The photochemical degradation of the fungicide cymoxanil {2-cyano-N-[(ethylamino)carbonyl]-2-(methoxyimino) acetamide} was studied in aqueous buffer solution (pH 5.9 ± 0.1) under UV light and in laboratory conditions. The degradation followed a pseudo-first-order kinetic with significant correlation coefficient. The main photoproducts were separated and tentatively identified by HPLC/UV and HPLC/MS data, as 3-ethyl-4-(methoxyamino)-2,5-dioxo-4-imidazolidinecarbonitrile, 1-ethyl-5-(methoxyimino)-2,4-imidazolidin-2,4-dione, ethylimidazolidinetrione and {[(ethylamino)carbonyl]-amino}oxoacetic acid. A photolysis pathway of cymoxanil is proposed.

High-performance liquid chromatographic mass spectrometric identification of the photoproducts of cymoxanil / Morrica, Patrizia; Fidente, Paola; Seccia, Serenella. - In: BIOMEDICAL CHROMATOGRAPHY. - ISSN 0269-3879. - ELETTRONICO. - 19:(2005), pp. 506-512. [10.1002/bmc.471]

High-performance liquid chromatographic mass spectrometric identification of the photoproducts of cymoxanil.

MORRICA, PATRIZIA;FIDENTE, PAOLA;SECCIA, SERENELLA
2005

Abstract

The photochemical degradation of the fungicide cymoxanil {2-cyano-N-[(ethylamino)carbonyl]-2-(methoxyimino) acetamide} was studied in aqueous buffer solution (pH 5.9 ± 0.1) under UV light and in laboratory conditions. The degradation followed a pseudo-first-order kinetic with significant correlation coefficient. The main photoproducts were separated and tentatively identified by HPLC/UV and HPLC/MS data, as 3-ethyl-4-(methoxyamino)-2,5-dioxo-4-imidazolidinecarbonitrile, 1-ethyl-5-(methoxyimino)-2,4-imidazolidin-2,4-dione, ethylimidazolidinetrione and {[(ethylamino)carbonyl]-amino}oxoacetic acid. A photolysis pathway of cymoxanil is proposed.
2005
High-performance liquid chromatographic mass spectrometric identification of the photoproducts of cymoxanil / Morrica, Patrizia; Fidente, Paola; Seccia, Serenella. - In: BIOMEDICAL CHROMATOGRAPHY. - ISSN 0269-3879. - ELETTRONICO. - 19:(2005), pp. 506-512. [10.1002/bmc.471]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/337934
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