product name
4-氨基苯甲酸, ReagentPlus®, 99%
质量水平
产品线
ReagentPlus®
检测方案
99%
形式
solid
反应适用性
reaction type: solution phase peptide synthesis
mp
187-189 °C (lit.)
溶解性
95% ethanol: soluble 5%, clear to slightly hazy, colorless to yellow
密度
1.374 g/mL at 25 °C (lit.)
应用
peptide synthesis
SMILES字符串
Nc1ccc(cc1)C(O)=O
InChI
1S/C7H7NO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,8H2,(H,9,10)
InChI key
ALYNCZNDIQEVRV-UHFFFAOYSA-N
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相关类别
一般描述
4-氨基苯甲酸 (4-ABA) 作为细菌辅助因子，参与叶酸的合成。它是一种通过线性氢键结合进行结构扩展的通用试剂，涉及羧酸和胺官能团。用氨基阳离子自由基法在玻碳电极 (GCE) 上制备了 4-ABA 单层膜。合成了 4-ABA 的分子加合物，用红外光谱和 X-射线衍射方法对其进行了表征。
应用
4-氨基苯甲酸可用于下列研究：
- 玻碳电极的共价修饰。
- 1，4-（2-氯亚苯基）氨基苯甲酸（席夫碱）的合成。
- 分光光度法测定微量多巴胺、甲基多巴和左旋多巴。
- 5-磺基水杨酸与 1：1 质子转移化合物的合成。
法律信息
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
危险声明
预防措施声明
危险分类
Aquatic Chronic 3
WGK
WGK 2
个人防护装备
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
The 1: 1 proton-transfer compound of 5-sulfosalicylic acid with 4-aminobenzoic acid.
Smith G, et al.
Acta Crystallographica Section E, Structure Reports Online, 61(2), 313-316 (2005)
Covalent modification of a glassy carbon surface by 4-aminobenzoic acid and its application in fabrication of a polyoxometalates-consisting monolayer and multilayer films.
Liu J, et al.
Langmuir, 16(19), 7471-7476 (2000)
Layer-by-layer assembly of multilayer films consisting of silicotungstate and a cationic redox polymer on 4-aminobenzoic acid modified glassy carbon electrode and their electrocatalytic effects.
Cheng L, et al.
Analytica Chimica Acta, 34(12), 1093-1100 (1999)
Gehad G Mohamed et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 62(4-5), 1140-1150 (2005-06-16)
Metal complexes of Schiff base derived from 2-thiophene carboxaldehyde and 2-aminobenzoic acid (HL) are reported and characterized based on elemental analyses, IR, 1H NMR, solid reflectance, magnetic moment, molar conductance and thermal analysis (TGA). The ligand dissociation as well as
Spectrophotometric determination of catecholamines based on their oxidation reaction followed by coupling with 4-aminobenzoic acid.
Madrakian T, et al.
Journal of the Brazilian Chemical Society, 17(7), 1259-1265 (2006)
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