United States                              .FINAL
               Environmental Protection                        ECAO-CIN-001 2
               Agency	August.  1988
 -^ __~ -        ^Z           K       •              Hev^sed  Uecember , iyy
oEPA       Research and
               Development
              DRINKING WATER CRITERIA DOCUMENT
              FOR TRICHLOROBENZENES
               Prepared for
              OFFICE OF WATER
               Prepared by
              Environmental Criteria and  Assessment Office
              Office of Health and Environmental Assessment
              U.S. Environmental Protection  Agency
              Cincinnati,  OH  45268
                         DRAFT:  00 NOT CITE OR QUOTE


                                 NOTICE

           This document I* a preliminary draft. It has not been formally released
        by the U.S.  Envlroraental  Protection Agency and should not at this stage be
        construed to represent Agency policy.  It Is being circulated for comments
        on Its technical accuracy and policy Implications.

-------
                                  DISCLAIMER
    This  document has  been reviewed  1n accordance  with  the  U.S.  Environ-
mental  Protection  Agency's  peer  and  administrative   review  policies  and
approved  for  publication.   Mention  of  trade  names  or commercial  products
does not constitute endorsement or recommendation for use.
                                       11

-------
                                   FOREWORD
    Section 1412  (b)(3)(A)  of  the Safe  Drinking Water  Act,  as amended  In
1986, requires  the  Administrator of  the  Environmental  Protection Agency  to
publish  maximum  contaminant  level  goals  (MCLGs)  and  promulgate  National
Primary  Drinking  Water  Regulations  for   each  contaminant,  which,  In  the
judgment of the  Administrator,  may have  an  adverse effect on  public  health
and  which  Is  known  or  anticipated to  occur  In  public  water   systems.   The
MCLG  Is  nonenforceable  and  Is set  at  a  level at  which  no known or  antici-
pated  adverse  health   effects   1n  humans  occur  and  which  allows  for  an
adequate margin of  safety.   Factors considered  1n  setting the  HCLG  Include
health effects data  and  sources  of exposure other than drinking  water.

    This document  provides   the  health effects  basis  to be  considered  1n
establishing the NCLG.   To achieve  this objective,  data  on pharmacoklnetlcs,
human exposure, acute and  chronic  toxlclty  to animals  and humans,  epidemi-
ology and mechanisms of toxlclty are evaluated.   Specific  emphasis  Is  placed
on  literature  data  providing dose-response  Information.  Thus,  while  the
literature  search and evaluation performed  In support  of this  document  has
been comprehensive,  only the  reports  considered  most pertinent  In  the  deri-
vation of  the MCLG  are  cited In the document.   The comprehensive  literature
data base  In  support of this document  Includes  Information  published  up  to
1985;  however,  more  recent  data  may  have  been  added  during  the  review
process.   Editorial  changes  were also  made In  1991  when this  document  was
finalized.

    When adequate health effects data exist, Health Advisory values  for less
than  lifetime  exposures   (1-day,   10-day  and  longer-term,    ~10X   of   an
Individual's lifetime)  are  Included In  this document.   These values  are  not
used  1n  setting  the MCLG,  but  serve  as  Informal guidance to  municipalities
and  other  organizations when  emergency  spills  or contamination  situations
occur.
                                                 Tudor Davis,  Director
                                                 Office of Science and
                                                 Technology
                                                 James Elder,  Director
                                                 Office of Ground Water
                                                 and Drinking  Water
                                      111

-------
                             DOCUMENT DEVELOPMENT


W. Bruce Pelrano, Document Manager and Principal  Author
Environmental Criteria and Assessment Office, Cincinnati
U.S. Environmental Protection Agency

John Clcmanec, Assistant Document Manager
Environmental Criteria and Assessment Office, Cincinnati
U.S. Environmental Protection Agency

Special Note:  This  document  was developed  from  the comprehensive Informa-
               tion  found  In  the Health Assessment  Document  for  Chlorinated
               Benzenes (EPA 600/8-84-015F).


Internal Scientific Reviewers and Contributors

David J. Relsman
Environmental Criteria and Assessment Office, Cincinnati
U.S. Environmental Protection Agency

Charles H. R1s III
Carcinogen Assessment Group, Washington, DC
U.S. Environmental Protection Agency

Seong T. Hwang
Exposure Assessment Group, Washington, DC
U.S. Environmental Protection Agency

Herbert H. Cornish
Ypsllantl. Michigan

Norman M. TMeff
University of Texas Medical Branch
Galveston, Texas

Shane S. Que Hee
Department of Environmental Health
University of Cincinnati
Cincinnati. Ohio

William L. Marcus
Office of Drinking Water, Washington, DC
U.S. Environmental Protection Agency
                                       1v

-------
Editorial Review

Erma R. Durden
Judith A. Olsen
Environmental Criteria and Assessment Office, Cincinnati
U.S. Environmental Protection Agency


Document Preparation

Technical  Support  Services  Staff,   Environmental  Criteria  and  Assessment
Office, Cincinnati

-------
                              TABLE OF  CONTENTS

                                                                      Page
  I.  SUMMARY	      1-1

 II.  PHYSICAL AND CHEMICAL PROPERTIES	     II-l

      CHEMICAL ANALYSIS  	     II-6

           Chemical Analysis 1n Water 	     II-7
           Chemical Analysis 1n Soil, Sediment and Chemical
           Waste Disposal Site Samples	     II-7
           Chemical Analysis In Fish and Other Foods	     II-7
           Chemical Analysis In Air . .	     II-8

      SUMMARY	     II-9

III.  TOXICOKINETICS	    III-l

      ABSORPTION	    IH-1
      DISTRIBUTION	    III-1
      METABOLISM	    III-2
      EXCRETION	    III-6

      SUMMARY	    III-9

 IV.  HUMAN EXPOSURE	     IV-1

  V.  HEALTH EFFECTS IN ANIMALS 	      V-l

      ACUTE TOXICITY	      V-l
      SUBCHRONIC TOXICITY 	      V-6
      CHRONIC TOXICITY	      V-15
      MUTAGENICITY	      V-17
      CARCIN06ENICITY 	      V-18
      REPRODUCTIVE AND TERATOGENIC TOXICITY 	      V-19

      SUMMARY	      V-21

 VI.  HEALTH EFFECTS IN HUMANS	     VI-1

      SUMMARY	     VI-1

VII.  MECHANISMS OF TOXICITY	    VII-1

      SUMMARY	    VII-3
                                     vl

-------
                          TABLE OF CONTENTS  (cont.)

                                                                       Page
VIII.  QUANTIFICATION OF TOXICOLOGIC EFFECTS 	   VIII-1

       INTRODUCTION	VIII-1
       NONCARCINOGENIC EFFECTS 	   V11I-6
       QUANTIFICATION OF NONCARCINOGENIC EFFECTS 	   VIII-7

            Derivation of 1-Day HA 	   VIII-7
            Derivation of 10-Day HA	VIII-12
            Derivation of Longer-term HA 	   VIII-14
            Assessment of Lifetime Exposure and Derivation of
            a DWEL	VIII-18

       CARCINOGENIC EFFECTS	VIII-19
       EXISTING GUIDELINES, RECOMMENDATIONS AND STANDARDS	VIII-19

            Occupational 	   VIII-19
            Transportation and Regulations 	   VIII-20
            Solid Waste Regulations	VIII-20
            Water	VIII-21

       SUMMARY 	   VIII-21

  IX.  REFERENCES	     IX-1
                                     vll

-------
                                LIST  OF TABLES


 No.                                Title
  II-l   Synonyms,  Trade Names and Identification Numbers of
         the Trlchlorobenzenes	    H-3

  II-2   Physical Properties of the Trlchlorobenzenes	    II-4

  II-3   Vapor Pressures and Vapor Densities  of  the
         Trlchlorobenzenes	    H-5

 III-l   Distribution of "C-Labeled 1,2.4-Trlchlorobenzene
         1n Rat Tissues After Oral Dosing  with  181.5 mg/kg/day
         for 7 Days	   IH-3

   V-l   Summary of Subchronlc and Chronic Toxldty Studies
         on Trlchlorobenzenes	     V-7

VIII-1   Summary of Subchronlc and Chronic Toxldty Studies
         on Trlchlorobenzenes	VIII-8

VIII-2   Toxlclty Data for Threshold Estimates  	  VIII-10

VIII-3   Summary of the Data for 1,2,4-Trlchlorobenzene  Used
         to Derive HA and DWEL	VIII-22
                                     vlll

-------
                            LIST OF ABBREVIATIONS

BUN                     Blood  urea  nHrogen
DUEL                    Drinking water  equivalent  level
EPN                     O-ethyl-0-p-nltrophenyl  phenylphosphothlonate
G-6-P                   Glucose-6-phosphatase
GC                      Gas  chromatography
GC/MS                   Gas  chromatography/mass  spectrometry
GI                      Gastrointestinal
1.p.                    IntraperUoneal
1.v.                    Intravenous
LDH                     Lactic dehydrogenase
LOAEL                   Lowest-observed-adverse-effect  level
NOAEL                   No-observed-adverse-effect level
NOEL                    No-observed-effect level
RfD                     Reference dose
SAP                     Serum  alkaline  phosphatase
SGOT                    Serum  glutamlc  oxaloacetlc transamlnase
SGPT                    Serum  glutamlc  pyruvlc transamlnase
wt                      Height
                                      1x

-------
                                  I.   SUMMARY

    The  trlchlorobenzenes are  a  group  of  three  chemical  Isomers  In  which
three  chlorine atoms  have  been  added  to  a benzene  ring.   The  1,2,3-  and
1,3,5-trlchlorobenzenes  are  normally  solid while  1,2,4-tr1chlorobenzene  1s
normally  a  liquid  at  25°C.  The  trlchlorobenzenes  are only  slightly  solu-
ble  In water  (6.6-34.6  mg/l at  25CC).   The trlchlorobenzenes  are  produced
In  relatively  small amounts  (1.3-7  million kg/year) and are  used primarily
as  chemical  Intermediates,  solvents,  Insecticides,  and  coolants  and Insula-
tors  In  electrical  equipment.   Analysis  of the  trlchlorobenzenes  In  water
normally  Involves  a solvent extraction and  cleanup  method followed by  gas
chromatography   (GC)   or   gas   chromatography/mass   spectrometry   (GC/HS)
analysis.  The  water analysis methods are  slightly  modified  for  analysis  of
trlchlorobenzenes In soil  and food.

    The   limited   comparative   pharmacoklnetlc   data   available  on   the
trlchlorobenzenes  prevent   specification  of  the  absorption,  distribution,
metabolism and  excretion  of the  Individual  Isomers.   The  trlchlorobenzenes
appear  to enter  the systemic  circulation readily by  Inhalation,  Ingestlon
and  dermal  absorption;  however,  data were  not  available  to  quantltate  the
rates  of  these processes  nor  of  any  of  the  pharmacoklnetlc  processes.
Initial  distribution of  the trlchlorobenzenes  and metabolites  Is  mainly  to
the  liver, kidneys  and adrenals,  followed  by migration  to  adipose tissue  or
metabolism  to  polar  compounds  that  are  more  readily  excreted.   From  the
available data,  It  seems  relatively clear  that  metabolism  In  at least  three
species  has  a  common  first  step,  the  production  of  an arene  oxide  Inter-
mediate.   Subsequent  metabolic   steps,   however,  vary  among  the  species
examined, at least  for the most  studied  Isomer,  1,2,4-trIchlorobenzene.

03720                                1-1                              04/05/91

-------
    In general, the pharmacoklnetlcs of  the  tMchlorobenzencs  are  similar  to
those  described  for  the  other halogenated  anomalies.   These compounds  arr
Upophlllc and their metabolism and excretion  depends on  their conversion  to
polar  Intermediates.   In  addition, their  Upophlllc character  provides  for
ready  absorption from  the gastrointestinal tract  and Initial  distribution  to
the  more  highly  perfused   tissues,  particularly   the  liver,  kidneys  and
adrenal  and  thyroid  glands,  after  which they  arc  either  metabolized  and
excreted or redistributed to adipose tissue  or skin. Additional experiments
are needed to clarify  the relationship of  these  studies  to  the metabolism of
trlchlorobenzenes In humans.

    The effects In mammals  of  acute exposure  by  various  loutcs  to  trlchloro-
benzenes Include local Irritation, convulsions and  death.  Livers,  kidneys,
adrenals,  mucous  membranes  and  brain  ganglion  cells  appear to  be  target
organs with effects Including  edema, necrosis,  fatty Infiltration  of livers,
Increased organ weights, porphyrin Induction  and mlcrosomal  enzyme  Induction.

    Quantitative data   on  the toxic  effects  of  trlchlorobenzene  following
subchronlc  exposure  by  various   routes  were  obtained  in   a   variety   of
species.  In general,   these  studies Indicate  that the liver,  kidney,  adrenal
glands   and    thyroid   glands  are   target   organs.     Oral   gavage   of
1,2,4-tr1chlorobenzene  at   53.5   mg/kg   (10   ppm)   for  95  days   Induced
vacuollzatlon  of  the  zona  fasdculata  of  the  adrenal  cortex  In  several
rats.  One  study Identified 14.8 mg/kg/day  of  1,2,4-tMchlorobenzene as  a
no-observed-adverse-effect   level   (NOAEL)   In rats,  while   another   study
reported that  some  rats exposed  by  Inhalation to 1,3,5-trlchlorobenzene  at
1000 mg/m3  for 13  weeks  showed  squamous metaplasia and focal  hyperplasla


03720                               1-2                               01/03/92

-------
of the  respiratory epithelium, which appeared  to  be  reversible.   Subchronlc
oral  studies have  also  shown that  the trlchlorobenzenes  Induce  transient
hepatic  xenoblotlc metabolism  and  porphyrla.   Subchronlc dermal  exposure
resulted In mild to moderate Irritation  .

    One  chronic  study,  on the  effects  of  tMchlorobenzene  painted on  the
skin of mice  for  2 years, reported Increased mortality  In females  at the  low
dose (30X solution  In  acetone) and In both sexes  at the high dose  (60%  solu-
tion).

    Results  of two  reports on  mutagenlclty tests  with Salmonella  typhlmurlum
test strains  were  negative.  However,  this  test system  Is generally  Insensi-
tive  to chlorinated  compounds.   One cardnogen1c1ty  study,  a 2-year  skin
painting study  In mice,  failed  to demonstrate a   conclusive  tumoMgenlc  ef-
fect.  A multlgeneratlon study of the reproductive effects  of  oral  exposure
of rats  to  trlchlorobenzene  failed to  show effects  on  reproduction.  Oral
teratogenlclty studies  In  rats  showed  mild  osteogenlc  changes In  pups  and
significantly  retarded  embryonic  development  as  measured  by  fetal growth
parameters.

    Human exposure  to  1,2,4-trlchlorobenzene at 3-5 ppm  causes eye  and res-
piratory Irritation.   The only other  data on human  exposure are  Individual
case reports  of  aplastlc anemia of persons  exposed occupatlonally or domes-
tically.

    No  health advisories  (HAs) or  lifetime  drinking  water  equivalent levels
(DWELs)  are  suggested  for  the  1,2,3- and  1,3,5-trfchlorobenzene  Isomers
because of Insufficient  data being available  for evaluation.

03720                               1-3                              12/23/91

-------
    The 1-day  HA  for 1,2,4-trlchlorobenzene of 1 mg/l  for  a  10 kg child Is
based on a study  In  which  female Wlstar rats were given  single  oral doses of
1,2,4-trkhlorobenzene and  were  then evaluated 24  hours  later.  The 10-day
HA  for  1,2,4-tr khlorobenzene of  1  mg/ft  for  a 10  kg  child  Is  based  on a
study  In  which male  CD  rats were given  1,2,4-tr khlorobenzene for  14 days
and   were   then   evaluated   for    effects.    The   longer-term  HAs    for
1,2,4-trlchlorobenzene of  1 mg/l  for  a  10 kg child  and  5  mg/a for  a  70
kg  adult  are  based  on a  study  In which  CD-I  rats were  exposed orally to
1,2,4-trkhlorobenzene for  95 days  and  evaluated  for  reproductive  effects
and  organ  weight  changes.   A DUEL  for  1,2,4-trlchlorobenzene  of  0.4 mg/a
for  a  70  kg  adult   Is  derived from  an  RfD  of  0.01  mg/kg/day (verified
12/12/91)   from the   same 95-day  reproductive  study.  The  data  available on
1,2,4-trlchlorobenzene Is  Inadequate for  making  any conclusions  about  Us
potential   carclnogenklty  In humans.  The trlchlorobenzenes  are classified
as  U.S.  EPA Group  D compounds  at this  time,  that Is,  available  data  are
Insufficient.   This   Information  was  verified by   the  CRAVE  workgroup  1n
October 1988.
03720                               I  4                             01/03/92

-------
                     II.   PHYSICAL  AND CHEMICAL  PROPERTIES

    The  trlchlorobenzenes are  a  group  of  three chemical  Isomers  In which
three  chlorine  substltuents  have  been  added  to  a   benzene   ring.   The
trlchlorobenzenes  are  only  slightly  soluble  In  water  (6.6-34.6  mg/l at
25°C).   The  trlchlorobenzenes  are  produced  1n   relatively  small   amounts
(1.3-7 million  kg/year  Is  the estimated 1983  production)  (U.S.  EPA, 1983;
Chlorobenzene Producers  Association.  1984)  and are used primarily as  chemi-
cal  Intermediates,  solvents.  Insecticides,  and coolants and Insulators 1n
electrical equipment  (Hawley,  1977;  Sllmak  et al.,  1980).   Trlchlorobenzenes
have  been  detected  In all environmental media  Including drinking water, and
have  been  found to bloaccumulate  In  fish (U.S. EPA, 1985).  In  addition to
the exposure  of humans during the manufacture  and  use  of  trlchlorobenzenes,
exposure could  result from  Inhalation  of  contaminated  air  and Ingestlon of
contaminated  food and water.

    The  chemical structures  of  the  trlchlorobenzenes  are  shown In  Figure
II-l.  Synonyms, trade  names  and  Identification numbers for  the trlchloro-
benzenes are  found  In Table II-l.   Some of  the physical and chemical  proper-
ties  of  the  trlchlorobenzenes  are  found In  Tables  II-2  and  II-3.   1,2,3-Trl-
chlorobenzene 1s a  white crystalline solid  (platelets  from alcohol)  that  Is
volatile with steam.   It  Is  slightly soluble  (31.5 mg/i) at  25°C  1n water,
slightly  soluble In  alcohol,  soluble  1n benzene  and  carbon  dlsulflde,  and
very  soluble  1n ether  (NLM.  1981a; Yalkowsky  and Valvanl. 1980).

