1976
DOI: 10.1016/s0021-9673(00)82297-9
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Gas chromatographic separation and analysis of trimethylsilyl derivatives of some naturally occurring non-volatile phenolic compounds and related substances

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Cited by 57 publications
(13 citation statements)
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“…The phenolic acids remaining were then converted to trimethylsilyl derivatives and analyzed on a 200 cm by 2 mm i.d. glass column filled with 3 % OV-25 coated on a 60-80 mesh Chromosorb W support installed in a Varian 3700 gas chromatograph fitted with a flame ionization detector (Vande Casteele et al 1976). The column was temperature programmed from 100 to 260 "C at 6 C" min-l with an initial hold of 5 min.…”
Section: Methodsmentioning
confidence: 99%
“…The phenolic acids remaining were then converted to trimethylsilyl derivatives and analyzed on a 200 cm by 2 mm i.d. glass column filled with 3 % OV-25 coated on a 60-80 mesh Chromosorb W support installed in a Varian 3700 gas chromatograph fitted with a flame ionization detector (Vande Casteele et al 1976). The column was temperature programmed from 100 to 260 "C at 6 C" min-l with an initial hold of 5 min.…”
Section: Methodsmentioning
confidence: 99%
“…In all cases, the final temperature was kept for 10 min. All the samples analyzed were derivatized with BSTFA prior to injection (adapted from Casteele et al, 1976;Popova et al, 2005). The compounds were characterized by mass spectral interpretation and automatic comparison with a spectra library, and, if available, reference compounds were co-chromatographed in order to confirm the retention times.…”
Section: Hrgc-ms Analysismentioning
confidence: 99%
“…Phenolic acids were separated and determined by a gas chromatograph equipped with FID according to the method of Casteele (5).…”
Section: Phenolic Compound Determination and Gas Chromatographic Sepamentioning
confidence: 99%