Items 21 to 30 of 426 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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L-Cystine disodium salt, anhydrous | 64704-23-0 | sc-295275 sc-295275A sc-295275B sc-295275C | 25 g 100 g 1 kg 10 kg | $31.00 $107.00 $1020.00 $9690.00 | ||
L-Cystine disodium salt, anhydrous, is a crystalline salt characterized by its unique zwitterionic nature, which facilitates specific molecular interactions in aqueous environments. This compound exhibits notable solubility due to its ionic character, allowing it to participate in various biochemical pathways. Its distinct structural arrangement influences the stability of protein folding and can modulate redox reactions, showcasing its role in maintaining cellular homeostasis. | ||||||
MK-886 sodium salt | 118427-55-7 | sc-200608B sc-200608 sc-200608A | 1 mg 5 mg 25 mg | $46.00 $93.00 $371.00 | 3 | |
MK-886 sodium salt is a distinctive ionic compound that exhibits strong electrostatic interactions due to its charged nature. This salt demonstrates enhanced solubility in polar solvents, promoting its reactivity in various chemical environments. Its unique structural features allow for specific binding interactions, influencing reaction kinetics and facilitating complex formation. The compound's behavior as a salt enhances its stability and reactivity, making it a subject of interest in various chemical studies. | ||||||
Guanidine Hydrochloride | 50-01-1 | sc-202637 sc-202637A | 100 g 1 kg | $60.00 $195.00 | 1 | |
Guanidine Hydrochloride is a notable ionic compound characterized by its ability to disrupt hydrogen bonding networks in aqueous solutions. This property enhances protein solubility and stability, making it a useful agent in denaturing proteins. Its high solubility in water and polar solvents facilitates rapid diffusion and interaction with biomolecules, influencing reaction pathways and kinetics. The compound's unique ionic interactions contribute to its role in various biochemical processes. | ||||||
α-Methylserotonin maleate salt | 97469-12-0 | sc-254929 sc-254929A | 10 mg 50 mg | $101.00 $421.00 | ||
α-Methylserotonin maleate salt is a distinctive ionic compound that exhibits strong electrostatic interactions, enhancing its solubility in polar solvents. This salt form facilitates the formation of stable complexes with various biomolecules, influencing their conformational dynamics. Its unique structural features allow for selective binding to specific receptors, potentially altering signaling pathways. The compound's behavior in solution is characterized by rapid dissociation, impacting reaction kinetics and molecular interactions. | ||||||
Butyrylcholine chloride | 2963-78-2 | sc-255007 sc-255007A | 10 g 25 g | $54.00 $138.00 | ||
Butyrylcholine chloride is a quaternary ammonium salt that demonstrates significant ionic character, leading to enhanced solubility in aqueous environments. Its structure promotes strong dipole-dipole interactions, which can influence the stability of molecular assemblies. The compound exhibits rapid hydrolysis in the presence of nucleophiles, affecting its reactivity and interaction with surrounding molecules. This dynamic behavior contributes to its role in modulating electrochemical gradients across membranes. | ||||||
Sodium carbonate, anhydrous | 497-19-8 | sc-203382 sc-203382A sc-203382B | 500 g 1 kg 2.5 kg | $25.00 $79.00 $122.00 | ||
Sodium carbonate, anhydrous, is a versatile salt characterized by its ability to act as a strong base in aqueous solutions, facilitating various acid-base reactions. Its crystalline structure allows for efficient packing, influencing its solubility and reactivity. The compound engages in ion exchange processes, enhancing its role in buffering systems. Additionally, it exhibits unique thermal properties, enabling it to participate in endothermic reactions, which can affect reaction kinetics in diverse chemical environments. | ||||||
Sodium (S)-3-hydroxybutyrate | 127604-16-4 | sc-236887 | 1 g | $194.00 | ||
Sodium (S)-3-hydroxybutyrate is a chiral salt that exhibits unique interactions due to its hydroxyl and carboxylate groups, promoting hydrogen bonding and ionic interactions in solution. This compound participates in metabolic pathways, influencing energy production and substrate utilization. Its solubility in water enhances its reactivity, allowing for rapid dissociation and interaction with other ions, which can affect reaction dynamics in biochemical systems. | ||||||
Ammonium Acetate | 631-61-8 | sc-203818 sc-203818A sc-203818B sc-203818C sc-203818D | 100 g 500 g 1 kg 2.5 kg 5 kg | $43.00 $139.00 $209.00 $408.00 $714.00 | 1 | |
Ammonium acetate is a versatile salt characterized by its ability to form hydrogen bonds and engage in ionic interactions, which enhance its solubility in polar solvents. This compound can act as a buffering agent, stabilizing pH levels in various environments. Its unique structure allows for distinct coordination with metal ions, influencing reaction kinetics and pathways in complexation reactions. Additionally, it can participate in crystallization processes, affecting the morphology of solid-state materials. | ||||||
Sodium periodate | 7790-28-5 | sc-203399 sc-203399A sc-203399B | 5 g 100 g 500 g | $45.00 $143.00 $364.00 | 1 | |
Sodium periodate is a distinctive salt known for its strong oxidizing properties, particularly in organic synthesis. It readily participates in oxidation-reduction reactions, facilitating the cleavage of carbon-carbon bonds. The compound exhibits unique interactions with hydroxyl groups, leading to the formation of periodate esters. Its crystalline structure contributes to its stability and reactivity, making it a key player in various chemical transformations, including the selective oxidation of alcohols. | ||||||
Hafnium ethoxide | 13428-80-3 | sc-269229 | 5 g | $197.00 | ||
Hafnium ethoxide is a notable salt characterized by its ability to form stable complexes with various ligands, enhancing its reactivity in coordination chemistry. It exhibits unique hydrolysis behavior, leading to the formation of hafnium oxides in aqueous environments. The compound's distinct molecular interactions facilitate the generation of hafnium-based thin films, which are crucial in advanced material applications. Its reactivity is influenced by steric factors, impacting its kinetics in polymerization processes. |