
Fatty Acids
Fatty acids are carboxylic acids with long hydrocarbon chains, which can be either saturated or unsaturated. They are essential components of lipids, serving as key building blocks for complex lipids, energy sources, and signaling molecules. Fatty acids are involved in various biological processes, including metabolism, cell membrane structure, and inflammation. At CymitQuimica, we offer a diverse range of high-quality fatty acids to support your research in lipid biochemistry, nutrition, and related fields.
Subcategories of "Fatty Acids"
Products of "Fatty Acids"
Sort by
rac 1,2-Bis-palmitoyl-3-chloropropanediol-D5
CAS:Controlled ProductApplications rac 1,2-Bis-palmitoyl-3-chloropropanediol-D5 was useful for establishing an analytical method for quantifying free and ester bound 2-, 3-MCPD, and esterified glycidol in fishery products. References Karl, H., et al.: Eur. J. Lipid Sci. Technol., 118, 406 (2016)Formula:C352H5H62ClO4Color and Shape:White To Light YellowMolecular weight:592.39rac-1-Linoleoyl-2-stearoyl-3-chloropropanediol-d5
CAS:Controlled ProductApplications Labelled lipids. New lipids in food protein hydrolyzates.Formula:C39H66D5ClO4Color and Shape:NeatMolecular weight:644.46Heptanoic Acid
CAS:Formula:C7H14O2Purity:>98.0%(T)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:130.19Palmitoyl Chloride
CAS:Controlled ProductStability Moisture Sensitive Applications Palmitoyl Chloride was used as a polymeric carriers for plasmid DNA (pDNA) delivery to 293T cells. References Remant, B.K.C., et al.: J. Biomaterials. Sci. Poly. Ed., 22, 873 (2011); Allard, E., et al.: Int. J. Pharma., 379, 217 (2009);Formula:C16H31ClOColor and Shape:Light YellowMolecular weight:274.879(Z),11(Z)-Octadecadienoic acid
CAS:Formula:C18H32O2Purity:>98%Color and Shape:SolidMolecular weight:280.45Propargyl chloride
CAS:Propargyl chloride is a chemical that is used as an inhibitor in organic synthesis. It can be used to synthesize compounds with reactive groups such as alkenes, ketones, and amines. Propargyl chloride reacts with the hydroxyl group of an alcohol to form a propargyl alcohol. The reaction mechanism involves intramolecular hydrogen bonding between the hydroxyl group of the propargyl chloride and the carbon atom adjacent to it. Kinetic energy is required for this reaction to occur. The product of this reaction can then react with other molecules in order to form new compounds. Propargyl chloride has been shown to have therapeutic effects on chronic coughs due its ability to reduce the amount of kinetic energy needed for respiratory tract cells, which may have reduced coughing frequency. END>>Formula:C3H3ClPurity:Min. 95%Color and Shape:Colorless Yellow Clear LiquidMolecular weight:74.51 g/molthreo-9,10-Dihydroxyhexadecanoic acid
CAS:Formula:C16H32O4Purity:>98%Color and Shape:In solution, EthanolMolecular weight:288.4213(S)-Hydroxy-6(Z),9(Z),11(E)-octadecatrienoic acid
CAS:Formula:C18H30O3Purity:>98%Color and Shape:LiquidMolecular weight:294.43Vinyl Laurate (stabilized with MEHQ)
CAS:Formula:C14H26O2Purity:>99.0%(GC)Color and Shape:Colorless to Light yellow clear liquidMolecular weight:226.36Cholesterol Propionate
CAS:Formula:C30H50O2Purity:>95.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:442.731-Cyclopropyl-6,7-difluoro-1,4-dihydro-8-hydroxy-4-oxo-3-quinolinecarboxylic Acid Ethyl Ester
CAS:Controlled ProductApplications 1-Cyclopropyl-6,7-difluoro-1,4-dihydro-8-hydroxy-4-oxo-3-quinolinecarboxylic Acid Ethyl Ester is used in the synthesis of antibacterials. References Phillips, O. et al.: Exp. Opin. Ther. Pat., 19, 529 (2009);Formula:C15H13F2NO4Color and Shape:NeatMolecular weight:309.265(5Z,8Z,11Z,14Z)-Methyl icosa-5,8,11,14-tetraenoate
CAS:Formula:C21H34O2Purity:90%Color and Shape:LiquidMolecular weight:318.4935Clindamycin palmitate hydrochloride
CAS:Clindamycin palmitate hydrochloride is an antimicrobial agent that has been used to treat infectious diseases, such as streptococcal pharyngitis. It binds to the 50S ribosomal subunit through a covalent linkage with the amino acid palmitate. The structural analysis of this drug has shown that it is a prodrug form of clindamycin, which is activated by hydrolysis in vivo. Clindamycin palmitate hydrochloride has been shown to be effective against Streptococcus pyogenes, and its efficacy may be due to the high affinity of clindamycin for binding to streptococci.Formula:C34H64Cl2N2O6SPurity:Min. 95%Molecular weight:698.38621Ref: 3D-FC148929
Discontinued product