123056
4-(2-氨基)苯乙胺
97%
别名:
4-氨基苯乙胺
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关于此项目
线性分子式:
H2NC6H4CH2CH2NH2
化学文摘社编号:
分子量:
136.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
236-739-2
Beilstein/REAXYS Number:
1099913
MDL number:
Assay:
97%
InChI key
LNPMZQXEPNWCMG-UHFFFAOYSA-N
InChI
1S/C8H12N2/c9-6-5-7-1-3-8(10)4-2-7/h1-4H,5-6,9-10H2
SMILES string
NCCc1ccc(N)cc1
assay
97%
refractive index
n20/D 1.591 (lit.)
bp
103 °C/0.3 mmHg (lit.)
mp
28-31 °C (lit.)
density
1.034 g/mL at 25 °C (lit.)
functional group
amine
Quality Level
General description
4-（2-氨基乙基）苯胺可通过还原胺化作用与碳水化合物偶联生成修饰的碳水化合物。
Application
4-（2-氨基乙基）苯胺已被用于丝素蛋白的化学改性以调整丝的整体亲水性和结构。它已被用作缩聚反应的试剂。
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Amanda R Murphy et al.
Biomaterials, 29(19), 2829-2838 (2008-04-18)
A simple chemical modification method using diazonium coupling chemistry was developed to tailor the structure and hydrophilicity of silk fibroin protein. The extent of modification using several aniline derivatives was characterized using UV-vis and 1H NMR spectroscopies, and the resulting
Isabella A Lobo et al.
Physical chemistry chemical physics : PCCP, 14(25), 9219-9229 (2012-05-31)
The neurotransmitter analogue p-aminophenethylamine (APEA) illustrates many of the pitfalls and challenges associated with spectroscopic and conformational analysis of flexible molecules. The combined experimental-theoretical study presented here resolves a long-standing controversy over its conformational energetic preferences. Jet-cooled resonance enhanced two-photon
Polymer Journal, 23, 1511-1511 (1991)
Macromolecules, 27, 1289-1289 (1994)
M Reyes-Parada et al.
Biochemical pharmacology, 47(8), 1365-1371 (1994-04-20)
The in vitro and ex vivo monoamine oxidase (MAO) inhibitory effects of (+/-)4-dimethylamino-alpha-methyl-phenethylamine (4-DMAA) and (+/-)4-methylamino-alpha-methyl-phenethylamine (4-MAA) were reassessed, in comparison with the previously unstudied achiral parent compound, 4-dimethyl-aminophenethylamine (4-DMAPEA) and with a salt of 4-DMAA enriched in the levo
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