WebDiafenthiuron reference standards, CAS number: 80060-09-9, for unparalleled analytical testing within the food and beverage sector. Buy online at LGC Standards. ... Forensic & Toxicology. LoGiCal. Drugs, metabolites & related standards. Test with confidence. Our Products View all. New psychoactive substances (NPS) WebEFSA - Wiley Online Library
Molecular Toxicology 9
WebApr 1, 1996 · Diafenthiuron was practically nontoxic to P. maculiventris when applied topically. However, both ingestion and residual contact caused severe mortality. In general, adults were more sensitive to diafenthiuron than 5th-instar nymphs. For imidacloprid, toxicity decreased in order of topical exposure > ingestion > residual contact. WebJan 27, 2024 · Diafenthiuron. Unknown. EPA Applications/Systems. Below are the EPA applications/systems, statutes/regulations, or other sources that track or regulate this substance. This table shows how each list refers to the substance. To view more metadata about the specific Synonym, click on the Synonym. EPA Applications/Systems. curcumin with black seed oil
DIAFENTHIURON - National Center for Advancing Translational …
WebPesticides have been blamed as the principal factor responsible for biological disequilibrium favoring the population increase of Panonychus citri (McGregor) in Brazilian citrus groves. In order to generate subsidies for the integrated management of this pest, we evaluated the lethal and sublethal effects of pesticides used in citrus on P. citri. Diafenthiuron has shown high efficacy against many important agricultural pests, including mites, aphids, thrips, and whiteflies. ... This considerably decreases the time frame of possible exposure and therefore reduces inducible toxicity by Diafenthiuron metabolism. Toxicology assessments and … See more Diafenthioron is a pesticide, specifically an insecticide. It is a chemical compound which belongs to the thiourea group. See more Diafenthiuron is an aromatic ether of molecular weight 384.6 g/mole and containing two 6-carbon rings attached to an oxygen and … See more Diafenthiuron itself is not the active compound in the process of action. Diafenthiuron photochemically transforms into its highly reactive metabolite, carbodiimide, which covalently and irreversibly binds to microsomal glucose-6-phosphate … See more Diafenthiuron was introduced to the market in 1990 by a pharmaceutical company called Ciba-Geigy in Switzerland and due to rising … See more The synthesis of diafenthiuron includes a fenol reacting with 2,6-diisopropyl-4-chloroaniline, creating the intermediate product 2,6-diisopropyl-4-phenoxyaniline. 2,6-Diisopropyl-4 … See more Diafenthiuron can be metabolized by the P450 cytochrome in the liver but can also be activated by light in insects to carbodiimide (its … See more Efficacy Diafenthiuron has shown high efficacy against many important agricultural pests, including mites, aphids, thrips, and whiteflies. Several studies have demonstrated the efficacy of diafenthiuron in controlling … See more curcumin with black pepper