Items 361 to 370 of 426 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Tetramethylammonium hexafluorophosphate | 558-32-7 | sc-237064 | 25 g | $93.00 | ||
Tetramethylammonium hexafluorophosphate is a quaternary ammonium salt known for its ionic nature and high solubility in polar solvents. Its unique structure allows for strong ion pairing, which influences its behavior in electrochemical applications. The hexafluorophosphate anion exhibits significant electron-withdrawing properties, enhancing the stability of the cation in various environments. This salt also plays a role in facilitating charge transfer processes, making it a subject of interest in ionic liquid research. | ||||||
Tetramethylammonium tetrafluoroborate | 661-36-9 | sc-251203 | 25 g | $95.00 | ||
Tetramethylammonium tetrafluoroborate is a quaternary ammonium salt characterized by its high ionic conductivity and solubility in polar solvents. The tetrafluoroborate anion contributes to its unique electrochemical properties, promoting efficient ion transport. This salt exhibits strong ion pairing and distinct molecular interactions, which can influence reaction kinetics in various chemical processes. Its stability and behavior in solution make it a notable subject in studies of ionic liquids and electrolyte systems. | ||||||
Cerium(III) acetate hydrate | 206996-60-3 | sc-252552 | 50 g | $53.00 | ||
Cerium(III) acetate hydrate is a coordination compound that showcases unique interactions between cerium ions and acetate ligands, leading to distinctive solvation dynamics. The presence of water molecules in its structure enhances its hygroscopic nature, facilitating the formation of stable complexes. This compound exhibits interesting redox properties, allowing it to participate in various electron transfer reactions. Its crystalline form contributes to its thermal stability and influences its reactivity in different chemical environments. | ||||||
Pentylmagnesium bromide solution | 693-25-4 | sc-236330 sc-236330A | 100 ml 800 ml | $125.00 $392.00 | ||
Pentylmagnesium bromide solution is a Grignard reagent characterized by its strong nucleophilic properties, enabling it to engage in rapid carbon-carbon bond formation. The solution exhibits unique reactivity with electrophiles, facilitating the formation of complex organic structures. Its high reactivity is influenced by the presence of the magnesium atom, which enhances the electron density on the pentyl group. Additionally, the solution's stability is affected by solvent interactions, impacting its overall reactivity profile in synthetic pathways. | ||||||
Isobutylmagnesium bromide solution | 926-62-5 | sc-235400 | 100 ml | $39.00 | ||
Isobutylmagnesium bromide solution is a highly reactive Grignard reagent known for its exceptional ability to act as a nucleophile in organic synthesis. The presence of the magnesium center significantly polarizes the carbon-bromine bond, enhancing its reactivity towards electrophiles. This solution exhibits unique solvation dynamics, which can influence its reactivity and selectivity in various synthetic pathways. Its distinct steric and electronic properties allow for the formation of branched carbon chains, making it a versatile tool in complex organic transformations. | ||||||
Sodium chlorodifluoroacetate | 1895-39-2 | sc-229295 | 25 g | $73.00 | ||
Sodium chlorodifluoroacetate is a distinctive salt characterized by its strong electronegative fluorine atoms, which impart unique reactivity and stability. The compound exhibits notable ionic interactions, enhancing its solubility in polar solvents. Its behavior as an acid halide allows for selective acylation reactions, where it can participate in nucleophilic attacks, leading to the formation of various derivatives. The presence of the chlorodifluoroacetate moiety influences reaction kinetics, making it a subject of interest in synthetic chemistry. | ||||||
Tetramethylammonium nitrate | 1941-24-8 | sc-237068 | 10 g | $85.00 | ||
Tetramethylammonium nitrate is a unique salt that showcases significant ionic character due to its quaternary ammonium structure. This compound exhibits strong solvation effects, enhancing its solubility in various solvents. Its ability to act as a non-nucleophilic counterion allows for the stabilization of reactive species in solution. Additionally, the compound's distinct molecular interactions can influence reaction pathways, making it a noteworthy subject in studies of ionic liquids and electrochemistry. | ||||||
Tetraethylammonium nitrate | 1941-26-0 | sc-237034 | 10 g | $165.00 | ||
Tetraethylammonium nitrate is a fascinating salt characterized by its quaternary ammonium framework, which imparts notable ionic properties. This compound demonstrates unique electrostatic interactions that can modulate the behavior of ions in solution, influencing reaction kinetics. Its high solubility in polar solvents facilitates the formation of ionic aggregates, which can alter the dynamics of chemical reactions. The compound's distinct structural features make it an intriguing candidate for exploring ionic conductivity and phase behavior in various chemical environments. | ||||||
Tetrabutylammonium nitrate | 1941-27-1 | sc-237019 | 2 g | $26.00 | ||
Tetrabutylammonium nitrate is a distinctive salt featuring a bulky quaternary ammonium cation that enhances its solubility in organic solvents. This compound exhibits unique ion-pairing dynamics, which can significantly influence reaction mechanisms and rates. Its ability to stabilize charged species in solution allows for the exploration of complexation and solvation effects. Additionally, the steric hindrance of the butyl groups contributes to its role in modulating ionic interactions, making it a subject of interest in studies of ionic transport and phase transitions. | ||||||
Trimethyloctylammonium bromide | 2083-68-3 | sc-229595 | 5 g | $43.00 | ||
Trimethyloctylammonium bromide is a quaternary ammonium salt characterized by its long hydrophobic octyl chain, which imparts unique surfactant properties. This compound exhibits strong ion-pairing capabilities, facilitating the formation of micelles in solution. Its distinct molecular structure enhances solubilization of nonpolar substances, while the trimethyl groups contribute to its stability and reactivity. The interplay between hydrophobic and ionic interactions makes it a key player in studies of interfacial phenomena and phase behavior. |