Items 291 to 300 of 468 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Magnesium fluoride | 7783-40-6 | sc-250278 | 25 g | $67.00 | ||
Magnesium fluoride serves as a versatile synthetic reagent, notable for its role in facilitating ionic interactions and stabilizing transition states during reactions. Its unique lattice structure enhances the solubility of various metal ions, promoting catalytic activity in diverse chemical processes. The compound exhibits distinct optical properties, making it useful in photonic applications. Additionally, its low reactivity with moisture allows for controlled environments in synthetic pathways, ensuring consistent outcomes. | ||||||
Sodium bromate | 7789-38-0 | sc-251012 | 100 g | $204.00 | ||
Sodium bromate serves as a versatile synthetic reagent, notable for its strong oxidizing properties that facilitate a range of organic transformations. It participates in radical reactions, often generating bromine radicals that can initiate polymerization or functionalization processes. Its ability to act as a brominating agent allows for selective halogenation, while its solubility in water enhances its reactivity in aqueous environments, making it a key player in various synthetic pathways. | ||||||
Calcium fluoride | 7789-75-5 | sc-239464 | 5 g | $69.00 | ||
Calcium fluoride is a unique synthetic reagent characterized by its ability to form stable complexes with metal ions, enhancing catalytic processes. Its low solubility in water allows for controlled release in reactions, making it effective in solid-state synthesis. The compound exhibits distinct ionic interactions, which can influence reaction kinetics and pathways, particularly in the formation of fluorinated organic compounds. Its crystalline structure contributes to its utility in various synthetic applications. | ||||||
Potassium disulfate | 7790-62-7 | sc-250750 | 25 g | $61.00 | ||
Potassium disulfate serves as a versatile synthetic reagent, notable for its ability to facilitate oxidation reactions through the generation of reactive sulfate species. Its strong oxidizing properties enable it to participate in diverse chemical transformations, often accelerating reaction rates. The compound's unique ability to stabilize intermediates through ionic interactions enhances selectivity in synthesis. Additionally, its hygroscopic nature allows for moisture retention, influencing reaction environments and outcomes. | ||||||
Iodine monochloride solution (Wijs′ chloride) | 7790-99-0 | sc-300832 sc-300832A | 500 ml 1 L | $137.00 $179.00 | ||
Iodine monochloride solution, known as Wijs' chloride, is a potent synthetic reagent characterized by its ability to engage in halogenation reactions. This compound exhibits unique reactivity due to the presence of both iodine and chlorine, allowing for selective electrophilic attacks on organic substrates. Its distinct molecular interactions facilitate the formation of stable intermediates, while its polar nature enhances solubility in various solvents, influencing reaction kinetics and pathways. | ||||||
Tetrabutylammonium acetate | 10534-59-5 | sc-258214 | 25 g | $100.00 | ||
Tetrabutylammonium acetate serves as a versatile synthetic reagent, notable for its ability to stabilize charged intermediates during organic transformations. Its quaternary ammonium structure enhances solubility in polar and non-polar solvents, promoting diverse reaction pathways. The acetate moiety can act as a nucleophile, facilitating acylation reactions. Additionally, its unique ionic interactions can influence reaction rates and selectivity, making it a valuable tool in synthetic chemistry. | ||||||
Borane dimethyl sulfide complex | 13292-87-0 | sc-252505 sc-252505A | 25 ml 100 ml | $49.00 $134.00 | ||
Borane dimethyl sulfide complex is a potent synthetic reagent characterized by its ability to facilitate hydroboration reactions with high regioselectivity. The presence of dimethyl sulfide enhances the stability of the borane, allowing for controlled reactivity in various organic transformations. Its unique coordination chemistry enables effective interactions with alkenes and alkynes, promoting rapid addition reactions. This complex also exhibits distinctive kinetic properties, influencing reaction mechanisms and product distributions in synthetic applications. | ||||||
Sodium selenate | 13410-01-0 | sc-251052A sc-251052 sc-251052B sc-251052C | 25 g 100 g 500 g 1 kg | $52.00 $187.00 $332.00 $599.00 | ||
Sodium selenate serves as a versatile synthetic reagent, notable for its role in oxidation reactions and as a source of selenate ions. Its unique ability to participate in redox processes allows for the selective transformation of organic substrates. The compound exhibits distinct solubility characteristics, enhancing its reactivity in aqueous environments. Additionally, its interactions with nucleophiles can lead to the formation of selenoesters, showcasing its utility in synthetic pathways. | ||||||
Ethylenediaminetetraacetic acid disodium magnesium salt | 14402-88-1 | sc-228092 sc-228092A | 50 g 250 g | $57.00 $240.00 | ||
Ethylenediaminetetraacetic acid disodium magnesium salt functions as a synthetic reagent with a unique chelating ability, effectively binding metal ions through its multiple coordination sites. This property facilitates the stabilization of metal complexes, influencing reaction kinetics and selectivity in various synthetic pathways. Its solubility in water enhances its reactivity, allowing for efficient interactions with transition metals, which can lead to the formation of stable complexes and influence catalytic processes. | ||||||
Tetrabutylphosphonium hydroxide solution | 14518-69-5 | sc-251164 | 100 ml | $140.00 | ||
Tetrabutylphosphonium hydroxide solution serves as a versatile synthetic reagent, characterized by its ability to act as a phase transfer catalyst. Its unique structure promotes the solubilization of ionic compounds in organic solvents, enhancing reaction rates and selectivity. The quaternary ammonium nature facilitates strong ionic interactions, enabling efficient nucleophilic substitutions and facilitating the formation of complex organic molecules. Its high viscosity and low volatility further contribute to its effectiveness in various synthetic applications. | ||||||