Atomfair tert-Butyl phenoxyperoxyacetate C12H16O4

Description tert-Butyl phenoxyperoxyacetate (CAS No. 5961-88-6) is a high-purity organic peroxide with the molecular formula C12H16O4. This compound, also known by its IUPAC name tert-butyl 2-phenoxyethaneperoxoate , is a specialized reagent widely used in polymerization, cross-linking, and oxidative reactions. It is characterized by its stable yet reactive peroxy group, making it valuable in controlled radical reactions and material synthesis. Available in rigorously tested batches, this product is ideal for researchers requiring precise and consistent performance in advanced chemical applications. Proper storage under inert conditions is recommended to maintain stability and efficacy.

Description

tert-Butyl phenoxyperoxyacetate (CAS No. 5961-88-6) is a high-purity organic peroxide with the molecular formula C₁₂H₁₆O₄. This compound, also known by its IUPAC name tert-butyl 2-phenoxyethaneperoxoate, is a specialized reagent widely used in polymerization, cross-linking, and oxidative reactions. It is characterized by its stable yet reactive peroxy group, making it valuable in controlled radical reactions and material synthesis. Available in rigorously tested batches, this product is ideal for researchers requiring precise and consistent performance in advanced chemical applications. Proper storage under inert conditions is recommended to maintain stability and efficacy.

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 employed as a radical initiator in polymerization processes, particularly for styrenic and acrylic monomers. Its controlled decomposition properties make it suitable for synthesizing polymers with specific molecular weights and architectures. Additionally, it is used in organic synthesis for selective oxidative transformations. Researchers also utilize it in cross-linking applications to modify material properties in coatings and adhesives.

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