Items 191 to 200 of 377 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Phenolphthalein bisphosphate tetrasodium salt | 68807-90-9 | sc-206042 sc-206042A | 1 g 5 g | $37.00 $107.00 | ||
Phenolphthalein bisphosphate tetrasodium salt is a phosphorus compound characterized by its unique ability to form stable complexes with metal ions, enhancing its reactivity in various chemical systems. Its distinct phosphonate groups facilitate strong ionic interactions, influencing solubility and stability in aqueous environments. The compound exhibits notable pH-dependent behavior, transitioning between forms that can significantly alter its reactivity and interaction pathways in complex biochemical processes. | ||||||
Sodium hexametaphosphate | 68915-31-1 | sc-253584 sc-253584A | 250 g 5 kg | $42.00 $158.00 | ||
Sodium hexametaphosphate is a versatile phosphorus compound known for its ability to act as a dispersing agent due to its unique chain-like structure. This compound exhibits strong chelating properties, allowing it to bind with metal ions and modify their solubility. Its amorphous nature contributes to its low hygroscopicity, while its anionic character enhances its interactions with cationic species, influencing reaction kinetics and stability in various environments. | ||||||
D-Mannose 6-phosphate sodium salt | 70442-25-0 | sc-221501 sc-221501A | 100 mg 1 g | $250.00 $1234.00 | ||
D-Mannose 6-phosphate sodium salt is a distinctive phosphorus compound characterized by its phosphorylated sugar structure, which facilitates specific enzymatic interactions. This compound plays a crucial role in metabolic pathways, influencing carbohydrate metabolism and energy transfer. Its ionic nature enhances solubility in aqueous environments, promoting rapid diffusion and reactivity. Additionally, the presence of the phosphate group can modulate molecular recognition processes, impacting cellular signaling dynamics. | ||||||
Carbamyl phosphate disodium salt | 72461-86-0 | sc-234278 | 1 g | $343.00 | 1 | |
Carbamyl phosphate disodium salt is a notable phosphorus compound distinguished by its role in nitrogen metabolism. Its unique structure allows for the formation of carbamoyl groups, which participate in key biochemical reactions, including the urea cycle. The compound exhibits high reactivity due to its charged phosphate moieties, facilitating interactions with various biomolecules. This reactivity is essential for the regulation of metabolic pathways, influencing nitrogen assimilation and energy dynamics within cells. | ||||||
Tetraethyl Difluoromethylenebisphosphonate | 78715-58-9 | sc-208429 | 50 mg | $527.00 | ||
Tetraethyl Difluoromethylenebisphosphonate is a phosphorus compound characterized by its unique difluoromethylene group, which enhances its reactivity and stability in various chemical environments. The compound exhibits distinct molecular interactions, particularly through its phosphonate moieties, allowing for the formation of stable complexes with metal ions. Its kinetic behavior is influenced by the presence of fluorine atoms, which can modulate reaction rates and pathways, making it a subject of interest in studies of phosphorus chemistry. | ||||||
Phosphazene base P1-t-Bu | 81675-81-2 | sc-253268 | 5 ml | $393.00 | ||
Phosphazene base P1-t-Bu is a notable phosphorus compound distinguished by its unique cyclic structure, which facilitates strong hydrogen bonding and enhances its basicity. This compound exhibits remarkable stability and reactivity, particularly in nucleophilic substitution reactions. Its sterically hindered t-butyl groups contribute to its selectivity in various chemical transformations, while its ability to form stable adducts with electrophiles showcases its versatility in synthetic pathways. | ||||||
N,N-diethyl-1,5-dihydro-2,4,3-benzodioxaphosphepin-3-amine | 82372-35-8 | sc-236221 | 1 g | $130.00 | ||
N,N-diethyl-1,5-dihydro-2,4,3-benzodioxaphosphepin-3-amine is a distinctive phosphorus compound characterized by its fused dioxaphosphepin framework, which promotes unique electronic properties. This compound exhibits intriguing reactivity patterns, particularly in electrophilic aromatic substitution, due to its electron-rich amine functionality. Its ability to engage in coordination with transition metals enhances its role in catalysis, while the presence of diethyl groups influences steric effects, impacting reaction kinetics and selectivity in synthetic applications. | ||||||
Anilinium hypophosphite | 82395-88-8 | sc-233875 | 25 g | $71.00 | ||
Anilinium hypophosphite is a notable phosphorus compound featuring an anilinium cation that enhances its solubility and reactivity in various environments. The compound exhibits unique hydrogen bonding interactions, which can influence its stability and reactivity in solution. Its phosphite moiety allows for distinct pathways in nucleophilic substitution reactions, while the aromatic ring contributes to its electronic properties, facilitating diverse chemical transformations. | ||||||
2-(Trimethylsilyl)ethoxymethyl-triphenylphosphonium chloride | 82495-75-8 | sc-237889 | 1 g | $41.00 | ||
2-(Trimethylsilyl)ethoxymethyl-triphenylphosphonium chloride is a phosphorus compound characterized by its unique trimethylsilyl and triphenylphosphonium groups, which enhance its lipophilicity and reactivity. The presence of the phosphonium cation facilitates strong ionic interactions, promoting efficient nucleophilic attack in various reactions. Its ethoxymethyl group provides steric hindrance, influencing reaction kinetics and selectivity, while the overall structure allows for versatile coordination chemistry. | ||||||
2,4-Diamino-6,7-diisopropylpteridine phosphate salt | 84176-65-8 | sc-230929A sc-230929 | 100 mg 1 g | $56.00 $403.00 | ||
2,4-Diamino-6,7-diisopropylpteridine phosphate salt is a phosphorus compound notable for its intricate molecular structure, which fosters unique hydrogen bonding interactions. The presence of amino groups enhances its solubility in polar solvents, while the diisopropyl substituents contribute to steric bulk, affecting its reactivity and stability. This compound exhibits distinct pathways in biochemical processes, influencing reaction rates and selectivity through its phosphate moiety, which can engage in phosphorylation reactions. | ||||||