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Common NameHexythiazox
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中文通用名噻螨酮
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IUPAC(4RS,5RS)-5-(4-chlorophenyl)-N-cyclohexyl-4-methyl-2-oxo-1,3-thiazolidine-3-carboxamide
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CAStrans-5-(4-chlorophenyl)-N-cyclohexyl-4-methyl-2-oxo-3-thiazolidinecarboxamide
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CAS No.78587-05-0
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Molecular FormulaC17H21ClN2O2S
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Molecular Structure
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Category
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ActivityAcaricide/Miticide
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PremixHexythiazox+Diafenthiuron
Fenpropathrin+hexythiazox
Bifenthrin+Hexythiazox
Flowable, wettable powder, emulsifiable concentrate.
Premix partners:Dicofol; Propargite
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Physical PropertiesMolecular weight:352.9g/mol; Physical form:Colourless crystals. Melting point:108.0-108.5℃; Vapour pressure:0.0034 mPa (20℃); Henry constant:2.40×10-3Pa m3 mol-1 (calc.); Partition coefficient(n-octanol and water):logP = 2.53; Solubility:In water 0.5 mg/l (20℃). In chloroform 1379, xylene 362, methanol 206, acetone 160, acetonitrile 28.6, hexane 4 (all in g/l, 20℃).; Stability:Stable to light, air and heat, and in acidic and alkaline media. Stable to 300℃. Aqueous solution in sunlight DT50 16.7 d.
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ToxicologyOral Acute oral LD50 for rats and mice >5000 mg/kg.Skin and eye Acute percutaneous LD50 for rats >5000 mg/kg. Mild eye irritant; non-irritating to skin (rabbits).Non-sensitising to skin (guinea pigs).Inhalation LC50 (4 h) for rats >2 mg/l air.
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Environmental ProfileEcotoxicology:
Birds Acute oral LD50 for mallard ducks >2510, Japanese quail >5000 mg/kg.Dietary LC50 (8 d) for mallard ducks and bobwhite quail >5620 mg/kg diet.Fish LC50 (96 h) for rainbow trout >300, bluegill sunfish 11.6 mg/l; (48 h) for carp 3.7 mg/l.Daphnia LC50 (48 h) 1.2 mg/l.Bees Not toxic to bees.LD50 by topical application >200 mg/bee.
Environmental fate:
Animals The main metabolite in urine and faeces is 5-(4-chlorophenyl)-N-(cis-4-hydroxycyclohexyl)-4-methyl-trans-2-oxothiazolidine-3-carboxamide. Soil/Environment DT50 in clay loam at 15℃, 8 d. In soil, undergoes oxidation to the corresponding hydroxy and carbonyl compounds. Koc 6200. -
Transport InformationSignal Word:CAUTION; Hazard Class:III(Slightly hazardous)
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