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2-(4-Aminophenyl)-1H-benzimidazol-5-amine (APBIA) CAS 7621-86-5

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2-(4-Aminophenyl)-1H-benzimidazol-5-amine (APBIA) CAS 7621-86-5

Synonyms: 2-(4-Aminophenyl)-5-aminobenzimidazole; 5-Amino-2-(4-aminophenyl)benzimidazole; 1H-Benzimidazol-5-amine, 2-(4-aminophenyl)-; 1H-Benzimidazol-6-amine, 2-(4-aminophenyl)-; 2-(4-Aminophenyl)-1H-benzo[d]imidazol-5-amine; 5(6)-Amino-2-(p-aminophenyl)benzimidazole; 

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Product Details

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2-(4-Aminophenyl)-1H-benzimidazol-5-amine (APBIA), CAS 7621-86-5, is a benzimidazole derivative and diamine monomer known for its solubility in organic solvents, low toxicity, and potential biological activities, making it suitable as an intermediate in polymer synthesis and pharmaceutical development.

Basic Information of APBIA

Product Name2-(4-Aminophenyl)-1H-benzimidazol-5-amine
Abbreviation

APBIA

CAS Number

7621-86-5

Molecular FormulaC13H12N4
Molecular Weight224.26 g/mol
AppearancePale Beige to Pale Brown Solid
Purity≥99%
Package1kg/bottle, 20kg/drum, or customized
Molecular formulaAPBIA Molecular Structure

 

Key Properties

  • High thermal stability, thanks to the benzimidazole core structure

  • Dual amino functionality for polymerization and crosslinking capability

  • Good chemical resistance and stability in harsh environments

  • Potential for incorporation in functional membranes (e.g. proton exchange)

  • Moderate polarity, enabling interactions in composite / interface systems


Key Applications of APBIA

  • Battery Materials: Used as a component in aerogel lithium battery separators and for preparing sulfonated polyimides containing benzimidazole (SPIBIs) combined with polyhedral oligomeric silsesquioxane glycidyl ethers (G-POSS) to create organic-inorganic hybrid proton exchange membranes (PEMs).

  • High-Performance Polymers: Serves as a monomer to optimize polyimide properties, enhancing performance in materials requiring thermal stability and mechanical strength.

  • Pharmaceuticals: Employed in drug development for anti-cancer agents (inhibiting kinases in cancer signaling pathways), antiviral compounds (e.g., against hepatitis C virus), and anti-inflammatory drugs (inhibiting cyclooxygenase enzymes); valued for its bioavailability and low toxicity.

  • Organic Synthesis: Acts as a versatile intermediate in pharmaceutical research and organic synthesis, facilitating the creation of novel compounds.


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