Items 21 to 30 of 33 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Sodium 1-tetradecanesulfonate | 6994-45-2 | sc-250995 | 10 g | $159.00 | ||
Sodium 1-tetradecanesulfonate serves as a versatile ion pair reagent, distinguished by its extended hydrophobic tail that facilitates the formation of stable ion pairs in polar solvents. This compound enhances the solubility of ionic species, promoting unique molecular interactions that can alter reaction pathways. Its structural properties enable effective shielding of charged groups, influencing reaction kinetics and enabling the study of dynamic equilibria in complex chemical environments. | ||||||
Sodium 1-octadecanesulfonate | 13893-34-0 | sc-250992 | 5 g | $298.00 | ||
Sodium 1-octadecanesulfonate is a prominent ion pair reagent characterized by its long hydrophobic chain, which significantly influences solvation dynamics. This compound promotes the stabilization of ionic species through hydrophobic interactions, enhancing their reactivity in various media. Its unique structure allows for selective ion pairing, which can modify reaction mechanisms and facilitate the exploration of charge transfer processes, making it a valuable tool in studying complex ionic interactions. | ||||||
Tetraethylammonium hydrogen sulfate | 16873-13-5 | sc-253669 | 10 g | $210.00 | 1 | |
Tetraethylammonium hydrogen sulfate serves as a versatile ion pair reagent, notable for its ability to form stable ion pairs through strong electrostatic interactions. Its quaternary ammonium structure enhances solubility in polar solvents, facilitating the transport of charged species. This compound can influence reaction kinetics by altering the effective concentration of ions, thereby modulating reaction pathways and enabling the study of ionic behavior in diverse chemical environments. | ||||||
Sodium pentanesulfonate | 22767-49-3 | sc-258174 sc-258174A | 5 g 25 g | $60.00 $166.00 | ||
Sodium pentanesulfonate acts as an effective ion pair reagent, characterized by its ability to stabilize ionic species through hydrophobic interactions and ionic bonding. Its unique structure promotes solubility in aqueous environments, enhancing the mobility of ions. This compound can significantly influence reaction dynamics by modifying the local ionic atmosphere, thereby affecting the rates and mechanisms of various chemical reactions. Its distinct properties allow for nuanced exploration of ion interactions in solution. | ||||||
Sodium 1-nonanesulfonate | 35192-74-6 | sc-253571 | 10 g | $136.00 | ||
Sodium 1-nonanesulfonate serves as a versatile ion pair reagent, distinguished by its long hydrophobic tail that enhances the solvation of ionic species. This compound facilitates the formation of stable ion pairs, promoting selective ion interactions and influencing reaction pathways. Its unique amphiphilic nature allows for effective modulation of electrostatic environments, thereby altering reaction kinetics and enhancing the efficiency of charge transfer processes in various chemical systems. | ||||||
Tetramethylammonium bisulfate | 80526-82-5 | sc-251197A sc-251197 | 10 g 50 g | $149.00 $550.00 | ||
Tetramethylammonium bisulfate acts as a potent ion pair reagent, characterized by its quaternary ammonium structure that enhances ionic solubility and stability. This compound promotes the formation of ion pairs through strong electrostatic interactions, effectively shielding charges and facilitating selective ion transport. Its unique ability to modulate the local dielectric environment influences reaction dynamics, enabling faster kinetics and improved selectivity in various chemical reactions. | ||||||
Tetrahexylammonium dihydrogen phosphate solution | 87700-05-8 | sc-258226 | 1 each | $1620.00 | ||
Tetrahexylammonium dihydrogen phosphate solution serves as an effective ion pair reagent, distinguished by its long-chain alkyl groups that enhance hydrophobic interactions. This compound stabilizes ionic species through solvation, promoting the formation of ion pairs in polar solvents. Its unique structural features allow for tailored electrostatic environments, which can significantly influence reaction pathways and enhance selectivity in complex chemical systems. The solution's viscosity and density further contribute to its behavior in various ionic interactions. | ||||||
Trimethyltetradecylammonium hydrogen sulfate | 104903-23-3 | sc-237352 | 10 g | $309.00 | ||
Trimethyltetradecylammonium hydrogen sulfate functions as a versatile ion pair reagent, characterized by its quaternary ammonium structure that facilitates strong electrostatic interactions. The long tetradecyl chain enhances lipophilicity, promoting solubilization of ionic compounds in non-polar environments. This compound exhibits unique aggregation behavior, influencing reaction kinetics and selectivity by stabilizing transient ionic states, thereby altering the dynamics of chemical transformations in solution. | ||||||
Sodium 1-hexanesulfonate monohydrate | 207300-91-2 | sc-250991 sc-250991A | 2.5 g 10 g | $42.00 $136.00 | ||
Sodium 1-hexanesulfonate monohydrate serves as an effective ion pair reagent, distinguished by its sulfonate group that enhances solubility in aqueous environments. The hexane chain contributes to its hydrophobic character, allowing for selective interactions with various ionic species. This compound exhibits unique micellar properties, which can modulate reaction pathways and improve the efficiency of ion exchange processes, ultimately influencing the kinetics of chemical reactions in solution. | ||||||
Sodium 1-pentanesulfonate monohydrate | 207605-40-1 | sc-253572 sc-253572A | 5 g 25 g | $58.00 $103.00 | ||
Sodium 1-pentanesulfonate monohydrate functions as a versatile ion pair reagent, characterized by its unique pentane chain that balances hydrophilicity and hydrophobicity. This structure facilitates specific ion interactions, promoting the formation of stable ion pairs in solution. Its ability to influence solvation dynamics enhances reaction kinetics, while the sulfonate moiety aids in stabilizing charged intermediates, thereby optimizing various chemical pathways and improving overall reaction efficiency. | ||||||