Abstract
Triglycerides, together with nine synthetic phenolic antioxidants most commonly used to prevent oxidation of edible oils and fats, as well as the natural antioxidants tocopherols andα-tocopherol acetate, were separated by high performance liquid chromatography by means of a reversed phase C18-column and gradient elution with water/acetonitrile/methanol/isopropanol. Besides dilution of the oil with isopropanol/hexane, no further example preparation was required. UV detection was applied. The synthetic antioxidants propyldodecylgallate, octyldodecylgallate, dodecylgallate, 3-tert-butyl-4-hydroxyanisol,tert-butylhydroquinone, 3,5-di-terf-butyl-4-hydroxytoluene, 2,6-di-tert-butyl-4-hydroxymethyl-phenol, 2,4,5-trihydroxybutyrophenone and nordihydro-quaiaretic acid, as well asα- andδ-tocopherol andα-tocopherol acetate were base-line separated;β- andγ-tocopherol, however, eluted together. The triglycerides, detected at λ = 215 nm, were separated according to then-partition number. The absorption at λ = 215 nm revealed saturated and unsaturated triglycerides. The absorption at λ = 280 nm indicated triglycerides with conjugated unsaturation, relating information about refining and heat treatment of the oil. Oxidized unsaturated triglycerides showed absorption at γ = 230 nm. Triglycerides of ricinoleic acid, a hydroxymonoun-saturated acid, gave identical UV spectra. The simultaneous detection of antioxidants and triglycerides may be used to study inhibition effects by antioxidants in oils.
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Andrikopoulos, N.K., Brueschweiler, H., Felber, H. et al. HPLC analysis of phenolic antioxidants, tocopherols and triglycerides. J Am Oil Chem Soc 68, 359–364 (1991). https://doi.org/10.1007/BF02663750
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DOI: https://doi.org/10.1007/BF02663750