LDjo 22
C H NO P 3-Hydroxy-N,N-dimethyl-ots-
crotonamide dimethyl phosphate
Ref.
1
2
3
4
5
6
AJ
AJ
AN
AC
67
69
71
67
15
17
9
5
465
56
44
213
4
4
3
20
c
a
c,o
...
H
(CH30)2P-0-C=c-C-N(CH3).
CH,
2380 DIELDRIN (HEOD)
Mol. Wl. 237
U«« Insectic.
ID50 22
CioHoC1c° !,2,3,4,10,10-Hexachloro-ero-6,7-epoxy-
12 o fa i A n-, c c 7 Q c "
Ref.
ezo-5,8-dimethanonaphthalene
1
2
3
4
5
6
C
A
AP
AL
AL
65
69
69
I
58
52
52
266
1220
1280
2
2
2
2
It
uv
0
b,c
bof
29
-------
Code Common Name Emp. Form. Chemical Name
Structure
2386 DIETHYL PHOSPHATE cjHnO.P 0,0-Diethyl phosphate
(DEP)
Mol. Wl. 154
Use Derivative
Ref.
2395 DIFENZOOUAT (Avenqe) C..H-
Mol.Wl. 360
Use Herbic.
U>50 470
Ref.
2406 OIFLUBENZURON C H
(TH-6040, Dimilin) 14 -
Mol. Wl. 311
Use Growth Regulat.
I t>50 10,000+
Ref.
2416 DIMETHIRIMOL (Milcurb) C H
Mol. Wl. 209
Use Fungic.
1 050 2,350
Ref.
A B C DEF
1
2
3
4
5
6
A
74
6.A,(2),
4
m
O
/ 1
(C2H50)2 P— OH
0N.SO 1 ,2-Dimethyl -3,5-di phenyl -1 H-
pyrazolium methyl sulfate
A B C DEF
1
2
3
4
5
6
i | CH3OSO3
H3C CH3
N 0 F Cl l-(4-Chlorophenyl)-3-(2,6-
^ difluorobenzoyl )urea
A B C D E F
1
2
3
4
5
6
AL
74
57/6
1269
16
0
r(. " '-r>
\=/ o o — •
F
ON 5-n-Butyl-2-dimethylamino-
4-Fydroxy-6-methyl pyrimid i ne
n(CH2)3CH3
ABC DEF ,_, ,, J^ r>H
1
2
3
4
5
6
7E
11J2
a
^l l'
1 1
N N
N(CH3)2
2420 DIMETHOATE (Cygon) C H NO PS 0,0-Diniethyl S-(N-methylcar=
b '' J ' bamoylmethyl) phosphorodithioate
Mol.Wl. 229
Uie Insectic. S
Acaric.
10,0 215
A B C DEF
1
2
3
C
AL
AL
74
72
II
57
55
930
1280
4,1!
3,4
4
jol
de
ajop
5
•f- ^J
(CH30)2P-S-CH2-C-N-CH3
H
Cl
30
-------
Code Common Name Emp. Form. Chemical Name
Structure
2458 DIMETHYL PHOSPHATE
(DMP)
C H O.P 0,0-Dimethyl phosphate
Mol.WI. 126
UM Derivative
A 8
D E F
R.f.
1
2
3
4
5
6
A
74
6,A,(2),
(a)
4
m
(CH3O)2P— OH
2460 DIMETHYL PHTHALATE C H 0, Dimethyl phthalate
- 10 10 4
Mel. Wt. 194
UM Insect Repel 1 ant
L DSO 8,200
A B
D E F
1
2
3
4
5
6
AN
WO
GD
74
70
72
12/3
46/2
68/6
149
137
180
10
3
10
X
X
j
COOCH3
2551 DINITRAMINE (Cobex) C,,H,,F,N.O. N4,N4-Diethyl-Ii,a,a-trifluoro-
H "»
Mol.Wt. 322
UM Herbic.
10 50 3,000
,,,,
" IJ
3,5-dinitrotoluene-2,4-diamine
A B
D E F
Rof.
1
2
3
4
5
6
AJ
WD
72
74
20/6
97
1222
103
2
2
a,u
u
NH2
NO2
2560 DINOCAP (Karathane)
Mo I. Wt- 364
„„ Fungi c. I
"** Mitic.
LD«o 980
2-(l-Methylheptyl )-4,6-
dinitrophenyl crotonate
A B
R.f.
D E F
1
2
3
4
5
A
AL
RD
70
71
53
9
887
761
3
11
w
ef
9
O-C-CH=CH 0-C-CH=CH
and.
N02 C8H17
2:1 ratio
-------
Code Common Name Emp. Form.
Chemical Name
Structure
2760 DINOSEB (DNBP)
2- (sea-Butyl )-4,6-dinitrophenol
Mol. Wt. 240
Ute Herbic.
L Duo 37-50
A B
Ref.
Off
1
2
3
4
5
6
AC
67
5
385
20
.—
OH
C-CH2-CH3
NO2
2566 DINOSEB ACETATE (Aretit) C ,H N 0 2-(see-Butyl)-4,6-dinitro=
12 14 2 6
phenyl acetate
N02 0-CH3
Mol. Wt. 282 1
A B C D E F ^#^ \.
Oie Herbic.
L DJO 65
Ref.
1
2
3
4
5
6
4E
12
w
1
2580 DIOXATHION (Delnav)
Mol.Wt. 456.5
LDjo 23-43
C19H9K°KP9S4 S.,i'-£.-Dioxane-2,3-diyl
'' ' 0,0-diethyl phosphorodithioate
(cts and trans isomers)
A B
ff
Ref.
1
2
3
4
5
6
C
AL
AL
69
71
11
52
54
522
513
12
3
3
ej
eh
eh
2600 DIPHACINONE
16
2-Di phenylacetyl-1 ,3-lndandlone
Mol. Wt. 340
Ute Rodentic.
LDso 3.2-5.1
Ref.
1
2
3
4
5
6
AJ
BF
WD
WD
75
67
73
71
23/1
14/1
79
57/2
72
103
217
319
2
14
11)4
11
jl
1
X
X
2620 DIPHENAMID (Enide)
Mol.Wt. 239
U»e Herbic.
I D50 1,000
C,,H,,NO N,N-D1methyl-2,2-d1phenyl=
"16"17
acetamide
A B
Ref.
D E F
1
2
3
4
5
6
C
AJ
AJ
AJ
AC
66
69
74
67
II
14
17
22
5
312
56
79
375
3
3
2
12
20
def
a
a
tu
-
(/
O"
O
t-C-N(CH3).
3/2
-------
Code Common Name Emp. Form.
Chemical Name
Structure
2640 DIPHENYL MERCURY C12H1C)Hg Diphenyl mercury
Mol.Wt. 355
Uie Fungic.
500
Rof.
1
1
3
4
5
t>
AB
AI
71
71
43
1
950
85
7
10
k
k
2660 DIQUAT DIBROMIDE
Mol.Wt. 362
ID50
Herbic. &
Desiccant
400
C12H12Br2VH2°
Ref.
6,7-Dihydrodipyrido[l,2-a:
2',1'-cjpyrazidiinium
dibromidei monohydrate
1
2
3
4
5
6
C
AJ
BA
AJ
AC
66
66
74
67
II
14
91
22
5
377
625
863
397
12
15
12
3
20
1
f
at
u
—
r^T\
2Br~
•H2O
2720 DISULFOTON (Di-Syston)
0,0-Diethyl S-[2-(ethylth1o)=
ethyl] phosphorodithioate
Mol. Wl. 274
U'e Insectic.
IDs,, 12.5
R«f.
1
2
3
4
5
6
C
AL
AL
AJ
AL
AJ
74
69
71
69
68
II
57/5
52/6
19/6
52/1
16/6
1033
1231
1196
157
895
9
4
4
3
4
9
bdeg
t
ano
f
a
a
(Q,H50)2P-S(CH2)2-S-C2H5
2721 DITHIANON (Thynon)
C14H4N2°2S2 2,3-Dicarbonitrile-l,
4-dithiaanthraquinone
Mol.Wt. 296
U»« Fungic.
10,0 638
Ref.
A B C D E F
1
2
3
4
5
6
2A
12
X
o
CN
o
2740 DIURON
_ y |U ^ ^ - .-, - 7 ~r..~..J . ,
1 -dimethyl urea
Mol.Wt. 233 Q
Use Herbic.
LDso 3,400
Ref.
A B C D E F
1
2
3
4
5
6
/r\ 9
° \ 7-N-C-N(CH3)2
\=v (H
-------
Code Common Name Emp. Form. Chemical Name
Structure
2770 DNOC
Mol. Wt. 198
,, Insectic. &
u" Fungic.
L D,o 30
4,6-D1nitro-o-cresol
A B
Off
Ref.
1
1
3
4
5
6
AL
AJ
AJ
68
71
73
51
19
21
24
1181
295
2
11
2
a
a
m
2780 DODINE (Carpene)
C H N 0 n-Dodecylguanidine acetate
Mol. Wt. 287
Use Fungic.
I D50 1 ,000
A B
D E F
Ref.
1
2
3
4
5
6
B
C
AL
73
'4.122-
.125
II
56
299
12
11
e
t
NH
Ci2H25-NH-C-NH2- CH3-COOH
2792 DRAZOXOLON (Ganocide) C.-H-O-N-Cl 4-(2-Chlorophenylhydrazono)-
Mol Wt 238
Use Fungic.
I DSO 126
10823
3-methyl-5-isoxazolone
A B
D E F
Ref.
1
2
3
4
5
6
41
12
a
-N = C C— CH3
2860 DSMA
CH AsO Na0.6H 0 Disodium methanearsonate,
u nu_.un_
hexahydrate
Mol.Wt. 292
Use Herbic.
LDso 1,000
A B
D E F
Ref.
1
2
3
4
5
6
ZF
ZB
AL
AJ
9E
69
69
68
72
33/2
22
51/6
20/2
279
51
1300
341
21
21
18
8
18
abu
a,u
w
w
X
CH3-As(ONa)2 -6H2O
2940 2,4-D, ACID
Mol.Wt. 221
Use Herbic.
I D50 500
C H Cl 0, 2,4-Dichlorophenoxyacetic acid
O D £0
A B
D E F
Ref.
1
2
3
4
5
6
C
A
AL
AJ
AJ
AJ
69
71
71
74
II
5, A, (4),
52
19 •
19
22
187
73
186
453
2,6
2
2
2
2
2
bceu
mt
t
u
u
t,u
0-CH2COOH
-------
Code Common Name Emp. Form.
Chemical Name
Structure
2960 2,4-D, BUTOXYETHANOL CUH18C12°4 2,4-Dichlorophenoxyacetic acid,
ETHER ESTERS butoxy ethanol ether esters
59.3% n-Butoxyethyl ester 0.5% Butoxyethanol ]f
39.6% IsoButoxyethyl ester 0,6% 2,4-D, add **. f-t_> f s\l/~u \ rifru \ S~LJ
Mot. wt. 321 U-v_n2»~ vJ(j~n2jj(JV-n2;3t,H3
ABC D E F r, ^k
Use Herbic.
I Ojo 800
Ref.
1
2
3
4
5
6
See
2940
T^ >
^Sx^
Cl
2980 2,4-D BUTYL ESTERS C H Cl 0 2,4-Dichlorophenoxyacetic
(MIXED)* 12 14 2 3 Acid, butyl esters
*Free acid 0.423 Other isomers 0.20% _
n-butyl alcohol 0.66 O
ABC D E F QCH2C-0(CH2)3CH,
Use Herbic.
L DSO 500
Ref.
1
2
3
4
5
6
AL
69
52
See also
2940
187
2
t
j^^^V
s5^ ^-~r\
1 H
^Sv JJ
^^^ ^^^
Cl
2985 2,4-D, DIETHANOL= C, ?H-| yCUNOc 2,4-Dichlorophenoxyacetic
AMINE SALT (Weedar 64D) acid, diethanolamine salt
/(CH2)2OH
Mol.Wt. 326
Use Herbic.
IDjo
Ref.
2990 2,4-D, DIMETHYLAMINE SALT C}
A B C D E F
1
2
3
4
5
6
AJ
65
13
See also
2940
123
2
b
OCH2COOH-NH >
1 X(CH2)2OH
f^*^ ^^^~S
T
L^^J
y^
Cl
nH. Cl.NO, 2,4-Dichlorophenoxyacetic
J acid, dimethylamine salt
Mol. Wt. 266 Q
.... A B C D E F /^==^
Use Hsroi c.
L D.0 500
Ref.
1
2
3
4
5
6
AK
AY
AD
AV
68
71
72
-
60/7
4/4
7/(2-3)
71-2382
See also
2940
827
199
115
-
2
2
2, 1C
10
t
ktu
ku
t
CK VO-CK -con~H N+crn ^
~\ // 2 ^CH3«
3000 2,4-D, ISOBUTYL ESTERS C H..C1 0, 2,4-Dichlorophenoxyacetic
(MIXED)* 12 t4 2 3 acid, isobutyl esters
*Free acid 0.13S; other Isomers 0.86% O
MclW1'277 ABC „ E F 0-CH2C-0-CH2CH(CH3)2
Use Herbic.
I D50 500
1
2
AL
69
52
See also
187
2
t
-x^\
r ]-ci
Ref.
35
-------
Code Common Name Emp. Form.
Chemical Name
Structure
3020 2,4-D, ISOOCTYL ESTERS C,CH
(MIXED)* lb
j.CljO, 2,4-Dichlorophenoxyacetic
acid, isooctyl esters
*Free acid 0.08% Other isomers 0.20X O
Ethyl hexyl alcohol 1.6% II
Moi.wt. 333 O-CH2-C-O(CH2)5CH(CH3)2
A B C 0 E F ^J^
Use Herbic.
!• DSO 500
Ref.
3040 2,4-D, ISOPROPYL ESTER C,,H
1
2
3
4
5
6
AL
69
52
See also
2940
187
2
t
r rc|
Cl
.Cl-0, 2,4-Dichlorophenoxyacetic
acid, isopropyl ester
0
II
M...W,. 263 A B c D E F 0-CH2-C-0-CH(CH3)2
Use Herbic.
IDso 700
Ref.
1
2
3
4
5
6
AL
69
52
See also
2940
187
2
t
r >ci
L T
^ /i
ir
Cl
3060 2,4-D, PROPYLENE GLYCOL 1. Clt-H?nCl?0. 2,4-Dichlorophenoxyacetic
BUTYL ETHER ESTERS acid, propylene glycol butyl
2' C18H26('12('5 ether esters
Mol.Wt. 358 (average) 3' '
Use Herbic.
<•*> so 500
Ref.
3080 2,4-DB, ACID CIQH]
21H32C12°6
A B C D E F
1
2
3
4
5
6
AL
69
52
See also
2940
187
2
t
0-CH2-C-oL(CH2)3oJx(CH2)3CH3
T 1 X = 1,2,3
^•^^^
^v^
Cl
Cl 0 4-(2,4-Dichlorophenoxy)
u ' J butyric acid
M.I. wi. 249 0(CH2)3COOH
A B C D E F ^y~~^ _
Use Herbic.
I D50 400
Ref.
1
2
3
4
5
6
AJ
AC
71
67
19
5
1181
369
11
20
a
...
r T
IN. J
^S^
Cl
3100 2,4-DB, BUTYL ESTER C,.HlnC1.0- 4-(2,4-Dichlorophenoxy)butyric
acid, butyl ester
O
Mol.Wt 305
Use Herbic.
IDjo ca. 400
Ref.
A B C D E F
.
2
3
4
5
6
See
3080
0(CH2)3-C-0(CH2)3-CH3
x*^^^s\
\ | Cl
L J
^>^^^
Cl
-------
Code Common Name Emp. Form. Chemical Name
Structure
3120 2,4-DB, ISOBUTYL ESTER C H. Cl 0 4-(2,4-Dichlorophenoxy)butyric
14 IB i J acid, isobutyl ester
O
M.I.WI. 305 O(CH2)3-C-O-CH2-CH(CH
ABCOEF X
U«e Herbic.
I.DSO ca. 400
Ref.
3140 2,4-DB, ISOOCTYL ESTER C H
1
2
3
4
5
6
See
3080
.f^^^ ^^ _ -
i^ M~
<5s. Jj
Cl
Cl 0 4-(2,4-D7chlorophenoxy)butyric
acid, isooctyl ester
O
MOI.W.. 361 O(CH2)3-C-O(CH2)sCH(CH3)2
A B C D E F ^A^
Ute Herbic.
I t>50 500
Ref.
1
2
3
4
5
6
See
3080
f>^ >CI
NSs. ^
Cl
3180 ENDOSULFAN (Thiodan) CnH£ClcO,S 6,7,8,9,10,10-Hexachloro-
(MIXED ISOMERS) 9 b b j 1 ,5,5a,6,9,9a-hexahydro-6,9-
methano-2,4>3-benzodioxa-
thiepin 3-oxide „
Mol. Wi. 407 .. J^ r-u 0
Use Insectic.
L D50 18-43
Ref.
3200 ENDOSULFAN I C-hU
9 6
A B C D E F IT 1 > ^n2wx
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
adef
c,u
a
t
ktu
he-* s=o
'N^^CH 0
*ci * 2
1,0, S The early eluting, low melting
(106°C) isomer of Endosulfan
Mol.Wi. 407 "]\
U Isomer of te<-h A B C D E F [V
endosul fan
IDs,, 18-43
Ref.
2
3
4
5
6
See
3180
*Y^1 A
M /
,^ 1 \
I
o-s-o
n
0
-------
Code Common Name Emp. Form.
Chemical Name
Structure
3240 ENDOTHALL, ACID
C H 0, 7-Oxabicyclo(2.2.1)heptane-2,3-
B dicarboxylic acid monohydrate
Mol. Wt. 204
U«» Herbic.
I I>50 51
R«f.
1
2
3
4
5
6
c
AJ
73
II
21/5
842
6
1
9
t,u
COOH
.H20
3260 ENDR1N
Mol. Wt. 381
U» Insectic.
IDso 10
C12H8C16°
Ref.
1,2,3,4,10,10-Hexachloro-6,7-epoxy-1,
4,4a,5,6,7,8,8a-octahydro-l,4-eudo,
erccfo-5,8-dimethanonaphthalene
1
2
3
4
5
6
C
A
AL
M.
AD
AL
69
69
72
74
I
52
52
8
57
1220
1280
169
585
2
2
2
2
2
2
a
jltu
be
acj
ktu
ktu
3280 EPN
. H..NO.PS 0-Ethyl 0-p_-ni'trophenyl phenyl =
phosphonothloate
Mol.Wt. 323
Acaric. &
Insectic.
42
Rut.
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
3300 EPTC (Eptam)
S-Ethyl dipropylthiocarbamate
Mol.Wl. 189
Use Herbic.
IDso 1,631
R>f.
1
2
3
4
5
6
C
AL
AJ
RC
WO
71
68
71
72
II
54/6
16/5
36,4
64/2
1366
839
84
383
6
4,9
2,3
3
11,17
de
>de
fg
f
r
X
O
II
C2H5-S-ON(C3H7).
7)1
3320 ERBON (Baron)
2-(2,4,5-Trichlorophenoxy)
ethyl 2,2-dichloropropionate
Mol. Wt. 366
Ufa Herbic.
LD50 1,120
R.f.
1
2
3
4
5
6
AJ
AJ
AL
69
70
71
17
18
54
1171
845
327
2
2
2
Imn
j
X
Cl
[ "1
cKAi
-------
Code Common Name Emp. Form.
Chemical Name
Structure
4
3330 ETHEPHON (CEPHA) C-HCC103P (Z-ChloroethvUnhosphnnlr add
Mol. Wi. 144.5
A B C D E F ^
Use Growth Regulat.
L DJO 4,229
Ref.
1
2
3
4
5
6
WD
AJ
AL
AJ
71
73
70
75
60/2
21
53/4
23/2
219
742
730
290
11
3
9
9
g
mno
ef
e
\*r
u
CICH2CH2P(OH)2
3335 ETHIOLATE (Prefox) C^jNOS S-Ethyl diethylthiocarbamate
Mol.Wl. 161
U» Herblc.
1050 400
Ref.
3340 ETHION CnH00
A B c D E F (r.wJ. M r c r u
1
2
3
4
5
6
3Z
4
c
II •* s
O
O.P-S. O.O.O'.O'-Tetraethyl S.S1-
methylene bisphosphoro=
dithloate
Mol.Wt. 384.5
Insectic. 8
04 Mitic.
IDjo 27-65
Ref.
3359 ETHIRIMOL (Mil stem) C H
A B C D E F
1
2
3
4
5
6
C
C
AL
AL
67
74
I
II
50
57
430
1033
12
2,17
2
4
a
de
ae
t
S S
T T
(C2H5O)2P-S-CH2-S-P(OC2H5)2
ON 5-Butyl-2-(ethylamino)-6-
hydroxy-4-methylpyrimidine
(CH2)3CH3
Mol. W). 209 1
A B C D E F HiCv. /"^^ ^.OH
U*e Fungic.
L Ofo 4,000
(female rats)
Ref.
1
2
3
4
5
6
41
9
be
II I
IN N
~~^^'
j^
H-N-C2H5
5880 ETHOPROP (Mocap) C0H,nO,PS, 0-Ethyl S,S,-dipropyl
8 phosphorodithioate
Mol. Wt. 242
A B C D E F (-)
U»e Nematoc.
I Djg 30-56
Ref.
1
2
3
4
5
6
C
II
6
cde
C2H50-P-(SC3H7)2
39
-------
Code Common Name Emp. Form. Chemical Name
Structure
3380 ETHYLHEXANEDIOL C8H18°2 2-Ethyl-l,3-hexanediol
Mol.Wl. 146
U«e Insect Repellant
ll>50 ca. 2,600
Ref.
A B C Off
1
2
3
4
5
6
AJ
59
1
259
12
X
C2H5
HO-CH2-C-CH-C3H7
H OH
3400 ETHYLMERCURY CHLORIDE C,H,HgCl Ethylmercury chloride
(Ceresan) i b
Mol.Wl. 265
U»e Fungi c.
I. DM 30
A B C D I f
Ref.
1
2
3
4
5
6
A
A
Wft
AB
68
71
13A
13B
22
43
2277
950
2
13
2
2
kin
t
k
K
CH,CH,-Hg-CI
3420 EXD (Herbisar)
C H 02$4 Diethyl dithiobis(thionoformate)
Mol. Wl. 242
Uie Herbic.
L Df0 603
A B C D E F
Ref.
C2H5-OC-S-S-CO-C2H5
s s
3440 FAMPHUR
Mol. Wt. 325
Use Insectic.
L D50 35
CinH,,NOl-PS, 0-[p-(dimethylsulfamoyl )=
lu phenyl] 0,0-dimethyl
phosphorothioate
A B C Off
Ref.
1
2
3
4
5
6
C
AO
67
II
15
920
3
3
]
jlo
0-P(OCH3)
'3'2
0=S-N(CH3)2
6
3460 FENAC
HcCKOo 2,3,6-Trichlorophenylacetic acid
Mol.Wl. 239.5
U«e Herbic.
LDM 3,000
A B C D E F
Ref.
1
2
3
4
5
6
AJ
67
15
208
2
u
Cl Cl
CH2-COOH
40
-------
Code Common Name Emp. Form.
Chemical Name
Structure
2020 FENAMINOSULF (Dexon) C H.-N.OjSNa p-(Dimethylamino)benzene.
diazo sodium sulfonate
Mol.Wl. 251 f, j,
U» Fungic.
I "50 60
R«l.
A B C D E F
1
2
3
4
5
6
.
(CH3)2N-^J^N=N_s03Na
3480 FENITROTHION (Sumithion) C.H.-NO.PS 0,0-Dimethyl 0-(4-nitro-m-
^ " b tollyl) phosphorothioate
s
Mol.Wl. 277 f / \
U»e Insectic.
I DM 250
R«f.
3500 FENSULFOTHION (Dasanit) C,,
A B C D E F
1
2
3
4
5
6
AL
AJ
AD
AL
AL
AP
74
69
72
74
74
71
57/6
17/2
8/1
57/6
57/6
64
1282
271
10
1272
1285
1394
4
2
4
4
4
4
ktu
ao
au
t
ae
>mno
(CH30)2P-0-<( \-H02
CH3
HO PS, 0,0-Diethyl 0-[p-(methylsulfinyl )
phenyl] phosphorothioate
Mol. Wl. 308
Us» Insectic.
ID,,, 2-11
R«l.
A B C D E F b , v O
1
2
3
4
5
6
C
AJ
AJ
AJ
AC
72
71
71
73
II
20/6
19/3
19/2
7
1219
456
342
253
9,11
3
4
4
20
a
u
a,f
aco
—
(C2H5O)2P-O-<\ A*-S-CH3
\\ //
3520 FENTHION (Baytex) C,nH,503PS- 0,0-Dimethyl 0-[4-(methylthio -
m-tolyl] phosphorothioate
Mol.Wl. 278 / v S
A B C D E F / \ T
U«« Insectic.
IDso 215
R«f.
1
2
3
4
5
6
C
AL
AJ
AJ
AD
AG
69
66
68
71
67
II
52/6
14/6
16/3
6/1
1/8
1231
619
399
55
639
9,4
4
2
4
4
2,4
,0
IOU
u
10
X
t
H3C-S-A />-0-P(OCH3)2
CH3
3527 FENTIN ACETATE ConH10O.Sn Triphenyltin acetate
(Brestan) 20 18 2
Mol.Wl. 409 ^\
n.. Fungic., Algic. S
U" Molluscic.
A B C D E F
1
we
7Z
78/1
41
15
a
v^\
/ \ C_./~\ /-/^ /-LJ
140-491
1
2
3
4
5
6
we
BF
WB
AE
4E
72
70
74
-
78/1
17/11
71/1
66-750032
41
1059
192
-
15
15
14
10
15
a
t
af
c
aef
-------
Code Common Name Emp. Form. Chemical Name
Structure
3540 FENTIN HYDROXIDE
(Outer)
Mol. Wt. 367
Use Fungic.
500
C,nH.,OSn Triphenyltin hydroxide
lo lo
DEF
1
2
3
4
5
6
C
81
II
12
12
jh
"ghu
V //
SnOH
3600 FERBAM
C H N SgFe Ferric dimethyldithiocarbamate
Mol. Wt. 416.5
Ute Fungic.
I D50 4,000
A B
D E F
Ref.
1
2
3
4
5
6
C
AL
AL
WD
BE
GF
69
69
64
71
71
II
52/6
52/1
14
2/6
14
1276
249
348
249
707
12
4
12
10
12
12
a
a
X
X
X
a
s
(CH3)2-N-C-S-
Fe
0407 FLUCHLORALIN (Basalin) C H . C1F ,N,0. N-Propyl-N-( 2-chloroethyl )-a,a,a-
'' J trif1uoro-2,6-dinitro-p-toluidine
Mol.Wt. 356 / <->2
Uie Herbic.
IDjo 1,550
Ref.
A B C D 1 F
1
2
3
4
5
6
1Q
1,2
agti
// \ XCH2-CH
F3CX7 %
\ / NCH2-Ch
IN^2
3620 FLUOMETURON (Cotoran) C H F N 0 1 ,1 -Dimethyl-3-(a,a,a-tri=
fluoro-m-tolyl)urea
o
A . c „ s f H-N-£-N(CH3)2
Use Herbic.
I.DSO 11,100
Ref.
3623 FLUORIDAMID (Sustar 2-S) C1QH
1
2
3
4
5
6
c
WD
AJ
BH
WD
69
69
71
68
II
44
17
11
36
419
1409
111
234
12
11
10
12
2
91
u
w
u
X
(f^
^>CF3
11N2°3F3 N-4-Methyl-3-[[(l,l,l-trifluoromethyl)=
sul fonyl ]amino]phenyl ]acetamide .-^
II
Mol. Wt. 264 NHCCH3
U Plant Growth ABCDEF J^
Regulator
L D50 9,230
Ref.
