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Atomfair tert-Butyl phenoxyperoxyacetate C12H16O4

Description tert-Butyl phenoxyperoxyacetate (CAS No. 5961-88-6) is a highly specialized organic peroxide with the molecular formula C12H16O4. This compound, also known by its IUPAC name tert-butyl 2-phenoxyethaneperoxoate , is a valuable reagent in synthetic chemistry and polymerization processes. It is characterized by its tert-butyl peroxyester functional group, which imparts reactivity as a radical initiator. The product is supplied as a high-purity material, ensuring consistency in research and industrial applications. Proper handling and storage under recommended conditions are essential due to its peroxide nature. Ideal for researchers and chemists working in advanced organic synthesis, material science, and polymer chemistry.

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Description

Description

tert-Butyl phenoxyperoxyacetate (CAS No. 5961-88-6) is a highly specialized organic peroxide with the molecular formula C12H16O4. This compound, also known by its IUPAC name tert-butyl 2-phenoxyethaneperoxoate, is a valuable reagent in synthetic chemistry and polymerization processes. It is characterized by its tert-butyl peroxyester functional group, which imparts reactivity as a radical initiator. The product is supplied as a high-purity material, ensuring consistency in research and industrial applications. Proper handling and storage under recommended conditions are essential due to its peroxide nature. Ideal for researchers and chemists working in advanced organic synthesis, material science, and polymer chemistry.

  • CAS No: 5961-88-6
  • Molecular Formula: C12H16O4
  • Molecular Weight: 224.25
  • Exact Mass: 224.10485899
  • Monoisotopic Mass: 224.10485899
  • IUPAC Name: tert-butyl 2-phenoxyethaneperoxoate
  • SMILES: CC(C)(C)OOC(=O)COC1=CC=CC=C1
  • Synonyms: tert-Butyl phenoxyperoxyacetate, 5789-77-5, HW7A4V2GKV, EINECS 227-325-2, UNII-HW7A4V2GKV

Application

tert-Butyl phenoxyperoxyacetate is primarily used as a radical initiator in polymerization reactions, enabling controlled synthesis of polymers and copolymers. It finds application in the production of specialty plastics, resins, and elastomers where precise radical initiation is critical. Researchers also utilize it in organic synthesis for the construction of complex molecular architectures. Its stability under controlled conditions makes it suitable for both laboratory-scale experiments and industrial processes.

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