4-氨基安替比林氧化偶联分光光度法测定氨基酚异构体

R. Al-Luhaiby, Mohammed S. Al-Enizzi
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引用次数: 0

摘要

建立了一种测定氨基酚异构体(邻氨基酚、间氨基酚和对氨基酚)的分光光度法。该方法是基于这些化合物与4-氨基安替比林(4-AAP)在硫酸铜作为氧化剂的存在下,在碱介质中氧化偶联反应,形成红棕色。产物对邻氨基酚、间氨基酚和对氨基酚的最大吸收波长分别为440 nm、480 nm和445 nm。在1-20、1-24和1-7 μg浓度范围内,摩尔吸光度分别为8.632×10、9.33×10和9.1449 ×10 l.mol.cm。以上化合物分别为Ml。加样回收率在98.38% ~ 101.01%之间,相对标准偏差< 1.6。氨基苯酚同分异构体与4-AAP的比例为1:2。邻氨基酚、间氨基酚和对氨基酚的稳定常数分别为7.4 ×10、3.27×10和9.94×10 l.mol,表明产品具有良好的稳定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spectrophotometric Determination of Aminophenol Isomers Via Oxidative Coupling Reaction with 4-Aminoantipyrine
A spectrophotometric method has been developed for the determination of aminophenol isomers (o-aminophenol, m-aminophenol and p-aminophenol). The method is based on oxidative coupling reaction of these compounds with 4-aminoantipyrine (4-AAP) in the presence of cupper sulphate as oxidizing agent in alkaine medium forming a reddish brown colour. The products show maximum absorption at 440 nm, 480 nm and 445 nm for o-aminophenol, m-aminophenol and p-aminophenol respectively. The molar absorptivities are 8.632×10 ,9.33×10 and 9.1449 ×10 l.mol.cm for concentrations obeyed Beer’s law in the range 1-20, 1-24 and 1-7 μg.ml for the above compounds respectively. The average recovery was ranged between 98.38% and 101.01% with relative standard deviation < 1.6 for all the studied compounds. The 4-AAP products were formed in the ratio of 1:2 aminophenol isomers : 4-AAP. The stability constant of the products was 7.4 ×10, 3.27×10 and 9.94×10 l.mol for o-aminophenol, m-aminophenol and p-aminophenol products respectively indicating the good stability of these products.
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