Please use this identifier to cite or link to this item: http://dspace.unimap.edu.my:80/xmlui/handle/123456789/7187
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dc.contributor.authorWaldron, Keith William-
dc.contributor.authorParr, Adrian J.-
dc.contributor.authorNg, Annie-
dc.contributor.authorRalph, John-
dc.date.accessioned2009-11-05T04:00:48Z-
dc.date.available2009-11-05T04:00:48Z-
dc.date.issued1996-
dc.identifier.citationPhytochemical Analysis, vol.7, 1996, pages 305-312.en_US
dc.identifier.issn0958-0344-
dc.identifier.urihttp://dspace.unimap.edu.my/123456789/7187-
dc.description.abstractAn optimized high performance liquid chromatography (HPLC) procedure has been developed for the analysis and quantification of all of the known ferulic acid dehydrodimers, and the principle phenolic aldehydes and acids, found in the cell walls of higher plants. The HPLC system uses an ODS2 reverse phase column (5 μm particle size) eluted with a methanol, acetonitrile and water gradient with detection at 280 nm. In addition to providing baseline resolution of most components, the method employs a spectrometric detector which enables the precise identification of eluted components through the analysis of their spectral properties. Analysis of the cell wall phenolics of wheat straw stem (Triticum vulgare) was carried out using this method which is highly versatile and, for certain components, more sensitive than the current gas chromatography-mass spectrometry methodology.en_US
dc.language.isoenen_US
dc.publisherJohn Wiley & Sons, Ltd.en_US
dc.subjectHigh performance liquid chromatographyen_US
dc.subjectDiod array detectionen_US
dc.subjectCell wallsen_US
dc.subjectPhenolicsen_US
dc.subjectDehydrodimersen_US
dc.subjectFerulic aciden_US
dc.subjectPlant cell wallsen_US
dc.subjectBiophysicsen_US
dc.titleCell wall esterified phenolic dimers: Identification and quantification by reverse phase high performance liquid chromatography and diode array detectionen_US
dc.typeArticleen_US
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