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首页> 外文期刊>Analytical methods >A simple pre-column derivatization method for the determination of mancozeb technical (fungicide) by reverse phase HPLC-UV
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A simple pre-column derivatization method for the determination of mancozeb technical (fungicide) by reverse phase HPLC-UV

机译:通过反相HPLC-UV测定ManCozeb技术(杀真菌剂)的简单柱衍生化方法

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摘要

A simple and fast pre-column derivatization high performance liquid chromatographic method for the technical analysis of mancozeb was developed and validated in the present study. The mobile phase consists of a mixture of acetonitrile and 0.1% (v/v) formic acid in the proportion 60 : 40. This was found to give a sharp peak of the S-ethyl derivative of mancozeb (S-ethyl ethylene bis-dithiocarbamate) at a retention time of 9.12 minutes. HPLC analysis of mancozeb was carried out at a wavelength of 272 nm with a flow rate of 1.0 mL per minute. The linear regression analysis data for the calibration curve showed a good linear relationship with a regression coefficient of 0.999 in the concentration range of 8.2 mg L-1 to 32.3 mg L-1 for the derivative of mancozeb technical. The method was validated for specificity, linearity, precision and accuracy.
机译:在本研究中开发并验证了一种简单且快速的预柱衍生高性能液相色谱法,用于ManCozeb的技术分析和验证。 流动相由乙腈和0.1%(v / v)甲酸的混合物组成,比例60:40。这被认为是Mancozeb的S-乙基衍生物的尖峰(S-乙基乙烯双二氨基甲酸酯 )在9.12分钟的保留时间。 ManCozeb的HPLC分析在272nm的波长下进行,流速每分钟1.0ml。 用于校准曲线的线性回归分析数据显示出浓度范围为0.999的回归系数为8.2mg的L-1至32.3mg L-1的回归系数,用于Mancozeb技术的衍生物。 该方法验证了特异性,线性度,精度和准确性。

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