1-Hexylpyridinium triflate, >99%

Price range: $549.12 through $4,414.08

Product Code: IL-0181-HP

CAS NO: 623167-81-7

  • Chemical Formula: C12H18F3NO3S
  • Synonyms: N-Hexylpyridinium triflate, 1-Hexylpyridinium trifluoromethanesulfonate, HexPy OTf
  • Aromatic
Clear

SUM Formula: C12H18F3NO3S

Molecular Weight: 313.34

Melting Point: 63°C

Purity: >99%

  • SUM Formula: C12H18F3NO3S
  • Molecular Weight: 313.34
  • Melting Point: 63°C

1-Hexylpyridinium triflate, CAS: 623167-81-7

Key Applications:

Solvent and Reaction Medium

  • Functions as a hydrophobic ionic liquid with strong thermal and electrochemical stability, enabling use in moisture‑sensitive and high‑temperature transformations.
  • Supports acid‑catalyzed reactions where the triflate anion provides low nucleophilicity and high stability.
  • Useful for biphasic catalysis and extraction systems requiring tunable polarity and low volatility.

Electrochemical Systems

  • Serves as a conductive medium for electrochemical studies, benefiting from the pyridinium cation’s stability and the triflate anion’s wide electrochemical window.
  • Suitable for ion‑transport studies, electrodeposition research, and electrolyte formulation in prototype devices.

Materials Science and Polymer Processing

  • Acts as a processing aid for polymers, particularly in systems requiring ionic plasticization or enhanced ion mobility.
  • Supports the formation of ionogels and polymer–ionic liquid composites with improved mechanical and conductive properties.
  • Useful in templating and nanostructuring applications where ionic liquids influence morphology and porosity.

Catalysis and Organic Synthesis

  • Provides a non‑volatile, recyclable medium for Lewis and Brønsted acid‑driven transformations.
  • Enhances selectivity in alkylation, esterification, and rearrangement reactions due to its polarity and low coordinating nature.
  • Can solubilize both organic substrates and metal catalysts, enabling homogeneous catalytic systems.

Separation Science

  • Employed in liquid–liquid extraction systems for selective partitioning of aromatic, sulfur‑containing, or metal‑ion species.
  • Useful in chromatographic method development where ionic liquids modify retention behavior or act as mobile‑phase additives.

Thermal and Transport Studies

  • Suitable for fundamental research on viscosity, ion mobility, and phase behavior in pyridinium‑based ionic liquids.
  • Provides a model system for studying structure–property relationships in ionic liquids with medium‑length alkyl chains.

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Additional information

Weight 25 g
Qty

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