S-(3)-Hydroxymyristic Acid, Methyl Ester (CAS 76835-67-1)

S-(3)-Hydroxymyristic Acid, Methyl Ester, with the CAS number 76835-67-1, is a chiral molecule characterized by the presence of a hydroxyl group on the third carbon of a myristic acid chain, which has been esterified with methanol. This molecular structure imparts specific physical and chemical properties due to its chirality, represented by the S-configuration. This ester′s structure is pivotal for researchers studying lipid biochemistry and the synthesis of complex lipid molecules, particularly in understanding the stereochemical effects in biochemical reactions and processes. In research, this compound has been employed to investigate the role of hydroxylated fatty acids in various non-medical systems, such as in industrial applications where the understanding of lipid interactions at surfaces and interfaces is crucial. The ester group enhances the molecule′s solubility in organic solvents, facilitating its use in experiments involving chromatography and spectroscopy to analyze lipid behavior and interactions. Furthermore, S-(3)-Hydroxymyristic Acid, Methyl Ester serves as a model compound in the study of the enzymatic processes that modify fatty acids, helping to explain the mechanisms by which specific enzymes recognize and act upon chiral molecules, thereby influencing the synthesis and breakdown of complex lipid structures in varied applications. This research contributes significantly to the broader field of organic chemistry, where the synthesis of stereochemically precise molecules can lead to the development of better materials and catalysts.