Description

5,10,15,20-Tetrakis(4-(1H-imidazol-1-yl)phenyl)porphyrin (CAS: 1311998-62-5) is a high-purity synthetic porphyrin derivative with the molecular formula C₅₆H₃₈N₁₂. This compound features a porphyrin core symmetrically functionalized with four imidazole-substituted phenyl groups, making it an excellent candidate for coordination chemistry, catalysis, and material science applications. Its rigid, planar structure and electron-rich aromatic system enable strong interactions with metal ions, facilitating the formation of stable metalloporphyrin complexes. Ideal for researchers in supramolecular chemistry, photodynamic therapy, and organic electronics, this product is supplied as a dark purple solid with ≥95% purity (HPLC). Store under inert conditions at -20°C to ensure long-term stability.

Properties

• CAS Number: 1311998-62-5
• Complexity: 1380
• IUPAC Name: 5,10,15,20-tetrakis(4-imidazol-1-ylphenyl)-21,23-dihydroporphyrin
• InChI: InChI=1S/C56H38N12/c1-9-41(65-29-25-57-33-65)10-2-37(1)53-45-17-19-47(61-45)54(38-3-11-42(12-4-38)66-30-26-58-34-66)49-21-23-51(63-49)56(40-7-15-44(16-8-40)68-32-28-60-36-68)52-24-22-50(64-52)55(48-20-18-46(53)62-48)39-5-13-43(14-6-39)67-31-27-59-35-67/h1-36,61,64H
• InChI Key: YSEHAJSQGBWKME-UHFFFAOYSA-N
• Exact Mass: 878.33423926
• Molecular Formula: C56H38N12
• Molecular Weight: 879.0
• SMILES: C1=CC(=CC=C1C2=C3C=CC(=C(C4=NC(=C(C5=CC=C(N5)C(=C6C=CC2=N6)C7=CC=C(C=C7)N8C=CN=C8)C9=CC=C(C=C9)N1C=CN=C1)C=C4)C1=CC=C(C=C1)N1C=CN=C1)N3)N1C=CN=C1
• Topological: 129
• Monoisotopic Mass: 878.33423926
• Synonyms: 1311998-62-5, 5,10,15,20-Tetrakis(4-(1H-imidazol-1-yl)phenyl)porphyrin, 5,10,15,20-Tetrakis[4-(1H-imidazol-1-yl)phenyl]-21H,23H-porphine, 5,10,15,20-tetrakis(4-imidazol-1-ylphenyl)-21,23-dihydroporphyrin, 21H,23H-Porphine, 5,10,15,20-tetrakis[4-(1H-imidazol-1-yl)phenyl]-, YSCH0019, CS-0111005, E81366

Application

This porphyrin derivative is widely used in the development of metal-organic frameworks (MOFs) due to its ability to coordinate with various transition metals. It serves as a photosensitizer in photodynamic therapy research, leveraging its strong absorbance in the visible spectrum. Additionally, it is employed in the synthesis of organic electronic materials, such as organic light-emitting diodes (OLEDs) and photovoltaic cells, owing to its excellent charge transport properties.

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