1973
DOI: 10.1007/978-3-642-97876-0
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The Chemistry of Organophosphorus Pesticides

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Cited by 126 publications
(28 citation statements)
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“…The compounds were protonated by lowering the pH to <1.25 (pK a for DMP = 1.25) [17,46,47] with HCl for efficient retention of DAPs in the SPE column. Although in previous studies [19,20] low recoveries were observed with HCl as the acidifying agent compared with acetic acid, our observation was in complete contrast.…”
Section: Resultsmentioning
confidence: 99%
“…The compounds were protonated by lowering the pH to <1.25 (pK a for DMP = 1.25) [17,46,47] with HCl for efficient retention of DAPs in the SPE column. Although in previous studies [19,20] low recoveries were observed with HCl as the acidifying agent compared with acetic acid, our observation was in complete contrast.…”
Section: Resultsmentioning
confidence: 99%
“…10) Compounds 11, 16 and 22 (including extra phosphorus atom) showed good inhibitions against all bacterial and fungal strains, while compounds 10, 14 and 20 (including sulfur atom) showed a degree of inhibition against only bacterial strains (Tables 1 and 2). This may be due to a combination between the extra phosphorus atoms withcompounds 9, 12 and 18 leading to a biocidal effects activity more that sulfur atom moieties.…”
Section: Diameter Of Zone Of Inhibition In MMmentioning
confidence: 93%
“…These compounds exert their biological action on arthropods by attacking the system of neural transmission and inhibiting the function of acetyl cholinesterase [16,17]. In particular, organophosphorus compounds including hydrophosphoryl group (H−P=O) are widely used in industry, agriculture and medicine.…”
Section: Introductionmentioning
confidence: 99%
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“…Other important classes of organic insecticides include organophosphates and carbamates [12]. The first synthetic organophosphates namely tabun and sarin were discovered by Kurkenthal and Schrader in Germany and were found to be toxic to aphids and sucking pests [13].…”
Section: Introductionmentioning
confidence: 99%