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To prevent growth of crabgrass, preemergent herbicides must be applied at a critical time. If they are applied to the soil too early, they get washed too deep into the soil or washed away by rainwater. If they are applied too late, the key enzyme inhibited is no longer active. The best control requires a second application about 6–8 weeks later.
Pages in category "Preemergent herbicides" The following 18 pages are in this category, out of 18 total. This list may not reflect recent changes. ...
Chlornidine is a preemergent herbicide.It is a dinitroaniline used in China [3] and India [4] on soybeans, corn, cotton, sorghum, and peanuts. [1]It is similar to other dinitroanilines and inhibits the emergence of soybeans less than any other dinitroaniline, though it had unimpressive control of velvet-leaf and giant foxtail.
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 ]
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 ...
Butralin is a preemergent herbicide used to control suckers on tobacco in the United States, [4] [5] Australia, [6] Mozambique and, for food crops also, China. [7] It is a dinitroaniline, first registered in the US in 1976. [8] It was used in the EU until a ban in 2009 due to its exotoxicity. [7] [9]
Trifluralin is a common pre-emergent selective herbicide, a dinitroaniline.With about 14 million pounds (6,400 t) used in the United States in 2001, [3] and 3–7 million pounds (1,400–3,200 t) in 2012, [4] it is one of the most widely used herbicides.
The use of DCPA as a herbicide was first described in a patent filed in 1958. [12] The material was prepared as had been described in a 1948 research paper by treating terephthaloyl chloride with chlorine to give tetrachloroterephthaloyl chloride which was then esterified with methanol. [13] C 6 H 4 (COCl) 2 + 4 Cl 2 + Fe (cat.) → C 6 Cl 4 ...
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