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incidence of mammary tumors. Control groups included a negative control (sesame oil only) and a positive control (7,12-dimethylbenz[a]anthracene). No tumors were observed in treated animals, but a 3% incidence was observed in the negative controls and 100% incidence in positive control animals. Osanai et al. (1976) treated 26 male ICR/JCL mice (plus 39 untreated control mice) with feed containing 0.1% 3,3’-dichlorobenzidine for 12 months with an interim sacrifice group at 6 months. Hepatomas were observed in all treated animals at 6 and 12 months (p < 0.01) and among control animals at an incidence of 0%, 9.5% (2/21) and 38.55% (5/13) at 6,12, and 18 months, respectively. Tatematse et al. (1977) fed 22 male Wistar rats a diet containing 0.3% 3,3’-dichlorobenzidine alone or in sequence with o-N-butyl-N-(4-hydroxybutyl)nitrosamine (0.1% in drinking water), N-[4-(5-nitro-2- furyl)-2-thiazolyl]formamide (0.15% in the diet) and N-fluorenylacetamide (0.025% in the drinking water) over a four week period. Twelve untreated animals served as controls. Animals were observed for a 40 week period. Only animals receiving combined exposures showed effects which included some bladder tumors and histological changes of the liver. Saffiotti et al. (1967) and Sellakumar et al. (1969) report on a feeding study in which Syrian golden hamsters (30/sex/group) were exposed to 0.1% or 0.3% 3,3’-dichlorobenzidine in feed; an untreated control group (30/sex) was included. No significant carcinogenic effects were observed in the 0.1% 3,3’-dichlorobenzidine group. The 0.3% 3,3’-dichlorobenzidine group, however, showed increased incidence of transitional cell carcinomas of the bladder (4/30 treated, 0/30 control; p = 0.056 by Fisher’s exact test). Other observations included some liver-cell and cholangiomatous tumors. A single study suggests that 3,3’-dichlorobenzidine may act as a transplacental carcinogen (Golub et al., 1974). Pregnant female BALB/c mice given 2 mg 3,3’-dichlorobenzidine (in 0.1 ml sesame oil) five times during the last week of pregnancy, showed increased incidence of lymphoid leukemia among the offspring of exposed animals (7/24 treated, 0/30 control; p < 0.01). This effect, however, could also have occurred by exposure via lactation. IV. DERIVATION OF CANCER POTENCY Basis for Cancer Potency An IARC (1982) review of the human epidemiological studies deemed them inadequate for evaluating carcinogenicity due to the relatively small size of the cohorts, inadequate time since first exposure, and/or incomplete follow-up of exposed workers. The only carcinogenesis studies amenable to the development of cancer potency values are those conducted by Stula et al. (1975, 1978) showing the induction of granulocytic leukemia, mammary adenocarcinoma, and Zymbal gland carcinoma in rats and papillary transitional cell carcinomas of the bladder and hepatocellular carcinomas in beagle dogs exposed to 3,3’-dichlorobenzidine. Limitations of the other available studies including poor study design, inadequate scope of endpoints, and unclear 249
interpretation of dose extrapolation, preclude the development of cancer potency values from these studies. Methodology The most sensitive experimentally determined endpoint for tumor development is mammary adenocarcinoma induction in female rats exposed to 3,3’-dichlorobenzidine (26/44 treated, 3/44 control) (Stula et al., 1975). A linearized multistage procedure (CDHS, 1985) applied to these data resulted in an estimation of the upper 95% confidence bound of cancer potency (q 1 * ) of 0.023 (mg/kgday) -1 . With a study duration of 49.9 weeks for females (T e ) and a natural lifespan assumption of 104 weeks (T), the cancer potency for animals (q animal ) was derived to be 0.21 (mg/kg-day) -1 from the following relationship: q animal = q 1 * × (T/T e ) 3 Human cancer potency (q human ) of 1.2 (mg/kg-day) -1 based upon body weight assumptions of 0.35 kg for female rats (bw a ) and 70 kg for humans (bw h ) and the following relationship: q human = q animal × (bw h /bw a ) 1/3 A unit risk value of 3.4 E-4 (µg/m 3 ) -1 based upon air concentrations was derived by <strong>OEHHA</strong>/ATES assuming a human breathing rate of 20 m 3 /day, a human body weight of 70 kg, and 100% fractional absorption after inhalation exposure. V. REFERENCES California Department of Health Services (CDHS). 1985. Guidelines for Chemical Carcinogen Risk Assessment and Their Scientific Rationale. CDHS, Health and Welfare Agency, Sacramento, CA. California Department of Health Services (CDHS). 1988. Proposition 65 Risk-Specific Levels: 3,3’- Dichlorobenzidine. Reproductive and Cancer Hazard Assessment Section (RCHAS), Office of Environmental Health Hazard Assessment (<strong>OEHHA</strong>), Berkeley, CA. Gadian T. 1975. Carcinogens in industry, with special reference to dichlorobenzidine. Chemistry and Industry 4 October, pp.821-831. Gerarde HW and Gerarde DF. 1974. Industrial experience with 3,3’-dichlorobenzidine. An epidemiological study of chemical manufacturing plant. J Occup Med 16:322-344. Golub NI, Kolesnichencko TS, and Shabad LM. 1974. Blastomogenic action of some nitrogencontaining compounds in the progeny of experimental mice. Bjull Eksp Biol Med 68:83-87. 250
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Air Toxics Hot Spots Program Risk A
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Prepared by: John D. Budroe, Ph.D.
