Bis(trifluoromethylsulfonyl)imide, 70% aqueous solution, >99%

Price range: $89.12 through $2,713.41

Product Code: KI-0055-HP

CAS NO: 82113-65-3

  • Chemical Formula: C2HF6NO4S2
  • Synonyms: HBTA, HTFSI, HNTf 2

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SUM Formula: C2HF6NO4S2

Molecular Weight: 281.16

Purity: >99%

  • SUM Formula: C2HF6NO4S2
  • Molecular Weight: 281.16

Bis(trifluoromethylsulfonyl)imide, CAS: 82113-65-3

Key Applications:

    • Reduced fuming and safer handling compared to anhydrous HTFSI.
    • Improved metering accuracy for neutralization reactions.
    • Lower volatility and easier integration into continuous‑flow or batch salt‑production systems.
    • Compatible with industrial‑scale purification and crystallization workflows for downstream TFSI⁻ salts.

      Electrolyte Manufacturing and Salt Precursor Processing

      • Used as a controlled‑strength precursor for generating TFSI⁻ salts through neutralization with lithium, sodium, potassium, ammonium, phosphonium, or imidazolium bases.
      • Aqueous format enables safer handling and more uniform stoichiometric control during salt formation, minimizing thermal load and avoiding direct handling of anhydrous HTFSI.
      • Supports scalable production of battery‑grade salts, ionic liquids, and deep eutectic electrolytes.

      Polymer and Membrane Functionalization

      • Acts as a sulfonylating and ion‑exchange reagent for preparing TFSI‑functionalized polymers, ionomers, and proton‑conducting membranes.
      • Aqueous medium improves compatibility with hydrophilic polymer backbones and reduces the need for aggressive organic solvents.

      Catalysis and Acid‑Mediated Transformations

      • Serves as a strong Brønsted acid for aqueous or biphasic catalytic systems requiring high acidity without introducing halides.
      • Enables acid‑catalyzed esterifications, rearrangements, and dehydration reactions where non‑nucleophilic counterions are essential.

      Surface Treatment and Materials Processing

      • Used to introduce TFSI⁻ into inorganic and hybrid materials through ion‑exchange or protonation pathways.
      • Supports preparation of TFSI‑doped metal oxides, conductive coatings, and surface‑modified nanoparticles.

      Electrochemical and Analytical Applications

      • Provides a controlled route to generate TFSI‑based electrolytes for supercapacitors, redox‑flow systems, and specialty electrochemical cells.
      • Aqueous form simplifies pH adjustment and ion‑exchange workflows in analytical chemistry and materials screening.

      Advantages of the Aqueous 70–72% Format

      • Reduced fuming and safer handling compared to anhydrous HTFSI.
      • Improved metering accuracy for neutralization reactions.
      • Lower volatility and easier integration into continuous‑flow or batch salt‑production systems.
      • Compatible with industrial‑scale purification and crystallization workflows for downstream TFSI⁻ salts.

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Additional information

Weight 25 g
Qty

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