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Atomfair Triphenylantimony C18H15Sb

Description Triphenylantimony (CAS No. 54010-75-2), also known as Triphenylstibane , is an organoantimony compound with the molecular formula C18H15Sb . This high-purity chemical is widely utilized in advanced research and industrial applications due to its role as a versatile reagent in organic synthesis and materials science. Triphenylantimony appears as a white to off-white crystalline solid and is sensitive to air and moisture, requiring storage under inert conditions. It serves as a precursor in the synthesis of antimony-containing polymers, catalysts, and semiconductor materials. Suitable for use in cross-coupling reactions, ligand design, and coordination chemistry, this compound is a valuable asset for…

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Description

Description

Triphenylantimony (CAS No. 54010-75-2), also known as Triphenylstibane, is an organoantimony compound with the molecular formula C18H15Sb. This high-purity chemical is widely utilized in advanced research and industrial applications due to its role as a versatile reagent in organic synthesis and materials science. Triphenylantimony appears as a white to off-white crystalline solid and is sensitive to air and moisture, requiring storage under inert conditions. It serves as a precursor in the synthesis of antimony-containing polymers, catalysts, and semiconductor materials. Suitable for use in cross-coupling reactions, ligand design, and coordination chemistry, this compound is a valuable asset for researchers in organometallic chemistry and nanotechnology. Each batch is rigorously tested for purity and consistency, ensuring reliable performance in sensitive applications.

  • CAS No: 54010-75-2
  • Molecular Formula: C18H15Sb
  • Molecular Weight: 353.1
  • Exact Mass: 352.02119
  • Monoisotopic Mass: 352.02119
  • IUPAC Name: triphenylstibane
  • SMILES: C1=CC=C(C=C1)[Sb](C2=CC=CC=C2)C3=CC=CC=C3
  • Synonyms: Triphenylantimony, 603-36-1, Triphenylstibane, TRIPHENYLSTIBINE, Stibine, triphenyl-

Application

Triphenylantimony is commonly employed as a reagent in the synthesis of organoantimony compounds and as a catalyst or co-catalyst in polymerization reactions. It finds use in the development of flame retardants due to antimony’s synergistic effects with halogens. Researchers also utilize it in the preparation of semiconductor materials and as a precursor for depositing antimony-containing thin films in electronic applications.

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