By John H. Montgomery
Very good source books are mixed to shape a unmarried entire database that provides 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 intensive exchange identify index. Profiles of every pesticide provide
This CD-ROM is an updated reference encouraged by means of the transforming into variety of learn courses and the continuing curiosity within the destiny, shipping, and remediation of detrimental components. Featured are environmental and physical/chemical facts on greater than three hundred compounds, together with insecticides, herbicides, and fungicides.
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Chemical/Physical. Hydrolyzes in acidic media releasing carbon disulfide. Decomposes in water forming ethylene thiourea (Hartley and Kidd, 1987). , 1983) emitting toxic fumes of nitrogen and sulfur oxides (Lewis, 1990; Sax and Lewis, 1987). Exposure Limits: NIOSH 10 mg/m3, IDLH 800 mg/m3; OSHA PEL: TWA 15 mg/m3; ACGIH TLV: TWA 10 mg/m3. Symptoms of Exposure: May cause irritation of skin and mucous membranes and renal damage. Formulation Types: Wettable powders. Toxicity: Moderately toxic to fish (Hartley and Kidd, 1987); acute oral LD50 for rats >17,000 mg/kg (Hartley and Kidd, 1987), 4,000 mg/kg (RTECS, 1985).
Formulation Types: Emulsifiable concentrate; water-dispersible granules. , 1983); acute oral LD50 for male and female rats is 81 and 67 mg/kg, respectively (Hartley and Kidd, 1987). Use: Nonsystemic insecticide. © 2000 CRC PRESS LLC FLUOMETURON Synonyms: C 2059; CIBA 2059; Cotoran; Cotoran multi 50WP; Cottonex; 1,1-Dimethyl3-(3-trifluoromethylphenyl)urea; N,N-Dimethyl-N′-(3-(trifluoromethyl)phenyl)urea; 1,1-Dimethyl-3-(α,α,α-trifluoro-m-tolyl)urea; Herbicide C-2059; Lanex; Meturon; Meturon 4L; NCI-C08695; Pakhtaran; N-(m-Trifluoromethylphenyl)-N′,N′-dimethylurea; N-(3Trifluoromethylphenyl)-N′,N′-dimethylurea; 3-(m-Trifluoromethylphenyl)-1,1-dimethylurea.
04,8]decane is the only product formed. , 1972). Heptachlor reacts with photochemically produced hydroxyl radicals in the atmosphere. At a concentration of 5 × 105 hydroxyl radicals/cm3, the atmospheric half-life was estimated to be about 6 hours (Atkinson, 1987). Chemical/Physical. Slowly releases hydrogen chloride in aqueous media (Hartley and Kidd, 1987; Kollig, 1993). 43 weeks, respectively (Chapman and Cole, 1982). , 1969). Heptachlor degraded in aqueous saturated calcium hypochlorite solution to 1-hydroxychlordene.
Agrochemicals Desk Reference by John H. Montgomery