CAS 174899-83-3

1-butil-3-metilimidazólio bis(trifluorometilsulfonil)imida

Descrição:

1-butil-3-metilimidazólio bis(trifluorometilsulfonil)imida, comumente referido como [BMIM][Tf2N], é um líquido iônico caracterizado por sua baixa volatilidade, alta estabilidade térmica e excelentes propriedades de solvatação. Apresenta um grupo butila e um grupo metila ligados ao cátion imidazólio, contribuindo para suas propriedades únicas. O ânion bis(trifluorometilsulfonil)imida é conhecido por seu forte caráter iônico e baixa viscosidade, tornando este líquido iônico particularmente útil em várias aplicações, incluindo eletroquímica, catálise e como solvente para reações orgânicas. Sua natureza não volátil e capacidade de dissolver uma ampla gama de compostos polares e não polares fazem dele uma alternativa atraente aos solventes orgânicos tradicionais. Além disso, [BMIM][Tf2N] exibe boa estabilidade eletroquímica, o que é benéfico para aplicações em baterias e supercapacitores. No geral, este composto é notável por seu perfil ambientalmente amigável, pois pode reduzir o uso de compostos orgânicos voláteis em processos químicos.

Fórmula: 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

Chave InChI: 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

Sinónimos:

• 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

Fórmula: C₁₀H₁₅F₆N₃O₄S₂

Pureza: >98.0%(T)(HPLC)

Cor e Forma: Colorless to Light orange to Yellow clear liquid

Peso molecular: 419.36

Ref: 3B-B2477

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

CAS: 174899-83-3

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

Pureza: 99%

Cor e Forma: Colourless Liquid

Peso molecular: 419.36g/mol

Ref: 54-PC56042

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

CAS: 174899-83-3

Fórmula: C₈H₁₅N₂·C₂F₆NO₄S₂

Peso molecular: 139.22 280.14

Ref: 4Z-I-078041

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

CAS: 174899-83-3

Pureza: 98%

Peso molecular: 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

Fórmula: C₁₀H₁₅F₆N₃O₄S₂

Pureza: Min. 98 Area-%

Cor e Forma: Clear Liquid

Peso molecular: 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.

Fórmula: C₁₀H₁₅F₆N₃O₄S₂

Cor e Forma: Solid

Peso molecular: 419.364

Ref: TM-T204101