Benzidine
RTECS #
DC9625000
CAS #
Updated
March 2019
Molecular Weight
184.26
Molecular Formula
C12H12N2
Synonyms
(1,1'-Biphenyl)-4,4'-diamine (9CI)
4,4'-Bianiline
4,4'-Biphenyldiamine
4,4'-Biphenylenediamine
4,4'-Diamino-1,1'-biphenyl
4,4'-Diaminobiphenyl
4,4'-Diaminodiphenyl
4,4'-Diphenylenediamine
Benzidin
Benzidin (Czech)
Benzidina (Italian)
Benzidine (ACGIH:OSHA)
Benzydyna (Polish)
Biphenyl, 4,4'-diamino-
C.I. 37225
C.I. Azoic Diazo Component 112
Fast Corinth Base B
NCI-C03361
p,p-Bianiline
p,p'-Diaminobiphenyl
p,p'-Dianiline
p-Diaminodiphenyl
RCRA waste number U021
4,4'-Bianiline
4,4'-Biphenyldiamine
4,4'-Biphenylenediamine
4,4'-Diamino-1,1'-biphenyl
4,4'-Diaminobiphenyl
4,4'-Diaminodiphenyl
4,4'-Diphenylenediamine
Benzidin
Benzidin (Czech)
Benzidina (Italian)
Benzidine (ACGIH:OSHA)
Benzydyna (Polish)
Biphenyl, 4,4'-diamino-
C.I. 37225
C.I. Azoic Diazo Component 112
Fast Corinth Base B
NCI-C03361
p,p-Bianiline
p,p'-Diaminobiphenyl
p,p'-Dianiline
p-Diaminodiphenyl
RCRA waste number U021
Mutation Data and Reference
System Test | Route/Organism/Tissue | Dose | Reference |
---|---|---|---|
body fluid assay | Salmonella typhimurium/rat | 250 µmol/kg | TXCYAC 21,223,1981 |
Cytogenetic Analysis | liver/rat | 12500 µg/L | PMRSDJ 1,570,1981 |
Cytogenetic Analysis | intraperitoneal/rat | 250 mg/kg | MUREAV 182,309,1987 |
Cytogenetic Analysis | intraperitoneal/other fish | 10 mg/kg | CBPCEE 82,489,1985 |
Cytogenetic Analysis | intraperitoneal/mouse | 25 mg/kg | MUREAV 320,69,1994 |
Cytogenetic Analysis | lymphocyte/mouse | 100 mg/L | MUREAV 320,69,1994 |
Cytogenetic Analysis | ovary/hamster | 160 mg/L | EMMUEG 10(Suppl 10),1,1987 |
DNA adduct | oral/mouse | 9600 µg/kg | CNREA8 42,2678,1982 |
DNA adduct | liver/mouse | 60 µmol/L | JJIND8 62,947,1979 |
DNA adduct | oral/Dog | 60 µmol/kg | EVHPAZ 49,125,1983 |
DNA adduct | other cell types/Dog | 100 µmol/L | CNREA8 44,1893,1984 |
DNA adduct | lymphocyte/human | 30 µmol/L | PNASA6 85,3513,1988 |
DNA adduct | parenteral/rat | 11600 µg/kg | CNREA8 42,2678,1982 |
DNA Damage | oral/rat | 200 mg/kg | ENMUDM 4,667,1982 |
DNA Damage | liver/rat | 3 mmol/L | SinJF# 26OCT1982 |
DNA Damage | intraperitoneal/rat | 63 mg/kg | CRNGDP 6,1285,1985 |
DNA Damage | fibroblast/human | 3 mmol/L | ENMUDM 7,267,1985 |
DNA Damage | /Bacillus subtilis | 2 mg/disc | PMRSDJ 1,175,1981 |
DNA Damage | lymphocyte/human | 100 µmol/L/2H | TOSCF2 72,283,2003 |
DNA Damage | other cell types/human | 0.37 µmol/L/12H | MUTAEX 28,515,2013 |
DNA Damage | oral/mouse | 160 mg/kg | MUREAV 440,1,1999 |
DNA Damage | intraperitoneal/mouse | 150 mg/kg | BSIBAC 56,1673,1980 |
DNA Damage | lung/hamster | 100 µmol/L/2H | BBRCA9 72,732,1976 |
DNA inhibition | oral/mouse | 20 gm/kg | ARGEAR 51,605,1981 |
DNA inhibition | oral/mouse | 200 mg/kg | MUREAV 46,305,1977 |
DNA inhibition | oral/rat | 100 µmol/kg | CRNGDP 8,1433,1987 |
DNA inhibition | HeLa cell/human | 600 µmol/L/30M-continuous | JEPTDQ 2(1),65,1978 |
DNA repair | /Escherichia coli | 1 mg/plate | MUREAV 54,101,1978 |
