1-Ethyl-2-methylpyridinium bis(trifluoromethylsulfonyl)imide, >99%
Price range: $202.34 through $11,340.61
Product Code: IL-0247-HPCAS NO: 712354-99-9
- Chemical Formula: C10H12F6N2O4S2
- Synonyms: 1-Ethyl-2-picolinium bis(trifluoromethylsulfonyl)imide, N-Ethyl-2-methylpyridinium bis(trifluoromethylsulfonyl)imide, Et2Pic BTA, Et-2-Pic BTA, Et2Pic NTf2, Et2Pic TFSI, Et2Pic BTI
- Weakly coordinating anion
- Hydrophobic
- Aromatic
Conductivity: 3.71 mS/cm (30 °C)
SUM Formula: C10H12F6N2O4S2
Molecular Weight: 402.33
Melting Point: <RT
Density: 1.51 g/cm³ (27 °C)
ECW: 4.4 V
Purity: >99%
Viscosity: 74.8 cP (25 °C)
- SUM Formula: C10H12F6N2O4S2
- Molecular Weight: 402.33
- Melting Point:
1-Ethyl-2-methylpyridinium bis(trifluoromethylsulfonyl)imide, CAS: 712354-99-9
Key Applications:
Electrochemical Systems
- High‑stability electrolyte component for lithium, sodium, and multivalent ion batteries where low viscosity and high ionic conductivity are required.
- Additive for high‑voltage electrolyte formulations, improving oxidative stability and suppressing parasitic reactions at electrode interfaces.
- Electrolyte medium for supercapacitors, particularly in devices requiring wide electrochemical windows and low volatility.
- Solvent or co‑solvent in electrodeposition baths, supporting uniform metal deposition and improved current efficiency.
Thermal & Chemical Stability Applications
- Heat‑transfer and thermal‑management fluids in systems requiring non‑flammability and high thermal stability.
- Reaction medium for high‑temperature or strongly electrophilic transformations, leveraging the TFSI anion’s exceptional chemical inertness.
- Solvent for catalytic processes, especially those involving transition‑metal complexes that benefit from weakly coordinating anions.
Separation Science & Extraction
- Phase‑transfer medium for metal ion extraction, including rare‑earth and precious‑metal separations.
- Selective solvent for hydrophobic analytes in liquid–liquid extraction workflows.
- Stationary‑phase modifier in chromatography, enhancing retention and selectivity for nonpolar or aromatic species.
Materials Science & Polymer Processing
- Plasticizer or processing aid for high‑performance polymers, improving flexibility and ionic mobility.
- Doping medium for conductive polymers such as PEDOT derivatives, enhancing conductivity and mechanical stability.
- Template or structuring solvent in the synthesis of porous materials, ionogels, and hybrid organic–inorganic matrices.
Surface & Interface Engineering
- Surface‑modification medium for tuning wettability, charge density, or interfacial adhesion on metals, oxides, and carbon materials.
- Electrochemical cleaning or passivation baths, benefiting from the ionic liquid’s low volatility and broad electrochemical window.
Analytical & Spectroscopic Uses
- Matrix or solvent for spectroscopic studies (NMR, IR, Raman) where low vapor pressure and high thermal stability are advantageous.
- Medium for studying ion–molecule interactions, proton transfer, and solvation dynamics due to its asymmetric pyridinium cation.
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