A novel 1H NMR spectroscopic method for determination of glycidyl fatty acid esters coexisting with acylglycerols

A new approach for determination of glycidyl fatty acid esters (GDEs) based on 1 H nuclear magnetic resonance ( 1 H NMR) spectroscopy was developed. The 1 H NMR spectra of the GDE standards were prepared and characterized. The quantification formula was then deduced from the characteristic signals of two epoxy methylene (CH 2 ) protons at chemical shifts 2.56 and 2.76 ppm. Tests on repeatability, reproducibility, and recovery were conducted and proved the reliability of the quantification method. This method was extended to GDEs mixed with oil matrices composed of different acylglycerols (GREs). The weighted average factor f w is introduced to calculate the fatty acid composition based on the stoichiometric proportion of the lipid component and its esterification degree. With the fatty acid composition determined, the molar percentage obtained from 1 H NMR can be converted to the weight percentage. This method is an analytical model for the determination of GDEs, with advantages such as easy operation and high accuracy. Practical applications: Heat treatment of edible oils in the refinery process can generate GDEs, a group of contaminants having potential risks to liberate a carcinogenic compound called glycidol during digestion of oil in the human body. It has become an important issue for the oil industry to develop an effective method for the determination of GDEs. The proposed 1 H NMR spectroscopic method is able to characterize and quantify GDEs in an accurate, rapid, and noninvasive way. With these advantages, the analytical results also provide quantitative criteria for subsequent concentration and mitigation of GDEs in refined edible oils. A novel 1 H NMR spectroscopic method was developed to determine glycidyl fatty acid esters (GDEs), a processing contaminant in refined edible oil.