By John H. Montgomery
Very good 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 alternate identify index. Profiles of every pesticide provide
This CD-ROM is an updated reference encouraged via the becoming variety of examine guides and the continuing curiosity within the destiny, shipping, and remediation of unsafe 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 Agrochemicals Desk Reference
1975; Cremlyn, 1991). N-Nitrosoglyphosate also formed from the nitrosation of glyphosate in soil solutions containing nitrite ions (Young and Kahn, 1978). The reported half-life of glyphosate in soil is <60 days (Hartley and Kidd, 1987). 022/day, respectively. , 1977). , 1975a; Normura and Hilton, 1977; Moshier and Penner, 1978). , 1981). Plant. , 1984). Photolytic. When an aqueous solution of glyphosate (1 ppm) was exposed to outdoor sunlight for 9 weeks (from August 12 through October 15, 1983), aminomethylphosphonic acid and ammonia formed as major and minor photoproducts, respectively (Lund-Høie and Friestad, 1986).
1989). Duke et al. (1991) reported that fluometuron degrades in plants via the following degradative pathway: fluometuron to N-methyl-N′-(3-(trifluoromethyl)phenyl)urea which undergoes demethylation to 3-(trifluoromethyl)phenylurea © 2000 CRC PRESS LLC followed by deamination and elimination of the ketone group to form 3-trifluoromethylaniline. Chemical/Physical. Emits toxic fumes of nitrogen oxides and fluorine when heated to decomposition (Sax and Lewis, 1987). Symptoms of Exposure: Dust may cause eye irritation.
2000 CRC PRESS LLC Uses: Soil insecticide used to control rootworms, wireworms, crickets and similar crop pests in vegetables, sorghum, ornamentals, cereals, maize, vines, olives, sugar beet, sugarcane, potatoes, groundnuts, tobacco, turf and fruit crops. © 2000 CRC PRESS LLC FORMALDEHYDE Synonyms: BFV; FA; Fannoform; Formalin; Formalin 40; Formalith; Formic aldehyde; Formol; Fyde; HOCH; Ivalon; Karsan; Lysoform; Methanal; Methyl aldehyde; Methylene glycol; Methylene oxide; Morbicid; NCI-C02799; Oxomethane; Oxymethylene; Paraform; Polyoxymethylene glycols; RCRA waste number U122; Superlysoform; UN 1198; UN 2209.