1-Butyl-2,3-dimethylimidazolium triflate, >98%

Price range: $278.87 through $3,848.60

Product Code: IL-0059-HP

CAS NO: 765910-73-4

  • Chemical Formula: C10H17F3N2O3S
  • Synonyms: BDiMIM OTf, Im114 OTf,1-butyl-2,3-dimethylimidazolium trifluoromethanesulfonate
  • Hydrophobic
  • Aromatic
Clear

SUM Formula: C10H17F3N2O3S

Molecular Weight: 302.32

Melting Point: 40 °C

Purity: >98%

  • SUM Formula: C10H17F3N2O3S
  • Molecular Weight: 302.32
  • Melting Point: 40 °C

1-Butyl-2,3-dimethylimidazolium triflate, CAS: 765910-73-4

Key Applications:

1. Catalysis and Organic Synthesis

  • Brønsted‑acidic reaction media for esterifications, acylations, alkylations, and dehydrations.
  • Solvent–catalyst hybrid for Friedel–Crafts reactions, Diels–Alder cycloadditions, and electrophilic aromatic substitutions.
  • Stabilizing medium for carbocationic and metal‑centered catalytic cycles, due to the triflate anion’s weak coordination.
  • Recyclable reaction solvent, reducing solvent waste in multi‑step synthesis.

2. Electrochemistry and Energy Materials

  • Electrolyte component in supercapacitors and electrochemical capacitors where high ionic conductivity and wide electrochemical windows are required.
  • Solvent for redox‑active species in flow‑battery research.
  • Medium for electrodeposition of metals or alloys where moisture‑sensitive or air‑sensitive conditions are needed.

3. Separation Science and Extraction

  • Selective extraction of metal ions, especially where hydrophobic ionic liquids improve phase separation.
  • Solvent for biomass fractionation, including lignin dissolution and carbohydrate processing.
  • CO₂ and SO₂ capture studies, leveraging the imidazolium cation’s tunable interactions with acidic gases.

4. Materials Processing

  • Template or structuring agent in polymer synthesis, block‑copolymer self‑assembly, and nanoparticle stabilization.
  • Plasticizer or ionic additive in polymer electrolytes and ion‑conducting films.
  • Medium for cellulose dissolution and regeneration, depending on the specific hydrogen‑bonding profile of the triflate system.

5. Spectroscopy and Physical Chemistry

  • Non‑volatile matrix for studying solvation dynamics, ion pairing, and transport properties.
  • Model system for benchmarking viscosity, conductivity, and thermal stability trends across substituted imidazolium ionic liquids.

6. Green Chemistry and Process Intensification

  • Replacement for volatile organic solvents in reactions requiring high temperature or strong acidity.
  • Recyclable reaction medium in continuous‑flow or biphasic catalytic systems.
  • Platform for immobilizing homogeneous catalysts, improving catalyst lifetime and recovery.

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Additional information

Weight 25 g
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