1-Ethyl-3-methylimidazolium chloride: Difference between revisions
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Script assisted update of identifiers for the Chem/Drugbox validation project (updated: 'ChEBI'). |
Updating {{chembox}} (no changed fields - added verified revid - updated 'DrugBank_Ref', 'UNII_Ref', 'ChEMBL_Ref', 'ChEBI_Ref', 'KEGG_Ref', 'StdInChI_Ref', 'StdInChIKey_Ref') per [[Wikipedia:WikiProject Chemicals/Chembox validation|Chem/Drugbox valid |
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| verifiedrevid = |
| verifiedrevid = 443256069 |
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| ImageFile = 1-ethyl-3-methylimidazolium chloride.png |
| ImageFile = 1-ethyl-3-methylimidazolium chloride.png |
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| Section1 = {{Chembox Identifiers |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChEBI_Ref = {{ebicite|correct|EBI}} |
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| ChEBI = 61326 |
| ChEBI = 61326 |
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| ChemSpiderID = 151883 |
| ChemSpiderID = 151883 |
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| InChIKey = NJMWOUFKYKNWDW-UHFFFAOYAA |
| InChIKey = NJMWOUFKYKNWDW-UHFFFAOYAA |
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| SMILES1 = CCn1cc[n+](c1)C |
| SMILES1 = CCn1cc[n+](c1)C |
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| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChI = 1S/C6H11N2/c1-3-8-5-4-7(2)6-8/h4-6H,3H2,1-2H3/q+1 |
| StdInChI = 1S/C6H11N2/c1-3-8-5-4-7(2)6-8/h4-6H,3H2,1-2H3/q+1 |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey = NJMWOUFKYKNWDW-UHFFFAOYSA-N |
| StdInChIKey = NJMWOUFKYKNWDW-UHFFFAOYSA-N |
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| CASNo = 65039-09-0 |
| CASNo = 65039-09-0 |
Revision as of 22:48, 5 August 2011
Names | |
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IUPAC name
3-Ethyl-1-methyl-3H-imidazol-1-ium chloride
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Other names
[EMIM]Cl
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.129.917 |
CompTox Dashboard (EPA)
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Properties | |
C6H11ClN2 | |
Molar mass | 146.62 g·mol−1 |
Melting point | 77-79 °C |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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1-Ethyl-3-methylimidazolium chloride or [EMIM]Cl is an ionic liquid that can be used in cellulose processing.[1][2] The cation consists of a five-membered ring with two nitrogen and three carbon atoms, i.e. a derivative of imidazole, with ethyl and methyl groups substituted at the two nitrogen atoms.[3] Its melting point is 77-79 °C.[4]
References
- ^ Scientists Propose a More Efficient Way to Make Ethanol, The New York Times, March 2, 2010
- ^ Joseph B. Binder and Ronald T. Raines (2010). "Fermentable sugars by chemical hydrolysis of biomass" (PDF). PNAS. 107 (10): 4516–4521. doi:10.1073/pnas.0912073107. PMID 20194793.
- ^ 1-Ethyl-3-methylimidazolium chloride, chemexper.com
- ^ MSDS