Widespread application of herbicides impacts surface water and groundwater. Their metabolites (e.g., desphenylchloridzon from chloridazon) may be persistent and even more polar than the parent herbicide, which increases the risk of groundwater contamination. When parent herbicides are still applied, metabolites are constantly formed and may in addition be degraded. Evaluating their degradation based on concentration measurements is, therefore, difficult. This study presents compound-specific stable isotope analysis (CSIA) of nitrogen and carbon isotope ratios at natural abundances as alternative analytical approach to track origin, formation and degradation of desphenylchloridazon (DPC), the major degradation product of the herbicide chloridazon. Methods were developed and validated for carbon and nitrogen isotope analysis (δ 13 C and δ 15 N) of DPC by liquid chromatography-isotope ratio mass spectrometry (LC-IRMS) and derivatization-gas chromatography-IRMS (GC-IRMS), respectively. Injecting standards directly onto an Atlantis LC-column resulted in reproducible δ 13 C isotope analysis (standard deviation < 0.5 ‰) by LC-IRMS with a limit of precise analysis of 996 ng DPC on-column. Accurate and reproducible δ 15 N analysis with a standard deviation < 0.4 ‰ was achieved by GC-IRMS after derivatization of > 100 ng DPC with 160-fold excess of (trimethylsilyl)diazomethane. Application of the method to environmental seepage water indicated that newly formed DPC could be distinguished from "old" DPC by different isotopic signatures of the two DPC sources.