1-Butyl-3-methylpyridinium triflate, >98%

Price range: $591.59 through $4,757.39

Product Code: IL-0179-HP

CAS NO: 857841-32-8

  • Chemical Formula: C11H16F3NO3S
  • Synonyms: Bu-3-Pic OTf, Bu3Pic OTf, 1-Butyl-3-methylpyridinium trifluoromethanesulfonate, 1-Butyl-3-picolinium triflate, N-Butyl-3-methylpyridinium triflate, N-Butyl-3-picolinium triflate
  • Hydrophoic
  • Aromatic
Clear

Conductivity: 2.35 mS/cm (30 °C)

SUM Formula: C11H16F3NO3S

Molecular Weight: 237.05

Melting Point: <RT

Density: 1.28 g/cm³ (25 °C)

Purity: >98%

Viscosity: 117 cP (25 °C)

  • SUM Formula: C11H16F3NO3S
  • Molecular Weight: 237.05
  • Melting Point:
  • Density: 1.28 g/cm³ (25 °C)
  • Viscosity: 117 cP (25 °C)

1-Butyl-3-methylpyridinium triflate, CAS: 857841-32-8

Key Applications:

Electrochemical Systems

  • Serves as a stable ionic medium for electrochemical studies requiring wide electrochemical windows and low volatility.
  • Supports ion transport in prototype electrolytes for capacitors, redox systems, and electrodeposition research.
  • Useful in evaluating ionic‑liquid–based interfaces due to its thermal stability and predictable conductivity profile.

Catalysis and Organic Synthesis

  • Functions as a non‑volatile reaction medium for acid‑catalyzed and transition‑metal‑catalyzed transformations.
  • Provides enhanced solvation for polar intermediates, enabling rate improvements in selected coupling, alkylation, and rearrangement reactions.
  • Suitable for biphasic catalysis where phase separation and product recovery are important.

Materials Science and Polymer Processing

  • Acts as a processing aid or plasticizing ionic component in polymer blends, ionogels, and hybrid materials.
  • Supports the formation of conductive films and membranes where ionic mobility and thermal robustness are required.
  • Enables dispersion and stabilization of nanoparticles in non‑aqueous matrices.

Separation Science

  • Employed as a tunable solvent or co‑solvent in liquid–liquid extraction systems targeting metal ions, organics, and specialty analytes.
  • Useful in chromatographic method development where ionic‑liquid additives improve peak shape, selectivity, or retention control.

Thermal and Transport Studies

  • Provides a model system for studying ion–ion and ion–solvent interactions due to its well‑defined cation/anion pairing.
  • Used in research on viscosity, conductivity, and diffusion behavior of pyridinium‑based ionic liquids.

Specialty Applications

  • Supports development of ionic‑liquid–based lubricants and anti‑wear additives for high‑temperature environments.
  • Investigated in CO₂ capture and gas‑solvation studies where triflate‑based ionic liquids offer predictable physicochemical behavior.

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Additional information

Weight 25 g
Qty

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