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Merck
CN

B25606

N-Benzylmethylamine

97%

Synonym(s):

N-Methylbenzylamine

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About This Item

Linear Formula:
C6H5CH2NHCH3
CAS Number:
103-67-3
Molecular Weight:
121.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24891660
EC Number:
203-133-4
Beilstein/REAXYS Number:
606221
MDL number:
MFCD00008289
Assay:
97%
Form:
liquid

Key Documents

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Product Name

N-Benzylmethylamine, 97%

InChI key

RIWRFSMVIUAEBX-UHFFFAOYSA-N

InChI

1S/C8H11N/c1-9-7-8-5-3-2-4-6-8/h2-6,9H,7H2,1H3

SMILES string

CNCc1ccccc1

assay

97%

form

liquid

refractive index

n20/D 1.522 (lit.)

bp

184-189 °C (lit.)

density

0.939 g/mL at 25 °C (lit.)

Quality Level

100

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pictograms

Health hazardCorrosion
GHS08,GHS05

signalword

Danger

Hazard Classifications

Resp. Sens. 1 - Skin Corr. 1B - Skin Sens. 1

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 1

flash_point_f

167.0 °F - closed cup

flash_point_c

75 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB7257
SDBB4831
STBL3501
STBK4198
STBK4075

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Steven Droge et al.
Environmental science & technology, 46(11), 5894-5901 (2012-05-01)
Sorption of organic cations to soil organic matter was studied using dynamic column experiments with different compositions of electrolytes in aqueous eluents. The sorption affinity of the tested variety of charged compounds, including primary, secondary, and tertiary amines and quaternary
Zinc deficiency and the induction of oesophageal tumors in rats by benzylmethylamine and sodium nitrite.
L Y Fong et al.
IARC scientific publications, (41)(41), 679-683 (1982-01-01)
F Karoum
British journal of pharmacology, 90(2), 335-345 (1987-02-01)
In an effort to explore the contribution of the metabolites of pargyline towards the in vivo inhibition of monoamine oxidase (MAO), the effects of pargyline and its major metabolites on the production and metabolism of a number of biogenic amines
H Weber et al.
Journal of chromatography, 307(1), 145-153 (1984-04-13)
The separation of racemic benoxaprofen into the two benoxaprofen enantiomers by preparative high-performance liquid chromatography and the application of the activated enantiomers as derivatization reagents for the simultaneous stereoselective determination of chiral amines in biological material is described. Activated (+)-
T Tahira et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 26(6), 511-516 (1988-06-01)
Thioproline, which is readily nitrosated to form nitrosothioproline, is expected to act as a nitrite scavenger. The effect of thioproline as an inhibitor of the carcinogenesis induced by N-nitroso-N-benzylmethylamine precursors was examined. Two groups of male F-344 rats were given
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