| Customization: | Available |
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| Appearance: | Oil Based |
| Source: | Organic Synthesis |
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Abamectin + Pyridaben of Insecticide Pesticide & Acaricide (18g/l+100g/l EC, 20g/l+150g/l EC)
Abamectin
Abamectin(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.
Pyridaben
Pyridaben is an insecticide and acaricide that is approved for use in the EU and many other countries. It has a low aqueous solubility, relatively volatile and, based on its chemical properties, is not expected to leach to groundwater. It tends not to persist in soils or water systems. It is moderately toxic to mammals and not expected to bioaccumulate. It is highly toxic to most aquatic organisms and honey bees but less so to earthworms and birds.
Description: An insecticide and acaricide affective against thrips, mites, aphids and leafhoppers
Example pests controlled: Spider mites; Rust mites; Pear Psylla; Whiteflies
Example applications: Field crops; Fruit trees; Strawberries; Ornamentals; Vegetables; Greenhouse crops including cucumbers, tomatoes & peppers
Chemical structure:
| Isomerism | - |
| Chemical formula | C19H25CIN2OS |
| Canonical SMILES | CC(C)(C)C1=CC=C(C=C1)CSC2=C(C(=O)N(N=C2)C(C)(C)C)Cl |
| Isomeric SMILES | No data |
| International Chemical Identifier key (InChIKey) | DWFZBUWUXWZWKD-UHFFFAOYSA-N |
| International Chemical Identifier (InChI) | InChI=1S/C19H25ClN2OS/c1-18(2,3)14-9-7-13(8-10-14)12-24-15-11-21-22(19(4,5)6)17(23)16(15)20/h7-11H,12H2,1-6H3 |
| Pesticide type | Insecticide, Acaricide |
| Substance group | Pyridazinone |
| Minimum active substance purity | 980 g/kg |
| Known relevant impurities | EU dossier - None declared |
| Substance origin | Synthetic |
| Mode of action | Non-systemic with rapid knock down action and long residual activity. Inhibitor of mitochondrial electron transport at complex I. |
| CAS RN | 96489-71-3 |
| EC number | 405-700-3 |
| CIPAC number | 583 |
| US EPA chemical code | 129105 |
| PubChem CID | 91754 |
| Molecular mass (g mol-1) | 364.93 |
| PIN (Preferred Identification Name) | - |
| IUPAC name | 2-tert-butyl-5-(4-tert-butylbenzylthio)-4-chloropyridazin-3(2H)-one |
| CAS name | 4-chloro-2-(1,1-dimethylethyl)-5-(((4-(1,1-dimethylethyl)phenyl)methyl)thio)-3(2H)-pyridazinone |
| Other status information | PAN listed Highly Hazardous Chemical |
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