Trioctylmethylammonium bis(trifluoromethylsulfonyl)imide

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Trioctylmethylammonium bis(trifluoromethylsulfonyl)imide
Trioctylmethylammonium bis(trifluoromethylsulfonyl)imide.png
Preferred IUPAC name
N-methyl-N,N-di(octyl)octan-1-aminium bis(trifluoromethanesulfonyl)azanide
Other names
Methyl-trioctylammonium bis(trifluoromethylsulfonyl)imide [1]
3D model (JSmol)
ECHA InfoCard 100.157.714 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 629-541-6
PubChem CID
  • InChI=1S/C25H54N.C2F6NO4S2/c1-5-8-11-14-17-20-23-26(4,24-21-18-15-12-9-6-2)25-22-19-16-13-10-7-3;3-1(4,5)14(10,11)9-15(12,13)2(6,7)8/h5-25H2,1-4H3;/q+1;-1 X mark.svgN
Molar mass 648.85 g·mol−1
GHS labelling: [2]
H315, H319, H335
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P332+P313, P337+P313, P362, P403+P233, P405
Flash point >110 °C
Related compounds
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Trioctylmethylammonium bis(trifluoromethylsulfonyl)imide is an ionic liquid [3] that is produced by Solvent Innovation, now part of EMD Chemicals.

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  1. See PubChem
  2. "Methyltrioctylammonium bis(trifluoromethylsulfonyl)imide". Retrieved 12 December 2021.
  3. Fraile, J. M.; Garcia, J. I.; Herrerias, C. I.; Mayoral, J. A.; Carrie, D.; Vaultier, M. (2001). "Enantioselective cyclopropanation reactions in ionic liquids". Tetrahedron: Asymmetry. 12 (13): 1891–1894. doi:10.1016/s0957-4166(01)00315-9. hdl: 10261/64635 .