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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

Approval Year

PubMed

PubMed

TitleDatePubMed
Transformation of BALB/c-3T3 cells: IV. Rank-ordered potency of 24 chemical responses detected in a sensitive new assay procedure.
1993 Jul
Tumor-promoting activity of 2,6-dimethylaniline in a two-stage nasal carcinogenesis model in N-bis(2-hydroxypropyl)nitrosamine-treated rats.
1999 Aug 3
Synthesis, characterization, and comparative 32P-postlabeling efficiencies of 2,6-dimethylaniline-DNA adducts.
2001 Feb
Plasma levels of lidocaine and prilocaine after application of Oraqix, a new intrapocket anesthetic, in patients with advanced periodontitis.
2001 May
Identification of DNA adducts using HPLC/MS/MS following in vitro and in vivo experiments with arylamines and nitroarenes.
2003 Oct
Update on olfactory mucosal metabolic enzymes: age-related changes and N-acetyltransferase activities.
2004
Synthesis, structure and pharmacology of acyl-2,6-xylidines.
2004 May-Jun
Alkylaniline-hemoglobin adducts and risk of non-smoking-related bladder cancer.
2004 Oct 6
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
N-(2,6-Dimethyl-phen-yl)benzene-sulfonamide.
2008 Aug 6
Kinetics and mechanism of 2,6-dimethyl-aniline degradation by hydroxyl radicals.
2009 Dec 30
N-[3-(2,6-Dimethylanilino)-1-methylbut-2-enylidene]-2,6-dimethylanilinium chloride.
2009 Jun 24
N-(2,6-Dimethyl-phen-yl)-2-(2-thien-yl)acetamide.
2009 Nov 25
N-(2,6-Dimethyl-phen-yl)maleamic acid.
2009 Oct 23
Iron-catalyzed dehydrogenative phosphonation of N,N-dimethylanilines.
2009 Oct 28
Separation and analysis of dimethylaniline isomers by supercritical fluid chromatography--electrospray ionization tandem mass spectrometry.
2009 Oct 9
Chemical oxidation of 2,6-dimethylaniline by electrochemically generated Fenton's reagent.
2010 Apr 15
N-(2,6-Dimethyl-phen-yl)-4-methyl-benzene-sulfonamide.
2010 Apr 24
N-(2,6-Dimethyl-phen-yl)succinimide.
2010 Jan 9
Patents
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
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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
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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
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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
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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
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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
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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
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