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This document is one of five docume
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TABLE OF CONTENTS PREFACE i INTRODU
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N-Nitrosodimethylamine 401 N-Nitros
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Hot Spots Unit Risk and Cancer Pote
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Additional ATES and PETS documents
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data. If several data sets (dose an
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US EPA Calculation of Carcinogenic
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exposure to a concentration of 1 µ
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incidences for each of the dose lev
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computes the surface area of a sphe
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Comparison of Hot Spots Cancer Unit
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Gold, L., de Veciana, M., Backman,
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Animal Studies Rats Woutersen et al
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ased on sufficient evidence of carc
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ACETAMIDE CAS No: 60-35-5 I. PHYSIC
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Methodology Expedited Proposition 6
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cancer mortality. However, US EPA (
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Table 2. Lung adenoma incidence in
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Table 3 (continued). Acrylamide-ind
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Robinson M, Bull RJ, Knutsen GL, Sh
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Also, a trend was observed correlat
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eported. Cause-specific expected de
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Bio/Dynamics Inc. conducted a study
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examination. Interim sacrifices wer
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Table 8. Tumor incidence in male an
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Gaffey WR and Strauss ME. 1981. A m
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(technical grade; 98% pure) by gava
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International Agency for Research o
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still alive in the low-dose control
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ANILINE CAS No: 62-53-3 I. PHYSICAL
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fibrosarcomas, stromal sarcomas, ca
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ARSENIC (INORGANIC) CAS No: 7440-38
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elationship between arsenic exposur
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al. (1988) did not induce lung tumo
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A risk assessment was also conducte
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Chen C, Chuang Y, You S, Lin T and
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Schrauzer G, White D, McGinness J,
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Table 1: Summary of epidemiologic s
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had at least one animal demonstrati
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mesothelioma, recommended lifetime
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National Institute for Occupational
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BENZENE CAS No: 71-43-2 I. PHYSICAL
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Animal Studies Available experiment
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Table 3: Summary of NTP bioassay re
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Table 4: Summary of benzene low-dos
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Maltoni C, Conti B and Cotti G. 198
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a benign tumor of the kidney. No ba
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al. (1968) found no tumors in lifet
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following relationship, where C(t 1
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Miakawa M. and Yoshida O. 1975. Pro
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human population and that BPDE-DNA
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demonstrated the tumor initiating a
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Table 4: Bronchoalveolar tumors fro
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Table 5: IARC groupings of PAHs, mi
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Table 6 (continued): IARC Group 3 P
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Potency Equivalency Factors (PEF) f
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This was rounded to a PEF of 0.1. 1
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experiment (Takayama et al., 1985)
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Deutsch-Wenzel RP, Brune H, Grimmer
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Krewski D, Thorslund T and Withey J
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U.S. Environmental Protection Agenc
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Sorahan et al. (1983) studied cance
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Lijinsky W. 1986. Chronic bioassay
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the drinking water (Schroeder and M
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Table II. Effective dose, upper-bou
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BIS(2-CHLOROETHYL)ETHER CAS No: 111
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IV. DERIVATION OF CANCER POTENCY Ba
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BIS(CHLOROMETHYL)ETHER CAS No: 542-
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Table 1. Bis(chloromethyl)ether-ind
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Drew RT, Laskin S, Kuschner M and N
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ates for the 1968 U.S. male populat
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Table 1: Incidence of primary tumor
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National Institute of Occupational
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was less than 0.05 when controlling
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up period. The final cohort include
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If the cadmium-exposed workers incl
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on personnel records (20%); (3) eva
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were exposed to a continuous (23.5
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procedure (NLIN), the parameters we
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International Agency for Research o
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Two reports were published on cance
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Mendel rats, respectively), and sub
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Eschenbrenner A and Miller E. 1946.
