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Tetrabutylammonium bis-trifluoromethanesulfonimidate

for electronic purposes, ≥99.0%

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Linear Formula:
(CH3CH2CH2CH2)4N[N(SO2CF3)2
CAS Number:
210230-40-3
Molecular Weight:
522.61
Beilstein:
8247973
MDL number:
MFCD01863113
UNSPSC Code:
26111700
PubChem Substance ID:
329769492
NACRES:
NB.61

grade

for electronic purposes

Quality Level

100

Assay

≥99.0% (qNMR)
≥99.0%

form

crystals

mp

90-95 °C

SMILES string

FC(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F.CCCC[N+](CCCC)(CCCC)CCCC

InChI

1S/C16H36N.C2F6NO4S2/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;3-1(4,5)14(10,11)9-15(12,13)2(6,7)8/h5-16H2,1-4H3;/q+1;-1

InChI key

CFAPFDTWIGBCQK-UHFFFAOYSA-N

Related Categories

General description

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Application


  • The cohesive properties and pyrolysis mechanism of an aprotic ionic liquid tetrabutylammonium bis(trifluoromethanesulfonyl)imide.: This study investigates the cohesive properties and thermal decomposition mechanism of tetrabutylammonium bis(trifluoromethanesulfonyl)imide, providing insights into its stability and potential applications in analytical and materials chemistry (Liu et al., 2023).

Other Notes

Novel type of electrolyte, used e.g. in electrical double layer capacitors

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Daniel Hirshberg et al.
ACS applied materials & interfaces, 10(13), 10860-10869 (2018-03-08)
Using UV-vis spectroscopy in conjunction with various electrochemical techniques, we have developed a new effective operando methodology for investigating the oxygen reduction reactions (ORRs) and their mechanisms in nonaqueous solutions. We can follow the in situ formation and presence of
M. Ue et al.
Journal of the Electrochemical Society, 141, 3366-3366 (1994)

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