Items 41 to 50 of 401 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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(+)-α-Tocopherol | 59-02-9 | sc-214454 sc-214454A sc-214454B | 10 g 25 g 100 g | $42.00 $61.00 $138.00 | ||
(+)-α-Tocopherol, a naturally occurring form of vitamin E, is a lipid characterized by its potent antioxidant properties. It integrates into cellular membranes, where it interacts with lipid bilayers, enhancing membrane fluidity and stability. This compound effectively scavenges free radicals, preventing oxidative damage to lipids. Its unique hydrophobic tail allows for deep insertion into membranes, influencing lipid peroxidation pathways and promoting cellular health through its protective mechanisms. | ||||||
Deoxycholic acid | 83-44-3 | sc-214865 sc-214865A sc-214865B | 5 g 25 g 1 kg | $36.00 $66.00 $923.00 | 4 | |
Deoxycholic acid is a bile acid that plays a crucial role in lipid metabolism and digestion. Its amphipathic nature allows it to interact with both hydrophilic and hydrophobic environments, promoting the emulsification of dietary fats. This compound can form micelles, enhancing the solubility of lipids in aqueous solutions. Furthermore, its ability to modulate membrane fluidity and permeability is significant in cellular processes, influencing lipid raft formation and protein interactions. | ||||||
Cholesteryl acetate | 604-35-3 | sc-214693 sc-214693A | 25 g 100 g | $112.00 $311.00 | ||
Cholesteryl acetate is a lipid that plays a crucial role in membrane dynamics and cellular signaling. Its esterified structure enhances hydrophobic interactions, allowing it to integrate seamlessly into lipid bilayers. This compound influences membrane fluidity and permeability, facilitating the transport of other lipids and proteins. Additionally, cholesteryl acetate can participate in lipid metabolism pathways, acting as a precursor in the synthesis of complex lipids, thereby impacting cellular function and homeostasis. | ||||||
Palmityl acetate | 629-70-9 | sc-215669 | 1 g | $60.00 | ||
Palmityl acetate is a lipid characterized by its long-chain fatty acid structure, which contributes to its unique hydrophobic properties. This compound exhibits strong van der Waals interactions, promoting stability within lipid membranes. Its presence can modulate membrane characteristics, influencing the behavior of surrounding molecules. Furthermore, palmityl acetate can participate in various metabolic pathways, serving as a substrate for enzymatic reactions that generate energy-rich compounds, thereby affecting cellular metabolism. | ||||||
Methyl melissate | 629-83-4 | sc-328872 sc-328872A | 100 mg 1 g | $209.00 $1142.00 | ||
Methyl melissate is a lipid distinguished by its ester functional group, which enhances its solubility in organic solvents. This compound exhibits unique hydrophobic interactions that facilitate the formation of micelles and lipid bilayers, crucial for cellular structure. Its reactivity as an acid halide allows for acylation reactions, influencing lipid metabolism and the synthesis of complex lipids. Additionally, methyl melissate can impact membrane fluidity, affecting protein dynamics and cellular signaling pathways. | ||||||
trans-Vaccenic acid | 693-72-1 | sc-216002 sc-216002A | 100 mg 1 g | $148.00 $633.00 | ||
Trans-vaccenic acid is a monounsaturated fatty acid characterized by its unique cis double bond configuration, which influences its fluidity and packing in lipid membranes. This structural feature enhances its role in modulating membrane properties, affecting permeability and protein interactions. As a precursor in the biosynthesis of longer-chain fatty acids, it participates in metabolic pathways that regulate energy storage and utilization. Its distinct hydrophobic nature also contributes to the formation of lipid rafts, impacting cellular signaling. | ||||||
Cholesta-3,5-diene | 747-90-0 | sc-211079 sc-211079A | 25 mg 100 mg | $173.00 $520.00 | ||
Cholesta-3,5-diene is a sterol derivative notable for its unique double bond configuration, which influences its interactions within lipid bilayers. This compound exhibits distinct hydrophobic characteristics that enhance membrane fluidity and stability. Its presence can alter lipid packing and affect the dynamics of membrane proteins, potentially influencing cellular signaling pathways. Additionally, it plays a role in the biosynthesis of cholesterol and other sterols, impacting lipid metabolism. | ||||||
Cholesteryl Linolenate | 2545-22-4 | sc-294020 | 100 mg | $70.00 | ||
Cholesteryl Linolenate is a lipid characterized by its long-chain fatty acid structure, which contributes to its unique amphiphilic properties. This compound can integrate into lipid membranes, affecting their fluidity and permeability. Its unsaturated fatty acid component introduces kinks in the hydrocarbon chains, promoting a more dynamic membrane environment. Furthermore, it participates in lipid metabolism pathways, influencing the synthesis and degradation of other lipids, thereby impacting cellular energy balance. | ||||||
Monoelaidin | 2716-53-2 | sc-295493 | 1 g | $167.00 | ||
Monoelaidin is a lipid that exhibits unique structural properties due to its monounsaturated fatty acid composition. This configuration allows for enhanced molecular packing, influencing the formation of lipid bilayers and micelles. Its hydrophobic tail interacts favorably with other lipids, promoting stability in membrane structures. Additionally, Monoelaidin can engage in specific intermolecular interactions, such as hydrogen bonding, which can modulate the physical characteristics of lipid aggregates and affect their behavior in various biochemical environments. | ||||||
Epoxidized soya bean oil | 8013-07-8 | sc-211421 sc-211421A | 500 mg 2.5 g | $71.00 $184.00 | ||
Epoxidized soybean oil is a modified lipid characterized by its epoxide groups, which introduce unique reactivity and enhance its compatibility with various substrates. The presence of these groups facilitates cross-linking reactions, leading to improved mechanical properties and thermal stability. Its polar nature allows for specific interactions with other polar molecules, influencing solubility and dispersion in formulations. This lipid's ability to form stable emulsions and its resistance to oxidative degradation further contribute to its distinctive behavior in diverse applications. |