DNA repair | /Saccharomyes cerevisiae | 100 mg/L | PMRSDJ 1,502,1981 |
DNA repair | other cell types/human | 0.37 µmol/L/12H | MUTAEX 28,515,2013 |
gene conversion and mitotic recombination | /Saccharomyes cerevisiae | 100 mg/L | PMRSDJ 1,491,1981 |
host-mediated assay | Salmonella typhimurium/rat | 1 mmol/kg | MUREAV 93,317,1982 |
host-mediated assay | Escherichia coli/mouse | 220 mg/kg | MUREAV 272,161,1992 |
micronucleus test | intraperitoneal/mouse | 6400 µg/kg | PMRSDJ 1,686,1981 |
micronucleus test | oral/mouse | 300 mg/kg | MUTAEX 2,267,1987 |
micronucleus test | intraperitoneal/other fish | 10 mg/kg | CYTBAI 47,147,1986 |
micronucleus test | subcutaneous/rat | 410 mg/kg | MUREAV 40,43,1976 |
micronucleus test | intraperitoneal/rat | 25 mg/kg | TXCYAC 57,217,1989 |
morphological transform | embryo/mouse | 2500 µg/L | TCMUD8 3,101,1983 |
morphological transform | embryo/hamster | 50 µg/L | CALEDQ 3,45,1977 |
morphological transform | kidney/hamster | 80 µg/L | BJCAAI 37,873,1978 |
morphological transform | fibroblast/mouse | 1 mg/L/21D (-enzymatic activation step) | EMMUEG 35,300,2000 |
mutation in mammalian somatic cells | lymphocyte/mouse | 500 µg/L | MUREAV 125,291,1984 |
mutation in microorganisms | /Salmonella typhimurium | 3 µg/plate (+enzymatic activation step) | TOSCF2 56,351,2000 |
mutation in microorganisms | /Salmonella typhimurium | 1 nmol/plate/20M | EMMUEG 38,268,2001 |
mutation in microorganisms | /Salmonella typhimurium | 4 mg/L/72H (+enzymatic activation step) | MUREAV 558,181,2004 |
mutation in microorganisms | /Salmonella typhimurium | 50 µmol/L/3H | TCMUD8 23,47,2003 |
mutation in microorganisms | /Salmonella typhimurium | 400 ng/plate (-enzymatic activation step) | MUREAV 175,11,1986 |
mutation in microorganisms | /Escherichia coli | 100 µg/plate (+enzymatic activation step) | PMRSDJ 1,387,1981 |
other mutation test systems | /Salmonella typhimurium | 567 mg/L | MUREAV 192,239,1987 |
other mutation test systems | other cell types/Dog | 100 µmol/L | CNREA8 44,1893,1984 |
other mutation test systems | intraperitoneal/mouse | 25 mg/kg | MUREAV 268,255,1992 |
other mutation test systems | intraperitoneal/mouse | 100 mg/kg | MUREAV 319,19,1993 |
phage inhibition capacity | /Escherichia coli | 100 mmol/L | MDMIAZ 31,11,1979 |
sex chromosome loss and nondisjunction | parenteral/Drosophila melanogaster | 5 mmol/L | MUREAV 56,31,1977 |
sex chromosome loss and nondisjunction | /Saccharomyes cerevisiae | 50 mg/L | PMRSDJ 1,468,1981 |
sister chromatid exchange | inhalation/man | 7 µg/m3/27W | POLEAQ 35,53,1980 |
sister chromatid exchange | lymphocyte/human | 2 mg/L | MUREAV 241,109,1990 |
sister chromatid exchange | intraperitoneal/mouse | 7700 µg/kg | MUREAV 108,225,1983 |
sister chromatid exchange | ovary/hamster | 5 mg/L | EMMUEG 10(Suppl 10),1,1987 |
specific locus test | ovary/hamster | 600 mg/L | PMRSDJ 1,594,1981 |
specific locus test | ovary/hamster | 25 mg/L/9D | EMMUEG 16,260,1990 |
specific locus test | oral/Drosophila melanogaster | 5 mmol/L/48H | MUREAV 222,359,1989 |
