299-84-3
Chemical Structure
Fenchlorphos
- CAS No.: 299-84-3
- Formula:C8H8Cl3O3PS
- Molecular Weight:321.55
IUPAC Name: O,O-dimethyl O-(2,4,5-trichlorophenyl) phosphorothioate
InChIKey: JHJOOSLFWRRSGU-UHFFFAOYSA-N
SMILES: S=P(OC)(OC)OC1=CC(Cl)=C(Cl)C=C1Cl
Biological Activity: Fenchlorphos, an organophosphate, is an insecticide. Fenchlorphos is an inhibitor of the enzyme acetylcholinesterase (AChE). Fenchlorphos is able to cause mitochondrial dysfunction[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Fenchlorphos | 98.44% | Fenchlorphos, an organophosphate, is an insecticide. Fenchlorphos is an inhibitor of the enzyme acetylcholinesterase (AChE). Fenchlorphos is able to cause mitochondrial dysfunction. | ||||||||||||||||||||
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Fenchlorphos (Standard) | ≥98% | Fenchlorphos (Standard) is the analytical standard of Fenchlorphos. This product is intended for research and analytical applications. Fenchlorphos, an organophosphate, is an insecticide. Fenchlorphos is an inhibitor of the enzyme acetylcholinesterase (AChE). Fenchlorphos is able to cause mitochondrial dysfunction. | ||||||||||||||||||||
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Dichlofenthion | Dichlofenthion is an organophosphorus (OP) pesticide. Dichlofenthion can be for the control of sheep maggot fly. | |||||||||||||||||||||
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Iodofenphos (Standard) | ≥98% | Iodofenphos (Standard) is the analytical standard of Iodofenphos. This product is intended for research and analytical applications. Iodofenphos (Jodfenphos) is an insecticide, that can be used as a protectant for stored grains. Iodofenphos is effective against grain pests, such as Sitophilus oryzae, Tribolium castaneum, and larvae of Trogoderma granarium, and has a significant residual toxicity, which could provide good insect control for several months. | ||||||||||||||||||||
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Cythioate | Cythioate is an organophosphorous insecticide and anthelmintic. Cythioate is an acetylcholinesterase inhibitor which interferes with neuromuscular transmission in ectoparastites. | |||||||||||||||||||||
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Bromofos | Bromofos is an active compound. | |||||||||||||||||||||
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Fenitrothion | 99.43% | Fenitrothion is a broad-spectrum and orally active insecticide/acaricide. Fenitrothion inhibits cholinesterase, AMPKα and IRS1/PI3K/AKT. Fenitrothion causes Apoptosis, reduces SOD activity. Fenitrothion shows insecticidal effect against Rhyzopertha dominica and Tribolium castaneum adults. Fenitrothion is widely used in cotton crops, vegetable crops, fruit crops and field crops, especially rice. Fenitrothion can be used for brain and spleen toxicology studies. | ||||||||||||||||||||
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Isochlorthion | Isochlorothion is an organic phosphorus pesticide. |
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Tolclofos-methyl | 98.52% | Tolclofos-methyl is an organophosphorus fungicide. Tolclofos-methyl undergoes photoinduced oxidative degradation to form oxo-analog derivatives. Tolclofos-methyl inhibits spore division in fungi and oomycetes, induces cytoplasmic leakage, and interferes with flagellar movement. Tolclofos-methyl is rapidly metabolized and excreted in rodents. Tolclofos-methyl can be used in studies related to fungal infections. | ||||||||||||||||||||
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Chlorthion | Chlorthion is an organic phosphorothionate insecticide. Chlorthion inhibits liver microsomal hydroxylation of testosterone. | |||||||||||||||||||||
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Fenthion sulfoxide | 98.02% | Fenthion sulfoxide is a metabolite of the organophosphate insecticide Fenthion. Fenthion sulfoxide can be formed from the transformation of Fenthion on grapes. | ||||||||||||||||||||
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O-(2,4-Dichlorophenyl) O-methyl isopropylphosphoramidothioate | O-(2,4-Dichlorophenyl) O-methyl isopropylphosphoramidothioate (Zytron) is a herbicide. At conventional application doses, Zytron exerts no adverse effects on molds, actinomycetes or soil bacteria in field plots or model systems. Zytron can be degraded by Aspergillus clavatus. | |||||||||||||||||||||
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References
- [1]. Nafstad I, et, al. Teratogenic effects of the organophosphorus compound fenchlorphos in rabbits. Acta Vet Scand. 1983;24(3):295-304. [Content Brief]
- [2]. Rimkus SA, et, al. A pharmacological screen for compounds that rescue the developmental lethality of a Drosophila ATM mutant. PLoS One. 2018 Jan 16;13(1):e0190821. [Content Brief]