711756
1-Ethyl-3-methylimidazolium trifluoromethanesulfonate
≥98% (H-NMR)
Synonym(s):
EMIM Otf
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Quality Level
Assay
≥98% (H-NMR)
form
liquid
impurities
≤0.5% water
refractive index
n20/D 1.435 (lit.)
bp
>350 °C (lit.)
density
1.387 g/mL at 25 °C (lit.)
functional group
fluoro
triflate
SMILES string
CCn1cc[n+](C)c1.[O-]S(=O)(=O)C(F)(F)F
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
InChI key
ZPTRYWVRCNOTAS-UHFFFAOYSA-M
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Application
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.
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point(F)
425.3 °F - closed cup
Flash Point(C)
218.5 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Heat capacities and excess enthalpies of 1-ethyl-3-methylimidazolium-based ionic liquids and water
Journal of Chemical and Engineering Data, 53.9, 2112-2119 (2008)
A study on IP2C actuators using ethylene glycol or EmI-Tf as solvent.
Smart Materials and Structures, 20(4), 045014-045014 (2011)
Capillary electrophoretic application of 1-alkyl-3-methylimidazolium-based ionic liquids
Analytical Chemistry, 73.16, 3838-3844 (2001)
Investigation of ionic liquids as reaction media for enzymatic enantioselective acylation of amines.
Journal of Molecular Catalysis. B, Enzymatic, 30(5), 189-194 (2004)
Ion-pair structure of vaporized ionic liquid studied by matrix-isolation FTIR spectroscopy with DFT calculations: A case of 1-ethyl-3-methylimidazolium trifluoromethanesulfonate
The Journal of Physical Chemistry A, 114.48, 12662-12666 (2010)
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