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344790-86-9

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344790-86-9 Structure

344790-86-9 Structure
IdentificationBack Directory
[Name]

1-BUTYL-3-METHYLPYRIDINIUM BIS(TRIFLUORM
[CAS]

344790-86-9
[Synonyms]

MBPy-FSI
B3MePyNTF2
[C4MPy]NTf2
MBPy-FSI 1M LiFSI
1-BUTYL-3-METHYLPYRIDINIUM BIS(TRIFLUORM
1-butyl-3-methylpyridinium bis-trifluormethanesulfonimide
N-Butyl-3-methylpyridinium bis(trifluormethylsulfonyl)imide
N-butyl-3-metylpyridinium bis((trifluoromethyl)sulfonyl)imide
1-Butyl-3-methylpyridinium Bis(trifluoromethylsulfonyl)imide
1-Butyl-3-methylpyridin-1-ium bis((trifluoromethyl)sulfonyl)amide
1-Butyl-3-methylpyridinium bis(trifluormethylsulphonyl)imide, 97%
bis(trifluoromethylsulfonyl)azanide:1-butyl-3-methylpyridin-1-ium
N-Butyl-3-MethylpyridiniuM bis(trifluoroMethylsulfonyl)iMide [BMPIM]
N-BUTYL-3-METHYLPYRIDINIUM BIS(TRIFLUOROMETHYLSULFONYL)IMIDE [BMPLM]
N-Butyl-3-methylpyridiniumbis(trifluoromethylsulfonyl)imide,99%[BMPIm]
1-Butyl-3-methylpyridinium bis(trifluormethylsulfonyl)imide >=97.0% (H-NMR)
[Molecular Formula]

C10H16N.C2F6NO4S2
[MDL Number]

MFCD03788916
[MOL File]

344790-86-9.mol
[Molecular Weight]

430.388
Chemical PropertiesBack Directory
[density ]

1,4 g/cm3
[storage temp. ]

RT, stored under nitrogen
[form ]

liquid
[color ]

colorless to pale yellow
[Specific Gravity]

1.4
[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
[InChIKey]

NOFBAVDIGCEKOQ-UHFFFAOYSA-N
[SMILES]

CCCC[n+]1cccc(C)c1.FC(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
[F ]

10-21
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

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.
  • As a solvent in the Ullmann homocoupling of aryl halides or aryl boronic acids using Cu nanoparticles.
  • To modify the carbon paste electrode applicable in the detection of dopamine in human serum and urine samples.
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