3-methyl-1-octyl-4-phenyl-triazolium bis((trifluoromethyl)sulfonyl)amide

Product Code: TzPhC8FS

CAS NO: Pending

  • SMILES: O=S(C(F)(F)F)([N-]S(=O)(C(F)(F)F)=O)=O.C[N+](C(C1=CC=CC=C1)=C2)=NN2CCCCCCCC
  • Chemical Formula: C19H26F6N4O4S2

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SUM Formula: C19H26F6N4O4S2

Molecular Weight: 552.55 g/mol

Purity: NA

  • SPECIFIC GRAVITY: 1.3551
  • SUM Formula: C19H26F6N4O4S2
  • Molecular Weight: 552.55 g/mol

3-methyl-1-octyl-4-phenyl-triazolium bis((trifluoromethyl)sulfonyl)amide

Key Applications:

  • 1. Electrochemical Systems

    • High‑stability electrolyte component in lithium, sodium, and multivalent ion batteries, leveraging the TFSI anion’s wide electrochemical window and the triazolium cation’s thermal robustness.
    • Ionic liquid additive for improving interfacial stability, SEI formation, and high‑temperature cycling performance.
    • Redox‑active medium for flow batteries and electrochemical reactors where aromatic substitution enhances charge‑transfer behavior.

    2. Catalysis and Organic Synthesis

    • Non‑volatile reaction medium for transition‑metal catalysis, including C–C and C–N coupling, where the phenyl‑substituted triazolium ring improves catalyst solubility and turnover.
    • Phase‑transfer catalyst in biphasic systems, benefiting from the long C8 chain and aromatic ring that tune hydrophobicity.
    • Stabilizing medium for carbene generation, particularly N‑heterocyclic carbene (NHC) chemistry, where triazolium precursors are valued for controlled deprotonation and ligand formation.

    3. Separation Science and Extraction

    • Selective extraction agent for metal ions (e.g., rare earths, transition metals), with the phenyl group enhancing π‑interactions and the TFSI anion providing low coordinating behavior.
    • Solvent for liquid–liquid extraction of hydrophobic organics, dyes, and aromatic compounds.
    • Stationary‑phase modifier in chromatography, enabling tunable polarity and enhanced retention of aromatic analytes.

    4. Materials Science and Polymer Integration

    • Plasticizer or ionic dopant in polymer electrolytes, ionogels, and conductive films.
    • Template or structure‑directing agent in nanoparticle synthesis, especially for noble metals where aromatic cations influence particle morphology.
    • Component in self‑assembled materials, leveraging amphiphilic behavior from the octyl chain and aromatic ring.

    5. Spectroscopy, Sensors, and Analytical Uses

    • Medium for spectroelectrochemical studies, offering high optical transparency and low volatility.
    • Ionic liquid matrix for sensors detecting aromatic pollutants or metal ions, where π‑stacking enhances analyte affinity.
    • Stabilizing environment for fluorescence and Raman studies requiring low background and high thermal stability.

    6. High‑Temperature and Vacuum Applications

    • Heat‑transfer and thermal‑stability medium in controlled environments where non‑flammability and low vapor pressure are essential.
    • Lubrication additive for high‑vacuum or high‑temperature systems, benefiting from TFSI’s chemical inertness.

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Additional information

Weight 2 g
Qty