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Very good source books are mixed to shape a unmarried finished 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 intensive alternate identify index. Profiles of every pesticide provide
This CD-ROM is an updated reference encouraged through the becoming variety of examine courses and the continuing curiosity within the destiny, delivery, and remediation of unsafe ingredients. Featured are environmental and physical/chemical facts on greater than three hundred compounds, together with insecticides, herbicides, and fungicides.
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Additional info for Agrochemical and pesticide desk reference
Harris (1969) concluded that heptachlor has a very low tendency to leach in soils. Groundwater. S. EPA (1986) heptachlor has a high potential to leach to groundwater. Plant. Heptachlor is converted to its epoxide on plant surfaces (Gannon and Decker, 1958). Photolytic. Sunlight and UV light converts heptachlor to photoheptachlor (Georgacakis and Khan, 1971). This is in agreement with Gore et al. (1971) who reported that heptachlor exhibited weakly absorption of UV light at wavelengths above 290 nm.
Symptoms of Exposure: In animals: tremors, convulsions, liver damage. Formulation Types: Emulsifiable concentrate; wettable powder; granules; dustable powder; seed treatment. 3 µg/L (Verschueren, 1983); acute oral LD50 for rats 147–220 mg/kg (Hartley and Kidd, 1987), 40 mg/kg (RTECS, 1985). Use: Insecticide for termite control. © 2000 CRC PRESS LLC HEPTACHLOR EPOXIDE Synonyms: ENT 25584; Epoxy heptachlor; HCE; 1,4,5,6,7,8,8-Heptachloro-2,3-epoxy2,3,3a,4,7,7a-hexahydro-4,7-methanoindene; 1,2,3,4,5,6,7,8,8-Heptachloro-2,3-epoxy3a,4,7,7a-tetrahydro-4,7-methanoindene; 5a,6,6a-Hexahydro-2,5-methano-2Hindeno[1,2-b]oxirene; 2,3,4,5,6,7,7-Heptachloro-1a,1b,5,5a,6,6a-hexahydro-2,5-methano-2H-oxireno[a]indene; Velsicol 53-CS-17.
33 × 10–4 mmHg at 25°C. Environmental Fate Biological. , 1969). In addition, hydrolysis produced hydroxychlordene with subsequent epoxidation yielding 1-hydroxy-2,3-epoxychlordene (Kearney and Kaufman, 1976). Heptachlor reacted with reduced hematin forming chlordene, which decomposed to hexachlorocyclopentadiene and cyclopentadiene (Baxter, 1990). , 1975). , 1981). When heptachlor (10 ppm) in sewage sludge was incubated under anaerobic conditions at 53°C for 24 hours, complete degradation was achieved (Hill and McCarty, 1967).