所有图片(2)
About This Item
线性分子式:
H2NC6H4CH2CH2NH2
CAS号:
分子量:
136.19
Beilstein:
1099913
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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质量水平
方案
97%
折射率
n20/D 1.591 (lit.)
沸点
103 °C/0.3 mmHg (lit.)
mp
28-31 °C (lit.)
密度
1.034 g/mL at 25 °C (lit.)
官能团
amine
SMILES字符串
NCCc1ccc(N)cc1
InChI
1S/C8H12N2/c9-6-5-7-1-3-8(10)4-2-7/h1-4H,5-6,9-10H2
InChI key
LNPMZQXEPNWCMG-UHFFFAOYSA-N
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一般描述
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。
应用
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。
警示用语:
Danger
危险声明
危险分类
Skin Corr. 1B
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 3
闪点(°F)
235.4 °F - closed cup
闪点(°C)
113 °C - closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
Mihaela Badea et al.
Biosensors & bioelectronics, 18(5-6), 689-698 (2003-04-23)
Glucose oxidase, lactate oxidase, L-aminoacid oxidase and alcohol oxidase were immobilised on new films based on 2,6-dihydroxynaphthalene (2,6-DHN) copolymerised with 2-(4-aminophenyl)-ethylamine (AP-EA) onto the Pt electrodes. The electropolymerisation was performed by cyclic voltammetry. Different scan rates and scan potential ranges
Chem. Abstr., 116, 106932j-106932j (1992)
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
Polymer Journal, 23, 1511-1511 (1991)
Macromolecules, 27, 1289-1289 (1994)
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