    1.2,4-Trlchlorobenzene  1s  a  colorless  liquid  at  25°C  but   at  somewhat
reduced  temperatures  may also take the  form of rhombic crystals  because Us


03730                              II-l                             09/12/88

-------
                                      Cl
                                           Cl
                                     Cl




1.2,3-TRICHLOROBENZENE     1,2,4-TRICHLOROBENZENE       1,3,5-TRICHLOROBENZENE
                                 FIGURE  II-l



                 Chemical  Structures of the TMchlorobenzenes
03730
II-2
09/24/85

-------
                                  TABLE II-l

  Synonyms, Trade Names and Identification Numbers of the Trlchlorobenzenes*
Chemical
Identification Number
Synonyms and Trade Names
 1.2,3-
 1,2.4-
  1.3,5-
CAS No. 87-61-6
CAS No. 120-82-1
TSL No. DC2100000
CAS No. 108-70-3
v1c-Tr1chlorobenzene
1,2,6-Trlchlorobenzene
v-Tr1chlorobenzene

Benzene, 1,2,4-trlchloro-
asym-Trlchlorobenzene
TCB
Trojchlorobenzen (Polish)
1,2,4-TMchlorobenzol
Hostetex L-Pec

s-Tr1chlorobenzene
sym-Trlchlorobenzene
TCB
TCBA
Benzene, 1,3,5-trlchloro-
*Source: NLM, 1981a.b, Toxicology Data Bank  (TDB)
03730
                 II-3
                 09/25/85

-------
                                                                                {  11-2
                                                          Physical Properties of the Trlchlorobenrenes*
0
0
Cheatcal
Trlchlorobenzene
1.2.3-
1.2.4-
1.3.5-

Holecular
Height

181.46
181.46
181.46

Helling
Point
CC)

52.6
16.95
63.4

Boiling
Point0

221
213.5
208.4

Dens1tyc
(g/flft)

1.69
1.45
1.39(64)1

Henry's Law
Constant x 1(T» Log P°d
(aim n* mol'1)

1.0d 4. 1*
1.42h 4.12*
NA NA

Hater
Solubility
(ng/t)e

31.59
34.69 ,
6.69

Flash
Point
CO

113
110
107

Index of
Refraction
at CC)

1.5776(19)
1.5717(20)
1.5662(19)
         'Data are fro* the NLH. 1981 a,b, Toxicology Data Bank (TDB).  except  as  noted.
         >>At 760 on
         CAI 20*C. except as noted
         facKay et al.. 1979
         *At K"t
         flsoaer unspecified
         flValkowsky and Valvanl. 1980
         *>Uarner et al.. 1980
         'Hansch and Leo. 1981
         JHorvath, 1982
         P» . Octanol/water partition coefficient at 25*C
         NA . Not available
CO
CO

-------
                                  TABLE I1-3

         Vapor Pressures and Vapor Densities of the Trlchlorobenzenes
     Chemical                Vapor Pressure            Specific Vapor  Density
                                 (mm Hg)                     (air = 1)
TMchlorobenzene
1.2,3-
1.2,4-
1.3,5-
0.07 at 25°Ca
1 at 40°Cb
0.29 at 25°Ca
1 at 38.4°Cb
0.15 at 25°Ca
10 mm at 78°Cb
6.26b
6.26b
6.26b
aNLM, 1981a,b; 1982

bSax, 1979
03730                               II-5                             09/24/85

-------
melting  point  occurs at 16.95°C.   It  possesses a distinctive  odor,  similar
to  that  of  l,4-d1chlorobenzene,  and 1s considered volatile  with  steam (NLM,
19815).   It  Is slightly soluble  In water, 34.6 mg/i at  25°C  (Yalkowsky and
Valvanl,  1980); mlsclble with  benzene,  petroleum ether  and carbon dlsulflde;
slightly  soluble  In  ethanol; and  very  soluble  In dlethyl  ether  (NLM,  1981b).
The  summer  sunlight  photolysis  half-life  for  1,2,4-trlchlorobenzene  In
surface waters at 40°  latitude has  been calculated  to be 450 years (Dulln et
al., 1986).  An Information  sheet  (Dow  Chemical  Company,  1979-1980)  listed a
purity of 100X for  Its product.   Kao  and Poffenberger  (1979)  reported that
commercial  1,2,4-trlchlorobenzene  may  contain  monochlorobenzene  (<0.1  wt
percent)  and  d1- and  tetrachlorobenzenes  (<0.5  wt  percent  and  <0.5  wt
percent) with the 1,2,4-trlchlorobenzene content being -97%.

    1,3,5-Trlchlorobenzene  takes   the   physical  form  of  white crystals  or
needles.   It  Is  very  slightly  soluble  (6.6  mg/l  at  25°C)   In   water;
sparingly  soluble  In  alcohol;  and  soluble  1n ether,   benzene,  petroleum
ether, carbon  dlsulflde  and glacial  acetic acid  (NLM,  1982;  Yalkowsky  and
Valvanl. 1980).

Chemical Analysis
    A solvent  extraction  and cleanup method  followed by GC or GC/MS  1s  the
most commonly  used  method  to Isolate trlchlorobenzenes  from water.   Methods.
that  are  slightly   modified  from  the  analytical  procedures  for  aquatic
samples  are  used for  the analysis  of trlchlorobenzenes  In soil and  food.
The  usual sampling  and  analytical  methods  for airborne  trlchlorobenzenes
Involve  the  adsorption  and concentration of  airborne  vapors on  sorbent-
packed  cartridges  followed  by  thermal  desorptlon   and   GC analysis  using


03730                               II-6                             09/12/88

-------
either  flame  1on1zat1on  detection,  electron  capture   (EC)  detection,   or
photolonlzatlon detection.   The  following sections  provide  examples  of  these
analytical methods.

    Chemical  Analysis  In Water.   The purge-trap technique does  not  provide
quantitative  recoveries   for  compounds   with  low  volatilities,   such   as
trlchlorobenzenes.   Therefore,  a  solvent extraction  and cleanup method  Is
normally  used  to  produce organic extracts suitable  for  GC/MS  analysis.   The
U.S.  EPA  (1982)  (Method  612)  has  recommended the  use of Florlsll  column
chromatography as a  cleanup step  before the  quantification  of  the samples by
GC  with   EC  detector.   This  recommended  method   1s  applicable  for   the
determination of trlchlorobenzenes  1n drinking water  and wastewater.

    Chemical  Analysis  1n   Soil.  Sediment and  Chemical  Waste  Disposal  Site
Samples.   The  solvent  extraction  method  was  used by  Lopez-Avlla  et  al.
(1983)  to determine trlchlorobenzenes  In  sediment  samples.   In this method,
the   solvent  extract   was  subjected   to   acid-base  fractlonatlon.    The
base/neutral  fraction  containing  the trlchlorobenzenes  was  fractionated by
silica  gel  chromatography.   The  final   separation  and quantification  was
accomplished  by  GC/MS.    The  recovery  of   1,2,4-trlchlorobenzene  by  this
method was 67X at a  spike  level of  400  ng/g  of  dry  sediment.

    Chemical  Analysis  1n Fish and  Other Foods.
       F1sh  — The  determination  of trlchlorobenzenes  1n  fish  samples  can
be  accomplished by  a solvent extraction method.  In  one  method,  Kuehl et al.
(1980)  subjected  the  solvent  extract  to  Florlsll  and  gel   permeation  on
chromatographlc separation,  followed by GC/MS  Identification and quantifica-
tion  of  trlchlorobenzene 1n fish  samples.

03730                               II-7                             09/12/88

-------
    Chemical Analysis  In  Air.   Lewis and  MacLeod  (1982) have developed  and
evaluated a portable  low-volume  air  sampling system for Indoor air  monitor-
Ing  of  sem1vo1at1le  organic  chemicals.   Two types  of sampling  cartridges
were  tested to  sample for  tHchlorobenzenes.  The  trlchlorobenzenes were
poorly  trapped  using  a   polyurethane   foam  (PUF)   plug,   with   collection
efficiencies of  6.6%.   However, using  a dual-sorbent  trap  consisting of  a
0.6 g  layer of  Tenax-GC   (35-60 mesh)  sandwiched between  two  3.8  cm  PUF
plugs, a  collection efficiency  of 98%  was obtained.   Theoretical  detection
limits,  using  GC/EC detection,  are  expected  to  be  at least one order  of
magnitude  lower  (In  the  range  of  0.06-0.1  pg/m3).   Storage  stability  of
the PUF cartridges  was  tested  under  adverse storage conditions.   The  amount
of trlchlorobenzenes recovered  from  the cartridges after 15 days  of  storage
at 32°C was 57%.   Oehme and Stray (1982),  however,  reported  high  recoveries
of 80,  94 and 115% for 1,2,3-, 1,2,4- and  1,3,5-tr1chlorobenzenes,  respec-
tively, with PUF  plugs.

    Langhorst  and NestMck  (1979)  used  an air sampling  tube  packed  with  two
sections of Amberllte  XAD-2 resin separated  by  a  sllanlzed glass wool  plug
to collect  the  trlchlorobenzenes.   The adsorbent was  desorbed  with  carbon
tetrachlorlde  and  analyzed by  GC  using  a photolonlzatlon detector.   Using
the method  described,  the minimum  detection  limits for  the  trlchlorobenzenes
were  30  ppb (v/v).   Collection  and  desorptlon efficiencies  for the  chloro-
benzenes  (air  concentrations  between  5 ppb  and  15  ppm)  were -95% with  a
precision of +12%.
03730                               II-8                             09/24/85

-------
Summary
    The  trlchlorobenzenes are  a group  of three  chemical  Isomers  1n  which
three  chlorine  substUuents have been  added  to a  benzene  ring.   The 1,2,3-
and  1,3,5-tr1ch1orobenzenes  are normally  solid  while 1,2,4-tr1chlorobenzene
1s  normally  a   liquid  at  25°C.   The  trlchlorobenzenes  are  only  slightly
soluble  1n  water   (6.6-34.6  mg/8.  at  25°C).   The  trlchlorobenzenes  are
produced  1n relatively  small  amounts (1.3-7  million  kg/year)  and  are  used
primarily  as chemical  Intermediates,  solvents,  Insecticides,  and  coolants
and  Insulators  1n  electrical  equipment.   Analysis  of  the trlchlorobenzenes
1n water  normally Involves a solvent extraction and cleanup  method  followed
by GC  or GC/MS  analysis.   The  water analysis methods  are slightly  modified
for analysis of trlchlorobenzenes 1n soil  and food.
03730                                I1-9                             09/24/85

-------
                             III.  TOXICOKINETICS

Absorption
    No quantitative  studies  on  the absorption of  the  trlchlorobenzenes  from
the  gastrointestinal  tract,  skin or   lungs  were  found.   Information  on
absorption may  be obtained from data  describing elimination.  Male  Charles
River rats  (16  In the group) excreted a  mean of 84X, and two  female  rhesus
monkeys excreted  a mean of 40%  of the orally (by gavage) administered  dose
of  10 mg  14C-l,2,4-tr1chlorobenzene/kg   1n  the 24-hour  urine, while  fecal
elimination accounted for only 11  and  IX,  respectively  (Llngg  et  al.,  1982).
The  results  Indicate  that  1n these  species, this  Isomer  Is  well  absorbed
from  the  gastrointestinal  tract.  Two Chinchilla female  rabbits  given  doses
of 500 mg 1,3,5-trlchlorobenzene/kg 1n arachls oil by  gavage  expired  -10X of
the  administered   dose  via  the  lungs over  a period  of 9  days  (Parke  and
Williams,  1960).   These Investigators also  observed elimination of  urinary
and fecal  metabolites, but quantities  or  percentages  were not  reported.

    That the trlchlorobenzenes are absorbed  by the respiratory tract and by
the skin can be Inferred from systemic effects  observed  In  toxldty  studies
using the  Inhalation (Kodba  et al.,  1981)  and dermal  (Brown  et al.,  1969)
routes  of  exposure.. • These  studies,  however,  were  not designed  to  give
Information on rates of absorption.

Distribution
    Smith  and   Carlson  (1980) examined  the  distribution of  14C-1,2,4-tM-
chlorobenzene In  groups of four male Sprague-Dawley rats on  days  1, 6,  11
and 16 after oral  dally dosing  with 181.5 mg/kg (1 mmol/kg)  1n corn  oil for


03740                                III-l                           09/26/85

-------
7  days.   Their  data  Indicate  that the  adrenals  Initially had  the  highest
concentration  of racholabel.   This  level declined rapidly; however,  by  day
11  H  was  less  than  twice  the background of the other  tissues.   Abdominal
fat  had   the  highest  concentration  at the  end  of day  1  (Table  III-l)  and
maintained  detectable  concentrations   (20%  of  the  day  1  level)  for  the
duration  of the  observation period  (16   days).   The  liver also  maintained
detectable  levels  throughout the recovery period, retaining -30%  of  the  day
1  level  by  day 16.  These  authors  also found that starvation  for  4 days  had
no  observed effect  on the  distribution   of  l4C-tr1chlorobenzene  1n  fat  or
liver.

    Parke and  Williams (1960)  reported the distribution of 1,3,5-trlchloro-
benzene  1n  one  rabbit on  day  8 following  oral  administration of a  single
dose of  500 mg/kg as  follows:   13% of the administered  dose was detected In
the  feces.  23% (4X  as  monochlorobenzene)  In the  gut.  5%  1n the  pelt,  5% In
depot fat (exclusive of pelt) and 22%  In  the  carcass.

Metabolism
    No metabolic  studies  following  the Inhalation of  trlchlorobenzenes were
available for  review,  but  the metabolic  fate following  oral  and/or  Intra-
venous  (1.v.)  or  Intraperltoneal   (1.p.) administration  has   been  charac-
terized  In  rabbits  (Jondorf et  al., 1955; Parke and Williams.  1960; Kohll et
al., 1976)  and 1n rats  and  monkeys  (L1ngg  et  al..  1982).

    Jondorf  et al.  (1955), using  spectrophotometrlc  analysis,  studied  the
metabolism  of  all  three  Isomers  of  trlchlorobenzene 1n groups  of  3 or  4
Chinchilla  rabbits   given a single oral  dose of  500  mg/kg  1n  arachls oil.


03740                                III-2                          09/26/85

-------
                                 TABLE  III-l
       Distribution  of  14C-Labeled  1,2,4-Trlchlorobenzene  In Rat Tissues
              after  Oral Dosing with 181.5 mg/kg/day for  7 Days3
Tissue
Abdominal fat
Liver
Adrenals0
Muscle
Kidney
Heart
Spleen

Day 1
2033+439
1075+87
754+132
400+30
1471+167
438+14
404+14
Activity (dpm/q t1ssue)b
Day 6 Day 11
642+54 342+10
442+22 308+21
246+22 d/
d/
404^43 d/
d/
d/

Day 16
408±39
317.+18





aSource:  Smith and Carlson, 1980
bEach value 1s the mean +. SE for 4 rats, except for abdominal fat on day 1,
 which was for three rats.
cTotal for both adrenals; they were not weighed.
dvalue less than twice background; further analyses were not performed.
03740                                III-3                           06/11/85

-------
The  results  Indicated  that  the  1,2,3- Isomer was metabolized to  2,3,4-trl-
chlorophenol (TCP),  to  3,4,5-TCP  to  a  lesser  degree,  and  to  small  amounts of
3,4,5-trlchlorocatechol.   During  the 5  days after  administration,  50% of the
dose was  excreted  In  the urine as  glucuronlc  acid  conjugates,  12% as sul-
furlc acid  (sulfate) conjugates  and  0.3% as 2.3,4-trlchlorophenylmercapturlc
acid.  The  5-day  urinary  metabolites  of 1,2,4-trlchlorobenzene were repre-
sented by  glucuronlde  conjugates  (27%),  sulfurlc  acid conjugates (11%) and
2,3,5- and 2,4,5-  trlchlorophenylmercaptuMc  add  (0.3%).  The major phenols
formed were  2,4,5- and  2,3,5-TCP.   For  the 1,3,5- Isomer.  20% was excreted
as glucuronlde  and 3% as  sulfurlc add conjugates.   No mercapturlc add was
found, 2.4,6-tMchlorophenol  was  the only phenol detected In the  urine, and
some unchanged  1,3,5-trlchlorobenzene  was present In the feces.   To further
characterize and  clarify the metabolic fate of  the 1.3,5- Isomer, Parke and
Williams (1960)  followed the 9-day urinary excretion 1n  2 or 3  female  Chin-
chilla  rabbits  treated orally with  a  single  dose   of  500  mg  of the 1so-
mer/kg.  For  the  first  3  days,  the  rabbits  eliminated 2,4,6-TCP  along with
some  minor  monochlorophenols,  while  from  day  4  to  9,  4-chlorophenol was
detected  more  prominently  along  with  2,4,6-TCP and  -1%  of  the  dose  as
4-chlorocatechol.

    Using GC/MS analysis,  KohH et al.  (1976)  examined  the metabolism of the
three  trlchlorobenzene  Isomers  following a  single  1.p.  Injection of  60-75
mg/kg  doses  In   vegetable  oil   to  male  rabbits  (number  and  strain not
reported).   In  agreement  with  the  results  of  Jondorf  et  al.  (1955), the
major   urinary    metabolites  of   1.2,4-tMchlorobenzene  were   2,4,5- and
2,3,5-TCP.   The  major  metabolite of  1,2,3-trlchlorobenzene was  2,3,4-TCP,
with  2,3,6-  and 3,4,5-TCP as  minor  urinary  metabolites.  The  1,3,5-  Isomer


03740                                II1-4                           09/12/88

-------
was metabolized to  2,3,5- and  2,4,6-TCP  and a third, more polar  metabolite,
was  tentatively  Identified  as  a  dlchlorobenzene  with  2  hydroxyl  and  1
methoxyl substHuents.

    Llngg  et  al.  (1982) Investigated  the metabolism of  1,2,4-trlchloroben-
zene  In  groups  of 16 male Charles  River  rats  and  groups  of 2  female  rhesus
monkeys following a single oral or  l.v. administration  of 10 mg/kg  doses  and
found  similar phenolic  metabolites  to those  observed  In  the rabbit.   These
researchers were also able to  characterize  some  species specific  conjugates.
An  Isomerlc pair  of  3.4,6-tr1chloro-3.5-cyclohexad1ene-l,2-d1ol  glucuronldes
accounted  for  48-61X  of  the  24-hour  urinary  metabolites  In  the  monkeys.
Also  found  were glucuronldes  of  2,4,5- and 2,3,5-TCP  and unconjugated TCP,
which  accounted  for 14-37  and  1-37X of  the urinary  metabolites,  respec-
tively.  In the rat, the 2.4,5- and 2,3,5-  Isomers  of  N-acetyl-S-(tr1chloro-
phenyl)-L-cyste1ne accounted  for  60-62%  of  the  urinary metabolites.   Minor
urinary metabolites  Included  2,4,5- and  2,3,5-trlchlorothlophenol  and free
2,3,5- and  2,3,4-TCP,  which  accounted for  28-33 and  1-1 OX  of  the  material
excreted, respectively.

    On  the  basis  of  the  studies of  Llngg et al.   (1982) and  Kohll et  al.
(1976), H  1s  apparent that  there  may be  differences  among  species  In  the
metabolism  of  1,2,4-tMchlorobenzene.   It  seems likely  that   these  differ-
ences  will  extend to  the  other  Isomers  of tHchlorobenzene  as  well.  Both
reports postulated  the  same  first  step  1n  metabolism  (I.e.,  Initial  forma-
tion of arene oxide  Intermediates), but  Indicated  differences  1n the  subse-
quent metabolic  reactions.   In the  rat, conjugation  of  the  Intermediate with
glutathlone was   postulated  to  account  for  the  sulfur-containing  urinary


03740                                111-5                           06/11/85

-------
metabolites.   In  the monkey,  hydrolysis  of  the arene  oxide  to  the  dlhydro-
diol and  the  absence of  sulfur-containing metabolites  seemed  to  preclude  the
Involvement  of glutathlone  (L1ngg  et al.,  1982).   As proposed by  Kohll  et
al.  (1976)  and Illustrated  In Figure III-l, formation of  the  Isomerlc  trl-
chlorophenols  from  the  arene  oxide Intermediates  can  proceed  either  by
direct opening of the C-0  bond or by  the  NIH shift of chlorine.

    Differences  In  the  rate of  metabolism of  the  different Isomers  within a
species  have been attributed  to the positions of  the  chlorine  atoms  on  the
benzene  ring, with  the  presence of  two  adjacent  unsubstHuted  carbon atoms
facilitating  the  formation of  the  arene  oxide  Intermediate.   Kalogenated
benzenes  without  adjacent unsubstltuted  carbons may still be metabolized  via
an  arene oxide Intermediate but at  a reduced  rate, and should  show evidence
of  a NIH  shift (Matthews  and Kato,  1979).

