Fungicide Pesticide & Repellent Copper Oxychloride 35% + Metalaxyl 15% WP
Copper Oxychloride
A widely used copper fungicide that is approved for use in many countries including at EU level. It has a low aqueous solubility and a low volatility. As a heavy metal, copper itself will not degrade in the environment. It is moderately toxic to mammals and most biodiversity.
Description: A protectant copper fungicide and bactericide used as a foliar spray
Example pests controlled: Leaf spot; Downy mildew
Example applications: Ornamentals; Beet crops; Olives; Grapes; Tomatoes
Chemical structure:
General status:
Metalaxyl
Description: A fungicide used to control diseases caused by air- and soil-bornePeronosporales in many different crops
Example pests controlled: Downy mildew; Foliar and tuber blight; Damping-off
Example applications: Many agricultural crops including tobacco, potaoes, soybean, onions, citrus, cucubits, tomatoes, cotton; Ornamentals; Turf
Chemical structure:
General status:
Copper Oxychloride
A widely used copper fungicide that is approved for use in many countries including at EU level. It has a low aqueous solubility and a low volatility. As a heavy metal, copper itself will not degrade in the environment. It is moderately toxic to mammals and most biodiversity.
Description: A protectant copper fungicide and bactericide used as a foliar spray
Example pests controlled: Leaf spot; Downy mildew
Example applications: Ornamentals; Beet crops; Olives; Grapes; Tomatoes
Chemical structure:
Isomerism | None |
Chemical formula | (ClCu2H3O3)2 |
Canonical SMILES | O(Cl)Cl.[Cu+2] |
Isomeric SMILES | No data |
International Chemical Identifier key (InChIKey) | CPOSXJRGXIJOHG-UHFFFAOYSA-I |
International Chemical Identifier (InChI) | InChI=1S/2ClH.2Cu.3H2O/h2*1H;;;3*1H2/q;;2*+2;;;/p-5 |
General status:
Pesticide type | Fungicide, Repellent |
Substance group | Inorganic compound |
Minimum active substance purity | >569 6/Kg total copper |
Known relevant impurities | EU 2018 dossier: May contain heavy metals including Pb, Cd, As, Ni, CO, Sb & Hg |
Substance origin | Synthetic |
Mode of action | Absorbed copper disrupts the enzyme systems of pathogens. Multi-site activity. |
CAS RN | 1332-40-7 |
EC number | 215-572-9 |
CIPAC number | 44.602 |
US EPA chemical code | - |
PubChem CID | 18629822 |
Molecular mass (g mol-1) | 427.14 |
PIN (Preferred Identification Name) | dicopper(II) chloride trihydroxide |
IUPAC name | dicopper chloride trioxide |
CAS name | copper chloride hydroxide |
Metalaxyl
Description: A fungicide used to control diseases caused by air- and soil-bornePeronosporales in many different crops
Example pests controlled: Downy mildew; Foliar and tuber blight; Damping-off
Example applications: Many agricultural crops including tobacco, potaoes, soybean, onions, citrus, cucubits, tomatoes, cotton; Ornamentals; Turf
Chemical structure:
Isomerism | A chiral molecule that exists in the R- and S-forms |
Chemical formula | C15H21NO4 |
Canonical SMILES | CC1=C(C(=CC=C1)C)N(C(C)C(=O)OC)C(=O)COC |
Isomeric SMILES | No data |
International Chemical Identifier key (InChIKey) | ZQEIXNIJLIKNTD-UHFFFAOYSA-N |
International Chemical Identifier (InChI) | InChI=1S/C15H21NO4/c1-10-7-6-8-11(2)14(10)16(13(17)9-19-4)12(3)15(18)20-5/h6-8,12H,9H2,1-5H3 |
General status:
Pesticide type | Fungicide |
Substance group | Phenylamide |
Minimum active substance purity | 950 g/kg |
Known relevant impurities | EU dossier: 2,6-dimenthylaniline < 1 g/kg |
Substance origin | Synthetic |
Mode of action | Systemic with curative and protective action, acts by suppressing sporangial formation, mycelial growth and the establishment of new infectons. Disrupts fungal nucleic acid synthesis - RNA ploymerase 1. |
CAS RN | 57837-19-1 |
EC number | 260-979-7 |
CIPAC number | 365 |
US EPA chemical code | 113501 |
PubChem CID | 42586 |
Molecular mass (g mol-1) | 279.33 |
PIN (Preferred Identification Name) | - |
IUPAC name | methyl N-(methoxyacetyl)-N-(2,6-xylyl)-DL-alaninate |
CAS name | methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)-DL-alaninate |
Other status information | Potential groundwater contaminant |