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  2. Roundup (herbicide) - Wikipedia

    en.wikipedia.org/wiki/Roundup_(herbicide)

    Roundup is a brand name of herbicide originally produced by Monsanto, which Bayer acquired in 2018. Prior to the late-2010s formulations, it used broad-spectrum glyphosate-based herbicides. [1]

  3. Pesticide formulation - Wikipedia

    en.wikipedia.org/wiki/Pesticide_formulation

    Other common formulations include granules (GR) and dusts (DP), although for improved safety the latter have been replaced by microgranules (MG e.g. for rice farmers in Japan). Specialist formulations are available for ultra-low volume spraying, fogging, fumigation, etc. Very occasionally, some pesticides (e.g.

  4. Preemergent herbicide - Wikipedia

    en.wikipedia.org/wiki/Preemergent_herbicide

    Preemergent herbicides are a form of chemical weed control which prevent germinated weed seedlings from becoming established. In some areas of the world, they are used to prevent crabgrass from appearing in lawns. [1] Preemergent herbicides are applied to lawns in the spring and autumn, to prevent the establishment of weed seeds. They will not ...

  5. Bifenthrin - Wikipedia

    en.wikipedia.org/wiki/Bifenthrin

    Bifenthrin has the longest known residual time in soil of insecticides currently on the market. It is a white, waxy solid with a faint sweet smell. It is chemically synthesized in various forms, including powder, granules and pellets. However, it is not naturally occurring. [1]

  6. Glyphosate - Wikipedia

    en.wikipedia.org/wiki/Glyphosate

    Landscaping company in Oklahoma applying a weed control product that contains glyphosate Glyphosate has four ionizable sites, with pKa values of 2.0, 2.6, 5.6 and 10.6. [ 83 ] Therefore, it is a zwitterion in aqueous solutions and is expected to exist almost entirely in zwitterionic forms in the environment.

  7. Carbaryl - Wikipedia

    en.wikipedia.org/wiki/Carbaryl

    Carbaryl is often inexpensively produced by direct reaction of methyl isocyanate with 1-naphthol. [5]C 10 H 7 OH + CH 3 NCO → C 10 H 7 OC(O)NHCH 3. Alternatively, 1-naphthol can be treated with excess phosgene to produce 1-naphthyl chloroformate, which is then converted to carbaryl by reaction with methylamine. [5]