Items 51 to 60 of 426 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Calcium chloride hexahydrate | 7774-34-7 | sc-239463 | 1 kg | $52.00 | ||
Calcium chloride hexahydrate is a highly soluble salt characterized by its ability to form strong ion-dipole interactions in aqueous solutions. Its crystalline lattice structure allows for efficient hydration, leading to significant thermal effects during dissolution. This compound exhibits notable deliquescence, absorbing water vapor from the air and transitioning into a liquid state. The presence of multiple water molecules enhances its ionic conductivity, making it effective in various ionic exchange processes. | ||||||
Sodium phosphate tribasic dodecahydrate | 10101-89-0 | sc-203403 sc-203403A | 500 g 2.5 kg | $54.00 $200.00 | ||
Sodium phosphate tribasic dodecahydrate is a versatile salt known for its ability to act as a buffering agent, maintaining pH stability in various environments. Its extensive hydration shell contributes to its solubility and facilitates ion mobility, enhancing its role in biochemical reactions. The compound's crystalline structure allows for the formation of hydrogen bonds, influencing its interaction with other molecules and affecting reaction kinetics in solution. | ||||||
Clodronate, Disodium Salt | 22560-50-5 | sc-202547 | 10 mg | $120.00 | 1 | |
Clodronate, Disodium Salt is a unique salt characterized by its ability to chelate metal ions, which can significantly alter the dynamics of ionic interactions in solution. Its dual anionic nature enhances solubility and promotes complex formation, influencing reaction pathways. The compound exhibits distinct thermal stability and hygroscopic properties, which can affect its behavior in various environments. Additionally, its crystalline lattice structure allows for specific molecular packing, impacting diffusion rates and reactivity. | ||||||
5-Nonyloxytryptamine oxalate | 157798-13-5 | sc-203480 sc-203480A | 10 mg 50 mg | $111.00 $627.00 | 2 | |
5-Nonyloxytryptamine oxalate is a distinctive salt known for its ability to engage in hydrogen bonding and π-π stacking interactions, which can influence solubility and stability in various solvents. Its unique alkoxy group enhances lipophilicity, facilitating membrane permeability. The compound's crystalline form exhibits anisotropic properties, affecting its dissolution kinetics and reactivity in different environments. Additionally, its ionic nature contributes to specific electrostatic interactions, shaping its behavior in complex systems. | ||||||
MJ33 | 1135306-36-3 | sc-221947 | 5 mg | $256.00 | 3 | |
MJ33 is a notable salt characterized by its strong ionic interactions, which enhance its solubility in polar solvents. The presence of halide ions facilitates unique coordination chemistry, allowing for the formation of stable complexes with metal ions. Its crystalline structure exhibits distinct optical properties, influencing light absorption and scattering. Furthermore, MJ33 demonstrates variable reactivity profiles, making it an intriguing subject for studying reaction mechanisms and kinetics in diverse chemical environments. | ||||||
Tiron | 149-45-1 | sc-253699 sc-253699A | 10 g 25 g | $28.00 $40.00 | 11 | |
Tiron is a distinctive salt known for its ability to form chelate complexes with metal ions, enhancing its stability and solubility in aqueous solutions. Its unique molecular structure allows for effective electron donation, facilitating redox reactions. The compound exhibits interesting electrochemical properties, making it a subject of study in various reaction pathways. Additionally, Tiron's crystalline form contributes to its specific thermal and mechanical characteristics, influencing its behavior in different environments. | ||||||
Sodium hydrogentartrate | 526-94-3 | sc-251027 sc-251027A sc-251027B | 5 g 250 g 1 kg | $15.00 $46.00 $140.00 | ||
Sodium hydrogentartrate is a notable salt characterized by its ability to act as a buffering agent, maintaining pH stability in various solutions. Its unique molecular interactions allow it to participate in complexation reactions, particularly with divalent metal ions, influencing solubility and reactivity. The compound's crystalline structure contributes to its hygroscopic nature, affecting its behavior in moisture-rich environments and altering its dissolution kinetics in aqueous media. | ||||||
Lithium carbonate | 554-13-2 | sc-203109 sc-203109A | 100 g 500 g | $59.00 $147.00 | ||
Lithium carbonate is a distinctive salt known for its high solubility in water, which facilitates rapid ion dissociation. Its ionic interactions lead to unique electrochemical properties, making it a subject of interest in various chemical processes. The compound exhibits a layered crystal structure, influencing its thermal stability and reactivity. Additionally, its ability to form stable complexes with certain anions can modify reaction pathways, enhancing its role in diverse chemical environments. | ||||||
Sodium L-lactate | 867-56-1 | sc-220120 sc-220120A sc-220120B sc-220120C | 5 g 25 g 500 g 1 kg | $87.00 $126.00 $349.00 $465.00 | 1 | |
Sodium L-lactate is a notable salt characterized by its ability to participate in various biochemical pathways due to its chiral nature. This compound exhibits strong hydrogen bonding capabilities, which can influence solvation dynamics and enhance its reactivity in enzymatic processes. Its hygroscopic properties allow it to absorb moisture from the environment, affecting its stability and interaction with other compounds. Additionally, it can act as a buffering agent, modulating pH levels in diverse chemical systems. | ||||||
(3-Bromopropyl)triethylammonium bromide | 3720-84-1 | sc-216421 | 5 g | $320.00 | ||
(3-Bromopropyl)triethylammonium bromide is a quaternary ammonium salt known for its unique ionic interactions, which enhance its solubility in polar solvents. The presence of the bromopropyl group introduces steric hindrance, influencing its reactivity and selectivity in nucleophilic substitution reactions. This compound can also form stable complexes with anions, affecting its behavior in various ionic environments. Its distinct molecular structure contributes to its role in phase transfer catalysis and ionic liquid formation. |