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14654

Sigma-Aldrich

1-Butyl-3-methylpyridinium bis(trifluormethylsulfonyl)imide

≥97.0% (H-NMR)

Synonym(s):

BMPIm

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About This Item

Empirical Formula (Hill Notation):
C12H16F6N2O4S2
CAS Number:
344790-86-9
Molecular Weight:
430.39
MDL number:
MFCD03788916
UNSPSC Code:
12352100
PubChem Substance ID:
57647185
NACRES:
NA.22

assay

≥97.0% (H-NMR)

form

liquid

impurities

<0.5% water

functional group

fluoro

SMILES string

CCCC[n+]1cccc(C)c1.FC(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F

InChI

1S/C10H16N.C2F6NO4S2/c1-3-4-7-11-8-5-6-10(2)9-11;3-1(4,5)14(10,11)9-15(12,13)2(6,7)8/h5-6,8-9H,3-4,7H2,1-2H3;/q+1;-1

InChI key

NOFBAVDIGCEKOQ-UHFFFAOYSA-N

Application

1-Butyl-3-methylpyridinium bis(trifluormethylsulfonyl)imide can be used:
  • In the modification of electrodes applicable in the detection of dopamine and uric acid in the human urine sample.[1]
  • As a solvent in the Ullmann homocoupling of aryl halides or aryl boronic acids using Cu nanoparticles.[2]
  • To modify the carbon paste electrode applicable in the detection of dopamine in human serum and urine samples.[3]

Physical form

fluorated, hydrophobic ionic liquid

Legal Information

Product protected by U.S. Patent 5,827,602 assigned to Covalent Associates, Inc. Woburn, MA, USA

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCC4594
BCBQ4633V
BCBN6589V
1383377V
1383377

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Evaluation of the usefulness of a novel electrochemical sensor in detecting uric acid and dopamine in the presence of ascorbic acid using a screen-printed carbon electrode modified with single walled carbon nanotubes and ionic liquids
Nagles E, et al.
Electrochimica Acta, 258, 512-523 (2017)
An effective and environment-friendly system for Cu NPs@ RGO-catalyzed C-C homocoupling of aryl halides or arylboronic acids in ionic liquids under microwave irradiation
Zhao H, et al.
Royal Society of Chemistry Advances, 6(47), 41108-41113 (2016)
Imidazolium-based ionic liquids as modifiers of carbon paste electrodes for trace-level voltammetric determination of dopamine in pharmaceutical preparations
vSekuljica S, et al.
Journal of Molecular Liquids, 306, 112900-112900 (2020)

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Ionic Liquids: Electrochemical Apps

Ionic Liquids serve as non-aqueous electrolytes in electrochemical applications, valued for their conductivity and stability.

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