B25606
N-Benzylmethylamine
97%
Synonym(s):
N-Methylbenzylamine
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5 ML
€36.70
100 ML
€44.40
500 ML
€80.00
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5 ML
€36.70
100 ML
€44.40
500 ML
€80.00
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
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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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
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 (+)-
R Siegler et al.
Journal of pharmaceutical and biomedical analysis, 7(1), 45-55 (1989-01-01)
DTAF has been used successfully to prepare fluorescent labelled reagents for fluorescence polarization immunoassays. Its applicability as a derivation reagent for direct fluorescence analysis of primary and secondary amines was evaluated. DTAF was shown to have spectral properties that closely
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