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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 2,6-XYLIDINE

SMILES

CC1=CC=CC(C)=C1N

InChI

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

HIDE SMILES / InChI

Approval Year

Unknown
139594
PubMed

PubMed

TitleDatePubMed
Hepatic effects of xylidine isomers in rats.
1979 Jan
Transformation of BALB/c-3T3 cells: IV. Rank-ordered potency of 24 chemical responses detected in a sensitive new assay procedure.
1993 Jul
An update of the National Toxicology Program database on nasal carcinogens.
1997 Oct 31
Determination of the levels of aromatic amines in indoor and outdoor air in Italy.
2001 Apr
Plasma levels of lidocaine and prilocaine after application of Oraqix, a new intrapocket anesthetic, in patients with advanced periodontitis.
2001 May
Determination of xylazine and its metabolites by GC-MS in equine urine for doping analysis.
2004 Apr 1
Liquid phase overtone spectral investigations of 2,6-dimethylaniline and 2,4-dimethylaniline-evidence for steric nature of the ortho effect and the consequent base weakening.
2004 Aug
Synthesis, structure and pharmacology of acyl-2,6-xylidines.
2004 May-Jun
Changes in production of lignin degrading enzymes during interactions between mycelia of the tropical decomposer basidiomycetes Marasmiellus troyanus and Marasmius pallescens.
2006 Feb
N-(5-Chloro-3-methyl-1-phenyl-1H-pyrazol-4-ylcarbon-yl)-N'-(2,6-dimethyl-phen-yl)thio-urea.
2007 Dec 6
N-(2,6-Dimethyl-phen-yl)succinamic acid.
2009 Feb 6
Separation and analysis of dimethylaniline isomers by supercritical fluid chromatography--electrospray ionization tandem mass spectrometry.
2009 Oct 9
N-(2,6-Dimethyl-phen-yl)succinimide.
2010 Jan 9
HPLC-DAD stability indicating determination of nitrofurazone and lidocaine hydrochloride in their combined topical dosage form.
2010 Sep
Patents

Patents

03966811
2
04034108
3
04046554
2
04147804
3
04188341
2
04203904
2
04243819
7
04275079
2
04291049
3
04411912
7
04740233
5
04751232
2
04855497
2
04960787
2
04981866
2
05051508
4
05064862
2
05374724
2
05382584
18
05461157
2
05464863
5
05639905
3
05889021
4
06103749
2
06355680
12
06579884
3
06646010
2
06924286
2
06958357
2
07186726
2
07449586
2
08252875
2
08481738
2
08653553
2
08710234
2
08754092
4
08785665
6
08796294
2
JP4751836B2
4
JPS60208972A
2
Name Type Language
2,6-XYLIDINE
HSDB  
Systematic Name English
2,6-DIMETHYLANILINE [USP IMPURITY]
Common Name English
2,6-DIMETHYLBENZENAMINE
Systematic Name English
BUPIVACAINE HYDROCHLORIDE IMPURITY F [EP IMPURITY]
Common Name English
XYLAZINE HYDROCHLORIDE IMPURITY A [EP IMPURITY]
Common Name English
XYLIDENE, 2,6-
Common Name English
2,6-DIMETHYLANILINE
Systematic Name English
MEPIVACAINE HYDROCHLORIDE IMPURITY A [EP IMPURITY]
Common Name English
XYLIDINE 2,6-DIMETHYLBENZENAMINE
MI  
Systematic Name English
2,6-DIMETHYLANILINE [IARC]
Common Name English
NCI-C56188
Code English
LIDOCAINE IMPURITY A [EP IMPURITY]
Common Name English
NSC-7098
Code English
O-XYLIDINE
Common Name English
ROPIVACAINE HYDROCHLORIDE MONOHYDRATE IMPURITY H [EP IMPURITY]
Common Name English
2,6-XYLIDINE [HSDB]
Common Name English
ROPIVACAINE RELATED COMPOUND A FREE BASE
Common Name English
LIDOCAINE HYDROCHLORIDE IMPURITY A [EP IMPURITY]
Common Name English
XYLIDINE 2,6-DIMETHYLBENZENAMINE [MI]
Common Name English
2-AMINO-1,3-XYLENE
Systematic Name English
BENZENAMINE, 2,6-DIMETHYL-
Systematic Name English
LIDOCAINE RELATED COMPOUND 2,6-DIMETHYLANILINE [USP IMPURITY]
Common Name English
1-AMINO-2,6-DIMETHYLBENZENE
Systematic Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 90502
Created by admin on Fri Dec 15 17:09:07 GMT 2023 , Edited by admin on Fri Dec 15 17:09:07 GMT 2023
Code System Code Type Description
WIKIPEDIA
2,6-XYLIDINE
Created by admin on Fri Dec 15 17:09:07 GMT 2023 , Edited by admin on Fri Dec 15 17:09:07 GMT 2023
PRIMARY
EPA CompTox
DTXSID8026307
Created by admin on Fri Dec 15 17:09:07 GMT 2023 , Edited by admin on Fri Dec 15 17:09:07 GMT 2023
PRIMARY
FDA UNII
4FT62OX08D
Created by admin on Fri Dec 15 17:09:07 GMT 2023 , Edited by admin on Fri Dec 15 17:09:07 GMT 2023
PRIMARY
CAS
87-62-7
Created by admin on Fri Dec 15 17:09:07 GMT 2023 , Edited by admin on Fri Dec 15 17:09:07 GMT 2023
PRIMARY
CHEBI
28738
Created by admin on Fri Dec 15 17:09:07 GMT 2023 , Edited by admin on Fri Dec 15 17:09:07 GMT 2023
PRIMARY
MESH
C007766
Created by admin on Fri Dec 15 17:09:07 GMT 2023 , Edited by admin on Fri Dec 15 17:09:07 GMT 2023
PRIMARY
MERCK INDEX
m11552
Created by admin on Fri Dec 15 17:09:07 GMT 2023 , Edited by admin on Fri Dec 15 17:09:07 GMT 2023
PRIMARY Merck Index
NSC
7098
Created by admin on Fri Dec 15 17:09:07 GMT 2023 , Edited by admin on Fri Dec 15 17:09:07 GMT 2023
PRIMARY
PUBCHEM
6896
Created by admin on Fri Dec 15 17:09:07 GMT 2023 , Edited by admin on Fri Dec 15 17:09:07 GMT 2023
PRIMARY
ECHA (EC/EINECS)
201-758-7
Created by admin on Fri Dec 15 17:09:07 GMT 2023 , Edited by admin on Fri Dec 15 17:09:07 GMT 2023
PRIMARY
HSDB
2094
Created by admin on Fri Dec 15 17:09:07 GMT 2023 , Edited by admin on Fri Dec 15 17:09:07 GMT 2023
PRIMARY
PARENT (METABOLITE INACTIVE)
Structure of LIDOCAINE
PARENT (METABOLITE)
Structure of D-2624
SALT/SOLVATE (PARENT)
Structure of 2,6-XYLIDINE HYDROCHLORIDE
SUBSTANCE RECORD
Structure of 2,6-XYLIDINE
NIH
NCATS
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ACCESSIBILITY
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