
doi: 10.1007/bf01985797
pmid: 4828552
The action of sunlight on dilute (1–10 ppm) aqueous solutions of the herbicide bromacil (5-bromo-3-sec-butyl-6-methyluracil) resulted in the formation of only one detectable photoproduct, 5-bromo-6-methyluracil, in very low yield. The almost quanitative recovery of starting material, even after prolonged periods of irradiation, indicated that bromacil was very stable toward sunlight. TheN-dealkylated photoproduct proved to be much less stable toward sunlight wave-lengths, forming principally 6-methyluracil. No 5-bromouracil was detected.
Chromatography, Gas, Photolysis, Spectrophotometry, Infrared, Herbicides, Bromine, Mass Spectrometry, Drug Stability, Dealkylation, Sunlight, Spectrophotometry, Ultraviolet, Chromatography, Thin Layer, Uracil
Chromatography, Gas, Photolysis, Spectrophotometry, Infrared, Herbicides, Bromine, Mass Spectrometry, Drug Stability, Dealkylation, Sunlight, Spectrophotometry, Ultraviolet, Chromatography, Thin Layer, Uracil
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