By John H. Montgomery
First-class 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 up to date reference encouraged through the turning out to be variety of learn courses and the ongoing curiosity within the destiny, delivery, and remediation of dangerous components. Featured are environmental and physical/chemical info on greater than three hundred compounds, together with insecticides, herbicides, and fungicides.
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Extra info for Agrochemicals Desk Reference
Properties: Liquid. 6 × 10–6 mmHg at 20°C. Environmental Fate Biological. , 1975). , 1981). This is consistent with the findings of Bowman et al. (1965). They observed that under laboratory conditions, heptachlor epoxide did not show any evidence of degradation when incubated in a variety of soils maintained at 45°C for 8 days. , 1965). , 1971). Photolytic. , 1972). Benson et al. (1971) reported a degradation yield of 99% when an acetone solution containing heptachlor epoxide was photolyzed at >300 nm for 11 hours.
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). , 1989), 3-(4-hydrocyclohexyl)-6-(methylamino)-1-methyl-1,3,5-triazine-2,4(1H,3H)dione, 3-cyclohexyl-1-methyl-1,3,5-triazine-2,4,6-(1H,3H,5H)trione, 3-(4-hydrocyclohexyl)-1methyl-1,3,5-triazine-2,4,6(1H,3H,5H)trione, 3-cyclohexyl-6-amino-1-methyl-1,3,5-triazine-2,4(1H,3H)dione and 3-cyclohexyl-6-(methylamino)-1,3,5-triazine-2,4(1H,3H)-dione (Rhodes, 1980a; Holt, 1981).
1989; Ashton and Monaco, 1991). Chemical/Physical. Fosamine-ammonium is stable as a dilute solution but decomposes in weak acidic media (Worthing and Hance, 1991), probably forming water-soluble salts. Symptoms of Exposure: May irritate eyes, nose, throat and skin. Formulation Types: Soluble concentrate (4 lb/gal). 4 g/kg (Ashton and Monaco, 1991). Uses: Nonselective contact herbicide used to control many woody and brush species on noncrop land. © 2000 CRC PRESS LLC FOSETYL-ALUMINUM Synonyms: Aliette; Aluminum tris(O-ethyl phosphonate); Efosite-AL; Epal; Fosetyl AL; LS 74783; Phosethyl; Phosethyl AL; RP 32545.
Agrochemicals Desk Reference by John H. Montgomery