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Malathion is a pesticide that is widely used in agriculture, residential landscaping, public recreation areas, and in public health pest control programs such as mosquito eradication. [5] In the US, it is the most commonly used organophosphate insecticide.
The industry-sponsored Insecticide Resistance Action Committee (IRAC) advises on the use of insecticides in crop protection and classifies the available compounds according to their chemical structures and mechanism of action so as to manage the risks of pesticide resistance developing. [4]
Banned in US for home and garden use. Should never be sprayed on flowering crops especially if bees are active and the crop requires pollination. Highly toxic Coumaphos [30] Checkmite Organophosphate: This is an insecticide that is used inside the beehive to combat varroa mites and small hive beetles, which are parasites of the honey bee ...
In addition, Malathion was no longer used alone, but mixed in a 4:1 ratio with Nu-Lure0 bait to attract insects to the area. [20] The period of infestation stretched from July 1989 through November 1990. [21]
The cotton stalks are shredded and plowed into the ground to eliminate their use as a winter shelter. During years 2 through 5, the automatic spraying is supplemented by an intensive trapping program (one trap per 1–2 acres), and malathion applications are made only in those fields where weevils are detected.
Also derivatives containing the thiophosphoryl group (P=S) include the pesticide malathion. The organophosphates prepared on the largest scale are the zinc dithiophosphates, as additives for motor oil. Several million kilograms of this coordination complex are produced annually by the reaction of phosphorus pentasulfide with alcohols. [6]
Azinphos-methyl is a neurotoxin derived from nerve agents developed during World War II. [4] It was first registered in the US in 1959 as an insecticide and is also used as active ingredient in organophosphate (OP) pesticides. [6]
Isomalathion is an impurity found in some batches of malathion. Whereas the structure of malation is, generically, RSP(S)(OCH 3) 2, the connectivity of isomalathion is RSPO(SCH 3)(OCH 3). It arises by heating malathion. Being significantly more toxic to humans than malathion, it has resulted in human poisonings. [1]
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