WebA sub-lethal dose (0.0075 mg L-1) of Diafenthiuron was applied under short (2, 4 and 8 days) and long term (16, 32 and 64 days) experimental conditions. Our results indicated … WebProper shipping name: Toxic solid, organic, n.o.s. (Diafenthiuron) UN classfication 6.1 Subsidiary hazard class Packing group II Marine pollutant Yes IMDG UN number UN2811 Proper shipping name: Toxic solid, organic, n.o.s. (Diafenthiuron) UN classfication 6.1 Subsidiary hazard class Packing group II Marine pollutant (Sea) Yes

Toxicity of diafenthiuron to honey bees in laboratory, semi-field …

WebDissipation of foliar residues of diafenthiuron and its metabolites. 2002 Jun. 12012060. Selectivity of pesticides used on cotton (Gossypium hirsutum) to Trichogramma … WebAcute Toxicity for Acrobat Fungicide Technical Acute Toxicity Study Results Toxicity Category Acute Oral - Rats LD50 = 3900 (3300-4500) mg/kg (M,F) III Acute Oral - Mice … he4ardle

Toxicity of Diafenthiuron and Imidacloprid to the Predatory Bug

WebDiafenthiuron, a broad-spectrum insecticide and acaricide used for agricultural crop protection, is highly toxic to nontarget organisms. However, the developmental … Webtoxicity study and a safety factor of 100. Dermal absorption was determined for the representative formulation, Ronstar® as 2 % for the concentrate and 3% for the in-use spray dilution based on an in vitro study performed with human skin. The level of operator exposure for the representative formulation at a maximum dose rate of 750 Acute toxicity: diafenthiuron can be highly toxic, especially to invertebrates such as crustaceans and insects. Exposure to high concentrations of diafenthiuron can cause rapid death in these organisms. Chronic toxicity: prolonged exposure to lower concentrations of diafenthiuron can lead to chronic effects. 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 nitrilo (tert-butylcarbamate) group substituting … See more Diafenthiuron itself is not the active compound in the process of action. Diafenthiuron photochemically transforms into its highly … See more Efficacy Diafenthiuron has shown high efficacy against many important agricultural pests, including mites, … See more Diafenthiuron was introduced to the market in 1990 by a pharmaceutical company called Ciba-Geigy in Switzerland and due to rising environmental concerns it is no longer approved in Switzerland and other countries of the European Union. However, until … See more The synthesis of diafenthiuron includes a fenol reacting with 2,6-diisopropyl-4-chloroaniline, creating the intermediate product 2,6 … 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 gold falls today show