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Details

Stereochemistry ACHIRAL
Molecular Formula C8H11N
Molecular Weight 121.1796
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3,4-Xylidine

SMILES

CC1=C(C)C=C(N)C=C1

InChI

InChIKey=DOLQYFPDPKPQSS-UHFFFAOYSA-N
InChI=1S/C8H11N/c1-6-3-4-8(9)5-7(6)2/h3-5H,9H2,1-2H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
N-{4-[(3,4-Dimethyl-phen-yl)sulfamo-yl]phen-yl}acetamide.
2010-07-31
N-(3,4-Dimethyl-phen-yl)benzene-sulfonamide.
2010-07-10
Investigating the mechanisms of aromatic amine-induced protein free radical formation by quantitative structure-activity relationships: implications for drug-induced agranulocytosis.
2010-05-17
4-Chloro-N-(3,4-dimethyl-phen-yl)benzene-sulfonamide.
2010-05-08
N-(3,4-Dimethyl-phen-yl)-2,4-dimethyl-benzene-sulfonamide.
2010-04-24
N-(3,4-Dimethyl-phen-yl)succinamic acid.
2010-01-23
N-(3,5-Dimethyl-phen-yl)-2,4-dimethyl-benzene-sulfonamide.
2009-11-28
N-(3,4-Dimethyl-phen-yl)maleamic acid.
2009-10-28
Separation and analysis of dimethylaniline isomers by supercritical fluid chromatography--electrospray ionization tandem mass spectrometry.
2009-10-09
2-(3,4-Dimethyl-anilino)acetohydrazide.
2009-09-30
N-(3,4-Dimethyl-phen-yl)-4-hydr-oxy-2-methyl-2H-1,2-benzothia-zine-3-carboxamide 1,1-dioxide.
2009-03-28
N-(3,4-Dimethyl-phen-yl)-4-methyl-benzene-sulfonamide.
2009-03-28
3,4-Dimethyl-anilinium chloride monohydrate.
2009-02-28
Semi-quantitative immunohistochemical analysis of male rat-specific alpha2u-globulin accumulation for chemical toxicity evaluation.
2006-02
Prediction of genotoxicity of chemical compounds by statistical learning methods.
2005-06
The effect of substituents on the phenyl portion of the imido ligand on the structure and properties of molybdenum(VI) imido complexes.
2002-11-18
Capture of a labile substrate by expulsion of water molecules from the active site of nicotinate mononucleotide:5,6-dimethylbenzimidazole phosphoribosyltransferase (CobT) from Salmonella enterica.
2002-10-25
Solid-phase microextraction of monocyclic aromatic amines using novel fibers coated with crown ether.
2001-11-16
Patents
Name Type Language
3,4-Xylidine
HSDB  
Systematic Name English
XYLIDINE 3,4-DIMETHYLBENZENAMINE
MI  
Preferred Name English
XYLIDINE, 3,4-
Systematic Name English
XYLIDINE 3,4-DIMETHYLBENZENAMINE [MI]
Common Name English
3,4-DIMETHYLANILINE
Systematic Name English
BENZENAMINE, 3,4-DIMETHYL-
Systematic Name English
1-AMINO-3,4-DIMETHYLBENZENE
Systematic Name English
NSC-41800
Code English
3,4-DIMETHYLBENZENAMINE
Systematic Name English
3,4-XYLIDINE [HSDB]
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
202-437-4
Created by admin on Mon Mar 31 18:56:49 GMT 2025 , Edited by admin on Mon Mar 31 18:56:49 GMT 2025
PRIMARY
HSDB
2095
Created by admin on Mon Mar 31 18:56:49 GMT 2025 , Edited by admin on Mon Mar 31 18:56:49 GMT 2025
PRIMARY
CAS
95-64-7
Created by admin on Mon Mar 31 18:56:49 GMT 2025 , Edited by admin on Mon Mar 31 18:56:49 GMT 2025
PRIMARY
WIKIPEDIA
3,4-XYLIDINE
Created by admin on Mon Mar 31 18:56:49 GMT 2025 , Edited by admin on Mon Mar 31 18:56:49 GMT 2025
PRIMARY
DRUG BANK
DB03018
Created by admin on Mon Mar 31 18:56:49 GMT 2025 , Edited by admin on Mon Mar 31 18:56:49 GMT 2025
PRIMARY
FDA UNII
R27I33AIDT
Created by admin on Mon Mar 31 18:56:49 GMT 2025 , Edited by admin on Mon Mar 31 18:56:49 GMT 2025
PRIMARY
CHEBI
39901
Created by admin on Mon Mar 31 18:56:49 GMT 2025 , Edited by admin on Mon Mar 31 18:56:49 GMT 2025
PRIMARY
PUBCHEM
7248
Created by admin on Mon Mar 31 18:56:49 GMT 2025 , Edited by admin on Mon Mar 31 18:56:49 GMT 2025
PRIMARY
MERCK INDEX
m11552
Created by admin on Mon Mar 31 18:56:49 GMT 2025 , Edited by admin on Mon Mar 31 18:56:49 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID3026308
Created by admin on Mon Mar 31 18:56:49 GMT 2025 , Edited by admin on Mon Mar 31 18:56:49 GMT 2025
PRIMARY
NSC
41800
Created by admin on Mon Mar 31 18:56:49 GMT 2025 , Edited by admin on Mon Mar 31 18:56:49 GMT 2025
PRIMARY