Choline bis(trifluoromethylsulfonyl)imide, >99%

Price range: $155.75 through $8,208.21

Product Code: IL-0110-HP

CAS NO: 827027-25-8

  • Chemical Fr: C7H14F6N2O4S2
  • Synonyms: Chol BTA, Chol NTf2, Chol TFSI, Chol BTI, N,N,N-thimethyl-N-(2-hydroxyethyl) ammonium bis(trifluoromethylsulfonyl)imide, 1,1,1-thimethyl-1-(2-hydroxyethyl) ammonium bis(trifluoromethylsulfonyl)imide
  • Weakly-coordinating anion
  • Hydrophobic
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Conductivity: 3.98 mS/cm (45 °C)

SUM Formula: C7H14F6N2O4S2

Molecular Weight: 368.32

Melting Point: 35-37 °C

Density: 1.508 (25 °C)

Purity: >99%

Viscosity: 49.5 cP (45 °C)

  • SUM Formula: C7H14F6N2O4S2
  • Molecular Weight: 368.32
  • Melting Point: 35-37 °C
  • Density: 1.508 (25 °C)
  • Viscosity: 49.5 cP (45 °C)

Choline bis(trifluoromethylsulfonyl)imide, CAS: 827027-25-8

Key Applications:

Electrolytes for Energy Storage

  • Serves as a high‑stability ionic liquid electrolyte component in lithium‑ion, sodium‑ion, and emerging multivalent battery systems.
  • Enhances ionic conductivity and electrochemical window in solid–liquid hybrid electrolytes.
  • Used in polymer gel electrolytes and ionogel matrices for flexible and solid‑state devices.

Electrochemical Devices & Interfaces

  • Employed in supercapacitor electrolytes to improve thermal stability and long‑term cycling performance.
  • Supports electrode surface engineering, including controlled SEI formation and interfacial ion transport studies.
  • Utilized in redox‑active systems for flow batteries and electrocatalytic platforms.

Catalysis & Green Chemistry

  • Functions as a thermally robust, non‑volatile reaction medium for acid‑ and base‑catalyzed transformations.
  • Applied in transition‑metal catalysis, including cross‑coupling, hydrogenation, and CO₂ conversion reactions.
  • Enables biphasic catalysis and catalyst recycling due to its immiscibility with many organic solvents.

Separation Science & Extraction

  • Used in liquid–liquid extraction of metal ions, particularly rare‑earth and transition‑metal species, due to strong TFSI⁻ coordination.
  • Supports selective extraction of hydrophobic organics and fluorinated compounds.
  • Applied in membrane‑based separations and supported ionic liquid phases (SILPs).

Materials Science & Polymer Engineering

  • Incorporated into polymer matrices to tune conductivity, mechanical flexibility, and thermal behavior.
  • Used in ionogels, block copolymers, and advanced dielectric materials.
  • Serves as a plasticizer or ionic dopant in conductive polymers and elastomers.

Surface & Colloid Science

  • Acts as a surfactant‑like ionic liquid for stabilizing dispersions of nanoparticles, carbon materials, and metal oxides.
  • Supports controlled self‑assembly and nanostructure formation in soft materials.

Analytical & Spectroscopic Applications

  • Provides a low‑volatility, high‑purity medium for NMR, FTIR, and electrochemical characterization.
  • Used in fundamental studies of ion pairing, solvation, and transport phenomena.

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Additional information

Weight 25 g
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