methoxyethane
{{Chembox
| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 431257039
| Name = Methoxyethane
| ImageFile = Ethylmethylether Structural Formulae.png
| ImageName = Skeletal formula
| ImageFile1 = Methoxyethane-3D-balls.png
| ImageFile2 = Methoxyethane-3D-vdW.png
| ImageName1 = Ball-and-stick model
| PIN = Methoxyethane{{cite book | title = Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book) | publisher = The Royal Society of Chemistry | date = 2014 | location = Cambridge | page = 703 | doi = 10.1039/9781849733069-00648 | isbn = 978-0-85404-182-4}}
| SystematicName =
| OtherNames = ethyl methyl ether
| IUPACName =
| Section1 = {{Chembox Identifiers
| SMILES = COCC
| CASNo_Ref = {{cascite|correct|??}}
| CASNo = 540-67-0
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = TF7D64JK16
| PubChem = 10903
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 10441
| ChEBI_Ref = {{ebicite|changed|EBI}}
| ChEBI = 39832
| InChI = 1/C3H8O/c1-3-4-2/h3H2,1-2H3
| InChIKey = XOBKSJJDNFUZPF-UHFFFAOYAP
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 1S/C3H8O/c1-3-4-2/h3H2,1-2H3
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = XOBKSJJDNFUZPF-UHFFFAOYSA-N
}}
| Section2 = {{Chembox Properties
| C=3 | H=8 | O=1
| Appearance = Colorless gas{{CRC91|page=3-248}}
| Density = 0.7251 g cm−3 (at 0 °C)
| Solubility =
| MeltingPtC = -113
| BoilingPtC = 7.4
| RefractIndex = 1.3420 (at 4 °C)
| pKa =
| pKb =
| Viscosity = 0.224 cP at 25 °C
}}
| Section3 = {{Chembox Structure
| MolShape =
| Dipole =
}}
| Section4 =
| Section5 =
| Section6 =
| Section7 = {{Chembox Hazards
| ExternalSDS = [http://encyclopedia.airliquide.com/sds/en/053_AL_EN.pdf External MSDS]
| MainHazards = Extremely Flammable (F+),
Liquefied gas
}}
| Section8 = {{Chembox Related
| OtherFunction_label = Ethers
| OtherFunction = Dimethyl ether
Diethyl ether
Methoxypropane
}}
}}
Methoxyethane, also known as ethyl methyl ether, is a colorless gaseous ether with the formula {{chem2|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{{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 }} and solvent{{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}} have been investigated.
References
{{Molecules detected in outer space}}
{{Authority control}}
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