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Atomfair Triallyl phosphate TAP C9H15O4P

Description Triallyl Phosphate (CAS No. 1623-19-4) is a high-purity organophosphorus compound with the molecular formula C9H15O4P and IUPAC name tris(prop-2-enyl) phosphate . This colorless to pale yellow liquid is widely utilized in polymer chemistry, flame retardancy, and crosslinking applications due to its trifunctional allyl groups. With a molecular weight of 218.18 g/mol, it exhibits excellent reactivity in radical polymerization and serves as a key intermediate in the synthesis of specialty polymers, adhesives, and coatings. Our product is rigorously tested for purity ( typically ??98% by GC ), ensuring optimal performance in advanced material science applications. Proper storage in amber glass…

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Description

Description

Triallyl Phosphate (CAS No. 1623-19-4) is a high-purity organophosphorus compound with the molecular formula C9H15O4P and IUPAC name tris(prop-2-enyl) phosphate. This colorless to pale yellow liquid is widely utilized in polymer chemistry, flame retardancy, and crosslinking applications due to its trifunctional allyl groups. With a molecular weight of 218.18 g/mol, it exhibits excellent reactivity in radical polymerization and serves as a key intermediate in the synthesis of specialty polymers, adhesives, and coatings. Our product is rigorously tested for purity (typically ??98% by GC), ensuring optimal performance in advanced material science applications. Proper storage in amber glass under inert atmosphere is recommended to maintain stability.

  • CAS No: 1623-19-4
  • Molecular Formula: C9H15O4P
  • Molecular Weight: 218.19
  • Exact Mass: 218.07079595
  • Monoisotopic Mass: 218.07079595
  • IUPAC Name: tris(prop-2-enyl) phosphate
  • SMILES: C=CCOP(=O)(OCC=C)OCC=C
  • Synonyms: TRIALLYL PHOSPHATE, Allyl phosphate, Triallyl orthophosphate, Phosphoric acid, tri-2-propenyl ester, PHOSPHORIC ACID TRIALLYL ESTER

Application

Triallyl phosphate is primarily employed as a reactive crosslinking agent in thermosetting resins and flame-retardant polymers. Its trifunctional structure enables efficient network formation in allyl-based polymerization systems, enhancing thermal and mechanical properties. The compound also finds use as a plasticizer modifier and as an intermediate for phosphorus-containing flame retardants. Researchers utilize it in photopolymerization studies due to its UV-sensitive allyl groups.

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