The hydrolysis and photolysis of the chiral fungicide mandipropamid were investigated, and the potential enantioselectivity of mandipropamid in solutions was further assessed. The aqueous solutions were filtered and directly injected into the liquid chromatography with tandem mass spectrometry. In the hydrolysis experiments, mandipropamid enantiomers hydrolyzed slowly in aquatic solutions with half-lives > 200 days; nevertheless, rise of the pH and incubation temperature could increase the hydrolysis rates more than 1.1 times (half-lives decreased from 495.1 to 216.6 days). Compared with the hydrolysis results, photolysis was found to be the main degradation pathway for mandipropamid in different solutions (half-lives < 14 h, except in pH = 5.05 buffer solution). Organic solvents were able to accelerate the photolysis of mandipropamid, but acidic solutions and the addition of flavonoids or inorganic salts significantly inhibited the photolysis of mandipropamid. During the hydrolysis and photolysis processes, the configuration of mandipropamid enantiomers was stable and five possible transformation products were identified by high resolution mass spectrometry. Due to the enantiomeric fraction values > 0.5, the hydrolysis and photolysis of mandipropamid were enantioselective, and S-( +)-mandipropamid preferentially disspated in certain aqueous solutions. The systematic evaluation of the hydrolysis and photolysis of mandipropamid enantiomers may provide more accurate data for better assessment of environmental and ecological risks in aquatic ecosystems.
Keywords: Aqueous solution; Hydrolysis; Mandipropamid; Photolysis; Transformation product.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.