| Weight | 411.325 g/mol |
|---|---|
| Formula | C21H24Cl2O4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 4 |
spirodiclofen (148477-71-8)
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- Genetic and biochemical analysis of a laboratory-selected spirodiclofen-resistant strain of Tetranychus urticae Koch (Acari: Tetranychidae) (Pest Management Science, 2009)
- Spirodiclofen resistance risk assessment in Tetranychus urticae (Acari: Tetranychidae): a biochemical approach (Pesticide Biochemistry and Physiology, 2002)
- Monitoring of resistance to spirodiclofen and five other acaricides in Panonychus citri collected from Chinese citrus orchards (Pest Management Science, 2010)
- Molecular analysis of resistance to acaricidal spirocyclic tetronic acids in Tetranychus urticae: CYP392E10 metabolizes spirodiclofen, but not its corresponding enol (Insect Biochemistry and Molecular Biology, 2013)
- Spirodiclofen and spiromesifen: Novel acaricidal and insecticidal tetronic acid derivatives with a new mode of action (Chimia, 2003)
- Effects of spirodiclofen on reproduction in a susceptible and resistant strain of Tetranychus urticae (Acari: Tetranychidae) (Experimental and Applied Acarology, 2009)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCC(C)(C)C(=O)OC1=C(C(=O)OC12CCCCC2)C3=C(C=C(C=C3)Cl)Cl
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InChIKeyDTDSAWVUFPGDMX-UHFFFAOYSA-N
- Pubchem - spirodiclofen
- Wikipedia - spirodiclofen
Spirodiclofen is an acaricide and insecticide used in agriculture to control mites and San Jose scale. In the United States, it is used on citrus, grapes, pome fruit, stone fruit, and tree nut crops. Spirodiclofen belongs to the tetronic acid class and acts by inhibiting lipid biosynthesis.
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