| Weight | 325.191 g/mol |
|---|---|
| Formula | C16H14Cl2O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 4 |
CHLOROBENZILATE (510-15-6)
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- Muscarinic receptor in house fly brain and its interaction with chlorobenzilate (Pesticide Biochemistry and Physiology, 1981)
- Worker environment research: residues from carbaryl, chlorobenzilate, dimethoate, and trichlorfon applied to citrus trees (Journal of Agricultural and Food Chemistry, 1979)
- Comparative metabolism of chlorobenzilate, chloropropylate, and bromopropylate acaricides by rat hepatic enzymes. (Canadian Journal of Physiology and Pharmacology, 1971)
- Exposure of spray applicators and mixer-loaders to chlorobenzilate miticide in Florida citrus groves (Archives of Environmental Contamination and Toxicology, 1983)
- Dissipation and Movement of Acaricide Chlorobenzilate in the Environment (Ecotoxicology and Environmental Safety, 1994)
- Acaricide Determination, Microdetermination of Acaricide Ethyl p,p-Dichlorobenzilate (Chlorobenzilate) (Journal of Agricultural and Food Chemistry, 1954)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H320: Causes eye irritation
Warning Serious eye damage/eye irritation - Category 2B - H373: Causes damage to organs through prolonged or repeated exposure
Warning Specific target organ toxicity, repeated exposure - Category 2 - H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 -
SMILESCCOC(=O)C(C1=CC=C(C=C1)Cl)(C2=CC=C(C=C2)Cl)O
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- Pubchem - CHLOROBENZILATE
- Wikipedia - chlorobenzilate
Chlorobenzilate is a pesticide that is not currently used in the USA or Europe. It was originally developed by Ciba-Geigy and introduced in 1952. It was used as an acaricide against mites on citrus trees, including deciduous fruit trees.
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CHLOROBENZILATE
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