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Methoxyethane

Names
Preferred IUPAC name Methoxyethane
Other names ethyl methyl ether
Identifiers
CAS Number	540-67-0
3D model (JSmol)	Interactive image
ChEBI	CHEBI:39832
ChemSpider	10441
ECHA InfoCard	100.128.000
PubChem CID	10903
UNII	TF7D64JK16
CompTox Dashboard (EPA)	DTXSID5074557
InChI InChI=1S/C3H8O/c1-3-4-2/h3H2,1-2H3Key: XOBKSJJDNFUZPF-UHFFFAOYSA-N InChI=1/C3H8O/c1-3-4-2/h3H2,1-2H3Key: XOBKSJJDNFUZPF-UHFFFAOYAP
SMILES COCC
Properties
Chemical formula	C3H8O
Molar mass	60.096 g·mol
Appearance	Colorless gas
Density	0.7251 g cm (at 0 °C)
Melting point	−113 °C (−171 °F; 160 K)
Boiling point	7.4 °C (45.3 °F; 280.5 K)
Refractive index (nD)	1.3420 (at 4 °C)
Viscosity	0.224 cP at 25 °C
Hazards
Occupational safety and health (OHS/OSH):
Main hazards	Extremely Flammable (F+), Liquefied gas
Safety data sheet (SDS)	External MSDS
Related compounds
Related Ethers	Dimethyl ether Diethyl ether Methoxypropane
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). N verify (what is  ?) Infobox references

Methoxyethane, also known as ethyl methyl ether, is a colorless gaseous ether with the formula CH₃OCH₂CH₃. Unlike the related dimethyl ether and diethyl ether, which are widely used and studied, this mixed alkyl ether has no current applications. It is a structural isomer of isopropyl alcohol. Its utility as an anesthetic and solvent have been investigated.

References

1. Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 703. doi:10.1039/9781849733069-00648. ISBN 978-0-85404-182-4.
2. ^ Haynes, William M. (2010). Handbook of Chemistry and Physics (91 ed.). Boca Raton, Florida, USA: CRC Press. p. 3-248. ISBN 978-1-43982077-3.
3. Bovill, J. G. (2008). "Inhalation Anaesthesia; From Diethyl Ether to Xenon". Modern Anesthetics. Handbook of Experimental Pharmacology. Vol. 182. Springer. pp. 121–142. doi:10.1007/978-3-540-74806-9_6. ISBN 978-3-540-72813-9. PMID 18175089.
4. Campion, Christopher L.; Li, Wentao; Lucht, Brett L. (2005). "Thermal Decomposition of LiPF[sub 6]-Based Electrolytes for Lithium-Ion Batteries". Journal of the Electrochemical Society. 152 (12): A2327. doi:10.1149/1.2083267.

v t e Molecules detected in outer space
Molecules	Diatomic Aluminium monochloride Aluminium monofluoride Aluminium(II) oxide Argonium Carbon cation Carbon monophosphide Carbon monosulfide Carbon monoxide Cyano radical Diatomic carbon Fluoromethylidynium Helium hydride ion Hydrogen chloride Hydrogen fluoride Hydrogen (molecular) Hydroxyl radical Iron(II) oxide Magnesium monohydride Methylidyne radical Nitric oxide Nitrogen (molecular) Imidogen Sulfur mononitride Oxygen (molecular) Phosphorus monoxide Phosphorus mononitride Potassium chloride Silicon carbide Silicon monoxide Silicon monosulfide Sodium chloride Sodium iodide Sulfanyl Sulfur monoxide Titanium(II) oxide Triatomic Aluminium(I) hydroxide Aluminium isocyanide Amino radical Carbon dioxide Carbonyl sulfide CCP radical Chloronium Diazenylium Dicarbon monoxide Disilicon carbide Ethynyl radical Formyl radical Hydrogen cyanide (HCN) Hydrogen isocyanide (HNC) Hydrogen sulfide Hydroperoxyl Iron cyanide Isoformyl Magnesium cyanide Magnesium isocyanide Methylene N2H Nitrous oxide Nitroxyl Ozone Methylidynephosphane Potassium cyanide Trihydrogen cation Sodium cyanide Sodium hydroxide Silicon carbonitride c-Silicon dicarbide SiNC Sulfur dioxide Thioformyl Thioxoethenylidene Titanium dioxide Tricarbon Water Four atoms Acetylene Ammonia Isocyanic acid Cyanoethynyl Formaldehyde Fulminic acid HCCN Hydrogen peroxide Hydromagnesium isocyanide Isocyanic acid Isothiocyanic acid Ketenyl Methylene amidogen Methyl cation Methyl radical Propynylidyne Protonated carbon dioxide Protonated hydrogen cyanide Silicon tricarbide Thioformaldehyde Tricarbon monoxide Tricarbon monosulfide Thiocyanic acid Five atoms Ammonium ion Butadiynyl Carbodiimide Cyanamide Cyanoacetylene Cyanoformaldehyde Cyanomethyl Cyclopropenylidene Formic acid Isocyanoacetylene Ketene Methane Methoxy radical Methylenimine Propadienylidene Protonated formaldehyde Silane Silicon-carbide cluster Six atoms Acetonitrile Cyanobutadiynyl radical E-Cyanomethanimine Cyclopropenone Diacetylene Ethylene Formamide HC4N Ketenimine Methanethiol Methanol Methyl isocyanide Pentynylidyne Propynal Protonated cyanoacetylene Seven atoms Acetaldehyde Acrylonitrile Vinyl cyanide Cyanodiacetylene Ethylene oxide Glycolonitrile Hexatriynyl radical Propyne Methylamine Methyl isocyanate Vinyl alcohol Eight atoms Acetic acid Aminoacetonitrile Cyanoallene Ethanimine Glycolaldehyde Hexapentaenylidene Methylcyanoacetylene Methyl formate Acrolein Nine atoms Acetamide Cyanohexatriyne Dimethyl ether Ethanol Methyldiacetylene Octatetraynyl radical Propene Ethanethiol Propionitrile N-Methylformamide Ten atoms or more Acetone Benzene Benzonitrile Buckminsterfullerene (C60, C60, fullerene, buckyball) C70 fullerene Cyanodecapentayne Ethylene glycol Ethyl formate Methyl acetate Methyl-cyano-diacetylene Methyltriacetylene Propionaldehyde Butyronitrile Pyrimidine Heptatrienyl radical
Deuterated molecules	Ammonia Ammonium ion Formaldehyde Formyl radical Heavy water Hydrogen cyanide Hydrogen deuteride Hydrogen isocyanide Propyne N2D Trihydrogen cation
Unconfirmed	Anthracene Dihydroxyacetone Methoxyethane Glycine Graphene Hemolithin H2NCO Linear C5 Naphthalene cation Phosphine Pyrene Silylidyne
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