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{{Chembox |
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| Verifiedfields = changed |
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| verifiedrevid = 409682494 |
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| Watchedfields = changed |
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| Name = Methoxyethane |
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| verifiedrevid = 431257039 |
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| ImageFile = Ethylmethylether Structural Formulae.png |
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| Name = Methoxyethane |
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| ImageName = Skeletal formula |
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| ImageFile = Ethylmethylether Structural Formulae.png |
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| ImageFile1 = Methoxyethane-3D-balls.png |
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| ImageName = Skeletal formula |
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| ImageName1 = Ball-and-stick model |
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| IUPACName = Methoxyethane |
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| ImageFile1 = Methoxyethane-3D-balls.png |
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| ImageFile2 = Methoxyethane-3D-vdW.png |
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| OtherNames = Methyl ethyl ether<br />Ethyl methyl ether |
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| ImageName1 = Ball-and-stick model |
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| Section1 = {{Chembox Identifiers |
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| PIN = Methoxyethane<ref name=iupac2013>{{cite book | title = Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book) | publisher = ] | date = 2014 | location = Cambridge | page = 703 | doi = 10.1039/9781849733069-00648 | isbn = 978-0-85404-182-4}}</ref> |
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| SMILES = COCC |
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| SystematicName = |
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| CASNo = 540-67-0 |
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| OtherNames = ethyl methyl ether |
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| PubChem = 10903 |
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| IUPACName = |
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}} |
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| Section2 = {{Chembox Properties |
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| Section1 = {{Chembox Identifiers |
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| SMILES = COCC |
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| C=3|H=8|O=1 |
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| CASNo_Ref = {{cascite|correct|??}} |
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| Appearance = Clear, colorless liquid |
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| Density = |
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| CASNo = 540-67-0 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| Solubility = |
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| UNII = TF7D64JK16 |
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| MeltingPtC = -139 |
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| BoilingPtC = 7.6 |
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| PubChem = 10903 |
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| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} |
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| pKa = |
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| ChemSpiderID = 10441 |
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| ChEBI_Ref = {{ebicite|changed|EBI}} |
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| Viscosity = 0.224 ] at 25 °C |
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| ChEBI = 39832 |
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| InChI = 1/C3H8O/c1-3-4-2/h3H2,1-2H3 |
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| Section3 = {{Chembox Structure |
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| InChIKey = XOBKSJJDNFUZPF-UHFFFAOYAP |
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| StdInChI = 1S/C3H8O/c1-3-4-2/h3H2,1-2H3 |
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| Section3 = {{Chembox Structure |
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| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} |
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| Dipole = |
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| StdInChIKey = XOBKSJJDNFUZPF-UHFFFAOYSA-N |
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| Section7 = {{Chembox Hazards |
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| Section2 = {{Chembox Properties |
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| ExternalMSDS = |
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| C=3 | H=8 | O=1 |
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| MainHazards = Extremely Flammable (F+),<br /> Liquefied gas |
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| Appearance = Colorless gas<ref name="CRC">{{CRC91|page=3-248}}</ref> |
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| Density = 0.7251 g cm<sup>−3</sup> (at 0 °C)<ref name="CRC" /> |
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| Section8 = {{Chembox Related |
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| Solubility = |
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| Function = ]s |
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| MeltingPtC = -113 |
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| OtherFunctn = ]<br />]<br />]}} |
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| BoilingPtC = 7.4 |
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| RefractIndex = 1.3420 (at 4 °C)<ref name="CRC" /> |
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| pKa = |
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| Viscosity = 0.224 ] at 25 °C |
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| Section7 = {{Chembox Hazards |
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| ExternalSDS = |
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| MainHazards = Extremely Flammable (F+),<br /> Liquefied gas |
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| Section8 = {{Chembox Related |
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| OtherFunction_label = ]s |
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| OtherFunction = ]<br />]<br />] |
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'''Methoxyethane''', also known as '''ethyl methyl ether''', is a colorless gaseous ] with the formula {{chem2|CH3OCH2CH3}}. Unlike the related ] and ], which are widely used and studied, this mixed alkyl ether has no current applications. It is a ] of ]. Its utility as an anesthetic<ref>{{cite book|chapter=Inhalation Anaesthesia; From Diethyl Ether to Xenon |author=Bovill, J. G.|title=Modern Anesthetics |series=Handbook of Experimental Pharmacology|year=2008|volume=182|issue=182 |pages=121–142|publisher=Springer|doi=10.1007/978-3-540-74806-9_6|pmid=18175089 |isbn=978-3-540-72813-9 }}</ref> and solvent<ref>{{cite journal |doi=10.1149/1.2083267|title=Thermal Decomposition of LiPF[sub 6]-Based Electrolytes for Lithium-Ion Batteries|year=2005|last1=Campion|first1=Christopher L.|last2=Li|first2=Wentao|last3=Lucht|first3=Brett L.|journal=Journal of the Electrochemical Society|volume=152|issue=12|pages=A2327|doi-access=free}}</ref> have been investigated. |
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'''Methoxyethane''', also known as '''ethyl methyl ether''', is an ] with a bonded ]. Methoxyethane is a colorless gaseous ] with a medicine-like odor. It is extremely flammable, and its inhalation may cause ] or dizzyness. As a ], it can react with ]s to form salts and reacts violently with ]s. |
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==References== |
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==References== |
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{{Molecules detected in outer space}} |
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{{Unreferenced|date=May 2010}} |
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{{Authority control}} |
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