Search results
Results from the WOW.Com Content Network
The 2024 IRAC poster of insecticide modes of action includes the majority of chemicals listed below. [5] The pesticide manual provides much information on pesticides. [6] [7] Many of the insecticides in the list are not in use.
Indian toxicity label system Toxicity symbol for European toxicity class I and class II. Toxicity class refers to a classification system for pesticides that has been created by a national or international government-related or -sponsored organization.
Toxicity labels [1] viz; red label, yellow label, blue label and green label are mandatory labels employed on pesticide containers in India identifying the level of toxicity (that is, the toxicity class) of the contained pesticide. [1] [2] [3] The schemes follows from the Insecticides Act of 1968 [1] and the Insecticides Rules of 1971.
Mexican Brand Insect Fluid, "Under the Insecticide Act of 1910" The Federal Insecticide Act (FIA) of 1910 was the first pesticide legislation enacted. [2] This legislation ensured quality pesticides by protecting farmers and consumers from fraudulent and/or adulterated products by manufacturers and distributors.
Buprofezin is an insecticide used for control of insect pests such as mealybugs, leafhoppers and whitefly on vegetable crops. It is a growth regulator, acting as an inhibitor of chitin synthase (IRAC group 16). [2]
Dimethoate is a widely used organophosphate insecticide and acaricide.It was patented and introduced in the 1950s by American Cyanamid.Like other organophosphates, dimethoate is an acetylcholinesterase inhibitor which disables cholinesterase, an enzyme essential for central nervous system function.
Aldicarb is a carbamate insecticide which is the active substance in the pesticide Temik. It is effective against thrips, aphids, spider mites, lygus, fleahoppers, and leafminers, but is primarily used as a nematicide. [2] Aldicarb is a cholinesterase inhibitor which prevents the breakdown of acetylcholine in the synapse.
Chlorfenapyr was developed by American Cyanamid from the natural product dioxapyrrolomycin, which was isolated from Streptomyces fumanus. [2]The United States Environmental Protection Agency initially denied registration in 2000 for use on cotton primarily because of concerns that the insecticide was toxic to birds and because effective alternatives were available. [3]