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 ยฐC)

SUM Formula: C7H9F6N3O4S2

Molecular Weight: 377.28

Melting Point: <RT

Purity: >98%

Viscosity: 106 cP (25 ยฐC)

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

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

1. Electrolytes for Highโ€‘Performance Energy Storage

  • Functions as a lowโ€‘viscosity ionic liquid electrolyte component for Liโ€‘ion, Naโ€‘ion, and Mgโ€‘ion batteries.
  • The TFSIโป anion provides wide electrochemical stability windows suitable for highโ€‘voltage cathodes.
  • Supports ionicโ€‘liquidโ€‘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 1,2โ€‘dimethyl substitution reduces crystallinity, improving lowโ€‘temperature performance.

3. Solvent and Coโ€‘solvent for Organic Synthesis

  • Acts as a nonโ€‘volatile, thermally robust reaction medium for transitionโ€‘metal catalysis, Cโ€“C coupling, and heterocycle functionalization.
  • The cationโ€™s steric and electronic profile can improve selectivity in organometallic transformations.

4. Extraction and Separation Processes

  • Effective in liquidโ€“liquid extraction of metal ions due to the hydrophobic TFSIโป anion.
  • Useful in COโ‚‚ 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, rareโ€‘earth metals, and reactive alloys.
  • Supports smooth, dendriteโ€‘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 cationโ€“anion interactions, solvation dynamics, and charge transport.
  • The 1,2โ€‘dimethyl substitution pattern provides a distinct benchmark for structureโ€“property correlation studies.

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Additional information

Weight 0.025 g
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