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Pyraclostrobin 133g/l + Cyproconazole 120g/l SC

产品介绍: PyraclostrobineIUPAC name methyl N-{2-[1-(4-chlorophenyl)pyrazol-3-yloxymethyl]phenyl}(N-methoxy)carbamateCAS RN [175013–18–0] Mol. wt. 387.8 M.f. C19H18ClN3O4  Chemical Group: methoxycarbamateCyproconazoleIUPAC name (2RS,3RS;2RS,3SR)-2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-olCAS RN [94361–06–5] unstated stereochemistry, formerly [113096–99–4]; [94361–07–6] (2RS,3SR)- isomers  Mol. wt. 291.8 M.f. C15H18ClN3O  Chemical Group:  triazole
 

Pyraclostrobin 133g/l + Cyproconazole 120g/l SC

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  • Specification
  • Applications

Pyraclostrobine

IUPAC name methyl N-{2-[1-(4-chlorophenyl)pyrazol-3-yloxymethyl]phenyl}(N-methoxy)carbamate

CAS RN [175013–18–0] 

Mol. wt. 387.8 

M.f. C19H18ClN3O4  

Chemical Group: methoxycarbamate


Cyproconazole

IUPAC name (2RS,3RS;2RS,3SR)-2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol

CAS RN [94361–06–5] unstated stereochemistry, formerly [113096–99–4]; [94361–07–6] (2RS,3SR)- isomers  

Mol. wt. 291.8 

M.f. C15H18ClN3O  

Chemical Group:  triazole


Pyraclostrobin 133g/l + Cyproconazole 120g/l SC

Mode of action 

Pyraclostrobine  Fungicide with protectant, curative and translaminar properties. Also causes physiological effects like delayed senescence, greener leaves, better tolerance against biotic and abiotic stress, as well as more efficient use of water and nitrogen. 

Cyproconazole Systemic fungicide with protective, curative, and eradicant action. Absorbed rapidly by the plant, with translocation acropetally.

Uses   Control of major plant pathogens such as Septoria, rust, powdery mildew, Rhynchosporium, Cercospora and Ramularia in cereals and sugar beet.

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