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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 3,5-XYLIDINE

SMILES

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

InChI

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

HIDE SMILES / InChI

Molecular Formula C8H11N
Molecular Weight 121.1796
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
N-(3,5-Dimethyl-phen-yl)succinamic acid.
2010-12-24
1-(3,5-Dimethyl-phen-yl)-4,5-dimethyl-2-phenyl-1H-imidazole hemihydrate.
2010-10-09
Monocyclic aromatic amines as potential human carcinogens: old is new again.
2010-01
Tetra-kis(3,5-xylidinium) dihydrogen cyclo-hexa-phosphate dihydrate.
2009-12-24
N-(3,5-Dimethyl-phen-yl)-4-methyl-benzene-sulfonamide.
2009-12-16
N-(3,5-Dimethyl-phen-yl)benzene-sulfonamide.
2009-11-28
Separation and analysis of dimethylaniline isomers by supercritical fluid chromatography--electrospray ionization tandem mass spectrometry.
2009-10-09
Ethyl 3-[(3,5-dimethyl-phen-yl)amino-carbon-yl]propanoate.
2009-07-29
Identification of adducts formed by reaction of N-acetoxy-3,5-dimethylaniline with DNA.
2007-11
Arylamine N-acetyltransferases: characterization of the substrate specificities and molecular interactions of environmental arylamines with human NAT1 and NAT2.
2007-09
Pi-Pi complexation of bupivacaine and analogues with aromatic receptors: implications for overdose remediation.
2007
Identification and characterization of functional rat arylamine N-acetyltransferase 3: comparisons with rat arylamine N-acetyltransferases 1 and 2.
2006-10
DNA adduct formation by 2,6-dimethyl-, 3,5-dimethyl-, and 3-ethylaniline in vivo in mice.
2006-08
Fabrication of a metal nanoparticles and polymer nanofibers composite material by an in situ chemical synthetic route.
2005-08-16
Alkylaniline-hemoglobin adducts and risk of non-smoking-related bladder cancer.
2004-10-06
2,4-disubstituted pyrimidines: a novel class of KDR kinase inhibitors.
2003-05-19
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:18:52 GMT 2025
Edited
by admin
on Mon Mar 31 19:18:52 GMT 2025
Record UNII
1418BR6T2H
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3,5-XYLIDINE
HSDB  
Systematic Name English
XYLIDINE 3,5-DIMETHYLBENZENAMINE
MI  
Preferred Name English
3,5-XYLIDENE-
Common Name English
NSC-26880
Code English
XYLIDINE 3,5-DIMETHYLBENZENAMINE [MI]
Common Name English
XYLIDENE, 3,5-
Common Name English
3,5-DIMETHYLANILINE
Systematic Name English
1-AMINO-3,5-DIMETHYLBENZENE
Systematic Name English
BENZENAMINE, 3,5-DIMETHYL-
Systematic Name English
3,5-XYLIDINE [HSDB]
Common Name English
Code System Code Type Description
MESH
C514328
Created by admin on Mon Mar 31 19:18:52 GMT 2025 , Edited by admin on Mon Mar 31 19:18:52 GMT 2025
PRIMARY
WIKIPEDIA
3,5-Xylidine
Created by admin on Mon Mar 31 19:18:52 GMT 2025 , Edited by admin on Mon Mar 31 19:18:52 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-607-0
Created by admin on Mon Mar 31 19:18:52 GMT 2025 , Edited by admin on Mon Mar 31 19:18:52 GMT 2025
PRIMARY
HSDB
2096
Created by admin on Mon Mar 31 19:18:52 GMT 2025 , Edited by admin on Mon Mar 31 19:18:52 GMT 2025
PRIMARY
PUBCHEM
7949
Created by admin on Mon Mar 31 19:18:52 GMT 2025 , Edited by admin on Mon Mar 31 19:18:52 GMT 2025
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NSC
26880
Created by admin on Mon Mar 31 19:18:52 GMT 2025 , Edited by admin on Mon Mar 31 19:18:52 GMT 2025
PRIMARY
CAS
108-69-0
Created by admin on Mon Mar 31 19:18:52 GMT 2025 , Edited by admin on Mon Mar 31 19:18:52 GMT 2025
PRIMARY
MERCK INDEX
m11552
Created by admin on Mon Mar 31 19:18:52 GMT 2025 , Edited by admin on Mon Mar 31 19:18:52 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID8026309
Created by admin on Mon Mar 31 19:18:52 GMT 2025 , Edited by admin on Mon Mar 31 19:18:52 GMT 2025
PRIMARY
FDA UNII
1418BR6T2H
Created by admin on Mon Mar 31 19:18:52 GMT 2025 , Edited by admin on Mon Mar 31 19:18:52 GMT 2025
PRIMARY