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Determination of 3-chloro-N-chloro-N-(3,4-dimethyl-5-isoxazolyl)-4-amine-1,2-naphthoquinone in presence of its degradation products using second derivative spectrophotometry

✍ Scribed by Viviana G. Dabbene; Margarita C. Briñón; M.M. de Bertorello


Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
618 KB
Volume
318
Category
Article
ISSN
0003-2670

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✦ Synopsis


A rapid, selective and accurate method for stability determination of 3-chloro-N-chloro-N-(3,4-dimethyl-5-isoxazolyl)-4-amine-1,2-naphthoquinone (lb) in the presence of its degradation products by using second derivative UV spectrophotometry was developed. The validity of this method was proved using synthetic mixtures of the intact drug with its decomposition products and by statistical analysis of the calibration data. Lack of interference between the signals was observed in an interaction study. The synthesis of lb and its degradation product 3-chloro-2-hydroxy-N-(3,4-dimethyl-Sisoxazolyl)-1,4-naphthoquinon-4-imine (2b) are also described.


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✍ Viviana G. Dabbene; Margarita C. Briñón; María M. De Bertorello 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 458 KB

The degradation kinetics of a new potential tripanocidal and anti bacterial agent, 3-bromo-2-hydroxy-K(3,4-dimethyl-5-isoxazolyl)-l,4naphthoquinon-4-imine (2), in 95% ethanol, was investigated between 35 and 50 "C under room-light and light-protected conditions. The decomposition product was isolate