727725
1-Butyl-1-methylpyrrolidinium trifluoromethanesulfonate
95%
Synonym(s):
BMPyrrOTf
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About This Item
Empirical Formula (Hill Notation):
C10H20F3NO3S
CAS Number:
Molecular Weight:
291.33
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
9820503
Product Name
1-Butyl-1-methylpyrrolidinium trifluoromethanesulfonate, 95%
InChI
1S/C9H20N.CHF3O3S/c1-3-4-7-10(2)8-5-6-9-10;2-1(3,4)8(5,6)7/h3-9H2,1-2H3;(H,5,6,7)/q+1;/p-1
SMILES string
[O-]S(=O)(=O)C(F)(F)F.CCCC[N+]1(C)CCCC1
InChI key
WZJDNKTZWIOOJE-UHFFFAOYSA-M
assay
≥95.0% (T)
95%
form
liquid
impurities
≤0.3% water
functional group
fluoro
triflate
Quality Level
Application
1-Butyl-1-methylpyrrolidinium trifluoromethanesulfonate ([BMPy][OTf]) is an ionic liquid that can be used as a solvent in:
([BMPy][OTf]) can also be used as an electrolyte in supercapacitor applications.
- Rhodium-catalyzed regioselective hydroformylation reactions.
- Direct asymmetric aldol condensation reaction.
- Desulfurization of fuels.
- Nucleophilic aromatic substitution reactions.
([BMPy][OTf]) can also be used as an electrolyte in supercapacitor applications.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Ionic liquids in supercapacitors
Brandt A, et al.
Mrs Bulletin, 38(7), 554-559 (2013)
Hydroformylation of 1-hexene with rhodium in non-aqueous ionic liquids: how to design the solvent and the ligand to the reaction
Favre F, et al.
Chemical Communications (Cambridge, England), 1360-1361 (2001)
Ionic liquids as designer solvents for nucleophilic aromatic substitutions
Newington I, et al.
Organic Letters, 9(25), 5247-5250 (2007)
Effect of the cation and anion of the ionic liquid on desulfurization of model fuels
Domanska U and Wlazlo M
Fuel: The Science and Technology of Fuel and Energy, 134(11-12), 114-125 (2014)
Andrzej Lewandowski et al.
Journal of solution chemistry, 42(2), 251-262 (2013-03-14)
The electrochemical behavior of cobaltocenium has been studied in a number of room temperature aprotic ionic liquids. Well defined, diffusion controlled, anodic and cathodic peaks were found for the Cc
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