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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

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.
[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)
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
[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)
M A Patrauchan et al.
Journal of applied microbiology, 94(2), 266-272 (2003-01-22)
The aim of this work was to study the biodegradation of benzyldimethylalkylammonium chloride (BAC) by Aeromonas hydrophila sp. K, an organism isolated from polluted soil and capable of utilizing BAC as sole source of carbon and energy. High performance liquid
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