Items 401 to 410 of 426 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Triphenylcarbenium pentachlorostannate | 15414-98-9 | sc-229614 | 5 g | $23.00 | ||
Triphenylcarbenium pentachlorostannate is a fascinating salt characterized by its robust cationic structure, which enhances its electrophilic reactivity. The presence of the pentachlorostannate anion introduces significant steric hindrance, influencing reaction kinetics and selectivity in electrophilic aromatic substitutions. Its unique molecular interactions allow for the formation of stable complexes with various nucleophiles, making it a subject of interest in studies of ionic and covalent bonding dynamics. | ||||||
Tetrabutylammonium bis(4-methyl-1,2-benzenedithiolato)nickelate | 15492-42-9 | sc-215948 | 250 mg | $205.00 | ||
Tetrabutylammonium bis(4-methyl-1,2-benzenedithiolato)nickelate is a distinctive salt known for its intricate coordination chemistry. The tetrabutylammonium cation provides a bulky, hydrophobic environment that stabilizes the nickel complex, enhancing solubility in organic solvents. The bis(4-methyl-1,2-benzenedithiolato) ligand exhibits strong chelation, facilitating unique electron transfer processes and influencing redox behavior. This compound's structural features promote intriguing interactions in various chemical environments. | ||||||
(R)-Phenoxybenzamine Hydrochloride | 16053-59-1 | sc-391970 | 5 mg | $320.00 | ||
(R)-Phenoxybenzamine Hydrochloride is a notable salt characterized by its chiral structure, which influences its interaction with biological systems. The hydrochloride form enhances solubility in aqueous environments, facilitating unique ionization behavior. Its phenoxy group contributes to distinctive π-π stacking interactions, while the amine functionality allows for hydrogen bonding, affecting reaction kinetics and stability. This compound's unique molecular architecture promotes diverse chemical reactivity and selectivity. | ||||||
Trimethylphenylammonium bromide | 16056-11-4 | sc-229598 | 100 g | $71.00 | ||
Trimethylphenylammonium bromide is a quaternary ammonium salt distinguished by its cationic nature, which enhances its solubility in polar solvents. The presence of the bulky trimethyl groups imparts steric hindrance, influencing molecular interactions and reactivity. This compound exhibits strong ionic interactions due to the bromide counterion, facilitating unique pathways in nucleophilic substitution reactions. Its amphiphilic characteristics enable it to stabilize interfaces, impacting surface tension and aggregation behavior in various systems. | ||||||
Tetrahexylammonium benzoate solution | 16436-29-6 | sc-229416 | 5 g | $194.00 | ||
Tetrahexylammonium benzoate solution is a quaternary ammonium salt characterized by its long-chain hexyl groups, which enhance hydrophobic interactions and solubility in organic solvents. The benzoate anion contributes to its unique reactivity, allowing for specific ion-pairing dynamics and facilitating complexation with various substrates. This compound exhibits distinct electrostatic properties, influencing its behavior in phase transfer catalysis and enhancing its role in interfacial phenomena. | ||||||
(4-Methylene-5-hexenyl)triphenyl-phosphonium Iodide | 17842-92-1 | sc-391257 | 25 mg | $360.00 | ||
(4-Methylene-5-hexenyl)triphenyl-phosphonium iodide is a distinctive salt characterized by its phosphonium cation, which enhances its reactivity through strong nucleophilic interactions. The presence of the iodide anion facilitates unique ion-pairing dynamics, influencing solubility and reactivity in various solvents. This compound exhibits interesting electrochemical properties, enabling specific pathways for electron transfer and promoting diverse reaction kinetics in organic synthesis. Its structural features contribute to intriguing photophysical behaviors, making it a subject of interest in chemical research. | ||||||
Sodium trimethylsilanolate | 18027-10-6 | sc-229324 sc-229324A | 25 g 100 g | $96.00 $409.00 | ||
Sodium trimethylsilanolate is a notable salt distinguished by its silanolate anion, which imparts unique reactivity through its ability to form strong hydrogen bonds and engage in nucleophilic substitution reactions. The trimethylsilyl group enhances its stability and solubility in organic solvents, facilitating diverse chemical transformations. This compound exhibits interesting coordination chemistry, allowing it to interact with metal ions and influence catalytic processes, making it a subject of interest in synthetic chemistry. | ||||||
Nitrilotriacetic acid trisodium salt monohydrate | 18662-53-8 | sc-236178 sc-236178A | 100 g 250 g | $21.00 $26.00 | ||
Nitrilotriacetic acid trisodium salt monohydrate is a versatile salt characterized by its chelating properties, enabling it to form stable complexes with metal ions. This interaction is facilitated by the presence of multiple carboxylate groups, which enhance its solubility in aqueous environments. The compound exhibits unique buffering capabilities, maintaining pH stability in various conditions. Its ionic nature contributes to its high conductivity in solution, making it significant in electrochemical applications. | ||||||
Dimethyldodecylethylammonium hydroxide solution | 19184-59-9 | sc-227907 | 500 ml | $475.00 | ||
Dimethyldodecylethylammonium hydroxide solution is a quaternary ammonium salt known for its surfactant properties, which arise from its long hydrophobic alkyl chain and positively charged ammonium group. This unique structure promotes strong interactions with both polar and non-polar substances, enhancing emulsification and dispersion. The compound exhibits significant surface activity, reducing surface tension in aqueous solutions, and demonstrates effective antimicrobial properties through membrane disruption mechanisms. | ||||||
Deterenol Hydrochloride | 23239-36-3 | sc-391328A sc-391328 | 1 mg 10 mg | $112.00 $388.00 | ||
Deterenol Hydrochloride is a quaternary ammonium salt characterized by its unique amphiphilic nature, which facilitates interactions between hydrophilic and hydrophobic environments. Its structure allows for effective ion pairing and solvation dynamics, enhancing its stability in various media. The compound exhibits notable electrostatic interactions, contributing to its ability to modulate surface properties and enhance phase behavior in complex mixtures, making it a versatile agent in diverse chemical contexts. |