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Atomfair 4,4′-Diamino-2,2′-bipyridine C10H10N4

Description 4,4′-Diamino-2,2′-bipyridine (CAS No. 18511-69-8) is a high-purity bipyridine derivative with the molecular formula C10H10N4. This compound, also known by its IUPAC name 2-(4-aminopyridin-2-yl)pyridin-4-amine , is a versatile bidentate ligand widely used in coordination chemistry and materials science. Its rigid bipyridine scaffold and dual amino functional groups make it an excellent building block for synthesizing metal-organic frameworks (MOFs), catalysts, and luminescent materials. The product is supplied as a fine crystalline powder with ??98% purity, ensuring optimal performance in research and industrial applications. Suitable for use in organic synthesis, photochemistry, and as a precursor for advanced polymeric materials.

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Description

Description

4,4′-Diamino-2,2′-bipyridine (CAS No. 18511-69-8) is a high-purity bipyridine derivative with the molecular formula C10H10N4. This compound, also known by its IUPAC name 2-(4-aminopyridin-2-yl)pyridin-4-amine, is a versatile bidentate ligand widely used in coordination chemistry and materials science. Its rigid bipyridine scaffold and dual amino functional groups make it an excellent building block for synthesizing metal-organic frameworks (MOFs), catalysts, and luminescent materials. The product is supplied as a fine crystalline powder with ??98% purity, ensuring optimal performance in research and industrial applications. Suitable for use in organic synthesis, photochemistry, and as a precursor for advanced polymeric materials.

  • CAS No: 18511-69-8
  • Molecular Formula: C10H10N4
  • Molecular Weight: 186.21
  • Exact Mass: 186.090546336
  • Monoisotopic Mass: 186.090546336
  • IUPAC Name: 2-(4-aminopyridin-2-yl)pyridin-4-amine
  • SMILES: C1=CN=C(C=C1N)C2=NC=CC(=C2)N
  • Synonyms: 18511-69-8, 4,4′-diamino-2,2′-bipyridine, 806-945-2, [2,2′-Bipyridine]-4,4′-diamine, 4,4′-diamino-2,2′-bipyridyl

Application

4,4′-Diamino-2,2′-bipyridine serves as a key ligand in transition metal catalysis, enabling efficient C-C coupling reactions. Its amino groups facilitate covalent attachment to surfaces or polymers for hybrid material design. Researchers utilize it in developing electrochemiluminescent sensors due to its redox-active bipyridine core. The compound is also employed in photovoltaic studies as an electron-accepting moiety in dye-sensitized solar cells.

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