CAS 174899-83-3

1-Butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide

Description:

1-Butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide, commonly referred to as [BMIM][Tf2N], is an ionic liquid characterized by its low volatility, high thermal stability, and excellent solvation properties. It features a butyl group and a methyl group attached to the imidazolium cation, contributing to its unique properties. The bis(trifluoromethylsulfonyl)imide anion is known for its strong ionic character and low viscosity, making this ionic liquid particularly useful in various applications, including electrochemistry, catalysis, and as a solvent for organic reactions. Its non-volatile nature and ability to dissolve a wide range of polar and non-polar compounds make it an attractive alternative to traditional organic solvents. Additionally, [BMIM][Tf2N] exhibits good electrochemical stability, which is beneficial for applications in batteries and supercapacitors. Overall, this compound is notable for its environmentally friendly profile, as it can reduce the use of volatile organic compounds in chemical processes.

Formula: C₈H₁₅N₂·C₂F₆NO₄S₂

InChI: InChI=1S/C8H15N2.C2F6NO4S2/c1-3-4-5-10-7-6-9(2)8-10;3-1(4,5)14(10,11)9-15(12,13)2(6,7)8/h6-8H,3-5H2,1-2H3;/q+1;-1

InChI key: InChIKey=INDFXCHYORWHLQ-UHFFFAOYSA-N

SMILES: S([N-]S(C(F)(F)F)(=O)=O)(C(F)(F)F)(=O)=O.C(CCC)[N+]1=CN(C)C=C1

Synonyms:

• 1-Butyl-3-Methylimidazolium Bis(Trifluorome.Sulfonyl)Imide
• 1-Butyl-3-Methylimidazolium Bis(Trifluoromethanesulfonyl)Imide
• 1-Butyl-3-methyl-1H-imidazol-3-ium bis((trifluoromethyl)sulfonyl)amide
• 1-Butyl-3-methyl-1H-imidazolium 1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide(1-)
• 1-Butyl-3-methyl-1H-imidazolium N,N-bis(trifluoromethanesulfonyl)imide
• 1-Butyl-3-methyl-1H-imidazolium N,N-bis[(trifluoromethyl)sulfonyl]amide
• 1-Butyl-3-methyl-1H-imidazolium salt with 1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide
• 1-Butyl-3-methyl-1H-imidazolium salt with 1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide (1:1)
• 1-Butyl-3-methylimidazolium N,N-bis(trifluoromethanesulfonyl)imide
• 1-Butyl-3-methylimidazolium N,N-bis(trifluoromethylsulfonyl)amide
• 1-Butyl-3-methylimidazolium bis((trifluoromethy)sulfonyl)imide
• 1-Butyl-3-methylimidazolium bis(trifluoromethane)sulfonimide
• 1-Butyl-3-methylimidazolium bis(trifluoromethanesulfonimide) salt
• 1-Butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide
• 1-Butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imidate
• 1-Butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide(1-)
• 1-Butyl-3-methylimidazolium bis(trifluoromethanesylfonyl)imide(1-)
• 1-Butyl-3-methylimidazolium bis(trifluoromethylsufonyl)imide
• 1-Butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide
• 1-Butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide(1-)
• 1-Butyl-3-methylimidazolium bis(triflyl)imide
• 1-Butyl-3-methylimidazolium bis[(trifluoromethyl)sulfonyl]amide
• 1-Butyl-3-methylimidazolium bistriflamide
• 1-Butyl-3-methylimidazolium bistriflimide
• 1-Butyl-3-methylimidazolium triflimide
• 1-Butyl-3-methylimidiazolium bis(trifluoromethanesulfonyl)imide
• 1-Methyl-3-butylimidazolium bis(trifluoromethylsulfonyl)imide
• 1-butyl-3-methyl-1H-imidazol-3-ium bis[(trifluoromethyl)sulfonyl]azanide
• 1-n-Butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide
• 1-n-Butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide
• 1H-Imidazolium, 1-butyl-3-methyl-, salt with 1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide (1:1)
• 1H-Imidazolium, 3-butyl-1-methyl-, salt with 1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide (1:1)
• 3-Butyl-1-methylimidazolium bis(trifluoromethanesulfonyl)imide
• 3-Butyl-1-methylimidazolium bis(trifluoromethylsulfonyl)imide
• BMIIm, BMIM TFSI
• Bmi-N 111
• Bmi-Tfsi
• Bmim bis(trifluoromethanesulfonyl)imide
• Bmim-Tfsi
• Butyl methyl imidazolium bis(trifluoromethyl)sulfonimide
• Methanesulfonamide, 1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]-, ion(1-), 1-butyl-3-methyl-1H-imidazolium
• [C₄Mim⁺][Tf₂N^-]

1-Butyl-3-methylimidazolium Bis(trifluoromethanesulfonyl)imide

CAS: 174899-83-3

Formula: C₁₀H₁₅F₆N₃O₄S₂

Purity: >98.0%(T)(HPLC)

Color and Shape: Colorless to Light orange to Yellow clear liquid

Molecular weight: 419.36

Ref: 3B-B2477

1-Butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide

CAS: 174899-83-3

1-Butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide

Purity: 99%

Color and Shape: Colourless Liquid

Molecular weight: 419.36g/mol

Ref: 54-PC56042

1-Butyl-3-Methylimidazolium Bis(trifluoromethylsulfonyl)imide

CAS: 174899-83-3

Formula: C₈H₁₅N₂·C₂F₆NO₄S₂

Molecular weight: 139.22 280.14

Ref: 4Z-I-078041

1-Butyl-3-methyl-1H-imidazol-3-ium bis((trifluoromethyl)sulfonyl)amide

CAS: 174899-83-3

Purity: 98%

Molecular weight: 419.04

Ref: 10-F551677

1-Butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide

CAS: 174899-83-3

1-Butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (BMIMTFSI) is a cationic electrolyte that is used in a variety of electrochemical applications. BMIMTFSI has been shown to be able to form hydrogen bonds with water and other hydroxyl groups. Hydrogen bonding interactions are important for the ionic conductivity of BMIMTFSI. These interactions allow the formation of an ionic solution in which the ions can conduct electricity. This property of BMIMTFSI makes it useful in electrochemical detectors, such as gas sensors and pH monitors, where it can be used to measure changes in pH or detect gases such as carbon dioxide or ammonia. The frequency shift of this material is due to its ability to undergo an acylation reaction, which is the addition of an acyl group onto a molecule. The activation energies for this process are determined by the chemical interactions between

Formula: C₁₀H₁₅F₆N₃O₄S₂

Purity: Min. 98 Area-%

Color and Shape: Clear Liquid

Molecular weight: 419.37 g/mol

Ref: 3D-FB60686

BMIM-TFSI

CAS: 174899-83-3

BMIM-TFSI (compound8) is an HIV-1 integrase inhibitor that effectively suppresses both the 3'-processing (3'-P) and strand transfer (ST) steps of the integration process. It is applicable in HIV-1 research.

Formula: C₁₀H₁₅F₆N₃O₄S₂

Color and Shape: Solid

Molecular weight: 419.364

Ref: TM-T204101