1,3-Bis(cyanomethyl)imidazolium chloride

95%

Reagent Code: #152689
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CAS Number 934047-83-3

science Other reagents with same CAS 934047-83-3

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inventory_2 Storage & Handling
Storage Room temperature, argon

description Product Description

Used as an ionic liquid precursor in electrochemical applications, particularly in batteries and supercapacitors due to its good thermal stability and ionic conductivity. It serves as a catalyst or solvent in organic synthesis, especially in reactions requiring mild and non-aqueous conditions. Its functionalized imidazolium structure makes it suitable for modifying electrodes in sensors, enhancing sensitivity and electron transfer. Also investigated in CO₂ capture systems where the nitrile groups contribute to selective gas interactions. Commonly employed in the preparation of supported ionic liquid-phase (SILP) catalysts for continuous flow processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿800.00
inventory 1g
10-20 days ฿5,010.00
inventory 5g
10-20 days ฿17,100.00
inventory 10g
10-20 days ฿29,650.00
inventory 25g
10-20 days ฿65,650.00

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1,3-Bis(cyanomethyl)imidazolium chloride
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Used as an ionic liquid precursor in electrochemical applications, particularly in batteries and supercapacitors due to its good thermal stability and ionic conductivity. It serves as a catalyst or solvent in organic synthesis, especially in reactions requiring mild and non-aqueous conditions. Its functionalized imidazolium structure makes it suitable for modifying electrodes in sensors, enhancing sensitivity and electron transfer. Also investigated in CO₂ capture systems where the nitrile groups contrib

Used as an ionic liquid precursor in electrochemical applications, particularly in batteries and supercapacitors due to its good thermal stability and ionic conductivity. It serves as a catalyst or solvent in organic synthesis, especially in reactions requiring mild and non-aqueous conditions. Its functionalized imidazolium structure makes it suitable for modifying electrodes in sensors, enhancing sensitivity and electron transfer. Also investigated in CO₂ capture systems where the nitrile groups contribute to selective gas interactions. Commonly employed in the preparation of supported ionic liquid-phase (SILP) catalysts for continuous flow processes.

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