B25606
N-苄甲胺
97%
别名:
N-甲基苄胺
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关于此项目
线性分子式:
C6H5CH2NHCH3
化学文摘社编号:
分子量:
121.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-133-4
Beilstein/REAXYS Number:
606221
MDL number:
Assay:
97%
Form:
liquid
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
Quality Level
refractive index
n20/D 1.522 (lit.)
bp
184-189 °C (lit.)
density
0.939 g/mL at 25 °C (lit.)
signalword
Danger
hcodes
Hazard Classifications
Resp. Sens. 1 - Skin Corr. 1B - Skin Sens. 1
存储类别
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
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)
Mechanism of aryl chloride amination: base-induced oxidative addition.
L M Alcazar-Roman et al.
Journal of the American Chemical Society, 123(51), 12905-12906 (2001-12-26)
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 (+)-
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
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