1.Name : azoxystrobin+cyproconazole+tebuconazole 11%+4%+12.5% FS
2.Chemical name
(2rs,3rs; 2rs,3sr)-2-(4-chloro-phenyl)-3-cyclopropyl-1-(1h-1,2,4-triazol-1-yl; triazole-1-ethanol,alpha-(4-chlorophenyl)-alpha-(1-cyclopropylethyl)-1h-2; alpha-(4-chlorophenyl)-alpha-(1-cyclopropylethyl)-1h-1,2,4-triazole-1-ethano; SHANDON
3.Molecular Weight : 291.78
5.Structure:
6.Technical Analysis
Suspension Rate |
Emulsifing Stability |
Wetting time |
Fineness(325mu) |
Low temp Stability |
Over75% |
Qualified |
Below40s |
Over98% |
Qualified |
7.Main formulation : Tebuconazole 43%SC/25%EC/25%EW/25%/40%WP/70%/80%WDG/6%ME and other compound formulations
8.Control Object :
This product is three triazole fungicide. Is a sterol demethylation inhibitor, has the function of prevention and treatment. For cereal crops, coffee, sugar beet, fruit trees and grapes on the Erysiphales, rust, the genus Neurospora spp., beak Cladosporium, Septoria, Venturia bacteria are effective. Fungicides and other mixed use, can be very good control of cereal eyespot disease, leaf spot and net blotch. Control wheat rust lasting for a period of 4 to 6 weeks, the prevention and control of powdery mildew of 3 ~ 4 weeks. Cereals, fruit and grape powdery mildew, peanuts, sugar beet leaf spot disease of apple scab and peanut white rot disease.
9.Technical Dosage Recommedation .For any further details,Pls contact our department plant protection for after-sales service:+86-513-55085866 Or write to us
Crop(Scope) |
Control Object |
Dosage |
Use Method |
Wheat |
Rust |
60-90g/ha |
Spray |
Wheat |
Stripe Rust |
75-112.5g/ha |
Spray |
Wheat |
Powdery Mildew |
93.75-121.875g/ha |
Spray |
Note :(1)Dosage of hectare =15*Mu dosage
(2)Total Effective Concentration(mg/Kg)=formulation content*1000000/
Formulation diluting times)
10. Colored Label in special package with Fluoride&HDPE bottles,Aluminum foil bags,water-soluble bags and cartons with pallets
IUPAC
(RS)-1-p-chlorophenyl-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol
CAS
α-[2-(4-chlorophenyl)ethyl]-α-(1,1-dimethylethyl)-1H-1,2,4-triazole-1-ethanol
CAS No.
107534-96-3
Molecular Formula
C16H22ClN3O
Category
Fungicides > Triazole fungicides
Activity
Fungicide
Tebuconazole is a systemic fungicide with protective and curative action. It is rapidly absorbed into the vegetative parts of the plant with translocation occurring acropetally.
CropUse
Tebuconazole is a fungicide for the control of smuts, bunt, seed rots and seedling blights on barley, oats and wheat as a seed treatment and for the control of Fusarium Head Blight on wheat as a post-emergent treatment.
Crop Uses:
| Cereals (target diseases: Rust species) |
125~250 g ai/ha |
| Cereals (target diseases: powdery mildew) |
200~250 g ai/ha |
| Cereals (target diseases: head scab) |
188~250 g ai/ha |
| Peanuts (target diseases: leaf spots) |
125~250 g ai/ha |
| Tea (target diseases: blister blight) |
25 g ai/ha |
| Bananas (target diseases: black leaf streak) |
100 g ai/ha |
Premix
Clothianidin+metalaxyl+prothioconazole+tebuconazole
Imidacloprid+imazalil+metalaxyl+tebuconazole
Imidacloprid+metalaxyl+tebuconazole
Imidacloprid+thiram+tebuconazole
Imidacloprid+tebuconazole
Trifloxystrobin+tebuconazole
Tebuconazole+fluoxastrobin
Chlorothalonil+tebuconazole
Fenaminstrobin+tebuconazole
Fluoxastrobin+prothioconazole+tebuconazole
Permethrin+dichlofluanid+tebuconazole
Permethrin+tebuconazole
Captan+tebuconazole
Azoxystrobin+tebuconazole
Tebuconazole+carbendazim
Tebuconazole+Prochloraz
tebuconazole+prothioconazole+metalaxyl+imidacloprid
Azoxystrobin+Metalaxyl+Tebuconazole
Pyraclostrobin+Tebuconazole
Tebuconazole+Prothioconazole+Metalaxyl
Thiophanate-methyl+Tebuconazole
Tebuconazole+Kresoxim-methyl
Emulsifiable concentrate, flowable, seed dressing, oil-water emulsion, water dispersible granule, wettable powder, emulsion for seed treatment.
