Styrene oxide
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IUPAC name
2-Phenyloxirane
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| Other names
Phenyloxirane; Epoxystyrene; Styryl oxide; Phenylethylene oxide
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| Identifiers | |
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3D model (JSmol)
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| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.002.252 |
| KEGG | |
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PubChem CID
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| Properties | |
| C8H8O | |
| Molar mass | 120.15 g·mol−1 |
| Appearance | Colorless to light yellow liquid |
| Density | 1.052 g/mL |
| Melting point | −37 °C (−35 °F; 236 K) |
| Boiling point | 194 °C (381 °F; 467 K) |
| Hazards | |
| Safety data sheet | Oxford University MSDS |
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EU classification (DSD) (outdated)
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Harmful (XN); Corrosive (C) |
| R-phrases (outdated) | R20 R22 R34 R36 R37 R38 |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| Infobox references | |
Styrene oxide is an epoxide derived from styrene. It can be prepared by epoxidation of styrene with peroxybenzoic acid, in the Prilezhaev reaction:
Styrene oxide is slightly soluble in water. Trace amount of acid in water causes hydrolysis to racemic phenylethyleneglycol via aryl cation. If the amount of water is not sufficient, acid-catalyzed isomerization for phenylacetaldehyde will occur.
Styrene oxide in the body is metabolized to mandelic acid, phenyl glyoxylic acid, benzoic acid and hippuric acid.
Since styrene oxide has a chiral center at the benzylic carbon atom, there are (R)-styrene oxide and (S)-styrene oxide. If optically pure reagent is used, only one optically pure compound will be obtained.
Styrene oxide is a main metabolite of styrene in humans or animals, resulting from oxidation by . It is considered possibly carcinogenic from gavaging significant amounts into mice and rats. Styrene oxide is subsequently hydrolyzed in vivo to styrene glycol by epoxide hydrolase.
Styrene oxide has a chiral center and thus two enantiomers. It has been reported that the two enantiomers had different toxicokinetics and toxicity. It was reported that the (R)-styrene oxide was preferentially formed in mice, especially in the lung, whereas the (S)-styrene oxide was preferentially generated in rats. In human volunteers, the cumulative excretion of the (S)-enantiomer of styrene glycol and mendelic acid were higher than the R form after exposure to styrene. In human liver microsomes, cytochrome P450-mediated styrene oxidation showed the production of more S enantiomer relative to the R enantiomer. It was also found that (S)-styrene oxide was preferentially hydrolyzed than the R enantiomer in human liver microsomes. Animal studies have shown that the (R)-enantiomer of styrene oxide was more toxic than the (S)-enantiomer in mice.
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