1
2
3
4
5
6
4Z
2
u
r ^i
I \ ,
T^
CH3
-------
Code Common Name imp. Form.
Chemical Name
Structure
3630
FLURECOL-n^ BUTYL ESTER
(Florencol)
C18H18°3
n-Butyl 9-hydroxyfluorene-
(9)-carboxylate
M«I.W|. 282
Uie Herbic.
ID M 5,000
Ref.
1
2
3
4
5
6
WD
AX
68
72
36/3
6
318
157
11
21
X
act
u
HO^COOQH,
3640 FOLEX (Merphos)
C12H27PS3 Trlbutyl Phosphorotrithiolte
Mol.Wt. 298.5
U»e Defoliant
ll>50 1,270
Ref.
1
2
3
4
5
6
AL
AL
5M
70
71
53/3
54/2
499
359
4
2,9
6
X
X
g
(C4H,S)3P
3660 FOLPET (Phaltan)
C H Cl NO S N-(Trichloromethylthio)
^ * J ' phthalimlde
Mol.Wt 297
U«e Fungic.
10,000
Ref.
1
2
3
4
5
6
C
AL
BA
70
72
II
53
97
154
713
12
2
2
d,e
a
e
N-S-CCI3
2910 FONOFOS (Dyfonate)
C10H15°PS2
0-Ethyl S-phenyl ethyl=
phosphonodithioate
Mol.Wt 246
Use Insectlc.
L D50 8-16
Ref.
1
2
3
4
5
6
C
AL
71
II
54
1086
9,11
4
a
0
/~\4«i*
3680
FORMETANATE HYDROCHLORIOE
(Carzol SP)
C11H15N302.HC1
m[[(Dimethyl ami no)methyl =
enelaminolphenyl methyl=
Q
Mol.Wi. 258 o-r-NH-n-l,
Acaric 8 A B C D E F O C NH LH3
Die "™' '*••*
Insectlc.
iDsc 20
Ref.
1
2
3
4
S
6
C
GA
II
2,11
2,12
e
a
r^i
L 1 A
•HCI
43
-------
Code Common Name Emp. Form.
Chemical Name
Structure
3722 FORMOTHION (Anthio) CfiH,
?N04P52 0,0-Dimethyl S-(N-methyl-N-formyl=
carbamoyl -methyl Jphosphorodithioate
Mol.WI. 257 CH3. O H S
ABCDEF \ II 1 II,
U» Insectic.
LDjo 365
Ref.
1
2
3
4
5
6
7M
3,9
aeu
IN — O — C — i> — PlLH3t
CH° H
3790 GIBBERELLIC ACID C19H22°6 Gibb-3-ene-l ,10-dicarboxyl ic acid,
2, 4a,7-tri hydroxy-1 -methyl -8 -methyl ene-
1 ,4a-lactone O
M0I Wf "M6 f^^l^ ' S
u Plant Growth A B C 0 E F | CO rtLj
Regulator
IDso — (relativ.
non- toxic)
Ref.
2
3
4
5
6
C
AF
AC
71
67
II
32/4
5
200 IB
413
1,1'
2
20
de
a
HO^XJX^S/X/
CH 1
3 COOH 1CH2
3801 GLVPHOSATE (Roundup) C3H8N05P N-(Phosphonomethyl Jglycine
Mel.Wl. 169 O /-)
ABCDEF V V
Uie Herbic.
L Dso 4,320
Ref.
1
2
3
4
5
6
5Q
4
b,c
HO — C — CH — N — CH2-P — OH
H OH
3860 HEPTACHLOR cirAC17 ] ,4,5,6,7,8,8-Heptachloro-
lu b ' 3a,4,7,7a-tetrahydro-4,7-
methanoindene
Mol.Wt. 373 *^X^S^
ABCDEF T ' 1 1
Use Insectic. [~~
LD,o 90
Ref.
1
2
3
4
5
6
A
C
C
AL
ftL
69
74
I
II
52
57
1220
585
2 -
2 a
12 a
2 b
2 k
It
uv
ou
df
,c
tu
—(_-*
*'\KXVX^
T T *ci
3880 HEPTACHLOR EPOXIDE C10H5C170 1 ,4,5,6,7,8,8-Heptachloro-2,
3-epoxy-2,3,3a,4,7,7a-hexa=
hydro-4 , 7-methanoi ndene
Mel.Wl. 389 xH^
. ABC DEF -ff 1 ^| f^
heptachlor
L D5o 40-60
Kef.
1
2
3
4
5
6
See
3860
~C- 1^0
*^^Sss. 1 s^ ^S>ss. .X^^
T T *ci
-------
Code Common Name Emp. Form. Chemical Name
Structure
3920 HEXACHLORQBENZENE (HCB)
Hexachlorobenzene
Mel. Wl. 285
U» Fungic.
L D
50
A B
Off
Ref.
1
2
3
4
5
6
A
C
AL
AL
AG
72
74
74
5,a.(l)&
12F
II
55
57
8
806
580
584
?
6
2
2
2
j
a
o,p
j
V
3940 HEXACHLOROPHENE (Nabac) C,,H Cl,0, 2,2'-Methylene bis(3,4,6-
13 6 6 ' trichlorophenol)
Mol.Wt. 407
Fungic., Bacteric.
A B
D E F
Die
& Acaric.
300
Ref.
1
2
3
4
5
6
AS
AL
AD
69
70
73
58
53
10
251
522
57
2
2
2
1
c
j
3960 1-HYDROXYCHLORDENE
C H Cl 0 t-exo, Hydroxy-4,5,6,7,8,8-hexachloro-
10 6 ° 3a,4,7,7a-tetrahydro-4,7-methanoindene
Mol.Wt. 355
Use
Heptachlor
derivative
2,400
A B
D E F
Ref.
1
2
3
4
5
6
A
C
AJ
72
4, A
II
20
328
2
2
2
X
a
aku
*CI
4011 IBP (Kitazin)
C. H,,0,PS 0,0-Diisopropyl S-benzyl
thiophosphate
Mol. Wt. 288
U»« Fungic.
I Dso 660 (mice)
Ref.
A B C D E F
1
2
3
4
5
6
r
UCH3 2CHOJ2 P —SCH
4040 IOXYNIL (Actril)
C?H I2NO 4-Hydroxy-3,5-diiodobenzonitrile
Mol.Wt. 371
U«« Herbic.
110
A B
0 E F
Ref.
1
2
3
4
5
6
AC
AL
AM
67
65
68
5
48/6
6/1
423
1173
9
20
2
2,3
X
X
-------
Code Common Name Emp. Form. Chemical Name
Structure
4070 ISOPROPALIN (Paarlan) Ci5H23N3°4 2,6-Dinitro-N,N-dipropylcumidine
N(C3H7)2
Mol.Wt. 309
Us* Herbic.
LDso 5,000+
Ref.
i
6420 KARBUTILATE (Tandex) C H
14
Mol.Wt. 279
U« Herbic.
l"50 3,000
Ref.
4166 LAMPRECIDE (TFN) C,H
Mol.Wt. 229
Uie Lamprey killer
1 DJO 370-440
Ref.
A B C D E F
1
2
3
4
5
6
AL
3E
74
57/3
645
3,12
?,11
w
a,u
NO m-(3,3-dimethylureido)=
i' J phenyl tert-butylcarbamate
A B C D E F
1
2
3
4
5
6
3Q
16
tu
10,F,Na 3-Trif 1 uoromethyl -4-ni tro=
phenol, sodium salt
A B C D E F
1
2
3
4
5
6
AL
74
57/2
387
2
k
°2NiTN02
CH(CH3)2
9V
, ^-O-C-N-C(CH3)3
\ — -/
HO
0-No
I
NO2
4180 LEAD ARSENATE PbHAs04 Acid lead arsenate
Mol.Wt. 347
Uie Insectic.
ID 50 100
Ref.
4185 LENACIL (Venzar) Cn,Hn
Mol.Wt. 234
Use Herbic.
I.DSO 11,000
A B C D E F
1
2
3
4
5
6
B
25.000-
.017
12
X
NO- 3-Cyclohexyl-6,7-dihydro-
IH-cyclopentapyrimidine-
2,4(3H,5H)-dione
A B C D E F
1
2
BC
66
17/3
121
3
af
H
I
QTT— r
— ^^H — \.
Ref.
-------
Code Common Name Emp. Form.
Chemical Name
Structure
4190 LEPTOPHOS (Phosvel)
Mol.Wt. 412
Uw Insectic.
IDso 53
C H BrC1.0.PS
IJ ' '
Ref.
0-(4-Bromo-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
g
d
ad
d,e
4220 LETHANE 384
8-Butoxy-B1-thiocyanodiethyl ether
Mel. Wl. 203
Uu Insectic.
L D
50
90
1
2
3
4
5
6
AJ
61
6
478
12
jo
C4H90(CH2)2-0-(CH2).1-S-CN
4240 LINURON (Lorox)
C.H.-Cl.N-O, 3-(3,4-D1chlorophenyl)-l-
* lu i ' i methoxy-1-methyl urea
Mol.Wt. 249
Uu Herbic.
LD,o 1,500
Kef.
1
2
3
4
5
6
C
AL
AD
AJ
WO
AC
66
67
69
71
67
II
49
2
17
57
5
452
75
1409
303
433
12
11,1
12
4
12
20
X
t
u
X
tu
—
=/ H N0-CH3
4260 MALATHION
Mol.Wt. 330
Uu Insectic.
l"50 1,000-1,375
Ref.
Dlethyl mercaptosucclnate,
3-ester with 0,0-dimethyl
phosphorodithioate
1
2
3
4
5
6
C
AL
AL
AJ
AL
AD
74
71
68
67
68
II
57
54
16
50
3
1033
513
361
581
247
12
4
4
4
3
2
de
t
a
ajo
0
?,SJ
S H
(CH30)2P-S-C-COOC2H5
CH2-COOC2H5
4300 MANEB
Mol.Wt *265
Uf» Fungic.
10!0 6,750
*Un1t mol. wt.
(Polymeric)
Manqanous ethyl ene-
bis(dithiocarbamate)
R.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
H H S
H-C-tW-S-
H-C-N-C-S-Mn-
H H S
47
-------
Code Common Name Emp. Form.
Chemical Name
Structure
4310 MCPA
CgHgClOj
(4-Chloro-2-methylphenoxy)-
acetic acid
Mol. Wl. 201
U«e Herbic.
1- O
w
700
Ref.
1
2
3
4
5
6
AL
WD
AC
69
71
67
52
57
5
187
303
439
2
11
20
t
tu
-
4360 MCPA, ISOCCTYL ESTER
C H CIO,
" " J
Isooctyl (4-chloro-
2-methylphenoxy)acetate
Mol.Wt. 313
Use Herbic.
I.DSO 700
Ref.
A B C D E F
)
2
3
4
5
6
See
4340
CH3
:H( \OCH2-C-0(CH2)5C(CH3)2
\=/ o
H
4380
MCPB
Mol.Wt. 229
Use Herbic.
LOso 700
C1,H13C1°3
Ref.
4-(4-Chloro-2-methyl=
phenoxy)butyric acid
1
2
3
4
5
6
AL
WD
GD
64
71
70
47
57
66
348
303
393
2
11
2
d
tu
a
0(CH2)3-COOH
4400
MCPP
C H ,C10 2-(4-Chloro-2-methyl=
'0 11 ^ phenoxy)propiom'c acid
Mol.WI. 215
Use Herbic.
650
Ref.
1
2
3
4
5
6
WD
AJ
71
71
57
19
303
1181
11
11
tu
abg
O-CH-COOH
4420 MCPP, ISOOCTYL ESTER C^H,
Mol. Wl. 327
Use Herbic.
1 °so ca- 65°
Ref.
CIO Isooctyl 2-(4-chloro-2-
' -> methylphenoxy)propionate
A B C D E F
1
2
3
4
5
6
See
4400
CH3
Q-CH-C-O(CH2)5CH(CH3)2
O
-------
Otto Cminon Name Emp. Form
Chemical Name
Structure
4441 MECARBAM (MC-474) ClnH
,nNO,-PS S-[N-Ethoxycarbonyl -N-methyl=
'" 3 carbamoylmethyl] 0,0-diethyl
phosphorodithioate
M.I.Wt. 297 S o
In-ectic & A B C D E F f V
Acaric.
ID50 36
Ref.
1
2
3
4
5
6
BA
69
94/1117
275
4,11
t
(C2H50)2 P-S— CH2— C — N— COOC2H5
CH3
4453 MENAZON (Azidithion) C H N 0 PS S-[(4,6-Diamino-l ,3,5-
6 12 5 2 2 triazin-2-yl)methyl]
0,0-dimethyl phosphorodithioate
NH2
Mol.Wt. 281 _ N i
"*• Aphicide
ID50 1,950
(female rats)
Ref.
ABC 0 E F , // \V
1
2
3
4
5
6
AC
AD
BA
73
73
69
7
10/5
94/1117
317
285
275
20
3
1,11
—
X
t
*C_H3U;2 V— 5 — CH2— ^ N
II N=^
s NH2
4460 MEOBAL ClnH.,.,NO, 3,4-Xylyl methyl carbamate
O-CO-NH-CH3
Mol.Wl. 179 II J
A B C D E F ^^\
U*e Insectic.
L DSO 290-380
Ref.
1630 MEPHOSFOLAN (Cytrolane) C0H
1
2
3
4
5
6
AJ
JB
73
70
21
35
178
72
11,
12
2
X
C
r^ 3
CH3
6N03PS2 P,P-Diethyl cyclic propylene
ester of phosphonodithio=
imidocarbonic acid
Mol. Wl. 269
A B C D E F „
Ute Insectic.
10,0 8.9
Ref.
0960 METALKAMATE (Bux) C,,H,
1
2
3
4
5
6
^-'S\ y
H3C^ (=N~P~(°C2H5)2
• s
gN02 Mixture of m-(l-ethylpropyl)=
phenyl methyl carbamate and m-
(1 -methyl butyl) phenyl methyl =
carbamate (ratio of 1:3) X^^ftyOCONHCHi
Mol.Wl. 205 fi T JL
.. A B C D E F [1 J and^^OCONHCH3
**»• Insectic.
ll>50 170
Ref.
1
2
3
4
5
6
C
II
11,
17
C
^r \\
H3C-C-(CH2)2CH3 ^?
H LJ r^fr^u ^"LJ ^
1 ' n ^\^*n2^-riT/2
-------
Code Common Name Emp. Form.
Chemical Name
Structure
6220 METHAM (SMDC)
Sodium N-methyldithiocarbatnate
Mol.Wt. 129
U*« Soil Fumigant
820
A B
D t f
Ref.
1
2
3
4
5
6
7Z
18
w
\J
CH3-NH-£-S-Na
4750 METHAMIDOPHOS (Monitor) C.H-NO.PS 0,S-Dimethyl phosphor^
amidothioate
Mel. Wl. 141
Ute Insectic.
L DJO 18.9-21
A B
Ref.
D E F
1
2
3
4
5
6
AL
AJ
GH
71
73
—
54/6
21/1
24/2
1396
143
252
9
4
3
afd
d
a
CH3O
4490 METHANEARSONIC ACID (MAA) CH3As03 Methyl arsonic acid
Mol.Wt. 140
U«« Herbic.
I.DSO 1,300
A B
D E F
Ref.
1
2
3
4
5
6
B
25.011-
.017
12
q
o
CH3-As(OH)2
4496 METHAZOLE (Probe)
Mol.Wt. 261
Ute Herbic.
I DM 1,350
C H Cl N 0 2-(3,4-Dichlorophenyl)-4-methyl-
» o f- f. J l,2,4-oxadiazolidine-3,5-dione
A B
D E F
Ref.
1
2
3
4
5
6
9A
2, If
g,u
Cl
N O
CH,
6340 METHIDATHION (Supracide) C.H N O.PS, S-[(2-methoxy-5-oxo-A2-
6 11 2 4 3 1>3i4_th1a(J1azoiin_/|_yi)=
methyl] 0,0-dimethyl phos=
phorodithioate
Mel.WI. 302
Use Insectic.
I "so 25-48
D E F
Ref.
I
2
3
4
5
6
AJ
AJ
69
70
17
18
565
164
6
4
b
c,P
w»
N N-CH2-S-P(OCH:
CH,O-
:/*
32
50
-------
fade Common Name Emp. Form.
Chemical Name
Structure
4500 METHIOCARB (Mesurol)
Mol. Wl. 225
Acaric. &
Insectic.
130-135
„
u"
10
,0
C-.H.^NO.S
" ls f
R»f.
4-(Methylthio)-3,5-xylyl
N-methylcarbamate
1
2
3
4
5
6
AL
AJ
AB
AL
WD
AL
74
72
72
69
70
73
57/4
20/2
44/12
52/5
49/2
56/3
570
443
2046
1054
215
713
3
2,3
11J4
4
2
2
d
X
tu
ad
idet
a
4520 METHOMYL (Lannate)
C,-Hlr.N.,0-,S S-Methyl N-[(methylcarba=
3 moyl)oxy] thioacetlmtdate
Mol.Wt. 162
Insectic.
„
u"
10,0
Nematoc.
'7-24
Ref.
1
2
3
4
5
6
C
AJ
AJ
JI
68
74
72
II
16
22
28
554
76
22
e
6
4
4
a.d
a
atu
f
4531 METHOPRENE (Altosid)
H34°3
Isopropyl (2E,4E)-ll-methoxy-
3,4,ll-trimethyl-2,4-dodecad1enoate
Mol.Wt.
Uie
IDjo
310
Insect Growth
Regulator
34,600+
Ref.
1
2
3
4
5
6
AP
AL
AJ
73
75
74
66/3
58/1
22/4
707
10
582
3
3,5
3
X
jko
tu
X
/°\l
i 9
4540 METHOXYCHLOR (Marlate)
2,2-Bis(p-methoxyphenyl)-
1 ,1 ,1-trichloroethane
Mol. Wt. 346
Uie Insectic.
L Oso 6,000
Ref.
1
2
3
4
5
6
B
BA
AL
AL
AL
69
69
72
72
24.128-
.152
94
52
55
55
900
1280
32
1058
12
2
2
2
2
e
u
a
k
k
oCH3
4560 NETHYLMERCURIC CHLORIDE CH,HgCl
Methylmercury chloride
Mol. Wt. 251
Use Fungic.
L D«o 30-35
Raf.
1
2
3
4
5
6
A
A
AB
WD
CA
71
74
70
13,A
13, B
43
97
50
950
65
597
2
13
10
2
13
jkln
t
k
1
cu
CH3-Hg-CI
-------
Common Name Emp. Form.
Chemical Name
Structure
4572 METHYLMERCURIC IODIDE CHjHgl Methylmercury iodide
Mel.Wt. 342.5
u«. Reagent In
Hg method
1050
Kef.
4631 HETOXURON (Dosanex) C1QH
A B C D E F
1
2
3
4
5
6
See
4560
CH3HgI
-CIN-O, 3-(3-Chloro-4-methoxy=
phenyl)-l,l-dimethylurea
Mol.WI. 289 C{ HO
ABC D E F > ^ V U
UM Herbic.
IDso 3,200
Ref.
4640 HEVINPHOS (Phosdrin) C^
1
2
3
4
5
6
7M
12
a be
fu
CH3OH( VN-C -N(CH3)2
\ — _/
,OfiP Methyl 3-hydroxy-aZp^a-
crotonate, dimethyl phosphate
Mol. Wl. 224
A B C D E F Q HO
U§e Insectic.
10,0 7
Ref.
7080 MEXACARBATE (Zectran) C,«H,,
1
2
3
4
5
6
B
AJ
BA
BA
70
67
68
24.174-
.180
18
92
93
401
578
691
17
3
12
11
d,e
a
V
a,f
(CH3o)2fi-o-c:=c-c
CH3 OCH3
NO. 4-Dimethylamino-3,5-xylyl
' ' methyl carbamate
O H
*•••*'• 222 ^ r M C-LJ
A B c D E F O-C-N-CH3
UM Insectic.
LDjO 15-63
*•«
1
2
3
4
5
6
10
U
M.
69
69
74
26
17
57/3
63
56
570
,6
2
3
a
a
a
r^N
\^\
N(CH3)2
4280 MH (Maleic Hydrazide) C/1H/1N,0, 6-Hydroxy-3-(2H)-pyridazinone
OH
M.I.Wt 112 ^A.
H^, , A B C 0 E F r^^M
Uf* Growth Regulator
LDM 2,340-6,950
«•».
1
2
3
4
B
AL
73
24.141-
.147
66
1164
12
11
f
af
k^N-H
u
O
52
-------
Code Common Name Emp. Form.
Chemical Name
Structure
4720 MIREX (Dechlorane)
Mol. Wl. 546
Uie Insectic.
I DSO 306
C10C11
Ref.
Dodecachlorooctahydro-1,3,
4-metheno-2H-cyclobuta[cd]=
pentalene
\
2
3
4
5
6
C
A
AL
AL
AJ
AL
63
75
73
73
II
10, A
46
58/3
21/6
56/3
884
557
1099
721
6
2
10
2
1
2
ajo
t
a
j
X
a,e
4740 MOLINATE (Ordram)
Mol. Wl. 187
Uu Herbic.
L D,o 660
CgH,7NOS S-Ethyl hexahydro-lH-
azepine-1-carbothioate
Ref.
1
2
3
4
5
6
C
AJ
AC
68
67
II
16
5
839
469
6
2
20
ct
t
—
O=C-S-C2H5
4747 HONALIDE (Potablan) C H C1NO N-(4-Chlorophenyl )-2,2-dimethyl=
pentanamide
Mol.Wl. 239.5
Uie Herbic.
IDjo 4,000
Ref.
A B C D E F
1
2
3
4
5
6
7Q
2
a
c,
H CH3
N -C -C -CH2 -CH2 -CH3
O CH3
0360 MONOCROTOPHOS (Azodrin)
Mol.Wt. 223
Use Insectic.
IDM 21
C7H14N05P
Ref.
Dimethyl phosphate of 3-
hydroxy-N-methyl-ris-cro=
tonamide
1
2
3
4
5
6
AJ
AJ
AD
AJ
AC
BA
67
68
74
66
67
73
15/3
16/6
11/5
14/2
5
98
465
899
434
145
193
194
4
3
4
16
12
21
a
a
a
a
X
a
O
(CH3O)2P-O H
i i
CH3-C=C-C=O
H-N-CH3
4751 MONOLINURON (Aresin)
CnH,,ClNO? 3-(p-Chlorophenyl)-l-methoxy-
1-methyl urea
911
Mol.Wl. 201
UM Herbic.
IDso 2,250
Kef.
1
2
3
4
5
6
GE
WD
WD
WD
71
71
69
67
256/3
63/2
44/2
27/1
194
364
419
296
9,15
18
1,2
10J1
11
X
X
X
au
/~V ? ?-CH»
Cl^ V-N-C-N-C
\~ —/
CH3
-------
Code Common Name Imp. Form.
Chemical Name
Structure
4760 MONURON
Mel. Wt. 199
U«e Herbic.
I- Dso 3,600
3-(p-Ch1orophenyl )-l ,l-d
methyl urea
AB
Ref.
ff
I
2
3
4
5
6
C
AL
WD
WD
AL
66
71
69
62
II
49
57
44
45/2
452
303
419
377
11,12
11)2
11
10J1
12
dei
t
tu
u
a
4780 MONURON- TCA (Urox)
C H Cl N 0, 3-(p-Chlorophenyl)-l,l-di=
" u 4 ' J methylurea trichloroacetate
"<"•*'• 362 ABC D E F H-N-C-N+H(CH3)2-OCOCI3
Use Herbic.
LDjQ 2,300
Ref.
4803 MORPHOTHION (Ekatin M) CgH1
1
2
3
4
5
6
See
4760
r i
UN. \
^z?/
T^
Cl
gO-PS, 0,0-Dimethyl 5-(morpholinocar=
bonylmethyl Jphosphorodithioate
Mol.Wt. 246
A B C D E F , , OH S
U» Insectic.
ID» 100-120
Ref.
.
3
3
4
5
6
/ \ II 1 II
O N-C-C-S-P(CH3O)2
H
4820 MSMA (Bueno) CH^AsNaO, Monosodium acid methanearsonate
Mol.Wt 162
ABCOEF O
U*e Herbic.
I D50 700
Ref.
4860 NALED (Dibrom) CdH?B
1
2
3
4
5
6
ZJ
If
IB
AJ
71
69
69
71
19
33/2
22
19/4
412
279
51
412
12
21
21
12
a
abu
ag
a
II Qf-J
3 $xONa
r,Cl.,O.P 1 ,2-Dibromo-2,2-dichloro=
ethyl dimethyl phosphate
Mol.WI. 381 m O .,
A B C D E F
U» Insectic.
IB» 430
1
2
C
AL
65
II
48
748
6
6
ade
de
T i
(CH3O)2P-O-C-CCI2Br
Br
Ref.
-------
Code Common Name Emp. Form.
Chemical Name
Structure
4880 NAPHTHALENE ACETAMIDE c12HnN0 1-Naphthalene-acetamide
Mel. Wt. 185
UM Growth Regulant
1,000
A B
Ro(.
E F
1
2
3
4
5
6
AC
67
5
455
10,
12
a
CH2-C-NH2
O
4900 NAA (Naphthalene
Acetic Acid)
C12H10°2
1-Naphthalene acetic acid
Mol. Wl. 186
U» Growth Regulant
I D,o 1,000
Ref.
1
2
3
4
5
6
C
AL
AJ
AL
AC
64
64
71
67
II
47
12
54
5
348
59
327
455
2,12
2
12
14
20
e
e
g
e
~
CH2COOH
4925 1-NAPHTHOL
1-Naphthol
Mol. Wl. 144
ii Derivative of
Carbaryl
2,590
Ref.
A B
1
2
3
4
5
6
A
AO
AL
71
70
7A
6
53
34
495
2
2
2
m
m
jo
2010 NAPROPAMIOE (Devrinol) C.-H^NO, 2-(a-Naphthoxy)-N,N-
Mol.Wt. 271
Ut* Herbic.
5,000
.-^,
Ref.
diethyl propionamide
A B
D E F
1
2
3
4
5
6
AF
7Z
82-84523
B
_
10
1
au
aju
0-CH-CN(C2H5)2
4920 NAPTALAM, SODIUM SALT C H NO.Na Sodium N-l-naphthyl=
Mel.Wl. 313
U«« Herbic.
IDjo ca. 177
18 12 3
phthalamate
A B
Ref.
1
2
3
4
5
6
AB
AJ
AC
53
58
64
25
6
4
1397
671
1
12
12
20
a
a
—
55
-------
Code Common Name Emp. Form.
Chemical Name
Structure
4940 NEBURON c,_H,
fiCl,N.O l-(n-Buty)-3-(3,4-dichloro=
phenyl )-l -methyl urea
O
II
K.I.WI. 275 H-N-C-N-QH,
U.. H L- A B C D E F ^\ CH,
**»• Heroic.
1-D50 11,000
Ref.
5020 NITRALIN (Planavin) C^H.,
1
2
3
4
5
<5
WD
WD
AL
WD
69
69
62
68
44
44
45/2
36
419
60
377
234
2,11
2
12
2
u
u
a
x
JL^ J
Cl'^jX/
Cl
QN,0,S 4-(Methylsulfonyl)-2,6-
a dinitro-N,N-dipropyUniline
Mol. Wl. 345 O yNOi
A B C D E F V ff—. JC'^2
UM Herbic.
L D,,, 2,000+
Ref.
1
2
3
4
5
6
C
ZB
AL
WO
73
72
70
II
26
55/5
53/2
390
913
397
2,11
19
12
11
d,9
u
w
X
CH,-S-N(CH2CH2CH3
l\={
0 N02
5031 NITRAPYRIN (N-Serve TG) C H NCI 2-Ch1oro-6-trichloromethyl=
6 J * pyridine (and related chlorinated
pyridines)
Mol.Wi. 231 -
A B C D E F x^^S,
Stabilizer
LOso 1,230
Ref.
