368466
4-氨基苄胺
99%
别名:
4-(氨甲基)苯胺, 4-氨基甲基苯胺, 4-氨基苯甲胺, 对(氨甲基)苯胺, 对氨基苄胺, 甲苯-α,4-二胺
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关于此项目
线性分子式:
H2NC6H4CH2NH2
化学文摘社编号:
分子量:
122.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
99%
Form:
liquid
InChI
1S/C7H10N2/c8-5-6-1-3-7(9)4-2-6/h1-4H,5,8-9H2
SMILES string
NCc1ccc(N)cc1
InChI key
BFWYZZPDZZGSLJ-UHFFFAOYSA-N
assay
99%
form
liquid
refractive index
n20/D 1.61 (lit.)
bp
101 °C/0.05 mmHg (lit.)
mp
37 °C
density
1.078 g/mL at 25 °C (lit.)
functional group
amine
Quality Level
General description
4-氨基苄胺是一种芳香胺。用亚硝酸钠在HCl水溶液中原位生成4-氨基苄基胺的重氮阳离子，该阳离子用于具有脂肪族胺基的芳基对玻璃碳电极的修饰。
Application
4-氨基苄胺可用于：
- 通过氧化偶联对单壁碳纳米管（SWCNT）进行电化学修饰
- 新型吖甲醛基氨基酸的制备
- 基于“荧光-间隔-（阴离子）受体”原理，合成两个新型荧光光致电子转移（PET）阴离子传感器
- SWCNTs 阳极耦合
- 通过与反应性前体聚合物聚（五氟苯基丙烯酸酯）（PPFPA）的双聚合物类似反应，合成含水杨醛基苯胺的聚丙烯酰胺系列
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
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
C B Carlson et al.
Bioorganic & medicinal chemistry letters, 10(17), 1979-1982 (2000-09-15)
The preparation of a novel acridine-based amino acid is reported. This N-Alloc-protected monomer can be coupled and deprotected under solid-phase peptide synthesis procedures to create acridine peptide conjugates as potential threading intercalators. A peptide containing this novel amino acid undergoes
Balasubramanian K, et al.
Advanced Materials, 15(18), 1515-1518 (2003)
Electrochemical modification of single carbon nanotubes.
Steven Earl Kooi et al.
Angewandte Chemie (International ed. in English), 41(8), 1353-1355 (2002-04-15)
Dual responsive chemosensors for anions: the combination of fluorescent PET (Photoinduced Electron Transfer) and colorimetric chemosensors in a single molecule.
Gunnlaugsson T, et al.
Tetrahedron Letters, 44(35), 6575-6578 (2003)
Tony Breton et al.
Langmuir : the ACS journal of surfaces and colloids, 24(16), 8711-8718 (2008-07-26)
The electrochemically induced functionalization of glassy carbon electrode by aryl groups having an aliphatic amine group was achieved by reduction of in situ generated diazonium cations in aqueous media. The corresponding diazonium cations of 4-aminobenzylamine, 2-aminobenzylamine, 4-(2-aminoethyl)aniline, N-methyl-1,2-phenylenediamine, and N
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