Items 111 to 120 of 122 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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2,2,2-Trifluoroethanol-d3 | 77253-67-9 | sc-256258 | 1 g | $210.00 | ||
2,2,2-Trifluoroethanol-d3 is a deuterated solvent known for its unique hydrogen bonding capabilities and high polarity, which significantly enhances solvation for polar and ionic species. The presence of trifluoromethyl groups imparts distinct electronic effects, promoting specific molecular interactions that can stabilize transition states in reactions. Its isotopic labeling allows for advanced NMR studies, providing insights into reaction mechanisms and dynamics. This solvent's unique properties make it a valuable tool in various chemical investigations. | ||||||
4-tert-Butyl-o-xylene | 7397-06-0 | sc-232989 | 5 ml | $32.00 | ||
4-tert-Butyl-o-xylene is a versatile solvent characterized by its branched alkyl structure, which enhances its hydrophobic interactions and solvation properties for non-polar compounds. Its unique steric hindrance allows for selective solvation, influencing reaction kinetics and pathways. The solvent's ability to stabilize radical intermediates and facilitate specific molecular interactions makes it particularly useful in various chemical processes, providing insights into reaction dynamics and mechanisms. | ||||||
Ethyl acetate-d8 | 117121-81-0 | sc-223977 sc-223977A | 500 mg 1 g | $184.00 $321.00 | ||
Ethyl acetate-d8 is a deuterated solvent known for its unique isotopic labeling, which enhances NMR spectroscopy applications. Its polar aprotic nature allows for effective solvation of a wide range of organic compounds, promoting efficient reaction kinetics. The presence of deuterium alters hydrogen bonding dynamics, leading to distinct molecular interactions that can influence reaction pathways. This solvent's low viscosity and high volatility further contribute to its utility in various analytical and synthetic processes. | ||||||
Acrylonitrile | 107-13-1 | sc-257067 sc-257067A sc-257067B | 5 ml 100 ml 500 ml | $24.00 $28.00 $50.00 | ||
Acrylonitrile is a versatile solvent characterized by its strong dipole moment, which facilitates interactions with polar and nonpolar solutes alike. Its ability to engage in hydrogen bonding enhances solvation dynamics, promoting rapid reaction kinetics. The compound's unique structure allows for selective reactivity, making it an effective medium for polymerization and other chemical transformations. Additionally, its moderate viscosity aids in efficient mixing and heat transfer during reactions. | ||||||
Chlorobenzene | 108-90-7 | sc-239517 sc-239517A | 250 ml 1 L | $44.00 $156.00 | ||
Chlorobenzene is a nonpolar solvent known for its unique aromatic structure, which allows for π-π stacking interactions with other aromatic compounds. This property enhances solubility for a range of organic materials, facilitating efficient extraction and purification processes. Its relatively low viscosity contributes to improved mass transfer rates, while its stability under various conditions makes it suitable for diverse chemical reactions, including nucleophilic substitutions. | ||||||
2-(Methylamino)ethanol | 109-83-1 | sc-237872 sc-237872A | 25 ml 250 ml | $20.00 $36.00 | ||
2-(Methylamino)ethanol is a polar solvent characterized by its ability to engage in hydrogen bonding due to the presence of both amino and hydroxyl groups. This dual functionality enhances its solvation capabilities, particularly for ionic and polar solutes. Its moderate viscosity allows for effective diffusion in reaction mixtures, promoting faster reaction kinetics. Additionally, its unique structure enables it to stabilize transition states, making it a versatile medium for various chemical transformations. | ||||||
Heptane | 142-82-5 | sc-250090 sc-250090A | 1 L 2 L | $122.00 $158.00 | ||
Heptane is a non-polar solvent known for its hydrophobic nature, which allows it to effectively dissolve non-polar compounds. Its linear structure facilitates efficient packing in liquid form, leading to low viscosity and high fluidity. This property enhances mass transfer rates in reactions. Heptane's weak van der Waals interactions contribute to its ability to minimize solvation effects, making it ideal for extracting and purifying organic compounds without interfering with their reactivity. | ||||||
3-Methoxy-3-methyl-1-butanol | 56539-66-3 | sc-238576 | 250 ml | $54.00 | ||
3-Methoxy-3-methyl-1-butanol is a versatile solvent characterized by its unique ability to engage in hydrogen bonding due to the presence of a methoxy group. This feature enhances its solvation capabilities, particularly for polar and semi-polar compounds. Its branched structure contributes to lower viscosity, promoting efficient mixing and mass transfer. Additionally, the solvent exhibits moderate polarity, allowing it to stabilize reactive intermediates in various chemical processes, thus influencing reaction kinetics favorably. | ||||||
Dipropylene Glycol Dimethyl Ether (mixture of isomers) | 111109-77-4 | sc-485865 | 25 ml | $29.00 | ||
Dipropylene Glycol Dimethyl Ether is a highly effective solvent known for its excellent solvating power across a range of polar and non-polar substances. Its unique isomeric structure facilitates strong dipole-dipole interactions, enhancing solubility and promoting rapid diffusion. The compound's low surface tension and high flash point contribute to its safety in various applications, while its ability to form stable emulsions makes it ideal for complex formulations. | ||||||
Perfluorokerosene, low boiling | sc-358500 | 10 g | $240.00 | |||
Perfluorokerosene is a unique solvent characterized by its exceptional chemical stability and low reactivity, attributed to the strong carbon-fluorine bonds. This compound exhibits remarkable hydrophobic properties, allowing it to effectively solvate non-polar substances while resisting moisture absorption. Its high density and low viscosity facilitate efficient mass transfer, making it suitable for applications requiring rapid phase separation. Additionally, its inert nature minimizes interference in sensitive reactions. |