1962
DOI: 10.1093/jaoac/45.1.92
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Characterization of Tocopherols in Vegetable Oils by Infrared Spectrophotometry

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1972
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“…For this reason, the molecular ions are shifted by a mass number of 6 between -tocopherol and -tocotrienol derivatives and similar changes occur in the subsequent compounds. No difference was observed between the positional isomers by mass spectrometry; however, the ß and isomers may be distinguished by their infrared spectra, since they have characteristic absorptions between 7.5 and 9.8 µ (Morris and Haenni, 1962). /3-Tocopherol has singlets at 8.1 and 8.65 µ, with shoulders at 8.47 and 8.55 µ and also doublets at 9.2 and 9.4 µ, whereas -tocopherol has two doublets at 8.05 and 8.25 µ, and 9.07 µ and 9.25 µ.…”
Section: Discussionmentioning
confidence: 98%
“…For this reason, the molecular ions are shifted by a mass number of 6 between -tocopherol and -tocotrienol derivatives and similar changes occur in the subsequent compounds. No difference was observed between the positional isomers by mass spectrometry; however, the ß and isomers may be distinguished by their infrared spectra, since they have characteristic absorptions between 7.5 and 9.8 µ (Morris and Haenni, 1962). /3-Tocopherol has singlets at 8.1 and 8.65 µ, with shoulders at 8.47 and 8.55 µ and also doublets at 9.2 and 9.4 µ, whereas -tocopherol has two doublets at 8.05 and 8.25 µ, and 9.07 µ and 9.25 µ.…”
Section: Discussionmentioning
confidence: 98%