U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C8H11N.ClH
Molecular Weight 157.641
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,6-XYLIDINE HYDROCHLORIDE

SMILES

Cl.CC1=CC=CC(C)=C1N

InChI

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

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

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

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
Oxidation of 2,6-dimethylaniline by recombinant human cytochrome P450s and human liver microsomes.
2001 Jun
Identification of DNA adducts using HPLC/MS/MS following in vitro and in vivo experiments with arylamines and nitroarenes.
2003 Oct
Pharmacokinetics of xylazine, 2,6-dimethylaniline, and tolazoline in tissues from yearling cattle and milk from mature dairy cows after sedation with xylazine hydrochloride and reversal with tolazoline hydrochloride.
2003 Summer
Update on olfactory mucosal metabolic enzymes: age-related changes and N-acetyltransferase activities.
2004
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
Metabolic activation of 2,6-xylidine in the nasal olfactory mucosa and the mucosa of the upper alimentary and respiratory tracts in rats.
2004 Oct
A kinetically controlled trans bifunctionalized organoimido derivative of the Lindqvist-type hexamolybdate: synthesis, spectroscopic characterization, and crystal structure of (n-Bu4N)2{trans-[Mo6O17(NAr)2]} (Ar = 2,6-dimethylphenyl).
2005 Dec 26
Production and characterization of laccase from Cyathus bulleri and its use in decolourization of recalcitrant textile dyes.
2006 Aug
Changes in production of lignin degrading enzymes during interactions between mycelia of the tropical decomposer basidiomycetes Marasmiellus troyanus and Marasmius pallescens.
2006 Feb
Pi-Pi complexation of bupivacaine and analogues with aromatic receptors: implications for overdose remediation.
2007
N-(5-Chloro-3-methyl-1-phenyl-1H-pyrazol-4-ylcarbon-yl)-N'-(2,6-dimethyl-phen-yl)thio-urea.
2007 Dec 6
Liquid-phase microextraction-gas chromatography-mass spectrometry for the determination of bromate, iodate, bromide and iodide in high-chloride matrix.
2007 May 4
2,6-Dimethyl-anilinium chloride monohydrate.
2008 Nov 29
N-(2,6-Dimethyl-phen-yl)succinamic acid.
2009 Feb 6
Ethyl 2-[(2,6-dimethyl-phen-yl)hydrazono]-3-oxobutanoate.
2009 Jun 10
N-[3-(2,6-Dimethylanilino)-1-methylbut-2-enylidene]-2,6-dimethylanilinium chloride.
2009 Jun 24
Mixed carbene-isocyanide Pd(II) complexes: synthesis, structures and reactivity towards nucleophiles.
2009 Mar 28
Chemical oxidation of 2,6-dimethylaniline in the fenton process.
2009 Nov 15
Chemical oxidation of 2,6-dimethylaniline by electrochemically generated Fenton's reagent.
2010 Apr 15
Monocyclic aromatic amines as potential human carcinogens: old is new again.
2010 Jan
Investigating the mechanisms of aromatic amine-induced protein free radical formation by quantitative structure-activity relationships: implications for drug-induced agranulocytosis.
2010 May 17
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:02:20 GMT 2023
Edited
by admin
on Fri Dec 15 19:02:20 GMT 2023
Record UNII
695APM3L5Y
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,6-XYLIDINE HYDROCHLORIDE
Systematic Name English
ROPIVACAINE RELATED COMPOUND A [USP-RS]
Common Name English
BENZENAMINE, 2,6-DIMETHYL-, HYDROCHLORIDE (1:1)
Systematic Name English
LIDOCAINE HYDROCHLORIDE RELATED COMPOUND 2,6-DIMETHYLANILINE HYDROCHLORIDE [USP IMPURITY]
Common Name English
2,6-DIMETHYLANILINE HYDROCHLORIDE
Systematic Name English
BENZENAMINE, 2,6-DIMETHYL-, HYDROCHLORIDE
Systematic Name English
ROPIVACAINE RELATED COMPOUND A [USP IMPURITY]
Common Name English
ROPIVACAINE RELATED COMPOUND A
USP   USP-RS  
Common Name English
2,6-XYLIDINE, HYDROCHLORIDE
Systematic Name English
2,6-DIMETHYLBENZENAMINE HYDROCHLORIDE
Systematic Name English
Code System Code Type Description
CAS
21436-98-6
Created by admin on Fri Dec 15 19:02:20 GMT 2023 , Edited by admin on Fri Dec 15 19:02:20 GMT 2023
PRIMARY
EPA CompTox
DTXSID80175705
Created by admin on Fri Dec 15 19:02:20 GMT 2023 , Edited by admin on Fri Dec 15 19:02:20 GMT 2023
PRIMARY
RS_ITEM_NUM
1605512
Created by admin on Fri Dec 15 19:02:20 GMT 2023 , Edited by admin on Fri Dec 15 19:02:20 GMT 2023
PRIMARY
PUBCHEM
88899
Created by admin on Fri Dec 15 19:02:20 GMT 2023 , Edited by admin on Fri Dec 15 19:02:20 GMT 2023
PRIMARY
ECHA (EC/EINECS)
244-388-1
Created by admin on Fri Dec 15 19:02:20 GMT 2023 , Edited by admin on Fri Dec 15 19:02:20 GMT 2023
PRIMARY
FDA UNII
695APM3L5Y
Created by admin on Fri Dec 15 19:02:20 GMT 2023 , Edited by admin on Fri Dec 15 19:02:20 GMT 2023
PRIMARY
MESH
C007766
Created by admin on Fri Dec 15 19:02:20 GMT 2023 , Edited by admin on Fri Dec 15 19:02:20 GMT 2023
PRIMARY
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