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

Details

Stereochemistry ACHIRAL
Molecular Formula C9H13N
Molecular Weight 135.2062
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N,N-DIMETHYLBENZYLAMINE

SMILES

CN(C)CC1=CC=CC=C1

InChI

InChIKey=XXBDWLFCJWSEKW-UHFFFAOYSA-N
InChI=1S/C9H13N/c1-10(2)8-9-6-4-3-5-7-9/h3-7H,8H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C9H13N
Molecular Weight 135.2062
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Dimethylbenzylamine is used as a catalyst for soft polyester-based polyurethane systems, semisolid foams, pre-polymerisation agents, to improve the effect of impregnation agents on cellulose fibres. Contact with skin causes burns

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Identification of alkyl dimethylbenzylammonium surfactants in water samples by solid-phase extraction followed by ion trap LC/MS and LC/MS/MS.
2001 Jun 15
Coordination chemistry of a chelating amidoximato ligand.
2001 Jun 4
Organometallics and quaternary ammonium salts affect calcium ion desorption from lecithin liposome membranes.
2001 May-Jun
Oxygenation of benzyldimethylamine by singlet oxygen. Products and mechanism.
2004 Dec 9
New palladium(II) and platinum(II) complexes with the model nucleobase 1-methylcytosine: antitumor activity and interactions with DNA.
2005 Oct 17
Electrophilic C-H activation at Cp*Ir: ancillary-ligand control of the mechanism of C-H activation.
2006 Apr 5
The mechanism of carbon dioxide catalysis in the hydrogen peroxide N-oxidation of amines.
2008 Feb 4
Easy access to bio-inspired osmium(II) complexes through electrophilic intramolecular C(sp2)-H bond cyclometalation.
2008 Jun 2
Methylated N-(4-N,N-dimethylaminobenzyl) chitosan for novel effective gene carriers.
2008 Sep
Computational and synthetic studies on the cyclometallation reaction of dimethylbenzylamine with [IrCl2Cp*]2: role of the chelating base.
2009 Aug 14
A new coordination tetra-mer of copper(I) iodide and benzyl-dimethyl-amine: tetra-μ(3)-iodido-tetra-kis[(benzyl-dimethyl-amine-κN)copper(I)].
2009 Jul 11
Chloridobis{2-[(dimethyl-amino)-meth-yl]phen-yl}anti-mony(III).
2009 Oct 17
Analysis of special surfactants by comprehensive two-dimensional gas chromatography coupled to time-of-flight mass spectrometry.
2010 Jan 29
Chlorido{2-[(dimethyl-amino)-methyl]phenyl-κC,N}(1-methyl-1H-imidazole-κN)palladium(II).
2010 Nov 24
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 02:17:02 GMT 2023
Edited
by admin
on Sat Dec 16 02:17:02 GMT 2023
Record UNII
TYP7AXQ1YJ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N,N-DIMETHYLBENZYLAMINE
Systematic Name English
NSC-5342
Code English
Code System Code Type Description
PUBCHEM
7681
Created by admin on Sat Dec 16 02:17:02 GMT 2023 , Edited by admin on Sat Dec 16 02:17:02 GMT 2023
PRIMARY
MESH
C045966
Created by admin on Sat Dec 16 02:17:02 GMT 2023 , Edited by admin on Sat Dec 16 02:17:02 GMT 2023
PRIMARY
EPA CompTox
DTXSID8021854
Created by admin on Sat Dec 16 02:17:02 GMT 2023 , Edited by admin on Sat Dec 16 02:17:02 GMT 2023
PRIMARY
FDA UNII
TYP7AXQ1YJ
Created by admin on Sat Dec 16 02:17:02 GMT 2023 , Edited by admin on Sat Dec 16 02:17:02 GMT 2023
PRIMARY
ECHA (EC/EINECS)
203-149-1
Created by admin on Sat Dec 16 02:17:02 GMT 2023 , Edited by admin on Sat Dec 16 02:17:02 GMT 2023
PRIMARY
CAS
103-83-3
Created by admin on Sat Dec 16 02:17:02 GMT 2023 , Edited by admin on Sat Dec 16 02:17:02 GMT 2023
PRIMARY
NSC
5342
Created by admin on Sat Dec 16 02:17:02 GMT 2023 , Edited by admin on Sat Dec 16 02:17:02 GMT 2023
PRIMARY
WIKIPEDIA
Dimethylbenzylamine
Created by admin on Sat Dec 16 02:17:02 GMT 2023 , Edited by admin on Sat Dec 16 02:17:02 GMT 2023
PRIMARY