Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/4183
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dc.contributor.authorMadhusudhan, G-
dc.contributor.authorNaidu, K Chinnam-
dc.contributor.authorKumar, B Anand-
dc.contributor.authorSatyanarayana, R-
dc.contributor.authorBalraju, V-
dc.date.accessioned2009-05-13T07:29:13Z-
dc.date.available2009-05-13T07:29:13Z-
dc.date.issued2009-05-
dc.identifier.issn0376-4699-
dc.identifier.urihttp://hdl.handle.net/123456789/4183-
dc.description741-745en_US
dc.description.abstractCarvedilol is prepared by different synthetic approaches. Almost in all the approaches the major impurities that are known in the literature A, B, C, D and E are listed in European pharmacopoeia. The control of pharmaceutical impurities is currently a critical issue to the pharmaceutical industry. In this publication, a description of these impurities and their origins in Carvedilol process are presented along with the preparation of impurity A.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJC-B Vol.48B(05) [May 2009]en_US
dc.subjectCarvedilolen_US
dc.subjectimpuritiesen_US
dc.subjectβ-adrenergic receptoren_US
dc.titleSynthesis of impurity A in Carvedilol: a β-adrenergic receptoren_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.48B(05) [May 2009]

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