Items 11 to 20 of 468 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Tridodecylmethylammonium chloride | 7173-54-8 | sc-255693 | 1 g | $173.00 | ||
Tridodecylmethylammonium chloride is a synthetic reagent characterized by its unique surfactant properties, which enhance solubilization and phase transfer in organic reactions. Its long hydrophobic alkyl chains promote strong molecular interactions, facilitating the formation of micelles and enhancing reaction kinetics in non-polar environments. This compound's quaternary ammonium structure imparts cationic characteristics, making it effective in stabilizing emulsions and influencing reaction pathways in complex mixtures. | ||||||
Nitronium tetrafluoroborate | 13826-86-3 | sc-250571 | 5 g | $84.00 | ||
Nitronium tetrafluoroborate serves as a potent synthetic reagent, notable for its strong electrophilic character, which facilitates nitration reactions. Its unique ability to generate nitronium ions enhances reactivity in aromatic systems, promoting selective substitution pathways. The compound's high ionic strength and stability contribute to its effectiveness in various organic transformations, while its low nucleophilicity minimizes side reactions, ensuring cleaner product profiles in synthetic applications. | ||||||
Potassium monopersulfate triple salt | 37222-66-5 | sc-236447 | 1 kg | $91.00 | ||
Potassium monopersulfate triple salt is a versatile synthetic reagent characterized by its strong oxidizing properties. It acts as a powerful oxidant in various chemical reactions, promoting electron transfer processes. The compound's unique ability to generate reactive sulfate radicals enhances its efficacy in oxidation pathways, facilitating the cleavage of C-H bonds. Its stability and solubility in aqueous environments make it suitable for diverse synthetic applications, ensuring efficient reaction kinetics and high selectivity. | ||||||
Cdk5 substrate | sc-3066 | 500 µg | $91.00 | 2 | ||
Cdk5 Substrate serves as a specialized synthetic reagent, notable for its role in modulating kinase activity through selective phosphorylation. This compound interacts uniquely with cyclin-dependent kinase 5, influencing signaling pathways that regulate neuronal function. Its ability to mimic natural substrates allows for precise studies of enzymatic mechanisms, while its structural features promote specific binding interactions, enhancing reaction rates and selectivity in biochemical assays. | ||||||
Sodium metasilicate nonahydrate | 13517-24-3 | sc-251033 | 500 g | $162.00 | ||
Sodium metasilicate nonahydrate is a versatile synthetic reagent characterized by its strong alkaline properties and ability to form silicate networks. It exhibits unique interactions with metal ions, facilitating the formation of stable complexes that enhance catalytic activity. Its high solubility in water promotes rapid dissolution, leading to efficient reaction kinetics in various chemical processes. Additionally, its hygroscopic nature allows it to maintain moisture, influencing reaction environments and outcomes. | ||||||
Woollins′ Reagent | 122039-27-4 | sc-229672 | 1 g | $79.00 | ||
Woollins' Reagent is a distinctive synthetic reagent known for its ability to facilitate the formation of organosilicon compounds through unique nucleophilic substitution pathways. It exhibits remarkable reactivity with electrophiles, enabling the generation of diverse carbon-silicon bonds. The reagent's solid-state properties contribute to its stability, while its selective reactivity allows for controlled transformations in complex organic syntheses. Its unique molecular interactions enhance reaction rates, making it a valuable tool in synthetic chemistry. | ||||||
Sodium Acetate, Anhydrous | 127-09-3 | sc-202340 sc-202340A sc-202340B | 250 g 1 kg 5 kg | $30.00 $92.00 $321.00 | 9 | |
Sodium Acetate, Anhydrous is a versatile synthetic reagent characterized by its ability to act as a buffering agent, stabilizing pH levels in various chemical reactions. Its ionic nature promotes solvation dynamics, enhancing reaction kinetics in aqueous environments. The compound's hygroscopic properties allow it to absorb moisture, influencing its reactivity and facilitating the formation of acetate derivatives. This reagent's unique interactions with metal ions can also lead to the formation of coordination complexes, expanding its utility in synthetic pathways. | ||||||
Barium iodide dihydrate | 7787-33-9 | sc-239273 | 50 g | $158.00 | ||
Barium iodide dihydrate serves as a potent synthetic reagent, notable for its role in facilitating halogenation reactions. Its crystalline structure promotes strong ionic interactions, enhancing solubility in polar solvents and accelerating reaction rates. The compound's ability to form stable complexes with various anions allows for selective reactivity in synthesis. Additionally, its hygroscopic nature influences the kinetics of reactions, making it a valuable component in diverse synthetic pathways. | ||||||
Ferrichrome Iron-free | 34787-28-5 | sc-255174 | 1 mg | $79.00 | 5 | |
Ferrichrome Iron-free is a synthetic reagent characterized by its unique chelating properties, enabling it to form stable complexes with metal ions. This compound exhibits distinct molecular interactions that enhance its reactivity in various synthetic pathways. Its ability to modulate electron transfer processes contributes to its effectiveness in catalyzing reactions. Furthermore, the compound's solubility in aqueous environments facilitates rapid kinetics, making it a versatile tool in synthetic chemistry. | ||||||
Phosphazene base P4-t-Bu solution | 111324-04-0 | sc-258013 sc-258013A sc-258013B | 1 ml 5 ml 25 ml | $148.00 $460.00 $1775.00 | ||
Phosphazene base P4-t-Bu solution is a highly effective synthetic reagent known for its exceptional nucleophilicity and ability to deprotonate a wide range of substrates. Its unique structure allows for strong interactions with electrophiles, promoting rapid reaction kinetics. The compound's sterically hindered nature enhances selectivity in reactions, while its solubility in organic solvents ensures compatibility with diverse reaction conditions, making it a powerful tool in synthetic organic chemistry. | ||||||