跳转至内容
Merck
所有图片(2)

主要文件

查看所有文档

123056

Sigma-Aldrich

4-(2-氨基)苯乙胺

97%

别名:

4-氨基苯乙胺

登录查看公司和协议定价
所有图片(2)

About This Item

线性分子式:
H2NC6H4CH2CH2NH2
CAS号:
13472-00-9
分子量:
136.19
Beilstein:
1099913
EC 号:
236-739-2
MDL编号:
MFCD00008194
UNSPSC代码:
12352100
PubChem化学物质编号:
24847518
NACRES:
NA.22

质量水平

200

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

正在寻找类似产品? 访问 产品对比指南

相关类别

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。

象形图

Corrosion
GHS05

警示用语：

Danger

危险声明

H314

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SHBP5669
SHBM8932
SHBK8914
SHBF0154V
04203KH

没有发现合适的版本？

如果您需要特殊版本，可通过批号或批次号查找具体证书。

搜索COA

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

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
Polymer Journal, 23, 1511-1511 (1991)
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
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
查看所有相关文献

我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持