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13365

Sigma-Aldrich

N,N-Dimethylbenzylamine

for protein sequence analysis, ≥99.5% (GC)

Synonym(s):

N-Benzyldimethylamine, BDMA, DMBA

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About This Item

Linear Formula:
C6H5CH2N(CH3)2
CAS Number:
103-83-3
Molecular Weight:
135.21
Beilstein:
1099620
EC Number:
203-149-1
MDL number:
MFCD00008329
UNSPSC Code:
12352200
PubChem Substance ID:
57647074
NACRES:
NA.26
Assay:
≥99.5% (GC)

grade

for protein sequence analysis

Assay

≥99.5% (GC)

refractive index

n20/D 1.501 (lit.)
n20/D 1.502

bp

183-184 °C/765 mmHg (lit.)

mp

−75 °C (lit.)

solubility

H2O: soluble

density

0.9 g/mL at 25 °C (lit.)

SMILES string

CN(C)Cc1ccccc1

InChI

1S/C9H13N/c1-10(2)8-9-6-4-3-5-7-9/h3-7H,8H2,1-2H3

InChI key

XXBDWLFCJWSEKW-UHFFFAOYSA-N

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Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

134.6 °F - closed cup

Flash Point(C)

57 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCBL0726V
1408050V
1408050
1173538
052383/1

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Y Kobayashi et al.
Organic letters, 3(14), 2253-2255 (2001-07-07)
[structure: see text] Examples of (13)C NMR desymmetrization of meso compounds are presented. On analysis of the NMR profiles of 1,3-diols, the additivity is recognized to predict the NMR profiles of 1,3,5-tirols.
Shuji Yasuike et al.
Chemical & pharmaceutical bulletin, 50(10), 1404-1406 (2002-10-10)
Novel, enantiomerically pure organoantimony compounds having a C-chiral amine moiety, (S)-(alpha-methyl-2-di-p-tolylstibanobenzyl)dimethylamine [AMSb] (2) and its (eta(6)-arene)chromium complex [AMSb-Cr(CO)(3)] (4), were prepared from common (S)-(alpha-methylbenzyl)dimethylamine (1) via its ortho-lithiated intermediates in short steps. The catalytic activity and enantioselectivity of the ligands
[Thin-layer chromatographic method for determination of N,N-dimethylbenzilamine in the air during sanitary and chemical studies of polymers].
L P Novitskaia et al.
Gigiena i sanitariia, (11)(11), 63-64 (1993-11-01)
[Optimization of biomimetic oxidation reactions achieved with the aid of an iodosylbenzene and meso-tetraphenylporphinatoiron (III): application to antergan].
F Pautet et al.
Pharmaceutica acta Helvetiae, 63(4-5), 140-144 (1988-01-01)
B Ståhlbom et al.
International archives of occupational and environmental health, 70(6), 393-398 (1997-01-01)
The aim of the present study was to develop a method for generation of dimethylbenzylamine (DMBA) atmospheres in an exposure chamber and to investigate the possibility of using urinary DMBA metabolites for biological monitoring of exposure to DMBA. A DMBA
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