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III. CARCINOGENIC EFFECTS Human Stu
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cancers, were less than expected. T
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and no cases of cancer (although cl
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There was a statistically significa
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NTP (1982a) also conducted an carci
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Several pathologists have independe
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hepatocellular adenoma/carcinoma tu
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carcinogenic potency may decline in
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Cochrane W, Singh J and Miles W. 19
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North Atlantic Treaty Organization,
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CHLORINATED PARAFFINS (average chai
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ased on dose-response data for beni
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chloroform in drinking water with k
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Overall, the present epidemiologica
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female dogs received toothpaste bas
Page 207 and 208: Calculated q 1 * values from the ab
Page 209 and 210: Hogan MD, Chi Py, Hoel DG and Mitch
Page 211 and 212: Table 1. Study design summary for N
Page 213 and 214: V. REFERENCES California Environmen
Page 215 and 216: toluidine. Followup of this subcoho
Page 217 and 218: feeding studies on by NCI (1979) us
Page 219 and 220: CHROMIUM (HEXAVALENT) CAS No: 18540
Page 221 and 222: expected rate may be inflated becau
Page 223 and 224: Oral Borneff et al. (1968) exposed
Page 225 and 226: CREOSOTE (COAL TAR-DERIVED) CAS No:
Page 227 and 228: from an inhalation exposure study (
Page 229 and 230: U.S. Environmental Protection Agenc
Page 231 and 232: Table 1. Study design summary for N
Page 233 and 234: Methodology Expedited Proposition 6
Page 235 and 236: Table 1. Experimental design for ca
Page 237 and 238: Hazardous Substance Data Bank (HSDB
Page 239 and 240: Table 1: Tumor induction in Fischer
Page 241 and 242: Hazardous Substance Data Bank (HSDB
Page 243 and 244: Table 1. Experimental design of 2,4
Page 245 and 246: Methodology Expedited Proposition 6
Page 247 and 248: Additional analysis of these data b
Page 249 and 250: IV. DERIVATION OF CANCER POTENCY Ba
Page 251 and 252: Jackson RJ, Greene CJ, Thomas JT, M
Page 253 and 254: Table 1. Tumor incidence in rats ex
Page 255 and 256: Girard R, Tolot F, Martin P and Bou
Page 257: exposed more than 16 years before t
Page 261 and 262: 1, 1-DICHLOROETHANE CAS No: 75-34-3
Page 263 and 264: Table 1b. Study design for carcinog
Page 265 and 266: National Cancer Institute (NCI) 197
Page 267 and 268: mice, hepatocellular carcinoma inci
Page 269 and 270: V. REFERENCES California Department
Page 271 and 272: DAB/day by gavage for the life of t
Page 273 and 274: 2,4-DINITROTOLUENE CAS No: 121-14-2
Page 275 and 276: Ellis et al.(1979) (also reported b
Page 277 and 278: Final Statement of Reasons for OAL,
Page 279 and 280: to the small sample size and short
Page 281 and 282: In an inhalation study, Torkelson e
Page 283 and 284: V. REFERENCES American Conference o
Page 285 and 286: EPICHLOROHYDRIN CAS No: 106-89-8 I.
