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Details

Stereochemistry ACHIRAL
Molecular Formula C14H15N3
Molecular Weight 225.289
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of O-AMINOAZOTOLUENE

SMILES

CC1=CC=CC=C1\N=N\C2=CC=C(N)C(C)=C2

InChI

InChIKey=PFRYFZZSECNQOL-WUKNDPDISA-N
InChI=1S/C14H15N3/c1-10-5-3-4-6-14(10)17-16-12-7-8-13(15)11(2)9-12/h3-9H,15H2,1-2H3/b17-16+

HIDE SMILES / InChI

Molecular Formula C14H15N3
Molecular Weight 225.289
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Ortho-aminoazotoluene activates mouse constitutive androstane receptor (mCAR) and increases expression of mCAR target genes.
2011-08-15
Biological Basis of Differential Susceptibility to Hepatocarcinogenesis among Mouse Strains.
2009-03
Species-specific effects of the hepatocarcinogens 3'-methyl-4-dimethyl-aminoazobenzene and ortho-aminoazotoluene in mouse and rat liver.
2005-12
o-Aminoazotoluene does induce the enzymes of its own mutagenic activation in mouse liver.
2005-07-01
[Different sensitivity of inbred mice to hepatocarcinogen ortho-aminoazotoluene may be due to differences in the negative control mechanisms of hepatocyte proliferation].
2004
[mRNA level and cytochrome P450 1A activity in the liver of C57BL mice induced by various xenobiotics].
2003-10-18
Species specific hepatocarcinogen inhibition of the glucocorticoid induction of tyrosine aminotransferase gene in mouse and rat liver.
2003-05
Cytochrome P4501A1 and 1A2 gene expression in the liver of 3-methylcholanthrene- and o-aminoazotoluene-treated mice: a comparison between PAH-responsive and PAH-nonresponsive strains.
2003-05
[Effect of the hepatocarcinogen ortho-aminoazotoluene on induction of tyrosine-aminotransferase by glucocorticoids in mouse liver].
2001-07-11
Involvement of transcription factor HNF3gamma in the effect of o-aminoazotoluene on glucocorticoid induction of tyrosine aminotransferase in mice sensitive to its hepatocarcinogenic action.
2001-05
Expression of CYP1A in liver of A/Sn and CC57BR mice differing in sensitivity to hepatocarcinogenesis induced by o-aminoazotoluene.
2000-06
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 21:03:45 GMT 2025
Edited
by admin
on Mon Mar 31 21:03:45 GMT 2025
Record UNII
QHZ900P7ZA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
C.I. 11160
Preferred Name English
O-AMINOAZOTOLUENE
MI  
Common Name English
BENZENAMINE, 2-METHYL-4-((2-METHYLPHENYL)AZO)-
Systematic Name English
2-METHYL-4-((O-TOLYL)AZO)ANILINE
Common Name English
NSC-26821
Code English
4-(O-TOLYLAZO)-O-TOLUIDINE
Common Name English
OIL YELLOW 21
Common Name English
HIDACO OIL YELLOW
Common Name English
2-AMINOAZOTOLUENE
Systematic Name English
O-AMINOAZOTOLUENE [MI]
Common Name English
SOMALIA YELLOW R
Common Name English
FAST YELLOW AT
Common Name English
C.I. SOLVENT YELLOW 3
Common Name English
O-TOLUIDINE, 4-O-TOLYLAZO-
Common Name English
2-METHYL-4-((2-METHYLPHENYL)DIAZENYL)AMINE
Common Name English
TOLUAZOTOLUIDINE
Common Name English
ORGANOL YELLOW 2T
Common Name English
2,3'-DIMETHYL-4'-AMINOAZOBENZENE
Systematic Name English
4-AMINO-2',3-DIMETHYLAZOBENZENE
Systematic Name English
FAT YELLOW B
Common Name English
BRASILAZINA OIL YELLOW R
Common Name English
5-(O-TOLYLAZO)-2-AMINOTOLUENE
Common Name English
NSC-1797
Code English
SOLVENT YELLOW 3
Common Name English
2',3-DIMETHYL-4-AMINOAZOBENZENE
Systematic Name English
BENZENAMINE, 2-METHYL-4-((2-METHYLPHENYL)AZO)-, (E)-
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C45178
Created by admin on Mon Mar 31 21:03:45 GMT 2025 , Edited by admin on Mon Mar 31 21:03:45 GMT 2025
Code System Code Type Description
PUBCHEM
7340
Created by admin on Mon Mar 31 21:03:45 GMT 2025 , Edited by admin on Mon Mar 31 21:03:45 GMT 2025
PRIMARY
HSDB
97-56-3
Created by admin on Mon Mar 31 21:03:45 GMT 2025 , Edited by admin on Mon Mar 31 21:03:45 GMT 2025
PRIMARY
CAS
61550-68-3
Created by admin on Mon Mar 31 21:03:45 GMT 2025 , Edited by admin on Mon Mar 31 21:03:45 GMT 2025
PRIMARY
MESH
D009762
Created by admin on Mon Mar 31 21:03:45 GMT 2025 , Edited by admin on Mon Mar 31 21:03:45 GMT 2025
PRIMARY
MERCK INDEX
m1685
Created by admin on Mon Mar 31 21:03:45 GMT 2025 , Edited by admin on Mon Mar 31 21:03:45 GMT 2025
PRIMARY Merck Index
CAS
97-56-3
Created by admin on Mon Mar 31 21:03:45 GMT 2025 , Edited by admin on Mon Mar 31 21:03:45 GMT 2025
NON-SPECIFIC STEREOCHEMISTRY
FDA UNII
QHZ900P7ZA
Created by admin on Mon Mar 31 21:03:45 GMT 2025 , Edited by admin on Mon Mar 31 21:03:45 GMT 2025
PRIMARY
NSC
26821
Created by admin on Mon Mar 31 21:03:45 GMT 2025 , Edited by admin on Mon Mar 31 21:03:45 GMT 2025
PRIMARY
SMS_ID
300000053426
Created by admin on Mon Mar 31 21:03:45 GMT 2025 , Edited by admin on Mon Mar 31 21:03:45 GMT 2025
PRIMARY
EPA CompTox
DTXSID1020069
Created by admin on Mon Mar 31 21:03:45 GMT 2025 , Edited by admin on Mon Mar 31 21:03:45 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-591-2
Created by admin on Mon Mar 31 21:03:45 GMT 2025 , Edited by admin on Mon Mar 31 21:03:45 GMT 2025
PRIMARY
NCI_THESAURUS
C29845
Created by admin on Mon Mar 31 21:03:45 GMT 2025 , Edited by admin on Mon Mar 31 21:03:45 GMT 2025
PRIMARY
NSC
1797
Created by admin on Mon Mar 31 21:03:45 GMT 2025 , Edited by admin on Mon Mar 31 21:03:45 GMT 2025
PRIMARY