By Michael A. Kamrin, John H. Montgomery
First-class source books are mixed to shape a unmarried entire database that gives summaries of environmental properties
The Agrochemicals and insecticides table Reference on CD-ROM comprises particular information regarding 137 insecticides, serving as a primer of environmental toxicology and an in depth alternate identify index. Profiles of every pesticide provide
This CD-ROM is an up to date reference encouraged through the becoming variety of learn guides and the continuing curiosity within the destiny, delivery, and remediation of dangerous components. Featured are environmental and physical/chemical information on greater than three hundred compounds, together with insecticides, herbicides, and fungicides.
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Additional info for Agrochemical and pesticide desk reference
Stable at temperatures below 210°C (Worthing and Hance, 1991). Emits very toxic fumes of phosphorus and sulfur oxides when heated to decomposition (Sax and Lewis, 1987; Lewis, 1990). , 1967). 2 mg/m3. Formulation Types: Emulsifiable concentrate; wettable powder; granules; dustable powder; fogging concentrate. 9 mg/L (Hartley and Kidd, 1987); acute oral LD50 for male and female rats 375 and 290 mg/kg, respectively (Hartley and Kidd, 1987), 180 mg/kg (RTECS, 1985). Uses: Insecticide for control of fruit flies, leaf hoppers and cereal bugs.
1976). , 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.
30; RTECS: XY7850000. Properties: Colorless to white, odorless crystals. 4 × 10–5 mmHg at 86°C. 4 Source: Rhodes, 1980a. Environmental Fate Soil/Plant. Biodegrades in soil and natural waters releasing carbon dioxide. The reported half-life in soil is 1 to 6 months (Hartley and Kidd, 1987). Rhodes (1980a) found that the persistence of hexazinone varied from 4 weeks in a Delaware sandy loam to 24 weeks in a Mississippi silt loam. Hexazinone is subject to microbial degradation (Rhodes, 1980a; Feng, 1987).
Agrochemical and pesticide desk reference by Michael A. Kamrin, John H. Montgomery