Excretion
    Llngg  et al. (1982)  measured  the 24-hour  excretion  of radioactivity 1n
the urine and feces  of  16 male  Charles River  rats  and  2  rhesus monkeys given
a  single 10  mg/kg  l.v.  or  oral dose of i4C-l,2,4-tr1chlorobenzene.  In  the
rat,  84X of  the oral  dose and 78X  of   the l.v.  dose were  excreted  In   the
urine  by 24  hours;  11  and  7X,  respectively,  were the amounts  Identified In
the feces In the same  period.  In  the monkeys, 4OX of the oral dose and  22%
of  the Injected dose'appeared In  the urine and <1% In the feces.  Smith  and
Carlson   (1980)   orally  administered  181.5  mg/kg/day  (1   mmol/kg/day)  of
14C-l,2,4-tr1chlorobenzene  In corn  oil  to 4  Sprague-Dawley  rats  for  7 days
and followed  the  excretion of  radioactivity  In the  feces  and  In the urine
during administration and  up  to 21  days after the  first  dose.  Fecal elimi-
nation rose  slightly  during  the  first  3  days  of dosing, after  which 1t

03740                                 III-6                          09/26/85

-------
                                  1. 1. 3-TCB
                                         \
                                Cl
                   OH
                        Cl
                 I I i-IW
 \
                                         Cl
                                   1 4- ICP
                                                 \
                                                 HO
                                                          Cl
                                                   1 « i-t«
                                                                           Cl' ^N^^ ^Cl



                                                                              1 I-TCS
                                                                       a
                                                                            OH
                                                                     I « I-TCP
/       \       /
                                                                                        OH
                                                                                    Cl
                                                                                             Cl
                                                                                      1 1 S-1CP
                                                                                                              MO
                                                                                                                  Cl


                                                                                                                I 4 S-fC*
                                                                                                        1CB • TNICNLOIIMiNfiNE

                                                                                                        ICf • IHICHLOROMCMOl
00
en
                                                         FIGURE III-l
HetaboDc Pathways for Trkhlorobeniene (TCB)  Isomers Through
              Arene Oxide  Intermediates  In Rabbits

           Source:  Adapted from Kohll et al.,  1976

-------
declined  rapidly  and was  essentially  complete  at  15  days  of  collection,
accounting  for  -4% of the  total  dose.   Urinary excretion followed a similar
pattern;  however,  at  21  days after  the  first  dose,  radioactivity was still
detectable.   Total urinary excretion to  this  time  accounted for  ~72X of the
total  administered  radioactivity.    As  noted  by  L1ngg  et  al.  (1982),  the
differences   In  the   excretion  rate  between  the   rat   and monkey  may  be
attributable  to  their different  pathways  of  metabolism,   since  the  monkey
required  two  steps beyond the arene oxide to produce Its urinary metabolite,
while  the rat required only one.

    Differences  In the rates of excretion  between  the  Isomers  of trlchloro-
benzene  have  also been  reported.   Jondorf  et  al.  (1955)  found that rabbits
given  oral  doses  of  500  mg/kg of  1,2,3-,  1,2,4-  or 1,3,5-trlchlorobenzene
excreted 78,  42  or 9%, respectively, of the administered dose as monophenols
In the 5-day urine collection.

    U.S. EPA  (1980),  using data from Williams  (1959)  and Parke and Williams
(1960),  estimated  the following half-lives  of  excretion In  the  rabbit:   2,
5.5  and  8.5  days  for  1,2,3-,  1,2,4- and  1,3,5-trlchlorobenzene,  respec-
tively.   The  rate of metabolism and  subsequent   excretion  Is  most  likely
related to  the position  of the chlorine atoms on the benzene ring.  Matthews
and  Kato (1979)  hypothesized  that  two adjacent unsubstltuted  carbon  atoms
facilitate  the  formation  of  the arene  oxide Intermediate  and  Increase  the
rate of metabolism and excretion.
03740                                 II1-8                           08/24/88

-------
Summary
    The limited comparative pharmacoklnetlc data available on the  trlchloro-
benzenes prevent  specification of  the  absorption, distribution,  metabolism
and excretion  of  the  Individual  Isomers.  The  tMchlorobenzenes  appear  to
enter   the  systemic  circulation readily by  Inhalation,  1ngest1on  and  dermal
absorption;  however,  data  were  not  available to  quantUate  the  rates  of
these   processes nor  of  any of the  pharmacoklnetlc processes.   Initial  dis-
tribution of  the  trlchlorobenzenes  and metabolites Is  mainly  to  the  liver,
kidneys and  adrenals, followed by migration to adipose tissue or  metabolism
to polar compounds that are more readily  excreted.  From  the available data,
It seems  relatively  clear  that metabolism  In at  least  three  species  has  a
common  first  step,  the production  of an arene  oxide  Intermediate.   Subse-
quent   metabolic steps,  however,  vary  among the species  examined, at  least
for the most studied  Isomer, 1,2,4-trUhlorobenzene.

    In general, the pharmacoklnetlcs of the trlchlorobenzenes are  similar  to
those   described for  the halogenated aromatlcs by  Matthews  and Kato  (1979).
The authors  observed  that these compounds are  Upophlllc  and   that  their
metabolism  and  excretion  depends  on  their conversion  to  polar  Intermedi-
ates.   In addition, their  Upophlllc  character provides  for ready  absorption
from the gastrointestinal  tract and  Initial distribution to the more  highly
perfused tissues,  particularly the liver, after which they are either  metap-
ollzed and excreted or  redistributed  to adipose tissue or skin.   Additional
experiments  are needed  to clarify the  relationship  of  these studies  to the
metabolism of trlchlorobenzenes In humans.
03740                                III-9                           09/26/85

-------
                              IV.  HUNAN EXPOSURE

    This  chapter will  be  submitted  by  the  Science and  Technology Branch,
Criteria and Standards  Division.  Office of  Drinking Water.
 03750                                 IV-1                            06/11/85

-------
                        V.  HEALTH EFFECTS IN ANIMALS
Acute ToxIcUv
    Studies  of  the  acute  toxlclty  of  the   trlchlorobenzenes   have   been
performed In several species  using various  routes  of  administration.

    Information on  the effects of acute  Inhalation exposure to  trlchloroben-
zenes  Is  limited.  In  an  abstract  of  a study from the Russian  literature
(Gurfeln and Pavlova, 1960), a single high Inhalation exposure  (exposures  of
0.005-0.01  mg/8,  In air or  5-10 mg/m3  were  used) of  an unspecified  Isomer
of trlchlorobenzene to  rats  resulted In Immediate nervousness, and  plnkness
of mouth,  ears and paws.   These  effects  were followed  by  convulsions and
death  within  30  minutes.  wUh  edema of  livers  and  kidneys  observed  upon
necropsy.   Unpublished  results  of  a study  performed  by  Treon (1950)  were
reported by Coate et al. (1977) and  Indicated  that  the  target  organs of  non-
lethal  acute  Inhalation exposure to  trlchlorobenzenes  (a weight-to-weight
mixture  of  854 1,2,3- and  92X 1,2,4-trlchlorobenzene)  In  cats, dogs,  rats,
rabbits and guinea  pigs Included  the liver,  ganglion cells at  all  levels  of
the brain,  and mucous membranes.   Lethal doses resulted In local  Irritation
of the  lungs  and  functional  changes 1n respiration In animals dying after
exposure.  Levels and duration of  exposure  were not  given.
    Brown et  al.  (1969)  reported  the single-dose  oral  LD5Q for  1,2,4-trl-
chlorobenzene  In  CFE rats  to be  756 mg/kg  (95X confidence limits  556-939
mg/kg).   In  CF mice,  the single-dose oral  LD_0 was  766  mg/kg (95X  confi-
dence  limits  601-979 mg/kg).  Death  occurred within  5  days In  rats and  3
days 1n mice.
03760                                V-l                              09/12/88

-------
    Rlmlngton  and  Zlegler  (1963)  studied the porphyrla-lnduclng ability of
1,2,4- and  1,2,3-trlchlorobenzenes  administered  by  gavage  to  male  albino
rats for various time  periods  (5-15  days).   Doses  of  the  Isomers  were  gradu-
ally Increased until porphyrln excretion was  high but fatalities were  few.
Porphyrla  was  Induced  by  1,2,4-tMchlorobenzene when  the  Isomer was  given
for 15 days  at 730 mg/kg (3 rats) as evidenced by peak elevations In urinary
coproporphyrln,  uroporphyrln,  porphoblUnogen  and  i-am1nolevul1n1c   add.
At  a dose  of  500 mg/kg  for  10  days  (1n  5 rats),  peak  liver  levels  of  copro-
porphyrln,  protoporphyrln,  uroporphyrln  and catalase were reached.   For  the
1,2,3-Isomer,  urinary  excretion of these Indicators peaked at 785  mg/kg  for
7 days (3  rats), but to a  lesser extent  than for the 1,2,4-lsomer.   Only the
liver  uroporphyrln  levels   were  Increased   by  administration  of  1,2,3-tM-
chlorobenzene  at  this  dose and  duration.   Glutathlone was  found to  have  a
protective effect  on tMchlorobenzene-lnduced porphyrla.

    Brown  et  al.   (1969)   determined  the  single-dose  percutaneous  LO.Q  In
CFE rats  (4 of each sex)  to be  6139 mg/kg  (95X confidence  limits  4299-9056
mg/kg)  for  1,2,4-tr1chlorobenzene  administered  topically  on  the  shaved
dorsolumbar  skin  and  covered  with  an  Impermeable  dressing.   All  deaths
occurred  within 5  days.   In skin Irritation studies, 1,2,4-tr1chlorobenzene
was applied to the skin of rabbits and guinea  pigs.  In the  first experi-
ment,  two  2x2 cm  patches  of  lint,  each containing  1  mi of  the  compound,
were applied to the shaved backs of  rabbits (4  of each sex)  for  6 hours/day
for  3  consecutive  days  and   covered  with  an  Impermeable  dressing.   For
another  experiment, rabbits (1 of each  sex) and guinea pigs  (5  of each sex)
received   single   uncovered applications  of  1,2,4-tr1chlorobenzene  on  the
shaved  mlddorsal   skin  (1 ml  for  rabbits,  0.5  mi for  guinea  pigs)  5


03760                                V-2                            09/25/85

-------
days/week for  3 weeks.   The  results Indicated that trlchlorobenzene was  not
very  Irritating,  although HssuHng  was  noted  during  the 3-week  exposure.
Some  guinea  pigs  that died during  the  3-week regimen had focal necrosis  of
the liver.

    Hepatotoxlc effects  (fatty  Infiltration  and  necrosis)  were reported  by
Cameron et al.  (1937)  following  s.c.  and/or  1.v. Injection of  500  mg  (range
of  doses  was  1-500 mg)  trlchlorobenzene  1n  liquid  paraffin  to  rats;  the
toxlclty was less than that of mono-  and  o-d1chlorobenzene.   Further details
of strain, number of animals  or  Isomers  were not  reported.

    Robinson  et  al.   (1981),  In  an  acute  toxlclty study  to  assess  the
Increased adrenal weight  that  was  noted  1n a multlgeneratlon  study,  admin-
istered to groups composed of 9-10  preweanlng female  Charles  River  rats 1.p.
Injections of  0,  250 or  500 mg  of 1,2,4-trlchlorobenzene/kg In corn  oil  at
22, 23 and 24  days  of  age.   Significant changes  (p<0.05)  from control  values
were  observed  upon  necropsy at  25 days  of  age  as follows:  decreased body
weight and  Increased  adrenal  weight  at  the high dose; decreased uterus  and
Increased liver weights at both  doses.

    Male  Holtzman  rats (number  not  specified) were  given  single  Intraperl-
toneal Injections of  1,2,4-  or  1,3,5-tMchlorobenzene at  a dose of  37 mg/kg
(5  mmol/kg)  as a 50X solution   1n  sesame oil In a volume of  1 ml/kg (Yang
et  al.,  1979).  Controls received  an equal volume of sesame oil.   After  24
hours,  the  femoral   veins and  the  common  bile  duct  were cannulated.   Both
Isomers  produced  significant   Increases   (p<0.05)  1n  bile  duct-pancreatic
fluid  (BDPF)  flow with the  1,2,4-  Isomer being  4 times more  effective than


03760                                V-3                             09/25/85

-------
the  1,3,5-  Isomer.   SGPT activity was elevated by  treatment with  1,3,5-trl-
chlorobenzene and bile  Flow was  elevated  by the 1.2,4- Isomer.   Both  Isomers
caused a decrease In BDPF protein concentration.

    Several  studies  have demonstrated  the  ability of  the  tdchlorobenzenes
to enhance  xenoblotlc  metabolism.   Carlson, In a series of  reports  (Carlson
and  Tardlff,  1976;  Carlson, 1977a,  1978,  1981;  Smith  and Carlson,  1980),
examined the ability of  1,2,4-tMchlorobenzene  to  Induce a  variety of  mlcro-
somal  functions  and  enzymes  Including  cytochrome  c  reductase,   0-ethyl
0-p-nltrophenyl   phenylphosphothlonate   (EPN)   detoxification,   cytochrome
P-450, glucuronyltransferase,  benzopyrene hydroxylase and  azoreductase.   In
a  14-day study  by  Carlson and  Tardlff  (1976),  dally  doses  of  1,2,4-trl-
chlorobenzene  In corn   oil  were administered  orally  to  groups  of  6 male
albino rats  at  10,  20  and  40  rug/kg.  All  the above functions and  enzymes
Increased  significantly  (p<0.05)  except  benzopyrene  hydroxylase.    In  a
90-day  study  by  the   same  Investigators,  all  the  functions  and   enzyme
activities.   Including   benzopyrene  hydroxylase.   Increased   significantly
(p<0.05)  at  10-40  mg/kg/day  and  remained significantly  elevated  after  a
30-day  recovery  period.   In  a  similar  study,  Smith  and  Carlson   (1980)
administered  1,2,4-trlchlorobenzene  at  181.5   mg/kg/day  (1 mmol/kg/day)   to
rats  for 7  days,  and  measured  recovery  at   1,  6,  11  and 16 days.  EPN
detoxification   was  still   significantly  (p<0.05)   elevated   at  11   days;
p-n1troan1sole  demethylatlon at  16 days; cytochrome  c reductase at  6  days;
and  cytochrome   P-450  at 11 days.   In  a similar  study by Carlson  (1977a),
14-day administration  of 1.3,5-tHchlorobenzene at  100-200  mg/kg/day  signif-
icantly  (p<0.05)  Increased EPN  detoxification,  UDP  glucuronyltransferase,
and  cytochrome  c  reductase,   and   significantly  decreased  hepatic   G-6-P;


03760                                 V-4                             08/24/88

-------
 benzopyrene  hydroxylase,  azoreductase  and  serum  Isocltrate  dehydrogenase
 were not  significantly  affected  at  200 mg/kg/day.   In the same  study, jhn
 vivo hepatotoxlclty  of  carbon  tetrachlorlde  (one  dose of  0.5 ml/kg)  was
 significantly  (p<0.05)   enhanced  by   14-day   pretreatment   of   rats  with
 1,2,4-trlchlorobenzene.   Glucose-6-phosphatase  activity  was  significantly
 (p<0.05)   decreased   by   pretreatment  with   1,2,4-trlchlorobenzene   at  5
 mg/kg/day,  and Isocltrate dehydrogenase was  decreased  by  pretreatment at 20
 mg/kg/day.

     The  1,2,4- Isomer, and to  a  lesser  extent  the  1,3,5-  Isomer,  were also
 shown  to  Induce hepatic  esterases  (Carlson  et al., 1979; Carlson, 1980).  In
 studies  similar  to  those  previously described,  rats  receiving dally oral
 doses  of  18.2  mg  1somer/kg  (0.1  mmol/kg)  for  14  days were  killed  24 hours
 later  and  hepatic  mlcrosomes  were  prepared.   The  l,2,4-1somer  was  an
 effective  Inducer  of  both acetanlllde esterase  and  acetanlllde hydroxylase,
 while  the  l,3,5-1somer Induced  only  the  esterase and to a lesser degree than
 did  1,2,4-trlchlorobenzene  (Carlson  et  al.,  1979).   The  l,2,4-1somer also
 Induced hepatic arylesterase,  while  1,3,5-tMchlorobenzene  did  not  (Carlson,
 1980).  Pretreatment  of  rats  with 181.5 mg/kg/day (1  mmol/kg/day)  of  either
 Isomer resulted 1n Induction of procalne esterase (Carlson et al., 1979).

     In  a   series  of  experiments,  Arlyoshl   et  al.  (1975a,b,c)  studied  the
 effects of the trlchlorobenzenes  on  Induction of  hepatic  mlcrosomal  pro-
 teins, phosphollplds  and  enzymes,  especially 1n relation to  the  activity of
 4-am1nolevul1n1c  acid synthetase,  the  rate  limiting  enzyme  1n  the  bio-
 synthesis   of   heme.   The  three trlchlorobenzene  Isomers  were  administered
orally to  groups  of  2-6  female Hlstar rats at a dose  of  250  mg/kg/day for  3
days, after  which the rats  were  killed  and mlcrosomes were prepared.   The

03760                                V-5                              09/24/85

-------
results  Indicated that  trlchlorobenzenes  Increased  the  levels of mlcrosomal
proteins,  phosphollplds  and cytochrome P-450, and enhanced the activities of
aniline   hydroxylase,   amlnopyrlne  demethylase  and  i-amlnolevullnlc  acid
synthetase, with  the  1,2,4-lsomer being the most effective (Arlyoshl  et al..
1975a,b).   The  dose  response of these effects to 1,2,4-trlchlorobenzene were
determined  (Arlyoshl   et  al.,  1975c)  for  groups  of  2-6  female  Wlstar  rats
treated  orally  with  single doses of  0,  125,  250,  500,  750,  1000 and  1500
mg/kg.   The results  Indicated  that 24  hours  after  the administration of the
Isomer,  mlcrosomal  protein was  elevated  at >750 mg/kg and  glycogen  content
was decreased at  >500 mg/kg.   The activities  of amlnopyrlne demethylase and
aniline  hydroxylase  and  the  content  of  cytochrome  P-450 were  Increased  at
>250 mg/kg, as was i-amlnolevullnlc acid  synthetase activity.

Subchronlc  Toxldtv
    The  effects of  trlchlorobenzene  following subchronlc  Inhalation,  as  well
as oral  and dermal exposure,  have been Investigated  In a variety of species.
ToxIcHy data for the  trlchlorobenzenes can be found In Table V-l.

