Items 181 to 190 of 377 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Calcium glycerophosphate | 28917-82-0 | sc-268663 | 250 g | $104.00 | ||
Calcium glycerophosphate is a phosphorus compound characterized by its ability to form chelate complexes with metal ions, enhancing its stability and solubility in aqueous environments. This compound participates in unique ionic interactions, influencing its behavior in biological systems. Its hygroscopic nature allows it to absorb moisture, which can affect its reactivity and storage conditions. Additionally, it plays a role in buffering systems, maintaining pH balance in various chemical contexts. | ||||||
Acephate | 30560-19-1 | sc-203800 | 50 mg | $60.00 | ||
Acephate is a phosphorus compound notable for its unique ability to undergo hydrolysis, leading to the formation of active metabolites that interact with biological systems. Its structure allows for specific nucleophilic attack pathways, influencing reaction kinetics and degradation rates in various environments. The compound exhibits polar characteristics, enhancing its solubility in water and facilitating its movement through different media. Additionally, Acephate's reactivity with nucleophiles contributes to its diverse chemical behavior. | ||||||
Phosphoenolpyruvic acid, tris(cyclohexylammonium) salt | 35556-70-8 | sc-208169 sc-208169A | 250 mg 500 mg | $35.00 $94.00 | ||
Phosphoenolpyruvic acid, tris(cyclohexylammonium) salt is a phosphorus compound characterized by its unique ability to participate in enzymatic reactions, particularly in metabolic pathways. Its structure promotes specific interactions with enzymes, influencing catalytic efficiency and substrate specificity. The compound's amphiphilic nature enhances its solubility in organic solvents, facilitating its role in biochemical processes. Additionally, its stability under various conditions allows for controlled reactivity in synthetic applications. | ||||||
Chlorodiisopropylphosphine | 40244-90-4 | sc-234329 sc-234329A | 5 g 25 g | $87.00 $229.00 | ||
Chlorodiisopropylphosphine is a phosphorus compound notable for its reactivity as a nucleophile, engaging in diverse substitution reactions. Its sterically hindered structure influences reaction kinetics, often leading to selective pathways in synthesis. The compound exhibits unique interactions with electrophiles, enhancing its utility in forming phosphine oxides and other derivatives. Its liquid state and moderate volatility contribute to its handling in various chemical environments, making it a versatile reagent in organic synthesis. | ||||||
(1-Octyl)triphenylphosphonium bromide | 42036-78-2 | sc-273428 | 5 g | $200.00 | ||
(1-Octyl)triphenylphosphonium bromide is a phosphorus compound characterized by its unique cationic structure, which enhances its solubility in organic solvents. The triphenylphosphonium moiety facilitates strong interactions with anions, promoting ion-pairing dynamics. This compound exhibits distinct behavior in phase transfer catalysis, where it can effectively shuttle reactants across immiscible phases. Its hydrophobic octyl chain contributes to its ability to stabilize intermediates, influencing reaction pathways and kinetics in various organic transformations. | ||||||
Bis(4-methylumbelliferyl)phosphate | 51379-07-8 | sc-280624 sc-280624A | 250 mg 500 mg | $250.00 $450.00 | ||
Bis(4-methylumbelliferyl)phosphate is a phosphorus compound notable for its fluorescent properties, which arise from the 4-methylumbelliferyl groups. This compound exhibits unique interactions with metal ions, leading to enhanced luminescence and potential applications in sensing. Its reactivity is influenced by the presence of phosphate groups, which can participate in hydrolysis and esterification reactions, affecting reaction rates and mechanisms in biochemical pathways. The compound's structural features also allow for specific binding interactions, making it a subject of interest in studies of molecular recognition. | ||||||
L-Alanyl-L-1-aminoethylphosphonic acid | 60668-24-8 | sc-257647 | 250 mg | $217.00 | ||
L-Alanyl-L-1-aminoethylphosphonic acid is a phosphorus compound characterized by its unique ability to form stable complexes with various cations, influencing its solubility and reactivity. The presence of the aminoethyl group enhances its interaction with biological molecules, facilitating specific binding events. Its kinetic behavior in hydrolytic reactions is notable, as it can act as a substrate for enzymatic processes, impacting metabolic pathways. The compound's structural configuration allows for diverse conformational states, contributing to its dynamic chemical behavior. | ||||||
Triphenylphosphine-3,3′,3′′-trisulfonic acid trisodium salt | 63995-70-0 | sc-356176 sc-356176A | 250 mg 1 g | $175.00 $289.00 | ||
Triphenylphosphine-3,3',3''-trisulfonic acid trisodium salt is a phosphorus compound distinguished by its strong ionic character and ability to engage in electrostatic interactions. Its sulfonic acid groups enhance solubility in polar solvents, promoting unique reactivity patterns. The compound exhibits notable stability in aqueous environments, facilitating its role in various catalytic processes. Additionally, its steric bulk influences reaction kinetics, allowing for selective pathways in chemical transformations. | ||||||
Lithium diphenylphosphide solution | 65567-06-8 | sc-235507 | 100 ml | $191.00 | ||
Lithium diphenylphosphide solution is a phosphorus compound characterized by its unique coordination chemistry and reactivity. The presence of lithium ions enhances its nucleophilicity, enabling it to participate in a variety of organometallic reactions. This solution exhibits distinct solvation dynamics, which influence its interaction with electrophiles. Its ability to stabilize reactive intermediates allows for efficient pathways in synthetic transformations, making it a versatile reagent in organic synthesis. | ||||||
Alendronate acid | 66376-36-1 | sc-337520 | 5 g | $135.00 | 2 | |
Alendronate acid is a phosphorus compound notable for its strong affinity for hydroxyapatite, a key component of bone mineral. This interaction facilitates its unique ability to inhibit bone resorption through specific binding mechanisms. The compound exhibits distinct acid-base properties, allowing it to engage in proton transfer reactions. Its structural features enable selective interactions with metal ions, influencing its reactivity and stability in various chemical environments. | ||||||