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The imidazolinone herbicides were first discovered in the 1970s. The first U.S. patent was awarded in 1980 for imazamethabenz-methyl. Imazaquin, imazapyr, imazapic, and imazethpyr followed suit and received patents in 1989. Imazamox, the last of the six, received its U.S. patent in 1994. [4]
Imazapic is a chemical used as an herbicide. It controls many broad leaf weeds and controls or suppresses some grasses in pasture, rangeland and certain types of turf. It has a half-life of around 120 days in soil. [1] [2] Imazapic is considered an environmental hazard due to its harmful effects on aquatic life. [3]
This is a list of herbicides.These are chemical compounds which have been registered as herbicides.The names on the list are the ISO common name for the active ingredient which is formulated into the branded product sold to end-users. [1]
Imazapyr is a non-selective herbicide used for the control of a broad range of weeds including terrestrial annual and perennial grasses and broadleaved herbs, woody species, and riparian and emergent aquatic species. [1] It is used to control annual and perennial grass and broadleaved weeds, brush, vines and many deciduous trees.
If applied when preemergent herbicide is needed, the fertilizer may burn or stress the lawn. If applied after the lawn "green-up", weed seeds will have already germinated and the herbicide will be ineffective. [3] Preemergants do not prevent seeds from germinating, they prevent cell division, and prevent vital parts of the weed from forming
Indaziflam composes all or part of the a.i. of several herbicides from Bayer Environmental Science (now owned by Cinven, aka Envu, per Bayer's and Envu's websites), [18] [19] including Rejuvra, [20] the Esplanade [21] line (sometimes mixed with diquat dibromide and glyphosate isopropylamine), [22] Marengo, [23] [24] Specticle, [25] [24] and Bayer CropScience (the inventor of the ingredient ...
In the same report, it added the "yield loss plus increased herbicide cost may result in an average estimated loss of $28 per acre" if atrazine were unavailable to corn farmers. [4] In 2006, the EPA concluded that the triazine herbicides posed "no harm that would result to the general U.S. population, infants, children or other... consumers." [5]
3-Amino-1,2,4-triazole (3-AT) is a heterocyclic organic compound that consists of 1,2,4-triazole with an amino group as a substituent.. 3-AT is a competitive inhibitor of the product of the HIS3 gene, imidazoleglycerol-phosphate dehydratase.