    Koclba  et  al.  (1981)  exposed  20 male  Sprague-Dawley  rats, 4 male  New
Zealand  rabbits and  2 male beagle dogs  by  Inhalation  to 1,2,4-trlchloroben-
zene  (99.4% pure) at levels  of 0,  223 mg/m3  (30  ppm)  or  742 mg/m3  (100
ppm)  for  7 hours/day, 5  days/week for a  total  of 30 exposures  In 44 days.
There  were no  significant effects on body  weight,  hematologic Indices  or
serum  biochemistry tests.  Upon necropsy, gross and  comprehensive hlstologlc
examination revealed  no  significant  treatment-related effects  In any of the
species.   At  the  742  mg/m3 level,  Increased  liver weights  were detected  In
dogs  and rats  and  Increased kidney  weights  In rats.  Urinary  excretion  of


03760                                 V-6                             04/05/91

-------
                                  F V-l



Sunary of Subchronlc and Chronic Toxic Ity Studies on Trlchlorobenzenes
CO
-J
o»
o


<
«j



8/81/80
Species Route Dose
Rat Inhalation 10. 100 or
1000 ng/n*
of 1.3.5-TCB
Rats, rabbits. Inhalation 223 or 742 ng/m«
two dogs of 1.2.4-TCB
Rat Inhalation 22.3 or
74.2 ng/n«
of 1.2.4-TCB
Rat Inhalation 186. 371 or
742 ng/m»
of 1.2.4-TCB
Rabbits. Inhalation 186. 371 or
monkeys 742 mg/m*
of 1.2.4-TCB
Monkey oral 1. 5. 25. 90.
125 or 173.6
•g/kg/day
of 1.2.4-TCB
Rat oral 50. 100 or
200 rag/kg/day
of 1.2.4-TCB
Rat oral 10. 20 or
40 ng/kg/day
of 1.2.4-TCB
House oral 600 ppm diet
(0.078 ng/kg/
day) of
1.2.4-TCB

Duration
6 hr/day. 5 day/wk
for up to 13 uk
7 hr/day. 5 day/wk;
total of 30 expo-
sures In 44 days
6 hr/day. 5 day/uk.
3 on
7 hr/day. 5 day/uk.
26 uk
7 hr/day. 5 day/uk.
26 uk
30 days
30. 60. 90 or
120 days
90 days
6 on

Effects Reference
No hepatotoxlclty; three high-dose rats had Sasnore et al.. 1983
squanous metaplasia and focal hyperplasla
of respiratory epithelium, believed to be
reversible
Increase In urinary excretion of porphyrla Koclba et al.. 1981
In exposed rats; Increase In liver weights
In high-dose rats and dogs; Increased kid-
ney weights In high-dose rats
Increase In urinary porphyrln excretion In Uatanabe et al.. 1978
high-dose rats; no effects In 22.3 ng/n»
group
Enlarged hepatocytes and nondose-dependent Coate et al.. 1977
hepatocytes vacuollzatlon. liver granuloma,
biliary hyperplasla and kidney hyaline de-
generation at 4 and 13 uk; no hlstopathology
evident at 26 uk
No treatment related changes at 26 uk Coate et al.. 1977
<25 ng/kg/day - no effects observed; Smith et al., 1978
>90 ng/kg/day - observed toxic Ity and death
Increases In liver weights, liver porphyrlns Carlson. 1977b
and urine porphyrlns. dose and tine related
Increase In llver-to-body weight ratio In Carlson and Tardlff,
high-dose group; changes In enzyme actlva- 1976
tton at all doses
No effects Goto et al.. 1972


-------
                                                                         TABLE V-l  (cont.)
o»
o
Species
Guinea pig
House
Rats
Rats
Route
dermal
dermal
oral
(drinking
water)
oral
Dose
0.5 in/day
of 1.2.4-TCB
0.03 mft/palnt-
Ing of 30 and
60X solution In
acetone of
1.2.4-TCB
25. 100 or
400 ng/t
of 1.2.4-TCB
36. 120. 360 or
1200 mg/kg/day
of 1.2.4-TCB
Duration
5 day/wk. 3 wk
2 tlnes/wk. 2 yr
F0 to F2
generations
days 9-13 of
gestation
Effects
Death following extensor convulsion; livers
showed necrotlc foci
Painting Induced excitability, panting and
epidermal thickening, Inflammation and
keratlnlzatlon; Increased organ weights and
mortality
Enlarged adrenals In FQ and FI generations
1200 ng/kg dose all dead by the 3rd day.
360 ng/kg dose caused 22Jt mortality In
dams and moderate hepatocellular hyper-
Reference
Brown et al.. 1969
Vamamoto et al.. 1982
Robinson et al.. 1981
Kltchln and Ebron.
1983
CD
          Rabbits
dermal        30. 150 or
              450 mg/kg/day
              of 1.2.3-TCB
              (30%) and 1.2.4-
              TCB (70X)
5 day/wk. 4 wk
trophy and non-significant Increases In
embryonic lethality and significantly
retarded embryonic development. 36 and
120 mg/kg groups not observed for embryonic
effects, but slight hepatocellular hyper-
trophy was reported In one 120 mg/kg dam

Dose-related skin Irritation; Increase In
urinary coproporphyrln In high-dose males
and slight pallor of liver In males and
females
                                                                                                                                  Rao et al..  1982
          1.2.3-TCB  -  1.2.3-trlchlorobenzene;  1.2.4-TCB  .  1.2.4-trlchlorobenzene;  1.3.5-TCB = 1.3.5-trtchlorobenzene
is*
tn
CD
in

-------
porphyMn was Increased  In  rats  exposed to 1,2,4-trlchlorobenzene at 223  or
742  mg/m3,  which  the  Investigators   Interpreted  as   a   compound-specific
physiologic effect rather  than a  toxic  effect.   A follow-up study  supported
this  Interpretation.   The  same   Investigators   exposed  male   and  female
Sprague-Dawley rats  to 1,2,4-tMchlorobenzene at  0,  22.3 mg/m3  (3 ppm)  or
74.2  mg/m3  (10   ppm)   for  6  hours/day,   5  days/week   for  3  months.   The
results,  which   were  reported  In  an  abstract  (Watanabe  et   al.,  1978).
Indicated that urinary excretion of porphyrlns was slightly  Increased 1n the
74.2 mg/m3  group during exposure,  but  returned  to control range 2-4 months
postexposure.  Since  this  appeared  to  be  the  most  sensitive  Indicator  In
rats,  and  exposure   to  trlchlorobenzene  at  22.3  mg/m3  did  not   cause
Increased  porphyrln  excretion,  22.3  mg/m3  was   considered  a   no-observed-
adverse-effect level  (NOAEL)  for  rats  by the  authors.

    Sasmore  et  al.   (1983)  exposed male  and female  outbred  albino CD  rats
(20/group) to 1,3,5-trlchlorobenzene  vapor  at 0,  10,  100 or 1000 mg/m3 for
6 hours/day,  5  days/week  for  up  to 13 weeks.   No significant  effects  were
observed on  body weights,  food consumption,  standard hematologlc and clini-
cal  chemistry  parameters or  on  methemoglobin  and porphyrln levels.   In  a
subgroup  of  five animals/sex/group  killed  after  4  weeks  of  exposure, the
only altered  experimental   parameter  was  an Increase  1n the  llver-to-body
weight  ratios  In the male  1000  mg/m3  group,   but  this  effect  was not
observed at  13  weeks.   Since  gross and microscopic  pathologic  examinations
of  the  liver  revealed  no  treatment-related   abnormalities,   the   authors
concluded  that   the  exposure  did  not  cause  hepatotoxldty.    Microscopic
examinations,  however,  revealed   that  three  high-dose  rats  had   squamous
metaplasia and  focal  hyperplasla  of  the respiratory  epithelium, which the
authors believed  to  be  reversible.

03760                                V-9                             04/05/91

-------
    Coate  et  al.  (1977)  exposed groups  of 30 male  Sprague-Dawley  rats,  16
male New  Zealand rabbits and 9  male  monkeys  (Hacaca  fasclcularls) to 99.07%
pure  1,2,4-trlchlorobenzene vapor  at  levels  of  0,  186 mg/m3  (25 ppm),  371
mg/m3  (50  ppm)  or  742 mg/m3  (100 ppm)  for  7  hours/day,  5  days/week  for
26  weeks.   Pulmonary  function  and  operant behavior  tests  In  the  monkeys.
ophthalmic  examinations  In  the  rabbits and monkeys,  and measurements of body
weight, hematologlc  Indices and serum biochemistry parameters  In all species
were conducted  before and  during the exposure period.   Subgroups of 5 rats
each were  killed after  4  and  13 weeks of  exposure;  all  remaining rats were
killed  after  26 weeks  for  hlstologlc  examination of  selected  tissues.   No
treatment-related  effects  at any observation time were  seen with respect  to
body  weight,  survival,  hematology   or   serum  chemistry  for  any  of  the
species.   No  ophthalmic changes  were  observed  In rabbits or  monkeys.   Pul-
monary  function  and  operant behavior were  unaffected In monkeys.  Hlstologlc
examination  of  rat  tissues  revealed  that   treated  animals   had  enlarged
hepatocytes that were  more  prominent at 4  weeks than at  13 weeks  after expo-
sure,  and  at  371   and  742 mg/m3  than  at  186  mg/m3.   Other  changes  In
treated rats  that  did not  appear  to be dose-dependent were vacuollzatlon of
hepatocytes at  4 and  13 weeks,  slightly  more  severe granuloma of the liver
at  4 weeks  and  biliary hyperplasla at 4 and 13 weeks.  A nondose-related In-
crease  In  the severity  of  kidney  hyaline  degeneration  was  observed In test
rats  at 4  weeks.    This  lesion  was  slightly more  severe In  the high-dose
group  at  13 weeks.  These  effects  appeared to  be transient; rats necropsled
after  26  weeks  of exposure had none of these changes.   Likewise, hlstologlc
examination  of  selected   tissues   from   rabbits  and  monkeys   revealed  no
treatment-related  changes after 26  weeks  of exposure.
03760                                 V-10                           04/05/91

-------
    Carlson and  Tardlff  (1976) assessed  the  effects of  14-  or  90-day oral
administration of  1,2,4-tMchlorobenzene  1n corn  oil compared with corn oil
controls 1n male  CO  rats.   In the 14-day studies, the effects examined were
lethality,  hepatotoxlclty  and the  Influence  on  hexabarbltal  sleeping time
and other parameters of xenoblotlc metabolism.  A dose of 600 mg/kg/day, the
highest dose administered, caused no deaths during the 14-day administration
period.  Hepatotoxlclty  was  evaluated  by  dosing  at  0,  150,  300  or  600
mg/kg/day and  determining  serum  Isodtrate  dehydrogenase and liver glucose-
6-phosphatase  activities.   Although no  dose-related changes In  serum Iso-
dtrate  dehydrogenase activity  was  observed,  liver glucose-6-phosphatase
activity was  significantly decreased at  >300 mg/kg  (p<0.05).  Hexabarbltal
sleeping time  was significantly decreased  at 600 mg/kg/day  (the  only dose
examined);  this  effect persisted  through  a  14-day recovery period.   In rats
receiving 14  dally doses  at 0, 10,  20  or 40  mg/kg,  there was a significant
dose-related   Increase  In  llver-to-body  weight  ratio  at  >10   mg/kg/day
(p<0.05).  Significant dose-related  Increases were also observed  1n  activi-
ties or  contents  of  cytochrome c  reductase  (at >10  mg/kg), cytochrome P-450
(at >20  mg/kg),  glucuronyltransferase  (at  >20  mg/kg),  azoreductase  (at >10
mg/kg) and  the  rate  of  detoxlcatlon of EPN  (at  >10 mg/kg).  These  results
Indicated that  the doses,  while causing  a  slight degree of  hepatic  Injury,
significantly enhanced xenoblotlc  metabolism.

    In the 90-day  studies  by  Carlson and  Tardlff  (1976),  the  effects  of oral
dosing of  male CD rats (6 animals/group) at  0,  10,  20 or 40 mg/kg/day with
1.2,4-trlchlorobenzene 1n  corn oil  on weight gain,  liver weight,  hemoglobin
content, packed  cell volume and the  Indicators  of  xenoblotlc  metabolism were
evaluated.   No effects on  weight  gain and no consistent  alteration  In hemo-
globin content or  packed  cell volume were observed.  At  40 mg/kg,  there was

03760                                V-ll                             09/24/85

-------
a statistically  significant Increase (p<0.05)  1n llver-to-body  weight  ratios
that persisted  throughout  a 30-day recovery period.   Following  90-day  admin-
istration, cytochrome  c  reductase activity was  Increased at >10 mg/kg,  with
recovery after  30  days;  cytochrome P-450 levels  Increased at >20 mg/kg,  fol-
lowed  by  recovery;  glucuronyltransferase activity decreased  at  >10  mg/kg;
EPN  detoxlcatlon  Increased  at  >20  mg/kg;  benzopyrene hydroxylase  activity
Increased  2-fold  at  40  mg/kg;  and azoreductase  activity  Increased at  >10
mg/kg.

    Groups of  5 female rats (strain not  reported) received dally  oral  doses
of  0,  50, 100  or  200 mg  1,2,4-trlchlorobenzene/kg/day  1n  corn oil for  30,
60, 90 or  120  days (Carlson,  1977b).  Significant  Increases were observed 1n
liver  porphyrlns  at  >100  mg/kg  after  30  days  exposure  and  1n  urinary
porphyrlns at  200  mg/kg after  30 days.  For the  30-day  study,  slight  but
significant  Increases were also  observed  1n liver  weights  at  200  mg/kg.
When the  compound  was administered  for  60  days, only  the liver weights  were
Increased.   The  administration  of  1,2,4-tMchlorobenzene   for   90   days
resulted  1n  slight but significant  Increases  1n liver weights  at  >50  mg/kg,
In  liver  porphyrlns at  >100 mg/kg and 1n urine  porphyrlns  at 200  mg/kg.   A
significant  Increase was observed for  liver  porphyrlns when the compound was
given  at  >50  mg/kg for  120 days.  The excretion of 6-am1nolevul1n1c  add
and porphoblUnogen  In the  urine was not Increased at  any dose  given for any
duration.  When  the author compared the 1,2,4-trlchlorobenzene results  with
the  results  for  hexachlorobenzene, he  concluded  that the  tMchlorobenzene
Induced porphyMa  was  very  small compared with the hexachlorobenzene Induced
porphyrla (Carlson, 1977b).
03760                                V-12                            09/24/85

-------
    A 90-day oral study by Smith et al.  (1978),  reported  In an abstract, was
reviewed by  U.S. EPA  (1980),  who  gave  further  details of  the  study after
communication with  the authors.  Rhesus  monkeys  (4/group) were given  1,2,4-
trlchlorobenzene In  dally  oral  doses of  1,  5,  25, 90,  125  or  173.6  mg/kg.
No toxic effects were observed at  <25 mg/kg, while  doses of >90 mg/kg were
observed to be toxic, and  the 173.6 mg/kg  dose was  lethal within  20-30 days.
There were  no deaths  observed  In  the 1,  5 and 25  mg/kg groups; one death
occurred  In  each  of  the  90  mg/kg  and  125  mg/kg  groups  and  two  deaths
occurred In  the 173.6 mg/kg  group.   Animals on  the highest dose exhibited
severe  weight  loss  and  predeath  fine tremors.  All  of  the  animals  In  the
highest  dose group  had  elevated  BUN,   Naf.  K*.  CPK,  SGOT, SGPT.  LDH  and
alkaline phosphatase  as  well  as hypercalcemla and hyperphosphatemla  from  30
days on.  Smith  et  al.  (1978) have been using the urinary pattern of  chlor-
guanlde  metabolites  as  an  Indication   of  cytochrome  P-450  dependent drug
metabolism.   At  the  high  doses,  monkeys  showed  evidence  of  the  hepatic
Induction as well as  Increased  clearance of  l.v. doses  of labeled 1,2,4-trl-
chlorobenzene.   Further   Information  on  the  study  (U.S.  EPA,  1980) gave
evidence of  liver  enzyme  Induction  In  the 90,  125 and  173.6 mg/kg  animals.
There  were   some  pathologic   changes  noted  In  the  livers  of  the  high-dose
groups,  primarily  a  fatty Infiltration.  The  point at  which  there  was  no
effect  related  to  the  compound was  at  the  5 mg/kg  level.   Since  only  an
abstract of  this study  was  available and  since the Interpretation  of  this
study  was  complicated by  the use  of  other  drugs and  weight  losses  In  the
control  animals,  a  valid  no-observed-effect  level (NOEL) cannot  be derived
from these data.
03760                                V-13                            04/05/91

-------
    Two  subchronlc  studies  have assessed the dermal  toxlclty of  the tMchlo-
robenzenes.   Powers et  al.  (1975) applied  technical  grade 1,2,4-trlchloro-
benzene  at  concentrations of 5 or 25% In petroleum ether, or 100% l,2,4-tr1-
chlorobenzene  topically  1n  0.2  ma volumes  to the  ventral  surface of  the
ears  of  New  Zealand  rabbits   (groups  of 12  each),  3  times  weekly for  13
weeks; a  control  group received petroleum ether only.   Rabbits  exposed  to 5%
trlchlorobenzene  and  controls   had  slight  redness  and  scaling.   Dermal
responses at  25  and 100% of the compound Included slight to severe erythema,
severe  scaling,  desquamatlon,  encrustation,  and some  hair loss  and scarring.
The  responses were characterized  by  acanthosls  and  keratosls,  typical  of
moderate  to  severe   Irritation   and  probably  attributable  to  degreaslng
(defattlng) action.  No  overt  signs  of  systemic  toxlclty were  noted,  body
weight  gain was  comparable 1n  all  groups,  and  none  of the animals  showed
meaningful  changes  In  gross pathology.   The  Investigators noted  that  this
contrasted  with  the findings of  Brown et  al.  (1969),  who reported that  some
guinea  pigs,  exposed  topically  to  1,2,4-tMchlorobenzene  at 0.5  ml/day,  5
days/ week  for 3  weeks,  died following  extensor convulsions and  their  livers
showed  necrotlc  foci.   This difference  1n results may  be  attributed  to  the
site of  application (Brown et al., 1969.  used  the dorsal mldllne for  appli-
cation,  a  more  extensive  exposure site),  the volume  applied  (0.5 ml  vs.
0.2  ma),  the species  used,  and  the  more frequent  (5  times/week  vs.  3
times/  week)  application, although  the  total  number  of exposures  was  less
(5x3 weeks  vs. 3x13 weeks).

    Rao  et  al.  (1982)  applied  technical  grade trlchlorobenzene  [1,2,4-  (70%)
and 1,2,3-tMchlorobenzene  (30%)]  5  days/week  for 4  weeks,  at doses of  0,
30, 150  or  450 mg/kg/day, to the dorsal  skin (4x4 Inch area) of  groups  (5 of
each sex)  of  New Zealand rabbits weighing ~3 kg.  One  rabbit died  after  18

03760                                V-14                            09/24/85

-------
applications, but  the  Investigators were  unable to determine  the cause  of
death  by  either  gross  or  hlstologlc  examination.   Gross  and  hlstologlc
examination of the  skin  showed  evidence of moderate Irritation  at  the  high-
est dose  and less  Irritation at  the lower doses.  This  Irritation  evidence
consisted  of  epidermal  scaling,  thickening,  fissures,  ulcers and  erythema.
No  treatment-related  change was  observed In  clinical  chemistry  (BUN,  glu-
cose.  SGPT,  SAP)   or  hematology.   A  slight  but  significant  Increase  1n
urinary  coproporphyrln  was  observed In high-dose  males  (450 mg/kg/day)  at
day 24;  none was seen In  females.   This slight  porphyrla and a  slight  gen-
eralized pallor of  the liver  (3/5 males,  4/4  females) were  the only signs  of
systemic  toxlclty.   Extensive  hlstologlc  examination  of  numerous  tissues
failed  to  show  any  treatment-related  abnormalities.   The  volume  of  tr1-
chlorobenzene applied at  the dose levels  In this study can  be calculated  as
=0.06  ml  (30 mg/kg).  0.31  ml  (150  mg/kg)  and  0.93  ml   (450  mg/kg)  by
multiplying  the  dose  In  g/kg by the weight of the  rabbits  (3 kg)  and divid-
ing by the density of trlchlorobenzene  (1.45 g/mi).

Chronic Toxldty
    No  studies   on  the  effects  of  the tMchlorobenzenes following  chronic
oral  or  Inhalation exposure  were available for  review;  however,  a  chronic
skin  painting study was  encountered.  Goto et  al. (1972)  conducted a 6-month
feeding  study In mice using hexachlorocyclohexane  Isomers and their  metabo-
lites.   Including   1,2.4-trlchlorobenzene.  Male  mice   (20/group)  of  the
ICR-JCL  strain (age at  Initiation  5 weeks, average  weight 26.5 g) received a
diet  containing  600  ppm  of  trlchlorobenzene  (78  yg of  compound/kg  body
weight,  assuming mice consume  13%  of  their body weight  In  food  per day).
 03760                                V-15                            08/24/88

-------
The  weight gain  of  treated  mice did  not differ  from controls during  the
6-month  exposure.   At  26 weeks,  10  mice were  killed  and liver, heart  and
kidneys were  weighed; no abnormal weight changes were observed.   Macroscopic
and  hlstologlc  examination of  the liver  revealed  no hepatic tumors  or  any
other lesions.

