38912
Dimethyl ether
puriss., ≥99.9% (GC)
Synonym(s):
Methyl ether
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About This Item
Linear Formula:
(CH3)2O
CAS Number:
Molecular Weight:
46.07
Beilstein:
1730743
EC Number:
MDL number:
UNSPSC Code:
12142100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
vapor density
1.62 (vs air)
vapor pressure
>760 mmHg ( 25 °C)
grade
puriss.
Assay
≥99.9% (GC)
autoignition temp.
662 °F
expl. lim.
27 %
bp
−24.8 °C (lit.)
mp
−141 °C (lit.)
SMILES string
COC
InChI
1S/C2H6O/c1-3-2/h1-2H3
InChI key
LCGLNKUTAGEVQW-UHFFFAOYSA-N
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General description
Dimethyl ether (DME) is the simplest aliphatic ether used as a reactant as well as a solvent in organic synthesis. It is also used as a precursor for the preparation of important useful organic compounds such as dimethyl carbonate, methyl acetate, propylene and chloromethyl ether.
Application
DME can be used as a precursor for the preparation of versatile methylating agents such as dimethyl sulfate and trimethyloxonium tetrafluoroborate.
Packaging
Cylinder with net 1.1 kg
DIN 477 nr.1
Other Notes
Sales restrictions may apply
Recommended products
Z742161 DIN 1 Regulator OR 99112 outlet Valve
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Gas 1A - Press. Gas Liquefied gas
Storage Class Code
2A - Gases
WGK
WGK 1
Flash Point(F)
-41.8 °F - closed cup
Flash Point(C)
-41 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Organic Syntheses, 50(4), 1019-1023 (1988)
Direct dimethyl ether synthesis
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Journal of natural gas chemistry, 12(4), 219-227 (2003)
Dimethyl ether (DME) as an alternative fuel
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Journal of Power Sources, 156(2), 497-511 (2006)
Kazuyuki Oshita et al.
Chemosphere, 78(9), 1148-1154 (2010-01-02)
We investigated whether polychlorinated biphenyls (PCBs) and water could be simultaneously removed from river sediment by solvent extraction using liquefied dimethyl ether (DME) as the extractant. DME exists in a gaseous state at normal temperature and pressure and can dissolve
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