Quantitative nuclear magnetic resonance (QNMR) spectroscopy for assessing the purity of technical grade agrochemicals: 2,4-dichlorophenoxyacetic acid (2,4-D) and sodium 2,2-dichloropropionate (Dalapon sodium)

被引:79
作者
Wells, RJ
Hook, JM [1 ]
Al-Deen, TS
Hibbert, DB
机构
[1] Univ New S Wales, NMR Facil, Sydney, NSW 2052, Australia
[2] Univ New S Wales, Sch Chem Sci, Sydney, NSW 2052, Australia
[3] Artfern Agrochem Dev Pty Ltd, Laurel, MD 20723 USA
关键词
quantitative NMR; QNMR; impurity profiling; 2,4-dichlorophenoxyacetic acid (2,4-D); Dalapon sodium; sodium 2,2-dichloropropionate; dimethyl sulfone (DMSO2); primary analytical ratio method; internal standard; uncertainty budget;
D O I
10.1021/jf0114379
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Comparison of quantitative NMR spectroscopy (QNMR) with chromatographic methods such as gas chromatography (GC) or high-pressure liquid chromatography (HPLC) for the determination of the purity of and impurities in technical grade agrochemicals, 2,4-dichlorophenoxyacetic acid (2,4-D), 1, and Dalapon sodium (sodium 2,2-dichloropropionate), 10, has revealed that QNMR is more precise and accurate than the chromatographic methods. Quantitative impurity profiling of technical grade 1 is rapid and accurate using 600 MHz H-1 NMR. Extra dispersion at the relatively high frequency allowed full assignment of the NMR spectrum of 1 and its related organic impurities in technical samples, The percentage purity of 1 was measured by the difference QNMR method, which involves summing the amounts of impurities and subtracting from 100%. Results are superior in consistency to those obtained by chromatographic methods. The percentage purity of Dalapon sodium, 10, in technical grade batches is readily obtained by 1H QNMR, using either the difference method or the internal standard method, using dimethyl sulfone (DMSO2) internally as a reference material, that is chemically unrelated to the analyte. The latter method also allows the simultaneous identification and quantification of impurities, many of which are either not accessible to or detectable by the chromatographic methods. Uncertainty budgets for the QNMR method are presented and demonstrate that the major contributors to uncertainty lie in the weighing of the chemicals and in purity of the standard reference material prior to the QNMR experiment.
引用
收藏
页码:3366 / 3374
页数:9
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