Agrochemicals Desk Reference by John H. Montgomery

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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

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

    This CD-ROM is an updated reference encouraged by means of the becoming variety of examine courses and the ongoing curiosity within the destiny, delivery, and remediation of harmful components. Featured are environmental and physical/chemical information on greater than three hundred compounds, together with insecticides, herbicides, and fungicides.
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    0); vp: negligible at 20–25°C. Environmental Fate Plant. Decomposes in plants to ethylene thiourea, ethylene thiuram monosulfide, ethylene thiuram disulfide and sulfur (Hartley and Kidd, 1987). 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.

    1 mg/m3. Formulation Types: Emulsifiable concentrate; granules. 4 mg/kg, respectively (Hartley and Kidd, 1987), 8 mg/kg (RTECS, 1985). Use: Nematocide. © 2000 CRC PRESS LLC FENBUTATIN OXIDE Synonyms: Bendex; Bis(tris(β,β-dimethylphenethyl)tin)oxide; Bis(tris(2-methyl-2-phenylpropyl)tin)oxide; Di(tri(2,2-dimethyl-2-phenylpropyl)tin)oxide; ENT 27738; Hexakis(β,β-dimethylphenethyl)distannoxane; Hexakis(2-methyl-2-phenylpropyl)distannoxane; SD 14114; Shell SD-14114; Torque; Vendex. 70; RTECS: JN8770000.

    Emits toxic fumes of phosphorus and sulfur oxides when heated to decomposition (Sax and Lewis, 1987; Lewis, 1990). Isomerizes readily to the O,S-diethyl isomer (Worthing and Hance, 1991). 0, were 69, 77, 87 and 58 weeks, respectively (Chapman and Cole, 1982). 1 mg/m3. Formulation Types: Emulsifiable concentrate; dustable powder; granules; wettable powder. 2 mg/kg, respectively (Hartley and Kidd, 1987), 2 mg/kg (RTECS, 1985). © 2000 CRC PRESS LLC Uses: Nematocide and pesticide used to control free-living, cyst-forming and root-knot nematotodes and soil insects in vegetable and fruit crops.

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