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Merck
CN

724416

Sigma-Aldrich

1,2-Dimethyl-3-propylimidazolium bis(trifluoromethylsulfonyl)imide

for energy applications

Synonym(s):

DMPIIm

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About This Item

Empirical Formula (Hill Notation):
C10H15F6N3O4S2
CAS Number:
169051-76-7
Molecular Weight:
419.36
MDL number:
MFCD03788922
UNSPSC Code:
26111700
PubChem Substance ID:
329764084
NACRES:
NA.23

Key Documents

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Assay

99.9% trace metals basis

form

liquid

impurities

≤0.5% H2O

refractive index

n20/D 1.433

mp

15 °C (lit.)

density

1.436 g/mL at 25 °C

application(s)

battery manufacturing

SMILES string

CCC[n+]1ccn(C)c1C.FC(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F

InChI

1S/C8H15N2.C2F6NO4S2/c1-4-5-10-7-6-9(3)8(10)2;3-1(4,5)14(10,11)9-15(12,13)2(6,7)8/h6-7H,4-5H2,1-3H3;/q+1;-1

InChI key

XOZHIVUWCICHSQ-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319

Precautionary Statements

P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKBQ1447V
MKBK1805V
MKBH9838V
MKBH5267V
MKBD9431

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Shiro Seki et al.
The journal of physical chemistry. B, 110(21), 10228-10230 (2006-05-26)
Highly reversible, safe lithium secondary batteries that use imidazolium-cation-based room-temperature ionic liquid as an electrolyte and lithium metal as an anode material were realized by the molecular design. To achieve higher reduction stability, an electron-donating substituent was introduced to promote
Navarra, M. A.; Panero, S.; Scrosati, B.
Electrochemical and Solid-State Letters, 8, A324-A324 (2005)
Koch, V. R.; Nanjundiah, C.; Appetecchi, G. Battista; Scrosati, B.
Journal of the Electrochemical Society, 142, L116-L116 (1995)
Ueki, Takeshi; Arai, Asako Ayusawa; Kodama, Kiochi
Pure and Applied Chemistry. Chimie Pure Et Appliquee, 81, 1829-1829 (2009)

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