Fatty Acids
Items 61 to 70 of 98 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
4,5-dehydro Docosahexaenoic Acid | 660429-97-0 | sc-220993 | 25 µg | $142.00 | ||
4,5-dehydro Docosahexaenoic Acid is a unique fatty acid characterized by its distinct unsaturation, which enhances its fluidity and membrane incorporation. This structural feature allows it to engage in specific molecular interactions with lipid bilayers, influencing membrane dynamics and protein function. Its reactivity can lead to the formation of specialized lipid mediators, playing a crucial role in cellular communication and metabolic regulation. The compound's behavior as a fatty acid highlights its importance in cellular architecture and signaling pathways. | ||||||
trans-11-Eicosenoic acid | 62322-84-3 | sc-213082 sc-213082A sc-213082B sc-213082C | 50 mg 100 mg 500 mg 1 g | $60.00 $90.00 $200.00 $300.00 | ||
Trans-11-Eicosenoic acid is a monounsaturated fatty acid notable for its unique cis-configuration, which contributes to its distinct physical properties and reactivity. This structural arrangement facilitates specific interactions with proteins and enzymes, influencing lipid metabolism and energy storage pathways. Its presence in various biological membranes can modulate fluidity and permeability, impacting cellular signaling and the function of membrane-bound receptors. The compound's behavior as a fatty acid underscores its role in maintaining cellular integrity and function. | ||||||
Linoleic Acid | 60-33-3 | sc-200788 sc-200788A sc-200788B sc-200788C | 100 mg 1 g 5 g 25 g | $33.00 $63.00 $163.00 $275.00 | 4 | |
Linoleic acid is a polyunsaturated fatty acid characterized by its two double bonds, which introduce kinks in its hydrocarbon chain, enhancing fluidity in lipid bilayers. This structural feature allows for unique interactions with membrane proteins, influencing their conformation and activity. Additionally, linoleic acid serves as a precursor for bioactive lipids, participating in signaling pathways that regulate inflammation and cellular responses. Its reactivity in oxidative processes further underscores its role in cellular dynamics. | ||||||
Iodoacetic acid | 64-69-7 | sc-215183 sc-215183A | 10 g 25 g | $56.00 $97.00 | ||
Iodoacetic acid is a halogenated fatty acid that exhibits unique reactivity due to the presence of the iodine atom, which enhances its electrophilic character. This property facilitates nucleophilic attack by thiols and amines, leading to the formation of stable adducts. Its ability to disrupt hydrogen bonding in lipid environments can alter membrane integrity and fluidity. Additionally, iodoacetic acid participates in various biochemical pathways, influencing metabolic processes through its interactions with key enzymes. | ||||||
C16 Dihydroceramide | 5966-29-0 | sc-210985 | 5 mg | $320.00 | 1 | |
C16 Dihydroceramide is a distinctive fatty acid known for its role in cellular signaling and membrane dynamics. Its long hydrocarbon chain contributes to its hydrophobic characteristics, enabling it to integrate into lipid bilayers and influence membrane fluidity. This compound participates in unique metabolic pathways, acting as a precursor in sphingolipid biosynthesis. Its interactions with proteins can modulate cellular responses, highlighting its importance in lipid-mediated signaling processes. | ||||||
Butyric acid | 107-92-6 | sc-214640 sc-214640A | 1 kg 10 kg | $63.00 $174.00 | ||
Butyric acid is a short-chain fatty acid characterized by its distinctive hydrophobic and hydrophilic regions, allowing it to engage in unique molecular interactions. It plays a significant role in cellular signaling and energy metabolism, influencing gene expression and cellular differentiation. Its ability to form hydrogen bonds enhances its solubility in polar solvents, while its hydrophobic tail facilitates interactions with lipid membranes, impacting membrane fluidity and permeability. | ||||||
3,7,11,15-Tetramethylhexadeca-2,6,10,14-tetraenoic Acid Ethyl Ester (Mixture of Isomers) | 60437-17-4 | sc-470665 | 250 mg | $360.00 | ||
3,7,11,15-Tetramethylhexadeca-2,6,10,14-tetraenoic Acid Ethyl Ester is a complex fatty acid ester known for its unique isomeric forms, which can influence its reactivity and interaction with biological membranes. The presence of multiple double bonds contributes to its fluidity and stability, allowing for diverse conformations. This compound can participate in various lipid metabolic pathways, affecting membrane dynamics and cellular signaling through its interactions with lipid bilayers. | ||||||
Stearoyl Ethanolamide | 111-57-9 | sc-205515 sc-205515A | 5 mg 10 mg | $85.00 $153.00 | ||
Stearoyl Ethanolamide is a fatty acid derivative characterized by its unique amide bond, which enhances its solubility and interaction with lipid environments. This compound exhibits distinct molecular interactions, promoting hydrogen bonding and van der Waals forces that influence membrane fluidity. Its structural properties allow it to modulate lipid metabolism and cellular signaling pathways, impacting the dynamics of membrane-associated processes and cellular responses. | ||||||
10-Undecenoic acid | 112-38-9 | sc-213573 sc-213573A | 100 ml 500 ml | $33.00 $173.00 | ||
10-Undecenoic acid is a fatty acid notable for its unsaturated carbon chain, which introduces unique reactivity and molecular flexibility. This compound can participate in various addition reactions due to its double bond, facilitating interactions with other lipids and biomolecules. Its hydrophobic nature influences micelle formation and lipid bilayer stability, while its distinct chain length contributes to specific phase behavior in lipid mixtures, affecting overall membrane characteristics. | ||||||
Elaidic Acid | 112-79-8 | sc-205309 sc-205309A | 50 mg 100 mg | $20.00 $39.00 | 1 | |
Elaidic acid is a trans fatty acid characterized by its unique geometric configuration, which influences its interactions with biological membranes. The trans double bond alters the packing efficiency of lipid bilayers, leading to increased rigidity compared to cis fatty acids. This structural distinction affects membrane fluidity and permeability, impacting cellular processes. Additionally, elaidic acid can undergo oxidation reactions, generating reactive intermediates that may influence lipid metabolism and signaling pathways. | ||||||