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
UNSPSC Code:
12142100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-065-8
Beilstein/REAXYS Number:
1730743
MDL number:
Assay:
≥99.9% (GC)
vapor density
1.62 (vs air)
Quality Level
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.)
functional group
ether
SMILES string
COC
InChI
1S/C2H6O/c1-3-2/h1-2H3
InChI key
LCGLNKUTAGEVQW-UHFFFAOYSA-N
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
Z742161 DIN 1 Regulator OR 99112 outlet Valve
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signalword
Danger
hcodes
Hazard Classifications
Flam. Gas 1A - Press. Gas Liquefied gas
Storage Class
2A - Gases
wgk
WGK 1
flash_point_f
-41.8 °F - closed cup
flash_point_c
-41 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves
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Dimethyl ether
Muller M, et al.
Ullmann's Encyclopedia of Industrial Chemistry, 156(2), 497-511 (2000)
Trimethyloxonium tetrafluoroborate
Curphey, TJ
Organic Syntheses, 50(4), 1019-1023 (1988)
Direct dimethyl ether synthesis
Ogawa T, et al.
Journal of natural gas chemistry, 12(4), 219-227 (2003)