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Chemical Identification
Common Name
Fenbuconazole
中文通用名
腈苯唑
IUPAC
(RS)-4-(4-chlorophenyl)-2-phenyl-2-(1H-1,2,4-triazol-1-ylmethyl)butyronitrile
CAS
α-[2-(4-chlorophenyl)ethyl]-α-phenyl-1H-1,2,4-triazole-1-propanenitrile
CAS No.
114369-43-6
Molecular Formula
C19H17ClN4
Molecular Structure
Category
Activity
Fungicide
Fenbuconazole is effective against ascomycetes, basidiomycetes and deuteromycetes. Following foliar application, the compound is translocated acropetally. Fenbuconazole has residual activity lasting 4-5 weeks. The optimum timing for protectant applications in wheat is at GS 38-45.


In field trials, fenbuconazole gave similar levels of disease control at lower application rates when compared with other azoles.
CropUse
CropUses:
apples, cereals, fruits (including vines), nuts, oilseed rape, ornamentals, pears, sugar beets, turf, vegetables, vines

Cereals

75-125 g ai/ha

Oilseed rape

60-75 g ai/ha

Sugar beet

65-280 g ai/ha

Peanuts

75-150 g ai/ha

Rice

50-150 g ai/ha

Turf

75-250 g ai/1,000m2

Vines

30-45 g ai/ha

Nuts

18-25 g ai/ha

Fruit

50-75 g ai/ha

Ornamentals

5-10 g ai/ha

Vegetables

50-100 g ai/ha

Premix

Emulsifiable concentrate (EC) ;Emulsion-in-water (EW) ;Suspension concentrate (SC);Wettable powder (WP) 
Premix Parters: 
cypermethrin; dimethoate; esfenvalerate; fenobucarb; fenvalerate; methabenzthiazuron; permethrin; tetramethrin; trichlorfon;

Physical Properties
Molecular weight:336.8; Physical form:Colourless crystals. Melting point:124-126 °C; Vapour pressure:0.005 mPa (20 °C); Partition coefficient(n-octanol and water):logP = 3.23; Solubility:In water 0.2 mg/l (25 °C). Soluble in common organic solvents such as ketones, esters, alcohols, and aromatic hydrocarbons. Insoluble in aliphatic hydrocarbons.; Stability:Stable to hydrolysis in the dark, DT50 >2210 d ( pH 5), 3740 d ( pH 7), 1370 d ( pH 9). Thermostable up to 300 °C.;
Toxicology
Oral:Acute oral LD50 for rats >2000 mg/ kg. Percutaneous:Acute percutaneous LD50 for rats >5000 mg/kg. Non-irritating to eyes and skin ( tech.); severe irritant to eyes and skin (EC formulation) (rabbits). Inhalation: LC50 (4 h) for rats >2.1 mg/l air (for tech.). ADI:0.005 mg/ kg.
Environmental Profile
Ecotoxicology: 
Bees: LC50 (96 h, dust exposure) >0.29 mg/bee.Birds:Dietary LC50 (8 d) for bobwhite quail 4050, mallard ducks 2110 mg/ kg diet. LC50 (21 d) for bobwhite quail 2150 mg/ kg daily.Fish: LC50 (96 h) for bluegill sunfish 0.68 mg/l ( tech.). 

Environmental fate: 
Soil:Soil adsorption Koc 2100-9000 (clay, loam, sand, sandy loam, silty clay loam).Plant:In peanuts, degraded by three routes: oxidation at the benzylic carbon, leading to oxidative degradation products including a ketone and some lactones, substitution on the carbon next to the triazole ring, leading to triazolylalanine and triazolylacetic a
Transport Information
Signal Word:CAUTION; Hazard Class:III(Slightly hazardous)

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