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2. Cumene process - Wikipedia

   en.wikipedia.org/wiki/Cumene_process

   This latter cumene converts into cumene radical and feeds back into subsequent chain formations of cumene hydroperoxides. A pressure of 5 atm is used to ensure that the unstable peroxide is kept in liquid state. Cumene hydroperoxide undergoes a rearrangement reaction in an acidic medium (the Hock rearrangement) to give phenol and acetone. In ...

3. Cumene hydroperoxide - Wikipedia

   en.wikipedia.org/wiki/Cumene_hydroperoxide

   Cumene hydroperoxide is an intermediate in the cumene process for producing phenol and acetone from benzene and propene. Cumene hydroperoxide is a radical initiator for production of acrylates. [5] Cumene hydroperoxide is involved as an organic peroxide in the production of propylene oxide by the oxidation of propene. This technology was ...

4. Phenol Peels Are Great Anti-Aging Skin Treatments, But They ...

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5. Chemical peel - Wikipedia

   en.wikipedia.org/wiki/Chemical_peel

   A phenol-croton oil is a type of chemical peel. [7] The term "phenol-croton oil peel" has replaced the vague term "phenol peel" in medical literature. It was originally used on a clandestine basis by early Hollywood stars in the 1920s and was incorporated into mainstream practice in the 1960s by Thomas Baker and Howard Gordon. [8]

6. Acetophenone - Wikipedia

   en.wikipedia.org/wiki/Acetophenone

   Acetophenone is formed as a byproduct of the cumene process, the industrial route for the synthesis of phenol and acetone.In the Hock rearrangement of isopropylbenzene hydroperoxide, migration of a methyl group rather than the phenyl group gives acetophenone and methanol as a result of an alternate rearrangement of the intermediate:

7. Cumene - Wikipedia

   en.wikipedia.org/wiki/Cumene

   Cumene (isopropylbenzene) is an organic compound that contains a benzene ring with an isopropyl substituent. It is a constituent of crude oil and refined fuels. It is a flammable colorless liquid that has a boiling point of 152 °C.

8. 2,4,6-Tri-tert-butylphenol - Wikipedia

   en.wikipedia.org/wiki/2,4,6-Tri-tert-butylphenol

   2,4,6-Tri-tert-butylphenol (2,4,6-TTBP) is a phenol symmetrically substituted with three tert-butyl groups and thus strongly sterically hindered. 2,4,6-TTBP is a readily oxidizable aromatic compound and a weak acid. It oxidizes to give the deep-blue 2,4,6-tri-tert-butylphenoxy radical.

9. Phenol - Wikipedia

   en.wikipedia.org/wiki/Phenol

   Phenol and its vapors are corrosive to the eyes, the skin, and the respiratory tract. [60] Its corrosive effect on skin and mucous membranes is due to a protein-degenerating effect. [49] Repeated or prolonged skin contact with phenol may cause dermatitis, or even second and third-degree burns. [61] Inhalation of phenol vapor may cause lung ...