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Details

Stereochemistry ACHIRAL
Molecular Formula C7H10N2.2ClH
Molecular Weight 195.09
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,4-Diaminotoluene dihydrochloride

SMILES

Cl.Cl.CC1=CC=C(N)C=C1N

InChI

InChIKey=FSSFFQIVJQERFY-UHFFFAOYSA-N
InChI=1S/C7H10N2.2ClH/c1-5-2-3-6(8)4-7(5)9;;/h2-4H,8-9H2,1H3;2*1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C7H10N2
Molecular Weight 122.1677
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Validation of a genotoxicity test based on p53R2 gene expression in human lymphoblastoid cells.
2011-09-18
New short term prediction method for chemical carcinogenicity by hepatic transcript profiling following 28-day toxicity tests in rats.
2011
High-density real-time PCR-based in vivo toxicogenomic screen to predict organ-specific toxicity.
2011
Toxicogenomics applied to in vitro carcinogenicity testing with Balb/c 3T3 cells revealed a gene signature predictive of chemical carcinogens.
2010-11
Analysis of primary aromatic amines originated from azo dyes in commercial textile products in Japan.
2010-08
Evaluation of a liver micronucleus assay in young rats (IV): a study using a double-dosing/single-sampling method by the Collaborative Study Group for the Micronucleus Test (CSGMT)/Japanese Environmental Mutagen Society (JEMS)-Mammalian Mutagenicity Study Group (MMS).
2010-04-30
Safety evaluation of food contact paper and board using chemical tests and in vitro bioassays: role of known and unknown substances.
2010-03
Integration of in vivo genotoxicity and short-term carcinogenicity assays using F344 gpt delta transgenic rats: in vivo mutagenicity of 2,4-diaminotoluene and 2,6-diaminotoluene structural isomers.
2010-03
The GSTP1 Ile105 Val polymorphism modifies the metabolism of toluene di-isocyanate.
2010-02
Validation of a liquid chromatography-mass spectrometry method for determining the migration of primary aromatic amines from cooking utensils and its application to actual samples.
2010-01
Determination of aromatic amines in food products and composite food packaging bags by capillary electrophoresis coupled with transient isotachophoretic stacking.
2009-10-23
Graphite- and soot-mediated reduction of 2,4-dinitrotoluene and hexahydro-1,3,5-trinitro-1,3,5-triazine.
2009-09-15
Current implant surface technology: an examination of their nanostructure and their influence on fibroblast alignment and biocompatibility.
2009-06-16
Is toluene diamine a sensitizer and is there cross-reactivity between toluene diamine and toluene diisocyanate?
2009-06
[Application of IR spectrum to the research on mechanism of synthesis of 2,4-toluene dicarbamate catalyzed by zinc acetate].
2009-02
Evaluation of a liver micronucleus assay with 12 chemicals using young rats (II): a study by the Collaborative Study Group for the Micronucleus Test/Japanese Environmental Mutagen Society-Mammalian Mutagenicity Study Group.
2009-01
Syrian hamster embryo (SHE) cell transformation assay with conditioned media (without X-ray irradiated feeder layer) using 2,4-diaminotoluene, 2,6-diaminotoluene and chloral hydrate.
2008-07-31
Single-step treatment of 2,4-dinitrotoluene via zero-valent metal reduction and chemical oxidation.
2008-06-30
Experimental evidence for in situ natural attenuation of 2,4- and 2,6-dinitrotoluene in marine sediment.
2008-01
[Determination and analysis of toluene diisocyanate metabolites in mice using gas chromatography-mass spectrometry].
2007-09
Biological monitoring of TDI-derived amines in polyurethane foam production.
2007-09
Removal of dinitrotoluenes from water via reduction with iron and peroxidase-catalyzed oxidative polymerization: a comparison between Arthromyces ramosus peroxidase and soybean peroxidase.
2007-04
Increasing selectivity for TNT-based explosive detection by synchronous luminescence and derivative spectroscopy with quantum yields of selected aromatic amines.
2007-01
Effects of toluene-2,4-diamine on red sea bream, Pagrus major: biochemical and histological evaluation.
2007
