Dimethyl ether
|  | |||
| Names | |||
|---|---|---|---|
| Preferred IUPAC name Methoxymethane | |||
| Other names Dimethyl ether R-E170 Demeon Dimethyl oxide Dymel A Methyl ether Methyl oxide Mether Wood ether | |||
| Identifiers | |||
| 3D model (JSmol) | |||
| Abbreviations | DME | ||
| 1730743 | |||
| ChEBI | |||
| ChEMBL | |||
| ChemSpider | |||
| ECHA InfoCard | 100.003.696 | ||
| EC Number | 
 | ||
| KEGG | |||
| MeSH | Dimethyl+ether | ||
| PubChem CID | |||
| RTECS number | 
 | ||
| UNII | |||
| UN number | 1033 | ||
| CompTox Dashboard (EPA) | |||
| 
 | |||
| 
 | |||
| Properties | |||
| C2H6O | |||
| Molar mass | 46.069 g·mol−1 | ||
| Appearance | Colorless gas | ||
| Odor | Ethereal | ||
| Density | 2.1146 kg m−3 (gas, 0 °C, 1013 mbar) 0.735 g/mL (liquid, −25 °C) | ||
| Melting point | −141 °C; −222 °F; 132 K | ||
| Boiling point | −24 °C; −11 °F; 249 K | ||
| 71 g/L (at 20 °C (68 °F)) | |||
| log P | 0.022 | ||
| Vapor pressure | 592.8 kPa | ||
| −26.3×10−6 cm3 mol−1 | |||
| 1.30 D | |||
| Thermochemistry | |||
| Heat capacity (C) | 65.57 J K−1 mol−1 | ||
| Std enthalpy of formation (ΔfH⦵298) | −184.1 kJ mol−1 | ||
| Std enthalpy of combustion (ΔcH⦵298) | −1460.4 kJ mol−1 | ||
| Hazards | |||
| GHS labelling: | |||
| Danger | |||
| H220 | |||
| P210, P377, P381, P403 | |||
| NFPA 704 (fire diamond) | |||
| Flash point | −41 °C (−42 °F; 232 K) | ||
| 350 °C (662 °F; 623 K) | |||
| Explosive limits | 27 % | ||
| Safety data sheet (SDS) | ≥99% Sigma-Aldrich | ||
| Related compounds | |||
| Related ethers | Diethyl ether | ||
| Related compounds | Ethanol | ||
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |||
Dimethyl ether (DME; also known as methoxymethane) is the organic compound with the formula CH3OCH3, (sometimes ambiguously simplified to C2H6O as it is an isomer of ethanol). The simplest ether, it is a colorless gas that is a useful precursor to other organic compounds and an aerosol propellant that is currently being demonstrated for use in a variety of fuel applications.
Dimethyl ether was first synthesised by Jean-Baptiste Dumas and Eugene Péligot in 1835 by distillation of methanol and sulfuric acid.