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  2. Quizalofop - Wikipedia

    en.wikipedia.org/wiki/Quizalofop

    Quizalofop is a chlorophenxy and phenoxy herbicide that works by inhibition of acetyl-CoA-carboxylase to selectively control grasses, without affecting broadleaf crops. It may be shortened to QPE, from Quizalofop-P-Ethyl. [3] It is a Group 1 / A / A herbicide, used in Australia, [4] Morocco and Europe. [1]

  3. 4-Hydroxyphenylpyruvate dioxygenase inhibitor - Wikipedia

    en.wikipedia.org/wiki/4-hydroxyphenylpyruvate_di...

    In 1990 sulcotrione was introduced for post- emergence weed control in corn. Isoxaflutole opened the market more broadly for HPPD inhibitors when it was introduced in 1996 for corn and sugarcane, and for use as a pre-emergence herbicide that could control broadleaf weeds as did sulcotrione, but also additional grass weeds.

  4. Ioxynil - Wikipedia

    en.wikipedia.org/wiki/Ioxynil

    Ioxynil is a post-emergent [4] selective nitrile herbicide. It is used in Australia, New Zealand [5] and Japan [6] to control broadleaf weeds via the inhibition of photosynthesis. It is used notably on onion crops, [7] among others, normally at 300–900 g/Ha. [8] It was introduced in 1966.

  5. Pendimethalin - Wikipedia

    en.wikipedia.org/wiki/Pendimethalin

    Pendimethalin acts in both pre-weed-emergence and early post-emergence. Pendimethalin is absorbed into roots and shoots, inhibits cell division and prevents growth, [10] to prevent weeds from emerging, particularly during the development phase of the crop.

  6. Diflufenican - Wikipedia

    en.wikipedia.org/wiki/Diflufenican

    Diflufenican has shown control over: wild radish, wild turnip, turnip weed, [6] multiply herbicide resistant waterhemp [7] (applied pre-emergence), hedge mustard, Indian hedge mustard, charlock, deadnettle, prickly lettuce, pheasant's eye, [11] Galium aparine, ivy-leaved speedwell and Veronica persica; [10] and suppression of capeweed, crassula ...

  7. Bromoxynil - Wikipedia

    en.wikipedia.org/wiki/Bromoxynil

    Under aerobic conditions in soils or pure cultures, products of bromoxynil degradation often retain the original bromine groups. The herbicide, and one of its common degradation products (3,5-dibromo-4-hydroxybenzoic acid) have been shown to undergo metabolic reductive dehalogenation by the microorganism Desulfitobacterium chlororespirans. [6]

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