1
1
3
4
5
6
2Z
2
acj
1 1
CI3C N Cl
5040 NITROFEN (TDK) C H Cl NO 2,4-Dichlorophenyl-
12 7 2 3 p-ni trophenyl ether
NUI.Wt. 284 ^Cl
UM Herbic.
IDjo 3,580
Ref.
A B C D E F
1
2
3
4
5
6
C
II
2,12
af
a^yo^y^
5060 4-NITROPHENOL (PNP) C,HrNO, 4-Ni trophenol
1 DO 3
OH
Mol. Wl. 139 s^
UM Parathion
Derivative
A B C D E F
1
A
6,A,(2),
. (b)
2
m
r 1
i
2
3
4
5
6
A
AD
AJ
AJ
AL
70
71
73
74
6,A,(2),
5 'b'
19
21
57
329
758
295
1288
2
2
2
2
2
m
m
0
m
m
NCh
-------
Code Common Hame Emp. Form. Chemical Name
Structure
5080 trans-NONACHLOR C,,,H,
C10 1-ato, 2-endc, -3-exo
a 4,5,6,7,8.8-Nonachloro-
3a,4,7,7a-tetrahydro-4,7- • »
methanoindane X
Mai. Wl. 444 .. _A"
Compon. of tech.
u" chlordane
L DJO 500
Kef.
5136 NORFLURAZON (Evital) C^Hg
1
2
3
4
5
6
A B C D E F J} / \
C
I
2
X
^1 / *
LK *°
*
C1F,N,0 4-Chl oro-5- (methyl ami no )-2-
U,o,a-trifluoro-m-tolyl)-
(2H)-pyridazinone
Mol.Wf. 304 ^.f3
A B C 0 t f ^, ^ N v X
Un Herbic.
IDso 9,300
R.f.
1
2
3
4
5
6
7M
2
egu
/ \_ ./ )— N
\ / \ ^ \,,
O"^ ^Cl
5148 ORYZALIN (Surflan) C,.H, N.O,S 3,5-Dinitro-N4,N4-
12 18 4 6 dipropylsulfanilamide
Mal.WI. 346 O (
ABCDEF 1 / \
0» Herbic.
IDjo 10,000+
Kef.
5176 OXADIAZON (Ronstar) ClrH,
1
2
4
5
6
3E
2
acu
HsN I "v_/C3H
o — \
NO2
3N203CI2 2-tert-6utyl-4-(2,4-
dichloro-5-isopropoxyphenyl)-
A^-T ,3,4-oxadiazol in-5-one
H
Mol. Wl. 345 1
U«e Herbic.
L D50 8,000+
R.f.
5186 OXAMYL (Vydate) C-H,.
A B C D E F
1
2
3
4
5
6
71
2
ajoi
(CH3)2C-0 °
-------
Code Common Name Emp. Form.
Chemical Name
Structure
5187 OXAMYL OXIME
C5H10N2°2S Methyl N1,N'-dimethyl-N-
hydroxy-1-thi'ooxamimi'date
Mol.Wl. 148
u Oxamyl
Derivative
Ref.
1
2
3
4
5
6
A
See
5186
o
(CH3)2N-C-C=N-OH
SCH3
OXYCHLORDANE
Mol.Wl. 424
Use
LDjo
Hetabol. of
chlordane
457
Ref.
1-eco, 2-endo, 4,5,6,7,8,8-Octachloro-
2,'3-aro-epoxy-2,3,3a,4,7,7a-
hexahydro-4,7rmethanoindene
1
2
3
4
5
6
AD
AD
AD
AJ
AJ
AD
70
73
71
73
72
72
5
10/3
5/6
21/6
20/2
7/1
521
208
521
1099
395
33
20
2
V-
1
2
2
—
jo
jou
X
j
X
5220 OXYDEMETON METHYL
(Metasystox R)
C6H15°4PS2
S-[2-(ethylsulfinyl)ethyl]-
0,0-dimethyl phosphorothioate
Mol. Wt. 246
Ute Insectic.
t 050 70
1
2
3
4
5
6
AL
AD
WD
BA
BA
WD
69
71
70
69
67
69
52/1
6/1
48/3
94/1122
92/1092
44/2
157
55
468
805
170
414
4
4
7
11J7
11
11
a
X
a
X
a
X
o o
(CH30)2P-S(CH2)2-S-CH2CH3
480CL OXYTHIOQUINOX
(Morestan)
Mol. Wt. 234
Ute Mitic.
ID50 3,000
Ref.
6-Methyl-2,3-quinoxa=
linedithiol cyclic-5,
S-dithiocarbonate
1
2
3
4
5
6
AL
AC
GH
AL
JC
71
67
68
69
69
54/5
5
20/2
52/1
18/11
1122
277
550
151
1344
2
12
2
11J7
2
de
w
de
t
X
C=0
5240 PARAQUAT DICHLORIDE
(Gramoxone)
C H, .CO, 1,1'-Qimethyl-4,4'-tn=
'' i pyridillum dichloride
Mol.Wt. 257
ABC D E F
Use Heroic.
ID 50 150
Ref.
1
2
3
4
5
6
c
AJ
AJ
AL
AC
74
74
74
67
II
22
22
57
5
863
79
202
473
12
3
12
12
20
fg
u
tu
tu
—
2cr
58
-------
Code Common Name Etnp. Form.
Chemical Name
Structure
5245 PARATHION ETHYL
Met.Wf. 291
Use Insectic.
11>30 3-30
C,0H,,N05PS 0,0-Diethyl-0-p-nitro=
phenyl phosphorothioate
C '
Kef.
1
2
3
4
5
6
A
C
AL
AL
AJ
BA
74
74
69
72
8A.10A
II
57
57
17
97
930
1033
1066
378
4
12J5
3,4
4
3
2
tv
sdej
de
t
b
ad
-P(OC2H5)2
4580 PARATHION METHYL
Mel. Wl. 263
Die Insectic.
LD50 9-25
Ref.
Phenyl phosphorothioate
1
2
3
4
5
6
See
5245
0-P(OCH3)2
5251
PARINOL (Parnon)
Mol. Wt. 330
Use Fungic.
I DJO 5,000
C18H13C12NO c,>c,-Bis(p-chlorophenyl)-3-
pyridine methanol
A B
Ref.
E F
1
2
3
4
5
6
AL
70
53/4
747
2,3,
12
aeu
5280 PCNB (Quintozene)
Mel.Wi. 295.5
Use Fungic.
12,000
Pentachloronitrobenzene
Ref.
1
2
3
4
5
6
C
AJ
BA
AL
AD
WD
67
72
72
74
74
II
15/4
97/1154
55/4
11/6
93/1
648
378
794
567
91
2,1;
2J
2
2
2
2
eg
aefu
de
c
u
a
NO
5260 PCP (Pentachlorophenol)
Mol.Wt.
Use
266
Herbic., Wood
Preservat.
125-210
Ref.
2,3,4,5,6-PentachTorophenol
1
2
3
4
5
6
A
AJ
BG
AD
AL
AC
69
70
73
74
67
5A(3b,4a)
17
4
10
57
5
871
533
57
389
313
2
2
5
2
2
20
Imt
ktu
jt
j
t
--
59
-------
Code Common Name Emp. Form.
Chemical Name
Structure
5300 PEBULATE (Tillam) C^H^NOS S-Propyl butylethyl =
thiocarbamate
Mol. Wl. 203
Uto A B C D E F Q CH2CH3
W*tl HerDi Co
L DSO 1,100
Ref.
5366 PERFLUIDONE (Destun) C H
1
2
3
4
5
6
C
II
6
adf
CH3(CH2)2S-C-N(CH2)3CH3
-NO.F-S- 1 ,1 ,l-Trifluoro-N-[2-methyl-
4- (phenyl sul fonyl ) phenyl ]me thane -
sulfonamide
Mol. Wl. 379
ABC D E F / ^ f, ^
Ute Herbic.
L D50 92° (mouse)
Ref.
]
2
3
4
5
6
42
2
gu
f Vso2-^ VNHSO.C
CH3
5380 PERTHANE C -H..C1,, 1 ,1 -Dichloro-2,2-bis(p-
ethyl phenyl) ethane
Mol.Wl. 307 , , H , *
Use Insectic.
LDso 8,170
Ref.
5400 PHENCAPTON C H
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
HA j \^j yCiHs
CHCI2
Cl 0 PS 0,0-Diethyl-S-(2,5-dichloro=
5223 phenyl thiomethyl ) phosphoro=
thiolothionate
Mol.Wl. 377 S-CH2-S-P(OC2H5)2
A B C D E F _. ^ »
Use Acaric.
I.DSO 65-182
Ref.
5410 PHENMEDIPHAM C,,H,
(Betanal) 16 '
1
2
3
4
5
6
BA
BA
69
67
94/1117
92/1092
275
170
4
11
t
a
T n
\ ^^~CI
^\^^ >-l
fiN 0 Methyl m-hydroxycarbanilate
m-methyl carbani 1 ate
Mol.Wl. 300 , . O H
u^,-, A B c D e F // Vo_r_N1_/r\v
L DJO 8,000+
Ref.
i
2
3
4
5
6
BH
7Q
70
10/4
340
10J2
10
a
f
CH3-O-C-N-H
60
-------
Code Common Name Emp. Form. Chemical Name
Structure
5420 PHENOTHIAZINE
Dibenzo-1 ,4-thiazine
Mol. Wt. 199
Ute Insectic.
L 0,0 5,000
A B C D E F
Ref.
1
2
3
4
5
6
B
AL
69
33.086-
.092
52
162
12
12
c
a
5680 PHENYLMERCURIC ACETATE CnH00,Hg Phenylmercury acetate
(Common name PMA) 8 8 2
Mol.Wl. 337
Uie Fungic.
ID 50 16-60
A B C D E F
Ref.
1
2
3
4
5
6
A
AB
71
13B
43
950
13
t
k
Hg-0-C-CH3
5460 PHENYLMERCURIC BORATE CgHyBHgOj Phenylmercury borate
Mol.Wt. 339
Ute Fungic.
I.DSO L.T.100
A B C D E F
Ref.
1
2
3
4
5
6
A
BA
JE
69
68
13B
94
14
143
131
13
21
10
t
cfj
a
Hg-0-
Hg-0-B(OH)2
5480 PHENYLMERCURIC CHLORIDE C H HgCl Phenylmercury chloride
Mol.Wl. 313
U" Fungic.
60
A B C D E F
Ref.
1
2
3
4
5
6
See
5680
5485 PHENYLMERCURIC HYDROXIDE C HrHgOH Phenylmercury hydroxide
—-~~ 6 J
Mol. Wl. 295
U»e Fungic.
I- OKI L.T.100
A B C D E F
Ref.
1
2
3
4
5
6
See
5680
-------
Code Common Name Emp. Form.
Chemical Name
Structure
5487 PHENYLMERCURIC IODIDE C£HcHgI Phenylmercury iodide
Mol.Wt. 405
., e Reagent in
Hg method
LDso — (Toxic)
Ref.
A B C 0 E F
1
2
3
4
5
6
See
5680
O-H.-,
5490 PHENYLPHENOL c,oH,n° 0-Phenyl phenol
(Dowicide 1) 12 10
Mol.Wt. 170
Use A"rl'c'. &
Fungic,
LDM 2,480
Ref.
5500 PHORATE (Thimet) C,^,
Mol. Wt. 260
Use Insectic.
1 DSO 1-5
Ref.
5520 PHOSALONE (Zolone) C H
Mol. Wt. 368
Use Insectic.
L D50 135
A B C Off
1
2
3
4
5
6
C
BA
AL
AL
70
71
73
II
95
54
56
490
975
299
12
12
12
def
i
de
b
) PS 0,0-Diethyl S-[(ethyl thio)=
methyl Jphosphorodithioate
A B C D E F
1
2
3
4
5
6
C
AL
AL
AD
AJ
AP
69
74
69
67
70
52
57
4
15
63
1231
1033
224
192
52
3,4
4
4
4
2
9
ajo
bcor
t
j
dc
u
f^^Tf^l
l^-J ^V./^
s
(C2H50)2P-S-CH2-S-C2H5
C1NO PS S-[(6-Chloro-2-oxo-3-ben=
5 4 2 zoxazolinyl )methyl] 0,0-
diethyl phosphorodi thioate /-\
A B C D E F
1
2
C
AJ
71
II
19
742
2,3
11
2
e
e
11
0 N-CH2S-P(OC2H5)2
Ref.
Cl
1610 PHOSFOLAN (Cyolane)
C H NO^PS P.P-Diethyl cyclic ethylene
ester of phosphonodithio=
imidocarbonic acid
Mol.Wt. 255 _ O
Use Insectic.
LD50 8,9
Ref.
A B C DEF /3^ . . J!
1
2
3
4
5
6
r
I s
-------
Code Common Name Emp. Form.
Chemical Name
Structure
4000 PHOSHET (Imidan)
C H NO.PS, 0,0-Dimethyl-S-phthalimi=
11 12 4 2
domethyl phosphorodithioate
Mol.WI. 317
A B C D 6 F
Use Insectic.
IDso 147
Ref.
1
2
3
4
5
6
C
AJ
AL
AL
AC
68
69
74
67
II
16
52
57
5
796
522
1033
257
4,12
4
3
4
20
bej
a
a
t
...
5580 PHOSPHAMIDON C.-H, C1NO,P 2-Chloro-N,N-diethyl-3-hydroxy=
(Dimecron) crotonamide dimethyl phosphate
Mol.WI. 300
A B C 0 E F
Use Insectic.
LDjo 15-33
Ref.
5600 PICLORAM (Tordon) C,H,C
1
2
3
4
5
6
C
ZD
71
II
37
All
12,17
20
deh
—
IN 0. 4-Amino-3,5,6-trichloropicolinic
J i acid
Mol. Wl. 241.5
Use Herbic.
I DJO 8,200
Ref.
5640 PIPERALIN (Pipron) Clf.H0
A B C D E F
1
2
3
4
5
6
AJ
BA
WD
ZA
AC
67
67
70
70
67
15
92
53/2
23
5
469
371
367
323
507
2
2
2
2
20
c
au
b
tu
—
Cl NO 3-(2-Methylpiperidino)propyl-
' z ' 3,4-dichlorobenzoate
Mol.Wl. 330
ABC Of
Use Fungic.
LDjo 2,500
Ref.
1
2
3
4
5
6
F
5620 PIPERONVL BUTOXIDE c1QH,n°i; a-[2-(butoxyethoxy)ethoxy]-
19 30 5 4,5-methylenedioxy-2-propyl=
toluene
Mol.WI. 338.5
A B C D E F
Use Synergist
LDjo 7,500
1
2
C
AB
75
II
47/4
674
12
3
c
fo
R.f.
H
N-C-S-P(OCH3)2
H
-------
Code Common Name Emp. Form.
Chemical Name
Structure
5632 PIRIMICARB (Pirimor) C11H18N4°2 2-(Dimethylamino)-5,6-dimethyl-
4- pyrimidinyl dimethylcarbamate
CH °
Mol.Wl. 238 | II
A B C D E F CH ^\ ,O— C— NlCh
usw April c.
I Dso 147
Ref
1
2
3
4
5
6
41
9
a
1 1
^^V^
N(CH3)2
t
5642 PIRIMIPHOS ETHYL C,.,H,
(Primicid)
.N,0,PS 0-[2-(Diethylamino -6-methyl-4-
J pyrimidinyl] 0,0-diethyl
phosphorothioate
(~ H
Mol. Wl. 333 1 n3
A B C D E F J^
Use Insectic.
I 050 140-200
Ref.
1
2
3
4
5
6
41
4,9
au
S | N
C2H50)2P-0X^N;^N(C2
5643 PIRIMIPHOS-METHYL C, ,H,nN,0-,PS 0-[2-(Diethylamino)-6-methyl -4-
(Actellic) M<;UJJ pyrimidinyl] 0,0-dimethyl
phosphorothioate
S
Mol.Wl. 305 ||
AB C DEF ..„ _ /-, _ n Ir^r-L.
Use Insectic.
LDW 2,050
Ref.
1
2
3
4
5
41
AW
74
11/1
17
4,9
10
ajot
c
M3L.\,^ \/
T if
1 II
N. N
V
N(C2H5)2
POLYCHLORI MATED BIPHENYLS
5700 AROCLOR 1016
C.0H-.CK Polychlorinated biphenyl with
12 ' 3 41.5?. Cl
Mol.Wt. 257.5
Use Industrial
LDjo 2,300
1
2
3
4
5
6
AL
AD
At,
AJ
AD
AL
74
71
70
73
69
73
57
6
42
21
4
56
576
377
1483
87
128
188
2
2
2
2
2
5
k
j
t
k
X
X
-------
Code Common Name Emp. Form. Chemical Name
Structure
5701 AROCLOR 1221
C ,H nCl, . Polychlorinated biphenyl with
12 8.8 1.2 m cl
Mol.WI. 196
Ufe Industrial
I "so 3,980 (undiluted)
A B C D E f
Ref.
1
2
3
4
5
6
See
5700
ci
,2
5702 AROCLOR 1232
CT>HO icli n Polychlorinated biphenyl with
12 8.1 1.9 m C1
Mol. Wl. 219
U«e Industrial
I D50 4,470 (undiluted)
A B C D t f
1
2
3
4
5
6
See
5700
Cl
1.9
5703 AROCLOR 1242
C,,H, nCl, , Polychlorinated biphenyl with
,,, n, ,
12 6.9 3.1
42|8 c,
Mol.W). 258
Uie Industrial
l*>50 8,650 (undiluted)
ABC Off
Ref.
1
2
3
4
5
6
See
5700
/~X^~
5704 AROCLOR 1248
C,_H
12 6.1 3.9
Polychlorinated biphenyl with
48% Cl
Mol.Wt. 289
Use Industrial
LDso 11,000 (undiluted)
Ref.
A B C Off
1
2
3
4
5
6
See
5700
5705 AROCLOR 1254
C.-H.C1,
12 5 b
Polychlorinated biphenyl with
54% Cl
Mol.WI. 326
Use Industrial
11,900 (undiluted)
Ref.
A B C D I f
1
2
3
4
5
6
See
5700
65
-------
Code Common Name Emp. Form. Chemical Name
Structure
5706 AROCLOR 1260 C^H.
..Cl Polychlorinated biphenyl with
•' 6-J 60% Cl
Mol. Wt. 371 fi *\ ft >\
Use Industrial
LD50 10,000 (50% sol.
in corn oi 1 )
Re*.
5707 AROCLOR 1262 C^H,
2
3
4
5
6
See
5700
\— - / \ ?(
CI6.3
9C1C D Polychlorinated biphenyl with
•^ b'B 62% Cl
Mol.Wl. 388
AS C D E F f, ^ ft ^
Use industrial
IDjo 11,300 (50% sol.
in corn oil)
Ref.
.
1
2
3
4
5
6
See
5700
// \\ // Vv
\ / \ \)
V^ __/ \ . /\
6.8
POLYCHLORINATED NAPHTHALENES
5720 HALOWAX 1000
c 7*-li T Polychlorinated naphthalene
"•' U with 26« CL
Mol.Wt. 171.5
Use Industrial
IDjo
A 8 C D E F
Ref.
5721 HALOWAX 1001
C H Cl Polychlorinated naphthalene
10 4.5 3.5 Wlth 5OT cl
Mol. Wl. 249
u«« Industrial
I D50
A B C D E F
Ref.
66
-------
Code Common Name Emp. Form. Chemical Name
Structure
5722 HALOWAX 1013 ClnH, ,C1. . Polychlorinated naphthalene
10 3.b 4.4 wUh 5M n
Mol. Wt. 279
u«« Industrial
LDjo —
A B C D I f
Hef.
5723 ' HALOWAX 1014
C-,^H^ ccljr c Polychlorinated naphthalene
10 2.5 5.5 with 6M C1
Mol.Wt. 314
Uie Industrial
A B C
Ref.
5724 HALOWAX 1051
C, H Cl Polychlorinated naphthalene
10 0.1 7.9 Wlth 7W C1
Mol.Wt. 400
Use Industrial
IDM
A B C D I f
Ref.
5725 HALOWAX 1099
IU 4.^ i.u Wlth 52« ci
Mol. Wt. 258
A B C D E F
U*e Industrial
l D50
Ref.
1
2
3
4
5
6
67
-------
Code Common Name Emp. Form. Chemical Name
Structure
5728 POTASSIUM AZIDE KM Potassium azide
(Kazoe), (See 6172-NaN3) 3
Mol. Wl. 81.1
Herbic., Fungic.,
Ule Nematoc., Insectic.
L 0,0 60-80
R.f.
5731 POTASSIUM DIETHYL DI= C.H,
THIOPHOSPHATE (KDEDTP) 4 '
A B C D E F
1
2
3
4
5
6
7A
12
au
K — N=N=N
Q02PS2K Do
Mol.Wt. 224 c
n v Organophosphorous
derivative
R.f.
5732 POTASSIUM DIETHYL CAH1
A B C D E F
1
2
3
4
5
6
A
6,A,(2),
(a)
4
m
*j
\\
(C2H5O)2 P — S — K
gOjPSK DO
Mol.Wt. 208 S
Organophosphorous
Use derivative
R.f.
A B C D E F
1
2
3
4
5
6
A
6,A,(2),
(a)
4
m
I
(C2H5O)2 P— O— K
5733 POTASSIUM DIMETHYL DI= C.H PS K Do
THIOPHOSPHATE (KDMDTP) ' b i
Mol.Wt. 196
Organophosphorous
e derivative
I DJO
R.f.
5734 POTASSIUM DIMETHYL C_H
THIOPHOSPHATE (KDMTP) '
A B C D E F
1
2
3
4
5
6
A
6, A, (2),
(a)
4
m
II
(CH3O)2 P— S — K
6°3PSK D°
Mol. Wl. 180 <;
., Organophosphorous
derivative
L D50 —
Ref.
A B C D E F
1
2
3
4
5
6
A
6, A, (2),
(a)
4
m
*j
II
(CH30)2 P— O-
-------
Code Common Name Emp. Form.
Chemical Name
Structure
5752 PROMECARB C H NO,, m-Cym-5yl methyl carbamate
(Carbamult) u "' L
Mol.Wt. 207 CH(CH3)2
ABC D E F ^ , 0 H
Use Insectic.
I DM 78-90
Ref.
1
2
3
4
5
6
BE
AL
AL
7Q
70
74
73
I
57/3
56/3
197
570
713
12
3
2
2
j
ad
a
a
/ \ " '
^^0-C-N-CH3
/
CH3
5760 PROMETON (Pramitol) C H NO 2,4-Bis(isopropylamino -
10 19 5 6-methoxy-s-triazine
OCH3
Mol. Wl. 225 JL
A B C D E F M^ K.I
Uie Herbic.
LOso 2,980
Ref
5780 PROHETRYN (Caparol) C,nH1
1
2
3
4
5
6
AJ
ZJ
ZD
74
69
70
22
17
32
139
309
371
2
19
20
f
d
II
(CH } C-NI'^ x^N-C(CH )
J * 1 IN | *
H H
aHfS 2,4-Bis(isopropylamino -
' 6-(methylthio)-s-triazine
SCH3
Mol. Wl. 241 ^~>^
A B C D E F N*^ N
Uu Herbic.
I D,o 3,800
Ref.
1
2
3
4
5
6
C
AJ
65
II
13/2
120
6,12
10
ajot
X
H | H
(CH3)2C-Ny%K|./^N-C(CH )
H H
4090 PRONAHIDE (Kerb) C H Cl.NO 3,5-Dichloro-N-(l ,1-dimethyl-
2-propynyl )benzamide
Mol.Wt. 256 CL
Use Herbic.
ID» 8,350
Ref.
A B C D E F
1
2
3
4
5
6
AL
AJ
72
72
55
20
802
1233
2
2
ajo
pu
jmn
op
f\?-K-C-CSCH
cH7^ ih3
5820 PROPACHLOR (Ramrod) C H.4C1NO 2-Chloro-N-isopropylacetanil ide
Mol.Wt. 212
UM Herbic.
LDjo 1 ,580
Ref.
A 8 C D E F
1
2
3
4
5
6
C
II
3
a
r, \\ CH(CH3)2
V VN-C-CH2CI
\ — / 6
69
-------
Code Common Name Emp. Form.
Chemical Name
Structure
5840 PROPANIL (Rogue)
Mol.Wt. 218
Use Herbic.
LDso 1,384
C H Cl.NO 3,4-Dichloroproplonanilide
Ref.
1
2
3
4
5
6
C
AD
ZJ
RE
65
70
73
II
3
18
32
7
464
77
2,12
2
2
11
:jop
0
cu
dk
^\ O
\N-C-
C2H5
5160 PROPARGITE (Omite)
Mol. Wt. 350.5
Use Acarlc.
L Dso 2,200
Re*.
2-(p-terf-Buty1phenoxy)cyclohexyl =
2-propynyl sulfite
1
2
3
4
5
6
C
AC
AJ
AJ
AD
73
72
71
73
11
7
20/1
19/5
12/6
355
59
894
641
6
20
4
4
16
eh
-
aeh
e
e
C(CH3):
O-S-O-CH2-C=CH
H
O
5800 PROPAZINE (Milogard)
Mol.Wt. 230
Use Herbic.
5,000
2-Chloro-4,6-bis(isopropylamino)
s-trlazlne
1
2
3
4
5
6
C
AJ
AJ
74
65
II
22
13
139
120
12
2
21
be
f
be
H
Cl
H
^-C(CH3)2
H
5860 PROPHAM (IPC)
C H NO Isopropyl N-phenylcarbamate
Mol.Wt. 179
U»« Herbic.
ID50 4,250
1
2
3
4
5
6
AJ
GB
69
73
17
9
1062
261
12
12
a
a
O
N-C-O-CH(CH
H
32
0440 PROPOXUR (Baygon)
Mol. Wl. 209
Use Insectic.
L DSO 100,
;
C11H15N°3
Ref.
cj-Isopropoxyphenyl
N-methylcarbamate
1
2
3
4
5
6
AL
AJ
AC
AJ
AL
AJ
75
72
73
73
73
72
58/3
20/6
7
17
56/6
20/6
562
1269
163
56
1319
1265
2
2
20
2
2
2
aef
jo
-
a
u
a
-------
Code Common Name Emp. Form.
Chemical Name
Structure
5882 PROTECT C,,H£
Mol.Wt. 198
Use Seed Protectant
I DM 12,300
Ref.
5905 PYRACARBOLIO (Sicarol) C^H
Mol.Wt. 203
Ut« Fungic.
LDso 15,000?
Ref.
5925 PYRAZON (Pyramin) C10Hg
Mol.Wt. 222
Use Herbic.
L DM 2 , 500
Ref.
5932 PYRAZOPHOS (Afugan) C.,H
Mol. Wt. 349
U»e Fungic.
L Dso 140-632
Ref.
5940 PYRETHRINS MIXTL
Mol. Wt. ---
U«e Insectic.
I D50 820-2,600
0, 1,8-Naphthalic anhydride
3
f/ — ^\ ^
A B C D E F (' \ f
1
2
3
4
5
6
3Z
2
a
tn
, cOo 3 ,4-Di hydro-6-methyl -N-phenyl -
2H-pyran-5-carboxamide
OH
ABCDEF || // ^
1
2
3
4
5
6
C1N,0 5-Amino-4-chloro-2-
phenyl-3(2H)-pyridazinone
A B C D E F
2
3
4
5
6
AF
BH
68
71
29/3
11/4
8993
257
21
19
u
X
nN OrPS 2-(0,0-Oiethyl thionophosph
5-methyl-6-carbethoxy-pyraz
(1 ,5a)pyrimidine
A B C D E F
1
2
3
4
5
6
GE
WD
4E
73
70
267/3
49/2
173
325
2,3
11
4
a
X
a
RE Standardized mixture of
pyrethrins I and II (Mixed
esters of pyrethrolone
A £ C D E F
1
2
C
D
II
2,12
21
ajo
a
Dryl)-
Dlo=
o
II
C2H5O— C ^^
\ ^f'^-fi M
HaC^jsi-^^X^o— P(OC2H ),
f,\
** "T"'
^..^w, ""V.1^.