Unscheduled DNA Synthesis | liver/human | 10 mg/L | MUREAV 206,91,1988 |
Unscheduled DNA Synthesis | HeLa cell/human | 100 µmol/L | CNREA8 38,2621,1978 |
Unscheduled DNA Synthesis | fibroblast/human | 160 µg/L | PMRSDJ 1,528,1981 |
Unscheduled DNA Synthesis | oral/rat | 200 mg/kg | ENMUDM 4,553,1982 |
Unscheduled DNA Synthesis | liver/rat | 100 nmol/L | MUREAV 136,255,1984 |
Unscheduled DNA Synthesis | other cell types/rabbit | 100 µmol/L | CRNGDP 8,401,1987 |
Unscheduled DNA Synthesis | liver/rabbit | 1 µmol/L | CNREA8 43,3120,1983 |
Unscheduled DNA Synthesis | liver/hamster | 20 nmol/L | MUREAV 136,255,1984 |
Tumorigenic Data and References
Route/Organism | Dose | Effect | Reference |
---|---|---|---|
inhalation/man | lowest published toxic concentration: 17600 µg/m3/14Y- continuous | Tumorigenic: Carcinogenic by RTECS criteria Kidney, Ureter, and Bladder: Hematuria Kidney, Ureter, and Bladder: Bladder tumors | AEHLAU 27,1,1973 |
inhalation/rat | lowest published toxic concentration: 10 mg/m3/56W- intermittent | Tumorigenic: Equivocal tumorigenic agent by RTECS criteria Liver: Tumors Blood: Leukemia | BEXBAN 69,68,1970 |
intratracheal/rat | lowest published toxic dose: 315 mg/kg/34W | Tumorigenic: Equivocal tumorigenic agent by RTECS criteria Liver: Tumors Skin and Appendages: Tumors | BEXBAN 69,68,1970 |
oral/hamster | lowest published toxic dose: 75 mg/kg/3Y- continuous | Tumorigenic: Equivocal tumorigenic agent by RTECS criteria Liver: Tumors | 85DAAC 5,129,1966 |
oral/rat | lowest published toxic dose: 108 mg/kg/27D- intermittent | Tumorigenic: Carcinogenic by RTECS criteria Skin and Appendages: Tumors | CNREA8 28,924,1968 |
oral/rat | toxic dose: 25560 ng/kg/2Y- continuous | Tumorigenic: Equivocal tumorigenic agent by RTECS criteria Liver: Tumors | EKSODD 9(4),73,1987 |
subcutaneous/mouse | lowest published toxic dose: 8400 mg/kg/35W- intermittent | Tumorigenic: Equivocal tumorigenic agent by RTECS criteria Lung, Thorax, or Respiration: Tumors Liver: Tumors | VOONAW 17(5),61,1971 |
subcutaneous/mouse | toxic dose: 1620 gm/kg/45W- intermittent | Tumorigenic: Equivocal tumorigenic agent by RTECS criteria Liver: Tumors | AICCA6 7,46,1950 |
subcutaneous/rat | toxic dose: 850 mg/kg/32W- intermittent | Tumorigenic: Equivocal tumorigenic agent by RTECS criteria Liver: Tumors Skin and Appendages: Tumors | VOONAW 20(2),53,1974 |
subcutaneous/rat | toxic dose: 800 mg/kg/60W- intermittent | Tumorigenic: Equivocal tumorigenic agent by RTECS criteria Ear: Tumors Blood: Tumors | VOONAW 20(8),69,1974 |
subcutaneous/rat | toxic dose: 2025 mg/kg/27W- intermittent | Tumorigenic: Carcinogenic by RTECS criteria Ear: Tumors Liver: Tumors | CANCAR 3,789,1950 |
subcutaneous/rat | lowest published toxic dose: 1200 mg/kg/26W- intermittent | Tumorigenic: Carcinogenic by RTECS criteria Tumorigenic: Tumors at site of application | VOONAW 10(5),50,1964 |
subcutaneous/rat | lowest published toxic dose: 1425 mg/kg/57W- intermittent | Tumorigenic: Carcinogenic by RTECS criteria Skin and Appendages: Tumors | VOONC* 37,60,1991 |
