Agrochemicals Desk Reference by John H. Montgomery

By John H. Montgomery

First-class 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 comprises particular information regarding 137 insecticides, serving as a primer of environmental toxicology and an in depth exchange identify index. Profiles of every pesticide provide

  • regulatory information
  • toxicity assessments
  • environmental destiny data
  • physical properties
  • acceptable publicity restrict values

    This CD-ROM is an up to date reference encouraged by way of the starting to be variety of study guides and the continuing curiosity within the destiny, delivery, 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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    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). The half-lives in a sandy soil and clay were 1 and 6 months, respectively (Rhodes, 1980a).

    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. Eichelberger and Lichtenberg (1971) reported heptachlor (10 µg/L) in river water, kept in a sealed jar under sunlight and fluorescent light, was completely converted to 1-hydroxychlordene.

    1983). Plant. , 1980). Surface Water. , 1983). Chemical/Physical. Undergoes hydrolysis at the ester bond (Hartley and Kidd, 1987). , 1983) probably releasing toxic fumes of nitrogen and chlorine. Formulation Types: Emulsifiable concentrate; suspension concentrate. 0 ppb (formulated product) (Coats and O’Donnell-Jeffrey, 1979); acute oral LD50 for rats 451 mg/kg (dimethylsulfoxide) (Hartley and Kidd, 1987). Use: Insecticide used against a wide variety of pests. © 2000 CRC PRESS LLC FERBAM Synonyms: Aafertis; Bercema Fertam 50; Carbamate; Dimethylcarbamodithioc acid iron complex; Dimethylcarbamodithioc acid iron(3+) salt; Dimethyldithiocarbamic acid iron salt; Dimethyldithiocarbamic acid iron(3+) salt; ENT 14689; Ferbam 50; Ferbame; Ferbam, iron salt; Ferbeck; Ferberk; Fermate; Fermate ferbam fungicide; Fermocide; Ferradow; Ferric dimethyldithiocarbamate; Fuklasin; Fuklasin ultra; Hexaferb; Hokmate; Iron flowable; Iron tris(dimethyldithiocarbamate); Karbam black; Trifungol; Tris(dimethylcarbamodithioato-S,S′)iron; Tris(dimethyldithiocarbamato)iron; Vancide FE95.

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