Page 287 and 288: espiratory tumors were noted in the
Page 289 and 290: Table 4. Epichlorohydrin-induced fo
Page 291 and 292: Konishi Y, Kawabata A, Denda A, Ike
Page 293 and 294: exposed to arsenicals for 20 months
Page 295 and 296: espectively (all statistically sign
Page 297 and 298: ETHYLENE DICHLORIDE CAS No: 107-06-
Page 299 and 300: Several factors have been suggested
Page 301 and 302: U.S. Environmental Protection Agenc
Page 303 and 304: myelogenous leukemias (4 and 8 year
Page 305 and 306: statistically significant. CDHS not
Page 307 and 308: combined with the incidence in the
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incidence of primary brain tumors.
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Table 6 (continued): Organ/Sex Mali
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An Upper 95% Confidence Limit (UCL)
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ETHYLENE THIOUREA (ETU) CAS No: 96-
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male and female rats. Tumor inciden
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FORMALDEHYDE CAS No: 50-00-0 I. PHY
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presented an extension of a previou
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Methodology In developing a spectru
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Casanova M, Morgan KT, Steinhagen W
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Tobe M, Kaneko T, Uchida Y, Kamata
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Table 1. Hexachlorobenzene-induced
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50 pups (F 1 ) of each sex were ran
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Ertürk E, Lambrecht RW, Peters HA,
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Table 1. Liver hepatoma incidence i
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1988). An airborne unit risk factor
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HYDRAZINE CAS No: 302-01-2 I. PHYSI
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Methodology Inhalation A linearized
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LEAD AND LEAD COMPOUNDS (INORGANIC)
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and other occupational carcinogens
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y inhalation is similar for rats an
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Goyer RA. 1992. Nephrotoxicity and
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LINDANE (g-Hexachlorocyclohexane) C
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Using these relationships, a human
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METHYL TERT-BUTYL ETHER (MTBE) CAS
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Tumor incidences according to the r
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kidney changes indicative of chroni
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Interspecies scaling for oral doses
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Table 4 (continued): Dose Response
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Experimental Pathology Laboratories
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Animal Studies Male and female HaM/
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Gold L, Sawyer C, Magaw R, Backman
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Using the statistical tests (one-ta
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Table 1: Methylene chloride-induced
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Significant treatment-related incre
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National Toxicology Program (NTP) 1
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noted; however, the study duration
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Crump KS, Howe RB, Van Landingham C
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Table 1. Michler’s ketone-induced
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NICKEL AND NICKEL COMPOUNDS CAS No:
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the high exposure group was 14.0. A
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male and 121 female rats, was expos
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2.1 - 2.6 × 10 -4 (µg/m 3 ) -1 .
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U.S. Environmental Protection Agenc
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The increased incidence of bladder
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A linearized multistage procedure w
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N-NITROSO-N-METHYLETHYLAMINE CAS No
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Hazardous Substance Data Bank (HSDB
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propylamine in drinking water at 0.
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N-NITROSODIETHYLAMINE CAS No: 55-18
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Table 2. Treatment groups, concentr
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California Department of Health Ser
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animals and the second generation t
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ationale for selection of the OEHHA
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A unit risk value based upon air co
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N-NITROSODIPHENYLAMINE CAS No: 86-3
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Methodology Dosage estimates of NDP
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Crump KS, Howe RB. 1984. The multis
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Table 1. P-Nitrosodiphenylamine-ind
