Abamectin 20g/l + Methoxyfenozide 80g/l SC of Insecticide PesticideAbamectinAbamectin(Avermectin B1)
Synonyms: Avermectin B1; Abamectinum; Affirm; Avermectin B(sub 1); Zephyr; Vertimec; Avomec; Avid; Agrimek; Agri-MEK
CAS: 71751-41-2
Formula: C48H72O14; C47H70O14
Molecular Weight: (873.09); (859.06)
EINECS: 265-610-3
Density: 1.244 g/cm3
Melting Point: 0-155 ° C
Boiling Point: 940.912 ° C at 760 mmHg
Flash Point: 268.073 ° C
Usage: Abamectin is used to control insect and mite pests of a range of agronomic, fruit, vegetable
Introduction:Abamectin is a mixture of avermectins containing more than 80% avermectin B1a and less than 20% avermectin B1b. These two components, B1a and B1b have very similar biological and toxicological properties. The avermectins are insecticidal or anthelmintic compounds derived from the soil bacterium Streptomyces avermitilis. Abamectin is a natural fermentation product of this bacterium. Abamectin is used to control insect and mite pests of a range of agronomic, fruit, vegetable and ornamental crops, and it is used by homeowners for control of fire ants. Abamectin is also used as a veterinary antihelmintic. Resistance to abamectin based antihelmintics, although a growing problem, is not as common as to other classes of veterinary antihelmintics.
MethoxyfenozideAn insectide approved for use in the EU and many other countries on a broad range of fruit and vegetables. It has a low aqueous solubility and a low volatility. Based on its chemical properties there is a high risk of leaching to groundwater and under some conditions it may be persistent in soil systems. It has a low oral toxicity to mammals and no significant risk issues to human health have been identified. It has a low toxicity to birds and honeybees but is relatively more toxic to aquatic species and earthworms.
Description: An insecticide used to control various insects including moths and butterflies
Example pests controlled: Codling moth; Lesser appleworm; Oriental fruit moth; Leafrollers; Loopers; Cotton bollworm; Armyworm; Bud moths
Example applications: Leafy vegetables; Fresh herbs; Lettuce; Salads; Herbs; Brassicas; Cotton; Pome fruit; Grapes; Sweetcorn; Maize; Peppers; Aubergines
Chemical structure: | Isomerism | - |
| Chemical formula | C22H28N2O3 |
| Canonical SMILES | CC1=CC(=CC(=C1)C(=O)N(C(C)(C)C)NC(=O)C2=C(C(=CC=C2)OC)C)C |
| Isomeric SMILES | No data |
| International Chemical Identifier key (InChIKey) | QCAWEPFNJXQPAN-UHFFFAOYSA-N |
| International Chemical Identifier (InChI) | InChI=1S/C22H28N2O3/c1-14-11-15(2)13-17(12-14)21(26)24(22(4,5)6)23-20(25)18-9-8-10-19(27-7)16(18)3/h8-13H,1-7H3,(H,23,25) |
| Pesticide type | Insecticide |
| Substance group | Diacylhydrazine |
| Minimum active substance purity | 970 g/kg |
| Known relevant impurities | EU dossier - butylhydrazine |
| Substance origin | Synthetic |
| Mode of action | A moulting accelerator that is an agonist of the hormone 20-hydroxyecdysone |
| CAS RN | 161050-58-4 |
| EC number | - |
| CIPAC number | 656 |
| US EPA chemical code | 121027 |
| PubChem CID | 105010 |
| Molecular mass (g mol-1) | 368.47 |
| PIN (Preferred Identification Name) | - |
| IUPAC name | N-tert-butyl-N'-(3-methoxy-o-toluoyl)-3,5-xylohydrazide |
| CAS name | 3-methoxy-2-methylbenzoic acid 2-(3,5-dimethylbenzoyl)-2-(1,1-dimethylethyl)hydrazide |