SEE ALSO...
Items 131 to 140 of 172 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
1-Ethyl-3-methylimidazolium acetate | 143314-17-4 | sc-237539 | 5 g | $137.00 | ||
1-Ethyl-3-methylimidazolium acetate, as an ionic liquid, showcases exceptional ionic conductivity and a high degree of solvation power due to its unique imidazolium cation structure. The acetate anion facilitates strong hydrogen bonding interactions, enhancing its ability to stabilize charged species. This ionic liquid exhibits a low tendency for crystallization, allowing for a wide liquid range, which can significantly impact reaction kinetics and mass transport in various chemical environments. | ||||||
1-Ethyl-3-methylimidazolium trifluoromethanesulfonate | 145022-44-2 | sc-237550 sc-237550A | 5 g 100 g | $95.00 $600.00 | ||
1-Ethyl-3-methylimidazolium trifluoromethanesulfonate, an ionic liquid, is characterized by its remarkable electrochemical stability and low viscosity, which promote efficient ion transport. The trifluoromethanesulfonate anion contributes to its strong Lewis acidity, enabling unique interactions with various substrates. This ionic liquid's ability to dissolve a wide range of polar and nonpolar compounds enhances its versatility in facilitating diverse chemical reactions and optimizing catalytic processes. | ||||||
1,2-Dimethyl-3-propylimidazolium tris(trifluoromethylsulfonyl)methide | 169051-77-8 | sc-251557 | 1 g | $323.00 | ||
1,2-Dimethyl-3-propylimidazolium tris(trifluoromethylsulfonyl)methide exhibits exceptional ionic conductivity and thermal stability, making it a prime candidate for electrochemical applications. The unique tris(trifluoromethylsulfonyl)methide anion enhances its Lewis basicity, facilitating strong interactions with cationic species. This ionic liquid's ability to form stable solvate complexes allows for tailored reaction pathways, promoting efficient catalysis and selective reactivity in various chemical environments. | ||||||
1-Hexyl-3-methylimidazolium chloride | 171058-17-6 | sc-251511 | 5 g | $54.00 | ||
1-Hexyl-3-methylimidazolium chloride is characterized by its unique ability to form hydrogen bonds and engage in strong ion-dipole interactions, which significantly influence its solvation properties. This ionic liquid exhibits a high degree of viscosity, affecting diffusion rates and reaction kinetics. Its chloride anion contributes to a diverse range of coordination complexes, enhancing its role in facilitating charge transfer processes and promoting unique pathways in various chemical reactions. | ||||||
1-Butyl-3-methylimidazolium hexafluorophosphate | 174501-64-5 | sc-251490 sc-251490A | 5 g 50 g | $97.00 $251.00 | ||
1-Butyl-3-methylimidazolium hexafluorophosphate stands out due to its exceptional ionic conductivity and low vapor pressure, making it a stable medium for electrochemical applications. The hexafluorophosphate anion enhances its ability to solvate a variety of cations, promoting unique ion pairing and aggregation behaviors. This ionic liquid exhibits significant thermal stability and a wide electrochemical window, facilitating diverse reaction mechanisms and enhancing mass transport in various systems. | ||||||
1-Ethyl-2,3-dimethylimidazolium trifluoromethanesulfonate | 174899-72-0 | sc-222693 sc-222693A | 5 g 50 g | $262.00 $835.00 | ||
1-Ethyl-2,3-dimethylimidazolium trifluoromethanesulfonate exhibits remarkable solvation properties, enabling efficient ion transport and unique molecular interactions. The trifluoromethanesulfonate anion contributes to its strong hydrogen bonding capabilities, influencing reaction kinetics and enhancing the stability of reactive intermediates. This ionic liquid's low viscosity and high ionic mobility facilitate rapid diffusion processes, making it an intriguing medium for various chemical transformations. | ||||||
1-Ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide | 174899-82-2 | sc-251507 | 1 g | $223.00 | ||
1-Ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide showcases exceptional electrochemical stability and a wide electrochemical window, making it ideal for applications requiring robust ionic conductivity. The unique bis(trifluoromethylsulfonyl)imide anion promotes strong ion pairing and enhances the liquid's ability to solvate a variety of cations. Its tunable viscosity and low volatility contribute to efficient mass transport, enabling diverse catalytic processes and enhancing reaction rates in complex systems. | ||||||
1-Butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide | 174899-83-3 | sc-251489 | 1 g | $141.00 | ||
1-Butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide exhibits remarkable ionic characteristics, characterized by its ability to form strong hydrogen bonds and facilitate ion mobility. The unique structure of the imidazolium cation allows for effective solvation of various anions, enhancing ionic interactions. Its low viscosity and high thermal stability promote efficient charge transport, making it suitable for electrochemical applications and facilitating rapid reaction kinetics in diverse chemical environments. | ||||||
1-Butyl-3-methylimidazolium nitrate | 179075-88-8 | sc-222683 sc-222683A | 5 g 50 g | $233.00 $688.00 | ||
1-Butyl-3-methylimidazolium nitrate is a distinctive ionic liquid known for its strong ionic interactions and ability to stabilize various anions through specific solvation dynamics. The imidazolium cation's unique architecture promotes effective charge delocalization, enhancing conductivity. Its favorable viscosity and density characteristics contribute to efficient mass transport, while its capacity to engage in diverse molecular interactions allows for tailored reactivity in various chemical processes. | ||||||
1-Butyl-2,3-dimethylimidazolium hexafluorophosphate | 227617-70-1 | sc-251488 | 5 g | $79.00 | ||
1-Butyl-2,3-dimethylimidazolium hexafluorophosphate is a notable ionic liquid characterized by its high ionic conductivity and low volatility. The presence of the hexafluorophosphate anion facilitates strong electrostatic interactions, enhancing its ability to dissolve a wide range of polar and non-polar compounds. Its unique molecular structure allows for significant tunability in viscosity and thermal stability, making it suitable for various electrochemical applications and reaction environments. | ||||||