Items 371 to 380 of 426 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
1-Naphthyl phosphate, disodium salt | 2183-17-7 | sc-206185 sc-206185A | 100 mg 1 g | $52.00 $113.00 | ||
1-Naphthyl phosphate, disodium salt, is a versatile salt known for its ability to engage in specific molecular interactions, particularly through its aromatic naphthyl group. This compound exhibits unique solubility characteristics, allowing it to participate in various reaction pathways. Its ionic nature enhances its reactivity, facilitating rapid hydrolysis in aqueous environments. The distinct electronic properties of the naphthyl moiety contribute to its role in complexation and coordination chemistry, making it an interesting subject for studies on molecular dynamics and reactivity patterns. | ||||||
Sodium methanesulfonate | 2386-57-4 | sc-236911 sc-236911A | 5 g 100 g | $37.00 $133.00 | ||
Sodium methanesulfonate is a distinctive salt characterized by its strong ionic interactions and high solubility in polar solvents. Its unique sulfonate group enhances its ability to stabilize transition states during chemical reactions, promoting efficient pathways in nucleophilic substitutions. The compound's low viscosity in solution allows for improved mass transfer, while its hygroscopic nature can influence reaction kinetics by modulating local concentrations of reactants. This behavior makes it a subject of interest in various chemical studies. | ||||||
Tetrapentylammonium iodide | 2498-20-6 | sc-237078 | 25 g | $74.00 | ||
Tetrapentylammonium iodide is a quaternary ammonium salt notable for its large, hydrophobic pentyl groups, which significantly influence its solubility and phase behavior in nonpolar solvents. The compound exhibits strong ionic interactions, leading to unique aggregation phenomena in solution. Its ability to form stable ion pairs can affect reaction kinetics, particularly in nucleophilic reactions, by altering the effective concentration of reactive species. Additionally, its distinct molecular structure contributes to its role in facilitating specific ion transport mechanisms. | ||||||
Barium trifluoromethanesulfonate | 2794-60-7 | sc-233914 | 5 g | $54.00 | ||
Barium trifluoromethanesulfonate is a highly soluble salt characterized by its strong ionic bonds and the presence of trifluoromethanesulfonate anions, which enhance its reactivity. The compound exhibits unique electrostatic interactions that can influence solvation dynamics and ion pairing in various media. Its distinct molecular architecture allows for selective coordination with other ions, potentially affecting reaction pathways and kinetics in complex chemical systems. | ||||||
Tetraheptylammonium iodide | 3535-83-9 | sc-237043 | 25 g | $224.00 | ||
Tetraheptylammonium iodide is a quaternary ammonium salt known for its unique surfactant properties and ability to form stable micelles in solution. The long heptyl chains contribute to its hydrophobic character, facilitating interactions with organic solvents. This compound exhibits interesting phase behavior and can influence the solubility of other ionic species, impacting reaction kinetics and equilibria in mixed solvent systems. Its distinct molecular structure allows for versatile applications in various chemical environments. | ||||||
Trimethyl-tetradecylammonium chloride | 4574-04-3 | sc-237339 | 5 g | $64.00 | ||
Trimethyl-tetradecylammonium chloride is a quaternary ammonium salt characterized by its long tetradecyl chain, which enhances its hydrophobic interactions and surface activity. This compound can effectively alter interfacial tension, promoting emulsification and stabilization in colloidal systems. Its unique molecular architecture facilitates ion pairing and influences the solubility of various compounds, thereby affecting reaction dynamics and equilibria in diverse chemical environments. | ||||||
Tetrapentylammonium hydroxide solution | 4598-61-2 | sc-237077 | 25 ml | $113.00 | ||
Tetrapentylammonium hydroxide solution is a quaternary ammonium salt notable for its unique amphiphilic properties, which arise from its pentyl chains. This structure enhances its ability to interact with both polar and nonpolar substances, facilitating complexation and solubilization processes. The hydroxide ion contributes to its strong basicity, promoting nucleophilic reactions and influencing the kinetics of various chemical transformations. Its distinct molecular interactions can significantly modify reaction pathways and equilibria in diverse systems. | ||||||
Methyltrioctylammonium chloride | 5137-55-3 | sc-235876 | 10 g | $128.00 | ||
Methyltrioctylammonium chloride is a quaternary ammonium salt characterized by its long octyl chains, which impart significant hydrophobicity. This structure enables the compound to form micelles in aqueous environments, enhancing its ability to encapsulate nonpolar molecules. The chloride ion facilitates ionic interactions, promoting solubility in polar solvents. Its unique molecular architecture influences phase behavior and enhances interfacial tension dynamics, making it a key player in various chemical processes. | ||||||
Benzyltripropylammonium chloride | 5197-87-5 | sc-234009 | 10 g | $65.00 | ||
Benzyltripropylammonium chloride is a quaternary ammonium salt distinguished by its benzyl and propyl groups, which contribute to its amphiphilic nature. This compound exhibits strong ionic interactions due to the presence of the chloride ion, enhancing its solubility in polar media. Its unique structure allows for effective surfactant properties, influencing adsorption at interfaces and stabilizing emulsions. Additionally, it can facilitate phase transfer reactions, showcasing its versatility in various chemical environments. | ||||||
Benzyltriethylammonium bromide | 5197-95-5 | sc-234006 | 25 g | $23.00 | ||
Benzyltriethylammonium bromide is a quaternary ammonium salt characterized by its bulky benzyl and ethyl groups, which enhance its lipophilicity. The bromide ion contributes to its ionic strength, promoting solubility in organic solvents. This compound exhibits unique behavior in phase transfer catalysis, enabling the migration of ionic species across immiscible phases. Its structure also facilitates strong van der Waals interactions, influencing molecular aggregation and stability in diverse chemical systems. | ||||||