Items 151 to 160 of 426 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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N-Allyl-(±)-SKF-38393 hydrobromide | 300561-58-4 | sc-224127 sc-224127A | 25 mg 100 mg | $211.00 $959.00 | ||
N-Allyl-(±)-SKF-38393 hydrobromide is a notable salt characterized by its unique ability to engage in specific molecular interactions that enhance its solubility in polar solvents. The presence of the hydrobromide moiety facilitates proton transfer processes, influencing its reactivity. This compound exhibits distinct conformational flexibility, which can affect its interaction with various substrates, potentially altering reaction pathways and kinetics in diverse chemical environments. | ||||||
N-Desmethyl Rosuvastatin Disodium Salt Monohydrate | sc-219129 | 1 mg | $380.00 | 1 | ||
N-Desmethyl Rosuvastatin Disodium Salt Monohydrate is a distinctive salt that showcases enhanced ionic interactions due to its disodium composition, promoting increased solubility in aqueous environments. Its monohydrate form contributes to unique hydration dynamics, influencing stability and reactivity. The compound's ability to form strong hydrogen bonds can affect its crystallization behavior, leading to variations in physical properties and potential reactivity in different chemical contexts. | ||||||
Benzyldimethyltetradecylammonium-d7 Chloride | 1219178-72-9 | sc-217741 | 10 mg | $300.00 | ||
Benzyldimethyltetradecylammonium-d7 Chloride is a quaternary ammonium salt characterized by its long hydrophobic alkyl chain, which enhances its surface-active properties. This compound exhibits unique molecular interactions, including strong electrostatic attractions and hydrophobic effects, facilitating its role in forming micelles. Its deuterated nature allows for distinct NMR spectroscopic analysis, providing insights into molecular dynamics and reaction pathways in various environments. | ||||||
Ethyltrimethylammonium iodide | 51-93-4 | sc-228099 | 25 g | $167.00 | ||
Ethyltrimethylammonium iodide is a quaternary ammonium salt notable for its ionic character and ability to form stable complexes with anions. Its structure promotes significant solvation effects, influencing reaction kinetics in polar solvents. The compound exhibits unique phase behavior, often acting as a surfactant, which can alter interfacial tension and enhance emulsification processes. Additionally, its ionic interactions contribute to its role in stabilizing colloidal systems. | ||||||
Haloperidol hydrochloride | 1511-16-6 | sc-203593 | 100 mg | $71.00 | 1 | |
Haloperidol hydrochloride is a quaternary ammonium salt characterized by its strong ionic interactions, which enhance solubility in polar solvents. The presence of the hydrochloride moiety facilitates hydrogen bonding, influencing its reactivity and stability in various environments. This compound exhibits unique electrostatic properties, allowing it to engage in specific molecular interactions that can affect aggregation behavior and phase transitions in solution. Its distinct crystalline structure contributes to its overall physical stability. | ||||||
Phenylhydrazine hydrochloride | 59-88-1 | sc-215707A sc-215707 | 10 g 25 g | $41.00 $61.00 | 3 | |
Phenylhydrazine hydrochloride is a hydrazine derivative that exhibits notable solubility in aqueous environments due to its ionic nature. The hydrochloride form enhances its ability to participate in hydrogen bonding, which can influence its reactivity in condensation reactions. This compound demonstrates unique kinetic behavior, often engaging in rapid redox processes. Its crystalline arrangement allows for specific packing interactions, impacting its thermal stability and reactivity in various chemical pathways. | ||||||
Sodium oxalate | 62-76-0 | sc-203396 sc-203396A | 100 g 500 g | $42.00 $136.00 | 5 | |
Sodium oxalate is a dicarboxylic acid salt that showcases interesting coordination chemistry, particularly with metal ions, forming stable complexes. Its ionic structure contributes to high solubility in water, facilitating its role in various chemical reactions. The compound exhibits distinct buffering properties, maintaining pH stability in solutions. Additionally, its crystalline form influences the rate of dissolution and reactivity, making it a key player in precipitation and complexation reactions. | ||||||
Sodium Pyruvate | 113-24-6 | sc-208397 sc-208397A | 5 g 25 g | $45.00 $65.00 | 14 | |
Sodium pyruvate, a key salt in biochemical pathways, acts as a crucial intermediate in cellular metabolism. Its unique ability to participate in redox reactions allows it to influence energy production and metabolic flux. The compound's ionic nature enhances its solubility, promoting rapid diffusion in aqueous environments. Furthermore, sodium pyruvate can engage in esterification reactions, showcasing its versatility in forming derivatives that can alter reaction kinetics and pathways. | ||||||
Benzethonium chloride | 121-54-0 | sc-239299 sc-239299A | 100 g 250 g | $53.00 $105.00 | 1 | |
Benzethonium chloride is a quaternary ammonium salt characterized by its amphiphilic nature, which facilitates interactions with both hydrophilic and hydrophobic environments. This dual affinity enhances its ability to disrupt lipid membranes, leading to unique surface-active properties. Its cationic structure allows for strong electrostatic interactions with anionic species, influencing adsorption dynamics and stability in various formulations. Additionally, it exhibits notable antimicrobial activity through membrane disruption mechanisms. | ||||||
Benzyldimethylhexadecylammonium chloride | 122-18-9 | sc-239325 sc-239325A sc-239325B | 25 g 100 g 500 g | $42.00 $107.00 $423.00 | ||
Benzyldimethylhexadecylammonium chloride is a quaternary ammonium salt known for its surfactant properties, which arise from its long hydrophobic alkyl chain and positively charged nitrogen. This unique structure promotes effective solubilization and emulsification, enhancing phase behavior in mixtures. Its strong cationic character enables robust interactions with negatively charged surfaces, influencing adsorption kinetics and stability. The compound also exhibits significant foaming properties, making it effective in altering interfacial tension. |