Items 81 to 90 of 426 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Potassium bromide | 7758-02-3 | sc-203348 sc-203348E sc-203348A sc-203348B sc-203348C sc-203348D | 100 g 250 g 500 g 2.5 kg 5 kg 10 kg | $46.00 $100.00 $154.00 $304.00 $520.00 $982.00 | ||
Potassium bromide is a highly soluble ionic compound characterized by its strong ionic interactions, which contribute to its stability in aqueous solutions. It exhibits notable dissociation in water, leading to a high degree of ion mobility that can influence reaction kinetics. The compound's crystalline lattice structure allows for efficient packing, enhancing its physical robustness. Additionally, it can participate in halogenation reactions, showcasing its reactivity as a source of bromide ions in various chemical processes. | ||||||
Ferrous Sulfate (Iron II Sulfate) Heptahydrate | 7782-63-0 | sc-211505 sc-211505A | 250 g 500 g | $72.00 $107.00 | ||
Ferrous sulfate heptahydrate is a crystalline salt known for its distinctive hydration properties, which contribute to its stability and solubility in water. The presence of water molecules in its structure facilitates unique hydrogen bonding interactions, enhancing its reactivity in redox reactions. This compound exhibits a characteristic greenish hue, indicative of its iron content, and its dissolution in aqueous environments leads to the release of ferrous ions, which can participate in various complexation reactions. | ||||||
Magnesium bromide | 7789-48-2 | sc-250274 sc-250274A | 10 g 50 g | $38.00 $114.00 | ||
Magnesium bromide is a hygroscopic salt that forms a crystalline structure, characterized by its ability to attract and retain moisture from the environment. This property enhances its solubility in polar solvents, facilitating ion dissociation into magnesium and bromide ions. The ionic interactions within its lattice contribute to its stability, while its reactivity in various chemical pathways allows it to participate in metathesis reactions, showcasing its versatility in diverse chemical contexts. | ||||||
Calcium Chloride, Dihydrate | 10035-04-8 | sc-202091 sc-202091A sc-202091B sc-202091C | 500 g 2 kg 10 kg 50 kg | $82.00 $214.00 $790.00 $2754.00 | 1 | |
Calcium chloride, dihydrate is a highly soluble ionic compound known for its strong hygroscopic nature, which allows it to absorb moisture effectively. Its crystalline form exhibits a unique lattice structure that influences its thermal properties and ion mobility. The compound readily dissociates into calcium and chloride ions in solution, promoting ionic interactions that enhance its reactivity in various chemical processes, including precipitation and complexation reactions. | ||||||
Thionin acetate salt | 78338-22-4 | sc-215973 sc-215973A sc-215973B sc-215973C | 5 g 25 g 100 g 250 g | $99.00 $362.00 $938.00 $1882.00 | 2 | |
Thionin acetate salt is a distinctive compound known for its vibrant color and unique electrochemical properties. Its structure allows for strong intermolecular hydrogen bonding, enhancing its stability in solution. The salt exhibits notable photophysical behavior, with specific absorption and emission spectra that are sensitive to environmental changes. This responsiveness to light and pH variations makes it an intriguing subject for studying molecular interactions and reaction kinetics in various chemical contexts. | ||||||
Hexadecyltrimethylammonium chloride | 112-02-7 | sc-235291 sc-235291A | 25 g 100 g | $80.00 $130.00 | ||
Hexadecyltrimethylammonium chloride is a quaternary ammonium salt characterized by its long hydrophobic alkyl chain, which influences its surfactant properties. This compound exhibits strong ionic interactions, promoting self-assembly into micelles in aqueous solutions. Its unique structure facilitates the formation of stable colloidal dispersions, enhancing its role in interfacial phenomena. Additionally, it demonstrates distinct thermal stability and solubility behavior, making it a subject of interest in studies of molecular aggregation and phase transitions. | ||||||
Cacodylic acid sodium salt trihydrate | 6131-99-3 | sc-293974 sc-293974A | 25 g 100 g | $102.00 $250.00 | 1 | |
Cacodylic acid sodium salt trihydrate is a unique organoarsenic compound that exhibits distinctive solubility characteristics due to its ionic nature. The presence of trihydrate enhances its stability and influences its reactivity in aqueous environments. This compound participates in specific ligand interactions, facilitating complex formation with metal ions. Its behavior in solution is marked by notable reaction kinetics, making it an intriguing subject for studies on molecular dynamics and environmental chemistry. | ||||||
Amprolium HCl | 137-88-2 | sc-391655 sc-391655A | 25 g 100 g | $82.00 $255.00 | 1 | |
Amprolium HCl is a distinctive compound characterized by its ability to form stable ionic interactions in aqueous solutions. As a salt, it exhibits enhanced solubility, which influences its reactivity and transport properties. The presence of chloride ions contributes to its unique behavior in complexation reactions, allowing it to engage in specific molecular interactions. Its kinetic profile reveals interesting pathways for ion exchange, making it a subject of interest in studies of ionic strength and solvation dynamics. | ||||||
Rabeprazole Sodium Salt | 117976-90-6 | sc-208255 | 10 mg | $130.00 | ||
Rabeprazole Sodium Salt is a notable compound recognized for its unique crystalline structure, which facilitates strong electrostatic interactions in solution. This salt demonstrates a high degree of solubility, enhancing its diffusion rates and reactivity in various environments. Its distinct ionization behavior allows for selective binding with other molecules, influencing reaction kinetics and pathways. The compound's stability under varying pH conditions further contributes to its intriguing chemical dynamics. | ||||||
Sodium bromoacetate | 1068-52-6 | sc-272479 | 5 g | $40.00 | ||
Sodium bromoacetate is a distinctive salt characterized by its ability to engage in nucleophilic substitution reactions due to the presence of the bromoacetate group. This compound exhibits strong ionic interactions, which enhance its solubility in polar solvents. Its reactivity is influenced by the electron-withdrawing nature of the bromine atom, facilitating the formation of intermediates in organic synthesis. Additionally, it can participate in esterification reactions, showcasing its versatility in various chemical pathways. |