Ref.
-------
Code Common Name Emp. Form.
Chemical Name
Structure
5966 QUINALPHOS (Ekalux)
C.-H N 0 PS 0,0-Diethyl 0-[qu1noxa=
12 15 2 3
11nyl-(2)] thionophosphate
Mol.Wl. 298
A B C Off
Use Insectic,
IDM 65-135
Ref.
6055 RESMETHRIN (SBP-1382) CnoH,
1
2
3
4
5
6
AD
GI
7M
74
69
11/2
22
121
218
9
10
21
ade
X
au
0 (5-Benzyl-3-furyl)methyl-2,2-di=
° methyl-3-(2-methyl propenyl )
cyclopropane-carboxyla!;e (approx.
70? trans, 30% cis isomers)
Mol.Wl. 338
A B C D E F
Use Insectic.
LDso ca. 1,500
Ref.
1
2
3
4
5
6
3Q
8
w
5980 RONNEL CnH0Cl,0,PS 0,0-Dlmethyl 0-(2,4,5-tri=
chlorophenyl ) phosphorothioate
Mol.Wl. 321.5
A B C D I f
U" Insectic.
!• °fO 1,740
Ref.
6000 ROTENONE C?1H?
1
2
3
4
5
6
C
C
A
AL
74
I
II
8B.10A
57
1033
11
12
4
4
a
e
tv
t
206 l,2,12,12a, Tetrahydro-2-isoprop=
enyl-8.9-dimethoxy-["i 1 benzo=
pyrano-[3,4-b]furo[2,3-b][l]
benzopyran-6(6aH)one
Mol. Wl. 394
A B C D E F
Use Insectic.
1 DJO 132
Ref.
1
2
3
4
5
6
AL
AN
AL
WD
73
70
69
74
56/6
8/5
52/1
95/2
1343
276
182
243
3
10
11
11,14
aw
a
a
X
6050 SALITHION C H 0 PS 2-Methoxy-4H-l ,3,2-benzo=
dioxaphosphorin-2-sulf ide
Mol.Wt. 216
A B C D E f
Use Insectic.
LDso 91 (mouse)
Ref.
1
2
3
4
5
6
JG
72
21
9
10
1
S—O—P(C2H50)2
CH3-C=CH
CH3
CH,
S
0-P(OCH3)2
Cl
H,CO
OCH
P-O-CH,
-------
Common Name Emp. Form.
Chemical Name
Structure
6100 SIDURON (Tupersan) c,,.H,nN,0 l-(2-Methylcyclohexyl)-
'4 '" <- 3-phenylurea
Mol. Wt. 232 ff \_|s(H-C-NH-{ )
ABCDEF \ / \ /
U(0 Herbic.
ID50 7,500+
Ref.
1
2
3
4
5
6
AJ
AM
7J
AL
69
66
69
74
17/5
4/11
17/1
57/1
1004
424
31
60
11
2
19
3
u
X
u
w
, , t
CH3
6120 SILVEX, ACID C0H7C1,0, 2-(2,4,5-Trichlorophenoxy)=:
[2-(2,4,5-TP)] ' ' J * propionic acid
CH3
Mol.Wt. 269.5 O-CH-COOH
ABCDEF A. f,
Uie Herbic.
I 050 650
Rof.
1
2
3
4
5
6
AJ
AX
IA
72
72
71
20
5
15
963
72
485
2
2
2
0
C
C
If J
JL J
Or^^
Cl
6130 SILVEX, ISOOCTYL ESTERS C]7H23C13°3 2-(2,4,5-Trichlorophenoxy)=
propionic acid, isooctyl
esters (mixed) ,~i_,
VH3
M...W,. 381.5 A . C D E F O'CH - COOC8H,7
U§e Herbic.
ID 50 400-800
Rof.
.
2
3
4
5
6
See
6120
^'\'C.
r I
o-^v^
T
a
6140 SILVEX, PROPYLENE GLYCOL C H Cl 0 2-(2,4.5-Trichlorophenoxy)=
BUTYL ETHER ESTERS 16 21 34 prop1onjc ac,-d> propylene
to glycol butyl ether esters QH
M.I.W.. 383.5-500 ^"""^ (W * ^^ O-CH-COO-(C3H6OJX-QH9
ABCDEF Ji^ ,_,
Uso Herbic.
l-Dso 650
Ref.
6160 SIMAZINE (Princep) C,H,0
1
2
3
4
5
6
See
6170
r ^ST"-'
1^ jf\
Cl^r Mixed esters
Cl
C1N. 2-Chloro-4,5,6-bis ethylamino)-
b s-triazine
a
Mol. Wl. 202 ^^
ABC D E F f\f^ N
Ut« Herbic.
I DM 5,000
1
2
C
AL
68
II
51
682
12
3
aceh
ctu
1
C2HsNH^Kix^NHC,H5
Ref.
73
-------
Code Common Name Emp. Form.
Chemical Name
Structure
6172 SODIUM AZIBE (Smite), NaN,
(See 2728 - KN3) J
Sodium azide
Mol. Wl. 65.02
u Herbic., Fungic.,
Nematoc., Insectic.
10JO 60-80
Ref.
A B
D E F
1
1
3
4
5
6
7A
12
au
No — N— N=N
2820 SODIUM PENTACHLOROPHENATE C.C1 rNaO.H_0 2,3.4.5,6-Pentachlorophenol .
(Dowicide G)
Mol.Wt. 306.5
Use Herbic.
210
6 5
A B
Ref.
sodium salt, monohydrate
1
2
3
4
5
6
AR
AL
AL
AJ
AJ
BG
66
74
69
73
69
70
31
56/2
52/2
21/2
17/4
4/8
742
389
294
295
871
533
21
2
2
2
2
2
e
t
jlm
m
ktu
kt
ONa-H2O
Cl
2800 SODIUM PHENYLPHENATE C,^HnNaO.H^O o-Phenyl phenol , sodium sal t,
(Dowicide A)
Mol.Wt. 210
Uie Fungic.
IDfo 1,160
12 9
monohydrate
A B
Ref.
E F
1
2
3
4
5
6
c
AL
71
II
54
See also
5490
975
12
11
def
de
ONa-Hp
3740 STIROFOS (Gardona)
Mol.Wt. 366
Use Insectic.
L D,o 4,000
C H Cl 0 P 2-Chloro-l-(2,4,5-trichloro=
10 9 4 4 phenyljvinyl dimethyl phosphate
Ref.
1
2
3
4
5
6
C
AP
70
II
63
1355
9
2
e
n
CIHC=C-0-P(OCH3):
32
6222 STREPTOMYCIN SULFATE C H N
(Agri-Strep) 21 39
3H,SO
Mol. Wl. 1457
Use Bacterioc.
L D50 —
24
[t-StrepL line, O-.'- eo\v-_'- mrihv :iminu)-o-I^c!' copvranos-
v!-f 1— ^^0-:-dc i >\ -S-C- . n nu 1- o- l^h \ofnrnnosvl-( 1 —4 )-
'V \''^i-inrint] .ifiuuj plhvK -irllatc CJ::j) l,all).
ABC D E F
Ref.
1
2
3
4
5
6
C
AL
AL
JI
72
70
71
II
55/4
53/1
11
714
54
133
19
17,19
19
3
e
g
g
X
HOHjC
-------
Code Common Name Emp. Form.
Chemical Name
Structure
6240 STROBANE CmHiiC17 Polychlorinates of camphene,
10 " ' pinene and related terpenes
(average)
Mol.Wt. 379 (average)
A B C D E F
Use Insectic.
LDM 200
Ref.
6300 SULFOXIDE C,nH,
1
2
3
4
5
6
C
II
12
9
OS l-Methyl-2-(3,4-methylane=
dioxyphenyl jethyl octyl sulfoxide
Mol.Wl. 324.5
. ABCDEF ^ ^f^ ,-,_, ,-L, crV/~i i \
Use Synergist
toy, 2,000-2,500
Ref.
1
2
3
4
5
6
AL
GM
64
47
264
21
11
X
:jop
H C ' \ If 2 ' ^v^-ni'>
^O-ks?. Jj 3
^•^^^
6360 SURECIDE (S4087) C H NO PS 0-(p-Cyanophenyl ) 0-ethyl
lb " ' phenylphosphonothioate
S
Mol.Wl. 303 C2H5O-P O
ABCDEF ,X 1
Use Insectic.
I "so 1,000
Ref.
1
2
3
4
5
6
8A
4,9
ac*>
r i r^^i
bs. J K
^xN/ ^vS /
T^
CN
6435 TECNAZENE (Fusarex) C HC1«NO, 2,3,5,6-Tetrachloronitrobenzene
Mol.Wt. 261
Fungic. &
u" Growth Regul.
IDj,, 100
Ref.
0020 TEMEPHOS (Abate) C, H
16 2
t £
A B C D E F
1
2
3
4
5
6
41
2
af
NO?
I T
*/"!
* '^^^Nv ^^^t
^^-^"^
OPS 0,0-Dimethyl phosphorothioate
u ° ^ J 0,0-diester with 4,4'-
thiodiphenol
Mol.Wt. 466
.... ABCDEF S S
Use Ins PC tic.
LDjo 4,000
1
2
WD
AB
71
71
59
43
1053
3
16
t
tw
. II /^X /^^N ''
(CHsOfeP-O-/ \_s_/ .VO-PI
^3'2
Ref.
-------
Code Common Name Emp. Form. Chemical Name
Structure
6540 TEPP
CHOP Tetraethyl pyrophosphate
o iU / £
Mol. Wt. 290
Us* Insectic.
LDso 1
A B
Off
Ref.
1
2
3
4
5
6
AL
70
53
1036
3
de
O O
(C2H50)2-P-0-P-(OC2H5)2
6560 TERBACIL (Sinbar) ' C H C1N,0, 3-(tert-Butyl)-5-chloro-6-
'91322
Mol. Wl. 217
Use Herbic.
ID50 5,000-7,500
methyluracil
A B
D I f
1
1
3
4
5
6
C
AO
68
II
16
54
6
6
be
aj
3980 TERBUTRYN (Igran) c,nH,As 2-(t«-t-Buty1amino)-4-(ethyl =
10 19
ami no)-6-(methylthio)~s-triazine
Mol.Wt. 241
U»e Herbic.
IDjo 2,100-2,900
D E f
S-CH3
6590 TERRAZOLE
C..H..C1 ,N,OS 5-Ethoxy-3-trichloromethyl-
.... ,
5 5 J
1,2,4-thladiazole
Mol.Wt. 247.5
Ui« Fungi c.
2,000 (mice)
D E F
Ref.
1
2
3
4
5
6
61
2
au
N
6600 TETRADIFON (Tedion)
Cl.O.S 4-Chlorophenyl 2,4,4-tri=
6 ' chlorophenyl sulfone
Mol. Wl. 356
Use Mitic.
I DM 5,000
D E F
Ref.
1
2
3
4
5
6
C
AL
AL
63
73
II
46
56
177
296
6,12
6
20
de
de
-
-------
Code Common Name Emo. Form.
Chemical Name
Structure
6630 TETRASUL (Animert)
C,,H,C1.S S-p-Chlorophenyl 2,4,5-
'264 trichlorophenyl sulfide
Mol.Wt. 324
Us* Acaric.
IDso 12,600
A B
D E F
Ref.
1
2
3
4
5
6
C
AL
FB
JA
JC
6V
73
69
74
69
II
56
62/635
38/2
18/11
296
75
279
1344
2
20
2,17
1,11
2
3
e
—
t
X
X
w
6640 THANITE
1 O 1 ^ C-
Mol.Wt. 253
ABC D
U» Insectic.
LDM 1,603
Ref.
1
2
3
4
5
6
AL
70
53/3
499
E
4
f
X
CH3 O
O-C-CH2-S-CN
C(Chi)2
6660 THIABENDAZOLE (Mertect) C H N S 2-(4'-Thiazolyl) benzimidazole
Mol.Wt. 201
Use
I D50 3,100
Fungic. 8
Anthelmintic.
Ref.
D E F
1
2
3
4
5
6
C
AL
AJ
AZ
72
72
71
II
55
20
84
1239
1227
272
14
11,14
12,14
12
ef
eg
e
e
6663 THIOFANOX (DS-15647) CnH.pN.O.S 3,3-Dimethyl-l-(methylthi'o)-2-buta=
W9"18"2U2
mone 0-[(methyl ami no)-carbonyl]oxime
Mol. Wt. 218
Use Insectic.
ID50 8.5
Ref.
A B C D E F
1
2
3
4
5
6
ZU
4
afg
tu
(cH3)3c—c:
O H
II I
—O—C —N—CH3
H2—S—CH3
6665 THIOMETON (Ekatln)
C H 0 PS 0,0-Dimethyl S-[2-(ethylthio)
° la ' J ethyl] phosphorodithloate
Mol.Wl. 246
Use Insectic.
IDso 107
.>
' Ref.
A B C D E F
1
2
3
4
5
6
7M
3
u
(CH3O)2 P-S-C2H4-S -C2H5
77
-------
Code Common Name Emp. Form.
Chemical Name
Structure
6670 THIOPHANATE C H
NOS l,2-Bis(3-ethoxycarbonyl-
8442 2-thioureido)benzene
Mol.Wt. 370 S O
ABC D E F ^ t ... Jl .... i
Use Fungic.
IDjo 15,000 (mice)
Ref.
6671 THIOPHANATE METHYL C,,H,
1
2
3
4
5
6
5Z
11
ade
U^ AMU r KH-I r n r M
-^/-NH-t. MM c u i_2n5
S 0
NOS. 1 ,2-Bis(3-methoxycarbonyl-
2-th ioureido) benzene
Mel. Wl. 342 S O
r . A B c D E F ^\_KiH-r-MH-r-n-a-i.,
Use Fungic.
L Den ^ Rid fmirol
1 i*50 J,si4 ^micej
Ref.
1
2
3
4
5
6
5Z
12
ade
l"*i _X_v_ILJ /" K.II 1 f~ r*"^ f H
^^~^ ii u
S O
6680 THIRAM (Arasan) C H^N^ Tetramethyl thiuram disulfide
Mol. Wt. 240
A 8 C Off
Use Fungic.
L D50 780
Ref.
1
2
3
4
5
6
C
B
AL
AL
AL
IB
69
70
71
70
II
12.000-
.206
52
53
54
45
1226
519
327
220
12
12
4
12
20
12
cde
a
c
...
X
s s
(CH3)2N-C-S-S-c!:-N(CH3)2
6740 TOXAPHENE A mixture of chlorinated camnhpnp
compounds of uncertain identity
(combined chlorine 67-69")
Mol.Wt. — -
A B C D E F
Use Insectic,
LDso 90
Ref.
2
3
4
5
6
C
AL
BG
AD
AJ
70
70
68
60
II
53
4
3
8
524
547
71
286
12
M2
10
2
12
e
b
ktu
a
a
6770 TRIALLATE C H Cl NOS S-(2,3,3-Trichloroal lyl )di=
10 1° 3 isopropyl thiocarbamate
Mol.Wt. 305
A B C D E F n
Use Herbic,
ID,,, 1,675-2,165
Ref.
1
2
3
4
5
6
AJ
WD
FB
67
74
69
15
97
62
935
103
214
2
2
2
cu
u
t
[(CH3)2CH]2N-C-S-CH2CCI=C
78
-------
Code Common Name Emp. Form.
Chemical Name
Structure
6777 TRIAZOPHOS (Hostathion) C H N OPS 0,0-Diethyl 0-(l-phenyl-lH-
12 16 3 3 1,2,4-triazol-3-yl)phos=
Uu
Mol.Wt. 313
Insectic., Mitic.,
Nema toe.
L Dso 82
Raf.
phorothioate
1
2
3
4
5
6
GE
4E
73
267/3
173
2,3
4
a
a
N —N
L 1 t
^NA_T
6780 TRICHLORFON (Dylox)
C4H8C13P04
Dimethyl (2,2,2-trichloro-l-
hydroxyethyl)phosphonate
Mol. Wt. 257
Uu Insectic.
t DM «0
Raf.
1
2
3
4
5
6
C
AD
AJ
AJ
AD
AJ
74
73
66
71
68
II
11/1
21/6
14/5
6/1
16/5
78
1095
508
55
808
2,6
4
4
2
4
11J7
ajo
j
atu
adj
X
X
O
(CHP)2P-CH-CCI3
OH
6890 2,4,5-TRICHLOROPHENOL
(Dowicide 2)
Mol.Wt. 197.5
Uta Fungic.
LD,o ca. 800
C H Cl 0 2,4,5-Trichlorophenol
633
Raf.
A B
D E F
1
2
3
4
5
6
AJ
72
20
963
2,6
0
6792 TRIDEMORPH (Calixin)
C H NO N-Tridecyl-2,6-di=
'' 39 methylmorpholine
Mel.WI. 297.5
Uia Fungic.
LD,o 650
Raf.
A B C D I f
1
2
3
4
5
6
CH,
6800 TRIFLURALIN (Treflan)
C H F N 0 a,a,ci-Trifluoro-2,6-dinitro-
13 16 3 3 4 N,N-dipropyl-p-toluidine
Mel. Wt. 335
U»» Herbic.
1 "so 3,700
Raf.
1
2
3
4
5
6
C
AJ
AJ
WO
WD
AN
74
72
74
71
72
II
22
20
97
57
10
79
829
103
303
176
2,11
12
2
2
11
2
be
tu
u
u
tu
u
N(CH2CH2CH3)2
CF,
-------
Code Common Name Emp. Form.
Chemical Name
Structure
6822 TRIFORINE (CELA W524) C._H,
10 1
.Cl.N.O,, N,N'-[l-4-Piperazinediyl-bis>
* (2,2,2-trichloroethylene)]-bis- u
(formamide) Y
fl C
Mol. Wt. 435 3 7
.. _ . _ A B C D E F ^NK
use rungic.
L DJO 16,000
Ref.
1
2
3
4
5
6
f j]
\ /
1
CI3-C —
H
6840 2,4,5-T, ACID C H Cl 0 2,4,5-Trichlorophenoxyacetic acid
— -^— — • 85 33
MU m/~\
-NH-CHO
M.I.W.. 255.5 ABC D E F Q-CH2COOH
Uie Herbic.
IDfO 500
Ref.
6860 2,4,5-T BUTOXYETHANOL C,.H,
ETHER ESTERS '4 '
1
2
3
4
5
6
AJ
AL
WO
AI
BE
WD
74
69
71
71
72
72
22
52
57
1
3/4
69
453
187
303
23
371
204
2
2
11
2
6
2
tu
t
tu
m
d
u
QNXX'
r
T
\.
s
1
[
Cl
?C1.0. 2,4,5-Trichlorophenoxyacetic acid,
mixed ether esters of butoxyethanol
and isobutoxyethanol
o
Y
Mol.Wt. 355.5 OCH2CO(CH,)2O(CH2),CHn
A B C D E F ^#^CI O
Use Herbic.
LDso ca. 500
Ref.
6870 2,4,5-T, BUTYL ESTERS C,0H,
1
2
3
4
5
6
See
6840
JLJ Sad. OCH2CO(CH2)2OCHCH2CH3
^ ^VQ CH3
K^ U
1^^
Cl
Cl 0_ 2,4,5-Trichlorophenoxyacetic
333 acid, butyl esters (mixed)
Mol.Wt. 312 Cl
Use Herbic.
H>50 ca. 500
Ref.
A B C D E F
1
2
3
4
5
6
See
6840
o
y=/
cf
6880 2,4,5-T, ISOOCTYL C H Cl 0 2,4,5-Trichlorophenoxyacetic
ESTERS '6 21 33 acid, isooctyl esters (mixed)
o
)-OCH2COC4H9
MOI. wt. 368 O-CH2-COO-C8H17
A B C D E F r.t ^*\
Uie Herbic.
L D50 ca. 500
Ref.
.
2
3
4
5
6
See
6840
...
V-l-J^
^S\NH JS
T^
Cl
1
[
C
-|
-1
80
-------
Code Common Name Emp. Form.
Chemical Name
Structure
6885 2,4,5-T, PROPYLENE GLYCOL 1. C,,H. 0C1,0, 2,4,5-Trichlorophenoxy=
BUTYL ETHER ESTERS u ls J * acetic add, propylene
2. C.,.H,,,C1..0, glycol butyl ether esters _
, r I n o {m1xe'd) 9 r 1 , »
Mol.Wt. 3925 (average) 3- C21H32C13°6 OCH,CO RCH2)3OL(CH2)-
ABC DEF I L -1* *
U» Herbic.
ID 50 ca. 500
Ret.
6895 2,4,5-T, TRIETHYL- C H
AMINE SALT '4 '•
1
2
3
4
5
6
AJ
69
17
See also
6840
1168
6
1m
f^^^ x-i.a.
1
>•• JLv^ J
CI'^-X
Cl
Cl 0 N 2,4,5-Trichlorophenoxyacetic
0 J J acid, triethylamine salt
M.I.WI. 357 OCH2COOH-N(C2H5)3
A B C DEF ^^ r,
Uie Herbic.
LDjo 500 (acid basis)
Kef.
6900 4-(2,4,5-TB) C H,
1
2
3
4
5
6
See
6840
C'^V^
a
Cl.O. 4-(2,4,5-Trichlorophenoxy)=
butyric acid
M.,.w,.284 0(CH2)3CCOH
U» Herbic.
1 BSO 650
R«f
A B C DEF
1
2
3
4
5
6
Clri
I
^x^X^CI
Cl
6920 2.3,6-TBA C H Cl 0. 2.3.6-Trichlorobenzoic acid
'3 32 an(j reiated compounds:
2,3,6-TBA 60.65% 2,4,6-TBA 2,6%
2,4,5-TBA 26.3 Tetra and dichloro-
Mol.Wi. 225 2,3,4-TBA 9.35 benzoic acids 1.1% COOH
A B C DEF ^
U«» Herbfc.
1 DSO ca. 750
R«f
1
2
3
4
5
6
AL
AJ
WD
71
68
71
t
54/4
16/6
57/2
966
908
303
2,6
2
11
efo
ac
u
r ii
I \
%v
CI3
7013 VENDEX Sn?OCfinH?R Hexakis (B,B-dimethylphenethyl )-
distannoxane
Mol.Wt. 1052
Uu Hi tic.
LOjo 2630
Ref.
ABC DEF , , , CH3 ^ „ CH3 , ,
1
2
3
4
5
6
(I Vc -CH2-JSn-O-Sn(-CH2-C -\
^-^CH3 *4 ^- 2 083^^
i)3CH3
-------
Code Common Name Emp. Form.
Chemical Name
Structure
7020 VERNOLATE (Vernam)
C, H_,NOS S-Propyl N,N-dipropyl=
10 21
thiocarbamate
Mol.Wt. 203
Use Herbic.
LDM 1,800
Ref.
1
2
3
4
5
6
C
AJ
7Z
AC
60
67
II
8
5
214
537
6
12
4
20
fg
a
cf
-
CH3(CH2)2-S-C-N(C3H7)2
7060 WARFARIN
Mol.Wt. 308
Use Rodentic.
IDso 323
C19H16°4
R«f.
3-(a-Acetonylbenzyl)-
4-hydroxycoumarin
1
2
3
4
5
6
BA
OC
67
69
92
18
192
943
12
15
X
X
7120 ZINEB
Mol. Wt. 276
U»e Fungic.
I C>50 5,200*
(C H N S Zn) Zinc ethylenebisdithio=
(polymeric)
carbamate
Ref.
1
2
3
4
5
6
C
AL
AL
AJ
67
71
72
II
50
54
20
1102
1120
967
12
12
12
2
X
a
c,f
e
\S
-S-^-NH-CH,
CH,-NH-C-S-Zn-
7100 ZIRAM
C H N 5 Zn Zinc dimethyldithiocarbamate
Mol. Wl. 306
Use Fungic.
I D50 1,400
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
-------
Code Common Name Emp. Form.
Chemical Name
Structure
ADDENDA
0425 BENTAZON {Basagran)
3-Isopropyl-lH-2,l,3-benzothia=
diazin-(4)3H-one 2,2-dioxlde
Mol. Wl. 240
U» Herbic.
I DSO 1,100
Ref.
1
2
3
4
5
6
WD
1Q
73
76/1
272
11
1,4
X
igtu
,CH3
SO,
4840 NABAM
Disodium ethylene bis=
(dithiocarbamate)
Mol.Wt. 256
U» Fungic.
395
Rof.
1
2
3
4
5
6
AL
GF
69
71
52
14
162
707
12
12
a
a
s
CH2-NH-C-S-Na
CHj-NH-C-S-Na
S
83
-------
Section I,b
LIST OF COMPOUNDS DELETED FROM STOCK
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.
The following 88 compounds listed in our 1973 Index have been deleted
in this edition for one of the above reasons:
Akton
Alar
Aldicarb Oxime Sulfone
Aldicarb Oxime Sulfoxide
Aldicarb Sulfone
Aldicarb Sulfoxide
Amidithion
Ammonium Sulfamate
*
Banamite
Bandane
Basamaize
Benazolin
Benzomate
Binapacryl
Bismuth Subsalicylate
Bomyl
Bromoxynil Octanoate
Bulan
Buturon
Cartap Hydrochloride
*Anot
CECA
Chlorbromuron
Chlorflurenol
Chlormequat Chloride
Chioronitropropane
Chloropropylate
Chloroxuron
Chiorthiamid
Copper 8 Quinolate
Coumachlor
Coumatetralyl
Cyano (methylmercury) guanidine
Cyanox
DAEP
Dazomet
o,p'-DDA
Deet
Demeton (mixed isomers;
individual isomers
still stocked)
Desmetryn
84
-------
Oil an
Dimethrin
Dlnobuton
Di ram
Fenuron
Fenuron-TCA
Fluorodifen
Gophacide
Hexachloroacetone
Hormodin
lodofenphos
Isothan
Landrin-3,4,5 isomer
Landrin-2,3,5 isomer
Lethane 60
Memmi
Metabromuron
Methyl Carbophenothion
Metribuzin
MGK R 11
MGK 264
MGK 326
MGK R 874
Niclosamide
Norbormide
Norea
OCS-21693
Pentac
Phosfon
Rival
Plantvax
Plictran
Pro!an
Propyl Isome
Pyramat
Pyriclor
Sabadilla
Sulfaquinoxaline
Sulphenone
Sumitol
SWEP
Tabatrex
TCA
Terbutol
Tetramethrin
TIBA
Tutane
Vancide TH
Zoalene
85
-------
Section II
THE HANDLING AND STORAGE OF ORGANOPHOSPHOROUS PESTICIDES
Samples of organophosphorous pesticides that are to be used as analytical
standards should be carefully protected from possible decomposition. Because
the rate of decomposition increases with temperature, organophosphorous pesti-
cide standards should be refrigerated. They should be stored tightly closed in
a refrigerator kepts at 0°C to 5°C. Minute traces of moisture also enhance the
decomposition rate, so that the sealed bottles should be placed in a desiccator
while inside the refrigerator. If a desiccator cannot be spared, a large, wide-
mouth jar can be substituted by placing some desiccant in the bottom of the jar
and the standards bottles on a platform. This storage system minimizes moisture
pickup while helping prevent vapor from.permeating the entire refrigerator.
When a sample is removed from the refrigerator for use, its temperature
should be permitted to fully equilibrate with that of the room, preferably
under continuous desiccation. The sub-sample should be removed as quickly as
possible and the bottle resealed and returned to refrigerated storage as rapidly
as possible.
These compounds should most emphatically NOT be stored for undue periods
of time even at low temperature,, It is recommended that after a year the
standard be discarded in a safe manner and a fresh standard be requested, A
six-month period is even safer.
