1-Methyl-1-propylpiperidinium bis(trifluoromethylsulfonyl)imide

1-Methyl-1-propylpiperidinium bis(trifluoromethylsulfonyl)imide, >99.5%

Price range: $178.24 through $12,155.95

Product Code: IL-0045-UP

CAS NO: 608140-12-1

  • Chemical Formula: C11H20F6N2O4S2
  • Synonyms: N-Methyl-N-propylpiperidinium bis(trifluoromethylsulfonyl)imide, PMPip BTA, PMPip NTf2, PMPip TFSI, PMPip BTI, PIP13 TFSI
  • Weakly-coordinating anion
  • Hydrophobic

For High Purity of >99% refer to IL-0045-HP

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Category:

Conductivity: 2.12 mS/cm (30 °C)

SUM Formula: C11H20F6N2O4S2

Molecular Weight: 422.21

Melting Point: 8 °C

Density: 1.41 g/cm³ (23 °C)

ECW: 5.9 V

Purity: >99.5%

Viscosity: 176 cP (25 °C)

  • SUM Formula: C11H20F6N2O4S2
  • Molecular Weight: 422.21
  • Melting Point: 8 °C
  • Density: 1.41 g/cm³ (23 °C)
  • ECW: 5.9 V
  • Viscosity: 176 cP (25 °C)

Applications

1-Methyl-1-propylpiperidinium bis(trifluoromethylsulfonyl)imide, CAS: 608140-12-1

Key Applications:

Electrochemical Systems

  • Serves as a non‑volatile electrolyte component for high‑temperature lithium and sodium battery research.
  • Used as an ionically conductive medium in redox‑flow and hybrid flow battery development where oxidative stability is required.
  • Functions as a supporting electrolyte in electrosynthesis, electrodeposition, and high‑potential anodic processes.
  • Enables stable ionic environments for supercapacitors and double‑layer capacitor prototypes.

Materials Science and Polymer Processing

  • Acts as a plasticizer or ionic mobility enhancer in polymer electrolytes, ionogels, and block‑copolymer membranes.
  • Supports fabrication of high‑temperature, low‑flammability polymer systems due to its negligible vapor pressure and thermal resilience.
  • Used in templating and dispersion of nanomaterials, including carbon nanostructures and metal oxides, where hydrophobic ionic liquids improve colloidal stability.

Catalysis and Synthesis

  • Provides a stable, inert medium for transition‑metal catalysis, especially reactions requiring moisture‑free, high‑temperature conditions.
  • Employed in biphasic catalysis where phase separation between hydrophobic ionic liquids and polar reactants improves catalyst recovery.
  • Useful in electro‑organic synthesis requiring wide electrochemical windows and low nucleophilicity.

Separation Science

  • Applied in liquid–liquid extraction systems for selective separation of metal ions, hydrophobic organics, and fluorinated species.
  • Utilized in gas absorption studies, including CO₂ solubility and transport measurements in hydrophobic ionic liquids.

Thermal and Transport Studies

  • Serves as a benchmark ionic liquid for evaluating ion transport, viscosity–conductivity relationships, and high‑temperature stability in piperidinium‑based systems.
  • Used in fundamental studies comparing saturated versus unsaturated cation families (piperidinium vs. imidazolium/pyrrolidinium).

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Additional information

Weight 0.025 g
Qty

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