Items 71 to 80 of 122 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Dimethyl sulfoxide-d6 | 2206-27-1 | sc-257361 sc-257361A sc-257361B sc-257361C | 5 g 25 g 100 g 1 kg | $66.00 $158.00 $413.00 $4600.00 | 1 | |
Dimethyl sulfoxide-d6 is a highly polar aprotic solvent known for its ability to dissolve a wide range of organic and inorganic compounds. Its unique molecular structure facilitates strong dipole-dipole interactions, enhancing solvation dynamics. The presence of deuterium allows for distinct NMR characteristics, aiding in the study of reaction mechanisms. Additionally, its high dielectric constant promotes ionic dissociation, making it effective in facilitating various chemical reactions and enhancing reaction kinetics. | ||||||
o-Xylene | 95-47-6 | sc-397231 sc-397231A sc-397231B | 250 ml 1 L 2.5 L | $67.00 $173.00 $367.00 | ||
o-Xylene is a non-polar aromatic hydrocarbon solvent characterized by its ability to solvate non-polar and moderately polar compounds through π-π stacking interactions. Its unique molecular structure allows for effective dispersion of solutes, enhancing the solubility of various organic materials. The solvent's low viscosity contributes to improved mass transfer rates in reactions, while its hydrophobic nature minimizes unwanted side reactions with water-sensitive compounds, making it a versatile choice in diverse chemical processes. | ||||||
Dichloromethane-d2 | 1665-00-5 | sc-257331 sc-257331A | 5 g 10 g | $120.00 $220.00 | ||
Dichloromethane-d2 is a polar aprotic solvent known for its ability to engage in dipole-dipole interactions, facilitating the solvation of a wide range of organic and inorganic compounds. Its unique isotopic labeling enhances NMR spectroscopy applications, providing clearer spectral data. The solvent's moderate volatility and density allow for efficient extraction processes, while its low surface tension promotes rapid wetting of solid substrates, optimizing reaction kinetics in various chemical environments. | ||||||
1,1,2,2-Tetrachloroethane | 79-34-5 | sc-356264 sc-356264A | 25 g 100 g | $39.00 $49.00 | ||
1,1,2,2-Tetrachloroethane is a non-polar solvent characterized by its strong van der Waals forces, which enable effective solvation of non-polar and moderately polar substances. Its high density and low viscosity contribute to enhanced mass transfer during extraction processes. The solvent's unique ability to stabilize radical intermediates makes it valuable in certain reaction pathways, while its inert nature minimizes unwanted side reactions, ensuring cleaner product yields in various chemical syntheses. | ||||||
Water-(18-O) (97% Isotopic Purity) | 14314-42-2 | sc-351853 sc-351853A | 1 g 10 g | $419.00 $2099.00 | 2 | |
Water-(18-O) (97% isotopic purity) serves as a unique solvent due to its distinct isotopic composition, which influences hydrogen bonding and molecular interactions. This isotopic variant exhibits altered reaction kinetics, enhancing the rate of certain chemical reactions through kinetic isotope effects. Its high polarity facilitates solvation of ionic and polar compounds, while its ability to participate in hydrogen bonding can stabilize transition states, leading to more efficient pathways in various chemical processes. | ||||||
1-Chlorobutane | 109-69-3 | sc-397740 | 200 ml | $68.00 | ||
1-Chlorobutane is a versatile solvent known for its ability to dissolve a wide range of organic compounds due to its moderate polarity. The presence of the chlorine atom enhances its dipole moment, facilitating unique solvation interactions that can stabilize transition states in chemical reactions. This solvent exhibits distinct reactivity patterns, particularly in nucleophilic substitution and elimination processes, making it a valuable medium for various synthetic pathways. Its relatively low viscosity contributes to efficient mixing and mass transfer in reaction systems. | ||||||
Dodecane | 112-40-3 | sc-397811 | 100 ml | $79.00 | ||
Dodecane, a linear alkane, exhibits remarkable solvation properties due to its extensive hydrocarbon chain, which facilitates effective solute-solvent interactions. Its nonpolar nature allows it to dissolve a variety of hydrophobic compounds, while the uniformity of its molecular structure minimizes steric hindrance, promoting efficient diffusion. Additionally, dodecane's high molecular weight contributes to its low volatility, making it an ideal medium for applications requiring stability and reduced evaporation rates. | ||||||
Benzyl alcohol-α-13C-α,α-d2 | 285977-71-1 | sc-257143 | 500 mg | $324.00 | ||
Benzyl alcohol-α-13C-α,α-d2 is a unique solvent characterized by its isotopic labeling, which alters molecular dynamics and enhances specific reaction pathways. The presence of deuterium modifies hydrogen bonding interactions, leading to distinct kinetic isotope effects that can influence reaction rates and mechanisms. Its non-polar aromatic structure allows for effective solvation of organic compounds, while its ability to engage in hydrogen bonding can stabilize intermediates, promoting efficient chemical transformations. | ||||||
Formic acid-D2 | 920-42-3 | sc-263339 | 5 ml | $177.00 | ||
Formic acid-D2 serves as a distinctive solvent, notable for its isotopic substitution that influences molecular interactions and reaction kinetics. The incorporation of deuterium alters the vibrational frequencies of the acid, enhancing its reactivity in certain chemical environments. This modification can lead to unique solvation effects, facilitating the stabilization of transition states and intermediates. Its polar nature allows for effective solvation of both polar and non-polar solutes, making it versatile in various chemical processes. | ||||||
Sulfolane | 126-33-0 | sc-251090 sc-251090A | 5 g 100 g | $23.00 $21.00 | ||
Sulfolane is a highly polar aprotic solvent characterized by its ability to dissolve a wide range of organic and inorganic compounds. Its unique structure promotes strong dipole-dipole interactions, enhancing solvation dynamics. The solvent's high dielectric constant facilitates ion dissociation, making it effective in supporting ionic reactions. Additionally, sulfolane exhibits low volatility, which minimizes evaporation losses during reactions, ensuring consistent concentration and improved reaction kinetics. |