A9878
4-氨基苯甲酸
≥99%, for peptide synthesis, ReagentPlus®
别名:
对氨基苯甲酸, PABA, 维生素 Bx, 维生素 H1
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关于此项目
线性分子式:
H2NC6H4CO2H
化学文摘社编号:
分子量:
137.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352106
EC Number:
205-753-0
MDL number:
Beilstein/REAXYS Number:
471605
产品名称
4-氨基苯甲酸, ReagentPlus®, ≥99%
InChI
1S/C7H7NO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,8H2,(H,9,10)
SMILES string
Nc1ccc(cc1)C(O)=O
InChI key
ALYNCZNDIQEVRV-UHFFFAOYSA-N
biological source
synthetic (organic)
product line
ReagentPlus®
assay
≥99%
form
powder
reaction suitability
reaction type: solution phase peptide synthesis
mp
187-189 °C (lit.)
solubility
ethanol: 50 mg/mL, clear, colorless to faintly yellow
density
1.374 g/mL at 25 °C (lit.)
application(s)
peptide synthesis
storage temp.
room temp
Quality Level
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Application
4-氨基苯甲酸被用于:
- 合成聚酰胺的结构单元
- 生产叶酸的底物
- 合成席夫碱
- 金属有机框架 (MOFs) 合成中的有机配体
General description
4-氨基苯甲酸，也被称为对氨基苯甲酸 (PABA)，是用于合成芳香胺和偶氮染料的前体。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
hcodes
pcodes
Hazard Classifications
Aquatic Chronic 3
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
339.8 °F - closed cup
flash_point_c
171 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Synthesis and antibacterial activity of some Schiff bases derived from 4-aminobenzoic acid.
Parekh J, et al.
J. Serb. Chem. Soc., 70(10), 1155-1155 (2005)
Electropolymerized 4-aminobenzoic acid based voltammetric sensor for the simultaneous determination of food azo dyes
G Ziyatdinova
Polymers, 14, 5429-5429 (2022)
Synthesis, Structure and Characterization of Some Metal Organic Framework Based on 4-Aminobenzoic Acid Schiff Base Linker
RJ Deghadi, et al.
Journal of Basic and Environmental Sciences, 8, 29-31 (2021)
Unsaturated polyamides prepared from 3-amino-or 4-carboxycinnamic acid and their heat curing to thermally stable resins
CD Diakoumakos
Polymer, 36, 387-392 (1995)
Simple conversion of aromatic amines into azides
Q Liu
Organic Letters, 5, 2571-2572 (2003)
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