Agrochemical pesticide fungicide azoxystrobin CAS 131860-33-8

Agrochemical Pesticide Fungicide Azoxystrobin CAS 131860-33-8DescriptionCommon NameAzoxystrobin  IUPACmethyl (E)-2-{2-[6-(2-cyanophenoxy)pyrimidin-4-yloxy]phenyl}-3-methoxyacrylate CASmethyl (αE)-2-[[6-(2-cyanophenoxy)-4-pyrimidinyl]oxy]-α-(methoxymethylene)benzeneacetate CAS No.131860-33-8 M

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Agrochemical Pesticide Fungicide Azoxystrobin CAS 131860-33-8


Common Name
Agrochemical Pesticide Fungicide Azoxystrobin CAS 131860-33-8
methyl (E)-2-{2-[6-(2-cyanophenoxy)pyrimidin-4-yloxy]phenyl}-3-methoxyacrylate
methyl (αE)-2-[[6-(2-cyanophenoxy)-4-pyrimidinyl]oxy]-α-(methoxymethylene)benzeneacetate
Molecular Formula
General Product Information
Fungicides > Strobilurin fungicides
Azoxystrobin is a systemic fungicide, active against AscomycetesBasidiomycetesDeuteromycetes andOomycetes. It has preventative, curative and translaminar properties and residual activity lasting for up to eight weeks on cereals. The product demonstrates slow, steady foliar uptake and moves only in the xylem. Azoxystrobin inhibits mycelial growth and also has anti-sporulant activity. It is particularly effective at the early stages of fungal development (especially at spore germination) due to its inhibition of energy production. The product is classified as a Group K fungicide.

Azoxystrobin has been found to be very toxic to Macintosh apple trees and any apple varieties derived from Macintosh; phytotoxicity has also been observed on some crabapples.
The product can be mixed with Ambush, Bravo, Captan, copper hydroxide, Dominex, Dipel, Karate, Larvin, Fortress (D0059), Talstar and Thiodan.
Azoxystrobin effectively controlled damping-off and foliar diseases of vegetables (e.g. lettuce, tomatoes) and ornamentals (e.g. roses, carnations) in Northern Italy.
Field trials in Taiwan showed promising control of a wide range of diseases of winter peppers and a 10% increase in yield following two or three applications of Amistar (25% SC).
Strobilurins and the structurally unrelated famoxadone and fenamidone form a cross-resistance group called Qol-STAR by FRAC. Rapid resistance first developed in Erisyphe graminis tritici and Sphaerotheca fuliginea, and is attributed to the same mutation. In controlled environment studies, resistant strains of the former were as fit as sensitive populations, but resistant strains of the latter were significantly less fit than sensitive wild-types. Results with Venturia inaequalis suggested a different resistance mechanism.
Isolates of Alternaria solani (early blight) collected from potato fields in the USA before and after the introduction of azoxystrobin showed large increases in EC50 correlating with lack of field efficacy.
In US cotton, in-furrow application of azoxystrobin improved seedling survival and, generally, final yield.
GR = Granule
SC = Suspension concentrate (=flowable concentrate)
WG = Water dispersible granules




Agrochemical Pesticide Fungicide Azoxystrobin CAS 131860-33-8

Agrochemical Pesticide Fungicide Azoxystrobin CAS 131860-33-8
Agrochemical Pesticide Fungicide Azoxystrobin CAS 131860-33-8



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Agrochemical Pesticide Fungicide Azoxystrobin CAS 131860-33-8
Agrochemical Pesticide Fungicide Azoxystrobin CAS 131860-33-8

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Agrochemical Pesticide Fungicide Azoxystrobin CAS 131860-33-8

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