WebDICOFOL is an organochlorine bridged diphenyl. Halogenated aliphatic compounds are moderately or very reactive. Halogenated organics generally become less reactive as … WebC-labeled p,p′-dicofol and o,p′-dicofol in separate experiments. The metabolites DCBP and DCBH were detected in tomatoes 21 days after treatment, but less was formed from the major dicofol isomer, -dicofol, than from -dicofol. p,po,p′′ Less than 1% TRR was comprised on DCBP and DCBH in the p,p′-dicofol experiment, while the sum
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WebSubstance Details Internal Tracking Number: 29157 Substance Type: Chemical Substance Systematic Name: Benzenemethanol, 4-chloro-.alpha.- (4-chlorophenyl)-.alpha.- (trichloromethyl)- CAS Number: 115-32-2 EPA Registry Name: Dicofol Molecular Weight: 370.49 Molecular Formula: C14H9Cl5O Additional Metadata WebJan 23, 2024 · In contrast, DDx levels measured downstream of Pieve Vergonte (1.28–97.97 ng g −1 d.w.) are comparable to those detected in other polluted sites, such as on the Cinca River in Spain , which are downstream of an industry which uses DDT as an intermediate in the production of dicofol, or such as the Fuchun reservoir of Qiantang River in China ...
Dicofol is an organochlorine pesticide that is chemically related to DDT. Dicofol is a miticide that is very effective against spider mite. Its production and use is banned internationally under the Stockholm Convention. One of the intermediates used in its production is DDT. This has caused criticism by many … See more Dicofol is structurally similar to DDT. It differs from DDT by the replacement of the hydrogen (H) on C-1 by a hydroxyl (OH) functional group. One of the intermediates used in its production is DDT. See more Dicofol is usually synthesized from technical DDT. During the synthesis, DDT is first chlorinated to an intermediate, Cl-DDT, followed by … See more Foliar spray on agricultural crops and ornamentals, and in or around agricultural and domestic buildings for mite control. It is formulated as emulsifiable concentrates, wettable powders, dusts, ready-to-use liquids, and aerosol sprays. In many countries, dicofol is … See more The Pesticide Survey, USA 1987 through 1996, reports that the total annual domestic agricultural usage of dicofol averaged about … See more Manufacturing-use dicofol products contain a number of DDT analogs as manufacturing impurities. These include the o,p' and p,p' isomers of DDT, DDE, DDD, and a substance called extra-chlorine DDT or Cl-DDT See more Dicofol first appeared in the scientific literature in 1956, and was introduced onto the market by the US-based multinational company Rohm & Haas in 1957. Other current … See more The California Department of Food and Agriculture has one of the world's most extensive incident reporting systems. Between 1982 and 1992, 38 incidents involving dicofol alone were reported: systemic 19 (50%); skin 10 (26%); eye 8 (21%); and … See more WebDicofol (WHO Pesticide Residues Series 4) DICOFOL JMPR 1974 Explanation Dicofol was evaluated by the Joint Meeting in 1968 with a minor amendment in 1970 …
WebDicofol (WHO Pesticide Residues Series 4) DICOFOL JMPR 1974 Explanation Dicofol was evaluated by the Joint Meeting in 1968 with a minor amendment in 1970 (FAO/WHO, 1969, 1971). Tolerances of 5 mg/kg were established for broad classes of fruit and vegetables, tea (dry manufactured) and hops. WebJan 15, 2024 · SUMMARY Dicofol is an organochloride acaricide. It has a low aqueous solubility, volatile and, based on its chemical properties, is unlikely to leach to groundwater. It is moderately persistent in soils but does not normally persist in water. It is moderately toxic to mammals and has a high tendency to bioaccumulate.
WebDicofol is an agricultural insecticide with 11 current product labels registered in the United States. It is structurally similar to DDT, but contains a central hydroxyl group that …
WebThis document presents the Agency's decision regarding the reregistration eligibility of the registered uses of dicofol. Section I is the introduction; Section II describes dicofol, its uses, data requirements and regulatory history; Section III discusses the human health and environmental assessment based on the data available to the Agency ... iphone hotspot setupWebDicofol is an organochlorine miticide that is used on a wide variety of crops, including cotton, citrus, tree nuts, beans, apples, stonefruit, cucurbits, wine grapes, strawberries, mint, and peppers. It is moderately persistent in the environment (U.S. EPA, 1998, p. 74). Workers involved in the manufacture and application of dicofol, and those ... iphone hotspot vs mifi performanceWebDicofol is a white or brown waxy solid. Chemical Properties. Pure dicofol is available as a white or gray powder or colorless solid crystals while the technical dicofol is a red-brown or amber viscous liquid with an odor like fresh-cut hay. Dicofol undergoes decomposition on burning or on contact with acids, acid fumes or bases, producing toxic ... iphone hotspot maximise compatibilityWebDicofol comprised the major portion of the residue, with some conversion to the metabolites DCBP and DCBH over time. In tomato experiments with a 21 day PHI, < 1% TRR was … iphone hotspot nameWebDicofol metabolites were found in kidney fat, liver, udder, brain, kidney lungs, blood, heart, omentum, bone marrow and muscles (Rohm and Haas, 1968). The feeding of dicofol to steers produces no significant residues in body fat at a level of 0.75 and 1.5 ppm. A feeding level of 3.0 ppm produces a definite residue of 0.32 ppm (Peoples, 1967). iphone hotspot timeoutWebapplication of dicofol on cultivated crops, orchards/vineyards, and turf, and expanded to include the total area where there is potential for direct or indirect effects to occur via off-site transport mechanisms. The extent of potential off-site … iphone hotspot über bluetoothWebPublic Health Statement for Dichlorvos. Spanish: Diclorvos. CAS#: 62-73-7. PDF Version [129 KB] This Public Health Statement is the summary chapter from the Toxicological … iphone hotspot usb windows 11