SEE ALSO...
Items 1 to 10 of 172 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Tetrabutylammonium nitrite | 26501-54-2 | sc-255643 | 10 g | $170.00 | ||
Tetrabutylammonium nitrite, as an ionic liquid, showcases remarkable solvation dynamics and ion mobility, which facilitate unique molecular interactions. Its structure promotes strong ion pairing and hydrogen bonding, leading to distinct reaction pathways in organic synthesis. The compound's low viscosity enhances mass transport, while its tunable properties allow for tailored reactivity in various chemical processes, making it a versatile medium for ionic reactions and catalysis. | ||||||
1-(Cyanomethyl)-3-methylimidazolium chloride | 154312-63-7 | sc-237447 | 5 g | $359.00 | ||
1-(Cyanomethyl)-3-methylimidazolium chloride, an ionic liquid, exhibits intriguing electrochemical properties due to its unique cation-anion interactions. The presence of the cyano group enhances dipole moments, promoting strong solvation effects and facilitating charge transfer processes. Its ability to stabilize reactive intermediates and influence reaction kinetics makes it a compelling medium for various chemical transformations. Additionally, its low vapor pressure contributes to a safer working environment in synthetic applications. | ||||||
1-Ethyl-2,3-dimethylimidazolium chloride | 92507-97-6 | sc-224653 | 5 g | $98.00 | ||
1-Ethyl-2,3-dimethylimidazolium chloride, an ionic liquid, showcases remarkable thermal stability and low viscosity, which enhance its fluidity and mass transport properties. The unique arrangement of its cation allows for effective hydrogen bonding and ion pairing, leading to distinctive solvation dynamics. This ionic liquid's ability to dissolve a wide range of polar and nonpolar compounds facilitates diverse reaction pathways, making it an intriguing candidate for innovative chemical processes. | ||||||
1-Butyl-3-methylimidazolium trifluoromethanesulfonate | 174899-66-2 | sc-251493 sc-251493A | 5 g 25 g | $220.00 $826.00 | ||
1-Butyl-3-methylimidazolium trifluoromethanesulfonate is an ionic liquid characterized by its strong ionic interactions and high ionic conductivity. The trifluoromethanesulfonate anion contributes to its unique solvation properties, promoting efficient ion transport and facilitating rapid reaction kinetics. Its ability to stabilize charged species enhances catalytic processes, while the cation's structural flexibility allows for diverse molecular interactions, making it a versatile medium for various chemical transformations. | ||||||
1-Butyl-3-methylimidazolium dibutyl phosphate | 663199-28-8 | sc-229782 sc-229782A | 5 g 50 g | $107.00 $450.00 | ||
1-Butyl-3-methylimidazolium dibutyl phosphate is an ionic liquid distinguished by its unique hydrogen bonding capabilities and polarizability. The dibutyl phosphate anion enhances its ability to solvate a wide range of polar and nonpolar compounds, promoting effective ion pairing and facilitating charge transfer. This ionic liquid exhibits low viscosity, which aids in mass transport during reactions, while its tunable properties allow for tailored interactions in diverse chemical environments. | ||||||
Cholin acetate | 14586-35-7 | sc-239544 sc-239544A | 5 g 50 g | $182.00 $766.00 | 1 | |
Choline acetate, as an ionic liquid, showcases remarkable ionic conductivity and a high degree of solvation for various ions. Its unique hydrogen bond network contributes to enhanced stability and reactivity, facilitating efficient ion transport. The presence of the acetate anion allows for versatile interactions with organic and inorganic substrates, promoting unique reaction pathways. Additionally, its low volatility and thermal stability make it suitable for diverse applications in electrochemistry and catalysis. | ||||||
Tetraethylammonium trifluoromethanesulfonate | 35895-69-3 | sc-253670 | 5 g | $71.00 | ||
Tetraethylammonium trifluoromethanesulfonate, as an ionic liquid, exhibits exceptional ionic mobility and a strong propensity for ion pairing, which enhances its electrochemical properties. The trifluoromethanesulfonate anion introduces significant dipole moments, leading to unique solvation dynamics and facilitating rapid ion exchange. Its distinctive molecular interactions promote efficient charge transfer and can influence reaction kinetics, making it a compelling medium for various chemical processes. | ||||||
1-Decyl-3-methylimidazolium chloride | 171058-18-7 | sc-224641 | 5 g | $55.00 | ||
1-Decyl-3-methylimidazolium chloride, as an ionic liquid, showcases remarkable viscosity and thermal stability, which contribute to its unique solvation characteristics. The long alkyl chain enhances hydrophobic interactions, while the imidazolium cation facilitates strong hydrogen bonding. This combination leads to distinctive phase behavior and tunable electrochemical properties, allowing for efficient ion transport and enhanced catalytic activity in diverse chemical environments. | ||||||
Triisobutylmethylphosphonium tosylate | 344774-05-6 | sc-237324 | 5 g | $209.00 | ||
Triisobutylmethylphosphonium tosylate, an ionic liquid, exhibits unique ionic interactions due to its bulky phosphonium cation and tosylate anion. The steric hindrance from the isobutyl groups results in low volatility and high ionic conductivity, promoting efficient ion mobility. Its ability to form stable solvate complexes enhances its role in facilitating various chemical reactions, while the strong dipole moment contributes to its distinctive solvent properties, enabling selective solvation and enhanced reaction kinetics. | ||||||
Trihexyltetradecylphosphonium bis(trifluoromethylsulfonyl)amide | 460092-03-9 | sc-253758 | 5 g | $77.00 | ||
Trihexyltetradecylphosphonium bis(trifluoromethylsulfonyl)amide is an ionic liquid characterized by its large, asymmetric phosphonium cation and highly polar bis(trifluoromethylsulfonyl)amide anion. This unique structure leads to significant ion pairing and strong intermolecular interactions, resulting in enhanced thermal stability and low viscosity. Its distinctive solvation properties facilitate the dissolution of a wide range of polar and nonpolar compounds, promoting diverse reaction pathways and improving reaction rates in various chemical processes. |