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 on 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, a physician should be consulted AT ONCE.
86
-------
Section III
PREPARATION AND STORAGE
OF PESTICIDE ANALYTICAL STANDARDS
A. 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, inverted I stopper, 30 ml, Corning 1560.
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.
8. Bottles, prescription, graduated, with molded plastic screw caps,
sizes 1/2 and 1 oz. (available from most wholesale drug suppliers).
9. Cap liners, Teflon, sizes 13, 15, and 18, Arthur H. Thomas 2390.
10. Primary pesticide standards. Available from the Repository at
Research Triangle Park, North Carolina in 1/4 oz. bottles with
foil-lined molded screw caps.
NOTE: The organophosphorous compounds are subject to a wide v? ^ cy
of oxidations, rearrangements, and hydrolytic reactions. Thes
should be stored in the refrigerator in a large air-tight container
(such as a wide-mouth mayonnaise jar), or in a desiccator, to mini-
mize moisture absorption, release of toxic vapors, or cross-contami-
nation. ALL HANDLING OF THESE STANDARDS SHOULD BE DONE WITH RUBBER
OR DISPOSABTE PLASTIC GLOVES. SKIN CONTACT WITH HIGH CONCENTRATES"
CA"N RESULT IN ILLNESS OR DEATH.
11. Isooctane (2,2,4-trimethylpentane) or hexane, pesticide quality,
distilled in glass.
NOTE: (1) A 10 u 1 injection of the solvent to be used should
result in a chromatogram with zero background.
87
-------
(2) Isooctane or hexane are both suitable for standard dilutions.
Isooctane, while more expensive, offers the advantage of a 100°C
boiling point and is therefore less subject to evaporation from
repeated opening of bottles, particularly of working standard
mixtures.
12. Benzene, pesticide quality, distilled in glass.
B. 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 hexane is suitable as the solvent for most of the
primary standards. A few compounds, however, dissolve in hexane
with great difficulty, but readily in benzene, with stirring and a
slight application of heat from the hot water bath. 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.
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
88
-------
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.
3o 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.
C. CONTAINERS FOR STANDARD SOLUTIONS
Volumetric flasks are, of course, the recommended glassware for prepa-
ration of all standard solutions. However, these containers are not
suitable for storage primarily for the following reasons:
1. An inordinate amount of valuable refrigerator space is required for
the storage of a 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. Although these bottles are expensive, large
numbers are not required in most laboratories. The cap has an inner
J joint that slips down over the outer J joint of the bottle, thus
affording complete protection of the mouth of the bottle from conta-
mination. The inverted-stopper bottles present one problem in the
tendency of the cap to pop off during the equilibration period from
freezer to room temperature. They require some watching.
89
-------
If desired, these same inverted-stopper bottles may be used for
storing the standards of intermediate concentration. However,
laboratories on a limited operating budget may prefer to use a
less expensive container such as the graduated prescription bottles
described in Item 8 of the equipment list. When the Teflon liners
are used (Item 9), these provide a wholly suitable container and
store well. The No. 15 liner is needed for the 1/2-oz. bottle cap
while the 1-oz. bottle cap takes a No. 18 liner.
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. prescription bottles
fitted with Teflon-lined screw caps. These should be stored in
the refrigerator at all times when not in use. Organochlorine
(OGC) working standards should be renewed monthly and the
organophosphorous (OGP) compounds semimonthly.
Method B
The working standard mixtures are transferred from the volumetric
flasks into 1-dram vials (Item 7) fitted with Teflon-line screw
caps (No. 13). The set of standards needed for immediate use
may be conveniently fitted in a small block of polystyrene into
which holes have been cut with a rattail file to a size that will
snugly accommodate the vials. The remainder of the filled vials
will be stored at -10 to -15°C.
The OGC 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 dis-
carded solutions. Vials of OGP solutions, however, should be
kept in the refrigerator at all times when not in use. Vials of
OGC compounds that are kept frozen can be held in the freezer for
up to 6 months, whereas frozen OGP compounds should be discarded
after 4 months.
90
-------
Table 1
SUGGESTED CONCENTRATIONS OF STANDARD SOLUTIONS
OF INTERMEDIATE CONCENTRATION
CHLORINATED
ng/yl
ORGANOPHOSPHOROUS
ng/pl
a-BHC 1
g-BHC 2
Lindane 1
Heptachlor 1
Aldrin 1
Heptachlor epoxide 1
o.p'-DDE 1
p.p'-DDE 2
Endosulfan 4
DDA (methyl ester) *
Dieldrin 2
o.p'-DDD 2
Endrin 4
Perthane *
p,p'-DDD 4
o.p'-DDT 4
p,p'-DDT 4
Oil an 10
Methoxychlor 10
Tetradifon 20
Mi rex 10
Chlordane 10
Toxaphene *
Mevinphos 50
Phorate 50
Dimethoate 40
Diazinon 20
Methyl parathion 10
Ethyl parathion 10
Malathion 20
Ethion 20
Carbophenothion 10
Azinphos (methyl or ethyl) *
Dichlorvos 2
Dioxathion 20
Ronnel 10
Fenthion 4
Phosphamidon 50
Folex 30
DEF 10
Phencapton 50
Monocrotophos *
EPN *
Imidan *
Coumaphos 50
Disulfoton 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 qualtiy). Isooctane should be considered because of its
higher boiling point, hence reduced possibility of evaporation of solvent
when container is repeatedly opened.
91
-------
Table 2. Commonly used dilution
concentrated soln. required per
Value at head of
values. Values in left columns are the ml of
100 ml to arrive at the cone, values given in the
each column is the concentration of the stock soln.
lug/ul
ml ng/ul
50
47.5
45
42.5
40
37.5
35
32.5
30
27.5
25
22.5
20
17.5
15
12.5
10
9.5
9
8.5
8
7.5
7
6.5
6
5.5
5
4.5
4
3.5
3
2.5
2
1.5
1
0.5
500
475
450
425
400
375
350
325
300
275
250
225
200
175
150
125
100
95
90
85
80
75
70
65
60
55
50
45
40
35
30
25
20
15
10
5
200 ng/pl
ml ng/yl
50
47.5
45
42.5
40
37.5
35
32.5
30
27.5
25
22.5
20
17.5
-15
12.5
10
9.5
9
8.5
8
7.5
7
6.5
6
5.5
5
4.5
4
3.5
3
2.5
2
1.5
1
0.5
100
95
90
85
80
75
70
65
60
55
50
45
40
35
30
25
20
19
18
17
16
15
14
13
12
11
10
9
8
7
6
5
4
3
2
1
20 ng/
ml p
5
4.875
4.75
4.625
4.5
4.375
4.25
4.125
4
3.875
3.75
3.625
3.5
3.375
3.25
3.125
3
2.875
2.75
2.625
2.5
2.375
2.25
2.125
2
1.875
1.75
1.625
1.5
1.375
1.25
1.125
1
0.875
0.75
0.625
0.5
ul
K/Ul
1,000
975
950
925
900
875
850
825
800
775
750
725
700
675
650
625
600
575
550
525
500
475
450
425
400
375
350
325
300
275
250
225
200
175
150
125
100
10 ng/iil
ml PK/yl
10
9
8
7
6
5
4.75
4.5
4.25
4
3.75
3.5
3.25
3
2.75
2.5
2.25
2
1.75
1.5
1.25
1
.95
.9
.85
.8
0.75
.7
.65
.6
.55
0.5
.45
.4
.35
.3
0.25
1,000
900
800
700
600
500
475
450
425
400
375
350
325
300
275
250
225
200
175
150
125
100
95
90
85
80
75
70
65
60
55
50
45
40
35
30
25
4 ng/ti
ml r
20
18.75
17.5
16.25
15
13.75
12.5
11.25
10
9.375
8.75
8.125
7.5
6.875
6.25
5.625
5
4.375
3.75
3.125
2.5
2.375
2.25
2.125
2
1.875
1.75
1.625
1.5
1.375
1.25
1.125
1.
.875
.75
.625
0.5
0.25
0.125
1
«/ui
800
750
700
650
600
550
500
450
400
375
350
325
300
275
250
225
200
175
150
125
100
95
90
85
80
75
70
65
60
55
50
45
40
35
30
25
20
10
5
2 ng/ul
ml pg/yl
35
32.5
30
27.5
25
22.5
20
17.75
17.5
16.25
15
13.75
12.5
11.25
10
8.75
7.5
6.25
5
4.75
4.5
4.25
4
3.75
3.50
3.25
3
2.75
2.5
2.25
2
1.75
1.5
1.25
1
.75
0.5
700
650
600
550
500
450
400
375
350
325
300
275
250
225
200
175
150
125
100
95
90
85
80
75
70
65
60
55
50
45
40
35
30
25
20
15
10
1 ng/ul
ml pg/yl
50
45
40
37.5
35
32.5
30
27.5
25
22.5
20
17.5
15
12.5
10
9.5
9
8.5
8
7.5
7
6.5
6
5.5
5
4.5
4
3.5
3
2.5
2
1.5
1
0.9
.8
.7
.6
.5
500
450
400
375
350
325
300
275
250
225
200
175
150
125
100
95
90
85
80
75
70
65
60
55
50
45
40
35
30
25
20
15
10
9
8
7
6
5
-------
Table 3
SUGGESTED MIXTURES FOR QUANTITATION OF SOME
COMMON CHLORINATED COMPOUNDS
Compound
A SERIES
Lindane
Aldrin
Dieldrin
osp'-DDT
P,P;-DDT
B SERIES
B-BHC
Aldrin
Heptachlor epoxide
p,p'-DDE
p,p'-DDD
C SERIES
ct-BHC
e-BHC
Aldrin
o.p'-DDE
o,p'-DDD
Concentration,
Al
1
5
5
10
15
15
B,
I
15
5
10
10
15
Cl
1
5
5
5
10
15
pi cograms
A2
C.
10
10
20
30
30
B?
c.
30
10
20
20
30
c2
C.
10
10
10
20
30
per micro liter
A3
O
20
20
40
60
60
B,
o
60
20
40
40
60
Co
O
20
20
20
40
- 60
93
-------
Section IV
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 biblio-
graphy 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: E = English, F = French, G = German, I = Italian,
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. Corneliussen, PE. Food and
Drug Administration, Washington, D.C.
Volume I, 1972 (Multiresidue)
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)
AF Dissertation Abstracts International (Section B: Sciences and
Engineering)
94
-------
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 Abstract 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 Sourthern 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
British (B...)
BA Analyst - E
BB Chemistry and Industry - E
BC Journal of the Science of Food and Agriculture - E
BD Journal of Stored Products Research - E
BE Pesticide Science - E
BF Talanta - E,F,G
BG Water Research - E
BH Weed Research - E,F,G
95
-------
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
Italian (I...)
IA Agrochemia - E,F,G,I,S
IB Industrie Conserve - I,E,F,G ("Canning Industry")
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 ("Medicine 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")
96
-------
A 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
West European—Miscellaneous (W...)
WA Acta Chemica Scandanavica - E
WB Analytica Chimica Acta - E
WC Annales de Gembloux - F
WD Journal of Chromatography - E,F,G
WE Journal of Radioanalytical Chemistry - E
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)
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
97
-------
F f Root Crop
g Oil-bearing Seeds (Cotton, Soybeans, etc.) or Vegetable Oils
h Nuts
i Trunk, Stalk (eg. sugarcane), or Paper
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 two 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 II appearing under
98
-------
the A heading identifies the American Cyanamid Company as the method source;
the symbol 3Q refers to the FMC Corporation, and so on. In these company
method citations, data under B , C , and D headings are omitted as they
are inapplicable.
99
-------
Section V
LIST OF CONTRIBUTING PESTICIDE PRODUCING COMPANIES
Code Company Code
1A Allied Chemical Corporation 5Q
IE Amchem Products, Inc. 6A
II American Cyanamid Company, Inc. 61
1M The Ansul Company 6M
1Q BASF Wyandotte Corporation 6Q
1Z Buckman Laboratories, Inc. 6S
2A Celamerck GMBH & Co. KG (W.Germ.) 6U
2C Cheminova (Denmark) 7A
2E Chempar Chemical Company, Inc. 7E
21 Chevron Chemical 71
2U Diamond Shamrock Corporation 7J
2Z Dow Chemical U.S.A. 7M
3A I.E. DuPont de Nemours & Co0 7Q
3E Elanco Products Company 7U
31 E. & M. Laboratories 7Z
3M Fike Chemicals, Inc. 8A
3Q FMC Corporation 8E
3Z Gulf Oil Chemical Company 81
4A Hercules, Inc. 8M
4E Hoechst, AG (West Germany) 8Q
41 ICI United States, Inc. 8U
4P Kumai Chemical (Japan) 8Z
4Z 3M Company 9A
5E McLaughlin Gormley King Co. 9E
51 Merck, Sharpe & Dohme 91
5K Miller Chemical & Fertilizer 9M
5M Mobil Chemical Company
Company
Monsanto Commercial Products Co.
Nor-Am Agricultural Products Co.
Olin Agricultural Division
S.B. Penick & Company
Pennwalt Corporation
Pepro 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 Co0, Inc.
West Agro-Chemical, Inc.
Zoecon Corporation
100
-------
Section VI
INDEX OF PESTICIDE EQUIVALENT NAMES
The list of over 2,400 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 avail-
able from our repository stock.
The common or generic name is one confirmed for oridnary 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 Ento-
mological 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 Zectran
to such tongue-twisters as carbophenothion, azinphos methyl and mexacarbate.
101
-------
PESTICIDE EQUIVALENT NAMES
NAME
Aatrex
Abate
Aba th ion
AC-4124
AC- 12880
AC-18682
AC-26691
AC-47031
AC-84777
Acarben
Acaralate
Acarin
Acarol
Accel arate
Accothion
Acephate
ACP 322
Acquinite
Acrex
Acriciol
Acrizane
Acrolein
Acronize
Acryl aldehyde
Actellic
Acti-Aid
Actidione
Actispray
Activol
Actril
Aerotheme TT
Afalon
Af es i n
Aflix
Afos
Afugan
Agallol
Agrimycin
Agrisil
Agri strep
Agritol
Agritox
Agrosan
Agrotec
Agrothion
Agrox
Agroxon
Akar
Alamos
Alanap
Alar
Aldicarb
Aldrin
Aldrite 4
Aldrosol
Alfacron
Alfa-tox
Ali pur
Alkron
Aileron
Allethrin
Allisan
Alltox
Allyveratrole
Altos id
Ambox
Ambush
Amcide
Amerol
Amethopterin
Ametrex
Ametryn
Amex 820
Amiben
Amidithion
Amid-thin W
Aminocarb
Aminotriazole
COMMON NAME
Atrazine
Temephos
Temephos
Dicapthon
Dimethoate
Prothoate
Cythioate
Phosfolan
Difenzoquat
Chlorobenzilate
Chloropropylate
Dicofol
Bromopropylate
Endothall
Fenitrothion
Acephate
Naptalam
Chloropicrin
Dinobuton
Binapacryl
Phenacridane chloride
Acrolein
Chlortetracycline
Acrolein
Pirimiphos-methyl
Cycloheximide
Cycloheximide
Cycloheximide
Gibberell ic acid
loxynil
Trichloroethane
Linuron
Monolinuron
Formothion
Mecarbam
Pyrazophos
MEMC
Streptomycin
Trichloronate
Streptomycin
Bacillus Thuringiensis
Trichloronate
PMA
2,4-D
Fenitrothion
Phenylmercury urea
MCPA
Chlorobenzilate
Azothoate
Naptalam
Daminozide
Aldicarb
Aldrin
Aldrin
Aldrin
lodofenphos
Methoxychlor & Diazinon
Cycloron & Chlorbufam
Parathion
Parathion
Allethrin
Dichloran
Toxaphene
Methyl eugenol
Hethoprene
Binapacryl
Aldicarb
AMS
Amitrole
Methotrexate
Ametryn
Ametryn
Dibutalin
Chloramben
Amidithion
Naphthalene acetamide
Aminocarb
Ami trol e
CODE
NUMBER
0420
0020
0020
2420
1621
1610
2395
1360
2340
3240
3480
0025
4920
0027
0027
5643
1600
1600
1600
3790
4040
4240
4751
3722
4441
5932
6222
6222
5680
2940
3480
4340
1360
4920
0060
0080
0080
0080
4540, 2080
5245
5245
0100
2260
6740
4531
0060
0200
0120
0120
0140
4880
0180
0200
NAME
Aminozide
Amiphos
Amitrole
Amizine
Amizol
Ammate
Amobam
Amoxone
Amrol
Ancymidol
Anilazine
An i ten
Anofex
Ansar 8100
Ansar 170
Anthio
Anthon
Anthraquinone
Anticarie
Anti-K
Antimilace
Antiphen
Antracol
Antu
Aphoxide
Apl-Luster
APO
Appex
Aquacide
Aqua-Kleen
Aqualin
Aquathol
Aqua-Vex
Aquinite
Arasan
Arathane
Aresin
A-Rest
Aretan
Aretit
Arisan
Aroclors
Arprocarb
Arrhenal
Arsinyl
ASP-51
Aspon
Aspor
Asulam
Asulox
Asuntol
ATA
Atgard
Atlacide
Atlas 'A1
Atra-Bor
Atranex
Atratol
Atrazine
Aureomycin
Avadex
Avadex BW
Avenge
Avicol
Avitrol
Avlothane
Axiom-n
Azak
Azidithion
Azinphos-ethyl
Azinphos-methyl
Aziprotryn
Azobenzene
Azobenzide
Azodrin
Azofume
COMMON NAME
Daminozide
DAEP
Amitrole
Simazine
Amitrole
AMS
Amobam
2,4-D, triethanolamine
Amitrole
Ancymidol
Anilazine
Fl urecol -n-butyl ester
DDT
DSMA
MSMA
Formothion
Trichlorfon
Anthraquinone
Hexachlorobenzene
Sulfa-quinoxaline
Metal dehyde
Dichlorophen
Propineb
Antu
Tepa
Thiabendazole
Tepa
StirofOo
Diquat
2,4-D
Acrolein
Endothall
Si 1 vex
Chloropicrin
Thiram
Dinocap
Monolinuron
Ancymidol
MEMC
Dinoseb-acetate
Buturon
Polychlorinated
biphenyls
Propoxur
DSMA
DSMA
Aspon
Aspon
Zineb
Asulam
Asulam
Coumaphos
Amitrole
Dichlorvos
Sodium chlorate
Sodium arsenite
Atrazine & Borate
Atrazine
Atrazine
Atrazine
Chlortetracycline
Dial late
Triallate
Difenzoquat
PCNB
4-AP
Hexachloroethane
Akton
Terbutol
Menazon
Azinphos-ethyl
Azinphos-methyl
Aziprotryn
Azobenzene
Azobenzene
Monocrotophos
Azobenzene
CODE
NUMBER
0200
6160
0200
0220
salt
0200
0230
2920
363C
1880
2860
4820
3722
5780
0250
3920
0260
6660
3740
2660
2940
0027
3240
6120
6680
2560
4751
0230
2566
5700-5707
0440
2860
2860
0300
0300
7120
0310
0310
1540
0200
2320
0420
0420
0420
2040
6770
2395
5280
4453
3840
3820
0340
0340
0360
0340
102
-------
NAME
B-995
Bakthane
Balan
Balfin
Banafine
Banex
Ban-Hoe
Banol
Bantrol
Banvel D
Banvel M
Banvel T
Barbamate
Barban
Barbasco
Baron
BAS 2903-H
Basagran
Basal In
Basamaize
Basinite
Basfapon
Basudin
Batasan
Bavistin
Bay 13/59
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 25634
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
Bay 77488
Bay 78418
Bay 79770
Bay 94337
Baygon
Bayluscide
Baymix
COMMON NAME
Daminocide
Bacillus Thuringiensis
Benefin
Benefin
Benefin
Dicamba
Lenacil & Propham
Carbanolate
loxynil
Dicamba
MCPA & Dicamba
Tricamba
Barban
Barban
Rotenone-conta^ning
plants
Erbon
Prynachlor
Bentazon
Fluchloralin
Prynachlor
Dinoseb
Dalapon-Na
Diazinon
Fentin acetate
BCM
Trichlorphon
Niclosamide
Tolyfluanid
Fenaminosulf
Propoxur
Demeton
Benquinox
Demeton-methyl
Azinphos-ethyl
Azinphos-methyl
Phenthoate
Disulfoton
Oxydemeton-methyl
Fenaminosulf
Oxydisulfoton
Hetasystox S
Fensulfothion
Coumatetralyl
Clonitralid
Fenthion
Propanil
Thioquinox
Fungi Ion
Phenthoate
Fuberidazole
Oxythioquinox
Trichloronate
Methiocarb
Gophacide
Propoxur
Fenitrothion
Aminocarb
Omethoate
Propineb
Dichlofluanid
Tolyfluanid
Allyxycarb
Benzthiazuron
Nemacur
Carbofuran
Methachlorphenprop
Methamidophos
Methabenzthiazuron
Quinalphos
Phoxim
