Información del producto
- 1H-Benzimidazol-5-amine, 2-(4-aminophenyl)-
- 1H-Benzimidazol-6-amine, 2-(4-aminophenyl)-
- 2-(4-Amino-phenyl)-1H-benzoimidazol-5-ylamine
- 2-(4-Aminophenyl)-1H-1,3-benzodiazol-5-amine
- 2-(4-Aminophenyl)-1H-1,3-benzodiazol-6-amine
- 2-(4-Aminophenyl)-1H-benzimidazol-5-amine
- 2-(4-Aminophenyl)-1H-benzimidazole-5-amine
- 2-(4-Aminophenyl)-1H-benzo[d]imidazol-5-amine
- 2-(4-Aminophenyl)-3H-benzimidazol-5-amine
- 2-(4-Aminophenyl)-5-aminobenzimidazole
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- 2-(4-aminophenyl)-1H-benzimidazol-6-amine
- 5(6)-Amino-2-(4′-aminophenyl)benzimidazole
- 5(6)-Amino-2-(p-aminophenyl)benzimidazole
- 5,4′-Diamino-2-phenylbenzimidazole
- 5-Amino-2-(4-aminobenzene)benzimidazole
- 5-Amino-2-(4-aminophenyl)-1H-benzimidazole
- 5-Amino-2-(4-aminophenyl)-benzimidazole
- 5-Amino-2-(4-aminophenyl)benzylimidazole
- 5-Amino-2-(p-aminophenyl)benzimidazole
- 6,4′-Diamino-2-phenylbenzimidazole
- Apbia
- Benzimidazole, 5(or 6)-amino-2-(p-aminophenyl)-
- Benzimidazole, 5-amino-2-(p-aminophenyl)-
- NSC 408148
5-Amino-2-(4-aminophenyl)benzimidazole is a chemical compound that is used in the synthesis of other compounds. It can be prepared by the reaction of 4-aminophenol with 2,5-dichlorobenzene imidazole followed by hydrogenation and purification. 5-Amino-2-(4-aminophenyl)benzimidazole has a high resistance to both UV and thermal degradation. It has been shown to have low solubility in water, but high solubility in organic solvents such as chloroform, ethyl acetate, and cyclohexane. This compound shows an orthorhombic crystal structure and reacts with proton (H+) or chloride ion. 5-Amino-2-(4-aminophenyl)benzimidazole is also used as a reagent for gel permeation chromatography in order to
Propiedades químicas
Consulta técnica sobre: 3D-HAA62186 5-Amino-2-(4-aminophenyl)benzimidazole
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