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  2. HRAC classification - Wikipedia

    en.wikipedia.org/wiki/HRAC_classification

    The Herbicide Resistance Action Committee (HRAC) classifies herbicides by their mode of action (MoA) to provide a uniform way for farmers and growers to identify the agents they use and better manage pesticide resistance around the world. [1] [2] It is run by CropLife International [3] in conjunction with the Weed Science Society of America ...

  3. List of herbicides - Wikipedia

    en.wikipedia.org/wiki/List_of_herbicides

    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 ]

  4. Cash-strapped US farmers switch to generic crop ... - AOL

    www.aol.com/news/cash-strapped-us-farmers-switch...

    If there is a generic option to brand-name herbicides, and the seeds that a farmer purchases can tolerate it, then it can makes sense to go with a less expensive product, said Mac Marshall ...

  5. Pendimethalin - Wikipedia

    en.wikipedia.org/wiki/Pendimethalin

    Herbicide options are limited for these minor crops, particularly in the vegetable sector. [4] Long-term field studies performed by the German government and institutions together with farmers call pendimethalin efficient for controlling blackgrass, regarding weed control efficacy, crop yield, treatment costs and environmental impact.

  6. Metolachlor - Wikipedia

    en.wikipedia.org/wiki/Metolachlor

    Metolachlor is a popular herbicide in the United States. [3] As originally formulated metolachlor was applied as a racemate , a 1:1 mixture of the ( S )- and ( R )-stereoisomers. The ( R )-enantiomer is less active, and modern production methods afford a higher concentration of S-metolachlor, thus current application rates are far lower than ...

  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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