Items 11 to 20 of 97 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Sodium carbonate decahydrate | 6132-02-1 | sc-251013 sc-251013A | 1 kg 2.5 kg | $73.00 $144.00 | ||
Sodium carbonate decahydrate exhibits unique properties as a sodium salt, characterized by its crystalline structure and high solubility in water. The extensive hydrogen bonding within its hydrated form enhances its thermal stability and influences its dissolution kinetics. This compound acts as a buffering agent, maintaining pH levels in various environments. Its ionic nature allows for effective ion exchange processes, making it a versatile participant in numerous chemical reactions. | ||||||
Sodium bicarbonate | 144-55-8 | sc-203271 sc-203271A sc-203271B sc-203271C sc-203271D | 25 g 500 g 1 kg 5 kg 25 kg | $20.00 $28.00 $42.00 $82.00 $683.00 | 1 | |
Sodium bicarbonate, as a sodium salt, showcases intriguing properties through its ability to engage in acid-base reactions. Its amphoteric nature allows it to react with both acids and bases, facilitating unique neutralization pathways. The compound's fine crystalline structure contributes to its rapid dissolution in aqueous solutions, promoting swift reaction kinetics. Additionally, its capacity to release carbon dioxide upon heating or reaction with acids highlights its role in gas evolution processes, making it a dynamic player in various chemical environments. | ||||||
Nitrilotriacetic acid trisodium salt monohydrate | 18662-53-8 | sc-236178 sc-236178A | 100 g 250 g | $21.00 $26.00 | ||
Nitrilotriacetic acid trisodium salt monohydrate exhibits distinctive chelating properties, effectively binding metal ions through its multiple carboxylate groups. This interaction enhances solubility and stability in aqueous solutions, facilitating complex formation. The compound's ionic nature contributes to its high conductivity in solution, while its monohydrate form influences hydration dynamics, impacting reaction rates and pathways in various chemical systems. Its unique structural features enable selective metal ion sequestration, showcasing its versatility in coordination chemistry. | ||||||
Sodium taurodeoxycholate Hydrate | 207737-97-1 | sc-253596 sc-253596A | 500 mg 1 g | $46.00 $71.00 | ||
Sodium taurodeoxycholate hydrate is a bile salt that plays a crucial role in emulsifying lipids, enhancing their solubility in aqueous environments. Its amphipathic structure allows it to interact with both hydrophilic and hydrophobic molecules, facilitating micelle formation. This compound exhibits unique surfactant properties, influencing membrane dynamics and permeability. Additionally, its hydration state affects molecular interactions, altering reaction kinetics and enhancing solubilization processes in biochemical systems. | ||||||
Sodium iodate | 7681-55-2 | sc-251029 sc-251029A | 100 g 500 g | $46.00 $185.00 | 1 | |
Sodium iodate is a versatile oxidizing agent that participates in redox reactions, showcasing distinct reactivity due to its iodine content. It can engage in halogenation processes, influencing the formation of iodinated organic compounds. The compound's ionic nature contributes to its solubility in water, facilitating its role in various chemical pathways. Its interactions with other halides can lead to unique coordination complexes, impacting reaction rates and mechanisms in synthetic chemistry. | ||||||
Methylxylenol Blue | 29412-85-9 | sc-475965 | 1 g | $204.00 | ||
Methylxylenol Blue is a synthetic dye characterized by its unique chromogenic properties, which allow it to undergo distinct colorimetric changes in response to pH variations. This compound exhibits strong interactions with metal ions, forming stable complexes that can alter its spectral properties. Its ability to participate in electron transfer processes enhances its reactivity, making it a valuable tool in analytical chemistry for monitoring redox states and environmental conditions. | ||||||
Molecular sieves, 4A, 1-2 mm (0.04-0.08 in) | 70955-01-0 | sc-476025A sc-476025 sc-476025B sc-476025C | 100 g 250 g 1 kg 5 kg | $23.00 $39.00 $148.00 $714.00 | ||
Molecular sieves, 4A, 1-2 mm, are crystalline aluminosilicates with a unique pore structure that selectively adsorb molecules based on size and polarity. Their high surface area and uniform pore openings facilitate efficient gas separation and drying processes. The sieves exhibit strong ionic interactions, particularly with cations, enhancing their ability to trap specific molecules. This selectivity is crucial for applications requiring precise molecular filtration and separation. | ||||||
Disodium 1-Naphthol-3,6-disulfonate | 20349-39-7 | sc-476817 | 25 g | $62.00 | ||
Disodium 1-Naphthol-3,6-disulfonate is a highly soluble compound characterized by its strong ionic nature and ability to form stable complexes with various metal ions. Its sulfonate groups enhance solvation, promoting rapid diffusion in aqueous environments. The compound exhibits unique chromogenic properties, allowing it to participate in specific redox reactions. Additionally, its molecular structure facilitates interactions with polar solvents, influencing reaction kinetics and enhancing its reactivity in diverse chemical pathways. | ||||||
Sodium orthosilicate | 13472-30-5 | sc-272493 | 1 kg | $65.00 | ||
Sodium orthosilicate is a versatile compound known for its unique silicate framework, which allows for strong hydrogen bonding and network formation in aqueous solutions. Its high reactivity stems from the presence of silanol groups, enabling it to engage in condensation reactions and polymerization processes. The compound's ability to interact with metal ions through coordination enhances its role in various catalytic pathways, while its amphoteric nature allows it to participate in both acidic and basic environments, influencing its solubility and stability. | ||||||
Phacolysine Sodium Salt | 3863-80-7 | sc-212541 | 10 mg | $280.00 | ||
Phacolysine Sodium Salt exhibits distinctive properties as a sodium salt, characterized by its ability to form stable complexes with various anions. This compound demonstrates unique solvation dynamics, enhancing its interaction with polar solvents. Its ionic nature facilitates rapid dissociation in solution, leading to increased ionic strength, which can influence reaction kinetics. Additionally, the compound's capacity for electrostatic interactions allows it to stabilize charged species, impacting its behavior in diverse chemical environments. |