(S)-3-Chloropropane-1,2-diyl Ditetradecanoate

(S)-3-Chloropropane-1,2-diyl ditetradecanoate is a chiral diester compound synthesized from 3-chloropropane-1,2-diol and tetradecanoic acid (myristic acid). This molecule features a central chiral carbon, providing a useful framework for studying stereochemical effects in biochemical reactions and processes. The presence of long-chain fatty acid esters makes it an amphiphilic molecule, which can interact with both hydrophilic and hydrophobic environments. In research, (S)-3-Chloropropane-1,2-diyl ditetradecanoate is utilized to investigate the role of stereochemistry in lipid-protein interactions and membrane dynamics. Its structural properties allow it to be incorporated into model membrane systems, such as liposomes or lipid bilayers, where it can modulate membrane fluidity, permeability, and protein association. Moreover, (S)-3-Chloropropane-1,2-diyl ditetradecanoate serves as a probe in exploring lipid metabolism pathways. It is employed in enzymatic studies to understand the specificity and kinetics of lipases and esterases that process chiral lipid substrates. Overall, (S)-3-Chloropropane-1,2-diyl ditetradecanoate is a valuable tool in biochemical research, providing insights into the stereochemical aspects of lipid interactions and enzymatic processes.