Differences in gene expression profiles in the liver between carcinogenic and non-carcinogenic isomers of compounds given to rats in a 28-day repeat-dose toxicity study.
2006-12-15
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Induction of LacZ mutations in Muta Mouse can distinguish carcinogenic from non-carcinogenic analogues of diaminotoluenes and nitronaphthalenes.
2006-09-19
Exposure of hairdressing apprentices to airborne hazardous substances.
2006-08-07
2,4-Toluene diisocyanate suppressed the calcium signaling of ligand gated ion channel receptors.
2006-02-15
Differences in the biotransformation of 2,4,6-trinitrotoluene (TNT) between wild and axenically grown isolates of Myriophyllum aquaticum.
2006
Different results of the Salmonella umu test between three isomers of phenylenediamine (PDA) derivatives.
2006
Risk evaluation of occupational exposure to methylene dianiline and toluene diamine in polyurethane foam.
2005-12
2,4-Diaminotoluene (2,4-DAT)-induced DNA damage, DNA repair and micronucleus formation in the human hepatoma cell line HepG2.
2005-09-15
Upper reference limits for biomarkers of exposure to aromatic diisocyanates.
2005-08
Improvement in the GC-MS method for determining urinary toluene-diamine and its application to the biological monitoring of workers exposed to toluene-diisocyanate.
2005-07
Hemoglobin adducts in workers exposed to nitrotoluenes.
2005-01
Hydrolytic stability of toluene diisocyanate and polymeric methylenediphenyl diisocyanate based polyureas under environmental conditions.
2004-02-15
2,4-Diaminotoluene.
2004
[Assessment of the emission of volatile organic compounds from polyurethane foams].
2004
Mutagenicity of nitroaromatic degradation compounds.
2003-10
Development, validation and characterization of an analytical method for the quantification of hydrolysable urinary metabolites and plasma protein adducts of 2,4- and 2,6-toluene diisocyanate, 1,5-naphthalene diisocyanate and 4,4'-methylenediphenyl diisocyanate.
2003-08-29
Toxicology of toluene diisocyanate.
2002-12
Evaluation of carcinogenic responses in the Eker rat following short-term exposure to selected nephrotoxins and carcinogens.
2002-10-10
Contact leukoderma secondary to occupational toluenediamine sulfate exposure.
2002-08
[Fast optimization of stepwise gradient conditions for ternary mobile phase in reversed-phase high performance liquid chromatography].
2002-07
2,4-Diaminotoluene.
2002
Interaction with the aromatic hydrocarbon receptor, CYP1A induction, and mutagenicity of a series of diaminotoluenes: implications for their carcinogenicity.
1996-07
Reduction and Acetylation of 2,4-Dinitrotoluene by a Pseudomonas aeruginosa Strain.
1996-07
Reproductive toxicity of 2,4-toluenediamine in the rat. 3. Effects on androgen-binding protein levels, selected seminiferous tubule characteristics, and spermatogenesis.
1988
Locus specificity of mutagenicity of 2,4-diaminotoluene in both L5178Y mouse lymphoma and AT3-2 Chinese hamster ovary cells.
1984-02
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:46:18 GMT 2025
Edited
by admin
on Mon Mar 31 21:46:18 GMT 2025
Record UNII
333A82EQ74
Record Status Validated (UNII)
Record Version
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Name Type Language
1,3-Benzenediamine, 4-methyl-, dihydrochloride
Preferred Name English
2,4-Diaminotoluene dihydrochloride
Systematic Name English
2,4-Tolylenediamine dihydrochloride
Systematic Name English
Toluene-2,4-diamine, dihydrochloride
Systematic Name English
1,3-Benzenediamine, 4-methyl-, hydrochloride (1:2)
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID9020403
Created by admin on Mon Mar 31 21:46:18 GMT 2025 , Edited by admin on Mon Mar 31 21:46:18 GMT 2025
PRIMARY
CAS
636-23-7
Created by admin on Mon Mar 31 21:46:18 GMT 2025 , Edited by admin on Mon Mar 31 21:46:18 GMT 2025
PRIMARY
PUBCHEM
71557
Created by admin on Mon Mar 31 21:46:18 GMT 2025 , Edited by admin on Mon Mar 31 21:46:18 GMT 2025
PRIMARY
FDA UNII
333A82EQ74
Created by admin on Mon Mar 31 21:46:18 GMT 2025 , Edited by admin on Mon Mar 31 21:46:18 GMT 2025
PRIMARY