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  2. 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.

  3. Triclopyr - Wikipedia

    en.wikipedia.org/wiki/Triclopyr

    Triclopyr is a selective weedkiller used to control dicotyledonous weeds (i.e. broadleaf plants) while leaving monocotyledonous plants (mostly bulbs, grasses and conifers) unaffected, [2] or to control rust fungus on soybean crops.

  4. Dicamba - Wikipedia

    en.wikipedia.org/wiki/Dicamba

    Dicamba is a selective and systemic herbicide that kills annual and perennial broadleaf weeds. [10] Its primary commercial applications are weed control for grain crops and turf areas. It is also used to control brush and bracken in pastures, as well as controlling legumes and cacti .

  5. 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 ]

  6. Herbicide - Wikipedia

    en.wikipedia.org/wiki/Herbicide

    One major complication to the use of herbicides for weed control is the ability of plants to evolve herbicide resistance, rendering the herbicides ineffective against target plants. Out of 31 known herbicide modes of action, weeds have evolved resistance to 21. 268 plant species are known to have evolved herbicide resistance at least once. [ 59 ]

  7. Phenoxy herbicide - Wikipedia

    en.wikipedia.org/wiki/Phenoxy_herbicide

    The best known phenoxy herbicides are (4-chloro-2-methylphenoxy)acetic acid , 2,4-dichlorophenoxyacetic acid (2,4-D) and 2,4,5-trichlorophenoxyacetic acid (2,4,5-T). [2] Analogues of each of these three compounds, with an extra methyl group attached next to the carboxylic acid , were subsequently commercialised as mecoprop , dichlorprop and ...

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