Trioctylmethylammonium bis(trifluoromethylsulfonyl)imide

Trioctylmethylammonium bis(trifluoromethylsulfonyl)imide
Names
	Preferred IUPAC name N-methyl-N,N-di(octyl)octan-1-aminium bis(trifluoromethanesulfonyl)azanide
	Other names Methyl-trioctylammonium bis(trifluoromethylsulfonyl)imide[citation needed]
Identifiers
CAS Number	375395-33-8 ;
3D model (JSmol)	Interactive image; Interactive image;
ChEMBL	ChEMBL561679 ;
ChemSpider	17339079 ;
ECHA InfoCard	100.157.714
PubChem CID	16211009;
UNII	939A0J7H68 ;
CompTox Dashboard (EPA)	DTXSID3047926 ;
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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EU classification (DSD) (outdated)	Xi
R-phrases (outdated)	R36/37/38
S-phrases (outdated)	S26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).
	(what is ?)
	Infobox references

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

References[]

^ 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.

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[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 (13): 1891–1894. doi:10.1016/s0957-4166(01)00315-9. hdl:10261/64635.

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