1-Butyl-2,3-dimethylimidazolium bis(trifluoromethylsulfonyl)imide, >99%

Price range: $96.16 through $6,366.66

Product Code: IL-0104-HP

CAS NO: 350493-08-2

  • Chemical Formula: C11H17F6N3O4S2
  • SYNONYMS: BMMIm NTf2
  • Weakly-coordinating anion
  • Hydrophobic
  • Aromatic
Clear

Conductivity: 1.96 mS/cm (25 °C)

SUM Formula: C11H17F6 N3O4S2

Molecular Weight: 433.39

Melting Point: -44 °C

Density: 1.42 g/cm³

ECW: 4.6 V

Purity: >99%

Viscosity: 98.0 cP

  • SUM Formula: C11H17F6 N3O4S2
  • Molecular Weight: 433.39
  • Melting Point: -44 °C
  • Density: 1.42 g/cm³
  • ECW: 4.6 V
  • Viscosity: 98.0 cP

1-Butyl-2,3-dimethylimidazolium bis(trifluoromethylsulfonyl)imide, CAS NO: 350493-08-2

Key Applications:

Electrochemical Applications

  • High‑voltage electrolytes for lithium, sodium, and multivalent metal batteries, leveraging wide electrochemical windows and low flammability.
  • Electrolyte additive or co‑solvent to improve SEI formation, ionic conductivity, and thermal stability in next‑generation cell chemistries.
  • Supercapacitor electrolytes, particularly for high‑temperature or high‑power systems requiring low volatility and stable ion transport.
  • Electrodeposition media for metals and alloys where controlled nucleation and smooth film formation are required.

Catalysis and Synthesis

  • Non‑coordinating reaction medium for acid‑sensitive or moisture‑sensitive transformations due to the weakly coordinating TFSI⁻ anion.
  • Phase‑transfer medium enabling enhanced solubility of organic substrates and transition‑metal complexes.
  • Support for homogeneous and biphasic catalysis, especially in C–C coupling, hydrogenation, and oxidation systems.
  • Stabilizing environment for reactive intermediates, benefiting mechanistic studies and high‑selectivity transformations.

Materials Science and Engineering

  • Polymer electrolyte component for ion‑conducting membranes, gels, and solid‑state devices requiring high thermal stability.
  • Plasticizer or ionic dopant in advanced polymers, improving conductivity and mechanical flexibility.
  • Processing aid for nanomaterials, including dispersion of carbon nanotubes, graphene, and metal nanoparticles.
  • Template or structuring medium in sol–gel and porous material synthesis where ionic liquids influence pore architecture.

Separation and Extraction

  • Hydrophobic extraction phase for metal ions, organometallic species, and hydrophobic organics.
  • Solvent for liquid–liquid extraction in systems requiring low miscibility with water and high chemical stability.
  • Selective dissolution medium for fluorinated compounds, aromatic species, and specialty polymers.

Thermal and Chemical Stability Applications

  • Heat‑transfer and thermal‑management fluids in niche systems requiring non‑volatile, thermally stable media.
  • Lubrication and anti‑wear additives in extreme environments where conventional lubricants degrade.
  • Stabilizing medium for high‑temperature spectroscopy, electrochemical testing, and reaction monitoring.

Analytical and Research Uses

  • Electrochemical probe solvent for studying redox couples, ion pairing, and charge‑transfer kinetics.
  • Medium for spectroscopic studies (NMR, IR, UV‑Vis) where low vapor pressure and chemical inertness are advantageous.
  • Reference formulation component in benchmarking ionic liquid behavior across cation/anion families.

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Additional information

Weight 25 g
Qty

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