    Yamamoto  et al.  (1982)  studied  the  toxldty  of 1,2,4-tMchlorobenzene
when  painted  on the  skin of  Slc:ddy  mice 2  times/week for 2 years.   Groups
consisted  of  75 mice/sex  receiving 0.03 ml  applications  of  the  compound  as
30  or  60% solutions  1n  acetone.  Controls  consisted of  50 mice/sex  and
received  only  acetone.    The  skin  painting  produced general  symptoms  of
excitability  and  panting,  local  skin  thickening,  keratlnlzatlon  and  Inflam-
mation  of  the epidermis.  These  effects  were not  observed In controls.   For
the  30% tHchlorobenzene  groups, mortality  was  Increased In females  (5/75
survived for  83 weeks compared  with  11/50 controls).   The mean survival  days
were  357il25.4  for  treated  females  compared with 423.8+145.0  for  controls
(p<0.01).   The  survival  of  males at  this  exposure  level was  not  signifi-
cantly  different  from that of  controls.  Spleen weights  were significantly
Increased  (p<0.05)  and   left  adrenal  weights  were  significantly  decreased
(p<0.01)  for  treated males  when compared  with  controls.   Hematologlc  and
blood  chemistry Indices  were  essentially unchanged  with the exception  of
decreased  red  blood  cell counts  1n  the  30%  treated  males (p<0.05)  and
decreased  Cl~ concentration  (p<0.01).    For  the  60% solution,  6/75  treated
females  survived   for  83  weeks.   Mean  survival  days  were  320.2+147.7  for
treated  females  compared with  423.8+.145.0 for controls  (p<0.001).   Eight  of
75  treated males  survived for  83 weeks compared with 9/50  control  males.
03760                                V-16                            09/25/85

-------
Mean survival  days  were  288.0^173.7  for  treated  males  and 363.9^173.9  for
controls  (p<0.05).   Significant differences  1n organ  weights  from  control
values  were  seen  In  the  spleens  of  males   (p<0.01)  and  the  adrenals  of
females  (p<0.05).   Hematologlc  and blood biochemistry  changes  were  seen  In
Increased  lymphocyte  counts  In  treated females  (p<0.05),  and  In  Increased
SGOT (p<0.05),  SGPT (p<0.001) and BUN  (p<0.01) for  treated males.

Hutaqenldty
    Schoeny et  al.  (1979)  and  Lawlor et al. (1979) examined the  mutagenlc
potential of 1,2,4-tMchlorobenzene In  Salmonella  typhlmurlum tester  strains
TA98,  TA100,  TA1535  and TA1537,  using the  plate  Incorporation  technique.
Schoeny et al.  (1979)  used  8 concentrations of trlchlorobenzene  ranging from
102  yg/plate  to  1.4x10=  tig/plate.    The   toxic  dose  was  determined  as
1599  yg/plate  (killing  of  one  or  more  strain  on  mutagenesls  plates).
Trlchlorobenzene was  negative for mutagenlcHy  In the absence and presence
of  S-9  mlcrosomal  fractions  from  unlnduced  rats,  from rats Induced  by the
polychlorlnated  blphenyl,  Aroclor  1254, and  from  rats  homologously  Induced
with trlchlorobenzene.

    The  study  of Lawlor  et  al.  (1979),  reported  In  an abstract, used the
TA1538  strain  of S.  typhlmurlum  1n  addition   to the  strains previously men-
tioned.   Negative  results were obtained for  five  unspecified  concentrations
tested  1n  the  presence  and  absence  of  rat  liver mlcrosomes  Induced  by
Aroclor  1254.   Because these  results were reported  1n an  abstract  without
the details of  the  experimental  procedures  used,  the results cannot be crit-
ically evaluated.
03760                                V-17                            09/25/85

-------
    The negative results  1n  the  Salmonella  hlstldlne  reversion  assay  are  not
unexpected  because  this   test   system  Is  generally   Insensitive  to  highly
chlorinated compounds (Rlnkus and Legator, 1980).

Carc1nogen1c1ty
    Yamamoto  et  al.  (1982) applied  1,2,4-tMchlorobenzene In acetone  to  the
skin of  Slc.ddy mice twice  weekly  for 2 years.  The  solution  of  1,2,4-tM-
chlorobenzene  was  60%  for  the  high  dose and 30%  for  the low dose  and  the
volume  applied was  0.03  mi/application.   Each  treated  group contained  75
animals  and  there were 50  control  animals  for  each  sex.  Growth rates  In
treated  and control  mice  were  comparable  through  83 weeks.   Mean  survival
days were  significantly reduced 1n  the 60%  1,2,4-trlchlorobenzene  groups  of
males and females and also 1n the 30X treatment group of females.

    Hlstopathology  showed  some  organ  sites  had  Increased  non-neoplastlc
lesions.  Assuming  that all  75  animals  1n the  treated  groups  were examined
and all  50  In the control groups were  examined,  there would be Increases  In
lesions  1n  the males In lung,  liver,  kidney,  adrenal,  spleen and  lymph  node
at  the  high  dose,  and 1n  all of  these  organs  except  lymph node  In  the
females  at   the  high  dose.    Unfortunately,  the  English  translation  of
Japanese  text 1s not  very  specific  1n  describing  the nature  of  the lesion
making  H   difficult  to use  this  Information  1n the Interpretation  of  the
tumor findings.

    No  single tumor  type was  Increased significantly  over the  control Inci-
dence  but   among  males  nine different  tumors were  found In  the  high-dose
group  as compared with  two  1n  the  low-dose  and two  1n  the  control  group.


03760                                 V-18                            09/25/85

-------
In females there were 11 different tumors  1n  the  high-dose  group  as  compared
with 3 1n the low-dose and 8  In  the  control  group.   The authors do not  state
whether  these  tumors  were all  found  In  different  Individual  animals  or
whether  these  were  multiple   tumors  In  the  same   animal.   Therefore,  the
actual  Incidence  In terms  of the  number of  tumor  bearing  animals  Is  not
known.

    Further  Information  from   this  study Is  necessary for  full  Interpreta-
tion.  This  single study  1s  clearly Inadequate  for making any  conclusions
about cardnogenldty 1n humans.

Reproductive and Teratogenlc Toxldty
    Studies  on  the reproductive  or teratogenlc effects  of  tMchlorobenzenes
following  Inhalation  exposure were  not  found  1n the  available  literature.
Robinson et  al.  (1981)  reported  a  multlgeneratlon study of  the reproductive
effects  of   1,2,4-tr1chlorobenzene  following  oral   administration.   Charles
River  rats  were  continuously   exposed to  the compound  at 0,  25,  100 or  400
ppm  1n  drinking   water.   The authors  calculated   the  dosages   for  the  F~
generation based on water consumption data  to be:   for females  at 29 days of
age, 8.3+0.8, 28.Oil.2,  133.2+.13.4 mg/kg/day, respectively; for  males  at 29
days  of  age,  8.5+.0.6,  27.6+1.6,   133.6+_15.6 mg/kg/day,  respectively;  for
females  at  83  days  of  age.   3.7+.0.1,  14.8+.1.0,  S3.6+.3.9 mg/kg/day,  respec-
tively;  for  males  at 83 days  of age,  2.5+0.1, 8.9+0.3. 33.0+0.4 mg/kg/day,
respectively.  The exposure  period  began with the  birth  of the F_  genera-
tion  and continued  through   32  days of  age  for the  F.  generation.   Each
treatment  group  consisted of  17-23  Utters.   No treatment-related  effects
were  noted  with  respect  to  fertility,  neonatal  weights,  maternal  weights,
litter sizes, preweanlng viability or postweanlng growth In  any generation.

03760                                V-19                            09/25/85

-------
Treatment-related  differences  were  seen  with  respect  to  food  Intake  and
water  consumption In  F. males and  females,  but  they were  Inconsistent  and
did  not  occur In other  generations.   Blood  chemistry  analyses  and locomotor
activity  measurements revealed no  overt hematologlc  or  neurologic  effects,
and  hlstologlc  examination  of  the  livers  and  kidneys  of  the  F,  genera-
tion  rats  revealed  no  damage.   At  the 400  ppm dose  level,  significantly
enlarged  adrenals  In both  sexes  of  the FQ  and F,  rats  were  observed  at
95 days  of  age (p<0.006).   A follow-up acute toxlclty study showed-that this
effect  could result  from  three dally  l.p.  Injections of 500  mg 1,2,4-trl-
chlorobenzene/kg.

    Black  et al.  (1983) reported  1n  an abstract a  teratogenlclty  study  1n
pregnant  Wlstar  rats using 1,2,4-, 1,2,3- or 1,3,5-trlchlorobenzene  adminis-
tered  by gavage In  doses  of 75-600 mg/kg on days 6-15  of  gestation (gesta-
tlonal  day  0 or  1  not  defined).   Upon  necropsy  (gestatlonal  day not speci-
fied),  thyroid  and  liver  lesions  and  reduced  hemoglobin  and  hematocrlt
values were  observed In treated dams  (doses  not  specified).   No teratogenlc
effects  were observed In  the pups; however, pups exposed  to  the 1,2,4- and
1.3,5- Isomers  (doses  not  specified) had mild osteogenlc changes.

    Kltchln  and  Ebron  (1983)  conducted  a  maternal  hepatic   toxlclty  and
embryotoxlclty  study  where  they  administered  1,2,4-trlchlorobenzene  (>99%
pure)  dissolved  1n  corn  oil (2  ml/kg) orally  to   pregnant  Sprague-Dawley
(CD  strain)  rats  (6  or  more/group) on  days  9-13 of gestation  and  the dams
were then  sacrificed on  day 14 of gestation.  The dosing groups were 0 (corn
oil only).  36.  120.  360 and  1200  mg/kg/day  1,2,4-trlchlorobenzene.   All  the
dams  1n  the 1200 mg/kg/day  group  died by the third day of dosing.   The 360


03760                                V-20                            04/05/91

-------
mg/kg/day  group were  observed with  a maternal  mortality rate  of  22%  and
greatly  reduced body  weight  gains.   Maternal  liver weights,  I1ver-to-body
weight  ratios  and hepatic  mlcrosomal  protein content  were  not  affected  by
1.2,4-trlchlorobenzene  administration.   1,2,4-Tr1chlorobenzene was  observed
to be  a strong Inducer of hepatic enzymes at  the  120 and  360  mg/kg/day dose
levels.   Liver histology  In  the  pregnant  dams  was  unremarkable 1n  the  36
mg/kg/day  group,  showed a slight  degree  of  hepatocellular hypertrophy  1n  1
of 9  rats  1n  the 120 mg/kg/day  group and  showed a moderate  hepatocellular
hypertrophy  1n 7  of  B rats 1n the 360 mg/kg/day  group.  The uteri  from only
the  0   and  360 mg/kg/day  groups  were examined   for  1,2,4-tr1chlorobenzene-
Induced  embryonic  effects.    No   statistically   significant  differences  In
resorptlon,  embryolethallty  or  abnormalities were  reported,  although  3/12
treated  Utters showed  embryolethallty as compared with 0/12  In  the control
litters.   Several  embryonic  parameters   were  significantly   decreased  by
1,2,4-trlchlorobenzene  treatment.   These  parameters   were   embryonic  head
length,  crown-rump  length,  somite number and  total  embryo protein content
(reduced 23X).

Summary
    The effects 1n mammals of  acute exposure  by  various routes to trlchloro-
benzenes  Include  local  Irritation, convulsions and  death.  Livers,  kidneys,
adrenals,  mucous  membranes  and   brain  ganglion   cells  appear   to be  target
organs   with  effects Including  edema, necrosis, fatty  Infiltration of livers,
Increased organ weights, porphyrln Induction  and  mlcrosomal enzyme Induction.
03760                                V-21                            09/25/85

-------
    Quantitative  data  on  the  toxic effects  of  trlchlorobenzene  following
subchronlc exposure  by  various  routes were obtained  In  a  variety  of species.
In  general,   these  studies  Indicate that  the liver and  kidney  are  target
organs.   Inhalation of  1,2,4-trlchlorobenzene at >74.2  mg/m3  (10 ppm)  for
6  hours/day,  5  days/week  for  up to 26  weeks  Induced hepatocytomegaly  and
hyaline  degeneration In  several  species   (Koclba  et  al.,  1981; Watanabe  et
al., 1978; Coate  et  al.,  1977),  although  these effects  may be to  some  extent
reversible.   One study   (Watanabe et  al.,  1978)  Identified  22.3  mg/m3  (3
ppm) as  a NOAEL In  rats.   Sasmore et  al.  (1983)  reported  that  some  rats
exposed  by  Inhalation to 1,3,5-tMchlorobenzene at  1000  mg/m3 for 13  weeks
showed squamous  metaplasia  and focal hyperplasla  of  the  respiratory epithe-
lium,  which  appeared to  be reversible.   Subchronlc  oral  studies  have  also
found  that   the  tMchlorobenzenes   Induce  hepatic  xenoblotlc   metabolism
(Carlson  and  Tardlff,  1976;  Smith  et al.,   1978)  and porphyrla  (Carlson.
1977b).  Subchronlc  dermal  exposure  resulted  In mild to  moderate  Irritation
(Powers et al.. 1975; Rao et al.. 1982).

    One  chronic  study,  on   the  effects  of  trlchlorobenzene  painted  on  the
skin of mice  for  2  years, reported  Increased mortality  In females  at the low
dose (30X solution  In acetone)  and  In  both sexes at  the high dose (60X solu-
tion)  (Yamamoto  et  al..  1982).   While  numbers of all tumor types  appeared to
be  Increased,  no significant  change was  detected for  any  Individual  tumor
type.   Thus,   the carcinogenic  results  from the  only  relevant  study  are
considered Inconclusive.

    Results of two  reports  on  mutagenlclty tests with Salmonella  typhlmurlum
test strains  were  negative  (Schoeny  et  al., 1979; Lawlor  et al.,  1979).
However, this  test  system Is generally  Insensitive to chlorinated  compounds.

03760                                V-22                            08/18/87

-------
A multlgeneratlon study of -the reproductive effects of oral exposure to trl-
chlorobenzene (Robinson et  al.,  1981)  failed  to show effects  on reproduc-
tion.  TeratogenlcUy studies after administration  by the oral route 1n rats
{Black et al.. 1983; KHchln and Ebron, 1983) showed mild osteogenlc changes
In  pups  and  significantly   retarded  embryonic   development  as  measured  by
growth parameters.
03760                                V-23                            09/25/85

-------
                         VI.  HEALTH  EFFECTS  IN HUMANS

    Information  on  the  health  effects of  tMchlorobenzenes  In  humans  Is
limited  to  case reports.   Rowe (1975) found  that  an Individual  exposed to
1,2,4-tMchlorobenzene  at  3-5  ppm  had  eye  and   respiratory   Irritation.
Glrard et  al.  (1969) reported  two  cases,  one In which a 68-year-old woman,
who often  soaked  her  husband's work clothes In  trlchlorobenzene, developed
aplastlc anemia,  and  the   other  In  which a  60-year-old  man, who  had been
occupatlonally exposed to  DDT as  well  as  to  mono-.  d1- and  trlchlorobenzenes
for over 30 years, developed  anemia.

Summary
    Limited data  are available  on  human exposure  to  trlchlorobenzenes.  No
conclusions can be drawn from this data.
03770                                VI-1                            09/12/88

-------
                         VII.  MECHANISMS OF  TOXICITY

    Several  studies  discussed 1n  Chapter V  on  acute  toxlclty  have  demon-
strated that  the  Isomers  of  trlchlorobenzene are capable of affecting  xeno-
blotlc  metabolism by  Inducing a  variety of  the  hepatic  drug-metabolizing
enzymes  In rats.   These  Include cytochrome  c  reductase, cytochrome  P-450,
glucuronyltransferase,  benzopyrene  hydroxylase,  azoreductase  (Carlson and
Tardlff. 1976; Carlson.  1977a, 1978.  1981;  Smith and Carlson, 1980;  Denomme
et  al.,  1983). acetanlUde  esterase  and acetanlUde  hydroxylase,  procalne
esterase  (Carlson  et al..  1979).  arylesterase  (Carlson. 1980).  mlcrosomal
proteins,  phosphollplds  and  amlnopyrene   hydroxylase   (Arlyoshl   et  al.,
1975a,b.c).   That  tMchlorobenzenes  enhance  xenoblotlc  metabolism has been
demonstrated  by  Smith and  Carlson  (1980) and  Carlson  (1977a),  who  showed
that administration  of  1,2,4- or  1,3,5-tMchlorobenzene to  groups of 4 male
Sprague-Dawley rats  for  7 days Increased EPN detoxlcatlon.   The  administra-
tion of 1,2,4-trlchlorobenzene to pregnant rats  was  also reported to  Induce
hepatic levels of  cytochrome P-450,  cytochrome c reductase, UOP  glucuronyl-
transferase and glutathlone S-transferase (Kltchln and  Ebron.  1983).

    Townsend  and  Carlson  (1981) demonstrated  that  1,2,4-trlchlorobenzene,
administered  by  gavage  1n  corn  oil  to groups  of  five  male  Swiss  mice at
181.5  mg/kg  (1 mmol/kg)  for 7 days,  Increased  the LD5Q and protected the
mice against  the  toxic  effects of malathlon,  malaoxon, parathlon and  para-
oxon when  graded  doses  of  these Insecticides were  administered on the day
following the last dose of trlchlorobenzene.
03780                                VII-1                            09/24/85

-------
    Experiments  comparing  the effects of  trlchlorobenzenes with  the  effects
of  phenobarbUal  and  3-methylcholanthrene  Indicated  that the  Inductions of
mlcrosomal  enzymes  by  trlchlorobenzenes  are  of  the  phenobarbltal   type
(Carlson, 1978).

    These data  suggest that  the  trlchlorobenzenes  stimulate the  drug  metabo-
lizing enzyme system  In  animals.   Thus,  these  compounds  would  be expected to
Increase  the  rate  of   their own metabolism, particularly  with  multiple expo-
sures,  resulting  In  Increased   production of  reactive  Intermediates  and
potentially a greater  toxic response.

    The  series   of  studies  by  AMyoshl  (1975a,b,c)  demonstrated that  trl-
chlorobenzenes  stimulated  the  activity  of   i-am1nolevu!1n1c  add  synthe-
tase.   Since  this  enzyme  Is  the rate-limiting step  1n heme  synthesis Us
elevated  activity  would  be expected to  result  In  the  production of  elevated
levels  of heme  precursors.   This  may  well account for at least  part of the
Increased  urinary  excretion  of  coproporphyrln, porphoblUnogen  and  uropor-
phyrln  In rats  treated  with  trlchlorobenzenes as  reported by  Rlmlngton and
Zlegler  (1963).   These authors also  reported  elevated levels of  these  heme
precursors 1n the  livers of treated rats.

    There  are some Indications  1n the  report  of  Powers et al.  (1975)  that
the  Irritant  effects  noted  In skin may be,  at least partially,  related to
the defattlng action of  the trlchlorobenzenes.
03780                                VII-2                           04/12/91

-------
Summary
    The mechanism of  toxlclty  for  trlchlorobenzene 1s not completely known.
The  cllnUal  effects  of  porphyMa  are  sometimes  observed  In  animals  and
humans  exposed  to   trlchlorobenzene,  but   to  a   lesser  extent  than  for
hexachlorobenzene.    The  capacity  of  trlchlorobenzene  to  stimulate  the
activity  of  i-am1nolevul1n1c  acid  synthetase  Is  well  documented.   Since
this enzyme  1s  the  rate-limiting step In heme  synthesis,  there Is a direct
link to excess porphyrln production.
03780                                VII-3                           04/30/91

-------
                 VIII.   QUANTIFICATION  OF TOXICOLOGIC EFFECTS

Introduction
    The  quantification  of  toxlcologlc effects  of  a  chemical  consists  of
separate  assessments  of  noncarclnogenlc  and  carcinogenic health  effects.
Chemicals  that do  not  produce  carcinogenic  effects  are believed  to  have  a
threshold  dose below which no adverse, noncarclnogenlc  health effects  occur,
while carcinogens are assumed  to act without a threshold.

