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Flutriafol

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Flutriafol Basic information
Flutriafol Chemical Properties
  • Melting point:130°
  • Boiling point:506.5±60.0 °C(Predicted)
  • Density 1.3015 (estimate)
  • vapor pressure 7.1 x l0-9 Pa (20 °C)
  • Flash point:2 °C
  • storage temp.  0-6°C
  • form neat
  • pka11.60±0.29(Predicted)
  • Water Solubility 130 mg l-1 (pH 7,20 °C)
  • Merck 13,4240
  • BRN 8155287
  • Stability:Stable. Incompatible with strong oxidizing agents.
  • InChIKeyJWUCHKBSVLQQCO-UHFFFAOYSA-N
  • CAS DataBase Reference76674-21-0(CAS DataBase Reference)
  • NIST Chemistry ReferenceFlutriafol(76674-21-0)
  • EPA Substance Registry SystemFlutriafol (76674-21-0)
Safety Information
  • Hazard Codes Xn,F
  • Risk Statements 22-36-20/21/22-11
  • Safety Statements 22-24/25-36-26
  • RIDADR UN 1648 3/PG 2
  • WGK Germany 3
  • RTECS XZ4825000
  • HS Code 29339900
  • ToxicityLD50 male, female rats (mg/kg): 1140, 1480 orally; rats, rabbits: >1000, >2000 percutaneously (Skidmore)
Flutriafol Usage And Synthesis
  • Chemical Propertiessolid
  • UsesFlutriafol is a systemic fungicide of the triazole class. Flutriafol has broad spectrum fungicidal activity and is used to control effectively cereal powdery mildew, cloud disease, leaf spot disease a nd rust disease.
  • UsesAgricultural fungicide.
  • UsesFlutriafol is used to control a wide variety of leaf and ear diseases in cereals. It is also used in seed treatment formulations to control the major soil-borne and seed-borne diseases of cereals.
  • Metabolic pathwayFlutriafol is stable to hydrolysis and to light and it is persistent in soils. In crops, the metabolites identified were derivatives of triazole.
  • DegradationFlutriafol, 1, is stable to hydrolysis at pH 5,7 and 9 in water at 50 °C over a period of 30 days in the dark.
    [14C-friazole]Flutriafoaln d [14C-carbinol]flutriafol were applied at a rate equivalent to 94 g ai ha-1 to samples of dry sandy loam soil distributed as a thin layer on 10 cm diameter glass plates. Samples were exposed to natural sunlight for 30 days or to alternating periods of 'black light' and darkness for 7 days. Recovery was 60-47% of applied radioactivity after 7 days artificial illumination and 74-85% after exposure to natural sunlight. All degradation products accounted for <5 %of the total applied radioactivity (PSD, 1996).
Flutriafol Preparation Products And Raw materials
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