Premix Parters: atrazine terbuthylazine; terbuthylazine; terbuthylazine terbutryn; alachlor; amitrole glyphosate; atrazine; atrazine terbumeton; bromoxynil; glyphosate; isoxaben; S-metolachlor; tembotrione; terbumeton; terbumeton terbutryn; terbutryn.
Physical Properties
Molecular weight:307.8 g/mol; Physical form:Colourless crystals; ( tech., colourless to light brown powder). Density:1.25 (26 °C); Composition:Racemate. Melting point:105 °C; Vapour pressure:1.7 × 10-3 mPa (20 °C) ( OECD 104); Henry constant:1 × 10-5 Pa m3 mol-1 (20 °C); Partition coefficient(n-octanol and water):logP = 3.7 (20 °C); Solubility:In water 36 mg/l ( pH 5-9, 20 °C). In dichloromethane >200, toluene 50-100, hexane <0.1 (all in g/l, 20 °C).; Stability:Stable to elevated temperatures, and to photolysis and hydrolysis in pure water, under sterile conditions; hydrolysis DT50 >1 y ( pH 4-9, 22 °C).
Toxicology
Oral:Acute oral LD50 for male rats 4000, female rats 1700, mice c. 3000 mg/kg.
Percutaneous:Acute percutaneous LD50 for rats >5000 mg/kg.
Non-irritating to skin; mild irritant to eyes (rabbits).
Inhalation: LC50 (4 h) for rats 0.37 mg/l air (aerosol), >5.1mg/l (dust).
Environmental Profile
Ecotoxicology:
Algae: ErC50 (96 h) for Scenedesmus subspicatus 4.01mg/l (static).Bees: LD50 (48 h) (oral) 175.8 μg/bee; (contact) 0.6 μg/bee.Birds:Acute oral LD50 for male Japanese quail 4438, female Japanese quail 2912, bobwhite quail 1988 mg/kg b.w. Dietary LC50 (5 d) for mallard ducks >4816, Daphnia: LC50 (48 h) 4.2 mg/l (flow through).Fish: LC50 (96 h) for rainbow trout 4.4, bluegill sunfish 5.7 mg/l (flow through).Worms:Acute LC50 (14 d) for Eisenia foetida 1381 mg/kg dry soil.Other aquatic spp.:No effect on Chironomus riparius at 0.1 mg/l (28 d).Other beneficial spp.:No adverse effects on ground dwellers, e.g. ground beetles (Poecilus cupreus) (adults and larvae) or on foliage dwellers, e.g. ladybirds (Coccinella septempunctata), up to 375 g/ha (EW 250 formulation).
Environmental fate:
Animals:After three days, elimination was almost complete (>99%). Tebuconazole was excreted with the urine and the faeces.Soil:The degradation of tebuconazole in soil was slow in laboratory studies. Under field conditions, the compound degraded much more rapidly, and did not accumulate in long-term studies (3-5 y). Since no residues could be detected in deeper soil layers of thesPlant:Metabolism studies on wheat, grapes and peanuts show that tebuconazole is the major terminal residue. The metabolites detected were mainly triazole-containing compounds of no toxicological relevance.
Acute oral LD50 (Japanese quail) |
4438 (male) |
Acute oral LD50 (Japanese quail) |
2912 (female) |
Acute oral LD50(bobwhite quail) |
1988 mg/kg b.w |
LC50 (rainbow trout) |
4.4 (96 h) |
LC50 (bluegill sunfish) |
5.7 mg/l |
LC50(Daphnia) |
4.2 mg/l (48 h) |
LD50 (Bees) |
175.8 μg/bee |
Transport Information
Signal Word:CAUTION; Hazard Class:III(Slightly hazardous)
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