1-Allyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide, >99%
Price range: $164.15 through $2,261.81
Product Code: IL-0239-HPCAS NO: 655249-87-9
- Chemical Formula: C9H11F6N3O4S2
- Synonyms: AllylMIM BTA, AllylMIM NTf 2, AllylMIM TFSI, AllylMIM BTI
- Weakly-coordinating anion
- Polymerizable
- Hydrophobic
- Aromatic
Conductivity: 8.871 mS/cm (30 ยฐC)
SUM Formula: C9H11F6N3O4S2
Molecular Weight: 403.32
Melting Point: <25 ยฐC
Density: 1.494 (29ยฐC)
ECW: 4.8V
Purity: >99%
Viscosity: 35 cP (25 ยฐC)
- SUM Formula: C9H11F6N3O4S2
- Molecular Weight: 403.32
- Melting Point: <25 ยฐC
- Density: 1.494 (29ยฐC)
- ECW: 4.8V
- Viscosity: 35 cP (25 ยฐC)
1-Allyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide, CAS: 655249-87-9
Key Applications:
Electrochemical Systems
- Serves as a highโconductivity ionic medium for supercapacitors, redoxโflow systems, and advanced electrochemical cells.
- Supports wide electrochemical windows, enabling stable operation in highโvoltage environments.
- Useful as a coโsolvent 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 ionโconducting polymer films.
Catalysis and Organic Synthesis
- Provides a tunable, lowโvolatility reaction medium for transitionโmetal 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 taskโspecific 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 thinโfilm devices.
- The allyl moiety allows covalent grafting onto surfaces via radical or photochemical pathways, enabling durable ionic interfaces.
Energy and Photonic Materials
- Employed in dyeโsensitized 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, nonโvolatile solvent for highโtemperature reactions and moistureโsensitive transformations.
- Compatible with a wide range of inorganic salts, enabling formulation of designer electrolytes and ionic mixtures.
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