185701
苄胺
ReagentPlus®, 99%
别名:
α-氨基甲苯
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线性分子式:
C6H5CH2NH2
化学文摘社编号:
分子量:
107.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-854-1
Beilstein/REAXYS Number:
741984
MDL number:
产品名称
苄胺, ReagentPlus®, 99%
InChI key
WGQKYBSKWIADBV-UHFFFAOYSA-N
InChI
1S/C7H9N/c8-6-7-4-2-1-3-5-7/h1-5H,6,8H2
SMILES string
NCc1ccccc1
product line
ReagentPlus®
assay
99%
form
liquid
refractive index
n20/D 1.543 (lit.)
bp
184-185 °C (lit.)
mp
10 °C (lit.)
solubility
alcohol: miscible
diethyl ether: miscible
water: miscible
density
0.981 g/mL at 25 °C (lit.)
Quality Level
Gene Information
human ... AOC3(8639)
mouse ... Aoc3(11754)
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Application
- 苄胺用于通过酰胺和酯形成反应改性烷硫醇单层，以附着在金属电极上。
- 它被用作载体电解质，通过毛细管电泳和间接紫外检测分离水样中的碱金属、碱土金属和铵阳离子。
- 它用于合成基于 N-（对-乙烯基苯甲酰基）-2-甲基丙氨酸、苯乙烯和二乙烯基苯的交联多孔共聚物载体。
General description
苄胺经过苄胺氧化酶和 B 型单胺氧化酶催化的氧化脱氨反应。
苯甲胺(BnNH2)是一种芳香胺，广泛用于生产有机精细化学品和多种药物化合物。它可在金属催化剂存在下，通过苯甲腈的氢化和苯甲醛的还原胺化制备而成。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
149.0 °F - closed cup
flash_point_c
65 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Hydrogenation of benzonitrile to benzylamine catalyzed by ruthenium hydride complexes with P- NH- NH- P tetradentate ligands: evidence for a hydridic- protonic outer sphere mechanism
Li Tianshu, et al.
Organometallics, 26(24), 5940-5949 (2007)
Aida Mohammadi et al.
Sensors (Basel, Switzerland), 18(10) (2018-10-14)
This study examines the improvements in surface-enhanced Raman scattering (SERS) performance achieved when silver nanodendritic structures are coated with various graphene-based materials, namely graphene oxide (GO), reduced graphene oxide (rGO), and graphene nanoplatelets (GNPs). The tests are performed on our
Benzylamine
Heuer, Lutz
Ullmann's Encyclopedia of Industrial Chemistry (2000)
Capillary electrophoresis of alkali and alkaline-earth cations with imidazole or benzylamine buffers.
Morin PCF and Dreux M.
Journal of Liquid Chromatography and Related Technologies, 17(18), 3869-3888 (1994)
A benzylamine oxidase distinct from monoamine oxidase B--widespread distribution in man and rat.
R Lewinsohn et al.
Biochemical pharmacology, 27(14), 1857-1863 (1978-01-01)
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