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
Identifiers
CAS Number	375395-33-8 ;
3D model (JSmol)	Interactive image; Interactive image;
ChEMBL	ChEMBL561679 ;
ChemSpider	17339079 ;
ECHA InfoCard	100.157.714
EC Number	629-541-6;
PubChem CID	16211009;
UNII	939A0J7H68 ;
CompTox Dashboard (EPA)	DTXSID3047926 ;
	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 Key: LAGQNGWYNLUQRI-UHFFFAOYSA-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
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H315, H319, H335
Precautionary statements	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	Bistriflimide
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

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

References

^ See PubChem
^ "Methyltrioctylammonium bis(trifluoromethylsulfonyl)imide". pubchem.ncbi.nlm.nih.gov. Retrieved 12 December 2021.
^ 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] See PubChem

[2] "Methyltrioctylammonium bis(trifluoromethylsulfonyl)imide". pubchem.ncbi.nlm.nih.gov. 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.

[3]

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