1-Methyl-3-pentylimidazolium bis(trifluoromethylsulfonyl)imide, >99%

Price range: $268.84 through $14,804.30

Product Code: IL-0300-HP

CAS NO: 280779-53-5

  • Chemical Formula: C11H17F6N3O4S2
  • Synonyms: PentMIM BTA, PentMIM NTf 2, PentMIM TFSI, PentMIM BTI, C 1 C 5 Im BTA, Im 15 BTA
  • Weakly-coordinating anion
  • Hydrophobic
  • Aromatic
Clear

Conductivity: 3.28 mS/cm (30°C)

SUM Formula: C11H17F6N3O4S2

Molecular Weight: 433.39

Melting Point: <RT

Purity: >99%

Viscosity: 59.3 cP (25 °C)

  • SUM Formula: C11H17F6N3O4S2
  • Molecular Weight: 433.39
  • Melting Point:
  • Viscosity: 59.3 cP (25 °C)

1-Methyl-3-pentylimidazolium bis(trifluoromethylsulfonyl)imide, CAS: 280779-53-5

Key Applications:

Electrochemical & Energy Applications

  • Electrolytes for high‑voltage lithium and sodium systems, leveraging the NTf₂⁻ anion’s wide electrochemical window and thermal stability.
  • Ion‑conductive media in supercapacitors, where moderate viscosity supports improved ion mobility compared to longer‑chain homologues.
  • Redox‑active electrolyte formulations for flow batteries and metal–air systems.

Catalysis & Synthesis

  • Reaction media for transition‑metal catalysis, including C–C coupling, hydrogenation, and oxidation reactions requiring non‑volatile, thermally robust solvents.
  • Phase‑transfer catalysis, where the C₅ chain provides tunable hydrophobicity for biphasic organic–aqueous systems.
  • Stabilization of reactive intermediates in organometallic and heterocycle synthesis.

Materials Science & Polymer Processing

  • Solvent and plasticizer for engineering polymers, including polyimides, polyacrylates, and fluorinated materials.
  • Template or structure‑directing agent in nanoparticle synthesis and porous material fabrication.
  • Processing aid for conductive composites, improving dispersion of carbon nanotubes, graphene, and metal oxides.

Separation & Extraction

  • Selective extraction of aromatic hydrocarbons, sulfur species, and metal ions due to strong π‑interaction and coordination capability.
  • CO₂ capture and gas separation media, benefiting from NTf₂⁻’s low coordinating nature and the cation’s moderate hydrophobicity.
  • Liquid–liquid extraction in bioprocessing, including purification of bioactive compounds and specialty organics.

Lubrication & Surface Engineering

  • High‑temperature, low‑volatility lubricant additive for metal–metal and metal–ceramic interfaces.
  • Anti‑wear and friction‑reducing films, where the ionic liquid forms stable boundary layers under load.
  • Surface treatment agent for corrosion‑resistant coatings.

Analytical & Laboratory Uses

  • Non‑aqueous mobile phase modifier in chromatography for enhanced separation of hydrophobic analytes.
  • Matrix or dispersive medium in spectroscopic and electroanalytical methods requiring low vapor pressure and high thermal stability.
  • Solvent for crystallization studies of organics and coordination complexes.

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Additional information

Weight 25 g
Qty

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