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Herbicides that act through multiple modes have multiple classifications, corresponding to each MoA. [8] For example, Quinmerac is classified as Group 4/29 (O/L) because it is both an Auxin mimic (Group 4 or O) and inhibits cellulose synthesis (Group 29 or L). [9]
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] The 2024 HRAC poster of herbicide modes of action includes ...
2,4-D, 2,4,5-T, and Aminopyralid are examples of synthetic auxin herbicides. ... If there is resistance to a single group of herbicides, then the use of herbicides ...
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.
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 fenoprop.
The activity of the 2-chloro-4-nitro analog was an outlier, and it was theorized that perhaps the nitro group was being reduced in vivo. The 4-methylsulfonyl group was then prepared to test this hypothesis, and what was to become the commercial herbicide Mikado (II) was prepared. The prospect of improving the biological activity with new ...