Trioctylmethylammonium bis(trifluoromethylsulfonyl)imide

Trioctylmethylammonium bis(trifluoromethylsulfonyl)imide

Names
Other names Methyl-trioctylammonium bis(trifluoromethylsulfonyl)imide[citation needed]
Identifiers
CAS Number	375395-33-8 Y
3D model (JSmol)	Interactive image Interactive image
ChEMBL	ChEMBL561679 ‹See TfM›N
ChemSpider	17339079 ‹See TfM›N
ECHA InfoCard	100.157.714
PubChem CID	16211009
InChI 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 ‹See TfM›N Key: LAGQNGWYNLUQRI-UHFFFAOYSA-N ‹See TfM›N
SMILES FC(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F.CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC O=S([N-]S(=O)(C(F)(F)F)=O)(C(F)(F)F)=O.CCCCCCCC[N+](CCCCCCCC)(C)CCCCCCCC
Properties
Chemical formula	C27H54F6N2O4S2
Molar mass	648.85 g·mol−1
Hazards
EU classification (DSD) (outdated)	Xi
R-phrases (outdated)	R36/37/38
S-phrases (outdated)	S26
Flash point	>110 °C
Related compounds
Related compounds	Bistriflimide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
‹See TfM›N verify (what is Y‹See TfM›N ?)
Infobox references

Trioctylmethylammonium bis(trifluoromethylsulfonyl)imide is an ionic liquid^[1] that is produced by Solvent Innovation, now part of EMD Chemicals.

References

1. 
   ^ 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: 1891–1894. doi:10.1016/s0957-4166(01)00315-9..mw-parser-output cite.citation{font-style:inherit}.mw-parser-output q{quotes:"""""""'""'"}.mw-parser-output code.cs1-code{color:inherit;background:inherit;border:inherit;padding:inherit}.mw-parser-output .cs1-lock-free a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-limited a,.mw-parser-output .cs1-lock-registration a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-subscription a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration{color:#555}.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration span{border-bottom:1px dotted;cursor:help}.mw-parser-output .cs1-hidden-error{display:none;font-size:100%}.mw-parser-output .cs1-visible-error{font-size:100%}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-format{font-size:95%}.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-left{padding-left:0.2em}.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-right{padding-right:0.2em}
   

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