1-Allyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide, >99%

Price range: $164.15 through $2,261.81

Product Code: IL-0239-HP

CAS NO: 655249-87-9

  • Chemical Formula: C9H11F6N3O4S2
  • Synonyms: AllylMIM BTA, AllylMIM NTf 2, AllylMIM TFSI, AllylMIM BTI
  • Weakly-coordinating anion
  • Polymerizable
  • Hydrophobic
  • Aromatic
Clear

Conductivity: 8.871 mS/cm (30 °C)

SUM Formula: C9H11F6N3O4S2

Molecular Weight: 403.32

Melting Point: <25 °C

Density: 1.494 (29°C)

ECW: 4.8V

Purity: >99%

Viscosity: 35 cP (25 °C)

  • SUM Formula: C9H11F6N3O4S2
  • Molecular Weight: 403.32
  • Melting Point: <25 °C
  • Density: 1.494 (29°C)
  • ECW: 4.8V
  • Viscosity: 35 cP (25 °C)

1-Allyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide, CAS: 655249-87-9

Key Applications:

Electrochemical Systems

  • Serves as a high‑conductivity ionic medium for supercapacitors, redox‑flow systems, and advanced electrochemical cells.
  • Supports wide electrochemical windows, enabling stable operation in high‑voltage environments.
  • Useful as a co‑solvent or electrolyte additive to improve ion mobility and reduce interfacial resistance.

Polymer and Materials Processing

  • Acts as a reactive ionic liquid for polymer modification, particularly where the allyl group enables covalent incorporation into polymer matrices.
  • Facilitates dissolution and processing of polar polymers, including cellulose derivatives and specialty engineering plastics.
  • Functions as a plasticizer or ionic dopant in ion‑conducting polymer films.

Catalysis and Organic Synthesis

  • Provides a tunable, low‑volatility reaction medium for transition‑metal catalysis, nucleophilic substitutions, and alkylation reactions.
  • The allyl substituent can participate in or stabilize reactive intermediates, offering unique selectivity profiles in certain catalytic cycles.
  • Enables biphasic catalysis where product separation is simplified due to immiscibility with common organic solvents.

Separation Science and Extraction

  • Effective as an extraction phase for metal ions, hydrophobic organics, and fluorinated species due to the hydrophobic TFSI anion.
  • Supports task‑specific extraction workflows where the allyl group can be leveraged for further functionalization or immobilization on solid supports.

Surface and Interface Engineering

  • Useful in forming ionically conductive surface films for sensors, coatings, and thin‑film devices.
  • The allyl moiety allows covalent grafting onto surfaces via radical or photochemical pathways, enabling durable ionic interfaces.

Energy and Photonic Materials

  • Employed in dye‑sensitized solar cells and related optoelectronic systems as a stable ionic medium with low volatility.
  • Enhances charge transport in composite materials containing conductive polymers or nanostructured carbon.

General Solvent and Processing Uses

  • Provides a thermally stable, non‑volatile solvent for high‑temperature reactions and moisture‑sensitive transformations.
  • Compatible with a wide range of inorganic salts, enabling formulation of designer electrolytes and ionic mixtures.

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Additional information

Weight 25 g
Qty

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