Azoxystrobin 8% + Dimethomorph 15% WG of Fungicide Pesticide
Azoxystrobin
Azoxystrobin is a broad-spectrum QoL fungicide that is approved for use at EU level. It has a low aqueous solubility, is non-volatile and imay leach to groundwater under certain conditions. It may be persistent in soil and can also be persistent in water systems if conditions are right. It has a low mammalian toxicity but may bioaccumulate. It is a skin and eye irritant. It is moderately toxic to birds, most aquatic life, honeybees and earthworms.
Description: A post-emergence broad spectrum strobilurin fungicide used mainly for cereals
Example pests controlled: Rusts; Powdery mildew; Black rot; Scab; Anthracnose; White mould; Peg rot; Early & late blight; Leaf spot; Rice blast; Botrytis
Example applications: Wheat; Fruit including grapes, citrus, strawberries, peaches; Sunflowers; Vegetables including onions, brassicas and curcubits; Potatoes; Cotton; pecans; Canola; Soybeans; Peanuts; Turf; Ornamentals
Chemical structure:
General status:
Dimethomorph
Description: A fungicide effective against various fungal pathogens in vines and other crops
Example pests controlled: Downy mildew; Anthracnose; Phytophthora cactorum, Septoria leaf spot; Late blight; Root rot; Crown rot
Example applications: Curcubits; Grapevines; Head lettuce; Onions; Potatoes; Fruit including blackberries, raspberries, strawberries, grapes
Chemical structure:
General status:
Azoxystrobin
Azoxystrobin is a broad-spectrum QoL fungicide that is approved for use at EU level. It has a low aqueous solubility, is non-volatile and imay leach to groundwater under certain conditions. It may be persistent in soil and can also be persistent in water systems if conditions are right. It has a low mammalian toxicity but may bioaccumulate. It is a skin and eye irritant. It is moderately toxic to birds, most aquatic life, honeybees and earthworms.
Description: A post-emergence broad spectrum strobilurin fungicide used mainly for cereals
Example pests controlled: Rusts; Powdery mildew; Black rot; Scab; Anthracnose; White mould; Peg rot; Early & late blight; Leaf spot; Rice blast; Botrytis
Example applications: Wheat; Fruit including grapes, citrus, strawberries, peaches; Sunflowers; Vegetables including onions, brassicas and curcubits; Potatoes; Cotton; pecans; Canola; Soybeans; Peanuts; Turf; Ornamentals
Chemical structure:
| Isomerism | Isomeric - E-form |
| Chemical formula | C22H17N3O5 |
| Canonical SMILES | COC=C(C1=CC=CC=C1OC2=NC=NC(=C2)OC3=CC=CC=C3C#N)C(=O)OC |
| Isomeric SMILES | CO/C=C(\C1=CC=CC=C1OC2=NC=NC(=C2)OC3=CC=CC=C3C#N)/C(=O)OC |
| International Chemical Identifier key (InChIKey) | WFDXOXNFNRHQEC-GHRIWEEISA-N |
| International Chemical Identifier (InChI) | InChI=1S/C22H17N3O5/c1-27-13-17(22(26)28-2)16-8-4-6-10-19(16)30-21-11-20(24-14-25-21)29-18-9-5-3-7-15(18)12-23/h3-11,13-14H,1-2H3/b17-13+ |
General status:
| Pesticide type | Fungicide |
| Substance group | Strobilurin |
| Minimum active substance purity | 965 g/kg |
| Known relevant impurities | EU dossier: Toluene |
| Substance origin | Synthetic |
| Mode of action | Systemic translaminar and protectant action having additional curative and eradicant properties. Respiration inhibitor (QoL fungicide). |
| CAS RN | 131860-33-8 |
| EC number | - |
| CIPAC number | 571 |
| US EPA chemical code | 128810 |
| PubChem CID | 3034285 |
| Molecular mass (g mol-1) | 403.4 |
| PIN (Preferred Identification Name) | methyl (2E)-2-(2-{[6-(2-cyanophenoxy)pyrimidin-4-yl]oxy}phenyl)-3-methoxyprop-2-enoate |
| IUPAC name | methyl (E)-2-{2-[6-(2-cyanophenoxy)pyrimidin-4-yloxy]phenyl}-3-methoxyacrylate |
| CAS name | methyl (αE)-2-[[6-(2-cyanophenoxy)-4-pyrimidinyl]oxy]-α-(methoxymethylene)benzeneacetate |
Dimethomorph
Description: A fungicide effective against various fungal pathogens in vines and other crops
Example pests controlled: Downy mildew; Anthracnose; Phytophthora cactorum, Septoria leaf spot; Late blight; Root rot; Crown rot
Example applications: Curcubits; Grapevines; Head lettuce; Onions; Potatoes; Fruit including blackberries, raspberries, strawberries, grapes
Chemical structure:
| Isomerism | Isomeric - a mixture of two isomers (E & Z) but only the Z-isomer has fungicidal activity |
| Chemical formula | C21H22ClNO4 |
| Canonical SMILES | COC1=C(C=C(C=C1)C(=CC(=O)N2CCOCC2)C3=CC=C(C=C3)Cl)OC |
| Isomeric SMILES | COC1=C(C=C(C=C1)/C(=C/C(=O)N2CCOCC2)/C3=CC=C(C=C3)Cl)OC |
| International Chemical Identifier key (InChIKey) | QNBTYORWCCMPQP-UHFFFAOYSA-N |
| International Chemical Identifier (InChI) | InChI=1S/C21H22ClNO4/c1-25-19-8-5-16(13-20(19)26-2)18(15-3-6-17(22)7-4-15)14-21(24)23-9-11-27-12-10-23/h3-8,13-14H,9-12H2,1-2H3/b18-14- |
General status:
| Pesticide type | Fungicide |
| Substance group | Morpholine |
| Minimum active substance purity | 965 g/kg (E/Z isomer ratio 44/56) |
| Known relevant impurities | EU dossier - None declared |
| Substance origin | Synthetic |
| Mode of action | Systemic with good protective activity. Cellulose synthesis inhibitor. |
| CAS RN | 110488-70-5 |
| EC number | 404-200-2 |
| CIPAC number | 483 |
| US EPA chemical code | 268800 |
| PubChem CID | 5889665 |
| Molecular mass (g mol-1) | 387.86 |
| PIN (Preferred Identification Name) | (2EZ)-3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)-1-(morpholin-4-yl)prop-2-en-1-one |
| IUPAC name | (EZ)-4-[3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)acryloyl]morpholine |
| CAS name | 4-(3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)-1-oxo-2-propenyl)morpholine |