B25606
N-Benzylmethylamine
97%
Synonym(s):
N-Methylbenzylamine
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About This Item
Linear Formula:
C6H5CH2NHCH3
CAS Number:
Molecular Weight:
121.18
Beilstein:
606221
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
form:
liquid
Assay:
97%
Recommended Products
Quality Level
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
Signal Word
Danger
Hazard Statements
Precautionary Statements
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
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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)
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
Suk Joong Lee et al.
Journal of the American Chemical Society, 128(7), 2178-2179 (2006-02-16)
Asymmetric syntheses of 4,5,6- and 3,4,5,6-substituted azepanes have been achieved by highly diastereoselective and enantioselective (-)-sparteine-mediated asymmetric lithiation-conjugate additions of N-Boc-N-(p-methoxyphenyl)-2,3-substituted allylamines to a beta-aryl alpha,beta-unsaturated ester followed by hydrolysis, cyclization, and reduction. Access to the enantiomeric adduct is provided
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 (+)-
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
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