Items 291 to 300 of 426 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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HEPPSO sodium salt | 89648-37-3 | sc-295141 sc-295141A | 25 g 100 g | $96.00 $309.00 | ||
HEPPSO sodium salt is a zwitterionic compound characterized by its unique buffering capacity and ability to stabilize pH in various environments. Its structure allows for effective ionic interactions, enhancing solubility in aqueous solutions. The presence of sulfonate groups contributes to its high ionic strength, facilitating electrostatic interactions. This compound also exhibits distinct chelating properties, influencing metal ion coordination and enhancing reaction pathways in complexation reactions. | ||||||
DL-Methionine beta-naphthylamide hydrochloride | 97405-58-8 | sc-294402 sc-294402A | 250 mg 1 g | $90.00 $275.00 | ||
DL-Methionine beta-naphthylamide hydrochloride is a salt that exhibits intriguing solubility characteristics due to its amphiphilic nature, promoting interactions with both polar and non-polar environments. Its unique molecular structure allows for specific hydrogen bonding and dipole-dipole interactions, enhancing its stability in solution. Additionally, the presence of the beta-naphthylamide moiety contributes to its ability to engage in π-π stacking, influencing reaction kinetics and molecular aggregation behavior. | ||||||
Malondialdehyde tetrabutylammonium salt | 100683-54-3 | sc-250289B sc-250289 sc-250289A sc-250289C | 100 mg 1 g 5 g 250 g | $95.00 $225.00 $655.00 $18360.00 | ||
Malondialdehyde tetrabutylammonium salt is a unique ionic compound characterized by its strong electrostatic interactions and hydrophobic properties due to the tetrabutylammonium cation. This salt exhibits enhanced solubility in organic solvents, facilitating its role in various chemical reactions. Its structure allows for significant ion pairing and stabilization of reactive intermediates, influencing reaction pathways and kinetics. The compound's ability to form micellar structures further enhances its reactivity and interaction with other molecular species. | ||||||
AS 101 | 106566-58-9 | sc-203825 sc-203825A | 10 mg 25 mg | $160.00 $575.00 | 4 | |
AS 101 is a distinctive salt that showcases remarkable ionic interactions, primarily driven by its unique cationic component. This compound exhibits a high degree of solvation, which enhances its reactivity in polar environments. Its ability to form stable complexes with various anions allows for selective ion exchange processes. Additionally, AS 101 demonstrates interesting phase behavior, contributing to its role in facilitating specific reaction mechanisms and influencing the kinetics of associated chemical transformations. | ||||||
Tetrabromophenol blue sodium salt | 108321-10-4 | sc-215946 sc-215946A | 1 g 5 g | $31.00 $90.00 | ||
Tetrabromophenol blue sodium salt is a notable salt characterized by its strong chromogenic properties, resulting from the presence of brominated phenolic groups. This compound exhibits unique electrostatic interactions, which enhance its solubility in aqueous solutions. Its distinct molecular structure allows for effective dyeing processes, as it can undergo reversible protonation, influencing its colorimetric behavior. Furthermore, it participates in complexation reactions, showcasing its versatility in various chemical environments. | ||||||
D-myo-Inositol-1,5,6-triphosphate, sodium salt | 120965-76-6 | sc-205286 sc-205286A | 100 µg 1 mg | $98.00 $785.00 | ||
D-myo-Inositol-1,5,6-triphosphate, sodium salt, is a unique salt that plays a pivotal role in cellular signaling pathways. Its structure facilitates specific interactions with phosphoinositide receptors, influencing intracellular calcium release. The compound exhibits high solubility in water, promoting rapid diffusion across membranes. Additionally, it participates in dynamic phosphorylation reactions, contributing to the regulation of various biochemical processes, highlighting its importance in cellular communication. | ||||||
IEM 1460 | 121034-89-7 | sc-204007 sc-204007A | 10 mg 50 mg | $128.00 $520.00 | ||
IEM 1460 is a distinctive salt characterized by its ability to form stable complexes with metal ions, enhancing its reactivity in various chemical environments. Its unique ionic structure allows for effective ion exchange processes, facilitating rapid interactions with other compounds. The salt exhibits notable hygroscopic properties, which can influence its stability and reactivity in different conditions. Furthermore, IEM 1460 participates in specific catalytic pathways, showcasing its versatility in diverse chemical reactions. | ||||||
Tetraphenylphosphonium hexafluoroantimonate | 124329-50-6 | sc-272588 | 5 g | $124.00 | ||
Tetraphenylphosphonium hexafluoroantimonate is a unique salt known for its strong ionic interactions and the ability to stabilize cationic species. Its bulky tetraphenylphosphonium cation enhances solubility in organic solvents, promoting diverse reactivity. The hexafluoroantimonate anion contributes to its distinctive electronic properties, enabling participation in electron transfer processes. This salt also exhibits interesting thermal stability, making it suitable for various synthetic applications. | ||||||
Resorufin β-D-glucuronide sodium salt | 125440-91-7 | sc-222248 sc-222248A | 1 mg 10 mg | $322.00 $1414.00 | ||
Resorufin β-D-glucuronide sodium salt is a distinctive compound characterized by its ability to undergo hydrolysis, leading to the release of resorufin, a fluorescent product. This transformation is influenced by pH and enzymatic activity, showcasing its role in biochemical pathways. The salt's solubility in aqueous environments facilitates its interaction with biological macromolecules, enhancing its reactivity and enabling specific molecular recognition processes. Its unique structural features contribute to its dynamic behavior in various chemical contexts. | ||||||
Alendronate sodium | 129318-43-0 | sc-300175 sc-300175A | 500 mg 1 g | $102.00 $153.00 | 1 | |
Alendronate sodium, a notable salt, exhibits strong ionic interactions that enhance its solubility in polar solvents. Its unique structure allows for specific binding to hydroxyapatite, a key component of bone mineral, facilitating distinct adsorption dynamics. The compound's stability in aqueous solutions promotes slow release kinetics, influencing its reactivity in various environments. Additionally, its capacity to form hydrogen bonds contributes to its overall molecular behavior, impacting its interactions in complex systems. |