Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5770
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dc.contributor.authorMruthyunjayaswamy B.H.M
dc.contributor.authorPatil S.M.M
dc.contributor.authorRaju S.A.
dc.date.accessioned2020-06-12T15:08:46Z-
dc.date.available2020-06-12T15:08:46Z-
dc.date.issued2003
dc.identifier.citationJournal of the Indian Chemical Society , Vol. 80 , 9 , p. 863 - 865en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5770-
dc.description.abstractThree new, simple and sensitive spectrophotometric methods I, II and III have been developed for the quantitative estimation of satranidazole by first reducing it with zinc granules and hydrochloric acid in ethanol followed by its reaction in situ with p-methylbenzaldehyde (Method-I) and salicylaldehyde (Method-II) in ethanol to form yellow chromogens with ?max 390 and 425 nm, which obeyed Beer's law in the concentration range 20-100 and 10-50 ?g/ml, respectively. Method-III is based on the reaction of diazotization of the reduced satranidazole and its subsequent coupling with N-(1-naphthyl)ethylenediamine dihydrochloride at room temperature to form a pink coloured chromogen exhibiting ?max at 508 nm which obeyed Beer's law in the concentration range 10-50 ?g/ml. These methods have been found to be applicable for quantitative estimation of satranidazole in bulk drugs and dosage formulations.en_US
dc.titleSpectrophotometric methods for the determination of satranidazoleen_US
dc.typeArticle
Appears in Collections:1. Journal Articles

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