    In  the  quantification  of  noncarclnogenlc   effects,   a  Reference  Dose
(RfD),  [formerly termed  the  Acceptable  Dally  Intake  (ADI)]  1s  calculated.
The RfD  Is an estimate  (with  uncertainty  spanning perhaps an  order  magni-
tude)  of  a  dally  exposure  to  the  human  population   (Including  sensitive
subgroups) that  1s  likely  to  be without an  appreciable risk  of deleterious
health effects during  a  lifetime.  The  RfD  Is derived  from  a no-observed-
adverse-effect   level   (NOAEL),  or   lowest-observed-adverse-effect   level
(LOAEL),  Identified from  a subchronlc or  chronic  study, and  divided  by  an
uncertainty  factor(s)  times a modifying factor.  The  RfD Is  calculated  as
follows:
     Dfn   	(NOAEL or LOAEL)	           ..   .   ..
     RfD = 	*	'	 =      mg/kg bw/day
           [Uncertainty  Factor(s) x Modifying Factor]   	  y  *      3
    Selection of  the  uncertainty factor to be employed In the calculation of
the RfD  Is  based upon professional  judgment,  while  considering  the entire
data base  of toxlcologlc effects  for  the  chemical.   In order to ensure that
uncertainty  factors  are  selected and  applied  In  a  consistent  manner,  the
03790                                 VIII-1                          04/05/91

-------
U.S.  EPA (1991)  employs  a modification  to  the  guidelines  proposed  by  the

National Academy of Sciences (NAS, 1977, 1980) as follows:


Standard Uncertainty Factors (UFs)

        Use a 10-fold  factor when  extrapolating  from valid experimental
        results from studies using prolonged exposure to average healthy
        humans.   This  factor  Is  Intended  to account for  the  variation
        In sensitivity among the members of the human population.   [10H]

        Use an  additional  10-fold  factor  when extrapolating  from valid
        results  of  long-term  studies  on  experimental  animals  when
        results of  studies  of  human exposure  are not available  or  are
        Inadequate.  This  factor  Is  Intended to  account  for  the  uncer-
        tainty  In  extrapolating  animal  data to the  case  of  humans.
        [10A]

        Use an  additional  10-fold factor  when  extrapolating from  less
        than  chronic  results  on experimental  animals when there  Is  no
        useful  long-term  human  data.   This  factor  Is  Intended  to
        account  for the  uncertainty  In  extrapolating  from  less  than
        chronic NOAELs to chronic NOAELs.   [10S]

        Use an  additional  10-fold factor  when deriving  an  RfD  from  a
        LOAEL Instead  of  a NOAEL.   This  factor   Is  Intended  to account
        for  the  uncertainty  In extrapolating  from  LOAELs  to  NOAELs.
        [10L]

Modifying Factor (MF)

        Use  professional  judgment  to  determine  another  uncertainty
        factor  (MF) that 1s greater  than  zero  and less  than  or  equal  to
        10.   The  magnitude  of  the  MF  depends  upon the  professional
        assessment  of  scientific  uncertainties  of  the  study  and  data
        base  not  explicitly treated  above, e.g.,  the  completeness  of
        the overall  data base  and the number of species tested.   The
        default value for the  MF 1s 1.


    The  uncertainty factor used  for  a  specific risk  assessment  Is  based

principally  upon   scientific   judgment   rather   than  scientific  fact  and

accounts  for   possible  Intra- and   Interspedes  differences.   Additional

considerations  not  Incorporated In  the NAS/ODW  guidelines for selection  of

an  uncertainty  factor   Include  the  use  of  a  less  than  lifetime  study  for

deriving an  RfD,  the  significance  of the  adverse  health  effects and  the

counterbalancing of beneficial  effects.
03790                                VI11-2                          04/05/91

-------
    From  the RfD.  a  Drinking  Water Equivalent  Level  (DUEL)  can  be  calcu-
lated.   The  DUEL   represents  a  medium  specific  (I.e.,  drinking  water)
lifetime  exposure at  which adverse, noncarclnogenlc health effects are  not
anticipated  to  occur.  The  DWEL  assumes 100% exposure  from drinking  water.
The DUEL  provides the  noncarclnogenlc  health  effects  basis  for  establishing
a  drinking  water standard.   For  Ingestlon data,  the  DUEL  Is  derived  as
follows:
                       
-------
    The  1-day HA  calculated  for  a  10  kg  child  assumes  a  single  acute
exposure to  the  chemical  and  1s  generally  derived from a  study of <7  days
duration.  The 10-day HA  assumes  a limited exposure period of  1-2  weeks  and
1s generally  derived  from a  study of <30 days duration.  The  longer-term HA
1s  derived  for  both  the  10  kg  child and  a  70  kg  adult and  assumes  an
exposure period  of  -7  years  (or  10% of  an  Individual's  lifetime).   The
longer-term  HA  Is  generally derived  from a  study of  subchronlc  duration
(exposure for 10% of animal's lifetime).

    The U.S.  EPA categorizes the  carcinogenic potential of  a chemical,  based
on the overall welght-of-evidence, according  to  the following scheme:
        Group  A:  Human  Carcinogen.   Sufficient   evidence  exists  from
        epidemiology  studies  to  support  a  causal association  between
        exposure  to the  chemical  and human cancer.
        Group  B:  Probable  Human  Carcinogen.   Sufficient  evidence  of
        carclnogenlclty  In  animals with  limited   (Group  Bl)  or  Inade-
        quate (Group B2) evidence In humans.
        Group  C:  Possible  Human   Carcinogen.    Limited   evidence  of
        carclnogenlclty  1n animals 1n the  absence  of human  data.
        Group D:  Not  Classified  as to  Human Carclnogenlclty.   Inade-
        quate human and animal evidence of carclnogenlclty  or  for which
        no  data are available.
        Group  E:   Evidence   of   Noncarclnogenlclty  for   Humans.    No
        evidence   of   carclnogenlclty  In   at  least  two  adequate  animal
        tests In  different  species  or In  both adequate  epldemlologlc
        and animal studies.
    If  toxlcologlc  evidence  leads  to  the classification of the  contaminant
as a  known,  probable  or  possible human  carcinogen, mathematical models  are
used  to calculate  the  estimated  excess  cancer   risk  associated  with  the
Ingestlon  of  the  contaminant  1n drinking water.   The data  used  In  these
03790                                VIII-4                          04/05/91

-------
estimates  usually  come  from  lifetime  exposure  studies  using animals.   In
order to  predict  the risk for humans from animal  data,  animal  doses  must  be
converted  to  equivalent  human doses.   This  conversion  Includes  correction
for  noncontlnuous exposure,  less  than  lifetime studies and  for  differences
1n  size.   The  factor  that compensates   for  the size difference Is the  cube
root of  the  ratio of the  animal and  human body weights.   It  Is  assumed  that
the  average  adult  human  body weight Is  70  kg and  that  the average  water
consumption of an adult  human  1s 2 a of water per day.

    For  contaminants  with  a carcinogenic  potential,   chemical  levels are
correlated with  a carcinogenic risk  estimate  by employing a  cancer  potency
(unit risk)  value  together  with  the assumption  for lifetime exposure  from
Ingest Ion of water.   The cancer  unit risk  Is  usually derived from a  linear-
ized multistage model with a 95%  upper  confidence limit providing  a low dose
estimate; that  Is,  the  true  risk  to humans, while  not  Identifiable,  Is not
likely  to exceed  the  upper  limit   estimate  and,  In  fact,  may  be  lower.
Excess cancer  risk  estimates may also be  calculated  using other  models  such
as  the  one-hit,  Welbull.  logH  and  problt.   There  Is  little basis   In the
current  understanding  of  the biologic  mechanisms  Involved  In  cancer  to
suggest that any  one  of  these models  Is  able to predict risk more accurately
than any  other.   Because each model  1s  based upon differing assumptions, the
estimates derived for each model can differ by several orders of magnitude.

    The  scientific  data  base used to calculate  and support  the  setting  of
cancer  risk  rate levels  has an  Inherent uncertainty  that  Is  due   to the
systematic and  random errors  In  scientific measurement.   In most  cases,  only
studies  using  experimental   animals  have  been performed.   Thus,  there  Is


03790                                VIII-5                          04/05/91

-------
uncertainty  when  the  data  are  extrapolated  to  humans.   When developing
cancer risk  rate  levels,  several other areas  of  uncertainty exist, such as
the  Incomplete  knowledge  concerning  the  health effects  of  contaminants In
drinking  water,   the   Impact  of  the  experimental  animal's  age,   sex  and
species,  the  nature  of the  target  organ system(s)  examined and the actual
rate of exposure  of  the  Internal targets  In experimental animals or humans.
Dose-response data usually  are  available only for  high  levels  of  exposure
and.  not for  the  lower levels of  exposure closer  to  where a  standard may be
set.   When  there Is  exposure  to  more  than  one  contaminant, additional
uncertainty results from a lack  of  Information about  possible  synerglstlc or
antagonistic effects.

Noncardnogenlc Effects
    A  number  of   biologic   endpolnts  have  been  Identified  In  short-term
studies  with  1,2,4-TCB   Including  transient  porphyrta,  transient hepatic
cellular  changes, and  Increase  1n adrenal  gland  weight  and  reproductive
effects (Coate et al., 1977; Koclba, 1981;  KUchln and  Ebron,  1983; Robinson
et  al.,  1981).   In  a reproductive study  In  rats,   25,  100 or  400 ppm of
1,2,4-trlchlorobenzene,  administered  to   the  parental  animals   In   their
drinking  water, produced  no reproductive, hematologlc  or neurologic effects
(Robinson  et  al., 1981).   Increased  adrenal gland  weight  occurred In  both
the  parents  and offspring  at the highest dose level.   This  change  was  found
to  be  associated  with vacuollzatlon of  the zona   fasdculata  of  the adrenal
cortex and  decreased  serum  cortlcosterone levels  (dcmanec,  1991).   Retarded
embryonic    development   was    observed     1n   pregnant    rats   receiving
1,2,4-trlchlorobenzene 360  mg/kg/day  on  days 9-13 of gestation  (K1tch1n and
Ebron, 1983).


03790                                VIII-6                           01/03/92

-------
    Hepatic porphyMa,  porphyrlnurla and hepatic cellular changes have  been
observed  following  the  administration  of  1,2,4-tMchlorobenzene but  these
changes either  occurred  at very high doses  or  were  transient.   Coate  et  al.
(1977)  reported a  study  1n  rats,  rabbits  and  cynomolgus  monkeys   (Hacaca
fasclcularls)  that  Involved   Inhalation exposure  for  26  weeks.   In  rats
hepatocytomegaly,  hepatic  vacuollzatlon  and  biliary  hyperplasla  were  seen at
4 weeks and 13  weeks  but not  at the completion of the study.   No significant
changes were  seen  1n  the rabbits  or  monkeys.  Carlson  (1977) reported a
study  In   rats  that  Investigated  the   potential  Induction  of  porphyla by
hexachlorobenzene,  trlchlorobenzene and dlchlorobenzene  when  given  by  oral
gavage  at  0, 50,  100  and 200  mg/kg/day.   Only hexachlorobenzene showed a
marked  ability  to Induce  porphyMa and the  author  determined  that  d1-  and
trlchlorobenzene  did not  share  this  property.  In  the  study  reported by
Carlson and Tardlff  (1976), male CD rats received 0,  10. 20  and  40 mg/kg/day
and  xenoblotlc  metabolism  was  measured  as  well  as  body   weight   and
hematologlc parameters.    There  was a dose-response  related  change  for  all
xenoblotlc enzymes  but  I1ver-to-body  weight ratio  was  only  affected at 40
mg/kg/day.

    Koclba et  al.  (1981)  reported a study  1n  which male rats,  rabbits  and
dogs  were  exposed   to   0,   30  or  100  ppm  (0,   223  or   742  mg/m3)  of
1,2,4-tMchlorobenzene  for 44  days.  No  significant  effects  were  observed
for  body  weight  gain,  hematologlc parameters,  serum biochemical tests or
microscopic  appearance   of  tissues.    A   reversible  Increase   1n   urinary
porphyrlns was  noted  but  the  authors  Interpreted  this change as  being a
compound-specific  physiologic effect rather than a  sign of  toxlclty.   In a
2-year  mouse  skin  painting study  (Yamamoto  et al.,  1982) a  slight  Increase

03790                                VIII-7                          01/03/92

-------
 1n  tumors  of  all sites was  reported,  but  no conclusions can be drawn  about
 carclnogenldty because of the lack of details  In  the  English  translation  of
 the text.

 Quantification of Noncardnoqenlc Effects
    Table  VIII-1  presents  a  summary of the  subchronlc and chronic  toxlclty
 studies  on  the tHchlorobenzenes that were  considered for  calculation of  a
 DWEL  for  each trlchlorobenzene.   Table VIII-2 presents  the toxlclty  thresh-
 old estimates  that  were  determined  from  the studies discussed In  Chapter  V.
 As  Indicated  by these tables  and Chapter  V,  very  little toxlclty data are
 available  to   derive  credible  HAs  or  DWELs  for  the  1,2,3- and  1,3,5-tM-
 chlorobenzenes  Isomers.   Therefore,  no  HAs  or  DWELs  are  recommended for
 these two trlchlorobenzene Isomers.

    Derivation  of  1-Dav  HA.    The   acute   studies  by  AMyoshl   et  al.
 (1975a,b,c) were  selected for  derivation  of  the  1-day HA  for  1.2.4-tM-
 chlorobenzene.

    In  a series  of experiments,  AMyoshl  et  al.  (1975a,b,c)  studied the
 effects  of  the  tMchlorobenzenes  on  Induction  of  hepatic  mlcrosomal pro-
 teins, phosphollplds and enzymes, especially  In  relation to the activity  of
 4-am1nolevul1n1c acid  synthetase,  the rate  limiting  enzyme  1n  the  biosyn-
 thesis of heme.  The three trlchlorobenzene  Isomers  were administered orally
 to groups of  2-6  female  Ulstar  rats at a dose  of  250  mg/kg/day for  3  days,
 after  which the  rats were  killed and mlcrosomes were  prepared.  The  results
 Indicated   that   trlchlorobenzenes   Increased   the   levels   of   mlcrosomal
 proteins, phosphollplds and cytochrome P-450, and enhanced the activities  of


03790                                 VIII-8                           01/03/92

-------
O)
-J
to
o
                              TABLE  VIII-1


Sunmary of Subchronlc and Chronic ToxicIty Studied on Trlchlorobenzenes
Species Route
Rat Inhalation
Rats, rabbits. Inhalation
two dogs
Rat Inhalation
Rat inhalation
Rabbits. Inhalation
murikpys
Monkey oral
Rat oral
Rat oral
House oral
Dose
10. 100 or
1000 ng/n*
of 1,3.5-TCB
223 or 742 ng/n»
of 1,2,4-TCB
22.3 or
74.2 rag/n»
of 1.2.4-TCB
186. 371 or
742 mg/ra»
of 1.2.4-TCB
186. 371 or
742 mg/rn*
of 1.2.4-TCB
1. 5. 25. 90.
12S or 173.6
mg/kg/day
of 1.P.4-TCB
50. 100 or
200 mg/kg/day
of 1.2.4-TCB
10. 20 or
40 mg/kg/day
of 1.2.4-TCB
600 ppm diet
(00/8 mg/kg/
day) of
!.?.« ICB
Duration
6 hours/day.
5 days/week for
up to 13 weeks
7 hours/day.
5 days/week; total
of 30 exposures In
44 days
6 hours/day,
5 days/week.
3 months
7 hours/day.
5 days /week,
26 weeks
7 hours/day.
5 days /week.
26 weeks
30 days
30. 60. 90 or
120 days
90 days
6 months
Effects Reference
No hepatotoxlclty; three high-dose rats had Sasmore et al., I9B3
squamous metaplasia and focal hyperplasta
of respiratory epithelium, believed to be
reversible
Increase In urinary excretion of porphyrla Koclba et al.. 1981
In exposed rats; Increase In liver weights
In high-dose rats and dogs; Increased kid-
ney weights In high-dose rats
Increase In urinary porphyrln excretion In Watanabe et al.. 1978
high-dose rats; no effects In 22.3 mg/m'
group
Enlarged hepatocytes and nondose-dependent Coate et al.. 1977
hepatocytes vacuoltzatlon. liver granuloma.
biliary hyperplasla and kidney hyaline de-
generation at 4 and 13 wk; no hlstopathology
evident at 26 wk
No treatment related changes at 26 wk Coate et al.. 1977
<25 mg/kg/day - no effects observed; Smith et al.. 1978
T25 mg/kg/day - observed toxic Ity and death
Increases In liver weights, liver porphyrlns Carlson. 1977b
and urine porphyrlns. dose and time related
Increase In llver-to-body weight ratio In Carlson and lardllf.
high-dose group; changes In enzyme actlva- 1976
lion at al 1 doses
No effects Goto et dl . 197?

-------
                                                                               TABLE VIII-1 (cont.)
u>
o
 I

o
Species
Guinea pig

Mouse




Rats


Rats








Rabbits




Route Dose
dermal 0.5 ml/day
of 1.2.4-TCB
dermal 0.03 mt /paint-
ing of 30 and
60Jt solution In
acetone of
1.2.4-TCB
oral 25. 100 or
(drinking 400 mg/l
water) of 1.2.4-TCB
oral 36. 120. 360 or
1200 mg/kg/day
of 1.2.4-TCB






dermal 30. 150 or
450 mg/kg/day
of 1.2.3-TCB
(30X) and
1.2,4-TCB (70X)
Duration
5 days/week.
3 weeks
2 times/week,
2 years



F0 to F2
generations

days 9-13 of
gestation







5 days/week,
4 weeks



Effects
Death following extensor convulsion; livers
showed necrotlc foci
Painting Induced excitability, panting and
epidermal thickening. Inflammation and
fceratlnlzatlon; Increased organ weights and
mortality

Increased adrenal weight 1n FQ and F|
generations

1200 mg/kg dose all dead by the 3rd day.
360 mg/kg dose caused 22X mortality In
dams and moderate hepatocellular hyper-
trophy and non-slqnlf leant Increases In
embryonic lethality and significantly
retarded embryonic development. 36 and
120 mg/kg groups not observed for embryonic
effects, but slight hepatocellular hyper-
trophy was reported In one 120 mg/kg dam
Dose-related skin Irritation; Increase In
urinary coproporphyrtn In high-dose males
and slight pallor of liver In males and
females

Reference
Brown et al.. 1969

Yamamoto et al.. 19B2




Robinson et al.. 1981


Kltchln and Ebron,
1983







Rao et al.. 1982




                 1.2.3-TCB = 1.2.3-trlchlorobenzene; 1.2,4-TCB = 1.2,4-trlchlorobenzene; 1.3.5-TCB = 1.3,5-trlchlorobeniene

-------
                                                                                   TABLE  VI11-2

                                                                      Toxlclty Data for  Threshold Estimates
Compound
1.2.4-Trlchlorobenzene
1,2.4-Trlchlorobenzene
1,3.5-Trlchlorobenzene
1,2.4-Trtchlorobenzene
Species Route
rat Inhalation
rabbit, monkey Inhalation
rat Inhalation
rat oral
Dose
Concentration
22.3 mg/m».
6 hour /day. 5 day/week
742 rag/m».
7 hour/day, 5 day/week
100 mg/m».
6 hour/day, 5 day/week
14.8 mg/kg/day
Dose
Duration
3 months
26 weeks
13 weeks
95 days/generation
2 generations
Effect
Level
NOAEL*
NOEL*
NOAEL*
NOAEL*
Reference
Watanabe el al.
197B
Coate et al..
1977
Sasmore et al..
1983
Robinson et al.
1981
                'Estimated toxlclty thresholds as determined In the respective Mammalian Toxlclty Sections  of  this  document.

                NOEL -  No-observed-effect level:   That  exposure  level at which  there are no  statistically  significant Increases  In  frequency or severity  ol
                effects between the exposed population and Its appropriate control.

                NOAEL  • No-observed-adverse-effect  level:   That  exposure  level  at which  there are  no  statistically  significant Increases  In  frequency  or
                severity of  adverse  effects  between  the  exposed  population and  Us  appropriate control.   Effects are produced at  this  dose,  but  they are not
                considered to be adverse.
IS)

-------
aniline  hydroxylase,   amlnopyrlne   demethylase  and  6-am1nolevul1n1c  add
synthetase. with  the  l,2,4-1somer being  the  most  effective  (Arlyoshl et al.,
1975a,b).  The  dose-response of  these effects  to  1,2,4-trlchlorobenzene were
determined  (AMyoshl  et  al., 1975c)  for  groups  of  2-6  female Wlstar rats
treated  orally  with  single  doses  of  0,  125,   250,  500,  750,  1000 and 1500
mg/kg.   The  results  Indicated that  24 hours after  the  administration of  the
Isomer,  mlcrosomal  protein was elevated at  >750  mg/kg and glycogen content
was decreased at  >500 mg/kg.  The activities of  amlnopyrlne demethylase  and
aniline  hydroxylase  and  the  content  of cytochrome  P-450 were Increased at
>250  mg/kg,  as  was  j-amlnolevullnlc acid  synthetase activity.   A slight
significant  Increase   In  6-am1nolevul1n1c   add  synthetase   activity   was
observed 1n  the  125  mg/kg group with  a  dose-related Increase  In activity In
the higher  dose levels.  The  125 mg/kg  dose can  be utilized as a NOAEL  for
the 1-day HA calculations.

