Please use this identifier to cite or link to this item: https://doi.org/10.1021/jf010339k
Title: Hydrolysis of terbufos using simulated environmental conditions: Rates, mechanisms, and product analysis
Authors: Hong, F.
Khin, Y.W. 
Pehkonen, S.O. 
Keywords: Di-tert-butyl disulfide
Formaldehyde
Microtox
Nucleophilic attack
O,O,S-triethyl phosphorodithioate
Toxicity
Issue Date: 2001
Source: Hong, F., Khin, Y.W., Pehkonen, S.O. (2001). Hydrolysis of terbufos using simulated environmental conditions: Rates, mechanisms, and product analysis. Journal of Agricultural and Food Chemistry 49 (12) : 5866-5873. ScholarBank@NUS Repository. https://doi.org/10.1021/jf010339k
Abstract: This study focuses on the hydrolysis of terbufos, an organophosphorus pesticide. Combining GCMS and wet chemistry methods, di-tert-butyl disulfide and formaldehyde were identified and quantified as major degradation products. Diethyl dithiophosphate was also indirectly identified as a degradation product under alkaline conditions. Hydrolysis rate constants of terbufos under homogeneous conditions were comparable to those of phorate and show relative insensitivity to pH under slightly acidic to neutral pH conditions, as the observed rate constants varied only in the range of (4.5-5.0) × 10-6 s-1 between pH 5.7 and 9.4; neutral hydrolysis is thus the most dominant hydrolysis pathway of terbufos in ambient waters. The mechanisms for terbufos hydrolysis and the formation of the major products and their temporal profiles are discussed. To assess the environmental impact of degradation products of this widely used pesticide, Microtox was used to analyze the toxicity of terbufos and two of its degradation products: diethyl dithiophosphate and di-tert-butyl disulfide; the EC50 of terbufos was found to be > 17 μM, whereas the EC50 of di-tert-butyl disulfide was 1.3 μM.
Source Title: Journal of Agricultural and Food Chemistry
URI: http://scholarbank.nus.edu.sg/handle/10635/92034
ISSN: 00218561
DOI: 10.1021/jf010339k
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