Ediphenfos
Chloraniformethane
Metribuzin
Propoxur
Clonitralid
Coumaphos
CODE
NUMBER
0480
0480
0480
2140
4185, 5860
4040
2140
4340, 2140
0400
0400
3320
0425
0407
2760
1660
2080
3527
6780
2020
0440
1981, 1982
3840
3820
2720
5220
2020
3500
0460
3520
5840
4800
4500
0440
3480
0180
1040
4750
5966
0440
0460
1540
NAME
Bayrusil
Baytan
Baytex
Baythion
BCPE
Belt
Benalan
Bencornox
Benefin
Benfluralin
Benlate
Benomyl
Bensofume
Bensulide
Bentazon
Benthiocerb
Bentranil
Benzac
Benzac 354
Benzadox
Benzahex
Benzene hexachloride
Benzex
Benzilan
Benzoylprop ethyl
Benzyl Benzoate
Berelex
Betanal
Betanal AM
Beta-naphthol
Betanex
Betasan
BHC
BHC, gamma
Bidisin
Bidrin
Bifenox
Big Dipper
Bilobran
Binnell
Bioquin
Bioresmethrin
Biostat PA
Biothion
Biotrol BTV
Biotrol-Plus
Biphenyl
Birlane
Bis-ethyl xanthogen
Black Leaf 40
Bladafume
Bladan
Bladex
Blattanex
Blue Vitriol
Blulan
B-Nine
Bo-Ana
Bol ero
Bordermaster
Borolin
Botran
Botrilex
Bovinex
Brasoran
Bravo
Brestan
Broadside
Brofene
Bromacil
Bromax
Bromochlorphos
Bromeflor
Bromex
Brominal
Bromodan
COMMON NAME
Quinalphos
MEMC
Fenthion
Phoxim
Dimite
Chlordane
Benefin
Benazolin
Benefin
Benefin
Benomyl
Benomyl
Azobenzene
Bensulide
Bentazon
BenthiQcarb
Bentrarfn
2,3,6-TBA
PBA
Benzado,",
BHC
BHC
BHC
Chlorobenzilate
Benzoylprop ethyl
Benzyl Benzoate
Gibberellic acid
Phenmedipham
Desmedipham
2-Naphthol
Desmedipham
Bensulide
BHC
Lindane
Methachlorphenprop
Dicrotophos
Bifenox
Diphenylamine
Monocrotophos, Dodine
& Dinocap 2780,
Benefin
Copper 8-Quinolate
Resmethrin
Oxytetracycline
Temephos
Bacillus Thuringiensis
Bacillus Thuringiensis
& Pyrethrins
Biphenyl
Chlorfenvinphos
EXD
Nicotine
Sulfotep
Pa rath ion
Cyanazine
Propoxur
Copper sulfate
Benefin
Daminozide
Famphur
Benthiocarb
MCPA
Picloram
Dichloran
PCNB
Trichlorfon
Aziprotryn
Chlorothalonil
Fentin acetate
MSMA & Sodium Cacodylate
Bromophos
B romac i 1
Chlorbromuron
Naled
Ethephon
Naled or Chlorbromuron 4860 or
Bromoxynil Octanoate
Bromocyclen
CODE
NUMBER
5966
3520
1200
0480
0480
0480
0500
0500
0340
0520
0425
0574
6920
0577
0600
0600
0600
1360
0578
0580
3790
5410
2006
4925
2006
0520
0600
0680
0700
0733
0360,
2560
0480
6055
0020
0740
1300
3420
5245
1552
0440
0480
3440
4340
5600
2260
5280
6780
1640
3527
0840
0800
4860
3330
—
103
-------
NAME
Bromofume
Brom-0-Gas
Bromophenoxim
Bromophos
Bromophos-ethyl
Bromopropylate
Bromoxynil
Bromsalans
Bronate
Brophene
Brozone
Brush-Rhap
BTV
Buctril
Bueno
Bui an
Bunema
Busan 72
Butachlor
Butacide '
Butopyronoxyl
Butralin
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
Cacodyllc acid
Calcium acid
methanearsonate
Calcium arsenate
Caldron
Calixin
Camphechlor
Cantrol
Caparol
Captafol
Captan
Caragard
Carbamult
Carbaryl
Carbatene
Carbendazim
Carbetamide
Carbicron
Carbofos
Carbofuran
Carbophenothion
Carboxin
Carbyne
Carfene
Carpene
Carpidor
Carzol SP
Casoron
Castrix
CDAA
CDEC
CDT
Cela A-36
Cela S-1942
COMMON NAME
Ethylene dibromide
Methyl bromide
Bromophenoxim
Bromophos
Bromophos-ethyl
Bromopropylate
Bromoxynil
Diaphene
MCPA & Bromoxynil
Bromophos
Methyl bromide &
Chloropicrin
2,4,5-T
Bacillus Thuringiensis
Bromoxynil Octanoate
MSMA
Bulan
Bunema
TCMTB
Butachlor
Piperonyl Butoxide
Indalone
Butralin
Butyl ate
2,4-DB
Buturon
Metal kamate
Dicrotophos
Monocrotophos
Chloroxuron
Fl uoraeturon
Amidithion
Metabromuron
Difenoxuron
Chlorbromuron
Fluorodifen
Aziprotryn
Carbaryl
Dioxacarb
Chlordimeform
Bromofenoxin
lodofenphos
Cacodylic acid
CAMA
Calcium arsenate
Dinoseb
Tridemorph
Toxaphene
MCPB
Prometryn
Captafol
Captan
Terbumeton
Promecarb
Carbaryl
Metiram
Carbendazim
Carbetamide
Dicrotophos
Malathion
Carbofuran
Carbophenothion
Carboxin
Barban
Azinphos-methyl
Dodine
Benef in
Formetanate hydrochloride
Dichlobenil
Crimidine
CDAA
CDEC
Simazine
Decafentin
Bromophos
CODE
NUMBER
0840
0860
0820
2060
4340, 0820
0840
6840
4820
0916
0922
5620
0933
0940
3080
0960
0700
0360
3620
1060
1480
0961
0980
2760
6792
6740
4380
5780
1000
1020
5752
1060
1071
1074
0700
4260
1040
1080
1100
0400
3820
2780
0480
3680
2200
1140
1160
6160
0840
NAME
Cela S-2225
Cela S-4084
Cela S-4087
Cela S-6000
Cela S-6115
Cela W-524
Celdion
Cel fume
Celmer
Celmide
Celmone
Celphos
CEPHA
Cercobin
Cercobin M
Ceredon
Ceregam
Cereline
Ceresan
Certrol
CET
Cevadine
Cevadilla
CGA 10832
Chemathion
Chem Bam
Chem-Hoe
Chem Neb
Chem-0-Bam
Chemox General
Chem Rice
Chem Zineb
Chinomethionate
Chinosol
Chinothionat
Chip-Cal
Chipco Buctril
Chipco Crab Kleen
Chipcote
Chipco Turf
Herbicide "D"
Chipco Turf
Herbicide MCPP
Chipco Turf Kleen
Chiptox
Chloramben
Chloranil
Chloranocryl
Chlorasol
Chlorbenside
Chlorbromuron
Chlor Chem T-590
Chlordane
Chlordecone
Chlordene
Chlordimeform
Chlorex
Chlorfenac
Chlorfenidim
Chlorfenson
Chlorfenvinphos
Chlorinat
Chlorinated
Camphene
Chlor Kil
Chlormephos
Chlormequat Chloride
Chi orobenzi late
Chloroble Forte
Chloroble M
Chlorocide
Chlorofenizon
Chloro IPC
Chloroneb
Chloro phacinone
COMMON NAME
Bromophos ethyl
Cyanox
Surecide
Cypromid
Cyprazine
Triforine
Fentiazon
Methyl bromide
MEMC
Ethyl dibromide
Naphthalene
acetic acid
Aluminum phosphide
Ethephon
Thiophanate
Thiophanate-methyl
Benquinox
Methoxy ethyl mercury
silicate
Benquinox
Ethyl mercury chloride
loxynil
Simazine
Sabadilla
Sabadilla
Profluralin
Malathion
Nabam
Propham
Maneb
Amobam
Dinoseb
Propanil
Zineb
Oxythioquinox
8-Quinolinol sulfate
Thioquinox
Calcium arsenate
Bromoxynil
DSMA
Methylmercury nitrite
2,4-D
MCPP
MCPP & 2,4-D
MCPA
Chloramben
Chloranil
Dicryl
Ethylene dichloride
Chlorbenside
Chlorbromuron
Toxaphene
Chlordane
Chlordecone
Chlordene
Chlordimeform
Dichlorethyl ether
Fenac
Monuron
Ovex or Chlorfenson
Chlorfenvinphos
Barban
Toxaphene
Chlordane
Chlormephos
Chlormequat chloride
Chi orobenzi late
Lindane, endosulfan,
copper oxide
Maneb
Chlorbenside
Ovex or Chlorfenson
Chlorpropham
Chloroneb
Chlorophacinone
CODE
NUMBER
0860
6360
1615
6822
4900
3330
6670
6671
3400
4040
6160
4260
4840
5860
4300
0220
2760
5840
7120
4800
0980
0820
2860
2940
4400
4400, 2940
4340
0140
1180
1340
6740
1200
1280
1260
1480
3460
4760
1300
0400
6740
1200
1316
1320
1360
4300
1340
1420
1380
1425
104
-------
NAME
Chlorophos
Chloromethane
Chlorophenothane
Chlor-0-Pic
Chloropropylate
Chlorothalonil
Chlorothene Nu
Chloroxone
Chloroxuron
Chlorparacide
Chlorphenami'di'ne
Chlorphos
Chlorpropham
Chlorpyrifos
Chlorsulphacide
Chlorthal-methyl
Chlorthiepin
Chromaphon
Chrysvon
CIBA 709
CIBA 1414
CIBA 8353
CIBA 8514
Cidial
Cinerin I,
allyl homolog
Ciodrin
Ciovap
CIPC
Citrazon
Clobber
Clonitralid
CMDP
CMPP
Cobex
Colloidex
Comite
Compound 448
Compound 1080
Compound 1081
Compound 4072
Compound 7744
Copper oxinate
Coprantol
Copro
Co-Ral
Corbit
Cornox CWK
Cornox RK
Corodane
Coromerc
Corothion
Corozate
Cotnion-ethyl
Cotnion-methyl
Cotoran
Coumachlor
Coumafene
Coumafuryl
Coumaphos
Coxysan
CP 4742
CP 6343
CP 15336
CP 31393
CP 50144
CP 53619
CPBS
CPCBS
Crab-E-Rad 100
Crag Fly Repel lant
Crag Fruit
Fungicide 341
Crag Fungicide 974
Crag Herbicide 1
COMMON NAME
Trichlorfon
Methyl chloride
DDT
Chloropicrin
Chloropropylate
Chlorothalonil
Trichloroethane
2,4-D
Chloroxuron
Chlorbenside
Chlordlmeform
Trichlorfon
Chlorpropham
Chlorpyrifos
Chlorbenside
DCPA
Endosulfan
Dition
Resmethrin
Dicrotophos
Monocrotophos
Oioxacarb
Chlordimeform
Phenthoate
Allethrin
Crotoxyphos
Crotoxyphos &
Dichlorvos 1500,
Chlorpropham
Benzomate
Cypromid
Clonitralid
Mevinphos
MCPP
Dinitramine
Copper oxychloride
Propargite
2-Phenyl cycl ohexanol
Sodium fluoroacetate
Fluoroacetamide
Chlorfenvinphos
Carbaryl
Copper 8-Quinolate
Copper oxychloride
Copper oxychloride sulfate
Coumaphos
Anthraquinone
Benazolin
Dichlorprop
Chlordane
Phenyl mercury
ethylenediamine
Parathion
Z i ram
Azinphos ethyl
Azinphos methyl
Fluometuron
Coumachlor
Warfarin
Coumafuryl
Coumaphos
Copper oxychloride
CDEC
DCAA
Diallate
Propachlor
Alachlor
Butachlor
Fenson
Ovex or Chlorfenson
DSMA
Butoxy polypropylene
glycol
Glyodin
Dazomet
Sesone
CODE
NUMBER
6780
1880
1640
2940
1340
1480
67SO
1420
2900
1340
1720
3180
6055
0700
0360
1480
0100
1500
2320
1420
0460
4640
4400
2551
5160
1300
1060
1540
0250
2309
1200
5245
7100
3840
3820
3620
7060
3720
1540
1160
1140
2040
5820
4160
0922
2860
NAME
Crag Herbicide 2
Crag Nemacide
Croneton
Crop Rider
Crotoxyphos
Crufomate
Cryolite
Cube
Cufram Z
Cuman
Cum' late
Cupramar
Cupravit
Cuprinol
CuproKylt
Cuprox
Curamil
Curaterr
Curitan
Cu-Sprex
Cyanazine
Cyanogas
Cycloate
Cyclodan
Cycloheximide
Cycl on
Cycocel
Cycoqan
Cyflee
Cygon
Cylan
Cymag
Cynem
Cyolane
Cyprazine
Cyprex
Cythioate
Cythion
Cytrol
Cytrolene
2,4-D
D-735
D-1221
DAC 893
Dacamine
Daconate
Daconil
Dacthal
DAEP
Dagadip
Dalapon
Dal-E-Rad 100
Dalf
Danex
Dapnene
Dasanit
DATC
Daxtron
Dazzel
2,4-OB
DBCP
2,6-DBN
DBP
DCMA
DCMOD
DCMU
DCNA
DCPA
DCPC
DCPM
DCU
DDA
ODD
DDE
DDMU
COMMON NAME
Dichloralurea
Dazomet
Ethiophencarp
2,4-D
Crotoxyphos
Crufomate
Cryolite
Rotenone
Cufraneb
Ziram
Copper 8-Quinolate
Copper oxychloride
Copper oxychloride
Copper naphthenates
Copper oxychloride
Copper oxychloride
Pyrazophos
Carbofuran
Dodine
Dichlobem'l
Cyanazine
Calcium cyanide
Cycloate
Endosulfan
Cycloheximide
Hydrocyanic acid
Chlormequat chloride
Chlormequat chloride
Cythioate
Dimethoate
Phosfolan
Sodium cyanide
Thionazin
Phosfolan
Cyprazine
Dodine
Cythioate
Malathion
Amitrole
Mephosfolan
2,4-D
Carboxin
Carbofuran
DCPA ,
Salts of 2,4-D &
2,4,5-T
MSMA
Chlorothalonil
DCPA
DAEP
Carbophenothion
Dalapon
DSMA
Parathion-methyl
Trichlorfon
Dimethoate
Fensulfothion
Diallate
Pyriclor
Diazinon
2,4-DB
Dibromochloropropane
Dichlobenil
Dibutyl Phthalate
Dicryl
Oxycarboxin
Diuron
Dichloran
DCPA
Dimite
Neotran
Dichloral urea
DDA
DDD
DDE
p,p'-DDD, olefin
CODE
NUMBER
2940
1500
6020
1546
6000
7100
5932
1040
2780
2200
1552
1591
3180
1600
1320
1320
1621
2420
1610
1610
1615
2780
1621
4260
0200
1630
2940
1100
1040
1720
4820
1640
1720
1080
1660
2860
4580
6780
2420
3500
2040
2080
3080
2090
2200
2120
5670
2740
2260
1720
1740
1750
1840, 1860
1800
105
-------
NAME
DDT
DDVE
DOVP
Dechlorane
De-Cut
Dedelo
Dedevap
Ded-Weed
DEF
De-Fend
De-Fol-Ate
De-Green
Deiquat
Del an
Delan-Col
Deleaf Defoliant
Delicia
Delnav
Delphene
Delsan
Demeton-0
Demeton-S
Demosan
Demos-L40
Demox
Dermaton
Derrin
Derris
Des-I-Cate
Desmedipham
2,4-DES-Na
De-Sprout
Dessin
Detamide
Dpthdiet
Dethmore
Devrinol
DEX
Dexon
Dextone X
Dextrone
DHA
Dial ifor
Diallate
Diametan
Dianat
Diaphene
Diazajet
Diazide
Diazinon
Diazoben
Diazel
Dibam
Dibrom
Dibromoethane
Dibutyl phthalate
Dibutyl succinate
Dicamba
Di-Captan
Dichlobenil
Dichlor
Dichlorfenidin
Dichlofenthion
Dichlone
Dichlorobenzene-o
Dichlorobenzene-p
Dichloroethane
Dichloronitroethane
Dichlorophenoxy-
acetic acid
Dichloropropane
Dichloropropene
Dichloropropionic
acid
Dichlorphenidim
Dichlorphos
COMMON NAME
DDT
Dichlorvos
Dichlorvos
Mi rex
MH
DDT
Dichlorvos
2,4-D, Dalapon-Na
& 2,4,5-T
DEF
Dimethoate
Magnesium chlorate
DEF
Diquat
Dithianon
Dithianon
Folex
Aluminum phosphide
Dioxathion
Deet
Thiram
Demeton-0
Demeton-S
Chloroneb
Dimethoate
Demeton
Dichlorvos
Rotenone
Rotenone
Endothall
Desmedipham
Sesone
MH
Dinobuton
Deet
Red Squill
Warfarin
Napropamide
EXD
Fenaminosulf
Paraquat dichloride
Diquat dibromide
Dihydroacetic acid
Dialifor
Diallate
Fulfogen
Dicamba
Diaphene
Diazinon
Diazinon
Diazinon
Fenaminosulf
Diazinon
Sodium dimethyl
dithiocarbamate
Naled
Ethylene dibromide
Dibutyl phthalate
Tabutrex
Dicamba
Dicapthon
Dichlobenil
Dichlobenil
Diuron
Dichlofenthion
Dichlone
Dichlorobenzene-o
Dichlorobenzene-p
Ethyl eno dichloride
Ethide
2,4-D
Propylene dichloride
Dichloropropene
Dalapon
Diuron
Dichlorvos
CODE
NUMBER
1880
2320
2320
4720
2280
1880
2320
2940,
1660, 6840
1940
2420
1940
2660
2721
2721
3640
2580
6680
1981
1982
1380
2420
1981, 1982
2320
6000
6000
3240
2006
4280
7060
2010
3420
2020
5240
2660
2035
2040
2140
2060
2080
2080
2080
2020
2080
4860
2120
2140
2200
2200
2740
2220
2180
2280
2300
2940
2306
1660
2740
2320
NAME
Dichlorprop
Dichlorvos
Diclotron
Dicofol
Dicrotophos
Dicurane
Dieldrin
Diethion
Diethquinalphion
Diethyl phosphate
Diethyl toluamide
Difenoxuron
Difenson
Difenthos
Difenzoquat
Diflubenzuron
Difolatan
Dihydropyrone
Dikar
Oil an
Dilan I
Dilan II
Dimecron
Dimelone
Dimephenthoate
Dimethan
Dimethirimol
Dimethoate
Dimethogen
Dimethylarsinic
acid
Dimethyl phosphate
Dimethyl phthalate
Dimetilan
Dimilin
Dinex
Dinitramine
Dinitrobutyl phenol
Dinitrocresol
Dinitrocyclohexyl-
phenol
Dinitro-o-sec-
amyl phenol
Dinocap
Dinofen
Dinoseb
Dinoseb acetate
Dinoseb methacrylate
Dinoterb acetate
Di-on
Dioxacarb
Dioxathion
Dipan
Dipel
Diphacin
Diphacinone
Diphenamid
Diphenyl
Diphenyl mercury
Dipropetryn
Dipterex
Diquat dibromide
Di rez
Dirimal
Disan
Disodium methane-
arsonate
Disparmone
Disulfoton
Disul-Na
Di-Syston
Disyston S
Disyston sulphoxide
Di-Tac
Dithane A-40
Dithane D-14
Dithane M-22
COMMON NAME
Dichlorprop
Dichlorvos
Dichlobenil &
Fluometuron
Dicofol
Dicrotophos
Chlorotoluron
Dieldrin
Ethion
Quinalphos
Diethyl phosphate
Deet
Difenoxuron
Ovex or Chlorfenson
Temephos
Difenzoquat
Diflubenzuron
Captafol
Indalone
Mancozeb & Dinocap
Dilan
Prolan
Bulan
Phosphamidon
Dimethyl carbate
Phenthoate
Dimetan
Dimethirimol
Dimethoate
Dimethoate
Cacodylic acid
Dimethyl phosphate
Dimethyl phthalate
Dimetilan
Diflubenzuron
Dinex
Dinitramine
Dinoseb
DNOC
Dinex
Dinosam
Dinocap
Dinobuton
Dinoseb
Dinoseb acetate
Binapacryl
Dinoterb acetate
Diuron
Dioxacarb
Dioxathion
Diphenatrile
Bacillus Thuringiensis
Diphacinone
Diphacinone
Diphenamid
Biphenyl
Diphenyl mercury
Dipropetryn
Trichlorfon
Diquat dibromide
Anilazine
Oryzalin
Bensulide
DSMA
Disparlure
Disulfoton
Sesone
Disulfoton
Oxydisulfoton
Oxydisulfoton
DSMA
Nabam
Nabam
Maneb
CODE
NUMBER
2309
2320
2200, 3620
2340
0700
2380
3340
5966
2386
0020
2395
2406
1000
5580
2416
2420
2420
0961
2458
2460
2480
2406
2551
2760
2770
2520
2560
2760
2566
2740
2580
2600
2600
2620
0740
2640
6780
2660
2920
5148
0520
2860
2720
2720
2860
4840
4840
4300
106
-------
NAME
Dithane M-45
Di thane Z-78
Dithianon
Dithio
Dithiod erne ton
Dithiomethon
Dithione
Dithiosystox
Ditranil
Dlurex
Diurol
Diuron
Divipan
DMA
DMC
DMP
DMTT
OMU
DN-111
DN-289
DNAP
DNBP
DNC
ONOC
DNOCHP
DNOSAP
DNOSPB
DO 14
Dodlne
Doquadlne
Do! Granule
Doom
OOP
Dorlone
Dormone
Dosanex
Double- Noctin
Dovip
Dowco 118
Dowco 132
Dowco 179
Dowco 213
Dow General
Dowfume W-85
Dowicide A
Dowicide B
Dowicide F
Dowicide G
Dowicide 1
Dowicide 2
Dowicide 2S
Dowicide 4
Dowicide 6
Dowicide 7
Dowlap
Dowpon
Dow Selective
Dowspray 9
DP-35
2,4-DP
DPA
Drat
Drawinol
Draza
Drazoxolon
DRB
Drinox
Drinox H-34
Drop Leaf
DSE
DSMA
DU 112307
DuBay 115HH
Duphar
OuPont
Insecticide 1179
Duraset
Dursban
COMMON NAME
Mancozeb
Zineb
Dithianon
Sul fotep
Disulfoton
Thiometon
Sul fotep
Disulfoton
Dichloran
Diuron
Diuron & Amitrole 2740,
Diuron
Dichlorvos
DSMA
Dimite
Dimethyl phthalate
Dazomet
Diuron
Dinex
Dinoseb
Dinosam
Dinoseb
DNOC
DNOC
Dinex
DNAP
Dinoseb
Propagite
Dodine
Dodine
Lindane
Milky disease spores
Dioctyl phthalate
Dichloropropene
2,4-D
Metoxuron
Captan & N-fixing bacteria
Famphur
Zytron
Crufomate
Chlorpyrifos
Plictran
Dinoseb
Ethyl dibromide
Sodium phenylphenate
Sodium trichlorophenate
Sodium tetrachlorophenate
Sodium pentachlorophenate
0-Phenyl phenol
2,4,5-Trichlorophenol
2,4,6-Trichlorophenol
2-Chloro-4-phenyl phenol
2,3,4,6-Tetrachlorophenol
PCP & other chlorophenols
Trichloronitrophenol
Dalapon-Na
Dinoseb
Styrene dibromide
Propanil
Dichlorprop
Propanil
Chlorophacinone
Dinobuton
Methiocarb
Drazoxolon
Nirit
Aldrin
Heptachlor
Sodium chlorate
Nabam
DSMA
Difluron
Ethylmercury iodide
Tetradifon
Methomyl
N-m-t
Chlorpyrifos
CODE
NUMBER
7120
2761
2720
6665
2720
2260
2740
0200
2740
2320
2860
2460
2740
2520
2760
2760
2770
2770
2520
2760
5160
2780
2780
0680
2306
2940
4631
3440
6020
2900
2760
2800
5490
6890
2840
1660
2760
5840
2309
5840
1425
4500
2792
0080
3860
4840
2860
6600
4520
2900
1
NAME
Du-Sprex
Du-Ter
Dyanap
Dybar
Dyfonate
Dylox
Dymid
Dynanap
Dynoram
Dyrene
E-500
E-600
E-605
E-838
E-1059
Easy Off-D
Ectoral
EDE
EDC
Ekalux
Ekatin
Ekatin M
Ektafos
El-119
El -179
El-241
El-273
El-531
Elancolan
Elgetol 30
Elgetol 318
Elocron
Elsan
Elvaron
EM-923
Embutox
EMC
Enmatas
Endosan
Endosulfan
Endothall
Endox
Endrin
Enide
Entex
EP-332
EP-333
EP-452
EP-475
Ephirsulphonate
EPN
Epoxyethane
Epoxypropane
Eptam
Eptapur
EPTC
Equigard
Equi no-Aid
Eradex
Erazidon
Erbon
Esteron
Esteron 245
Estone
Estonmite
Estox
Ethephon
Ethiolate
Ethion
Ethirinol
Ethodan
Ethohexadiol
Ethoprop
Ethrel
Ethyl Guthion
Ethyl hexanediol
COMMON NAME
Dichlobenil
Fentin hydroxide
Naptalam
Fenuron
Fonofos
Trichlorfon
Diphenamid
Dinoseb & Naptalam
Chloramben & Dinoseb
Anilazine
Ambithion
Paraoxon
Parathion
Potasan
Demeton
Folex
Ronnel
Ethyl ene dibromide
Ethyl ene di chloride
Quinalphos
Thiometon
Morphothion
Dicrotophos
Oryzalin
Isopropalin
Parinol
Triarimol
Ancymidol
Trifluralin
DNOC
Dinoseb
Dioxacarb
Phenthoate
Dichlofluanid
Genite
2,4-DB
Ethylmercury chloride
Malathion
Binapacryl
Endosulfan
Endothall
Coumatetralyl
Endrin
Diphenamid
Fenthion
Formetanate hydrochloride
Chlordimeform
Phenmedipham
Desmedipham
Ovex or Chlorfenson
EPN
Ethylene oxide
Propylene oxide
EPTC
Buturon
EPTC
Dichlorvos
Trichlorfon
Thioquinox
Thioquinox
Erbon
2,4-D
2,4,5-T
2,4-D
Ovex or Chlorfenson
Metasystox-S
Ethephon
Ethiolate
Ethion
Ethirinol
Ethion
Ethyl hexanediol
Ethoprop
Ethephon
Azinphos ethyl
Ethyl hexanedio^.
