CAS 174899-83-3

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

Descripción:

1-butil-3-metilimidazolio bis(trifluorometilsulfonil)imida, comúnmente conocido como [BMIM][Tf2N], es un líquido iónico caracterizado por su baja volatilidad, alta estabilidad térmica y excelentes propiedades de solvatación. Presenta un grupo butilo y un grupo metilo unidos al catión imidazolium, lo que contribuye a sus propiedades únicas. El anión bis(trifluorometilsulfonil)imida es conocido por su fuerte carácter iónico y baja viscosidad, lo que hace que este líquido iónico sea particularmente útil en diversas aplicaciones, incluyendo electroquímica, catálisis y como disolvente para reacciones orgánicas. Su naturaleza no volátil y su capacidad para disolver una amplia gama de compuestos polares y no polares lo convierten en una alternativa atractiva a los disolventes orgánicos tradicionales. Además, [BMIM][Tf2N] exhibe buena estabilidad electroquímica, lo que es beneficioso para aplicaciones en baterías y supercapacitores. En general, este compuesto es notable por su perfil ecológico, ya que puede reducir el uso de compuestos orgánicos volátiles en procesos 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

Clave 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)

Forma y color: 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%

Forma y color: 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-%

Forma y color: 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

Forma y color: Solid

Peso molecular: 419.364

Ref: TM-T204101