Butyltrimethylammonium bis(trifluoromethylsulfonyl)imide, >99.5%

Price range: $192.46 through $1,602.36

Product Code: IL-0032-UP

CAS NO: 258273-75-5

  • Chemical Formula: C9H18F6N2O4S2
  • Synonyms: N1114 BTA, N1114 NTf 2 , N1114 TFSI, N1114 BTI
  • Weakly-coordinating anion
  • Hydrophobic

For High-Purity of >99% Purity, refer to IL-0032-HP

Clear

Conductivity: 2.86 mS/cm

SUM Formula: C9H18F6N2O4S2

Molecular Weight: 396.37

Melting Point: 7 °C

Density: 1.40 g/cm³

ECW: 6.1 V

Purity: >99.%%

Viscosity: 99.5 cP

  • SUM Formula: C9H18F6N2O4S2
  • Molecular Weight: 396.37
  • Melting Point: 7 °C
  • Density: 1.40 g/cm³
  • ECW: 6.1 V
  • Viscosity: 99.5 cP

Butyltrimethylammonium bis(trifluoromethylsulfonyl)imide, CAS: 258273-75-5

Key Applications:

Electrochemical Systems

  • Serves as a high‑stability supporting electrolyte in non‑aqueous electrochemical cells, including lithium, sodium, and multivalent metal systems.
  • Enhances ionic conductivity and suppresses parasitic reactions in high‑voltage environments due to the TFSI anion’s oxidative robustness.
  • Used in electrodeposition studies where controlled ion mobility and low water content are essential.

Battery and Energy Storage Research

  • Functions as an additive or co‑salt in electrolyte formulations for next‑generation batteries, improving SEI formation and cycling stability.
  • Supports research on ionic‑liquid‑based electrolytes for solid‑state and hybrid solid–liquid systems.
  • Applied in redox‑flow battery development where wide electrochemical windows and thermal stability are required.

Materials Science and Polymer Processing

  • Acts as a dopant or ionic modifier in polymer matrices, enabling tunable conductivity in ion gels, block copolymers, and elastomeric materials.
  • Used in the preparation of polymer electrolytes and membranes with enhanced mechanical and electrochemical performance.
  • Facilitates ion‑exchange processes in advanced materials where hydrophobic, weakly coordinating anions are advantageous.

Catalysis and Synthesis

  • Employed as a phase‑transfer or ionic‑medium component in organic synthesis, particularly under low‑volatility or solvent‑free conditions.
  • Supports catalytic systems that benefit from the TFSI anion’s non‑coordinating nature, improving catalyst stability and turnover.
  • Useful in halide‑free reaction environments where minimal nucleophilicity is required.

Spectroscopy and Fundamental Studies

  • Provides a well‑defined cation–anion pair for benchmarking ion transport, solvation, and interfacial behavior in ionic liquid research.
  • Used in vibrational, NMR, and dielectric spectroscopy to study ion pairing and dynamic relaxation processes.
  • Serves as a model salt for computational and theoretical investigations of ionic liquids with quaternary ammonium cations.

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Additional information

Weight 25 g
Qty

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