Items 411 to 420 of 426 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Magnesium chromate hydrate | 23371-94-0 | sc-235547 | 500 g | $134.00 | ||
Magnesium chromate hydrate is a crystalline salt known for its distinctive coordination chemistry and vibrant yellow coloration. It exhibits strong ionic interactions, which influence its solubility and reactivity in aqueous environments. The compound participates in redox reactions, showcasing its ability to act as an oxidizing agent. Its unique lattice structure contributes to its thermal stability and influences the kinetics of reactions, making it an intriguing subject for studies in inorganic chemistry. | ||||||
(R)-(-)-Isobornylamine hydrochloride | 24629-78-5 | sc-229054 | 100 mg | $260.00 | ||
(R)-(-)-Isobornylamine hydrochloride is a chiral amine salt characterized by its unique stereochemistry, which facilitates specific molecular interactions in various chemical environments. Its ammonium group enhances hydrogen bonding capabilities, influencing solubility and reactivity. The compound exhibits distinct pathways in nucleophilic substitution reactions, showcasing its kinetic behavior. Additionally, its crystalline structure contributes to its stability and potential for forming diverse coordination complexes. | ||||||
Benzyltributylammonium bromide | 25316-59-0 | sc-227349 | 50 g | $99.00 | ||
Benzyltributylammonium bromide is a quaternary ammonium salt known for its ability to form ion pairs and facilitate phase transfer reactions. The bulky tributyl groups enhance hydrophobic interactions, promoting solubility in organic solvents. Its cationic nature allows for strong electrostatic interactions with anions, influencing reaction kinetics. The compound's unique structure enables it to act as a surfactant, stabilizing emulsions and enhancing the transport of ions across interfaces. | ||||||
(R)-(+)-α-[(3-Methoxy-1-methyl-3-oxo-1-propenyl)amino]-1,4-cyclohexadiene-1-acetic acid sodium salt | 26774-89-0 | sc-236598 sc-236598A | 1 g 10 g | $35.00 $207.00 | ||
(R)-(+)-α-[(3-Methoxy-1-methyl-3-oxo-1-propenyl)amino]-1,4-cyclohexadiene-1-acetic acid sodium salt exhibits distinctive solubility characteristics due to its ionic nature, allowing for effective dissociation in aqueous environments. The presence of the sodium ion enhances its stability and reactivity, facilitating specific molecular interactions that can influence reaction pathways. Its unique cyclohexadiene structure contributes to its reactivity, enabling participation in diverse chemical transformations. | ||||||
2-Acetyl-3,4,5,6-tetrahydropyridine Hydrochloride | 27300-28-3 | sc-391892 | 10 mg | $373.00 | ||
2-Acetyl-3,4,5,6-tetrahydropyridine Hydrochloride is characterized by its ability to form strong hydrogen bonds due to the presence of nitrogen and oxygen atoms in its structure. This salt exhibits enhanced solubility in polar solvents, promoting rapid ionization and facilitating unique reaction kinetics. Its tetrahydropyridine ring contributes to its reactivity, allowing it to engage in nucleophilic attacks and participate in various organic transformations, showcasing its versatility in chemical processes. | ||||||
Sulfosuccinic Acid Sodium Salt | 29454-16-8 | sc-396244 sc-396244A sc-396244B | 2 g 5 g 10 g | $390.00 $800.00 $1400.00 | ||
Sulfosuccinic Acid Sodium Salt is a versatile compound known for its unique surfactant properties, which arise from its anionic nature. The presence of sulfonate groups enhances its ability to interact with water molecules, leading to improved solubility and stability in aqueous environments. This salt exhibits distinct electrostatic interactions, allowing it to effectively reduce surface tension and stabilize emulsions. Its molecular structure facilitates complexation with metal ions, influencing reaction pathways and kinetics in various chemical systems. | ||||||
Tridodecylmethylammonium iodide | 29710-98-3 | sc-237291 | 25 g | $140.00 | ||
Tridodecylmethylammonium iodide is a quaternary ammonium salt characterized by its long hydrophobic alkyl chains, which impart unique surfactant properties. The cationic nature of the molecule promotes strong electrostatic interactions with anionic species, enhancing its ability to form stable micelles. This compound exhibits notable solubilization effects, facilitating the dispersion of hydrophobic substances in polar solvents. Its structural attributes also enable effective phase transfer catalysis, influencing reaction dynamics in organic synthesis. | ||||||
Demethyl Memantine Hydrochloride | 33103-93-4 | sc-391357 | 5 mg | $290.00 | ||
Demethyl Memantine Hydrochloride is a unique salt that exhibits distinct solubility characteristics due to its ionic nature. The presence of the hydrochloride moiety enhances its stability in aqueous environments, promoting favorable interactions with polar solvents. This compound demonstrates interesting ion-pairing behavior, which can influence its reactivity and transport properties. Additionally, its molecular structure allows for specific hydrogen bonding interactions, affecting its overall physicochemical behavior in various environments. | ||||||
Barium thiosulfate | 35112-53-9 | sc-233913 | 250 g | $97.00 | ||
Barium thiosulfate is a distinctive salt characterized by its ability to form strong ionic bonds, which influence its solubility and stability in various environments. The thiosulfate anion exhibits unique redox properties, allowing it to participate in electron transfer reactions. Its crystalline structure contributes to specific lattice energies, affecting dissolution rates. Additionally, the compound can engage in complexation with metal ions, altering its reactivity and interaction pathways in solution. | ||||||
3-(Trimethylsilyl)propionic Acid Sodium Salt | 37013-20-0 | sc-391489 | 100 mg | $320.00 | ||
3-(Trimethylsilyl)propionic Acid Sodium Salt is a notable salt recognized for its unique solvation dynamics and ionic interactions. The trimethylsilyl group enhances hydrophobic characteristics, influencing its behavior in polar solvents. This compound exhibits distinct buffering capacity, stabilizing pH levels in various environments. Its ability to form stable complexes with cations can modify reaction kinetics, making it a versatile participant in diverse chemical processes. |