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900804

Sigma-Aldrich

1-Butyl-2,3-dimethylimidazolium bis(trifluoromethylsulfonyl)imide

≥99%, H2O <500 ppm

Synonym(s):

1-Butyl-2,3-dimethylimidazolium bis(trifluoromethylsulfonyl)amide, 1-Butyl-2,3-dimethylimidazolium bistriflamide

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About This Item

Empirical Formula (Hill Notation):
C11H17F6N3O4S2
CAS Number:
350493-08-2
Molecular Weight:
433.39
MDL number:
MFCD30342166
UNSPSC Code:
12352107
NACRES:
NA.23

Quality Level

100

Assay

≥99%

form

liquid

composition

H2O, <500 ppm

impurities

≤500 ppm H2O

bp

430 °C (decomp(lit.))

mp

-76 °C (lit.)

density

1.4059 g/cm3

application(s)

battery manufacturing

InChI

1S/C9H17N2.C2F6NO4S2/c1-4-5-6-11-8-7-10(3)9(11)2;3-1(4,5)14(10,11)9-15(12,13)2(6,7)8/h7-8H,4-6H2,1-3H3;/q+1;-1

InChI key

UCCKRVYTJPMHRO-UHFFFAOYSA-N

Application

Ionic liquids (ILs) are molten salts with melting points lower than 100 °C. They usually consist of pair of organic cation and anion. ILs exhibit unique properties such as non-volatility, high thermal stability, and high ionic conductivity and find applications as electrolytes in lithium/sodium ion batteries and dye-sensitized solar cells. They are also used as media for synthesis of conducting polymers and intercalation electrode materials.

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Pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

Signal Word

Danger

Hazard Statements

H301,H318

Hazard Classifications

Acute Tox. 3 Oral - Eye Dam. 1

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

230.0 °F

Flash Point(C)

110 °C

Certificates of Analysis (COA)

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Ionic liquids and their solid-state analogues as materials for energy generation and storage.
MacFarlane DR, et al.
Nature Reviews. Materials, 1, 15005-15005 (2016)
Masayoshi Watanabe et al.
Chemical reviews, 117(10), 7190-7239 (2017-01-14)
Ionic liquids (ILs) are liquids consisting entirely of ions and can be further defined as molten salts having melting points lower than 100 °C. One of the most important research areas for IL utilization is undoubtedly their energy application, especially
Dandan Han et al.
Molecules (Basel, Switzerland), 15(4), 2405-2426 (2010-04-30)
Ionic liquids (ILs) have been applied in different areas of separation, such as ionic liquid supported membranes, as mobile phase additives and surface-bonded stationary phases in chromatography separations and as the extraction solvent in sample preparations, because they can be

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