    The  1-day  HA  for a  10  kg child  Is calculated using  the  24  hour oral
NOAEL of 125 mg/kg reported by AMyoshl et al.  (1975c) as  follows.
For a 10 kg child:
      i  -,   ...    (125 mq/kq/day x 10 kg)   , ...    .  .    .  .  .   ,
      1-day HA = J	  j*  *    '	^ =1.25 mg/l (rounded  to 1  mg/l)
where:
         125 mg/kg/day = NOAEL, based on the absence of adverse  effects
                        In rats (AMyoshl et al.,  1975c)
         10 kg         = assumed body weight of a child
         1 a/day       = assumed water consumption by a child
         1000          = uncertainty  factor,  1n accordance  with  NAS/ODW
                        and  Agency guidelines  for use  with  a NOAEL from
                        an animal study and to account for limited  data.

This HA  1s equivalent to  1 mg/day or 0.1 mg/kg/day.

03790                                VIII-12                         01/03/92

-------
    Derivation  of  10-Dav  HA.   The  Carlson  and  Tardlff  (1976)  study  was

chosen for derivation of the 10-day HA for 1,2,4-trlchlorobenzene.



    Carlson and Tardlff  (1976)  assessed  the effects of a  14-day oral  admin-

istration  of   1,2,4-trlchlorobenzene  In  corn  oil  compared  with  corn  oil

controls  1n male CD  rats.   In the 14-day  studies,  the  effects  examined  were

lethality, hepatotoxlclty  and  the  Influence on  hexabarbltal  sleeping  time

and other  parameters of xenoblotlc  metabolism.*  A dose  of  600  mg/kg/day,

the   highest   dose   administered,  caused   no   deaths   during  the   14-day

administration  period.   Hepatotoxlclty was  evaluated  by  dosing  at 0,  150,

300  or  600  mg/kg/day  and determining  serum  Isocltrate  dehydrogenase  and

liver  glucose-6-phosphatase activities.   Although  no dose-related  changes  In

serum    Isocltrate     dehydrogenase    activity    was     observed,     liver

glucose-6-phosphatase  activity  was  significantly  decreased  at  >300  mg/kg

(p<0.05).  Hexabarbltal  sleeping  time was  significantly decreased  at  600

mg/kg/day  (the  only  dose examined); this  effect persisted through a  14-day

recovery period.  In rats  receiving 14 dally  doses  at 0,  10,  20 or 40  mg/kg,

there  was  a  significant dose-related Increase  In  I1ver-to-body weight  ratio
*The  stimulation  of  the  xenoblotlc  metabolizing system  may be  considered
 primarily   a   physiologic   response,   although  1n   the   case   of   the
 trlchlorobenzenes   Increased   metabolism  of   subsequent   doses  and   the
 production  of  reactive  Intermediates  and  phenolic  metabolites  would  be
 expected  to enhance  toxldty.    In  addition,  the  elevated  activity  of
 6-am1nolevul1n1c   acid   synthetase,   the   rate  limiting   step  In   heme
 synthesis,  at  250  and 125  mg/kg dose  levels  suggests Increased  porphyrln
 synthesis.  This 1s  verified at higher  dose levels  In other  studies  where
 Increased   porphyrln  excretion   1n   the   urine  has   been   documented.
 Stimulation of  porphyrln  synthesis  may  be seriously  detrimental to  some
 portions of the  population.   The  use of drugs, such as  barbiturates,  that
 enhance   porphyrln   synthesis   are  contralndlcated   In   patients   with
 Intermittent porphyrla or  porphyMa  varlegata  (Goodman and  Oilman,  1985).
 Thus,  1n  addition   to  the   sparse   data,   the  potential  effects  of  the
 stimulation of heme  synthesis 1n man warrants  an additional  safety  factor
 of 10 1n this  calculation.
03790                                VIII-13                         01/03/92

-------
at  >10  mg/kg/day (p<0.05).   Significant dose-related  Increases  were  also
observed  In activities  or  contents  of  cytochrome  c  reductase (at  >10 mg/kg),
cytochrome  P-450  (at  >20  mg/kg),  glucuronyltransferase   (at  >20  mg/kg),
azoreductase  (at >10  mg/kg) and  the  rate  of  detoxlcatlon of  EPN  (at  >10
mg/kg).   These  results  Indicated  that   the  doses,  while  causing  a  slight
degree of  hepatic Injury,  significantly  enhanced  xenoblotlc metabolism.   The
dose  of  10 mg/kg/day  can be  considered  a  NOAEL since  none of  the  effects
observed at this  dose  can  be directly considered  adverse but rather adaptive
responses.

    The  10-day HA  for a  10 kg  child Is calculated  using the 14-day  oral
NOAEL of 10 mg/kg/day  reported by Carlson and Tardlff (1976) as  follows.
For a 10 kg child:
                  10-day HA = dO mq/kq/day x lOkq)   =
                                 100 x U/day
where:
        10 mg/kg/day = NOAEL, based on the absence of adverse effects
                       In  rats (Carlson and  Tardlff, 1976)
        10 kg        = assumed body weight of a child
        1 i/day      = assumed water consumption by a child
        100          = uncertainty  factor,  1n  accordance  with  NAS/ODW
                       and Agency  guidelines for  use with  a NOAEL  from
                       an  animal study.
This HA 1s equivalent  to 1 mg/day or 0.1  mg/kg/day.

    Derivation  of  Longer-term  HA.   Three  studies  were  evaluated  as  the
possible  basis  for  the derivation  of  longer-term HAs for  a 10  kg  child  or  a
70  kg adult.   Two  of  the studies were  oral  studies  (Carlson and Tardlff,
1976; Robinson  et al., 1981) and one was an Inhalation study (Kodba et al.,
1981).

03790                                VIII-14                        12/17/91

-------
    In the 90-day  study  by Carlson and  Tardlff  (1976),  the effects of oral
dosing of male  CD  rats (6 animals/group) at 0,  10,  20 or 40 mg/kg/day with
1,2,4-trlchlorobenzene In corn  oil  on  weight gain, liver weight, hemoglobin
content,  packed cell volume and the Indicators of  xenoblotlc metabolism were
evaluated.  No effects on weight  gain  and no consistent alteration  In hemo-
globin content or  packed  cell  volume  were observed.   At 40 mg/kg,  there was
a statistically significant Increase (p<0.05) 1n  llver-to-body weight ratios
that persisted throughout a 30-day recovery  period.  Following 90-day admin-
istration, cytochrome c reductase activity  was  Increased at >10 mg/kg. with
recovery  after  30  days;  cytochrome  P-450   levels  Increased  at  >20 mg/kg,
followed by recovery; glucuronyltransferase  activity decreased at >10 mg/kg;
EPN detoxlcatlon  Increased  at  >20  mg/kg;  benzopyrene hydroxylase  activity
Increased 2-fold  at 40  mg/kg;  and azoreductase activity  Increased at >10
mg/kg.

    The  Robinson  study (1981)  was  a  multlgeneratlon  reproductive   study  In
which dams received 0, 25, 100  or 400  ppm of 1,2,4-trlchlorobenzene (TCB)  In
the drinking  water.   Following birth  of the F. generation,  Utters of the
F.  and  FI  generations were  dosed  with 0, 25,  100  or  400  ppm  (0,  3.7,
14.8 or  53.6 mg/kg/day) of 1,2,4-trlchlorobenzene  for  95  days.   Subsequently
these  rats   were  bred  and   the   F.   generation  received  similar dosing.
Seventeen to  23  Utters/dose   group  were  used  for  the  study.   During the
study  maternal  weights,  litter  size,  neonatal  sex,  and  weights  were
recorded, as well  as  food and  water Intake.  Serum chemistry  determinations
for  glucose,   BUN,  creatlnlne,  Na,  K,   Cl. uric  acid,  CaP,  cholesterol,
trlglyceMde,  blUrubln,  alkaline  phosphatase,  ALT,  AST, LDH, CPK,  protein,
globulin  and  albumin  were made.   When  the  rats were  killed,  organ weights
for  liver,  kidney,  uterus,  adrenal   glands,  lung,  heart  and  gonads  were

03790                                VIII-15                         01/03/92

-------
recorded.   The  study  ended  when  the  F^  generation was  32  days  old.   A
significant  Increase  1n  adrenal  gland  weight  (11%  for males  and  13%  for
females)  was  noted  1n   the  FQ  and  F,  groups.   Further  Investigation  of
this effect  found  the adrenal gland  Increase  to be associated with  moderate
vacuollzatlon  of  the zona fasclculata of the  cortex  and decreased  levels  of
cortlcosterone  In   the   53.6  mg/kg/day  level  of  exposure  In  male  rats
(dcmanec, 1991).

    Koclba et  al.  (1981) reported a  study  In which  male rats,  rabbits  and
dogs  were   exposed   to   0,   30   or  100  ppm  (0,  223  or   742  mg/m3)   of
1,2,4-trlchlorobenzene  for  44  days.  No  significant  effects were  observed
for  body weight  gain,  hematologlc  parameters,  serum  biochemical   tests  or
microscopic  appearance   of   tissues.   A  reversible  Increase  In   urinary
porphyrlns was noted  but  the  authors  Interpreted this change  as  being  a
compound-specific physiologic effect  rather than a sign of toxlclty.

    The  study  by  Carlson  and  Tardlff (1976)  used the  oral route of exposure,
which  1s  preferred for  deriving  drinking  water  HAs,  but  this study  was
primarily  a  study  of  1,2,4-tr1chlorobenzene's ability  to  Induce xenoblotlc
metabolizing enzymes and  to alter  related parameters such as liver  weights.
The  critical adverse  effect  Induced  by  1,2,4-trlchlorobenzene  of  porphyrla
related  effects  was not  evaluated  In  this  study and therefore,  makes  this
study Inappropriate  for deriving  HAs.

    The  longer-term HAs   for a 10 kg child and a  70  kg  adult are calculated
on  the  basis  of  a  NOAEL of  14.8  mg/kg/day  as established  In  the  Robinson
study.


03790                                 VIII-16                         12/17/91

-------
    The longer-term HA for a 10 kg child 1s calculated as follows:
       Longer-tern, HA B l".6 ..q/kq/day)  «  10  Kq
                              1  I/day x 100
                                                    (rounded  to  1  mg/8.)
where:
       14.8 mg/kg/day = NOAEL, based  on  the absence of adverse effects
                        1n rats (Robinson et al., 1981)
       10 kg          = assumed body weight of a child
       1 l/day        = assumed water consumption by a child
       100            = uncertainty  factor,  In accordance with  NAS/ODW
                        and Agency guidelines  for  use  with  a NOAEL from
                        an animal study.

    The longer-term HA for a 70 kg adult 1s calculated as follows:
                 „.   (14.8 mg/kq/dav)  x 70  kg
     Longer-term HA  ="       	  = 5.18 mg/i
                          2 I/day x 100
                                                (rounded to  5 mg/i)
where:
        14.8 mg/kg/day = NOAEL, based on the absence of  adverse effects
                         In rats (Robinson  et al.. 1981)
        70 kg          = assumed body weight of an adult
        2 i/day        = assumed water consumption by an adult
        100            = uncertainty factor.  In  accordance with  NAS/ODW
                         and  Agency   guidelines  for  use with  a  NOAEL
                         from an animal study.

    Assessment  of Lifetime  Exposure  and   Derivation  of a   DWEL.   As  dis-
cussed In the longer-term HA  section  the Robinson  et  al.  (1981)  study Is the
most appropriate  to  derive a lifetime DUEL.   The  lifetime  DWEL  for a  70  kg
adult 1s calculated as follows.
       Step 1 - RfD Derivation
      RfD  =14'8lmQqo/0kq/daY  = 0.0148 mg/kg/day  (rounded  to 0.01 mg/kg/day)
03790                                VIII-17                         01/03/92

-------
where:
        14.8 mg/kg/day = NOAEL, based on  the  absence of adverse effects
                         1n rats (Robinson et al., 1981)
        1000        =  uncertainty  factor.  In  accordance  with  NAS/ODW
                       and  Agency  guidelines  for use with a  NOAEL  from
                       a subchronlc animal study.
        Step 2 - DUEL Derivation
                   0.01  mg/kq/dav x 70 kg
            DWEL =	       	*  =0.35 mg/l
                         2 I/day
                                              (rounded to  0.4  mg/i)
where:
        0.01 mg/kg/day = RfD
        70 kg          = assumed body weight  of an adult
        2 l/day        = assumed water consumption by an  adult

Carcinogenic Effects
    One study reported  by  Yamamato et al. (1982), where  30%  or  60% solutions
of  1,2.4-tMchlorobenzene   1n  acetone were applied  to the  skin  of  Slc.ddy
mice  twice weekly  for 2 years, was  evaluated by the Human Health  Assessment
Group  (HHAG) of  the U.S. EPA.  The  HHAG evaluation  of this  study  determined
that  Insufficient  Information was   presented  1n  this  study  to  allow  an
acceptable Interpretation  of the  data  to be made.  Also, this single study
was   found  to  be  clearly  Inadequate   for  making  any  conclusions about
carclnogenldty .In  humans.  Therefore,  the  trlchlorobenzenes are  classified
as U.S. EPA Group D compounds (U.S. EPA,  1991).
Existing Guidelines. Recommendations and Standards
    Occupational.    There   are  no   U.S.  workplace   standards   for   the
trlchlorobenzenes.
03790                                VIII-18                         01/03/92

-------
    The  ACGIH   has   recommended   a  celling   of   5  ppm  (40  mg/m3)   for
1,2,4-trlchlorobenzene (ACGIH,  1982), and NIOSH classified 1t as a  Group  III
pesticide.   Group III pesticides are less toxic than Group II pesticides  and
the  recommended  criteria  for  workplace  standards  are  less  stringent  than
those  recommended  for   Group   II  pesticides   (NIOSH.   1978).    The  British
Journal of  Industrial Medicine reported  a  provisional  operational  limit  of
25  ppm for  1,2,4-trlchlorobenzene  (Verschueren,  1977).   The  1971 TLV  for
1,2,3-trlchlorobenzene   Is   1.3   ppm  [10  mg/m3  (n.s.1.)]   for   the   USSR
(Verschueren, 1977).

    Trlchlorobenzenes have  been  designated  by  the  ITC  as TSCA  Section  4(e)
priority chemicals  (44  FR 70666).   Preliminary Assessment Information  Manu-
facturers  Reports  were  to  be  submitted to  the  U.S.  EPA  Office  of  Toxic
Substances by  November  19,  1982,  for  each  of  the  trlchlorobenzenes (40  CFR
712).

    The U.S.  EPA determined that, on  the basis of  present  Information,  TCB
Is  not  classifiable as  a  human  carcinogen;  It therefore Is placed In  Class
D.  This decision was verified by CRAVE 1n October  1988 (U.S.  EPA,  1991).

    Transportation  and   Regulations.   The  export   of  1,2,3- and  1,2,4-trl-
chlorobenzene  1s  regulated by DOT  through  the use  of  the Commodity Control
List (15 CFR 399).

    Solid  Haste  Regulations.    The  trlchlorobenzenes   are   designated  as
hazardous  constituents  of hazardous wastes from specific  sources  subject to
RCRA disposal  regulations  (40  CFR  261.32).   The hazardous waste In which the


03790                                VIII-19                         12/17/91

-------
trlchlorobenzenes  are  controlled  as part  of the hazardous  constituents  1s
from  the  distillation or fractlonatlon  column bottoms  from the production  of
chlorobenzene and  Is  designated as EPA Hazardous Waste No. K085.

    Mater.   The  U.S.  EPA  (1980),  In  an  Ambient  Water  Quality  Criteria
Document  for Chlorinated  Benzenes,  determined  that  "Reliable  tox1co!og1cal
data  on  which  to base  a  defensible  water  quality  criterion  do  not  exist  for
the trlchlorobenzenes.11  As a result of this  determination  no  criterion was
recommended  for any trlchlorobenzene Isomer.

Special Groups at Risk
    Only  anecdotal  Information regarding human  exposure  to  trlchlorobenzene
1s  available.   These  data  do not Indicate  special  groups that might be  at
risk.

Summary
    Health  advisories  and  a DWEL  for  1,2,4-tMchlorobenzene  In  drinking
water, based on noncarclnogenlc  toxlclty  data, are  given In Table  VIII-3.
No  HAs  or   DWELs  are  suggested  for  the  1,2,3-  and  1,3,5-trlchlorobenzene
Isomers  because  of  Insufficient  data  being  available for  evaluation.  The
1-day  HA  for 1,2,4-tMchlorobenzene  of  1  mg/s.  for  a 10  kg child  1s based
on a  study by Arlyoshl  et al. (1975c)  1n which female Wlstar rats  were given
single oral  doses  of  1.2,4-tMchlorobenzene  and  were then  evaluated.  The
10-day HA for  1,2,4-tr1chlorobenzene of  1  mg/i for a 10 kg child  1s based
on a  study  by Carlson  and Tardlff  (1976)  In  which  male CD  rats were given
1,2,4-trlchlorobenzene  for  14 days and  were then evaluated.   The  longer-term
03790                                VIII-20                         01/03/92

-------
o
CO
                                                                            TABLE VI11-3


                                             Sumnary of the Data for 1.2.4-Trlchlorobenzene Used to Derive HAs  and DUEL
Health Species/Route
Advisory
1-Oay rat/oral
10-Day rat/oral
Longer-term rat/oral
DWH rat/oral
Cdncer
potency
Dose Duration
(rag/kg bw/day)
12S single
dose
10 14 days
14.8 95 days/gen.
2 generations
14.8 95 days/gen.
2 generations


Value (mq/t)
Basis Uncertainty
factors Child Adult
NOAEL. higher doses 1000 1 NA
cause a greater number
of alterations
NOAEL. higher doses 100 1 NA
cause a greater number
of dose-related hepatic
changes
NOAEL. higher dose caused 100 1 5
Increased adrenal gland
weights
NOAEL. higher dose caused 1000 NA 0.4
Increased adrenal gland
weights
NR

Reference
Arlyoshl
el al.. 1975c
Carlson and
Tardiff. 1976
Robinson
et a).. 1981
Robinson
et al.. 1981


          *for  a  70 kg adult


          "For  a  10 kg child


          NA  =  Not  applicable;  NR = none recomnended
o
GO

-------
HAs  for   1,2,4-tMchlorobenzene  of  1  mg/l  for  a  10  kg  child  and  5  mg/j.
for a  70  kg adult  are  based on a  study  by  Robinson  et  al.  (1981)  In which
CD-I   rats   were  exposed   by   gavage  to  1,2,4-tMchlorobenzene   for   95
days/generation  for 2 generations  and  evaluated for reproductive effects  and
adrenal gland  changes.   An  oral RfD  of  1E-2 mg/kg/day  was derived  from  the
Robinson  study.   A DWEL for  1,2,4-tr1chlorobenzene of 0.4 mg/l  for  a 70 kg
adult  was  calculated  from the  same  Robinson et  al. (1981) study.   The data
available   on   1,2,4-tMchlorobenzene  are   Inadequate   for   making   any
conclusions about Us potential cardnogenlclty  In humans.
03790                                VIII-22                         01/03/92

-------
                               IX.  REFERENCES

ACGIH  (American  Conference  of  Governmental  Industrial  Hyglenlsts).   1982.
Threshold Limit Values  for  Chemical  Substances  In Work Air Adopted  by  ACGIH
for 1982.  Cincinnati. OH.   ISBN:  0-936712-39-2.

Arlyoshl, T.,  K.  Ideguchl,  Y. Ishlzuka, K.  Iwasakl  and M. Arakakl.  1975a.
Relationship between  chemical structure  and activity.   I.  Effects of  the
number  of  chlorine  atoms  In chlorinated   benzenes  on  the  components   of
drug-metabolizing system and the hepatic constituents.   Chem. Pharm.  Bull.
23(4): 817-823.

