Items 271 to 280 of 426 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Benzyldimethylhexylammonium chloride | 22559-57-5 | sc-227343 | 5 g | $198.00 | ||
Benzyldimethylhexylammonium chloride is a quaternary ammonium salt known for its amphiphilic nature, which allows it to interact effectively with both polar and nonpolar environments. Its unique structure promotes self-assembly into micelles, enhancing its surface activity. The compound exhibits strong electrostatic interactions, which can influence membrane permeability and stability. Additionally, its hydrophobic alkyl chains contribute to its ability to modulate interfacial tension in various systems. | ||||||
Zinc neodecanoate | 27253-29-8 | sc-272777 | 250 g | $126.00 | ||
Zinc neodecanoate is a versatile zinc salt characterized by its ability to act as a Lewis acid, facilitating various coordination interactions with organic substrates. Its unique structure allows for effective chelation with ligands, enhancing reaction rates in catalysis. The compound exhibits notable thermal stability and solubility in organic solvents, which can influence its reactivity in polymerization processes. Additionally, its role in promoting cross-linking reactions highlights its significance in material science applications. | ||||||
Calcium nitrate | 35054-52-5 | sc-234269 | 10 g | $82.00 | ||
Calcium nitrate is a hygroscopic salt that plays a crucial role in various chemical processes due to its ability to dissociate into calcium and nitrate ions in solution. This dissociation enhances ionic interactions, promoting nutrient uptake in plants and influencing soil chemistry. The compound's solubility in water allows for rapid ion exchange, making it effective in nutrient delivery systems. Its unique crystalline structure contributes to its stability and reactivity in diverse environmental conditions. | ||||||
2-Chloro-1,3-dimethylimidazolinium chloride | 37091-73-9 | sc-254191 sc-254191A | 5 g 25 g | $52.00 $180.00 | ||
2-Chloro-1,3-dimethylimidazolinium chloride is a versatile salt characterized by its ability to engage in nucleophilic substitution reactions due to the presence of the reactive chloro group. This compound exhibits strong ionic interactions, facilitating the formation of stable complexes with various anions. Its unique imidazolinium structure enhances its reactivity, making it a key player in facilitating coupling reactions and promoting efficient charge transfer in diverse chemical environments. | ||||||
Ammonium trifluoromethanesulfonate | 38542-94-8 | sc-233868 sc-233868A | 10 g 50 g | $96.00 $330.00 | ||
Ammonium trifluoromethanesulfonate is a distinctive salt known for its strong ionic character and the presence of trifluoromethanesulfonate, which imparts unique solvation properties. This compound exhibits significant hydrogen bonding capabilities, influencing its reactivity in various chemical pathways. Its high electronegativity enhances its role in facilitating electrophilic reactions, making it an effective catalyst in organic synthesis and promoting rapid reaction kinetics in polar solvents. | ||||||
(Iodomethyl)trimethylammonium iodide | 39741-91-8 | sc-279218 | 5 g | $66.00 | ||
(Iodomethyl)trimethylammonium iodide is a quaternary ammonium salt characterized by its strong ionic interactions and the presence of iodomethyl groups. This compound exhibits unique reactivity due to its ability to participate in nucleophilic substitution reactions, driven by the electrophilic nature of the iodomethyl moiety. Its solubility in polar solvents enhances its accessibility for various chemical transformations, making it a versatile intermediate in synthetic pathways. | ||||||
MES potassium salt | 39946-25-3 | sc-286156C sc-286156 sc-286156A sc-286156B | 5 g 25 g 50 g 100 g | $26.00 $55.00 $87.00 $130.00 | ||
MES potassium salt is a zwitterionic compound that exhibits unique buffering properties, maintaining pH stability in various environments. Its structure allows for strong hydrogen bonding and ionic interactions, facilitating solubility in aqueous solutions. The compound's ability to stabilize proteins and enzymes through electrostatic interactions enhances its role in biochemical applications. Additionally, its low toxicity and compatibility with biological systems make it an attractive choice for various experimental setups. | ||||||
2-Mercapto-4,6-dimethylpyrimidine sodium salt | 41840-27-1 | sc-265753 | 1 g | $20.00 | ||
2-Mercapto-4,6-dimethylpyrimidine sodium salt is a distinctive thiol compound that exhibits strong chelating properties due to its sulfur atom, enabling it to form stable complexes with metal ions. This salt demonstrates unique solubility characteristics in various solvents, influencing its reactivity in nucleophilic substitution reactions. Its ability to participate in redox processes highlights its role in electron transfer mechanisms, making it an intriguing subject for studying reaction kinetics and molecular interactions. | ||||||
Sodium ammonium phosphate tetrahydrate | 51750-73-3 | sc-296392 sc-296392A | 100 g 250 g | $20.00 $37.00 | ||
Sodium ammonium phosphate tetrahydrate is a versatile salt characterized by its ability to form hydrogen bonds, enhancing its solubility in aqueous environments. This compound exhibits unique ionic interactions that facilitate the stabilization of various cations, influencing its behavior in precipitation reactions. Its crystalline structure contributes to distinct thermal properties, while its hygroscopic nature allows it to absorb moisture, impacting its reactivity and storage conditions. | ||||||
Methyl-d3-magnesium iodide solution | 41251-37-0 | sc-235856 | 100 ml | $367.00 | ||
Methyl-d3-magnesium iodide solution is a highly reactive organometallic compound characterized by its strong nucleophilic properties. The presence of magnesium enhances its ability to participate in Grignard reactions, facilitating the formation of carbon-carbon bonds. Its unique isotopic labeling allows for precise tracking in synthetic pathways, providing insights into reaction mechanisms. The solution exhibits high reactivity with electrophiles, making it a versatile reagent in organic synthesis. |