Dioxolane
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| Names | |||
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| Preferred IUPAC name
1,3-Dioxolane | |||
| Systematic IUPAC name
1,3-Dioxacyclopentane | |||
| Other names
Dioxolane 5-Crown-2 Formal glycol | |||
| Identifiers | |||
3D model (JSmol) |
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| ChEBI | |||
| ChEMBL | |||
| ChemSpider | |||
| ECHA InfoCard | 100.010.422 | ||
| EC Number |
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PubChem CID |
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| UNII | |||
| UN number | 1166 | ||
CompTox Dashboard (EPA) |
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| Properties | |||
| C3H6O2 | |||
| Molar mass | 74.08 g/mol | ||
| Density | 1.06 g/cm3 | ||
| Melting point | −95 °C (−139 °F; 178 K) | ||
| Boiling point | 75 °C (167 °F; 348 K) | ||
| Hazards | |||
| GHS labelling: | |||
| Danger | |||
| H225 | |||
| P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, P501 | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |||
Dioxolane is a heterocyclic acetal with the chemical formula (CH2)2O2CH2. It is related to tetrahydrofuran (THF) by replacement of the methylene group (CH2) at the 2-position with an oxygen atom. The corresponding saturated 6-membered C4O2 rings are called dioxanes. The isomeric 1,2-dioxolane (wherein the two oxygen centers are adjacent) is a peroxide. 1,3-dioxolane is used as a solvent and as a comonomer in polyacetals.