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  2. Styrene oxide - Wikipedia

    en.wikipedia.org/wiki/Styrene_oxide

    Styrene oxide is a main metabolite of styrene in humans or animals, resulting from oxidation by cytochrome P450. It is considered possibly carcinogenic from gavaging significant amounts into mice and rats. [4] Styrene oxide is subsequently hydrolyzed in vivo to styrene glycol by epoxide hydrolase. [5]

  3. Styrene - Wikipedia

    en.wikipedia.org/wiki/Styrene

    Styrene is regarded as a "known carcinogen", especially in case of eye contact, but also in case of skin contact, of ingestion and of inhalation, according to several sources. [20] [33] [34] [35] Styrene is largely metabolized into styrene oxide in humans, resulting from oxidation by cytochrome P450.

  4. List of reagents - Wikipedia

    en.wikipedia.org/wiki/List_of_reagents

    a mineral acid with many industrial uses; commonly used in the laboratory preparation of hydrogen halides Phosphorus pentachloride: one of the most important phosphorus chlorides; a chlorinating reagent. Also used as a dehydrating agent for oximes which turn them into nitriles. Phosphorus tribromide: used for the conversion of alcohols to alkyl ...

  5. Styrene monooxygenase - Wikipedia

    en.wikipedia.org/wiki/Styrene_monooxygenase

    as the first step of the aerobic styrene degradation pathway. [1] The product 2-phenyloxirane is also known as styrene oxide and can be converted by a styrene oxide isomerase (SOI) to obtain phenylacetaldehyde, which can be transformed into the key-intermediate phenylacetic acid by a phenylacetaldehyde dehydrogenase (PAD).

  6. Poly(p-phenylene oxide) - Wikipedia

    en.wikipedia.org/wiki/Poly(p-phenylene_oxide)

    Poly(p-phenylene oxide) (PPO), poly(p-phenylene ether) (PPE), poly(oxy-2,6-dimethyl-1,4-phenylene), often referred to simply as polyphenylene oxide, is a high-temperature thermoplastic with the general formula (C 8 H 8 O) n. It is rarely used in its pure form due to difficulties in processing.

  7. Epoxide - Wikipedia

    en.wikipedia.org/wiki/Epoxide

    Typical laboratory operations employ the Prilezhaev reaction. [10] [11] This approach involves the oxidation of the alkene with a peroxyacid such as mCPBA. Illustrative is the epoxidation of styrene with perbenzoic acid to styrene oxide: [12] The stereochemistry of the reaction is quite sensitive.

  8. Styrene-oxide isomerase - Wikipedia

    en.wikipedia.org/wiki/Styrene-oxide_isomerase

    The systematic name of this enzyme class is styrene-oxide isomerase (epoxide-cleaving). This enzyme is also called SOI. This enzyme participates in styrene degradation and is the second step of the pathway after the epoxidation of styrene by styrene monooxygenase. SOI is an integral membrane protein consisting of four transmembrane helices.

  9. Dehydrogenation - Wikipedia

    en.wikipedia.org/wiki/Dehydrogenation

    One of the largest scale dehydrogenation reactions is the production of styrene by dehydrogenation of ethylbenzene. Typical dehydrogenation catalysts are based on iron(III) oxide, promoted by several percent potassium oxide or potassium carbonate. [4] C 6 H 5 CH 2 CH 3 → C 6 H 5 CH=CH 2 + H 2