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, HNTfย 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 continuousโ€‘flow or batch saltโ€‘production systems.
    • Compatible with industrialโ€‘scale purification and crystallization workflows for downstream TFSIโป salts.

      Electrolyte Manufacturing and Salt Precursor Processing

      • Used as a controlledโ€‘strength precursor for generating TFSIโป 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 batteryโ€‘grade salts, ionic liquids, and deep eutectic electrolytes.

      Polymer and Membrane Functionalization

      • Acts as a sulfonylating and ionโ€‘exchange reagent for preparing TFSIโ€‘functionalized polymers, ionomers, and protonโ€‘conducting membranes.
      • Aqueous medium improves compatibility with hydrophilic polymer backbones and reduces the need for aggressive organic solvents.

      Catalysis and Acidโ€‘Mediated Transformations

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

      Surface Treatment and Materials Processing

      • Used to introduce TFSIโป into inorganic and hybrid materials through ionโ€‘exchange or protonation pathways.
      • Supports preparation of TFSIโ€‘doped metal oxides, conductive coatings, and surfaceโ€‘modified nanoparticles.

      Electrochemical and Analytical Applications

      • Provides a controlled route to generate TFSIโ€‘based electrolytes for supercapacitors, redoxโ€‘flow systems, and specialty electrochemical cells.
      • Aqueous form simplifies pH adjustment and ionโ€‘exchange workflows in analytical chemistry and materials screening.

      Advantages of the Aqueous 70โ€“72% Format

      • Reduced fuming and safer handling compared to anhydrous HTFSI.
      • Improved metering accuracy for neutralization reactions.
      • Lower volatility and easier integration into continuousโ€‘flow or batch saltโ€‘production systems.
      • Compatible with industrialโ€‘scale purification and crystallization workflows for downstream TFSIโป salts.

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Additional information

Weight 25 g
Qty

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