邻苯二酚紫和铈离子分光光度法测定盐酸氯丙噻烯

B. Starczewska, J. Karpińska
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引用次数: 5

摘要

建立了两种测定盐酸氯原噻烯含量的方法。其中一种是利用氯代噻吩叔胺基氮原子的负电荷与有机化合物形成离子缔合配合物。所形成的络合物不溶于水,但溶于有机溶剂。该性质为建立一种新的提取-分光光度法测定氯原噻烯的方法奠定了基础。第二种方法是用Ce(IV)离子氧化氯原噻烯。盐酸氯丙噻烯在室温下被铈(IV)离子氧化,生成无色产物。采用分光光度法分别测定445 nm(萃取法)和268 nm(氧化法)的吸光度。提取-分光光度法可测定3.5 ~ 32.0µg/mL盐酸氯原噻烯的含量。氧化法在3.2 ~ 21.0µg/mL范围内符合Beer定律。该方法可用于药品溶液中氯原噻烯的含量测定。计算结果与官方程序计算结果吻合较好。
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SPECTROPHOTOMETRIC DETERMINATION OF CHLORPROTHIXENE HYDROCHLORIDE BY PYROCATECHOL VIOLET AND CERIC(IV) IONS
ABSTRACT Two methods for the determination of chlorprothixene hydrochloride are presented. One of them employs the liability of the chlorprothixene tertiary amine group nitrogen atom to form ion-association complexes with organic compounds. The formed complex is insoluble in water but well soluble in organic solvents. This property is the base of a new extractive-spectrophotometric method for chlorprothixene determination. The second method applied the oxidation reaction of chlorprothixene by Ce(IV) ions. Chlorprothixene hydrochloride is oxidised by ceric(IV) ions at room temperature with the formation of colourless products. Both reactions were followed spectrophotometrically by measuring the absorbance at 445 nm (extractive method) and at 268 nm (oxidative method). Extractive-spectrophotometric method allows to determine chlorprothixene hydrochloride in the range of 3.5–32.0 µg/mL. The oxidative method obeys Beer's law in the range of 3.2–21.0 µg/mL. The methods were successfully applied to the determination of chlorprothixene in pharmaceutical solutions. The results are in good agreement with those obtained by the official procedure.
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