Items 51 to 60 of 97 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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D-myo-Inositol-1,2,3,6-tetraphosphate, sodium salt | sc-223914 sc-223914A | 100 µg 500 µg | $165.00 $744.00 | |||
D-myo-Inositol-1,2,3,6-tetraphosphate, sodium salt, exhibits a unique structural configuration that facilitates its interaction with various cellular components, particularly in the regulation of phosphoinositide signaling pathways. The sodium ion enhances its hydrophilicity, promoting rapid cellular uptake and distribution. This compound is integral in orchestrating cellular responses through its ability to bind to specific proteins, influencing enzymatic activity and cellular homeostasis. Its dynamic role in cellular signaling underscores its importance in maintaining physiological balance. | ||||||
D-myo-Inositol-1,2,4,5,6-pentaphosphate, sodium salt | sc-223916 sc-223916A | 100 µg 500 µg | $220.00 $992.00 | |||
D-myo-Inositol-1,2,4,5,6-pentaphosphate, sodium salt, features a complex arrangement of phosphate groups that allows for versatile interactions with metal ions and proteins. The presence of sodium enhances its solubility, facilitating its diffusion across membranes. This compound plays a critical role in cellular signaling by modulating enzyme activity and influencing intracellular calcium levels. Its unique structure enables it to participate in diverse biochemical pathways, contributing to cellular regulation and signaling dynamics. | ||||||
Sodium Camptothecin | 25387-67-1 | sc-338592 | 1 g | $700.00 | ||
Sodium Camptothecin exhibits unique molecular interactions due to its lactone structure, which can undergo hydrolysis to form an active carboxylate form. This transformation is influenced by pH and ionic strength, affecting its reactivity. The sodium ion enhances solubility, promoting its diffusion in aqueous environments. Its distinct conformational flexibility allows for specific binding to target molecules, influencing reaction kinetics and enabling participation in various biochemical processes. | ||||||
Sodium aluminate | 11138-49-1 | sc-224288 sc-224288A sc-224288B sc-224288C | 2.5 kg 5 kg 10 kg 20 kg | $137.00 $159.00 $315.00 $630.00 | ||
Sodium aluminate is characterized by its ability to form complex ions with aluminum, facilitating unique interactions in aqueous solutions. Its amphoteric nature allows it to react with both acids and bases, leading to diverse pathways in precipitation and coagulation processes. The presence of sodium ions enhances its solubility, promoting effective dispersion in various media. Additionally, its role in altering pH levels can significantly influence reaction kinetics and the stability of colloidal systems. | ||||||
D-2(3)-Phosphoglyceric acid sodium salt | sc-397368 sc-397368A | 10 mg 100 mg | $72.00 $339.00 | |||
D-2(3)-Phosphoglyceric acid sodium salt exhibits unique properties as a sodium salt, particularly in its role as a key intermediate in metabolic pathways. Its anionic structure enables it to participate in enzyme-catalyzed reactions, influencing energy transfer and carbon metabolism. The sodium component enhances its solubility in biological systems, facilitating rapid diffusion and interaction with other biomolecules. This compound's reactivity is pivotal in regulating metabolic flux and maintaining cellular homeostasis. | ||||||
Sodium chromate tetrahydrate | 10034-82-9 | sc-224289 sc-224289A | 100 g 500 g | $41.00 $113.00 | ||
Sodium chromate tetrahydrate, as a sodium salt, showcases distinctive properties through its chromate anion, which engages in redox reactions and complexation with various metal ions. Its high solubility in water allows for efficient ion exchange and facilitates its role in oxidation processes. The compound's unique ability to form stable complexes with transition metals enhances its reactivity, making it a significant player in various chemical syntheses and environmental applications. | ||||||
Sodium permanganate monohydrate | 79048-36-5 | sc-236916 sc-236916A | 50 g 250 g | $70.00 $218.00 | ||
Sodium permanganate monohydrate, as a sodium salt, exhibits remarkable oxidative capabilities due to its permanganate ion, which participates in diverse redox reactions. Its strong oxidizing nature allows it to effectively break down organic compounds and engage in electron transfer processes. The compound's solubility in water promotes rapid reaction kinetics, enabling swift interactions with substrates. Additionally, its distinct purple color serves as a visual indicator of concentration and reactivity in various chemical environments. | ||||||
Sodium hexafluoroantimonate(V) | 16925-25-0 | sc-229300A sc-229300 sc-229300B sc-229300C sc-229300D | 1 g 25 g 100 g 250 g 1 kg | $12.00 $29.00 $50.00 $100.00 $200.00 | ||
Sodium hexafluoroantimonate(V) is a unique sodium salt characterized by its strong Lewis acidity, attributed to the presence of hexafluoroantimonate anions. This compound exhibits exceptional stability and low reactivity under ambient conditions, yet it can engage in complexation reactions with various ligands, enhancing its role in coordination chemistry. Its high electronegativity and polarizability facilitate intriguing interactions with electron-rich species, influencing reaction pathways and kinetics in diverse chemical systems. | ||||||
Disodium terephthalate | 10028-70-3 | sc-278995 | 5 g | $30.00 | ||
Disodium terephthalate is a sodium salt notable for its role in polymer chemistry, particularly in the synthesis of polyesters. Its structure allows for effective hydrogen bonding and π-π stacking interactions, which enhance the thermal stability and mechanical properties of resultant materials. The compound exhibits a high degree of solubility in polar solvents, facilitating its incorporation into various reaction pathways. Additionally, its ionic nature contributes to unique reactivity patterns in condensation reactions, influencing polymerization kinetics. | ||||||
Sodium cobalticarborane | 99492-72-5 | sc-229296 | 1 g | $106.00 | ||
Sodium cobalticarborane is a unique sodium compound characterized by its distinctive cluster structure, which facilitates electron delocalization and enhances its reactivity. This compound exhibits strong Lewis acid behavior, promoting various coordination interactions with nucleophiles. Its ability to stabilize transition states in reactions leads to accelerated kinetics, making it a valuable participant in organometallic chemistry. Furthermore, its solubility in non-polar solvents allows for diverse applications in synthetic pathways. |