1-Butyl-1-methylpiperidinium bis(trifluoromethylsulfonyl)imide, >99%

Price range: $116.07 through $5,758.00

Product Code: IL-0154-HP

CAS NO: 623580-02-9

  • Chemical Formula: C12H22F6N2O4S2
  • Synonyms: N-Butyl-N-methylpiperidinium bis(trifluoromethylsulfonyl)imide, BMPip BTA, BMPip NTf2, BMPip TFSI, BMPip BTI, PIP14 TFSI
  • Weakly-coordination anion
  • Hydrophobic
Clear

Conductivity: 0.84 mS/cm (25 °C)

SUM Formula: C12H22F6N2O4S2

Molecular Weight: 436.44

Melting Point: -76 °C

Density: 1.38 g/cm³

ECW: 3.7 V

Purity: >99%

Viscosity: 183 cP (20 °C)

  • SUM Formula: C12H22F6N2O4S2
  • Molecular Weight: 436.44
  • Melting Point: -76 °C
  • Density: 1.38 g/cm³
  • ECW: 3.7 V
  • Viscosity: 183 cP (20 °C)

1-Butyl-1-methylpiperidinium bis(trifluoromethylsulfonyl)imide, CAS: 623580-02-9

Key Applications:

Electrochemical Systems

  • High‑voltage electrolytes for lithium, sodium, and magnesium batteries, leveraging the wide electrochemical stability window of piperidinium–TFSI salts.
  • Ionic liquid electrolytes for supercapacitors and hybrid capacitors requiring low volatility and high thermal stability.
  • Electrolyte additives to improve interfacial stability, suppress dendrite formation, and enhance cycling performance in next‑generation metal‑anode systems.

High‑Temperature & Harsh‑Environment Media

  • Heat‑resistant ionic liquid matrices for processes operating above 150–200^\circC where conventional organic solvents degrade.
  • Stable media for high‑temperature spectroscopy and analytical methods requiring non‑volatile, chemically inert solvents.
  • Thermally robust lubricants and anti‑wear additives for extreme‑environment tribology.

Catalysis & Synthesis

  • Non‑coordinating reaction media for transition‑metal catalysis, especially where TFSI⁻ enhances catalyst lifetime.
  • Solvent or co‑solvent for halide‑sensitive transformations and organometallic reactions.
  • Phase‑transfer medium in biphasic systems requiring hydrophobic, non‑nucleophilic ionic liquids.

Separation & Extraction

  • Selective extraction of metal ions, particularly hydrophobic complexes of rare‑earth or transition metals.
  • Solvent systems for liquid–liquid extraction where low miscibility with water and high chemical stability are advantageous.
  • CO₂ capture and gas‑absorption studies, leveraging the tunable viscosity and hydrophobicity of the piperidinium–TFSI framework.

Materials Science & Surface Engineering

  • Template or structuring agent in polymer and nanoparticle synthesis, enabling controlled morphology and conductivity.
  • Plasticizer or ionic dopant for polymer electrolytes, ion gels, and flexible electronic materials.
  • Surface‑modification medium for creating hydrophobic, ion‑conductive coatings.

Industrial & Engineering Uses

  • Hydrophobic ionic liquid lubricant base stocks for aerospace, vacuum, and high‑temperature mechanical systems.
  • Dielectric fluids in specialized electronics requiring low flammability and high breakdown strength.
  • Antistatic and charge‑control additives in polymer processing and advanced manufacturing.

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Additional information

Weight 25 g
Qty

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