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Hydrolysis of organophosphate insecticides in aqueous media
Abstract Hydrolysis of crucron [0-(4-bromo-2-chorophenyl)-ethyl-s-n-propyl phosphorothioate], bromophos [0-(4-bromo-2,5-dichlorophenyl)0,0-dimethyl phosphorothioate] and fenitrothion [0,0-dimethyl-0-(4-nitro-m-tolyl phosphorothioate] was investigated in buffered aqueous media at various pH values. Rate constants and half-life studies revealed that these insecticides were relatively stable in acidic medium, and their stability decreased as the pH increased. The mode of decomposition of these compounds in acidic; the neutral medium is dealkylation which results in deakylated compounds and alcohols. In an alkaline medium they undergo hydrolysis resulting in the formation of phenol derivatives and dialkylphosphoric acid.
Hydrolysis of organophosphate insecticides in aqueous media
Abstract Hydrolysis of crucron [0-(4-bromo-2-chorophenyl)-ethyl-s-n-propyl phosphorothioate], bromophos [0-(4-bromo-2,5-dichlorophenyl)0,0-dimethyl phosphorothioate] and fenitrothion [0,0-dimethyl-0-(4-nitro-m-tolyl phosphorothioate] was investigated in buffered aqueous media at various pH values. Rate constants and half-life studies revealed that these insecticides were relatively stable in acidic medium, and their stability decreased as the pH increased. The mode of decomposition of these compounds in acidic; the neutral medium is dealkylation which results in deakylated compounds and alcohols. In an alkaline medium they undergo hydrolysis resulting in the formation of phenol derivatives and dialkylphosphoric acid.
Hydrolysis of organophosphate insecticides in aqueous media
Aly, Osama A. (author) / Badawy, Mohamed I. (author)
Environmental International ; 7 ; 373-377
1982-06-07
5 pages
Article (Journal)
Electronic Resource
English
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