Direct Determination of Endothall in Water Samples by IC–MS


The Application Notebook

The Application NotebookThe Application Notebook-08-02-2011
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Dionex Application note

Endothall is a widely used herbicide for both terrestrial and aquatic weeds. Exposure to endothall in excess of the maximum contamination level (MCL) can cause illness. Endothall is regulated by the US Environmental Protection Agency (EPA) at 100 ppb in drinking water, and by the California EPA at 0.58 mg/L, or 580 ppb, as the Public Health Goal. Current analytical methods described in EPA method 548.1 for the quantification of endothall in water samples involve time-consuming sample preparation and derivatization followed by a 20-min analysis by GC–MS or GC–FID.

This study describes the direct analysis of trace levels of endothall in water samples by ion chromatography–mass spectrometry (IC–MS). Water samples were directly injected for analysis and chromatographic separation was reduced to 10 min. The MSQ Plus mass spectrometer was operated in selected ion monitoring (SIM) mode, allowing minimum sample cleanup and ensuring sensitive (low ppb) and selective quantification. Isotope labelled glutaric acid (Glutarate–d6) was used as the internal standard to ensure quantification accuracy.

Results and Conclusion

As seen in Figure 1, endothall was retained and separated from seven commonly seen anions within 10 min, and was detected with great sensitivity and selectivity using SIM acquisition. This method features direct analysis without sample pretreatment and significantly reduces run time relative to GC methods, thus improving throughput. Sufficient sensitivity was achieved in this study to allow the routine quantification of endothall below the lowest regulated level (100 ppb by US EPA standards).

Figure 1: IC–MS of 20 ppb endothall spiked in a seven anions matrix: 0.2–1.5 ppm.

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