Fungicide Pesticide Propamocarb Hydrochloride 10% + Metalaxyl 15% WPMetalaxylDescription: 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 |
Propamocarb HydrochlorideDescription: A fungicide for specific control of Phycomycetes and effective against Phytophthora spp. and Pythium spp.
Example pests controlled: Late blight; Root rot; Damping off; Downy mildew (
Bremia lactucae); Mildew
Example applications: Turf; Ornamentals; Tobacco; Vegetables; Potatoes; Strawberries; Cucumbers; Tomato; Lettuce
Chemical structure: Isomerism | - |
Chemical formula | C9H21ClN2O2 |
Canonical SMILES | CCCOC(=O)NCCCN(C)C.Cl |
Isomeric SMILES | No data |
International Chemical Identifier key (InChIKey) | MKIMSXGUTQTKJU-UHFFFAOYSA-N |
International Chemical Identifier (InChI) | InChI=1S/C9H20N2O2.ClH/c1-4-8-13-9(12)10-6-5-7-11(2)3;/h4-8H2,1-3H3,(H,10,12);1H |
General status: Pesticide type | Fungicide |
Substance group | Carbamate |
Minimum active substance purity | 92-97% |
Known relevant impurities | EU dossier - None declared |
Substance origin | Synthetic |
Mode of action | Systemic, with protective action absorbed by roots and leaves and translocated. Lipid synthesis inhibitor. |
CAS RN | 25606-41-1 |
EC number | 247-125-9 |
CIPAC number | 399.601 |
US EPA chemical code | 119302 |
PubChem CID | 15575641 |
Molecular mass (g mol-1) | 224.73 |
PIN (Preferred Identification Name) | - |
IUPAC name | propyl 3-(dimethylamino)propylcarbamate hydrochloride |
CAS name | propyl (3-(dimethylamino)propyl)carbamate monohydrochloride |