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  2. 2,6-Dichlorobenzonitrile - Wikipedia

    en.wikipedia.org/wiki/2,6-Dichlorobenzonitrile

    1 Mechanism of action. 2 Safety. Toggle Safety subsection. 2.1 Residue. ... It is widely used as a herbicide and organic chemistry building block. [1] Mechanism of action

  3. Chlorsulfuron - Wikipedia

    en.wikipedia.org/wiki/Chlorsulfuron

    Chlorsulfuron is an ALS (acetolactate synthase) inhibitor herbicide, and is a sulfonylurea compound. [ 3 ] [ 4 ] It was discovered by George Levitt in February 1976 while working at DuPont , which was the patent assignee .

  4. 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]

  5. Herbicide - Wikipedia

    en.wikipedia.org/wiki/Herbicide

    Eventually the Herbicide Resistance Action Committee (HRAC) [29] and the Weed Science Society of America (WSSA) [30] developed a classification system. [31] [32] Groups in the WSSA and the HRAC systems are designated by numbers and letters, inform users awareness of herbicide mode of action and provide more accurate recommendations for ...

  6. 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 ...

  7. Paraquat - Wikipedia

    en.wikipedia.org/wiki/Paraquat

    Paraquat (trivial name; / ˈ p ær ə k w ɒ t /), or N,N′-dimethyl-4,4′-bipyridinium dichloride (systematic name), also known as methyl viologen, is a toxic organic compound with the chemical formula [(C 6 H 7 N) 2]Cl 2.

  8. Mode of action - Wikipedia

    en.wikipedia.org/wiki/Mode_of_action

    A mechanism of action of a chemical could be "binding to DNA" while its broader mode of action would be "transcriptional regulation". [3] However, there is no clear consensus and the term mode of action is also often used, especially in the study of pesticides, to describe molecular mechanisms such as action on specific nuclear receptors or ...

  9. Fomesafen - Wikipedia

    en.wikipedia.org/wiki/Fomesafen

    The detailed mechanism of action for fomesafen and related nitrophenyl ether herbicides was unknown at the time they were invented. The effects visible on whole plants are chlorosis and desiccation : several hypotheses were advanced regarding the molecular-level interactions which might explain these symptoms. [ 13 ]