2005
DOI: 10.1007/s10809-005-0155-1
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Retention Indices As the Best Reproducible Chromatographic Parameters for the Characterization of Phenolic Compounds in Reversed-Phase High-Performance Liquid Chromatography

Abstract: A comparison of various methods for presenting the retention parameters of analyzed compounds in reversed-phase HPLC under the conditions of stepwise gradient elution demonstrated that retention indices (RIs) based on a standard scale of n -alkyl phenyl ketones exhibited the best reproducibility. However, a new procedure for calculating extrapolated RI values under these conditions should be developed for determining the RIs of the most hydrophilic compounds, which are eluted from a column before a reference c… Show more

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Cited by 12 publications
(3 citation statements)
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“…•OH radical attack on phenol leads to the formation of several intermediates such as hydroquinone (HQ), catechol (CC), pyrogallol (PG), hydroxyhydroquinone (HHQ), resorcinol (RC), muconic acid (MU), p-benzoquinone (p-BQ), o-benzoquinone (o-BQ), and hydroxybenzoquinone (HBQ) [43,[66][67][68][69].…”
Section: Photocatalytic Degradation Of Phenolmentioning
confidence: 99%
“…•OH radical attack on phenol leads to the formation of several intermediates such as hydroquinone (HQ), catechol (CC), pyrogallol (PG), hydroxyhydroquinone (HHQ), resorcinol (RC), muconic acid (MU), p-benzoquinone (p-BQ), o-benzoquinone (o-BQ), and hydroxybenzoquinone (HBQ) [43,[66][67][68][69].…”
Section: Photocatalytic Degradation Of Phenolmentioning
confidence: 99%
“…It was interesting to compare the quantitative and qualitative composition of the phenolic fraction of the extracts and their antioxidant activity. Natural phenolic compounds (aromatic and polyaromatic compounds containing a phenolic hydroxyl [11]) were identified using a previously compiled database [12]. The database contained spectral and chromatographic properties for 74 phenolic compounds including aromatic alcohols, aldehydes, acids, methoxy-and acylated derivatives, flavanoids and their glycosides, coumarins, and furocoumarins.…”
Section: Resultsmentioning
confidence: 99%
“…There are several intermediates of degraded phenol that have toxicity in the environment reported in the existing literature [44]. In particular, the addition of hydroxyl radical resulted in hydroxy benzenes, and these intermediate species can further oxidize and lead to the highly substituted intermediates and the acidic intermediates after the cleavage of the ring [45][46][47]. The HPLC results provide a broader picture regarding the intermediates that formed under our experimental conditions, and it was further validated by the APCI-MS studies explained in the subsequent section.…”
Section: Hplc Analysismentioning
confidence: 99%