1,2-Dioxane
| Names | |
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| Preferred IUPAC name
1,2-Dioxane | |
| Other names
o-Dioxane | |
| Identifiers | |
3D model (JSmol) |
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| UNII | |
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| Properties | |
| C4H8O2 | |
| Molar mass | 88.106 g·mol−1 |
| Appearance | colorless liquid |
| Boiling point | 116–117 °C (241–243 °F; 389–390 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
1,2-Dioxane or o-dioxane is an organic compound with the molecular formula (CH2)4O2, classified as a cyclic peroxide. Its synthesis was reported in 1956 by Criegee and Müller, who prepared it by reacting butane-1,4-diol bis(methanesulfonate) with hydrogen peroxide and distilled it as a colorless liquid. Acids and bases decompose it to gamma-hydroxybutyraldehyde.
Substituted 1,2-dioxanes have also been prepared, and some have been isolated from natural sources.