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1-Ethyl-3-methylimidazolium trifluoromethanesulfonate

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Products Intro: Product Name:1-Ethyl-3-methylimidazolium trifluoromethanesulfonate
CAS:145022-44-2
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CAS:145022-44-2
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CAS:145022-44-2
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CAS:145022-44-2
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Products Intro: Product Name:1-Ethyl-3-methylimidazolium trifluoromethanesulfonate
CAS:145022-44-2
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1-Ethyl-3-methylimidazolium trifluoromethanesulfonate Basic information
Product Name:1-Ethyl-3-methylimidazolium trifluoromethanesulfonate
Synonyms:1-Ethyl-3-methylimidazolium trifluoromet;1-ETHYL-3-METHYLIMIDAZOLIUM TRIFLUOROMETHANESULFONATE 98+%;EMIM Otf;EMIM Otf 1-Ethyl-3-methylimidazolium Triflate;1-Ethyl-;1-Ethyl-3-methylimidazole Trifluoromethanesulfonate;Ethyl-3-MethyliMidazoliuM trifluoroMethanesulfo;1-Ethyl-3-MethyliMidazoliuM trifluoroMethanesulfonate >=98.0% (T)
CAS:145022-44-2
MF:C7H11F3N2O3S
MW:260.23
EINECS:680-002-1
Product Categories:Chemical Synthesis;Imidazolium;Specialty Synthesis;Imidazolium Compounds;Imidazolium Salts (Ionic Liquids);Ionic Liquids;Synthetic Organic Chemistry
Mol File:145022-44-2.mol
1-Ethyl-3-methylimidazolium trifluoromethanesulfonate Structure
1-Ethyl-3-methylimidazolium trifluoromethanesulfonate Chemical Properties
Melting point -12°C
Boiling point >350 °C (lit.)
density 1.387 g/mL at 25 °C (lit.)
refractive index n20/D 1.435(lit.)
Fp >230 °F
storage temp. Store below +30°C.
form clear liquid
color Colorless to Light yellow to Light orange
Water Solubility Soluble in water.
LogP-2.5--2.2 at 23℃ and pH6.8
CAS DataBase Reference145022-44-2(CAS DataBase Reference)
ECW3.9 V
Safety Information
Hazard Codes Xi
Risk Statements 36/38
Safety Statements 26-36-24/25
WGK Germany 3
9-21
HazardClass IRRITANT
HS Code 29332900
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
1-Ethyl-3-methylimidazolium trifluoromethanesulfonate Usage And Synthesis
Conductivity9.84 mS/cm
Chemical PropertiesColorless liquid
Uses1-Ethyl-3-methylimidazolium trifluoromethanesulfonate may be used as a solvent to produce ionic polymer-polymer composites (IP2C) and also in lipase-catalyzed enantioselective amine acylation with 4-pentenoic acid.
UsesRecently used in the preparation of hydrophobic, highly conductive ambient-temperature molten salts, and in the preparation of dual intercalating molten electrolyte batteries.
1-Ethyl-3-methylimidazolium trifluoromethanesulfonate Preparation Products And Raw materials
Tag:1-Ethyl-3-methylimidazolium trifluoromethanesulfonate(145022-44-2) Related Product Information
Ethanol Ethyl acetate Ethyl propionate Trifluoromethanesulfonic acid Scandium trifluoromethanesulfonate Pefloxacin mesylate Trifluoromethanesulfonic anhydride Ethylparaben Levofloxacin Methylate 2-Ethoxyethanol Sodium trifluoromethanesulfonate Ethyl formate COPPER(II) TRIFLUOROMETHANESULFONATE YTTERBIUM(III) TRIFLUOROMETHANESULFONATE HYDRATE ISOXADIFEN-ETHYL Trinexapac-ethyl Lithium trifluoromethanesulfonate Diethyl ether