1-Ethyl-3-methylpyridinium bis(trifluoromethylsulfonyl)imide, >99%

Price range: $149.93 through $8,208.21

Product Code: IL-0214-HP

CAS NO: 841251-37-4

  • Chemical Formula: C10H12F6N2O4S2
  • Synonyms: Et-3-Pic BTA, Et-3-Pic NTf2, Et-3-Pic TFSI, Et-3-Pic BTI, Et3Pic BTA, Et3Pic NTf2, Et3Pic TFSI, Et3Pic BTI, Ethyl-3-picolinium bis(trifluoromethylsulfonyl)imide, N-Ethyl-3-methylpyridinium bis(trifluoromethylsulfonyl)imide, N-Ethyl-3-picolinium bis(trifluoromethylsulfonyl)imide
  • Weakly-coordinating anion
  • Hydrophobic
  • Aromatic
Clear

Conductivity: 7.47 mS/cm (30 °C)

SUM Formula: C10H12F6N2O4S2

Molecular Weight: 402.33

Melting Point: 6 °C

Density: 1.48 g/cm³ (26 °C)

Purity: >99%

Viscosity: 36.6 cP (25 °C)

  • SUM Formula: C10H12F6N2O4S2
  • Molecular Weight: 402.33
  • Melting Point: 6 °C
  • Density: 1.48 g/cm³ (26 °C)
  • Viscosity: 36.6 cP (25 °C)

1-Ethyl-3-methylpyridinium bis(trifluoromethylsulfonyl)imide, CAS: 841251-37-4

Key Applications:

Electrochemical Systems

  • Serves as a high‑stability ionic liquid electrolyte for lithium, sodium, and multivalent metal batteries.
  • Provides wide electrochemical windows and low volatility, supporting high‑voltage cell designs.
  • Used as a conductive medium in supercapacitors, enabling improved ionic mobility and thermal resilience.
  • Functions as a stable solvent/electrolyte for electrodeposition of metals and alloys under moisture‑sensitive or high‑temperature conditions.

Catalysis and Organic Synthesis

  • Acts as a non‑volatile, thermally robust reaction medium for transition‑metal‑catalyzed transformations.
  • Supports acid‑sensitive and base‑sensitive reactions due to its weakly coordinating TFSI anion.
  • Enables biphasic catalysis and catalyst recycling workflows.
  • Useful for selective alkylation, nucleophilic substitution, and oxidative coupling reactions requiring controlled ionic environments.

Separation Science and Extraction

  • Employed in liquid–liquid extraction of metal ions, particularly rare‑earth and actinide species, due to its hydrophobicity and tunable coordination behavior.
  • Used in chromatographic method development as an ionic liquid additive to improve peak shape and separation efficiency.
  • Supports gas absorption studies, including CO₂ solubility and transport behavior in fluorinated ionic liquids.

Materials Science and Polymer Engineering

  • Incorporated into polymer matrices to enhance ionic conductivity, flexibility, and thermal stability.
  • Used in ionogel formation for flexible electronics, sensors, and solid‑state electrochemical devices.
  • Serves as a plasticizer or mobility‑enhancing additive in high‑performance polymer electrolytes.

Surface Science and Coatings

  • Provides controlled interfacial behavior for electrode modification, corrosion studies, and surface passivation research.
  • Used as a medium for forming uniform, defect‑minimized thin films via electrochemical or solution‑based deposition.
  • Supports lubrication studies where low vapor pressure and high thermal stability are required.

Spectroscopy and Fundamental Research

  • Employed as a reference ionic liquid for benchmarking transport properties (viscosity, conductivity, diffusion).
  • Used in vibrational, NMR, and dielectric spectroscopy to study ion pairing, solvation, and dynamic relaxation processes.
  • Supports computational and experimental investigations of structure–property relationships in pyridinium‑based ionic liquids.

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Additional information

Weight 25 g
Qty

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