2014
DOI: 10.1016/j.chroma.2014.10.051
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Ultraviolet–vis degradation of iprodione and estimation of the acute toxicity of its photodegradation products

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Cited by 22 publications
(12 citation statements)
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“…Media containing fully formed mycelium cells were supplemented with iprodione (Pestanal, Sigma-Aldrich) to a final concentration of 20 μM, the temperature was increased to 37 • C to induce the M→Y transition, and the transition was monitored in iprodionesupplemented and non-supplemented cultures by bright field microscopy at 5, 10, 24, 48, 72 and 96 h. Because iprodione is insoluble in water, dimethyl sulphoxide (DMSO) was used to solubilise the drug. Because the drug undergoes photodegradation in solution (Lassalle et al 2014), it was always freshly prepared and stored in the dark.…”
Section: Histidine Kinase Inhibition Assaymentioning
confidence: 99%
“…Media containing fully formed mycelium cells were supplemented with iprodione (Pestanal, Sigma-Aldrich) to a final concentration of 20 μM, the temperature was increased to 37 • C to induce the M→Y transition, and the transition was monitored in iprodionesupplemented and non-supplemented cultures by bright field microscopy at 5, 10, 24, 48, 72 and 96 h. Because iprodione is insoluble in water, dimethyl sulphoxide (DMSO) was used to solubilise the drug. Because the drug undergoes photodegradation in solution (Lassalle et al 2014), it was always freshly prepared and stored in the dark.…”
Section: Histidine Kinase Inhibition Assaymentioning
confidence: 99%
“…The inverse relationship between the target molecule and Cl-indicates an easily loss of Cl ring substituents, suggesting the HO• attack into the carbon-chloride bond as one of the firsts steps during IPR degradation. The susceptibility of these bonds have been also reported during the photodecomposition of IPR leading to the substitution of the Cl atoms by OH groups (Lassalle et al 2014). …”
Section: Main Degradation Pathwaysmentioning
confidence: 92%
“…It is mainly used against Botrytis on ornamentals plants such as carnation, chrysanthemum, and rose. It is also used in agricultural crops such as potato, tomato, and onion (Lassalle et al 2014).…”
mentioning
confidence: 99%
“…Some of them remain present in detectable amounts in commercial products such as grape juice . As they are directly applied on fruits and leaves, fungicides are exposed to direct sunlight and may undergo phototransformation processes . Fenbuconazole is part of the triazole molecules class, introduced as pesticides in the 1970s, that includes molecules containing the 1,2,4‐triazole moiety such as myclobutanil, propiconazol and tebuconazol .…”
mentioning
confidence: 99%
“…[7] As they are directly applied on fruits and leaves, fungicides are exposed to direct sunlight and may undergo phototransformation processes. [8][9][10] Fenbuconazole is part of the triazole molecules class, introduced as pesticides in the 1970s, that includes molecules containing the 1,2,4-triazole moiety such as myclobutanil, propiconazol and tebuconazol. [11,12] Applications of fenbuconazole pre-and post-harvest allow to inhibit various fungal diseases on fruits, vegetables and grain crops.…”
mentioning
confidence: 99%