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Details

Stereochemistry ACHIRAL
Molecular Formula C15H17N3
Molecular Weight 239.3156
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of 4-(DIMETHYLAMINO)-3'-METHYLAZOBENZENE

SMILES

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

InChI

InChIKey=LVTFSVIRYMXRSR-WUKNDPDISA-N
InChI=1S/C15H17N3/c1-12-5-4-6-14(11-12)17-16-13-7-9-15(10-8-13)18(2)3/h4-11H,1-3H3/b17-16+

HIDE SMILES / InChI

Molecular Formula C15H17N3
Molecular Weight 239.3156
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Promotion by dietary phenobarbital of hepatocarcinogenesis by 2-methyl-N,N-dimethyl-4-aminoazobenzene in the rat.
1979 Jan
Dose-response studies on promoting and anticarcinogenic effects of phenobarbital and DDT in the rat hepatocarcinogenesis.
1984 Dec
Promotion of hepatocarcinogenesis by suxibuzone in rats initiated with 3'-methyl-4-dimethylaminoazobenzene.
1987 Jul
Resistance of DRH strain rats to chemical carcinogenesis of liver: genetic analysis of later progression stage.
2002 Jan
[Quantitative analysis of p53 and related genes mRNA in rat hepatocarcinogenesis induced by 3'-Me-DAB].
2003 Jan
Species specific hepatocarcinogen inhibition of the glucocorticoid induction of tyrosine aminotransferase gene in mouse and rat liver.
2003 May
Detection of a smaller, 32-kDa 8-oxoguanine DNA glycosylase 1 in 3'-methyl-4-dimethylamino-azobenzene-treated mouse liver.
2004 Feb
Prevention of rat hepatocarcinogenesis by acyclic retinoid is accompanied by reduction in emergence of both TGF-alpha-expressing oval-like cells and activated hepatic stellate cells.
2005
Species-specific effects of the hepatocarcinogens 3'-methyl-4-dimethyl-aminoazobenzene and ortho-aminoazotoluene in mouse and rat liver.
2005 Dec
Formate excretion in urine of rats fed dimethylaminoazobenzene-rich diets: the possibility of formate formation from D-lactate.
2008 Jun
Chronic alcohol consumption prevents 8-hydroxyguanine accumulation in 3'-methyl-4-dimethylaminoazobenzene-treated mouse liver.
2009 Sep 18
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 08:55:24 GMT 2023
Edited
by admin
on Sat Dec 16 08:55:24 GMT 2023
Record UNII
SXK3ZE3U4Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-(DIMETHYLAMINO)-3'-METHYLAZOBENZENE
Systematic Name English
3'-METHYL-4-(DIMETHYLAMINE)AZOBENZENE
Common Name English
M'-METHYL-P-DIMETHYLAMINOAZOBENZENE
Common Name English
3'-METHYL-4-(N,N-DIMETHYLAMINO)AZOBENZENE
Systematic Name English
BENZENAMINE, N,N-DIMETHYL-4-((3-METHYLPHENYL)AZO)-
Systematic Name English
4-(N,N-DIMETHYLAMINO)-3'-METHYLAZOBENZENE
Systematic Name English
4-DIMETHYLAMINO-3'-METHYLAZOBENZENE
Systematic Name English
3'-METHYL-4-DIMETHYLAMINOAZOBENZENE
Systematic Name English
3'-METHYL-N,N-DIMETHYL-4-AMINOAZOBENZENE
Common Name English
N,N-DIMETHYL-4-(3-METHYLPHENYLAZO)ANILINE
Systematic Name English
ANILINE, N,N-DIMETHYL-P-(M-TOLYLAZO)-
Systematic Name English
N,N-DIMETHYL-P-(M-TOLYLAZO)ANILINE
Common Name English
NSC-59783
Code English
BENZENAMINE, N,N-DIMETHYL-4-(2-(3-METHYLPHENYL)DIAZENYL)-
Systematic Name English
ANILINE, N,N-DIMETHYL-P-(3'-METHYLPHENYLAZO)-
Systematic Name English
N,N-DIMETHYL-4-((3-METHYLPHENYL)AZO)BENZENAMINE
Systematic Name English
METHYLDIMETHYLAMINOAZOBENZENE
Systematic Name English
3',N,N-TRIMETHYL-4-AMINOAZOBENZENE
Common Name English
3-METHYL-4'-(DIMETHYLAMINO)AZOBENZENE [HSDB]
Common Name English
N,N-DIMETHYL-4-(M-TOLYLAZO)ANILINE
Systematic Name English
N,N,3'-TRIMETHYL-4-AMINOAZOBENZENE
Common Name English
Code System Code Type Description
FDA UNII
SXK3ZE3U4Q
Created by admin on Sat Dec 16 08:55:24 GMT 2023 , Edited by admin on Sat Dec 16 08:55:24 GMT 2023
PRIMARY
NSC
59783
Created by admin on Sat Dec 16 08:55:24 GMT 2023 , Edited by admin on Sat Dec 16 08:55:24 GMT 2023
PRIMARY
EPA CompTox
DTXSID8020838
Created by admin on Sat Dec 16 08:55:24 GMT 2023 , Edited by admin on Sat Dec 16 08:55:24 GMT 2023
PRIMARY
ECHA (EC/EINECS)
200-243-4
Created by admin on Sat Dec 16 08:55:24 GMT 2023 , Edited by admin on Sat Dec 16 08:55:24 GMT 2023
PRIMARY
HSDB
5071
Created by admin on Sat Dec 16 08:55:24 GMT 2023 , Edited by admin on Sat Dec 16 08:55:24 GMT 2023
PRIMARY
CAS
55-80-1
Created by admin on Sat Dec 16 08:55:24 GMT 2023 , Edited by admin on Sat Dec 16 08:55:24 GMT 2023
PRIMARY
CHEBI
76329
Created by admin on Sat Dec 16 08:55:24 GMT 2023 , Edited by admin on Sat Dec 16 08:55:24 GMT 2023
PRIMARY