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  2. Isoxaben - Wikipedia

    en.wikipedia.org/wiki/Isoxaben

    Isoxaben (N-[3-(1-ethyl-1-methylpropyl)-1,2-oxazol-5-yl]-2,6-dimethoxybenzamide) is an herbicide from the benzamide and isoxazole family. [1] It is intended for use in vineyards and tree nut orchards for the preemergence control of broadleaf weeds. [2]

  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. Pesticide regulation in the United States - Wikipedia

    en.wikipedia.org/wiki/Pesticide_regulation_in...

    The purpose of the label is to "provide clear directions for effective product performance while minimizing risk to human health and the environment." A label is a legally binding document that mandates how the pesticide can and must be used and failure to follow the label as written when using the pesticide is a federal offense. [4]

  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. 2,4-Dichlorophenoxyacetic acid - Wikipedia

    en.wikipedia.org/wiki/2,4-Dichlorophenoxyacetic_acid

    2,4-Dichlorophenoxyacetic acid is an organic compound with the chemical formula Cl 2 C 6 H 3 OCH 2 CO 2 H.It is usually referred to by its ISO common name 2,4-D. [4] It is a systemic herbicide that kills most broadleaf weeds by causing uncontrolled growth, but most grasses such as cereals, lawn turf, and grassland are relatively unaffected.

  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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