Cyproconazole+Trifloxystrobin

产品介绍： CyproconazoleIUPAC 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: triazoleTrifloxystrobinIUPAC name methyl (E)-methoxyimino-{(E)-α-[1-(α,α,α-trifluoro-m-tolyl)ethylideneaminooxy]-o-tolyl}acetateCAS RN [141517–21–7], formerly [221007–60–9] Mol. wt. 408.4 M.f. C20H19F3N2O4 Chemical Group: oximinoacetate

Cyproconazole 375g/l +Trifloxystrobin 165g/l SC

Cyproconazole 160g/l +Trifloxystrobin 375g/l SC

Information
Specification
Applications

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

Trifloxystrobin

IUPAC name methyl (E)-methoxyimino-{(E)-α-[1-(α,α,α-trifluoro-m-tolyl)ethylideneaminooxy]-o-tolyl}acetate

CAS RN [141517–21–7], formerly [221007–60–9]

Mol. wt. 408.4

M.f. C20H19F3N2O4

Chemical Group: oximinoacetate

Cyproconazole 375g/l +Trifloxystrobin 165g/l SC

Cyproconazole 160g/l +Trifloxystrobin 375g/l SC

Mode of action

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

Trifloxystrobin Mesostemic, broad-spectrum fungicide with mainly preventive activity. Particular characteristics are redistribution by superficial vapour movement and surface water, good rain-fastness, and residual activity.

Uses Registered for use in field crops: cereals, soya beans, corn, rice, cotton, peanuts, sugar beet and sunflowers; horticultural crops: pome fruit, stone fruit, tropical fruit, bananas, grapes, soft fruit, and many vegetables, as well as ornamentals and turf.