1,2-Dimethyl-3-propylimidazolium bis(trifluoromethylsulfonyl)imide, >99%

Price range: $179.73 through $9,858.65

Product Code: IL-0134-HP

CAS NO: 169051-76-7

  • Chemical Formula: C10H15F6N3O4S2
  • Synonyms: DMPIIm, PDiMIM BTA, PDiMIM NTf2, PDiMIM TFSI, PDiMIM BTI, IM113 BTA
  • Weakly-coordinating anion
  • Aromatic
  • Hydrophobic
Clear

Conductivity: 1.95 mS/cm (25 °C)

SUM Formula: C10H15F6N3O4S2

Molecular Weight: 419.36

Melting Point: 15 °C

Density: 1.45 g/cm³ (25 °C)

ECW: 4.6 V

HMIS Key: NA

Purity: >99%

Viscosity: 107 cP (25 °C)

  • SPECIFIC GRAVITY: NA
  • SUM Formula: C10H15F6N3O4S2
  • Molecular Weight: 419.36
  • Melting Point: 15 °C
  • Density: 1.45 g/cm³ (25 °C)
  • ECW: 4.6 V
  • HMIS KEY: NA
  • TSCA: NA
  • Viscosity: 107 cP (25 °C)

1,2-Dimethyl-3-propylimidazolium bis(trifluoromethylsulfonyl)imide, CAS: 169051-76-7

Key Applications

Electrochemical Systems

  • Serves as a high‑stability ionic liquid electrolyte component for lithium, sodium, and multivalent metal batteries, benefiting from the TFSI⁻ anion’s wide electrochemical window and low coordinating character.
  • Supports high‑temperature supercapacitor formulations where low volatility and strong thermal resilience are required.
  • Functions as a conductive medium in redox‑flow and hybrid flow battery research, particularly where cation structure influences viscosity and ion mobility.

Catalysis and Synthesis

  • Acts as a non‑volatile reaction medium for transition‑metal‑catalyzed transformations, including C–C and C–N coupling, hydrogenation, and selective oxidations.
  • Provides a tunable solvent environment for organocatalysis, enabling enhanced selectivity and recyclability.
  • Useful in biphasic catalysis where phase separation and catalyst retention are critical.

Materials Science and Polymer Processing

  • Employed as a plasticizer or ionic additive in polymer electrolytes, ionogels, and high‑performance elastomers.
  • Facilitates dispersion and stabilization of nanoparticles, carbon materials, and metal oxides due to its balanced polarity and low nucleophilicity.
  • Supports surface modification and thin‑film deposition processes where ionic liquids enable controlled morphology and reduced defect formation.

Separation Science and Extraction

  • Functions as an extraction medium for metal ions, hydrophobic organics, and fluorinated species, leveraging the hydrophobic TFSI⁻ anion.
  • Enables selective partitioning in liquid–liquid extraction systems, particularly for rare‑earth and transition‑metal separations.
  • Useful in gas absorption studies, including CO₂ capture, where cation substitution patterns influence solubility and transport.

Thermal and Chemical Stability Applications

  • Suitable for high‑temperature lubrication and tribological studies where non‑flammability and thermal endurance are required.
  • Serves as a stable medium for studying reaction kinetics under elevated temperatures or inert‑atmosphere conditions.
  • Supports high‑vacuum and high‑temperature environments where conventional solvents degrade or volatilize.

Analytical and Spectroscopic Uses

  • Provides a low‑volatility matrix for electrochemical impedance spectroscopy, NMR diffusion studies, and vibrational spectroscopy.
  • Useful in calibrating ion transport models due to its well‑defined cation structure and predictable physicochemical behavior.

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Additional information

Weight 25 g
Qty

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