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  2. Pyribenzoxim - Wikipedia

    en.wikipedia.org/wiki/Pyribenzoxim

    This article about an ester is a stub. You can help Wikipedia by expanding it.

  3. Glyphosate-based herbicides - Wikipedia

    en.wikipedia.org/wiki/Glyphosate-based_herbicides

    The glyphosate-based herbicide RoundUp (styled: Roundup) was developed in the 1970s by Monsanto. Glyphosate was first registered for use in the U.S. in 1974. [4] Glyphosate-based herbicides were initially used in a similar way to paraquat and diquat, as non-selective herbicides. Attempts were made to apply them to row crops, but problems with ...

  4. Indaziflam - Wikipedia

    en.wikipedia.org/wiki/Indaziflam

    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 ...

  5. Dicamba - Wikipedia

    en.wikipedia.org/wiki/Dicamba

    Brand names for formulations of this herbicide include Dianat, Banvel, Diablo, Oracle and Vanquish. This chemical compound is a chlorinated derivative of o -anisic acid . [ 5 ] It has been described as a "widely used, low-cost, environmentally friendly herbicide that does not persist in soils and shows little or no toxicity to wildlife and humans."

  6. Asulam - Wikipedia

    en.wikipedia.org/wiki/Asulam

    Asulam is a herbicide invented by May & Baker Ltd, internally called M&B9057, [1] that is used in horticulture and agriculture to kill bracken [2] [3] and docks. [4] It is also used as an antiviral agent. It is currently marketed, by United Phosphorus Ltd - UPL, as "Asulox" which contains 400 g/L of asulam sodium salt.

  7. Saflufenacil - Wikipedia

    en.wikipedia.org/wiki/Saflufenacil

    As described in the BASF patent, the key step in the preparation of saflufenacil involved the reaction between a substituted aniline and an oxazinone. 2-chloro-4-fluoro-5-aminobenzoic acid and 2-dimethylamino-4-(trifluoromethyl)-6H-1,3-oxazin-6-one were heated in acetic acid to form the ring systems of the herbicide in over 90% yield, with further standard chemical transformations to generate ...