2-Methyl-1-propylpyridinium bis(trifluoromethylsulfonyl)imide, >99%

Price range: $179.73 through $9,858.65

Product Code: IL-0248-HP

CAS NO: 1456877-99-8

  • Chemical Formula: C11H14F6N2O4S2
  • Synonyms: 1-Propyl-2-picolinium bis(trifluoromethylsulfonyl)imide, N-Propyl-2-methylpyridinium bis(trifluoromethylsulfonyl)imide,  Pro2Pic BTA, Pro-2-Pic BTA,  Pro2Pic NTf2, Pro2Pic TFSI, Pro2Pic BTI
  • Weakly-coordinating anion
  • Hydrophobic
  • Aromatic
Clear

Conductivity: 1.31 mS/cm (25 °C)

SUM Formula: C11H14F6N2O4S2

Molecular Weight: 416.36

Melting Point: <RT

Purity: >99%

Viscosity: 81.6 cP (25 °C)

  • SUM Formula: C11H14F6N2O4S2
  • Molecular Weight: 416.36
  • Melting Point:
  • Viscosity: 81.6 cP (25 °C)

2-Methyl-1-propylpyridinium bis(trifluoromethylsulfonyl)imide, CAS: 1456877-99-8

Key Applications:

Electrochemical Systems

  • High‑stability electrolyte component for lithium, sodium, and multivalent metal batteries, leveraging the TFSI⁻ anion’s wide electrochemical window.
  • Ionic‑liquid medium for supercapacitors requiring low volatility and strong thermal resilience.
  • Conductive additive in redox‑flow batteries to enhance ion mobility and suppress side reactions.

Thermal & Chemical Stability Applications

  • Heat‑transfer and thermal‑management fluids in high‑temperature or vacuum environments, where non‑flammability and low vapor pressure are essential.
  • Replacement for volatile organic solvents in high‑temperature synthesis, catalytic cycles, and controlled‑atmosphere reactions.

Catalysis & Organic Synthesis

  • Reaction medium for transition‑metal catalysis, including C–C and C–N bond‑forming reactions that benefit from ionic‑liquid stabilization.
  • Solvent for selective extraction, biphasic catalysis, and phase‑transfer processes, especially where hydrophobicity and chemical inertness are required.

Separation Science & Extraction

  • Hydrophobic ionic liquid for liquid–liquid extraction of metal ions, hydrophobic organics, and fluorinated species.
  • Tunable medium for chromatographic method development, particularly in ion‑pairing or non‑aqueous separations.

Materials Science & Polymer Engineering

  • Additive for ion‑conducting polymers, gels, and elastomers to improve conductivity, flexibility, and thermal stability.
  • Processing aid in membrane fabrication, enabling controlled microstructure and enhanced transport properties.

Surface Science & Nanotechnology

  • Stabilizing medium for nanoparticle synthesis, preventing aggregation and enabling narrow size distributions.
  • Ionic‑liquid phase for surface modification, thin‑film deposition, and interfacial engineering.

Tribology & Lubrication

  • High‑performance lubricant or lubricant additive for extreme‑pressure and high‑temperature environments, benefiting from TFSI⁻‑based ionic liquids’ low wear and friction coefficients.

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Additional information

Weight 25 g
Qty

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