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Atomfair Cyclohexanone peroxide C12H22O5
Description Cyclohexanone Peroxide ( CAS 12262-58-7 ) is a high-purity organic peroxide widely utilized in polymerization and crosslinking applications. With the molecular formula C12H22O5and IUPAC name 1-(1-hydroperoxycyclohexyl)peroxycyclohexan-1-ol , this compound serves as a highly efficient free-radical initiator. It is available in stabilized forms to ensure safe handling and storage. Ideal for industrial and research applications, Cyclohexanone Peroxide exhibits excellent reactivity in polymer synthesis, resin curing, and material modification processes. Its controlled decomposition properties make it suitable for precise reaction conditions.
Description
Description
Cyclohexanone Peroxide (CAS 12262-58-7) is a high-purity organic peroxide widely utilized in polymerization and crosslinking applications. With the molecular formula C12H22O5 and IUPAC name 1-(1-hydroperoxycyclohexyl)peroxycyclohexan-1-ol, this compound serves as a highly efficient free-radical initiator. It is available in stabilized forms to ensure safe handling and storage. Ideal for industrial and research applications, Cyclohexanone Peroxide exhibits excellent reactivity in polymer synthesis, resin curing, and material modification processes. Its controlled decomposition properties make it suitable for precise reaction conditions.
- CAS No: 12262-58-7
- Molecular Formula: C12H22O5
- Molecular Weight: 246.30
- Exact Mass: 246.14672380
- Monoisotopic Mass: 246.14672380
- IUPAC Name: 1-(1-hydroperoxycyclohexyl)peroxycyclohexan-1-ol
- SMILES: C1CCC(CC1)(O)OOC2(CCCCC2)OO
- Synonyms: CYCLOHEXANONE PEROXIDE, Perhexa P, 1-Hydroperoxycyclohexyl 1-hydroxycyclohexyl peroxide, 12262-58-7, Cyclohexanone, peroxide
Application
Cyclohexanone Peroxide is primarily used as a radical initiator in the polymerization of unsaturated polyester resins and vinyl monomers. It is also employed in the curing of fiberglass-reinforced plastics and thermosetting composites. Additionally, this peroxide finds applications in adhesive formulations and coatings due to its ability to initiate crosslinking at moderate temperatures. Researchers value its predictable decomposition kinetics for controlled polymerization studies.
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