Vitamin E Oxidation with Alkaline Ferricyanide
W. A. Skinner 1 and
P. Alaupovic 2
1 Department of Pharmaceutical Chemistry, Stanford Research Institute, Menlo Park, California
2 Cardiovascular Section, Oklahoma Medical Research Institute, and Department of Biochemistry, University of Oklahoma School of Medicine, Oklahoma City
Oxidation of dl-
-tocopherol or its model, 6-hydroxy-2,2,5,7,8-pentamethylchroman, with alkaline ferricyanide yields a variety of products. In addition to the known dimeric keto ether, two new products, compound A, a trimer, and compound B, an isomer of compound A, were ioslated. Ultraviolet and infrared absorption spectra and paper chromatography indicate that compound A might be identical with liver metabolite "O" which results from the addition of
-tocopherol to the diet.