Acute Toxicity Data and References
Route/Organism | Dose | Effect | Reference |
---|---|---|---|
intraperitoneal/mouse | lethal dose (50 percent kill): 110 mg/kg | PMRSDJ 1,682,1981 | |
oral/Dog | lowest published lethal dose: 200 mg/kg | AEXPBL 58,167,1907 | |
oral/mouse | lethal dose (50 percent kill): 214 mg/kg | NTIS** PB214-270 | |
oral/rabbit | lowest published lethal dose: 200 mg/kg | AEXPBL 58,167,1907 | |
oral/rat | lethal dose (50 percent kill): 309 mg/kg | NTIS** PB214-270 |
Reviews
Organization | Standard | Reference |
---|---|---|
American Conference of Governmental Industrial Hygienists (ACGIH) | Threshold Limit Value-Control as low as possible, skin | DTLVS* TLV/BEI,2013 |
American Conference of Governmental Industrial Hygienists (ACGIH) | Threshold Limit Value-Confirmed human carcinogen | DTLVS* TLV/BEI,2013 |
International Agency for Research on Cancer (IARC) | Cancer Review:Human Limited Evidence | IMEMDT 1,80,1972 |
International Agency for Research on Cancer (IARC) | Cancer Review:Animal Sufficient Evidence | IMEMDT 1,80,1972 |
International Agency for Research on Cancer (IARC) | Cancer Review:Animal Sufficient Evidence | IMEMDT 29,149,1982 |
International Agency for Research on Cancer (IARC) | Cancer Review:Human Sufficient Evidence | IMEMDT 29,149,1982 |
International Agency for Research on Cancer (IARC) | Cancer Review:Animal Sufficient Evidence | IMEMDT 99,245,2010 |
International Agency for Research on Cancer (IARC) | Cancer Review:Animal Sufficient Evidence | IMEMDT 100F,61,2012 |
International Agency for Research on Cancer (IARC) | Cancer Review:Human Sufficient Evidence | IMEMDT 99,245,2010 |
International Agency for Research on Cancer (IARC) | Cancer Review:Human Sufficient Evidence | IMEMDT 100F,61,2012 |
International Agency for Research on Cancer (IARC) | Cancer Review:Group 1 | IMSUDL 7,123,1987 |
International Agency for Research on Cancer (IARC) | Cancer Review:Group 1 | IMEMDT 100F,61,2012 |
International Agency for Research on Cancer (IARC) | Cancer Review:Group 1 | IMEMDT 99,245,2010 |
TOXICOLOGY REVIEW | EAHB** -,38,1974 | |
TOXICOLOGY REVIEW | KHZHAZ 12(2),85,1976 | |
TOXICOLOGY REVIEW | ADCSAJ 13,271,1970 | |
TOXICOLOGY REVIEW | BLFSBY 24,253,1983 | |
TOXICOLOGY REVIEW | TOLED5 127,321,2002 | |
TOXICOLOGY REVIEW | TOLED5 134,39,2002 | |
TOXICOLOGY REVIEW | MUREAV 567,347,2004 | |
TOXICOLOGY REVIEW | REPTED 19,547,2005 | |
TOXICOLOGY REVIEW | TCMUD8 23(Suppl 1),187,2003 | |
TOXICOLOGY REVIEW | MUREAV 588,88,2005 | |
TOXICOLOGY REVIEW | MUREAV 612,58,2006 | |
TOXICOLOGY REVIEW | ENTOX* -,255,2005 | |
TOXICOLOGY REVIEW | FCTOD7 44,1699,2006 | |
TOXICOLOGY REVIEW | ENTOX* -,104,2005 | |
TOXICOLOGY REVIEW | MUREAV 627,59,2007 | |
TOXICOLOGY REVIEW | MUREAV 627,10,2007 | |
TOXICOLOGY REVIEW | MUREAV 584,1,2005 | |
TOXICOLOGY REVIEW | JTPAE7 18,69,2005 | |
TOXICOLOGY REVIEW | HUTOX* -,649,1996 | |
TOXICOLOGY REVIEW | MUREAV 608,136,2006 | |
TOXICOLOGY REVIEW | MUREAV 681,51,2009 | |
TOXICOLOGY REVIEW | MUTAEX 23,271,2008 | |
