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1-Ethyl-3-methylimidazolium trifluoromethanesulfonate

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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
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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.)
Flash point:
>230 °F
storage temp. 
Store below +30°C.
form 
clear liquid
color 
Colorless to Light yellow to Light orange
Water Solubility 
Soluble in water.
InChI
InChI=1S/C6H11N2.CHF3O3S/c1-3-8-5-4-7(2)6-8;2-1(3,4)8(5,6)7/h4-6H,3H2,1-2H3;(H,5,6,7)/q+1;/p-1
InChIKey
ZPTRYWVRCNOTAS-UHFFFAOYSA-M
SMILES
N1(CC)C=C[N+](C)=C1.C(F)(F)(F)S([O-])(=O)=O
LogP
-2.5--2.2 at 23℃ and pH6.8
CAS DataBase Reference
145022-44-2(CAS DataBase Reference)
ECW
3.9 V
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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

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1-Ethyl-3-methylimidazolium trifluoromethanesulfonate Usage And Synthesis

Conductivity

9.84 mS/cm

Chemical Properties

Colorless liquid

Uses

Recently used in the preparation of hydrophobic, highly conductive ambient-temperature molten salts, and in the preparation of dual intercalating molten electrolyte batteries.

Uses

1-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.

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