1,2-Dimethylimidazolium bis(trifluoromethylsulfonyl)imide, >98%

Price range: $260.45 through $2,063.17

Product Code: IL-0278-SG

CAS NO: 353239-12-0

  • Chemical Fr: C7H9F6N3O4S2
  • Synonyms: DiMIM BTA, DiMIM NTf2, DiMIM TFSI, DiMIM BTI
  • Weakly-coordinating anion
  • Hydrophobic
  • Aromatic
  • Protic

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Clear

Conductivity: 1.08 mS/cm (25 °C)

SUM Formula: C7H9F6N3O4S2

Molecular Weight: 377.28

Melting Point: <RT

Purity: >98%

Viscosity: 106 cP (25 °C)

  • SPECIFIC GRAVITY: NA
  • SUM Formula: C7H9F6N3O4S2
  • Molecular Weight: 377.28
  • Melting Point:
  • Viscosity: 106 cP (25 °C)

1,2-Dimethylimidazolium bis(trifluoromethylsulfonyl)imide, CAS: 353239-12-0

1. Electrolytes for High‑Performance Energy Storage

  • Functions as a low‑viscosity ionic liquid electrolyte component for Li‑ion, Na‑ion, and Mg‑ion batteries.
  • The TFSI⁻ anion provides wide electrochemical stability windows suitable for high‑voltage cathodes.
  • Supports ionic‑liquid‑based gel polymer electrolytes requiring enhanced ion mobility.

2. Supercapacitors and Hybrid Capacitors

  • Serves as a stable ionic medium for EDLCs and pseudocapacitors with high ionic conductivity and thermal stability.
  • The 1,2‑dimethyl substitution reduces crystallinity, improving low‑temperature performance.

3. Solvent and Co‑solvent for Organic Synthesis

  • Acts as a non‑volatile, thermally robust reaction medium for transition‑metal catalysis, C–C coupling, and heterocycle functionalization.
  • The cation’s steric and electronic profile can improve selectivity in organometallic transformations.

4. Extraction and Separation Processes

  • Effective in liquid–liquid extraction of metal ions due to the hydrophobic TFSI⁻ anion.
  • Useful in CO₂ capture systems where imidazolium ionic liquids enhance absorption capacity and tunability.

5. Electrochemical Deposition and Surface Engineering

  • Provides a stable ionic environment for metal electrodeposition, including aluminum, rare‑earth metals, and reactive alloys.
  • Supports smooth, dendrite‑resistant deposition due to low water content and high thermal stability.

6. Polymer Processing and Advanced Materials

  • Functions as a plasticizer or ionic dopant in conductive polymers such as PEDOT and polyaniline.
  • Enhances mechanical flexibility and ionic conductivity in ionogels and polymer electrolytes.

7. Spectroscopy and Fundamental Research

  • Used as a model ionic liquid for studying cation–anion interactions, solvation dynamics, and charge transport.
  • The 1,2‑dimethyl substitution pattern provides a distinct benchmark for structure–property correlation studies.

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Additional information

Weight 25 g
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