1-Ethyl-2,3-dimethylimidazolium Bis(trifluoromethanesulfonyl)imide

98%

Reagent Code: #182201
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CAS Number 174899-90-2

science Other reagents with same CAS 174899-90-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 405.33 g/mol
Formula C₉H₁₃F₆N₃O₄S₂
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an ionic liquid in electrochemical applications such as batteries and supercapacitors due to its high ionic conductivity and wide electrochemical stability window. It serves as a solvent in organic synthesis, especially in reactions requiring non-volatile and thermally stable media. Commonly employed in green chemistry processes to replace volatile organic solvents, reducing environmental impact. Applied in separation processes, including extraction of metals and desulfurization of fuels. Also utilized in analytical chemistry as a buffer additive in capillary electrophoresis to improve separation efficiency.

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Test Parameter Specification
Appearance Colorless to light yellow liquid
NMR Conforms to Structure
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿4,330.00
inventory 25g
10-20 days ฿10,950.00
inventory 100g
10-20 days ฿33,120.00

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1-Ethyl-2,3-dimethylimidazolium Bis(trifluoromethanesulfonyl)imide
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Used as an ionic liquid in electrochemical applications such as batteries and supercapacitors due to its high ionic conductivity and wide electrochemical stability window. It serves as a solvent in organic synthesis, especially in reactions requiring non-volatile and thermally stable media. Commonly employed in green chemistry processes to replace volatile organic solvents, reducing environmental impact. Applied in separation processes, including extraction of metals and desulfurization of fuels. Also ut

Used as an ionic liquid in electrochemical applications such as batteries and supercapacitors due to its high ionic conductivity and wide electrochemical stability window. It serves as a solvent in organic synthesis, especially in reactions requiring non-volatile and thermally stable media. Commonly employed in green chemistry processes to replace volatile organic solvents, reducing environmental impact. Applied in separation processes, including extraction of metals and desulfurization of fuels. Also utilized in analytical chemistry as a buffer additive in capillary electrophoresis to improve separation efficiency.

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