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  2. Clopyralid - Wikipedia

    en.wikipedia.org/wiki/Clopyralid

    Clopyralid (3,6-dichloro-2-pyridinecarboxylic acid) is a selective herbicide used for control of broadleaf weeds, especially thistles and clovers.Clopyralid is in the picolinic acid family of herbicides, which also includes aminopyralid, picloram, triclopyr, and several less common herbicides.

  3. List of herbicides - Wikipedia

    en.wikipedia.org/wiki/List_of_herbicides

    The industry-sponsored Herbicide Resistance Action Committee (HRAC) advises on the use of herbicides in crop protection and classifies the available compounds according to their chemical structures and mechanism of action so as to manage the risks of pesticide resistance developing. [4]

  4. Trifluralin - Wikipedia

    en.wikipedia.org/wiki/Trifluralin

    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. Trifluralin is also used in Australia, [5] and New Zealand, [6] previously in the EU.

  5. 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 ...

  6. Alachlor - Wikipedia

    en.wikipedia.org/wiki/Alachlor

    Alachlor is an herbicide from the chloroacetanilide family. It is an odorless, white solid. The greatest use of alachlor is for control of annual grasses and broadleaf weeds in crops. Use of alachlor is illegal in the European Union [1] and no products containing alachlor are currently registered in the United States. [2]

  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 ...

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