1-Ethyl-2,3-dimethylimidazolium hexafluorophosphate

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Reagent Code: #182903
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CAS Number 292140-86-4

science Other reagents with same CAS 292140-86-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 270.16 g/mol
Formula C₇H₁₃F₆N₂P
badge Registry Numbers
MDL Number MFCD08458503
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an ionic liquid in catalysis and organic synthesis due to its high thermal stability and low vapor pressure. Commonly serves as a green solvent in reactions such as Heck coupling, Diels-Alder, and hydrogenation, where it enhances reaction rates and selectivity. Also applied in electrochemistry, including as an electrolyte in batteries and supercapacitors, owing to its wide electrochemical window and good ionic conductivity. Its non-volatile nature makes it suitable for use in separation processes and extraction of compounds, including metal ions and biomolecules. Additionally, employed in analytical chemistry for matrix-assisted laser desorption/ionization (MALDI) mass spectrometry and as a background electrolyte in capillary electrophoresis.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿420.00
inventory 25g
10-20 days ฿1,150.00
inventory 100g
10-20 days ฿4,280.00
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1-Ethyl-2,3-dimethylimidazolium hexafluorophosphate
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Used as an ionic liquid in catalysis and organic synthesis due to its high thermal stability and low vapor pressure. Commonly serves as a green solvent in reactions such as Heck coupling, Diels-Alder, and hydrogenation, where it enhances reaction rates and selectivity. Also applied in electrochemistry, including as an electrolyte in batteries and supercapacitors, owing to its wide electrochemical window and good ionic conductivity. Its non-volatile nature makes it suitable for use in separation processes

Used as an ionic liquid in catalysis and organic synthesis due to its high thermal stability and low vapor pressure. Commonly serves as a green solvent in reactions such as Heck coupling, Diels-Alder, and hydrogenation, where it enhances reaction rates and selectivity. Also applied in electrochemistry, including as an electrolyte in batteries and supercapacitors, owing to its wide electrochemical window and good ionic conductivity. Its non-volatile nature makes it suitable for use in separation processes and extraction of compounds, including metal ions and biomolecules. Additionally, employed in analytical chemistry for matrix-assisted laser desorption/ionization (MALDI) mass spectrometry and as a background electrolyte in capillary electrophoresis.

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