TOXICOLOGY REVIEW | MUTAEX 26,205,2011 | |
TOXICOLOGY REVIEW | MUREAV 733,39,2012 | |
TOXICOLOGY REVIEW | MUREAV 769,34,2014 | |
TOXICOLOGY REVIEW | MUREAV 786-788,14,2015 | |
TOXICOLOGY REVIEW | MUREAV 768,27,2016 | |
TOXICOLOGY REVIEW | MUREAV 802,1,2016 | |
TOXICOLOGY REVIEW | MUREAV 770,170,2016 | |
TOXICOLOGY REVIEW | RTOPDW 56,67,2010 | |
TOXICOLOGY REVIEW | MUTAEX 33,179,2018 | |
TOXICOLOGY REVIEW | RTOPDW 60,S1,2011 |
Standards and Regulations
Organization | Standard | Reference |
---|---|---|
Mine Safety and Health Administration (MSHA) STANDARD | skin-HUMAN CARCINOGEN, NO ASSIGNED time-weighted average | DTLWS* 3,11,1973 |
Occupational Exposure Limit IN ARGENTINA, BULGARIA, COLOMBIA, JORDAN check ACGIH TLV; | ||
Occupational Exposure Limit IN SINGAPORE, VIETNAM check ACGIH TLV | ||
Occupational Exposure Limit-AUSTRALIA | (Prohibited) Carcinogen, JUL2008 | |
Occupational Exposure Limit-BELGIUM | Skin, MAR2002 | |
Occupational Exposure Limit-FRANCE | VME 0.001 ppm (0.008 mg/m3), C1 Carcinogen, FEB2006 | |
Occupational Exposure Limit-HUNGARY | ceiling concentration 0.008 mg/m3, Carcinogen, SEP2000 | |
Occupational Exposure Limit-JAPAN | 1 carc, MAY2012 | |
Occupational Exposure Limit-KOREA | carcinogen, skin, 2006 | |
Occupational Exposure Limit-NEW ZEALAND | carcinogen, skin, JAN2002 | |
Occupational Exposure Limit-POLAND | MAC(time-weighted average) 0 mg/m3, MAC(short term exposure limit) 0 mg/m3, JAN1999 | |
Occupational Exposure Limit-SWEDEN | Group A Carcinogen, JUN2005 | |
Occupational Exposure Limit-SWITZERLAND | carc 1, JAN2011 | |
Occupational Safety and Health Administration (OSHA) Permissible Exposure Limit (Construction) | see Code of Federal Regulations (CFR) 29,1926.1110 | CFRGBR 29,1926,55,1994 |
Occupational Safety and Health Administration (OSHA) Permissible Exposure Limit (General Industry) | see Code of Federal Regulations (CFR) 29,1910.1010 | CFRGBR 29,1910.1000,1994 |
Occupational Safety and Health Administration (OSHA) Permissible Exposure Limit (Shipyards) | see Code of Federal Regulations (CFR) 29,1915.1010 | CFRGBR 29,1915.1000,1993 |
Occupational Safety and Health Administration (OSHA)-cancer suspect agent | CFRGBR 29,1910.1010,1987 |
NIOSH Documentation and Surveillance
Organization | Standard | Reference |
---|---|---|
National Institute for Occupational Safety and Health (NIOSH) Recommended Exposure Level TO BENZIDINE-air | Carcinogen use 29 Code of Federal Regulations (CFR) 1910.1010 | NIOSH* DHHS #95-121,1995 |
National Occupational Exposure Survey 1983 | Hazard Code 09830; Number of Industries 3; Total Number of Facilities 252; Number of Occupations 8; Total Number of Employees Exposed 1554; Total Number of Female Employees Exposed 426 | |
National Occupational Hazard Survey 1974 | Hazard Code 09830; Number of Industries 4; Total Number of Facilities 263; Number of Occupations 5; Total Number of Employees Exposed 1166 |
Status in Federal Agencies
Page last reviewed: November 16, 2018
Content
source: National Institute for Occupational Safety and Health