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  2. Cynodon dactylon - Wikipedia

    en.wikipedia.org/wiki/Cynodon_dactylon

    Bermuda grass is incredibly difficult to control in flower beds and most herbicides do not work. However, Ornamec, Ornamec 170, Turflon ester (tricyclopyr), and Imazapyr have shown some effectiveness. All of these items are difficult to find in retail stores, as they are primarily marketed to professional landscapers. [20]

  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. Diflufenican - Wikipedia

    en.wikipedia.org/wiki/Diflufenican

    Diflufenican (sometimes called DFF) is a herbicide used to control weeds including wild radish and wild turnip weeds or suppress capeweed, crassula, marshmallow or shepherd's purse, in clover pasture, lupins, lentils or field peas.

  5. Halosulfuron-methyl - Wikipedia

    en.wikipedia.org/wiki/Halosulfuron-methyl

    Halosulfuron-methyl is a sulfonylurea post-emergence herbicide used to control some annual and perennial broad-leaved weeds and sedges (such as nutsedge/nutgrass) in a range of crops (particularly rice), established landscape woody ornamentals and turfgrass. [citation needed] It is marketed under several tradenames including Sedgehammer [2] and ...

  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. Dimethyl tetrachloroterephthalate - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_tetrachlorotere...

    The use of DCPA as a herbicide was first described in a patent filed in 1958. [12] The material was prepared as had been described in a 1948 research paper by treating terephthaloyl chloride with chlorine to give tetrachloroterephthaloyl chloride which was then esterified with methanol. [13] C 6 H 4 (COCl) 2 + 4 Cl 2 + Fe (cat.) → C 6 Cl 4 ...