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Merck
CN

136921

N,N-Dimethylbenzylamine

98%

Synonym(s):

N-Benzyldimethylamine, BDMA, DMBA

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About This Item

Linear Formula:
C6H5CH2N(CH3)2
CAS Number:
Molecular Weight:
135.21
EC Number:
203-149-1
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
1099620
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InChI

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

InChI key

XXBDWLFCJWSEKW-UHFFFAOYSA-N

SMILES string

CN(C)Cc1ccccc1

assay

98%

refractive index

n20/D 1.501 (lit.)

bp

183-184 °C/765 mmHg (lit.)

mp

−75 °C (lit.)

density

0.9 g/mL at 25 °C (lit.)

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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

3 - Flammable liquids

wgk

WGK 2

flash_point_f

134.6 °F - closed cup

flash_point_c

57 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

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N Hayashi et al.
Organic letters, 3(14), 2249-2252 (2001-07-07)
[structure: see text] Three additional NMR databases, 1-3, in a chiral solvent are presented. The C.21-C.38 portion of oasomycin A is used to demonstrate the scope and limitation of the universal NMR database approach in a chiral solvent for assignment
B Ballantyne et al.
Drug and chemical toxicology, 8(1-2), 43-56 (1985-01-01)
N-Benzyl-N,N-dimethylamine (BDMA), a polyester foam catalyst, was determined to have LD50 values of 0.65 (0.48-0.88) ml/kg perorally in the rat, and 1.66 (1.35-2.04) ml/kg by 24-hr occluded dermal contact in rabbits. The Lt50 for saturated vapor atmosphere exposure of rats
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
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
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.

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