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Key Documents

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Safety Information

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

Quality Level

100

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

Signal Word

Danger

Hazard Statements

H314,H317,H334

Hazard Classifications

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

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

167.0 °F - closed cup

Flash Point(C)

75 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

B25606-500ML:
B25606-5ML:
B25606-100ML:
B25606-VAR:
B25606-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
STBL3501
STBK4198
STBK4075
STBJ9763
STBJ4452

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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 (+)-
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
Jennifer A Francesconi et al.
Behavioural brain research, 382, 112467-112467 (2020-01-10)
Male and female C57BL/6 J mice were tested on the predator odor response task, where they needed to cross through a chamber of scented bedding to reach a sucrose reward. Following the behavioral testing, mouse brains were immunohistochemically labeled for expression
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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