Diafenthiuron 32% + Thiacloprid 8% SC Insecticide Pesticide & Acaricide Miticide MolluscicideDiafenthiuronDiafenthiuron is an insecticide and acaricide without regulatory approval for use in the EU. It has a low aqueous solubility but is readily soluble in many organic solvents. It is volatile and, based on its chemical properties, it is unlikely to leach to groundwater. It is not persistent in most soil systems but may be very persistent in aquatic systems. It has a low mammalian toxicity but is moderate to highly toxic for most biodiversity including aquatic life, bees and worms.
Description: An insecticide and acaricide effective against phytophagous mites and other sucking pestsExample pests controlled: Aphids; Whiteflies; Spidermites; Diamondback moth; thrips; JassidsExample applications: Cotton; Fruit trees; Ornamentals; SoybeansChemical structure: | Isomerism | None |
| Chemical formula | C23H32N2OS |
| Canonical SMILES | CC(C)C1=CC(=CC(=C1NC(=S)NC(C)(C)C)C(C)C)OC2=CC=CC=C2 |
| Isomeric SMILES | No data |
| International Chemical Identifier key (InChIKey) | WOWBFOBYOAGEEA-UHFFFAOYSA-N |
| International Chemical Identifier (InChI) | InChI=1S/C23H32N2OS/c1-15(2)19-13-18(26-17-11-9-8-10-12-17)14-20(16(3)4)21(19)24-22(27)25-23(5,6)7/h8-16H,1-7H3,(H2,24,25,27) |
| Pesticide type | Insecticide, Acaricide, Miticide |
| Substance group | Thiourea |
| Minimum active substance purity | - |
| Known relevant impurities | - |
| Substance origin | Synthetic |
| Mode of action | Broad spectrum, contact and stomach action with some ovicidal activity, acts by inhibiting oxidative phosphorylation |
| CAS RN | 80060-09-9 |
| EC number | - |
| CIPAC number | 8097 |
| US EPA chemical code | - |
| PubChem CID | 3034380 |
| Molecular mass (g mol-1) | 384.58 |
| PIN (Preferred Identification Name) | N-tert-butyl-N'-[2,6-di(propan-2-yl)-4-phenoxyphenyl]carbonothioic diamide |
| IUPAC name | 1-tert-butyl-3-(2,6-diisopropyl-4-phenoxyphenyl)thiourea |
| CAS name | N-(2,6-bis(1-methylethyl)-4-phenoxyphenyl)-N'-(1,1-dimethylethyl)thiourea |
| Other status information | PAN Listed as Highly Hazardous Chemical |
Example pests controlled: Aphids; Pollen beetles; Blossom midge; Codling moth; Wireworm; Fruit fly
Example applications: Apples; Pears; Some citrus crops; Brussel sprouts; Cabbage; Cauliflower; Carrot; Parsnip; Peas; Potato; Oilseed rape
Chemical structure: | Isomerism | Isomeric - exists in the E- and Z- forms. Technical products are predominately comprised of the Z- form. |
| Chemical formula | C10H9CIN4S |
| Canonical SMILES | C1CSC(=NC#N)N1CC2=CN=C(C=C2)Cl |
| Isomeric SMILES | No data |
| International Chemical Identifier key (InChIKey) | HOKKPVIRMVDYPB-UVTDQMKNSA-N |
| International Chemical Identifier (InChI) | InChI=1S/C10H9ClN4S/c11-9-2-1-8(5-13-9)6-15-3-4-16-10(15)14-7-12/h1-2,5H,3-4,6H2/b14-10- |
| Pesticide type | Insecticide, Molluscicide |
| Substance group | Neonicotinoid |
| Minimum active substance purity | 975 g/kg |
| Known relevant impurities | EU and FAO dossiers - None declared |
| Substance origin | Synthetic |
| Mode of action | Contact and stomach action with some systemic properties. Acetylcholine receptor (nAChR) agonist. |
| CAS RN | 111988-49-9 |
| EC number | - |
| CIPAC number | 631 |
| US EPA chemical code | 014019 |
| PubChem CID | 115224 |
| Molecular mass (g mol-1) | 252.72 |
| PIN (Preferred Identification Name) | ((2Z)-3-((6-chloropyridin-3-yl)methyl)-1,3-thiazolidin-2-ylidene}cyanamide |
| IUPAC name | (Z)-3-(6-chloro-3-pyridylmethyl)-1,3-thiazolidin-2-ylidenecyanamide |
| CAS name | (Z)-(3-((6-chloro-3-pyridinyl)methyl)-2-thiazolidinylidene)cyanamide |
| Other status information | NOTE ban or usage restriction may be in place for use on flowering crops in some Member States |