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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:
Product Name
Dimethyl ether, ≥99%
InChI key
LCGLNKUTAGEVQW-UHFFFAOYSA-N
InChI
1S/C2H6O/c1-3-2/h1-2H3
SMILES string
COC
vapor density
1.62 (vs air)
vapor pressure
>760 mmHg ( 25 °C)
assay
≥99%
autoignition temp.
662 °F
expl. lim.
27 %
bp
−24.8 °C (lit.)
mp
−141 °C (lit.)
functional group
ether
Quality Level
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Application
DME can be used as precursor for the production dimethyl sulfate by treatment with sulfur trioxide. Dimethyl sulfate is employed as a versatile methylating agent in chemical synthesis. It is also used as a starting material for preparation of dimethyl sulfide, acetic acid, unsaturated and saturated hydrocarbons, and formadehyde.
Dimethyl ether (DME) can be used as a precursor to synthesize methyl acetate, oligomeric oxymethylene ethers (OMEs), polyoxymethylene dimethyl ethers (DMMx) and light olefins.
General description
Dimethyl ether (DME) is the simplest aliphatic ether used as a reactant as well as a solvent in organic synthesis. It is used as a precursor for the preparation of important useful organic compounds. DME is also used as an aerosol propellant.
Packaging
Supplied in a Sure/Pac™ cylinder and has a brass needle valve with a male 1/4" NPTF outlet thread installed. Before using the cylinder, ensure that the valve is closed, then remove the galvanized steel hex cap that seals the outlet valve.
Compatible with the following:
Compatible with the following:
Legal Information
Aldrich is a registered trademark of Sigma-Aldrich Co. LLC
Sure/Pac is a trademark of Sigma-Aldrich Co. LLC
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, multi-purpose combination respirator cartridge (US)
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Nature and Location of Carbonaceous Species in a Composite HZSM-5 Zeolite Catalyst during the Conversion of Dimethyl Ether into Light Olefins.
Iba?ez M, et al.
Catalysts, 7(9), 254-254 (2017)
Synthesis of Polyoxymethylene Dimethyl Ethers from Dimethyl Ether Direct Oxidation over Carbon?Based Catalysts.
Gao X-Y, et al.
ChemCatChem, 10(1), 273-279 (2018)
The carbonylation of dimethyl ether catalyzed by supported heteropoly acids: The role of Br?nsted acid properties.
Shen H, et al.
Catalysis Today (2018)
Carbonylation of dimethyl ether over Co-HMOR.
Ma M,et al.
Catalysis Science & Technology, 8(8), 2124-2130 (2018)
Dimethyl ether
Muller M, et al.
Ullmann's Encyclopedia of Industrial Chemistry (2000)
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