3-methyl-1-octyl-4-phenyl-triazolium bis((trifluoromethyl)sulfonyl)amide
Product Code: TzPhC8FSCAS 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
This is a custom synthesis product. Price upon request
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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:
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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.
Please contact us if you want to learn more or need assistance with your order.
Additional information
| Weight | 2 g |
|---|---|
| Qty |