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N-NITROSOMORPHOLINE CAS No: 59-89-2
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Page 429 and 430:
N-NITROSOPIPERIDINE CAS No: 100-75-
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Table 3. N-Nitrosopiperidine-induce
Page 433 and 434:
Crump KS, Howe RB, Van Landingham C
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testicular tumors were noted in the
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PARTICULATE MATTER FROM DIESEL-FUEL
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etired railroad workers who had had
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employment (χ 2 test for trend: p
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elevated smoking-adjusted risk esti
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Table 1 (continued): Reference Miln
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Table 1 (continued): Reference Damb
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Table 1 (continued): Reference Burn
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Table 1 (continued): Reference Raff
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Table 1 (continued): Epidemiologica
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Table 1 (continued): Epidemiologica
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Table 1 (continued): Reference Wegm
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Animal Studies Section 6.1 (Animal
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The variability, or heterogeneity,
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estimate for those studies for whic
Page 465 and 466:
Figure 1: Estimates of Relative Ris
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q 1 * = Excess relative risk × CA
Page 469 and 470:
Table 3: Number of Workers in the E
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u nexposed workers at zero concentr
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for each µg/m 3 of diesel exhaust
Page 475 and 476:
Table 4: Values from Unit Risk for
Page 477 and 478:
their findings that a reasonable es
Page 479 and 480:
Garshick E, Schenker M, Woskie S an
Page 481 and 482:
Lewis T, Green, FH MW, Burg J and L
Page 483 and 484:
Rothman K. 1986. Modern epidemiolog
Page 485 and 486:
PENTACHLOROPHENOL CAS No: 87-86-5 I
Page 487 and 488:
The default lifespan for mice is 10
Page 489 and 490:
documented. An excess risk from ski
Page 491 and 492:
B6C3F 1 mice and F344/N rats were e
Page 493 and 494:
This model, rather than a time depe
Page 495 and 496:
POLYCHLORINATED BIPHENYLS (PCBs) CA
Page 497 and 498:
several benign adenomatous lesions
Page 499 and 500:
Ito et al. (1973) exposed groups of
Page 501 and 502:
could not be characterized by chlor
Page 503 and 504:
exposure (all pathways and mixtures
Page 505 and 506:
National Toxicology Program 1993. T
Page 507 and 508:
Table 1. Potassium bromate-induced
Page 509 and 510:
1,3-PROPANE SULTONE CAS No: 1120-71
Page 511 and 512:
Page 513 and 514:
PROPYLENE OXIDE CAS No: 75-56-9 I.
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oxide. In the NTP carcinogenicity s
Page 517 and 518:
1,1,2,2-TETRACHLOROETHANE CAS No: 7
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assumed a body weight of 70 kg and
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total); an untreated control group
Page 523 and 524:
TOLUENE DIISOCYANATE CAS No: 26471-
Page 525 and 526:
Animal Studies The National Toxicol
Page 527 and 528:
Mortillaro PT and Schiavon M. 1982.
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male or female rats. Increases in h
Page 531 and 532:
TRICHLOROETHYLENE CAS No: 79-01-6 I
Page 533 and 534:
A mortality analysis of a cohort of
Page 535 and 536:
elative to that of the controls whi
Page 537 and 538:
applied or metabolized. The range o
Page 539 and 540:
Katz RM and Jowett D. 1981. Female
Page 541 and 542:
10,000 ppm 2,4,6-trichlorophenol in
Page 543 and 544:
Page 545 and 546:
Bionetics Research Laboratories. 19
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control; females: 6/10 exposed, 0/1
Page 549 and 550:
over controls (p < 0.04). Other tum
Page 551 and 552:
was increased (100/314 exposed vs.
Page 553 and 554:
Table 3. Cancer potency estimates f
Page 555 and 556:
Crouch E. 1983. Uncertainties in in
Page 557 and 558:
VINYL CHLORIDE CAS No: 75-01-4 I. P
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Table 1 (continued): A Summary of E
Page 561 and 562:
al., 1983). Histopathology of all o
Page 563 and 564:
Table 3: Tumor incidences in 100 pp
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experiment, animals were exposed to
Page 567 and 568:
Experiment BT1 Most previous risk a
Page 569 and 570:
No statistical analyses of mortalit
Page 571 and 572:
Table 11 gives unit risk estimates
Page 573 and 574:
Bertazzi PA, Villa A, Foa V, Saia B
Page 575 and 576:
Nicholson WJ, Hammond EC, Seidman H
Page 577 and 578:
immunotoxicity, reproductive toxici
Page 579 and 580:
scheme. TEFs for two major noncance
Page 581 and 582:
NATO/CCMS (1988a) Pilot Study on In
Page 583 and 584:
Table 2 Toxicity Equivalency Factor
Page 585 and 586:
Table 4 A Comparison of CTEF- and I
Page 587 and 588:
Office of Environmental Health Haza
Page 589 and 590:
Group 4: The agent is probably not
Page 591 and 592:
TECHNICAL SUPPORT DOCUMENT FOR DESC
Page 593 and 594:
US EPA IRIS Inhalation Unit Risk an
Page 595 and 596:
TECHNICAL SUPPORT DOCUMENT FOR DESC
Page 597 and 598:
as appropriate, and revise IRIS fil
Page 599 and 600:
Chemical Exposure Route Study Type
Page 601 and 602:
Page 603 and 604:
Page 605 and 606:
Methyl tert-butyl ether p. 5: Added
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