1-Hexyl-1-methylpyrrolidin-1-iumBis((trifluoromethyl)sulfonyl)amide

≥95%(T)(N)

Reagent Code: #197418
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CAS Number 380497-19-8

science Other reagents with same CAS 380497-19-8

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Weight 450.46 g/mol
Formula C₁₃H₂₄F₆N₂O₄S₂
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as an ionic liquid in electrochemical applications due to its high thermal stability and low volatility. Commonly employed as an electrolyte in lithium-ion batteries and supercapacitors, where it enhances ion conductivity and improves device safety by reducing flammability. Its wide electrochemical window makes it suitable for use in dye-sensitized solar cells and fuel cells. Also utilized as a green solvent in organic synthesis, facilitating reactions such as palladium-catalyzed cross-couplings without the need for volatile organic solvents. Stable under both acidic and basic conditions, it supports biphasic catalytic systems and enables easy product separation.

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inventory 5g
10-20 days ฿8,070.00

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1-Hexyl-1-methylpyrrolidin-1-iumBis((trifluoromethyl)sulfonyl)amide
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Used primarily as an ionic liquid in electrochemical applications due to its high thermal stability and low volatility. Commonly employed as an electrolyte in lithium-ion batteries and supercapacitors, where it enhances ion conductivity and improves device safety by reducing flammability. Its wide electrochemical window makes it suitable for use in dye-sensitized solar cells and fuel cells. Also utilized as a green solvent in organic synthesis, facilitating reactions such as palladium-catalyzed cross-cou

Used primarily as an ionic liquid in electrochemical applications due to its high thermal stability and low volatility. Commonly employed as an electrolyte in lithium-ion batteries and supercapacitors, where it enhances ion conductivity and improves device safety by reducing flammability. Its wide electrochemical window makes it suitable for use in dye-sensitized solar cells and fuel cells. Also utilized as a green solvent in organic synthesis, facilitating reactions such as palladium-catalyzed cross-couplings without the need for volatile organic solvents. Stable under both acidic and basic conditions, it supports biphasic catalytic systems and enables easy product separation.

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