Styrene oxide
 | |
| Names | |
|---|---|
| IUPAC name
2-Phenyloxirane | |
| Other names
Phenyloxirane; Epoxystyrene; Styryl oxide; Phenylethylene oxide | |
| Identifiers | |
96-09-3  | |
| ChEBI | CHEBI:17907  |
| Jmol interactive 3D | Image |
| KEGG | C02083 |
| PubChem | 7276 |
| |
| 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 |
| EU classification (DSD) |
Harmful (XN); Corrosive (C) |
| R-phrases | R20 R22 R34 R36 R37 R38 |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| verify (what is ?) | |
| 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:[1]
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.[2]
Styrene oxide in the body is metabolized to mandelic acid, phenyl glyoxylic acid, benzoic acid and hippuric acid.
Stereospecific reaction
Since styrene oxide has a chiral center at the benzylic carbon atom, there are (R)-styrene oxide and (S)-styrene oxide. In addition, nucleophiles always attack the secondary carbon of the oxirane ring because of stability of the intermediate and steric hindrance. If optically pure reagent is used, only one optically pure compound will be obtained.
Toxicology
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.[3] Styrene oxide is subsequently hydrolyzed in vivo to styrene glycol by epoxide hydrolase.[4]
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.
References
- ↑ Harold Hibbert and Pauline Burt (1941). "Styrene Oxide". Org. Synth.; Coll. Vol. 1, p. 494
- ↑ Verfahren zur Herstellung von Phenylacetaldehyden, BASF-Patent DE3546372A1 vom 2. Juli 1987
- ↑ EPA Styrene Oxide evaluation
- ↑ Kenneth C. Liebman (1975). "Metabolism and toxicity of styrene" (PDF). Environmental Health Perspectives 11: 115–119. doi:10.2307/3428333. JSTOR 3428333.