Names | |
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IUPAC name
1,2-Dimethoxyethane
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Other names
DME, glyme, Ethylene glycol dimethyl ether, monoglyme,
dimethyl glycol, dimethyl cellosolve |
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Identifiers | |
110-71-4 | |
3D model (Jmol) | Interactive image |
ChEBI | CHEBI:42263 |
ChemSpider | 13854808 |
ECHA InfoCard | 100.003.451 |
RTECS number | KI1451000 |
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Properties | |
C4H10O2 | |
Molar mass | 90.12 g·mol−1 |
Appearance | Colorless liquid |
Density | 0.8683 g/cm3 |
Melting point | −58 °C (−72 °F; 215 K) |
Boiling point | 85 °C (185 °F; 358 K) |
miscible | |
Hazards | |
EU classification (DSD)
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Flammable (F) Toxic (T) Repr. Cat. 2 |
R-phrases | R60, R61, R11, R19, R20 |
S-phrases | S53, S45 |
NFPA 704 | |
Flash point | −2 °C (28 °F; 271 K) |
Related compounds | |
Related Ethers
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Dimethoxymethane |
Related compounds
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Ethylene glycol 1,4-Dioxane Diethylene glycol dimethyl ether |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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what is ?) | (|
Infobox references | |
Dimethoxyethane, also known as glyme, monoglyme, dimethyl glycol, ethylene glycol dimethyl ether, dimethyl cellosolve, and DME, is a clear, colorless, aprotic, and liquid ether that is used as a solvent, especially in batteries. Dimethoxyethane is miscible with water.
Monoglyme may be manufactured by a number of methods:
Together with a high-permittivity solvent (e.g. propylene carbonate), dimethoxyethane is used as the low-viscosity component of the solvent for electrolytes of lithium batteries. In the laboratory, DME is used as a coordinating solvent.
Dimethoxyethane is often used as a higher boiling alternative to diethyl ether and THF. Dimethoxyethane forms chelate complexes with cations and acts as a bidentate ligand. It is therefore often used in organometallic chemistry like Grignard reactions, hydride reductions, and palladium-catalyzed reactions like Suzuki reactions and Stille couplings. Dimethoxyethane is also a good solvent for oligo- and polysaccharides.