By John H. Montgomery
First-class source books are mixed to shape a unmarried accomplished database that provides summaries of environmental properties
The Agrochemicals and insecticides table Reference on CD-ROM includes particular information regarding 137 insecticides, serving as a primer of environmental toxicology and an intensive exchange identify index. Profiles of every pesticide provide
This CD-ROM is an updated reference encouraged via the turning out to be variety of learn courses and the continuing curiosity within the destiny, delivery, and remediation of harmful components. Featured are environmental and physical/chemical info on greater than three hundred compounds, together with insecticides, herbicides, and fungicides.
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Properties: Colorless to amber liquid or brown oil with a faint garlic-like odor. 64 (air = 1); vp: 3 × 10–5 mmHg at 20°C. S. Department of Agriculture, 1990. Environmental Fate Biological. , 1988). Surface Water. , 1995). © 2000 CRC PRESS LLC Plant. In plants, fenthion oxidizes to the mesulfenfos and sulfone which further degrades to the sulfone phosphate before undergoing hydrolysis (Hartley and Kidd, 1987). Photolytic. Fenthion was oxidized to the corresponding sulfoxide and trace amounts (<5% yield) of sulfone when sorbed on soil and exposed to sunlight.
2 mg/L (Hartley and Kidd, 1987); acute oral LD50 for rats 10,000 mg/kg (RTECS, 1985). Use: Seed fungicide. © 2000 CRC PRESS LLC HEXAZINONE Synonyms: 3-Cyclohexyl-6-(dimethylamino)-1-methyl-1,3,5-triazine-2,4(1H,3H)dione; 3-Cyclohexyl-6-(dimethylamino)-1-methyl-s-triazine-2,4(1H,3H)-dione; DPX 3674; Velpar; Velpar K; Velpar L; Velpar RP; Velpar ULW; Velpar weed killer. 30; RTECS: XY7850000. Properties: Colorless to white, odorless crystals. 4 × 10–5 mmHg at 86°C. 4 Source: Rhodes, 1980a. Environmental Fate Soil/Plant.
1985). 7) (Choudhry and Hutzinger, 1984). 2) (Choudhry and Hutzinger, 1984). In another study, the irradiation (λ = 290–310 nm) of hexachlorobenzene in aqueous solution gave only pentachlorobenzene and possibly pentachlorophenol as the transformation products. The photolysis rate increased with the addition of naturally occurring substances (tryptophan and pond proteins) and abiotic sensitizers (diphenylamine and skatole) (Hirsch and Hutzinger, 1989). 7 nm monochromatic UV lamps, significant concentrations of pentachlorobenzene, all tetra-, tri- and dichlorobenzenes, chlorobenzene, benzene, phenol, hydrogen and chloride ions were formed.