CODE
NUMBER
2200
3540
4920
2910
6780
2620
2760, 4920
0140, 2760
2920
5245
1981, 1982
3640
5980
5966
6665
4803
0700
5148
4070
5251
0230
6800
2770
2760
3080
3400
4260
3180
3240
3260
2620
3520
3680
3680
51:0
2006
3280
3300
3300
2320
6780
3320
2940
6840
2940
3330
3335
3340
3359
3340
3380
5880
3330
3840
3380
107
-------
NAME
Ethyl mercury
chloride
Ethyl parathion
Ethyl pyrophosphate
Ethyl xanthogen
disulfide
Etilon
ETO
Etrofol
Etrofolan
Etrol ene
Eulava SM
Euparen
Euparen M
Eurex
Evik
Evital
EXD
Exothion
Exporsan
E-Z-Off
E-Z-Off D
F-319
F-461
Fac
Fac Super
Fair-Tac
Fall
Faladin
Falone
Famid
Famofos
Famphur
Faneron
Fanfos
Far-Go
Fatal
FBHC
Fen-all
Fenac
Fenaminosulf
Fenatrol
Fence Rider
Fenchlorfos
Fen id "in
Fenitrothion
Fenizon
Fenoflurazole
Fenolovo acetate
Fenophosphon
Fenoprop
Fensulfothion
Fenthion
Fentin acetate
Fentin hydroxide
Fenulon
Ferbam
Berberk
Fermate
Fermide 850
Fernasan
Fernesta
Fernimine
Fernoxone
Ferxone
Field Kleen Weed
Killer
Filariol
Finidim
Fitios B/77
Floral tone
Florel
Florencol
Florocid
Fluchloralin
COMMON NAME
Ethyl mercury
chloride
Parathion
TEPP
EXD
Parathion
Ethyl ene oxide
CPMC
MIPC
Ronnel
Magnesium fluosilicate
Dichlofluanid
Tolyfluanid
Cycloate
Ametryn
;Norflurazon
-EX~D
Endothion
Bensul ide
Magnesium chlorate
DEF
Hymexazol
Oxycarboxin
Prothoate
Prothoate & Ovex
n-Decanol
Sodium chlorate
2,4-DEP
2,4-DEP
Dioxacarb
Famphur
Famphur
Bromofenoxim
Famphur
Triallate
DCPA
BHC
2,3,6-TBA
Fenac
Fenaminosulf
Atrazine, Amitrole,
& Fenac
2,4,5-T
Ronnel
Fenuron
Fenitrothion
Fenson
Fenozaflor
Fentin acetate
Trichloronate
Si 1 vex
Fensulfothion
Fenthion
Fentin acetate
Fentin hydroxide
Fenuron
Ferbam
Ferbam
Ferbam
Thiram
Thiram
2,4-D
2,4-D
2,4-D
2,4-D
2,4-D
Bromophos ethyl
Fenuron
Ethoate-methyl
TIBA
Ethephon
Fl urecol -n-butyl ester
Sodium fluoride
Fluchloralin
CODE
NUMBER
3400
5245
6540
3420
5245
5980
1591
0120
5136
3420
0520
1940
5670
3440
3440
3440
6770
1720
0600
6920
3460
2020
0420,
0200, 3460
6840
5980
3480
3527
6120
3500
3520
3527
3540
3600
3600
3600
6680
6680
2940
2940
2940
2940
2940
0860
3330
3630
0407
NAME
Fluenyl
Fl uometuron
Fluorakil 100
Fluoridamid
Fluorodifen
Fluorogesarol
Fluoroparacide
Fl urecol -n-
butyl ester
FMC 10242
Folbex
Folcid
Folex
Folidol E-605
Folidol M
Folimat
Folithion
Folosan
Folpan
Folpet
Fonofos
Fores tan
Forlin
For-Mal 50
Formetanate
Hydrochloride
Formothion
Forron
Forstan
Forturf
Fos-Fall "A"
Fosfamid
Fosferno 50
Fosferno M50
Fostion
Fostion MM
Foxlene
Frescon
Frucote HC1 salt
Fruitone A
Fruitone CPA
Fruitone M
Fruitone T
Frumin Al
Fuklasin
Fumarin
Fumazone
Fundal EC
Fungiclor
Funginex
Fungo 50
Furadan
Furloe
Fusarex
FW-293
FW-734
FW-925
Fyfanon
6-11
G-18359
G-19258
G-22008
G-22870
G-23330
G-23611
G-23645
G-24163
G-24480
G-24622
G-27901
G-28029
G- 30026
G-30027
G-30028
G-30044
G-30130
COMMON NAME
Fl uenethyl
Fl uometuron
Fluoroacetamide
Fluoridamid
Fluorodifen
DFDT
Fluorobenside
Fl urecol -n-
butyl ester
Carbofuran
Chlorobenzilate
Captafol
Folex
Parathion
Parathion methyl
Omethoate
Fenitrothion
Tecnazene
Folpet
Folpet
Fonofos
Oxythioquinox
Lindane
Malathion
Formetanate
hydrochloride
Formothion
2,4,5-T
Oxythioquinox
Chlorothalonil
DEF
Dimethoate
Parathion
Parathion, methyl
Prothoate
Dimethoate
Pinolene
Trifenmorph
sec-Butyl amine
2,4,5-T
3-CPA
Naphthaleneacetic acid
Silvex
Disulfoton
Ziram
Coumafuryl
Dibromochloropropane
Chlordimeform
PCNB
Triforine
Thiophanate methyl
Carbofuran
Chlorpropham
Tecnazene
Dicofol
Propanil
Nitrofen
Malathion
Hexachlorophene
KIK
Dimetan
Pyrolan
Dimetilan
Pyramat
Isolan
Etoxinol
Chloropropylate
Diazinon
Pyrazinon
Trietazine
Phencapton
Norazine
Atrazine
Propazine
Simetone
Propanil
CODE
NUMBER
3620
3623
3630
1040
1360
1000
3640
5245
4580
3480
6435
3660
3660
2910
4800
0680
4260
3680
3722
6840
4800
1640
1940
2420
5245
4580
2420
6840
4900
6120
2720
7100
3720
2090
1480
5280
6822
6671
1040
1420
6435
2340
5840
5040
4260
3940
2080
5400
0420
5800
5840
108
-------
NAME
G-30344
G-30494
G-31435
G- 31 71 7
G-32293
G-32911
G-34161
G-34162
G- 34690
G- 36393
Galecron
Gallotox
Gamaphex
Garrml i n
Gamma BHC
Gammex
Gammexane
Ganoclde
Gardentox
Gardona
Gardoprim
Garlon
Garrathion
Gatnon
GC-1283
GC-2466
GC-3707
Genitol
Genitox
Gesabal
Gesadural
Gesafloc
Gesafram
Gesagard
Gesamil
Gesapax
Gesapon
Gesaprim
Gesapun
Gesaran
Gesarex
Gesarol
Gesatamin
Gesatop
Gibberellic acid
Gibrel
Gib-Tabs
Gib-Sol
GIX
Glyphosate
Glytac
Golden Decoy
Gralit 85
Gramevin
Gramonol
Gramoxone
Granol NM
Granosan
Granox NM
Granox PFM
Grocel
GS-13005
GS-13529
GS-14254
GS-14259
GS-14260
GS-16068
GS-19851
Guazatine
Gusathion M
Gusathion A
Guthion
Gypsine
Gyron
H-321
H-1313
COMMON NAME
Simazine
Methyl phencapton
Prometon
I pa tone
Atraton
Simetryn
Prometryn
Ametryn
Methometon
Metroprotryn
Chlordimeform
PMA
Lindane
Lindane
Lindane
Lindane
Lindane
Drazoxolon
Diazinon
Stirofos
Terbuthylazine
Si 1 vex
Carbophenothion
Benzthiazuron
Mi rex
Mucochloric anhydride
Bomyl
Genite
DDT
Ipazin
Simetone
Trietazine
Prometon
Prometryn
Propazine
Ametryn
DDT
Atrazine
Simazine
Metoproptryn
DDT
DDT
Atraton
Simazine
Gibberellic acid
Gibberellic acid
Gibberellic acid
Gibberellic acid
DFDT
Glyphosate
Glytac
Dichlorvos & Ronnel
Chloral chloroamide
Dalapon-Na
Paraquat & Monolinuron
Paraquat dichloride
Maneb & Lindane
Ethylmercury chloride
Maneb & HCB
Maneb & Captan
Gibberellic acid
Methidathion
Terbuthylazine
sec-Bumeton
Terbumeton
Terbutryn
Dipropetryn
Bromopropylate
Guazatine
Azinphos methyl
Azinphos ethyl
Azinphos methyl
Lead arsenate
DDT
Methiocarb
Dichlobenil
CODE
NUMBER
6160
5780
5780
0120
1480'
5680
0680
0680
0680
0680
0680
2792
2080
3740
6120
1080
4720
1880
5760
5780
5800
0120
1880
0420
6100
1880
1880
0320
6160
3790
3790
3790
3790
3801
3804
2320, 5980
1660
5240, 4751
5240
4300, 0680
3400
4300, 3920
4300, 1020
3790
6340
3980
3820
3840
3820
4180
1880
4500
2200
NAME
Halizan
Halowaxes
Halts
Hanane
Harven
HC-1281
HCA
HCB
HCCH
HCH
HCN
Hedonal
Hedonal DP
Hel iotox
HEOD
Heptachlor
Heptachlor epoxide
Heptamul
Herban
Herbicide 273
Herbisan
Herbizol
Hercules AC 528
Hercules AC5727
Hercules 7531
Hercules 9573
Hercules 14503
Herkol
Heteroauxin
HETP
Hexachlor
Hexachloran
Hexadrin
Hexafor
Hexanema
Hexasul
Hexathane
Hexathir
Hexavin
Hexazir
Hexyclan
HHDN
Hinosan
Hoe 2671
Hoe 2747
Hoe 2784
Hoe 2810
Hoe 2873
Hoe 2904
Hoe 2960
Hoe 2989, 6052,
6053, 13764
Homal
Hong Niem
Hopcide
Hormotuho
Hormotuho Special
Hostathion
Hydout
Hydram
Hydrogen phosphide
Hydrol
Hydro thol
1 -Hydro xychlordene
2-Hydroxydiphenyl
Hyvar
Hyvar X
IAA
IBA
IBP
IFC
COMMON NAME
Metal dehyde
Polychlorinated
naphthalenes
Bandane
Dimefox
Dihydroacetic acid
(Na salt)
2,3,6-TBA
Hexachloroacetone
Hexachlorobenzene
BHC
BHC
Hydrocyanic acid
Various formulations of
2,4-D, MCPA, MCPP,
2,4-DP & 2,4,5-T
Dichlorprop
Toxaphene & DDT
Dieldrin
Heptachlor
Heptachlor epoxide
Heptachlor
Norea
Endothall
EXD
Amitrole
Dioxathion
UC 10854
Norea
Terbutol
Dial if or
Dichlorvos
3-Indoleacetic acid
TEPP
BHC
BHC
Endrin
BHC
Dichlofenthion
Sulfur
Zineb
Thiram
Carbaryl
Ziram
BHC
Aldrin
Edifenphos
Endosulfan
Monol inuron
Binapacryl
Linuron
Pyrazophos
Dinoseb
Triazophos
Pyracarbolid
Thiram & thiophanate
methyl
PMA
CMPC
MCPA
MCPA & Dicamba
Triazophos
Endothall
Molinate
Phostoxin
Allyxycarb
Endothall
1-Hydroxychlordene
Phenyl phenol
Bromacil
Terbacil
3-Indoleacetic acid
Hormodin
IBP
Propham
CODE
NUMBER
6920
3920
0600
0600
2309
6740, 1880
2380
3860
3880
3860
5120
3240
3420
0200
2580
2035
2320
6540
0600
0600
3260
0600
2220
7120
6680
1060
7100
060D
0080
3180
4751
4240
2760
6777
5905
6680, 6671
5680
4340
4340, 2140
6777
3240
4740
3240
3960
5490
0800
6560
4011
5860
109
-------
NAME
Igran
Imidan
Imugan
Insectophene
Inverton 245
lodofenphos
loxym'l
IPC
Isco thane
Isobac 20
Isobenzan
Isocarb
Iso-Cornox
Isopestox
Isoprocil
Isopropalin
Isotox
IT-3233
IT-3456
Ivoset
Japidemic
Jodfenphos
Jolt
Kara thane
Karbaspray
Karbation
Karbofos
Karbutilate
Kannex
Karphos
Kartril T
Kauritil
Kazoe
Kel thane
Kemate
Kepone
Kerb
Kildip
Kill-All
Klllex
Kilmite 40
Kiloseb
Kiloprop
Kilsem
Kilval
Kitazin
Kleer-Lot
Kl oben
Klorex
KHH
Knoxweed
Kobutol
Kocide
Kop-Fume
Kop-Mite
Kopsol
Kop-Thiodan
Kop-Thion
Korax
Korlan
Kroma-Chlor
Krovar
Krysid
KUE 13032c
KUE 13183b
Kuron
Kurosal
Kwit
Kylar
Kypchlor
Kypfarin
COMMON NAME
Terbutryn
Phosmet
Chloranifor methane
Endosulfan
2.4,5-T
lodofenphos
loxynll
Propham
Dinocap
Isobac 20
Telodrin
Isocarb
MCPP
Mipafox
Isocil
Isopropalin
BHC
Fl urecol -n-butyl ester
CODE
NUMBER
3980
4000
3180
6840
4040
5860
2560
4400
4070
0600
3630
Chi orflurecol -methyl ester
Dinoseb acetate
Milky disease spores
lodofenphos
Ethoprop
Dinocap
Carbaryl
Metham
Malathion
Karbutilate
Diuron
Isoxathion
Diuron, aminotriazole
sodium thiocyanate
Copper oxychloride
Azide
Dicofol
Anilazine
Chlordecone
Pronomide
Dichlorprop
Sodium arsenite
Trimec
TEPP
Dinoseb
MCPP
MCPA
Vamidothion
IBP
Amitrole & Linuron
Neburon
Sodium chlorate
MH
EPIC & 2,4-D,
isooctyl ester
PCN8
Copper hydroxide
Ethylene dibromide
Chi orobenzi late
DDT
Endosulfan
Malathion
Chloronitropropane
Ronnel
Cadmium succinate &
potassium chromate
Diuron & Bromacil
ANTU
Dichlofluanid
Tolyfluanid
Silvex, PGBE esters
Si 1 vex
Ethion
Daminozide
Chlordane
Warfarin
2566
5880
2560
1060
6220
4260
6420
2740
1
5728 or 6172
2340
2920
1280
4090
2309
6540
2760
4400
4340
4011
0200, 4240
4940
2280
3300, 3020
5280
1360
1880
3180
4260
5980
2740, 0800
0260
6140
6120
3340
1200
7060
NAME
Kypfos
Kypman 80
Kypzine
Lambast
Lanbrol
Lamprecide
Lanex
Lannate
Lanoc CN
Lanslide
Lanstan
Larvacide
Larvatrol
Lasso
Lazo
Lead Arsenate
Lebaycid
Legumez Extra
Lenacil
Lepton
Leptophos
Lethane 384
LeyCornox
Leytosan
LH 3012
Lignasan
Limit
Lindafor
Lindagram
Lindane
Line Rider
Lintox
Linurex
Linuron
Liphadione
Liquiphene
Lironion
LM-91
Lonacol
Londax
Lorox
Lousewort
Lovozal
Lumeton
Luprisol
M-74
M-81
MAA
Machete
Mad
Mafu
Magnetic 70
Magron
Maintain
Maintain 3
Maintain CF 125
Malamar
Malaspray
Malathion
Maleic hydrazide
Malix
Maloran
Maneb
Maneba
Maneb gan
Manesan
Manzate
MAPO
Maposol
MAPS
Maretin
Marl ate
Manner
COMMON NAME
Malathion
Maneb
Zineb
MPMT
Fluemethyl
Lamprecide
Fl uometuron
Methomyl
Eulan
Lenacil & Linuron
Chi oroni tropropane
Chloropicrin
Bacillus Thuringiensis
Alachlor
Alachlor
Lead arsenate
Fenthion
Benazol in
Lenacil
Leptophos
Leptophos
Lethane 384
Benazol in
Phenyl mercury urea
Propineb
Ethyl mercury phosphate
CDAA & 2,4-D
Lindane
Lindane
Lindane or gamma BHC
2,4,5-T
Lindane
Linuron
Linuron
Chlorophacinone
PMA
Difenoxuron
Chlorophacinone
Zineb
Linuron & Propachlor
Linuron
Stavesacre
Fenozaflor
Metoprotryn
Propionic acid
Disulfoton
Thiometon
Methanearsonic acid
Butachlor
MSMA & 2,4-D
Dichlorvos
Sulfur
Magnesium chlorate
Bromacil
MH
Chi orflurecol -
methyl ester
Malathion
Malathion
Malathion
MH
Endosulfan
Chlorbromuron
Maneb
Maneb
Maneb
Maneb
Maneb
Metepa
Metham
Methiotepa
Naphthalaphos
Methoxychlor
Diuron
CODE
NUMBER
4260
4000
7120
4166
3620
4520
4185, 4240
4160
4160
4180
3520
4185
1190
419C
4220
1140, 2940
0680
0680
0680
6840
0680
4240
4240
1425
5680
1425
7120
4240, 5820
4240
2720
6665
4490
0922
4820, 2940
2320
0800
2280
4260
4260
4260
2280
3180
4300
4300
4300
4300
4300
6620
4540
2740
110
-------
NAME
Marpelon
Marvex
MAS
Matacil
Mataven
MB 9057
MB 10064
MBC
MC 25
MC 474
MC 1053
MC 1108
MC 1488
MC 1947
MC 2188
MC 2420
MCA 600
MC Defoliant
MCP
MCPA
MCPB
MCPES
MCPP
MEA
MeBr
Mecarbam
Mecopar
Mecopex
Mecoprop
Mediben
Medinoterb acetate
Meldane
Melprex
MEMA
Menazon
Mendrin
Menite
Meobal
MEP
Mephanac
Mephosfolan
Mepro
Mercaptodimethur
Mercaptofos
Mercaptophos
Mercaptothion
Merculine
Mercuram
Mercusol
Mergamma
Merpan
Merphos
Mersolite
Mertect
Merthon
Mesoranil
Mesurol
Metacide
Metadelphene
Metal dehyde
Metalkamate
Me tarn-sodium
Metaphos
Metaphoxide
Metapside
Metasystemox
Metasystox
Metasystox I
Metasystox II
Metasystox R
Metaxon
COMMON NAME
Lenacil & Benzthiazuron
Dichlorvos
Rhizoctol
Aminocarb
Difenzoquat
Asulam
Bromoxynil
Sodium chlorate
Guazatine
Mecarbam
Dinobuton
Dinoterb acetate
Medinoterb acetate
Dinocton-4
Chlormephos
Mecarphon
Mobam
Magnesium chlorate
MCPA
MCPA
MCPB
Methin
MCPP
Methoxyethylmercury
acetate
Methyl bromide
Mecarbam
The diethanolamine salts
of MCPP & 2,4-0
MCPP (K salt)
MCPP
Dicamba
Medinoterb acetate
Coumaphos
Dodine
Methoxyethylmercury
acetate
Menazon
Endrin
Mevinphos
Meobal
Fenitrothion
MCPA
Mephosfolan
MCPP
Methiocarb
Demeton-o
Demeton
Malathion
Phenylmercury
salicylate
Thiram
Phenylmercury
salicylate
BHC & organo Hg
compound
Captan
Folex
PMA
Thiabendazole
Polyethyl mercury
phosphate
Aziprotryn
Methiocarb
Methyl parathion
Deet
Metal dehyde
Metal kamate
Metham
Methyl parathion
Metepa
Methiotepa
Oxydemeton methyl
Demeton methyl
Demeton-o-methyl
Demeton-s-methyl
Oxydemeton methyl
MCPA
CODE
NUMBER
2320
0180
2395
0310
0820
4441
1316
4340
4340
4380
4400
4441
4400
2140
1540
2780
4453
3260
4640
4460
3480
4340
1630
4400
4500
1981
1981, 1982
4260
6680
1020
3640
5680
6660
4500
4580
0960
6620
4580
5220
5220
4340
NAME
Metham
Methamidophos
Methanearsonic acid
Methaphoxlde
Methar
Methazole
Methidathion
Methiocarb
Meth-0-Gas
Methomyl
Methoprene
Methoxone
Methoxychlor
Methoxy propazine
Methyl aphoxide
Methyl Guthion
Methyl isothlocyanate
Methylmercury
chloride
Methylmercury
Dicyanodiamide
Methylmercury iodide
Methyl Trlthion
Methyl thiotriazine
Meticide
Metilmerkapto-
fasocsid
Metmercapturon
Metoprotryn
Metoxuron
Metriben
Metron
Mevinphos
Mexacarbate
Mezene
MF-344
MGK Dog & Cat
Repel 1 ant
MGK R 326
MH
MH-30
MH 090
Micofume
Microzul
Midox
Mil bam
Mil -Col
Mil curb
Mildex
Milfaron
Mil go
Miller 531
Miller 658
Milogard
Mi Is tern
Mintacol
Mi rex
Mitigan
Mitox
2M-4Kh-M
MLT
Mobil awn
Mocap
Modown
Molina te
Monalide
Monex 3
Monitor .
Monoammonium
methanearsonate
Monocalcium
methanearsonate
Monocron
Monocrotophos
Monolinuron
Monosodium
methanearsonate
COMMON NAME
Metham
Methamidophos
Methanearsonic acid
Metepa
OSMA
Methazole
Methidathion
Methiocarb
Methyl bromide
Methomyl
Methoprene
MCPP
Methoxychlor
Prometon
Metepa f
Azinphos ffethyl
Metham
Methylmercury
chloride
Cyano (methylmercuri)
guanidine
Methylmercury iodide
Methyl carbophenothion
Desmetryn
Parathion-methyl
Oxydeme ton-methyl
Methiocarb
Metoprotryn
Metoxuron
Tricamba
Parathion-methyl
Mevinphos
Mexacarbate
Ziram
Koban
Methyl nonyl ketone
MGK R 326
MH
MH
Methiuron
Dazomet
Chlorophacinone
Chlorbenside
Ziram
Drazoxolon
Dimethirimol
Dinocap
Chloraniformethane
Ethirimol
Cd-Ca zinc chroma te
complex
Copper zinc chromate
Propazine
Ethirimol
Paraoxon
Mi rex
Dicofol
Chlorbenside
MCPB
Malathion
Dichlofenthion
Ethoprop
Bifenox
Molinate
Monalide
Diuron & MSMA
Methamidophos
MAMA
Calcium arsenite
Monocrotophos
Monocrotophos
Monolinuron
MSMA
CODE
NUMBER
6220
4750
4490
2860
4496
6340
4500
4520
4531
4400
4540
5760
3820
6620
4560
4572
4580
5220
4500
4631
4580
4640
7080
7100
2280
2280
1425
1340
7100
2792
2416
2560
3359
5800
3359
4720
2340
1340
4380
4260
2220
5880
0733
4740
4747
2740, 4820
4750
0360
0360
4751
4820
111
-------
NAME
Monoxone
Monurex
Monuron
Honuron-TCA
Morcram
Morestan
Morfoxon
Morkit
Horocide
Morphothion
Morphotox
Morsodren
Motox 6-3 Cotto.i
Spray
Moxie
MSMA
MTMC
Murbetex
Murfotox
Murvesoo
Muscatox
Mylone
Myprozine
N-2790
NAA
Nabac
Nabam
NAD
Naftil
Naled
Namilan
Nankor
Na NPA
1-Naphthol
Naphthyl phthalamic
acid
Naphthyl thiourea
Napromlde
Naptalam
Na TA
Natal
Navadel
NC-4780
NC-5016
NC-6897
Neburea
Neburex
Neburon
Neguvon
Nemacide
Nemafos
Nemafume
Nemagon
Nendrin
Neocid
Neocidol
Neo-Pynamin
Neoron
Nephis
New Mel
Nexagan
Nexion
NF 48
NIA 1240
NIA 2995
NIA 4512
NIA 4556
NIA 5488
NIA 5767
NIA 5961
NIA 5996
NIA 9044
NIA 10242
NIA 11092
NIA 17370
COMMON NAME
SMA
Monuron
Monuron
Monuron-TCA
Naptalam
Oxythioquinox
Morfamquat
Anthraquinone
Binapacryl
Morphothion
Morphothion
Cyano (methylmercuri)
guanidine
Toxaphene & Parathion,
methyl
Methoxychlor
MSMA — ..'
Tsumacide
Medinoterb acetate
Mecarbam
Fenson
Coumaphos
Dazomet
Pimaricin
Fonofos
Naphthaleneacetic acid
Hexachlorophene
Nabam
Naphthalene acetamide
Carbaryl & Ovex
Naled
Chlordane & Lindane
Ronnel
Naptalam
1-Naphthol
Naptalam,
ANTU
Napromide
Naptalam
TCA
TCA
Dioxathion
Fluoromidine
Fenozaflor
Ficam W
Neburon
Neburon
Neburon
Trichlorfon
Dichlofenthion
Zinophos
Dibromochlcropropane
Di bromoch 1 oropropane
Endrin
DDT
Diazinon
Tetramethrin
Bromopropyl ate
Ethylene dibromide
Ethylmercury sulfate
Bromophos ethyl
Bromophos
Thiophanates
Ethion
SWEP
Solan
Dicryl
Tetradifon
Endothion
Chloronitropropane
Dichlobenil
Binapacryl
Carbofuran
Karbutilate
Resmethrin
CODE
NUMBER
4760
4760
4780
4920
4800
0250
4803
4803
6740, 4580
4540
4820
4441
1540
2910
4900
3940
4840
4880
1060, --
4860
1200, 0680
5980
4920
4925
4920
0260
2010
4920
2580
4940
4940
4940
6780
2220
2090
2090
3260
1880
2080
0860
0840
6670, 6671
3340
6600
2200
1040
6420
6055
NAME
Niacides
Niagaramite
Niagara tran
Niagara thol
Nialate
Niclofen
Nicouline
Niklor
Nimitox
NIP
Ni pa-Thin
Niran
Niran
Ni trader
Nitralin
Nitrapyrin
Nitrofen
4-Nitro phenol
Nitropone C
Nitrox 80
Nix-Scald
No Bunt
No-Crab
Nogos
Noita-Koisumu
Nomersan
Nonachlor
No-Pest
Norax
Norea
Norflurazon
Nortron
Noruron
Novathion
Novigam
Novigam Super
NPA
NPD
NRDC-104
NTH
Nucidol
Nudrin
Nu-Film
Nuodex 84
N'lvacron
Nuvan
Nuvanol
Nuvanol N
Nu-Z
Oatax
Octacide
Octachlor
Octachlor epoxide
Octal ene
Octal ox
Off
Ohric
Oko
Oleocuivre
Oleoparaphene
Ordram
Orthene
Ortho 5353
Ortho 9006
Ortho 12420
Orthocide 406
Ortho-Klor
Ortho LM
preparations
Ortho MC
Orthophos
Ortho Phosphate
Defol iant
Orthoxenol
Oryzal in
COMMON NAME
Mercaptobenzothiazole
Aramite
Ovex
Endothall
Ethion
Nitrofen
Rotenone
Chloropicrin
Temephos
Nitrofen
Naptalam
Parathion
Chlordane
DNOC
Nitralin
Nitrapyrin
Nitrofen
4-Nitrophenol
Dinoseb
Parathion methyl
Ethoxyquin
Hexachl orobenzene
Calcium propanearsonate
Dichlorvos
DDT & Lindane
Thiram
Nonachlor
Dichlorvos
Chloroxuron
Norea
Norflurazon
Fluoromidine
Norea
Fenitrothion
Lindane
Pyrethrins & Pip.
Butoxide
Naptalam
Aspon
Resmethrin
Dimethyl phthalate
Diazinon
Methomyl
Pinolene
Mercaptobenzothiazole
Monocrotophos
Dichlorvos
Fenitrothion
lodofenphos
Zinc sulfate (basic)
Barban
MGK 264
Chlordane
Oxychlordane
Aldrin
Dieldrin
Deet
Dimethachlon
Dichlorvos
Copper oxides
Parathion
Molinate
Acephate
Metal kamate
Methamidophos
Acephate
Captan
Chlordane
Methylmercury
quinolinolate
Magnesium chlorate
Parathion
DEF
Phenyl phenol
Oryzal in
CODE
NUMBER
3240
3340
5040
6000
0020
5040
4920
5245
1200
5020
5031
5040
5060
2760
4580
3920
2320
1880, 0680
6680
5080
2320
5136
3480
0680
5940, 5620
4920
0300
6055
2460
2080
4520
0360
2320
3480
0400
1200
5200
0080
2380
2320
5245
4740
0025
0960
4750
0025
1020
1200
5245
1940
5490
5148
112
-------
NAME
OS-2046
Osmosalts
Osmosar
Outfox
Ovochlor
Ovotron
Oxadiazon
Oxamyl
Oxamyl oxi me
0x1 ne
Oxine-copper
Oxirane
Oxycarboxin
Oxychlordane
Oxycll
Oxydemeton methyl
Oxyquinoline
Oxythioquinox
P-1504
Paarlan
Padan
Pallethrin
Pamosol 2 Forte
Panoctine
Panodrin A-13
Panogen
Panoram D-31
Panthion
Papthion
Paracide
Paradow
Paramar
Para-Nitrophenol
Paraphos
Paraquat dichloride
Parathene
Parathion ethyl
Parathion methyl
Parawet
Parinol
Parnon
Parfox
Partron M
Parzate
Parzate C
Pa to ran
PCA
PCNB
PCP
PCPBS
PDB
PDQ
PDU
PEBC
Pebulate
Pedinex
Pencal
Penchlorol
Penite
Pennamine D
Penta
Pentachlorin
Pentachloronitro-
benzene
Pentachlorophenol
Pentachlorophenol,
Na salt
Pentacon
Pentanochlor
Penwar
Peprothion
Perchlorobenzene
Perecot
COMMON NAME
Mevinphos
Fluor Chrom Arsenate
Phenols
Cyprazlne
Chlorfenson or Ovex
Chlorfenson or Ovex
Oxadiazon
Oxamyl
Oxamyl oxlme
8-Qulnollnol sulfate
Copper 8-Qulnolate
Ethyl ene oxide
Oxycarboxin
Oxychlordane
Sodium chlorate
Oxydemeton methyl
8-Qu1nolinol
Oxythloquinox
Phosraet
Isopropalin
Cartap hydrochloride
Allethrln
Zineb
Guazatine
Cyano (methyl mercuri)
guanidine
MEMA
Dieldrin
Parathion
Phenthoate
p-Dichlorobenzene
p-Dichlorobenzene
Parathion
4-N1trophenol
Parathion
Paraquat dichloride
Parathion
Parathion
Parathion methyl
Parathion
Parinol
Parinol
Chlorophacinone
Parathion methyl
Nabam 8 Zineb
Zineb
Metabromuron
Pyrazon
PCNB
PCP
Fenson
Dichlorobenzene-p
MCPB
Fenuron
Pebulate
Pebulate
Dinex
Calcium arsenate
PCP
Sodium arsenite
2,4-D
PCP
DDT
PCNB
PCP
Sodium pentachloro-
phenate
PCP
Solan
PCP
DDT, Endosulfan &
Parathion methyl
Hexachlorobenzene
Copper oxides
CODE
NUMBER
4640
1615
5176
5186
5187 ,
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
5925
5280
5260
2300
4380
5300
5300
0980
5260
2940
5260
1880
5280
5260
2820
5260
5260
1880,
3180, 4580
3920
NAME
Perenox
Perfekthion
Perfluidone
Perthane
Pescombi
Pestan
Pestmaster EDB 85
Pestox III
Pestox XIV
Pestox XV
Pest Strip
PETD
PH 6040
Phal tan
Phenacide
Phenatox
Phencaptone
Phenmad
Phenmedipham
Phenotan
Phenothiazine
Phenpiazine
Phenthazine
Phentin acetate
Phenyl benzene
Phenyl mercury
acetate
Phenyl mercury
ammonium acetate
Phenyl mercury
borate
Phenyl mercury
chloride
Phenyl mercury
hydroxide
Phenyl mercury
iodide
Phenyl mercury-
8-oxyquinolate
Phenyl phenol
Pherocon GM
Phix
Phorate
Phosalone
Phosdrin
Phosfene
Phosfolan
Phosfon
Phoskil
Phosmet
Phosphamidon
Phosphine
Phosphopyron
Phos toxin
Phosvel
Phosvit
Phthalophos
Phthalthrin
Phyban H.C.
