Phosphorus Compounds
Items 1 to 10 of 377 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
D(−)-2-Amino-5-phosphonovaleric acid (D-AP5) | 79055-68-8 | sc-200434 | 5 mg | $95.00 | 2 | |
D(-)-2-Amino-5-phosphonovaleric acid (D-AP5) is a phosphorus compound characterized by its unique ability to selectively inhibit specific glutamate receptors, particularly NMDA receptors. This selectivity is attributed to its structural conformation, which allows for precise molecular interactions. D-AP5's kinetic properties facilitate rapid binding and unbinding, influencing synaptic transmission and neuronal signaling pathways. Its phosphonate group enhances solubility and reactivity, making it a notable compound in biochemical studies. | ||||||
β-Glycerophosphate disodium salt pentahydrate | 13408-09-8 | sc-203323 sc-203323A sc-203323B | 50 g 100 g 250 g | $87.00 $173.00 $265.00 | 36 | |
β-Glycerophosphate disodium salt pentahydrate is a phosphorus compound notable for its role in cellular energy metabolism and phosphate transfer. Its unique structure allows for effective interactions with various enzymes, influencing metabolic pathways. The compound exhibits high solubility, promoting its diffusion in biological systems. Additionally, its ability to act as a phosphate donor enhances its reactivity in biochemical reactions, making it a key player in energy-related processes. | ||||||
KDdiA-PC | 439904-34-4 | sc-391510 | 1 mg | $147.00 | ||
KDdiA-PC is a phosphorus compound characterized by its unique reactivity as an acid halide, facilitating nucleophilic acyl substitution reactions. Its structure promotes strong interactions with nucleophiles, leading to rapid reaction kinetics. The compound's ability to form stable intermediates enhances its role in synthetic pathways, while its polar nature contributes to solvation effects in various solvents. This behavior underscores its significance in chemical transformations involving phosphorus. | ||||||
(1-Decyl)triphenylphosphonium bromide | 32339-43-8 | sc-264801 sc-264801A | 2.5 g 25 g | $46.00 $96.00 | 10 | |
(1-Decyl)triphenylphosphonium bromide is a phosphorus compound notable for its distinctive cationic nature, which enhances its interaction with anionic species. The long decyl chain imparts hydrophobic characteristics, influencing solubility and aggregation behavior in nonpolar environments. Its triphenylphosphonium moiety facilitates electron transfer processes, making it a key player in redox reactions. Additionally, the compound exhibits unique thermal stability, allowing for diverse applications in organic synthesis. | ||||||
α-hydroxy Farnesyl Phosphonic Acid | 148796-53-6 | sc-205200 sc-205200A | 1 mg 5 mg | $138.00 $695.00 | ||
α-Hydroxy Farnesyl Phosphonic Acid is a phosphorus compound characterized by its unique ability to form stable complexes with metal ions, enhancing its reactivity in various catalytic processes. The presence of the hydroxy group allows for hydrogen bonding interactions, influencing solubility in polar solvents. Its distinct molecular structure promotes specific reaction pathways, particularly in esterification and phosphorylation reactions, showcasing its versatility in synthetic chemistry. | ||||||
Ethylenediaminetetra(methylenephosphonic acid) | 1429-50-1 | sc-300682 sc-300682A sc-300682B sc-300682C | 5 g 25 g 100 g 500 g | $37.00 $57.00 $128.00 $552.00 | 1 | |
Ethylenediaminetetra(methylenephosphonic acid) is a phosphorus compound notable for its chelating properties, enabling it to effectively bind with metal ions and stabilize them in solution. This compound exhibits strong acidity, facilitating proton transfer reactions and enhancing its role in complexation chemistry. Its unique molecular architecture allows for multiple coordination sites, influencing reaction kinetics and promoting diverse pathways in catalysis and environmental applications. | ||||||
Potassium Phosphate, Monobasic | 7778-77-0 | sc-203211 sc-203211A sc-203211B sc-203211C | 500 g 2 kg 5 kg 10 kg | $20.00 $50.00 $105.00 $475.00 | 3 | |
Potassium Phosphate, Monobasic is a phosphorus compound characterized by its ability to act as a buffering agent, maintaining pH stability in various environments. Its ionic nature allows for effective solvation and interaction with water molecules, enhancing its role in biochemical processes. The compound participates in energy transfer mechanisms, particularly in ATP synthesis, and exhibits distinct solubility properties that influence nutrient availability in agricultural contexts. | ||||||
Sodium phytate | 14306-25-3 | sc-203329 | 25 g | $120.00 | 2 | |
Sodium Phytate is a phosphorus compound notable for its chelating properties, enabling it to form stable complexes with metal ions. This interaction can influence nutrient bioavailability and soil chemistry. Its unique structure allows for effective sequestration of phosphorus, impacting its mobility in environmental systems. Additionally, Sodium Phytate exhibits distinct solubility characteristics, which can affect its reactivity and interactions in various biochemical pathways. | ||||||
GYY 4137 | 106740-09-4 | sc-224013 sc-224013A sc-224013B sc-224013C | 10 mg 25 mg 50 mg 100 mg | $78.00 $210.00 $330.00 $576.00 | 12 | |
GYY 4137 is a phosphorus compound characterized by its unique ability to modulate redox reactions through specific molecular interactions. It engages in distinct pathways that influence cellular signaling and energy metabolism. The compound's reactivity is enhanced by its structural features, allowing for rapid kinetics in various chemical environments. Its solubility profile further facilitates diverse interactions, impacting its behavior in biochemical systems and contributing to its role in phosphorus cycling. | ||||||
Demeton-S | 126-75-0 | sc-207520 | 100 mg | $300.00 | ||
Demeton-S is a phosphorus compound notable for its electrophilic nature, which allows it to readily participate in nucleophilic substitution reactions. Its unique structure enables it to interact with thiol groups, leading to the formation of stable adducts. This compound exhibits distinct reactivity patterns, influencing its behavior in various chemical environments. Additionally, its hydrophobic characteristics affect its distribution and interaction with biological membranes, impacting its overall chemical dynamics. | ||||||