Items 141 to 150 of 377 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Spermine diphosphate hydrate | 3891-79-0 | sc-253603 | 1 g | $204.00 | ||
Spermine diphosphate hydrate is a unique phosphorus compound characterized by its ability to form stable complexes with metal ions, enhancing its role in biochemical processes. Its diphosphate moiety contributes to high-energy phosphate transfer, crucial for various enzymatic reactions. The compound exhibits distinct kinetic properties, influencing reaction rates in metabolic pathways. Additionally, its hydrophilic nature promotes solubility, facilitating interactions with biomolecules and enhancing cellular signaling mechanisms. | ||||||
Methyl diphenylphosphinite | 4020-99-9 | sc-235821 | 1 g | $56.00 | ||
Methyl diphenylphosphinite is a notable phosphorus compound recognized for its role as a versatile ligand in coordination chemistry. It exhibits strong donor properties, allowing it to form stable complexes with transition metals, which can significantly alter the electronic properties of the metal centers. The compound's unique steric and electronic characteristics influence reaction kinetics, making it a key player in catalysis. Its lipophilic nature enhances solubility in organic solvents, promoting diverse reactivity in synthetic pathways. | ||||||
Tris(2-cyanoethyl)phosphine | 4023-53-4 | sc-280164 | 1 g | $122.00 | ||
Tris(2-cyanoethyl)phosphine is a distinctive phosphorus compound characterized by its ability to engage in nucleophilic reactions due to the presence of cyanoethyl groups. These groups enhance the electron density on the phosphorus atom, facilitating interactions with electrophiles. The compound's unique structure allows for the formation of stable intermediates in various chemical transformations, influencing reaction pathways and kinetics. Its polar nature also contributes to solubility in polar solvents, expanding its reactivity profile. | ||||||
Phosphoenolpyruvic acid, monopotassium salt | 4265-07-0 | sc-208168 sc-208168A sc-208168B | 100 mg 250 mg 1 g | $76.00 $152.00 $296.00 | 1 | |
Phosphoenolpyruvic acid, monopotassium salt, is a notable phosphorus compound that plays a crucial role in metabolic pathways, particularly in energy transfer and biosynthesis. Its unique enol phosphate structure allows for high-energy phosphate bond formation, which is pivotal in enzymatic reactions. The compound exhibits strong ionic interactions due to its potassium salt form, enhancing its solubility and reactivity in aqueous environments. This facilitates rapid participation in biochemical processes, influencing reaction rates and pathways. | ||||||
Tetradecyl Phosphonate | 4671-75-4 | sc-205519 sc-205519A | 100 mg 500 mg | $24.00 $113.00 | ||
Tetradecyl Phosphonate is a distinctive phosphorus compound characterized by its long hydrocarbon chain, which imparts unique amphiphilic properties. This structure promotes self-assembly in various environments, leading to the formation of micelles or vesicles. The compound exhibits significant reactivity through its phosphonate group, enabling it to participate in nucleophilic substitution reactions. Its interactions with metal ions can enhance catalytic activity, influencing reaction kinetics in complex systems. | ||||||
Propylphosphonic acid | 4672-38-2 | sc-236493 sc-236493A sc-236493B | 1 g 5 g 25 g | $87.00 $339.00 $1056.00 | ||
Propylphosphonic acid is a notable phosphorus compound distinguished by its ability to form strong hydrogen bonds due to its acidic proton and polar functional groups. This property enhances its solubility in polar solvents and facilitates interactions with various substrates. The compound exhibits unique reactivity patterns, particularly in esterification and phosphorylation reactions, where it acts as a potent electrophile. Its structural flexibility allows for diverse coordination with metal ions, influencing catalytic pathways and reaction dynamics. | ||||||
1-Dodecylphosphonic acid | 5137-70-2 | sc-273318 | 1 g | $45.00 | ||
1-Dodecylphosphonic acid is a unique phosphorus compound characterized by its long hydrophobic dodecyl chain, which imparts distinct amphiphilic properties. This structure promotes self-assembly in solution, leading to micelle formation and enhanced surface activity. The compound's phosphonic acid group exhibits strong affinity for metal ions, facilitating complexation and influencing adsorption processes. Its reactivity in condensation reactions highlights its potential in forming stable phosphonate esters, showcasing its versatility in synthetic pathways. | ||||||
4-Aminobenzylphosphonic acid | 5424-27-1 | sc-232399 | 250 mg | $70.00 | ||
4-Aminobenzylphosphonic acid is a distinctive phosphorus compound featuring an amino group that enhances its reactivity and solubility in polar environments. This compound engages in hydrogen bonding, which can influence its interaction with various substrates. Its phosphonic acid moiety allows for strong coordination with metal ions, promoting unique catalytic pathways. Additionally, the presence of the benzyl group contributes to its ability to stabilize intermediates in chemical reactions, showcasing its dynamic behavior in synthetic applications. | ||||||
O,O-Diethyl thiophosphate potassium salt | 5871-17-0 | sc-236223 | 5 g | $88.00 | ||
O,O-Diethyl thiophosphate potassium salt is a notable phosphorus compound characterized by its thiophosphate group, which imparts unique reactivity and stability. This compound exhibits strong nucleophilic properties, facilitating interactions with electrophiles in various chemical pathways. Its ionic nature enhances solubility in aqueous environments, promoting rapid reaction kinetics. The presence of ethyl groups contributes to steric effects, influencing molecular interactions and reactivity profiles in synthetic processes. | ||||||
N-(Phosphonomethyl)iminodiacetic acid | 5994-61-6 | sc-235955 | 250 g | $127.00 | ||
N-(Phosphonomethyl)iminodiacetic acid is a distinctive phosphorus compound featuring a phosphonomethyl group that enhances its chelating ability with metal ions. This compound exhibits strong coordination chemistry, forming stable complexes that can influence reaction pathways. Its unique structure allows for multiple protonation states, affecting its acidity and reactivity. Additionally, the presence of carboxylate groups contributes to its solubility and interaction dynamics in various environments, making it a versatile agent in chemical processes. |