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  2. Ohio State, Nationwide Children's proton therapy center ... - AOL

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    The $100-million proton therapy center is the first such treatment facility in central Ohio for adult and pediatric cancer patients. Ohio State, Nationwide Children's proton therapy center brings ...

  3. Cumene process - Wikipedia

    en.wikipedia.org/wiki/Cumene_process

    Cumene is oxidized in air, which removes the tertiary benzylic hydrogen from cumene and hence forms a cumene radical: The cumene radical then bonds with an oxygen molecule to give cumene peroxide radical, which in turn forms cumene hydroperoxide (C 6 H 5 C(CH 3) 2 O 2 H) by abstracting a benzylic hydrogen from another cumene molecule. This ...

  4. Cumene hydroperoxide - Wikipedia

    en.wikipedia.org/wiki/Cumene_hydroperoxide

    Products of decomposition of cumene hydroperoxide are methylstyrene, acetophenone, and 2-phenylpropan-2-ol. [3] It is produced by treatment of cumene with oxygen, an autoxidation. At temperatures >100 °C, oxygen is passed through liquid cumene: [4] C 6 H 5 (CH 3) 2 CH + O 2 → C 6 H 5 (CH 3) 2 COOH. Dicumyl peroxide is a side product.

  5. 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:

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

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  7. 2,4,6-Tri-tert-butylphenol - Wikipedia

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

    The oxidation of 2,4,6-tri-tert-butylphenol in the alkaline to the intensely blue-colored phenoxy radical can also occur with potassium ferricyanide. [1] [9] [6] The 2,4,6-tri-tert-butylphenoxy radical forms blue crystals on cooling to -70 °C which are stable at room temperature for several weeks and only gradually turn yellow. [9]

  8. Bisphenol A - Wikipedia

    en.wikipedia.org/wiki/Bisphenol_A

    An excess of phenol is used to ensure full condensation and to limit the formation of byproducts, such as Dianin's compound. BPA is fairly cheap to produce, as the synthesis benefits from a high atom economy and large amounts of both starting materials are available from the cumene process. [7]

  9. Naturally occurring phenols - Wikipedia

    en.wikipedia.org/wiki/Naturally_occurring_phenols

    In female elephants, the two compounds 3-ethyl phenol and 2-ethyl 4,5 dimethylphenol have been detected in urine samples. [70] Temporal glands secretion examination showed the presence of phenol, m-cresol and p-cresol (4-methyl phenol) during musth in male elephants. [71] [72] [73] p-Cresol and o-cresol are also components of the human sweat.