Phygon
Phyomone
Phystasol
Phytar 550
Phytomycin
Phytosol
Picfume
Pindone
Pinoran
Piperalin
Piperonyl Butoxide
Pipron
Pirimicarb
Pirimiphos ethyl
Pirimiphos methyl
Pirimor
Pi vac in
Pival
Pivaldione
COMMON NAME
Copper oxides
Dimethoate
Perfluidone
Perthane
Mecarbam
Mecarbam
Ethyl dibromide
Schradan
Dimefox
Mi pa fox
Dichlorvos
Met i ram
Diflubenzuron
Folpet
Toxaphene
Toxaphene
Phencapton
PMA
Phenmedipham
Dinoseb-acetate
Phenothiazine
Quinoxaline
Phenothiazine
Fentin acetate
Biphenyl
Phenylmercury
acetate
Setrete
Phenylmercury
borate
Phenylmercury
chloride
Phenylmercury
hydroxide
Phenylmercury
iodide
Quinex
Phenyl phenol
Disparlure
PMA
Phorate
Phosalone
Mevinphos
Mevinphos
Phosfolan
Chlorphonium
Parathion
Phosmet
Phosphamidon
Aluminum phosphide
Endothion
Phostoxin
Leptophos
Dichlorvos
Phosmet
Tetramethrin
MSMA
Dichlone
oc-Naphthylacetic acid
Trichloronate
Cacodylic acid
Streptomycin nitrate
Trichloronate
Chloropicrin
Pindone
Difenoxuron
Piperalin
Piperonyl Butoxide
Piperalin
Pirimicarb
Pirimiphos ethyl
Pirimiphos methyl
Pirimicarb
Pindone
Pindone
Pindone
CODE
NUMBER
2420
5366
5380
4441
4441
2320
2406
3660
6740
6740
5400
5680
5410
2566
5420
5420
3527
0740
5680
5460
5480
5485
5487
5490
5680
5500
5520
4640
4640
1610
5245
4000
5580
4190
2320
4000
4820
2180
0961
5640
5620
5640
5632
5642
5643
5632
113
-------
NAME
Pivalyn
P Kh NB
Planavin
Plantvax
Plus de Rltz
PMAS
PNP
Polaris
Polychlorinated
biphenyls
Polychlorinated
naphthalenes
Polychlorocamphene
Polymone 60
Polyram-Combi
Polyram-Ultra
Polyram Z
Polysol Forte
Pomasol Z Forte
Potablan
Potassium azide
Potassium di ethyl
dithiophosphate
Potassium diethyl
thiophosphate
Potassium dimethyl
dithiophosphate
Potassium dimethyl
thiophosphate
PP-062
PP-148
PP-149
PP-211
PP-5H
PP-675
PP-745
PP-781
Pramitol
Prebane
Pre-Beta 1
Pre-Beta 2
Prefar
Prefix
Preforan
Prefox
Premerge
Pre-San
Preventol
Preservit
Primatol
Primatol 025
Primatol A
Primatol P
Primatol Q
Primatol S
Primaze
Primin
Princep
Proban
Probe
Prodan
Profluralin
Profume
Prolan
Prolate
Pro! in
Promecarb
Prometon
Prometryn
Prometrex
Pronamide
Propachlor
Propanil
Propargite
Propazine
Propenal
Propham
Prophos
COMMON NAME
Pindone
PCNB
Nitralin
Oxycarboxin
Propanil
PMA
4-Nitrophenol
Glyphosine
Polychlorinated
biphenyls
Polychlorinated
naphthalenes
Toxaphene
MCPP & 2,4-D
Meti ram
Thiram
Zineb
Thiram
Ziram
Monalide
Potassium azide
Potassium diethyl
dithiophosphate
Potassium diethyl
thiophosphate
Potassium dimethyl
dithiophosphate
Potassium dimethyl
thiophosphate
Pirimicarb
Paraquat
Ethirimol
Pirimiphos ethyl
Pirimiphos methyl
Dimethirimol
Morfamquat
Drazoxolon
Prometon
Terbutryn
Pebulate & Dial late
Cycloate & Diallate
Bensulide
Chlorthiamid
Fluorodifen
Cyprazine & Ethiolate
Dinoseb
Bensul ide
Dichlorophen
Dazomet
Atraton
Prometon
Atrazine
Propazine
Prometryn
Simazine
Atrazine & Prometryn
Isolan
Simazine
Cythioate
Methazole
Sodium fluorosilicate
Profluralin
Methyl bromide
Oil an component
Phosmet
Warfarin
Promecarb
Prometon
Prometryn
Prometryn
Pronamide
Propachlor
Propanil
Propargite
Propazine
Acrolein
Propham
Ethoprop
CODE
NUMBER
5280
5020
5840
5680
5060
5700-5707
5720-5725
6740
4400, 2940
6680
7120
6680
7100
4747
5728
5731
5732
5733
5734
5632
5240
3359
5642
5643
2416
2792
5760
3980
5300, 2040
1591, 2040
0520
1615, 3335
2760
0520
0320
5760
0420
5800
5780
6660
0420, 5780
6160
1621
4496
4000
7060
5752
5760
5780
5780
4090
5820
5840
5160
5800
0027
5860
5880
NAME
Propi-Rhap
Prop-Job
Proponex D
Propoxur
Protect
Protex
Proxal
Prussic acid
PTF
PTMB
Puratized B-2
Pynamin
Pyracarbolid
Pyramin
Pyramin Plus
Pyrazon
Pyrethrins
Quel
Queletox
Quilan
Quinalphos
Quinex
Quinomethionate
Quinophenol
Quintozene
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-7465
Rabon
Rock Granular
Racumin
Radapon
Rad-E-Cate 25
Rad-E-Cate 35
Radoxone TL
Rametin
Rami k
Rampart
Ramrod
Ramucide
Randox
Rasikal
Raticate
Ratilan
Ratomet
Ravap
Raviac
Ravyon
Rawetin
Rax Water Soluble
RE 4355
Readex
Rebel ate
Reddon
Reducymol
Regim 8
Reglone
Regulox
Resistox
Resmethrin
COMMON NAME
Dichlorprop
Propanil
Amines of CMPP &
2,4-D
Propoxur
Protect
Rotenone
Trichlorfon
Hydrocyanic acid
Polyram
Danifos
Mercuric lactate
Allethrin
Pyracarbolid
Pyrazon
Pyrazon & Dalapon
Pyrazon
Pyrethrins
Ancymidol
Fenthion
Benefin
Quinalphos
Phenyl mercuric
oxyquinolate
Oxythioquinox
8-Quinolinol
PCNB
Arami te
Sulphenone
Carbophenothion
Phosmet
Azinphos ethyl
Azinphos methyl
Vernolate
Pebulate
Cycloate
Oxydemeton methyl
Bensulide
Molinate
Byram
Napropamide
Sti rof os
Fenac & Atrazine
Coumatetralyl
Dalapon Na
Sodium Cacodylate
Sodium Cacodulate &
cacodulic acid
Ammonium thiocyanate
Naphthalaphos
Diphacinone
Phorate
Propachlor
Chlorophacinone
CDAA
Sodium chlorate
Norbormide
Coumachlor
Chlorophacinone
Dichlorvos & Stirofos
Chlorophacinone
Carbaryl
Naphthalaphos
Warfarin
Naled
Thioquinox
Dimethoate
2,4,5-T
Ancymidol
TIBA
Diquat dibromide
MH
Coumaphos
Resmethrin
CODE
NUMBER
2309
5840
0440
5882
6000
6780
0100
5905
5925
5925, 1660
5925
5940
0230
3520
0480
5966
4800
5280
1080
4000
3840
3820
7020
5300
1591
5220
0520
4740
2010
3740
3460, 0420
1660
2600
5500
5820
1425
1140
1425
2320, 3740
1425
1060
7060
4860
2420
6840
0230
2660
2280
1540
6055
114
-------
NAME
Res-Q
Retard
RH-315
Rhodiatox
Rhomene
Rhonox
Rhothane
Rlcetrine
Roccal
Rodine
Rogor
Rogue
Ro-Neet
Ronstar
Rootone
Rospin
Rotenone
Rotox
Roundup
Roxion
Royal HH-30
Rozol
R.P. 11974
R.P. 17623
Ruelene
Rukseam
Ruphos
Rutgers 612
Rycel an
Ryzelan
S-276
S-410
S-767
S-1752
S-2940
S-4084
S-4087
S-4400
S-6000
S-9115
S-10165
S-15076
S-22012
SADH
Salithion
Salvo
SAN 9789
Sancap
Santar
Santobrite
Santochlor
Santoquin
Sapecron
Saphi-Col
Saphizon
Saphos
Sappiran
Saprol
Sarclex
Sarolex
Saturn
Sayfor A
Sayfos
SBP-1382
Seal dip
Sobering 4075
Schering 34615
Schering 35830
Schering 36056
Schering 36268
Schering 38107
Sclex
Scogal
COMMON NAME
Maneb, HCB &
Captan
MH
Pronamide
Parathion
MCPA
MCPA
ODD
Copper triethanol-
amine complex
Benzalkonium chloride
Red Squill
Dimethoate
Propanil
Cycloate
Oxadiazon
Naphthalene acetamide
Chloropropylate
Rotenone
Methyl bromide
Glyphosate
Dimethoate
MH
Chlorophacinone
Phosalone
Oxadiazon
Crufomate
DDT
Dioxathion
Ethyl hexanediol
Oryzalin
Oryzalin
Disulfoton
Metasystox S
Fensulfothion
Fenthion
Phenthoate
Cyanox
Surecide
Trichloronate
Cypromid
Cyprazine
Propanil
Ethiolate
Benzthiazuron
Daminozide
Sal ithion
2,4-D
Norf 1 urazon
Dipropetryn
Mercuric oxide
Sodium pentachloro-
phenate
Dichlorobenzene-p
Ethoxyquin
Chlorfenvinphos
Menazon
Menazon
Menazon
Ovex or Chlorfenson
Triforine
Linuron
Diazinon
Benthiocarb
Menazon
Menazon
Resmethrin
Diphenylamine
Phenmedipham
Promecarb
Monalide
Formetanate Hydrochloride
Chlordimeform
Desmedipham
Dichlozoline
Cyanazine & MCPA
CODE
NUMBER
4300,
3920, 1020
2280
4090
5245
4340
4340
1750
2420
5840
1591
5176
4880
6000
3801
2420
2280
1425
5520
5176
6020
1880
2580
3380
5148
5148
2720
3500
3520
6360
1615
5840
3335
6050
2940
5136
2820
2300
1300
4453
4453
4453
6822
4240
2080
0570
4453
4453
6055
5410
5752
4747
3680
1480
2006
1552,4340
^
NAME
SD 3562
SO 4294
SD 7859
SD 8447
SD 8530
SD 8786
SD 9098
SD 9129
SD 11831
SD 14114
SD 15418
SD 30053
Secbumeton
Seedrin
Select
Selinon
Semeron 25
Sencor
Sencoral
Sencorex
Sendran
Septene
SES
Sesoxane
Sevin
Sevithion
Shed-A-Leaf
Shinmerex
Short-stop E
Shoxin
SI-6505
Sicarol
Siduron
Silvanol
Si 1 vex
Silvi-Rhap
Silvisar 510
Silvisar 550
Simanex
Simazine
Sinbar
Sinituho
Sinox
Sinox General
Si stan
Slam
Slo-Gro
SMDC
Smite 86
Snip Fly Bands
Sodium Azide
Sofril
Soilbrom 85 8, 86
SDK
Solabar
Solo
Sol vi rex
SOPP
Soprabel
Sopracol 781
Sopragam
Sopranebe
Soprathion
Soprocide
Soyex
SP-1103
Spectracide
Spergon
Spotrete
Spra-Cal
Spring-Bak
Sprout Nip
Sprout-Stop
Spud-Nic
Squill
SR 73
SRA 5172
COMMON NAME
Dicrotophos
Crotoxyphos
Chlorfenvinphos
Stirofos
Landrin-3,4,5 Isomer
Landrin-2,3,5 Isomer
Akton
Monocrotophos
Nitralin
Vendex
Cyanazine
Benzoylprop ethyl
Secbumeton
Aldrin V,
Naptalam
DNOC
Desmetryn
Metribuzin
Metribuzin
Metribuzin
Propoxur
Carbaryl
Sesone
Sesamex
Carbaryl
Carbaryl & Parathion
methyl
Sodium chlorate
Phenylmercuric acetate
Terbutryn
Norbormide
Hydroxyisoxazole
Pyracarbolid
Siduron
Lindane
Si 1 vex
Silvex
Cacodylic acid
MSMA
Simazine
Simazine
Terbacil
PCP
DNOC
Dinoseb
Metham
Azothoate
MH
Metham
Azide
Dimetilan
Sodium Azide
Sulfur
Ethylene dibromide
Carbanolate
Barium polysulfide
Naptalam
Disulfoton
Sodium phenylphenate
Lead arsenate
Drazoxolon
Parathion & Lindane
Maneb
Parathion
BHC
Fluorodifen
Tetramethrin
Diazinon
Chloranil
Thiram
Calcium arsenate
Nabam
Chlorpropham
MH
Chlorpropham
Red Squill
Clonitralid
Methamidopfios
CODE
NUMBER
0700
1500
1300
3740
0360
5020
7013
1552
0578
0080
4920
2770
0440
1060
1060
1060, 4580
5680
3980
5905
6100
0680
6120
6120
0961
4820
6160
6160
6560
5260
2770
2760
6620
2280
6620
5728 or 6172
6172
4920
2720
2800
4180
2792
5245, 0680
4300
5245
0600
2080
1180
6680
0980
4840
1420
2280
1420
4750
115
-------
NAME
SRA 7312
Stam F-34
Stain M-4
Stannoplus
Stannoram
Stay-Kleen
Stlrofos
Stop Scald
Stops pot
Streptomycin Sulfate
Strobane
Strobane T
Stunt Man
Subitex
Sucker Stuff
Suffix
Sulfallate
Sulfasan
Sulf oxide
Sul foxyl
Sulkol
Sumithion
Sumitol
Sunclde
Super Crab-E-Rad
Super Crab-E-Rad
A.M.A.
Super Crab-E-Rad
Calar
Super Dal-E-Rad
Super Dal-E-Rad
Calar
Super De-Sprout
Sup'R Flo
Super Sucker Stuff
Supona
Supracide
Surcopur
Surecide
Surflan
Su Seguro Carpldor
Sustar 2-S
Sutan
Swat
Syllit
Synklor
Synthrin
Systemox
Systox
Sytam
Sytemp
2,4,5-T
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
Tabatrex
Tachigaren
Tag HL 331
Talan
Tamaron
Tandex
Tanone
Tartan
Tarzol
Task
Taterpex
Tayssato
2,3,6-TBA
TBCS-53
COMMON NAME
Quinalphos
Propanil
Propanil
Decafentln
Decafentin
Cyanazlne & Llnuron
Stirofos
Ethoxyquin
Phenylmercury chloride
Streptomycin Sulfate
Terpene polychlori nates
Terpene polychlorinates
(Toxaphene)
MH
Dinoseb
MH
Benzoylprop ethyl
CDEC
PD
SulTBxide
Sulfoxide
Sulfur
Fenitrothion
Secbumeton
Propoxur
Amine methanearsenates
Ammonium methane-
arsenates
Calcium acid
methanearsenates
Amine roethanearsenates
Calcium acid
methanearsenates
MH
Maneb
MH
Chlorfenvinphos
Methidathion
Propanil
Surecide
Oryzalin
Trifluralin
Fluoridamid
Butyl ate
Bomyl
Dodine
Chlordane
Resmethrin
Demeton
Demeton
Schradan
Toxaphene, Parathion &
Parathion methyl
2,4,5-T
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
Tabutrex
Hymexazol
Phenyl mercuric acetate
Dinobuton
Methamidophos
Karbutilate
Phenthoate
Cyanthoate
Fenozaflor
Dichlorvos
Chlorpropham
MEMC
2,3,6-TBA
Copper sulfate, basic
CODE
NUMBER
5966
5840
5840
1522, 4240
3740
5480
6222
6240
6740
2280
2760
6740
0578
1160
3420
6300
6300
3480
0440
6740
4300
6740
1300
6340
5840
6360
5148
6800
3623
0940
2780
1200
6055
1981, 1982
1981, 1982
6740,
5245, 4580
6840
6860
6870
6880
6885
5680
4750
6420
2320
1420
6920
NAME
TBTO
TBZ
TCB
TCMTB
TCNB
TCTP
TD-183
TDE
Tecnazene
Tecto
Tedion
Tekwaisa
Telodrin
Tel one
Tel one C
Tel var
TEM
Temephos
Temik
Tendex
Tenoran
TEPP
Terbacil
Terbucarb
Terbuthylazine
Termil
Terraclor
Terraclor Super X
Terra -Coat
Terracur
Terracur P
Terramitsin
Terramycin
Terra-Sytam
Terrazole
Tersan
Tersan 1991
Tersan SP
Tetrachlorophenol
Tetrachloroquinone
Tetrachlorothiophene
Tetrachlorvinphos
Tetradifon
Tetraethyl
pyrophosphate
Tetrasul
Tetron
TFN
TH 6040
Thanite
Thiabendazole
Thibenzole
Thifor
Thimer
Thimet
Thimul
Thiocron
Thiocron Extra
Thiodan
Thiodemeton
Thiodiphenylamine
Thiofanox
Thiometan
Thiometon
Thioneb
Thionex
Thiophal
Thiophanate
Thiophanate methyl
Thiophos
Thiotepp
Thiotex
Thiram
Thiramad
Thirasan
Thistrol
Thuricide
COMMON NAME
Butinox
Thiabendazole
Trichlorobenzene
TCMTB
Tecnazene
Penphene
Penphene
ODD
Tecnazene
Thiabendazole
Tetradifon
Parathion methyl
Isobenzan
Dichloropropene
Chloropicrin
Monuron
Tretamine
Temephos
Aldicarb
Propoxur
Chloroxuron
TEPP
Terbacil
Terbutol
Terbuthylazine
Chlorothalomil
PCNB
Terrazole
Terrazole
Thiadiazinthion
Fensulfothion
Oxytetracycline
Oxytetracycl ine
Dimefox
Terrazole
Thiram
Benomyl
Chloroneb
Tetrachlorophenol
Chloram'l
Penphene
Stirofos
Tetradifon
TEPP
Tetrasul
TEPP
Lamprecide
Diflubenzuron
Thanite
Thiabendazole
Thiabendazole
Endosulfan
Th i ram
Phorate
Endosulfan
Amidithion
Amidithion &
Fenitrothion
Endosulfan
Disulfoton
Phenothiazine
Thiofanox
Metasystox S
Thiometon
Meti ram
Endosulfan
Folpet
Thiophanate
Thiophanate methyl
Parathion
Sulfotep
Thiram
Thiram
Thiram
Thiram
MCPB
Bacillus Thuringiensis
CODE
NUMBER
6660
6435
1750
6435
6660
6600
4580
2306
4760
0020
0060
0440
6540
6560
1640
5280
6590
6590
3500
6590
6680
0500
1380
1180
3740
6600
6540
6630
6540
4166
2406
6640
6660
6660
3180
6680
5500
3180
3480
3180
2720
5420
6663
6665
3180
3660
6670
6671
5245
6680
6680
6680
6680
4380
116
-------
NAME
Thylate
Thynon
Tiazon
Tiezene
Tiguron
Tilarex
Ti 11 am
Tillamtox
Timbo
T1met
Tirampa
TMTDS
Tobaz
TDK
Tolban
Tomarin
Tomaset
Tomato tone
Tomorin
Topane
Tope i de
Topiclor 20
Topitox
Topsin
Topsin-M
Torac
Tordon
Tormona
Toxakil
Toxaphene
2,4,5-TP
TPTH
TPTOH
Trametan
Trefanocide
Treficon
Treflan
Trefmid
Tre-hold
Trey
Triallate
Triaram
Triasyn
Triazophos
Triazotion
Tribac
Tribactur
Triban
Tribetol
Tribunil
Tributon
Tricarbamix Z
Tricarnam
Trichlorfenson
Trichlorfon
Trichloroben-
zoic acid
2,4,5-Trichloro-
phenol
Trichlorpyrphos
Tri-Clor
Tricornox
Tridemorph
Tridex
Tridodine
Tri-Endothall
2,4,5-T, Triethyl-
amine salt
Trifene
Trifenson
Trifluralin
Triflurex
Trifocide
Triforine
Trifungol
Triherbide
Triherbide-CIPC
COMMON NAME
Thlram
Dlthianon
Dazomet
Zineb
Fenthion
PCNB & Qulntozene
Pebulate
Benqulnox
Rotenone
Phorate
Thiram
Thiram
Thlabendazole
Nitrofen
Profluralin
Coumafuryl
N-m-t
4-CPA
Coumachlor
Sodium phenylphenate
Benzadox
Chlordane
Chlorophacinone
Thiophanate
Thiophanate methyl
Dial ifor
Plcloram
2,4,5-T
Toxaphene
Toxaphene
Si 1 vex
Fentin hydroxide
Fentin hydroxide
Thiram
Trifluralin
Trifluralin
Trifluralin
Trifluralin &
Diphenamid
Naphthaleneacetic acid
Siduron
Triallate
Atram
Anilazine
Triazophos
Azinphos ethyl
2,3,6-TBA
Bacillus Thuringiensis
Pindone
Endothall & Propham
Methabenzthiazuron
2,4-D & 2,4,5-T
Ziram
Carbaryl
Ovex or Chlorfenson
Trichlorfon
2,3,6-TBA
2,4,5-Trichlorophenol
Chlorpyrifos
Chloropiorin
Benazol in
Tridemorph
EXD
Dodine
Endothall
2,4,5-T, Triethyl-
amine salt
Fenac
Fenson
Trifluralin
Trifluralin
DNOC
Triforine
Ferbam
Propham
Chlorpropham
CODE
NUMBER
6680
2721
7120
3520
5300
6000
5500
6680
6680
6660
5040
3720
2800
0577
1200
1425
6670
6671
2835
5600
6840
6740
6740
6120
3540
3540
6680
6800
6800
6800
6800, 2620
4900
6100
6770
2920
6777
3840
6920
3240, 5860
2940, 6840
7100
1060
6780
6920
6890
2900
6792
3420
2780
3240
6895
3460
6800
6800
2770
6822
3600
5860
1420
NAME
Tri-iodobenzoic acid
Trim
Trimangol
Trlmanoc
Trimaton
Trimetion
Trinox
Triofterol
Trioneb
Trioxone
Tri-PCNB
Tri-P.E.
Trl-Penar
Triphenyltin acetate
Triphenyltin
hydroxide
Triscabol
Trithion
Tritisan
Tritoftorol
Tri-VC 13
Trixabon
Trixan
Trizinoc
Trizone
Trol ene
Tronabor
Tropital
Tropotox
Truban
Trysban
Tserenox
Tsitrex
Tuads
Tuberite
Tubotoxin
Tugon
Tugon Fl iegen Kugel
Tumbleleaf
Tumex
Tupersan
Turf Fungicide
Tutane
U-27415
UC 7744
UC 10854
UC 19786
UC 20047A
UC 20299
UC 21149
UC 22463
Ultracide
Unden
Unipon
Uniroyal D 014
Urab
USB-3584
V-18
V-101
Valexon
Validacin
Vamidoate
Vancide FE-95
Vancide MZ
Vancide MZ-96
Vancide TM-95
Vancide TM Flowable
Vaponite
Vapor Card
Vapotone
COMMON NAME
TIBA
Trifluralin
Maneb
Manoc
Metham
Dimethoate
Trichlorfon
Zineb
Metiram
2,4,5-T
PCNB
Dimexan
Penar
Fentin acetate
Fentin hydroxide
Ziram
Carbophenothion
PCNB
Zineb
Dichlofenthion
Dimexan, Cycluron &
Chlorbufam
PCNB, Quintozene &
Thiram
Zinoc
Methyl bromide, Chloropicrin
& Propargyl bromide
Ronnel
Borax
Piprotal
MCPB
Terrazole
2,3,6-TBA
Benquinox
Dodine
Thiram
Propham
Rotenone
Trichlorfon
Propoxur
Sodium chlorate
8-Quinolinol
Siduron
Cyano (methylmercuri)
guanidine
sec-Butylamine
Banamite
Carbaryl
Hercules AC 5727
Dinobuton
Tranid
Prep
Aldicarb
Rowmate
Methidathion
Propoxur
Dalapon-Na
Propargite
Fenuron-TCA
Dinitramine
Tetrad if on
Tetrasul
Phoxim
Validamycin A
Vami doth ion
Ferbam
Ziram
Ziram
Thiram
Thiram
Dichlorvos
Pinolene
TEPP
CODE
NUMBER
6800
4300
6620
2420
6780
7120
6840
5280
3527
3540
7100
1080
5280
7120
2220
5980
4380
6590
6920
2780
6680
5860
6000
6780
0440
6100
1060
0060
6340
0440
1660
5160
2551
6600
6630
3600
7100
7100
6680
6680
2320
6540
117
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NAME
VC-13 Nemacide
VC 9-104
Vegadex
Veglben
Velsicol 58-CS-ll
Velsicol 1068
Vendex
Venzar
Veratridene
Veratrin
Veratrum
Vergemaster
Vernam
Vernolate
Vertron 2D
Vertron 2T
Vertron T
Vi-Cad
Viozene
ViPar
Vi-pex
Viricuivre
Vitavax
Volaton
Vondalhyde
Vondcaptan
Vondodine
Vondrax
Vonduci
Vonduron
Voronit
VPM
Vydate L oxamyl
Wacher S 1410
Wallop 6
Warbex
Watathion
Weed-Ag-Bar
Weedar
Weedazol
Weedbeads
Weed-E-Rad
Weedez Wonder Bar
Weed-Hoe
Weedol
Weedone
Weedozol
Weed-Rhap
Wepsyn
WL 17,731
WL 19,805
Wydac
Yomesan
Zassol
Z-C Spray
Zebtox
Zectran
Zelan
Zelio
Zephiran
Zerdane
Zerlate
Zidan
Zinc Uversol
Zineb
Zinophos
Zinosan
Ziram
Zirberk
COMMON NAME
Oichlofenthion
Ethoprop
CDEC
Chloramben
Dlcamba
Chlordane
Vendex
Lenacil
Sabadilla
Sabadilla
Hellebore
2,4-0
Vernolate
Vernolate
2,4-D
2,4,5-T
2,4,5-T
Cadmium chloride
Ronnel
MCPP 8, 2,4-D
MCPP (potassium salt)
Copper oxychloride
Carboxin
Phoxim
MH
Captan
Dodine
MH
Diuron
Diuron
Fuberidazole
Metham
Oxamyl
Dimefox
Propachlor &
Parathion
Famphur
Surecide
2,4-D
2,4-D 8. 2,4,5-T
Amitrole
Sodium pentachloro-
phenate
DSMA & MSMA
2,4-D
DSMA & MSMA
Paraquat dichloride
PCP, 2,4-D &
2,4,5-T
Amitrole
2,4-D
Triamiphos
Benzoylprop ethyl
Cyanazine
Propanil & Carbaryl
Niclosamide
Sodium cyanate
Ziram
Zineb
Mexacarbate
MCPA
Thallium sulfate
Benzalkonium chloride
DDT
Z i ram
Zineb
Zinc naphthenate
Zineb
Thionazin
Zineb
Ziram
Ziram
CODE
NUMBER
2220
5880
1160
0140
2140
1200
7013
4185
2940
7020
7020
2940
6840
6840
5980
4400, 2940
1100
2280
1020
2780
2280
2740
2740
6620
5186
5820, 5245
3440
6360
2940
2940, 6840
0200
2820
2860, 4820
2940
2860, 4820
5240
5260,
2940, 6840
0200
2940
0578
1552
5840, 1060
7100
7120
7080
4340
1880
7100
7120
7120
7120
7100
7100
NAME
Ziride
Zithlol
Zitox
Zobar
Zolone
Zoocoumarin
Zorial
Zotox Crab Grass
Killer
ZR-512
ZR-515
Zytox
COMMON NAME
Ziram
Malathion
Ziram
PBA
Phosalone
Warfarin
Norf 1 urazon
Arsenic acid
Altozar
Methoprene
Methyl bromide &
ethylene dibromide
CODE
NUMBER
7100
4260
7100
5520
7060
5136
4531
118
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TECHNICAL REPORT DATA
(Please read Instructions on the reverse before completing)
1. REPORT NO.
EPA 600/9-76-012
3. RECIPIENT'S ACCESSION-NO.
4. TITLE AND SUBTITLE
ANALYTICAL REFERENCE STANDARDS AND SUPPLEMENTAL DATA
for Pesticides and Other Selected Organic Compounds
5. REPORT DATE
May 1976
6. PERFORMING ORGANIZATION CODE
7. AUTHOR(S)
J. F. Thompson (Editor)
8. PERFORMING ORGANIZATION REPORT NO
9. PERFORMING ORGANIZATION NAME AND ADDRESS
Analytical Chemistry Branch
Environmental Toxicology Division
Health Effects Research Laboratory
Research Triangle Park, N.C. 27711
10. PROGRAM ELEMENT NO.
1EA615
11. CONTRACT/GRANT NO.
12. SPONSORING AGENCY NAME AND ADDRESS
Health Effects Research Laboratory
Office of Research and Development
U.S. Environmental Protection Agency
Research Triangle Park, N.C. 27711
13. TYPE OF REPORT AND PERIOD COVERED
14. SPONSORING AGENCY CODE
EPA-ORD
15, SUPPLEMENTARY NOTES
16. ABSTRACT
This manual lists several hundred compounds of analytical reference standards
of insecticides, herbicides, algicides, nematocides, rodenticides and fungi-
cides which are available, mostly in purified form, in subsamples of 100
milligrams to any bona fide pesticide laboratory in the world free of charge.
Also included in the manual are miscellaneous data pertinent to pesticidal
compounds such as precautionary 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 2,400 pesticide equiva-
lent names.
KEY WORDS AND DOCUMENT ANALYSIS
DESCRIPTORS
b.lDENTIFIERS/OPEN ENDED TERMS
c. COSATI Field/Group
standards
chemical analysis
pesticides
organic compounds
07 C, D
13. DISTRIBUTION STATEMENT
RELEASE TO PUBLIC
19. SECURITY CLASS (This Report/
UNCLASSIFIED
21. NO. OF PAGES
124
20. SECURITY CLASS (This page)
UNCLASSIFIED
EPA Form 2220-1 (9-73)
119
-------
ENVIRONMENTAL PROTECTION AGENCY
Technical Publications Branch
Office of Administration
Research Triangle Park, North Carolina 27711
POSTAGE AND FEES PAID
ENVIRONMENTAL PROTECTION AGENCY
EPA - 335
OFFICIAL BUSINESS
AN EQUAL OPPORTUNITY EMPLOYER
Return this sheet if you do NOT wish to receive this material
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PUBLICATION NO. EPA-600/9-76-012
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