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B25606

Sigma-Aldrich

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
Beilstein/REAXYS Number:
606221
EC Number:
203-133-4
MDL number:
MFCD00008289
UNSPSC Code:
12352100
PubChem Substance ID:
24891660
NACRES:
NA.22

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.)

SMILES string

CNCc1ccccc1

InChI

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

InChI key

RIWRFSMVIUAEBX-UHFFFAOYSA-N

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Related Categories

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_germany

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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C C Hsia et al.
Proceedings of the National Academy of Sciences of the United States of America, 78(3), 1878-1881 (1981-03-01)
Previous studies in Linxian, an area of China with a high incidence of esophageal carcinoma, showed that fungal infections are common in the esophageal epithelium of patients with either premalignant changes or early esophageal carcinoma. Fungi of the genus Candida
L Y Fong et al.
Journal of the National Cancer Institute, 72(2), 419-425 (1984-02-01)
Nine-week-old zinc-sufficient (100 mg zinc/kg feed) and zinc-deficient (7 mg zinc/kg feed) noninbred male Sprague-Dawley rats were given free access 5 days a week to deionized drinking water containing low (0.05%) or high (0.25%) quantities of benzylmethylamine (BMA) and concurrently
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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