Items 191 to 200 of 426 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Tetraethylammonium perchlorate | 2567-83-1 | sc-356122 sc-356122A | 10 g 50 g | $90.00 $268.00 | ||
Tetraethylammonium perchlorate is a quaternary ammonium salt characterized by its highly polar perchlorate anion, which contributes to its solubility in various solvents. The compound exhibits unique ionic interactions, facilitating the formation of ion pairs that can influence reaction pathways. Its structure allows for significant charge delocalization, enhancing its stability in solution. Additionally, the compound's low viscosity and high ionic conductivity make it suitable for applications requiring efficient ion transport. | ||||||
Hexyltrimethylammonium bromide | 2650-53-5 | sc-235321 | 25 g | $149.00 | ||
Hexyltrimethylammonium bromide is a quaternary ammonium salt notable for its hydrophobic hexyl chain, which enhances its surfactant properties. The bromide anion contributes to its ionic strength, promoting effective solvation in polar solvents. This compound exhibits unique self-assembly behavior, forming micelles that can encapsulate hydrophobic substances. Its distinct molecular interactions facilitate phase transfer reactions, making it a versatile agent in various chemical processes. | ||||||
Sodium glycolate | 2836-32-0 | sc-272481 | 100 g | $71.00 | ||
Sodium glycolate is a sodium salt characterized by its ability to form strong hydrogen bonds due to the presence of hydroxyl and carboxylate groups. This compound exhibits excellent solubility in water, enhancing its reactivity in aqueous environments. Its ionic nature allows for effective ion pairing and stabilization of transition states in reactions, influencing reaction kinetics. Additionally, sodium glycolate can participate in complexation with metal ions, altering their solubility and reactivity. | ||||||
Sodium trifluoromethanesulfonate | 2926-30-9 | sc-236927 | 5 g | $40.00 | ||
Sodium trifluoromethanesulfonate is a highly polar salt known for its strong ionic interactions and unique trifluoromethyl group, which enhances its electrophilic character. This compound exhibits remarkable solubility in polar solvents, facilitating its role in various chemical reactions. Its ability to stabilize charged intermediates and influence reaction pathways makes it a valuable reagent in organic synthesis. Additionally, the presence of the sulfonate group contributes to its distinctive reactivity profile, allowing for efficient nucleophilic substitutions. | ||||||
Glycidyltrimethylammonium chloride | 3033-77-0 | sc-235263 sc-235263A | 50 ml 250 ml | $66.00 $215.00 | ||
Glycidyltrimethylammonium chloride is a quaternary ammonium salt characterized by its strong ionic nature and the presence of a glycidyl group, which imparts unique reactivity. This compound exhibits significant solubility in polar media, promoting its participation in nucleophilic reactions. Its structure allows for effective stabilization of transition states, enhancing reaction kinetics. The trimethylammonium moiety contributes to its distinctive behavior in forming stable complexes with anionic species, influencing various chemical pathways. | ||||||
GDP-D-mannose | 3123-67-9 | sc-285856B sc-285856C sc-285856 sc-285856A sc-285856D | 5 mg 10 mg 25 mg 50 mg 100 mg | $175.00 $200.00 $430.00 $775.00 $1175.00 | ||
GDP-D-mannose is a nucleotide sugar that plays a crucial role in glycosylation processes. Its unique structure facilitates specific interactions with enzymes, enhancing substrate specificity and catalytic efficiency. The compound participates in metabolic pathways, particularly in the synthesis of polysaccharides, where it acts as a donor of mannose residues. Its ability to form hydrogen bonds and engage in conformational changes contributes to its reactivity and stability in biochemical environments. | ||||||
(3-Bromopropyl)trimethylammonium bromide | 3779-42-8 | sc-231560 | 25 g | $114.00 | ||
(3-Bromopropyl)trimethylammonium bromide is a quaternary ammonium salt characterized by its strong ionic interactions and hydrophilicity. The presence of the bromopropyl group enhances its ability to participate in nucleophilic substitution reactions, making it a versatile reagent in organic synthesis. Its unique structure allows for effective solvation in polar solvents, influencing reaction kinetics and facilitating the formation of stable intermediates. The compound's cationic nature promotes electrostatic interactions, which can significantly affect its behavior in various chemical environments. | ||||||
Potassium chlorate | 3811-04-9 | sc-203350 sc-203350A | 100 g 500 g | $52.00 $126.00 | ||
Potassium chlorate is a highly reactive salt known for its strong oxidizing properties, particularly in redox reactions. Its crystalline structure allows for efficient packing, which influences its solubility in water. The compound can decompose exothermically when heated or in the presence of reducing agents, leading to the release of oxygen. This behavior is attributed to the instability of the chlorate ion, which can participate in various electron transfer processes, enhancing its reactivity in diverse chemical environments. | ||||||
Erioglaucine disodium salt | 3844-45-9 | sc-218328 sc-218328A | 5 g 25 g | $26.00 $70.00 | ||
Erioglaucine disodium salt is a vibrant blue dye characterized by its unique interaction with light, which results in distinct absorption and fluorescence properties. Its ionic nature contributes to high solubility in aqueous solutions, facilitating rapid diffusion and interaction with other molecules. The compound exhibits specific binding affinities, influencing its behavior in complexation reactions. Additionally, its stability under various pH conditions allows for versatile applications in diverse chemical systems. | ||||||
Calcium Acetate Monohydrate | 5743-26-0 | sc-207391 sc-207391A | 100 g 500 g | $56.00 $184.00 | ||
Calcium Acetate Monohydrate is a hygroscopic salt that showcases unique solvation dynamics due to its monohydrate form, which influences its crystallization behavior. The presence of water molecules alters the lattice structure, enhancing its dissolution rate in polar solvents. This compound participates in ion exchange reactions, where calcium ions can readily interact with anions, affecting reaction kinetics. Its ability to form stable complexes with various ligands further highlights its role in diverse chemical environments. |