1966
DOI: 10.1093/jaoac/49.2.399
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Determination of Temik Residues in Raw Fruits and Vegetables

Abstract: Temik, 2-methyl-2-(methylthio) propionaldehyde O-(methylcarbamoyl)oxime, is a systemic pesticide effective both by topical application to the plant and by systemic translocation from treated soil. The method developed for residues of Temik in crops is based on extraction of the crops with chloroform, followed by cleanup involving both coagulation and liquid partitioning techniques. The analysis involves both base- and acid-catalyzed hydrolysis to liberate hydroxylamine, which is then oxidized by iodine to nitr… Show more

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Cited by 6 publications
(6 citation statements)
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“…c References for water solubilities quoted: Aldrin, Dieldrin (Shell Chemical Corp., 1965); DDT (Robeck et ai., 1965): Parathion (Popov, 1956); Diazinon, Disyston (Schrader, 1963); Carbaryl (UnionCarbide, 1963); Temik (Johnson & Stansbury, 1966). ""Differences observed between control cultures (EtOH treated) and 'compound' treated were significant at the 5 % (a) or 1 % (b) level.…”
Section: Resultsmentioning
confidence: 99%
“…c References for water solubilities quoted: Aldrin, Dieldrin (Shell Chemical Corp., 1965); DDT (Robeck et ai., 1965): Parathion (Popov, 1956); Diazinon, Disyston (Schrader, 1963); Carbaryl (UnionCarbide, 1963); Temik (Johnson & Stansbury, 1966). ""Differences observed between control cultures (EtOH treated) and 'compound' treated were significant at the 5 % (a) or 1 % (b) level.…”
Section: Resultsmentioning
confidence: 99%
“…Since the retention times of Temik oxime, the sulfoxide, and the sulfoxide oxime are close together, and these compounds cannot be separated by column chromatography, it is best to remove the oximes prior to the actual analysis. This study utilized acid hydrolysis to convert the oximes quantitatively to their respective aldehydes (Johnson and Stansbury, 1966), which do not interfere with the analysis. It has been reported that carbamates are stable under acid conditions (Cassil and Cullen, 1968;Coppedge et al, 1967) but are rapidly hydrolyzed to form their oximes under basic conditions (Johnson and Stansbury, 1966).…”
Section: Resultsmentioning
confidence: 99%
“…This study utilized acid hydrolysis to convert the oximes quantitatively to their respective aldehydes (Johnson and Stansbury, 1966), which do not interfere with the analysis. It has been reported that carbamates are stable under acid conditions (Cassil and Cullen, 1968;Coppedge et al, 1967) but are rapidly hydrolyzed to form their oximes under basic conditions (Johnson and Stansbury, 1966). Heating in aqueous acid solution also extracts the desired compounds from the crop materials, because Temik and its metabolites are soluble in water while the crop materials are not.…”
Section: Resultsmentioning
confidence: 99%
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“…The analytical procedure of Johnson and Stansbury (1966) was used in this investigation with certain modifications to improve sensitivity and to remove some interfering substances (Meagher et al, 1967). The technique releases the nitrogen of Temik compounds as nitrous acid to allow stoichiometric diazotization of sulfanilic acid, which in turn couples to form a related quantity of dye in solution that is measured spectrophotometrically.…”
Section: Inmentioning
confidence: 99%