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Atomfair Benzo[c]phenanthrene C18H12

Description Benzo[c]phenanthrene (CAS No. 195-19-7) is a polycyclic aromatic hydrocarbon (PAH) with the molecular formula C18H12. This high-purity compound is widely utilized in organic synthesis, material science, and environmental research due to its unique fused-ring aromatic structure. It is available in crystalline form with guaranteed purity levels suitable for analytical standards, chemical synthesis, and photophysical studies. Benzo[c]phenanthrene is rigorously tested via GC/MS, HPLC, and NMR to ensure compliance with research-grade specifications. Ideal for studying PAH reactivity, carcinogenicity, and optoelectronic properties.

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Description

Description

Benzo[c]phenanthrene (CAS No. 195-19-7) is a polycyclic aromatic hydrocarbon (PAH) with the molecular formula C18H12. This high-purity compound is widely utilized in organic synthesis, material science, and environmental research due to its unique fused-ring aromatic structure. It is available in crystalline form with guaranteed purity levels suitable for analytical standards, chemical synthesis, and photophysical studies. Benzo[c]phenanthrene is rigorously tested via GC/MS, HPLC, and NMR to ensure compliance with research-grade specifications. Ideal for studying PAH reactivity, carcinogenicity, and optoelectronic properties.

  • CAS No: 195-19-7
  • Molecular Formula: C18H12
  • Molecular Weight: 228.3
  • Exact Mass: 228.093900383
  • Monoisotopic Mass: 228.093900383
  • IUPAC Name: benzo[c]phenanthrene
  • SMILES: C1=CC=C2C(=C1)C=CC3=C2C4=CC=CC=C4C=C3
  • Synonyms: Benzo[c]phenanthrene, 195-19-7, BENZO(C)PHENANTHRENE, Tetrahelicene, 3,4-Benzophenanthrene

Application

Benzo[c]phenanthrene is primarily used as a model compound in environmental toxicology to study the metabolic activation and DNA adduct formation of polycyclic aromatic hydrocarbons. It serves as a key intermediate in organic synthesis for constructing helicenes and other chiral aromatic systems. Researchers also employ it in photophysical studies due to its extended ??-conjugation and fluorescence properties.

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