Items 121 to 130 of 426 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Lithium acetate | 546-89-4 | sc-235503 sc-235503A sc-235503B sc-235503C sc-235503D | 100 g 1 kg 2.5 kg 5 kg 10 kg | $87.00 $168.00 $372.00 $700.00 $1331.00 | ||
Lithium acetate is a distinctive salt known for its ability to form strong hydrogen bonds due to the presence of lithium ions, which can influence solvation dynamics in solution. This compound exhibits unique ionic interactions that enhance its reactivity, particularly in organic synthesis. Its low lattice energy contributes to its solubility, allowing for efficient ion dissociation. Additionally, lithium acetate can participate in various coordination complexes, affecting its behavior in different chemical environments. | ||||||
2-Ketobutyric acid, sodium salt | 2013-26-5 | sc-206463 sc-206463A | 5 g 25 g | $95.00 $328.00 | ||
2-Ketobutyric acid, sodium salt is a notable salt characterized by its capacity to engage in ionic interactions that facilitate its solubility in aqueous environments. The sodium ion enhances the compound's stability and reactivity, allowing it to participate in various biochemical pathways. Its unique structure promotes specific molecular interactions, influencing reaction kinetics and enabling it to act as a versatile intermediate in diverse chemical processes. | ||||||
Benzyldimethyloctylammonium chloride | 959-55-7 | sc-227344 sc-227344A | 5 g 100 g | $377.00 $4080.00 | ||
Benzyldimethyloctylammonium chloride is a quaternary ammonium salt characterized by its amphiphilic nature, which promotes unique surfactant properties. The long hydrophobic octyl chain enhances its ability to interact with lipid membranes, while the positively charged nitrogen facilitates electrostatic interactions with anionic species. This compound exhibits notable surface activity, lowering interfacial tension and enabling distinct micelle formation, which influences its behavior in various chemical environments. | ||||||
Xylometazoline hydrochloride | 1218-35-5 | sc-255719 | 5 g | $164.00 | ||
Xylometazoline hydrochloride is a zwitterionic compound that exhibits unique solubility characteristics due to its dual functional groups. The presence of a positively charged nitrogen atom allows for strong ionic interactions with polar solvents, enhancing its stability in aqueous environments. Its structural conformation facilitates specific hydrogen bonding, influencing its reactivity and interaction with other ionic species. This compound's ability to form stable complexes contributes to its distinct behavior in various chemical systems. | ||||||
Metaproterenol hemisulfate salt | 5874-97-5 | sc-257701 | 1 g | $600.00 | 2 | |
Metaproterenol hemisulfate salt is characterized by its ionic nature, which promotes strong electrostatic interactions in solution. The sulfate moiety enhances solubility in polar solvents, facilitating rapid diffusion and interaction with other charged species. Its molecular structure allows for specific conformational flexibility, influencing reaction kinetics and enabling unique pathways in ionic equilibria. This compound's ability to engage in hydrogen bonding further modulates its reactivity, making it a distinctive entity in chemical systems. | ||||||
Victoria blue R | 2185-86-6 | sc-216056 | 25 g | $57.00 | ||
Victoria blue R, as a salt, exhibits remarkable solubility in aqueous environments, attributed to its ionic character. The presence of multiple aromatic rings contributes to its strong π-π stacking interactions, enhancing stability in solution. Its unique chromophoric structure allows for distinct light absorption properties, influencing photochemical behavior. Additionally, the compound's ability to form complexes with metal ions can alter its reactivity, showcasing its versatility in various chemical contexts. | ||||||
Tetrabutylammonium sulfate solution | 2472-88-0 | sc-229395 sc-229395A sc-229395B | 100 ml 500 ml 2.5 L | $40.00 $135.00 $612.00 | ||
Tetrabutylammonium sulfate solution is characterized by its high ionic strength, which facilitates enhanced solvation dynamics in polar solvents. The bulky tetrabutylammonium cation promotes unique steric effects, influencing reaction pathways and kinetics. This compound exhibits strong ion-pairing interactions, which can stabilize transition states in various reactions. Its ability to modulate the dielectric environment also affects the solubility and reactivity of other ionic species, making it a versatile medium for electrochemical studies. | ||||||
Dimethyldioctylammonium Bromide | 3026-69-5 | sc-294358 sc-294358A | 5 g 25 g | $228.00 $678.00 | ||
Dimethyldioctylammonium Bromide is a quaternary ammonium salt known for its amphiphilic nature, which allows it to interact effectively with both polar and nonpolar environments. The long hydrocarbon chains enhance its surface activity, promoting micelle formation and altering interfacial tension. Its unique molecular structure facilitates strong van der Waals interactions, influencing solubility and stability in various formulations. Additionally, it exhibits significant ion exchange properties, impacting reaction dynamics in complex systems. | ||||||
Azumolene Sodium Salt | 105336-14-9 | sc-207313 | 10 mg | $330.00 | 2 | |
Azumolene Sodium Salt is a unique salt that exhibits distinctive solubility characteristics, allowing it to interact effectively with various solvents. Its ionic nature facilitates strong electrostatic interactions, enhancing its stability in solution. The compound's ability to form complexes with transition metals can influence catalytic pathways, while its specific anion-cation interactions may lead to unique crystallization behaviors. Additionally, its reactivity profile is shaped by the presence of functional groups that can participate in diverse chemical transformations. | ||||||
2-(Aminooxy)propane hydrochloride | 4490-81-7 | sc-298135 sc-298135A | 500 mg 1 g | $149.00 $269.00 | ||
2-(Aminooxy)propane hydrochloride is a distinctive salt characterized by its ability to engage in hydrogen bonding and nucleophilic interactions due to its aminooxy functional group. This compound exhibits notable reactivity in condensation reactions, facilitating the formation of stable adducts. Its ionic nature enhances solubility in polar solvents, promoting effective molecular interactions. The presence of the hydrochloride moiety contributes to its stability and influences its behavior in various chemical environments. |