1976
DOI: 10.5650/jos1956.25.764
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Evaluation of Heat Treated Frying Oils. I.

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1976
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“…Further discussions on these compounds as well as the cyclohexenyl compound (footnote g) will be given in a paper to be reported later. Peak 18 (F3) was a large peak and appered to be a mixture of those designated in the table and the following two types of compounds, which have also been isolated by Artman and Smith 3' A cyclohexyl compound having C3-ester and C9:1-hydrocarbon side chains with M=294 (2% intensity in the mass pattern obtained in the present study) and mje 279 (1) and 253 (1) indicating M-15 and M-31, respectively; and an 1,4-epoxy compound having C,H13 and C$ester side chains with M=310 (1), which has been shown to elute at a temperature close to that of the former compound'". Epoxy and hydroxylated compounds could be more readily detected than the conjugated systems by the present method of fractionation.…”
Section: Ir Nmr and Glc Of Pfa Fractionsupporting
confidence: 68%
“…Further discussions on these compounds as well as the cyclohexenyl compound (footnote g) will be given in a paper to be reported later. Peak 18 (F3) was a large peak and appered to be a mixture of those designated in the table and the following two types of compounds, which have also been isolated by Artman and Smith 3' A cyclohexyl compound having C3-ester and C9:1-hydrocarbon side chains with M=294 (2% intensity in the mass pattern obtained in the present study) and mje 279 (1) and 253 (1) indicating M-15 and M-31, respectively; and an 1,4-epoxy compound having C,H13 and C$ester side chains with M=310 (1), which has been shown to elute at a temperature close to that of the former compound'". Epoxy and hydroxylated compounds could be more readily detected than the conjugated systems by the present method of fractionation.…”
Section: Ir Nmr and Glc Of Pfa Fractionsupporting
confidence: 68%