Items 11 to 20 of 377 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Tetra-n-butylphosphonium iodide | 3115-66-0 | sc-272548 | 5 g | $71.00 | ||
Tetra-n-butylphosphonium iodide is a phosphorus compound characterized by its ionic nature, which facilitates strong electrostatic interactions in solution. Its bulky n-butyl groups enhance solubility in organic solvents, promoting unique phase transfer capabilities. This compound exhibits distinct reactivity in nucleophilic reactions, often acting as a phase transfer catalyst. Its ability to stabilize charged intermediates contributes to its effectiveness in various synthetic pathways, influencing reaction kinetics and selectivity. | ||||||
Naphthol AS-BI-phosphate | 1919-91-1 | sc-222042 sc-222042A | 100 mg 1 g | $96.00 $282.00 | 1 | |
Naphthol AS-BI-phosphate is a phosphorus compound notable for its unique ability to form stable complexes with metal ions, enhancing its role in catalysis. Its structure allows for effective hydrogen bonding, influencing solubility and reactivity in various solvents. The compound exhibits distinct behavior in electrophilic aromatic substitution reactions, where it can act as a powerful activating agent. Additionally, its phosphonate group contributes to its reactivity, facilitating diverse synthetic pathways. | ||||||
D-myo-Inositol-1,4,5-trisphosphate hexasodium salt | 108340-81-4 | sc-201522 | 1 mg | $135.00 | 1 | |
D-myo-Inositol-1,4,5-trisphosphate hexasodium salt is a phosphorus compound characterized by its role in cellular signaling pathways, particularly in calcium mobilization. Its unique structure allows for specific interactions with inositol trisphosphate receptors, influencing downstream signaling cascades. The compound's high solubility in aqueous environments enhances its bioavailability, while its anionic nature promotes interactions with cationic proteins, affecting various biochemical processes. | ||||||
Farnesyl pyrophosphate ammonium salt, in methanol | 13058-04-3 | sc-364722 | 200 µg | $86.00 | ||
Farnesyl pyrophosphate ammonium salt in methanol is a phosphorus compound notable for its involvement in lipid biosynthesis and protein prenylation. Its unique structure facilitates interactions with enzymes involved in isoprenoid metabolism, influencing cellular growth and differentiation. The compound exhibits distinct reactivity patterns, particularly in nucleophilic attack scenarios, and its solubility in methanol enhances its accessibility for various biochemical assays, promoting efficient reaction kinetics. | ||||||
Potassium Glycerophosphate Solution | 1319-69-3 | sc-281135 | 120 ml | $71.00 | ||
Potassium Glycerophosphate Solution is a phosphorus compound characterized by its role in cellular energy metabolism and phosphate transfer. Its unique ionic structure allows for effective interactions with biological membranes, enhancing permeability and facilitating nutrient transport. The compound exhibits notable buffering capacity, stabilizing pH levels in various environments. Additionally, its hygroscopic nature contributes to moisture retention, influencing biochemical pathways and reaction dynamics in aqueous systems. | ||||||
Tris(2,4,6-trimethoxyphenyl)phosphine | 91608-15-0 | sc-255706 | 2 g | $91.00 | ||
Tris(2,4,6-trimethoxyphenyl)phosphine is a phosphorus compound distinguished by its sterically hindered structure, which influences its reactivity and selectivity in organic synthesis. The presence of multiple methoxy groups enhances electron donation, facilitating nucleophilic attacks in various reactions. Its unique molecular geometry allows for specific interactions with electrophiles, promoting efficient reaction kinetics. Additionally, the compound's lipophilicity aids in solubility in organic solvents, impacting its behavior in diverse chemical environments. | ||||||
Tris(diethylamino)phosphine | 2283-11-6 | sc-251400 | 5 g | $82.00 | ||
Tris(diethylamino)phosphine is a phosphorus compound characterized by its unique tri-substituted amine structure, which imparts significant nucleophilicity. The diethylamino groups enhance electron density, enabling rapid interactions with electrophiles. This compound exhibits distinctive reactivity patterns, particularly in the formation of phosphonium salts and in facilitating various coupling reactions. Its solubility in organic solvents and ability to stabilize reactive intermediates further influence its behavior in synthetic pathways. | ||||||
TCEP, Hydrochloride | 51805-45-9 | sc-203290 sc-203290A | 1 g 25 g | $86.00 $816.00 | 13 | |
TCEP, Hydrochloride is a phosphorus compound notable for its strong reducing properties, particularly in the presence of disulfide bonds. Its unique structure allows for efficient electron transfer, making it a potent agent in redox reactions. The compound's stability in aqueous solutions and resistance to oxidation enhance its utility in various chemical processes. Additionally, TCEP's ability to maintain a low pH environment can influence reaction kinetics, promoting specific pathways in complex biochemical systems. | ||||||
Sodium pyrophosphate decahydrate | 13472-36-1 | sc-203404 sc-203404A sc-203404B sc-203404C | 100 g 500 g 1 kg 2.5 kg | $45.00 $150.00 $242.00 $370.00 | ||
Sodium pyrophosphate decahydrate is a phosphorus compound characterized by its ability to act as a buffering agent, stabilizing pH levels in various environments. Its unique chelating properties allow it to form complexes with metal ions, influencing solubility and reactivity. The compound exhibits hygroscopic behavior, readily absorbing moisture, which can affect its physical state and reactivity. Additionally, its role in promoting the formation of phosphoester bonds highlights its significance in biochemical pathways. | ||||||
Tris phosphate dibasic | 108321-11-5 | sc-301954 sc-301954A | 25 g 250 g | $316.00 $520.00 | ||
Tris phosphate dibasic is a phosphorus compound notable for its role in modulating ionic strength in solution, which can significantly influence reaction kinetics. Its ability to participate in hydrogen bonding enhances solubility and facilitates interactions with various biomolecules. The compound's distinct buffering capacity allows it to maintain stable pH levels, crucial for biochemical processes. Furthermore, its reactivity with metal ions can alter catalytic pathways, impacting overall system dynamics. |