Arlyoshl. T., K. Ideguchl,  K. Iwasakl and M.  Arakakl.   1975b.  Relationship
between  chemical  structure  and  activity.    II.   Influences  of  Isomers   In
dlchlorobenzene. trlchlorobenzene, and  tetrachlorobenzene on  the  activities
of drug-metabolizing enzymes.  Chem.  Pharm.  Bull.   23(4):  824-830.

Arlyoshl, T.,  K. Ideguchl.  K.  Iwasakl  and M. Arakakl.   1975c.  Relationship
between  chemical structure  and  activity.   III.  Dose-response  or  time-course
of Induction In mlcrosomal  enzymes following treatment with 1,2,4-trlchloro-
benzene.  Chem. Pharm. Bull.  23(4):  831-836.

Berger,  D.A.   1987.   1,2,4-TMchlorobenzene  health-based  maximum  contaminant
level  support  document,  in: Maximum  Contaminant Level  Recommendations  for
Hazardous Contaminants  In  Drinking  Water.    Appendix B.  Health-Based Maximum
Contaminant Level Support Documents.   March  26,  1987.   Section P.
03800                                IX-1                             08/20/87

-------
Black,  W.D.,  V.E.O.  Vall1.  J.A.  Ruddlck  and  D.C.  Vllleneuve.   1983.  The
toxldty  of  three  trlchlorobenzene  Isomers  In  pregnant  rats.   The Tox1-
cologlst.  3(1): 30.  (Abstr.)

Brown,  V.K.H.,  C.  Mulr  and  E. Thorpe.  1969.   The  acute toxlclty and  skin
Irritant  properties  of   1,2,4-trlchlorobenzene.    Ann.   Occup.  Hyg.   12:
209-212.

Cameron, G.R.,  J.C. Thomas,  S.A. Ashmore,  J.L. Buchan, E.H. Warre/i and  A.W.
McKlnney  Hughes.    1937.   The  toxlclty  of  certain  chlorine derivatives of
benzene, with  special reference to o-dlchlorobenzene.   J.  Pathol. Bacterlol.
44(2): 281-296.

Carlson, G.P.   1977a.   Halogenated benzenes, effect  on  xenoblotlc metabolism
and the toxlclty of other chemicals.  Ann.  N.Y. Acad. Scl.   298:  159-169.

Carlson, G.P.   1977b.  Chlorinated  benzene  Induction of  hepatic porphyMa.
ExpeMentla.  33(12): 1627-1629.

Carlson, G.P.   1978.  Induction of cytochrome  P-450  by  halogenated  benzenes.
Blochem. Pharmacol.  27(3): 361-363.

Carlson, G.P.   1980.  Effects  of  halogenated benzenes  on  arylesterase  activ-
ity  Ui  vivo  and  in  vitro.   Res.  Commun.  Chem.  Pathol.   Pharmacol.   30(2):
361-364.
03800                                IX-2                            08/20/87

-------
Carlson,  G.P.    1981.   Effects  of  halogenated  aromatic  compounds  on  the
metabolism of foreign organic compounds.  U.S. EPA Health Effects Res.  Lab.,
Cincinnati, OH.   EPA-600/1-81-010.   NTIS PB81-152522.

Carlson,  G.P.  and R.G. Tardlff.   1976.  Effect of  chlorinated benzenes on
the metabolism of foreign organic  compounds.  Toxlcol. Appl. Pharmacol.   36:
383-394.

Carlson,  G.P.. J.D.  Dzlezak  and  K.M. Johnson.  1979.  Effect of  halogenated
benzenes  on  acetanlllde  esterase,  acetanlllde   hydroxylase   and   procalne
esterase  1n rats.  Res. Commun.  Chem. Pathol.  Pharmacol.   25(1):  181-184.

Chlorobenzene Producers  Association.   1984.  Comments  of the  Chlorobenzene
Producers Association on the EPA Review Draft Health  Assessment  Document  for
Chlorinated Benzenes.  49 Fed. Reg.  18616  (May, 1984) Part  II.   Submitted to
U.S.  EPA, Environmental Criteria  and  Assessment  Office,  Cincinnati,  OH  on
July 30,  1984.

Clcmanec,    J.L.      1991.      Report     of     In-house     research    with
1.2,4-trlchlorobenzene; an  acute animal study.  Memorandum  to the  U.S.  EPA
RfD/RfC Work Group.  December, 1991.

Coate,  W.B.,  U.H. Schoenflsch.  T.R.  Lewis  and  U.M.  Busey.  1977.   Chronic,
Inhalation exposure  of  rats,  rabbits, and  monkeys  to 1,2,4-tMchlorobenzene.
Arch. Environ. Health.  32(6): 249-255.
03800                                IX-3                            01/03/92

-------
 S.T..  G.F.  Wolfe and C.C. Smith.  1918.  Toxlclty of 1,2,4-trlchloro-
'  1-i Rhesus monkeys:  Comparison  of  two in vivo methods for estimating
 ct-'Hy.   Toxlcol.  Appl.  Pharmacol.   45(1):  340.   {Abstr.J

     A., B. Leece,  3.  Gyorkos and K. Homonko.  1383.   PolychloMnated
   .-  :  phenol  congeners  as Inducers  of  rat  hepatic drug-metabolizing
    n  Immature  male Hlstar  rats.  Can.  J.  Physlol.  Pharmacol.   61:
      1   Company.   1979-1980.    Material  safety  data   sheets - mono-
      e,  o-dlchlorobenzene,  p-dlchlorobenzene,  1,2,4-trichlorobenzene,
      achlorobenzene.  Midland, HI.

      .  Orossman and T. Mill.  1986.   Products  and  quantum  yields  for
      F  chloroaromatlcs In water.   Environ. Scl.  Technol.   20:  72-77.

      jerova.  V.  and  H.C.  Hughes.    1983.   Species  differences   on
      ity of  Inhaled vapors and  gases.   Chapter  4.   In.: Modeling  of
      Exposure   to   Vapors:   Uptake,   Distribution  and   Elimination
        Press, Boca Raton, FL.

      F.  Tolot, P.  Martin  and J. Bourret.   1969.   Serious  blood dls-
      exposure   to  chlorine  derivatives  of  benzene  (A  report  of  7
      •led. Lyon.  50(1164): 771-773.  (Fre.)

       Gllman.   1985.   Goodman and Oilman's  The Pharmacological  Basis
      ics, 7th ed. MacMlllan Publishing  Company, New York.  p.  358.


                               IX-4                            01/03/92

-------
Goto,  M.,  H.  Hattorl,  T.  Mlyagawa  and  M.  Enomoto.   1972.   BeHrage zur
okologlschen chemle.  II.  Hepatoma-blldung  1n mausen nach verabrelchung von
HCH-lsomeren 1n hohen dosen.   Chemosphere.   6:  279-282.   (6er.)

Gurfeln, L.N.  and  Z.K.  Pavlova.   1960.   Maximum allowable concentration of
chlorinated  benzene  In  water  supplies.   Sanlt.  Okhrana  Vod.  Zagryaznenlya
Prom. Stochrayml Vodanrt.   (4): 117-127.   (Cited 1n CA 56:10601)

Hansch,  C.  and  A.3.  Leo.  1981.   Medchem Project.   Issue  No. 19.   Pamona
College, CA.

Hawley,  G.G.   1977.  Condensed  Chemical  Dictionary,  9th  ed.  Van  Nostrand
Relnhold Company, NY.

Horvath,  A.L.   1982.   Halogenated  Hydrocarbons.   Solubility  -  MlsclbHlty
with Water.  Marcel Oekker, Inc., NY.  p.  530.

Jondorf,  W.R.,  D.V. Parke  and R.T.  Williams.   1955.   Studies In  detoxlca-
tlon.    66.  The metabolism of  halogenobenzenes,  1,2,3-, 1,2,4- and  1,3,5-
tMchlorobenzenes.  Blochem. 3.  61: 512-521.

Kao,  C.I.  and  N.  Poffenberger.   1979.    Chlorinated  benzenes.    In.:  Klrk-
Othmer  Encyclopedia  of Chemical  Technology, 3rd ed., Vol.  5.   John Wiley and
Sons.  New York.  p. 797-808.

KHchln,  K.T.  and  H.T.  Ebron.  1983.  Maternal hepatic and embryonic effects
of  1,2,4-trlchlorobenzene  In  the rat.  Environ.  Res.  31: 362-373.


03800                                 IX-5                            01/03/92

-------
Kodba, R.J.,  B.K.J.  Leong and R.E. Hefner. Jr.  1981.  Subchronlc toxldty
study  of  1,2,4-trlchlorobenzene  1n the  rat.  rabbit  and  beagle  dog.   Drug
Chem. Toxlcol.  4(3): 229-249.

KohH.  J..  0. Jones  and S.  Safe.   1976.   The metabolism  of higher chlori-
nated benzene  Isomers.  Can.  J. Blochem.  54(3): 203-208.

Kuehl, D.W.,  E.N. Leonard.  K.J. Welch  and G.D.  Velth.   1980.   Identification
of hazardous  organic chemicals In  fish from the Ashtabula River, Ohio, and
Wabash River,  Indiana.  J. Ass.oc.  Off. Anal. Chem.   63(6):  1238-1244.

Langhorst,  M.L.  and  T.J.  Nestrlck.  1979.  Determination of  chlorobenzenes
In  air and  biological  samples  by  gas chromatography with  photolonlzatlon
detection.  Anal. Chem.  51(12): 2018-2025.

Lawlor, T.,  S.R. Haworth  and P.   Voytek.   1979.   Evaluation of  the genetic
activity  of  nine chlorinated phenols,  seven chlorinated benzenes, and  three
chlorinated hexanes.  Environ. Nutagen.  1: 143.  (Abstr.)

Lewis,  R.G.  and K.E.  MacLeod.   1982.   Portable  sampler  for pesticides and
semlvolatlle  Industrial organic chemicals In air.  Anal. Chem.   54:  310-315.

L1ngg, R.D..  U.H. Kaylor,  S.N.  Pyle et al.  1982.   Comparative metabolism of
1,2,4-tMchlorobenzene  In  the rat  and  Rhesus  monkey.   Drug  Metabol. Dlspos.
10(2): 134-141.
03800                                IX-6                            01/03/92

-------
Lopez-Avlla,  V., R. Northcutt. J.  Onstot,  M.  Wlckham and S. Billets.   1983.
Determination of  51  priority organic compounds  after  extraction from  stan-
dard reference materials.   Anal.  Chem.   55(6):  881-889.

MacKay,  D.,  W.Y.  Shlu  and R.P.  Sutherland.   1979.   Determination  of air-
water  Henry's  Law constants  for  hydrophobia  pollutants.   Environ.  Sc1.
Techno!.  13(3): 333-337.

Matthews, M.B.  and  S.  Kato.   1979.  The metabolism and  disposition  of  halo-
genated  aromatlcs.   Irr.  Ann N.Y.  Acad. Scl., Vol.  320.  Health Effects  of
Halogenated  Aromatic  Hydrocarbons, Int.  Symp.,  NY, June  24-27, 1978, W.J.
Nicholson and J.A. Moore,  Ed.   N.Y. Acad.  Scl.   p.  131-137.

NAS  (National Academy of Sciences).  1977.  Drinking Water  and  Health.   Safe
Drinking Water Committee,  NAS,  Washington. DC.   p.  667-673,  798-799.

NAS  (National Academy of Sciences).  1980.  Drinking Water  and  Health.   Vol.
3, p. 25-67.

NIOSH  (National  Institute  for  Occupational Safety  and  Health).   1978.   Cri-
teria  for  a  Recommended  Standard...Occupational  Exposure  During the  Manu-
facture  and  Formulations of  Pesticides.  Cincinnati, OH.  DHEW (NIOSH) Publ.
No.  78-174.

NLM  (National Library of  Medicine).   1981a.   1,2,3-TMchlorobenzene.   Toxi-
cology  Data  Base,  Bethesda, MD.  TDB No. 1502.
 03800                                IX-7                            01/03/92

-------
NLH  (National  Library of Medicine).   1981b.   1,2,4-Trlchlorobenzene.   Toxi-
cology Data Base, Bethesda, MD.  TOB No. 1105.

NLM  (National  Library  of  Medicine).   1982.   1,3,5-Trlchlorobenzene.   Toxi-
cology Data Base, Bethesda, MD.  TDB No. 0132.

Oehtne, M.  and H.  Stray.   1982.  Quantitative determination of  ultra-traces
of  chlorinated compounds  1n  high-volume air  samples  from the Arctic  using
polyurethane  foam as  collection  medium.  Fresenlus Z. Anal.  Chem.   311(7):
665-673.

Parke, D.V.  and  R.T. Williams.  1960.   Studies  In  detoxlcatlon.   LXXXI.  The
metabolism  of  halogenobenzenes: (a) penta- and  hexa-chlorobenzenes.  and  (b)
further observations  on 1,3,5-trlchlorobenzene.  Blochem.  J.  74:  5-9.

Powers, M.B.,  U.B. Coate  and T.R.  Lewis.  1975.   Repeated  topical  applica-
tions  of  1,2,4-trlchlorobenzene:  Effects  on rabbit  ears.   Arch.  Environ.
Health.  30: 165-167.

Rao,  K.S.,  K.A.   Johnson and  J.W.  Henck.  1982.  Subchronlc  dermal  toxldty
study  of  trlchlorobenzene   1n  the  rabbit.   Drug.   Chem.  Toxlcol.   5(3):
249-263.

Rlmlngton,  C.  and G. Zlegler.  1963.  Experimental  porphyrla In rats Induced
by  chlorinated benzenes.   Blochem. Pharmacol.  12:  1387-1397.
03800                                 IX-8                            01/03/92

-------
Rlnkus,  S.J.  and M.S. Legator.   1980.   The need  for  both  Ui  vitro and In
vivo  systems  1n  mutagenlcHy screening.  Ijn: Chemical Mutagens,  Vol.  6, A.
Hollander, Ed.  Plenum Press, New York.   p.  365-473.

Robinson, K.S., R.J. Kavlock, N. Chernoff and L.E. Gray.  1981.  Multlgener-
atlon  study of 1,2,4-tMchlorobenzene In rats.  J. Toxlcol.  Environ. Health.
8(3): 489-500.

Rowe, V.K.  1975.  Written communication.   (Cited  1n  U.S. EPA, 1980)

Sasmore,  D.P.,  C.  Mltoma, C.A.  Tyson and  J.S.  Johnson.   1983.  Subchronlc
Inhalation toxldty of  1,3,5-tMchlorobenzene.   Drug.  Chem.  Toxlcol.  6(3):
241-258.

Sax. N.I.  1979.   Dangerous  Properties  of  Industrial Materials, 5th ed. Van
Nostrand Relnhold Co..  NY.  p.  716.

Schoeny. R.S., C.C. Smith  and  J.C.  Loper.   1979.   Non-mutagen1c1ty for  Sal-
monella  of  the chlorinated  hydrocarbons  Arochlor  1254,  1,2,4-tMchloroben-
zene, ml rex and kepone.   Mutat.  Res.   68(2):  125-132.

Sllmak,  K.,   P.  Johnson  and V.  Hodge.   1980.   Materials  balance-task a4
chlorobenzenes.   U.S.   EPA,  Office  of  Toxic  Substances,   Washington,  DC.
EPA-560/13-80-001.

Smith, E.N. and  G.P.  Carlson.   1980.   Various pharmacoklnetlc parameters 1n
relation   to   enzyme-Inducing   abilities   of   1,2,4-trlchlorobenzene  and
1,2,4-trlbromobenzene.   J. Toxlcol.  Environ.  Health.  6(4): 737-749.

03800                                IX-9                            01/03/92

-------
SmHh,  C.C.,  S.T.  Cragg  and  G.F.  Wolfe.   1978.   Subacute  toxlclty   of
1,2,4-trlchlorobenzene (TCB) 1n subhuman pr_1mates.  Fed.  Proc.   37(3):  248.

Townsend, B.A.  and G.P.  Carlson.   1981.   Effect of halogenated benzenes  on
the  toxlclty and metabolism  of  malathlon,  malaoxon, parathlon and  paraoxon
In mice.  Toxlcol. Appl.  Pharmacol.  60(1):  52-61.

Treon,  J.   1950.  The  toxlclty  of tMchlorobenzene.  Ketterlng Lab.,  Univ.
of Cincinnati.   (Unpubl.  rep.)  (Cited 1n Coate et al..  1977)

U.S.  EPA.   1980.  Ambient Water  Quality  Criteria Document for Chlorinated
Benzenes.   Prepared  by  the Office of  Health and  Environmental Assessment.
Environmental Criteria  and Assessment Office. Cincinnati. OH  for  the  Office
of Water Regulations and Standards. Washington,  DC.  EPA 440/5-80-028.  NTIS
PB 81-117392.

U.S.  EPA.    1982.   Test  Methods:  Methods  of Organic  Chemical  Analysis   of
Municipal and  Industrial  Wastewater,  J.E.  Longbottom and  J.J.  Llchtenberg,
Ed.   Environ.  Monlt.  Sup.  Lab.,  Cincinnati, OH.   EPA  600/4-82-057.  NTIS
PB83-20-1798.

U.S.  EPA.   1983.  Chlorinated  benzenes  aggregates  derived from  Information
reported under  TSCA section  8(a).  Preliminary  assessment Information rule
(47  FR  26992)  using the techniques  for  aggregating data described  by  48  FR
27041.  Office of Toxic  Substances. Washington, DC.
03800                                IX-10                           01/03/92

-------
U.S.  EPA.    1985.   Health  Assessment  Document  for Chlorinated  Benzenes.
Office  of  Health  and Environmental  Assessment,  Environmental Criteria  and
Assessment Office. Cincinnati, OH.  EPA 600/8-84/015F.   NTIS PB 85-150332.

U.S.  EPA.   1986.    Guidelines  for  Carcinogen  Risk   Assessment.    Federal
Register.  51(185): 33992-34003.

U.S.  EPA.   1991.    Integrated  Risk   Information  System  (IRIS).    Online.
Office  of  Health  and Environmental  Assessment,  Environmental Criteria  and
Assessment Office, Cincinnati, OH.

Verschueren, K.   1977.   Handbook  of Environmental  Data  on Organic  Chemicals.
Von Nostrand Relnhold Co., New York.

Warner, H.P.,  J.M.  Cohen and J.C.  Ireland.   1980.   Determination  of  Henry's
Law  Constants  of  Selected Priority  Pollutants.   U.S.  EPA  Research  Report.
Cincinnati, OH.  EPA/600/D-87/229.  NTIS PB87-212684.

Watanabe,  P.G.,  R.J.  Koclba,  R.E.  Hefner,  Jr., H.O. Yakel  and B.K.J.  Leong.
1978.   Subchronlc  toxldty studies of 1,2,4-trlchlorobenzene In experimental
animals.  Toxlcol. Appl. Pharmacol.   45(1): 332-333.

Williams,  R.T.   1959.  The metabolism  of  halogenated  aromatic hydrocarbons.
jhn:  Detox1cat1on  Mechanisms,  2nd  ed.   John Wiley  and  Sons,  New  York.
p. 237-277.

Yalkowsky,  S.H.  and  S.C.  Valvanl.   1980.  Solubility and  partitioning.   I.
Solubility of nonelectrolytes 1n water.  J. Pharm. Set.  69(8): 912-922.

03800                                 IX-11                           01/03/92

-------
Yamamoto, H.,  Y. Ohno,  K.  Nakamorl,  T.  Okuyama,  S.  Imal  and  Y.  Tsubura.
1982.  Chronic  toxlclty and  carclnogenlclty  test of  1,2,4-trlchlorobenzene
on mice by dermal painting.   J.  Nara.  Med.  Assoc.   33:  132-145.   (Jap.)

Yang,  K.H.,  R.E. Peterson and  J.M.  Fujlmoto.  1979.   Increased bile  duct-
pancreatic  fluid  flow  In  benzene  and  halogenated  benzene-treated  rats.
Toxlcol.  Appl. Pharmacol.  47(3):  505-514.
03800                                IX-12                           01/03/92

-------