Demeton
PESTICIDE NAME: Demeton
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Trade name(s): Systox
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Manufacturer(s): Mobay Chemical Corporation
Agricultural Chemicals Division
P.O. Box 4913
Kansas City, MO. 64120
I. Basic information
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A. Molecular structure: C8H19O3PS2
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B. Chemical name: mixture of: 0,0-diethyl-0-[2-
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2(ethylthio)ethyl]phosphorothioate and
0,0-diethyl-S[2(ethylthio)ethyl]phosphorothioate N.B.:For the
purposes of the remainder of this discussion, the first component will
be denoted "O" and the second "S".
C. Derivatives: 0,0-dimethyl S-(2-ethyl-
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sulfinylethyl)phosphorothioate
2-(ethylsulfinyl)ethanethiol
2-(ethylsulfonyl)ethanethiol
bis[2-(ethylsulfinyl)-ethyl]disulfide
bis[2-(ethylsulfonyl)-ethyl]disulfide
bis[2-(ethylsulfinyl)-ethyl]sulfide
bis[2-(ethylsulfonyl)-ethyl]sulfide
D. Molecular weight: 258.3 g/mole
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E. Solubility in water: O:60 mg/l; S:2000mg/l
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F. Common physical appearance: light brown liquid
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G. Oral LD50(rat): 2-4 mg/kg
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H. Pesticide classification: organophosphate insecticide
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I. Restricted use list (N.Y.): yes
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EPA priority pesticide list: no
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J. Crop use: beans, celery, cabbage, cauliflower, broccoli,
Brussels sprouts, cucurbits, lettuce, endive, escarole, peas, peppers,
eggplant, tomato
II. Text
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Demeton is an organophosphate insecticide used on a variety of
vegetable crops but not widely treated in the scientific literature.
It appears to be rapidly degraded to its metabolites. No information
was available concerning adsorption and transport.
III. Soils information
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A. Degradation and transformation
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The literature does not contain extensive information on
degradation/transformation or adsorption/transport of demeton. One
study found that demeton was 65-98% (av = 86.1%) degraded 14d after
application. The variability depended upon the microorganisms present
in the soil. The sulfoxide was transformed to metabolites rather than
being mineralized(2).
B. Adsorption and transport
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No information was available concerning adsorption and transport
of demeton.
IV. References(*denotes key reference)
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1.Kuhr, R.J., A.C. Davis, and J.B. Bourke. 1974.
Bull.Environ.Contam. Toxicol. 11:3 224-30.
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*2.Ziegler, W., G. Engelhardt, P.R. Wallnofer, L. Oehlmann, and K.
Wagner. 1980. J.Agric.Food Chem. 28. 1102-6.
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