Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/46874
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dc.contributor.authorGoyal, R N-
dc.contributor.authorKumar, Anoop-
dc.date.accessioned2019-03-28T05:07:14Z-
dc.date.available2019-03-28T05:07:14Z-
dc.date.issued1989-11-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/46874-
dc.description949-952en_US
dc.description.abstractElectrochemical oxidation of 8-methylxanthine has been investigated in phosphate buffers of pH range (1.35-10.71) using various techniques such as linear and cyclic sweep voltammetry, coulometry, controlled potential electrolysis and spectral studies. Linear and cyclic sweep voltammetry of 8-methylxanthine exhibit one well-defined 2e, 2H+ oxidation peak (Ia). The first order rate constant for the disappearance of UV absorbing intermediate has been calculated. The products of controlled potential electrolysis have been separated in the pH range (1.35-4.57) and identified as alloxan and acetamidine. A tentative mechanism has been proposed to account for the observed experimental results.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.28A(11) [November 1989]en_US
dc.titleElectrochemical oxidation of 8-methylxanthine at stationary pyrolytic graphite electrodeen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.28A(11) [November 1989]

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