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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.
2,4-DB or 4-(2,4-dichlorophenoxy)butyric acid is a selective systemic phenoxy herbicide used to control many annual and perennial broad-leaf weeds in alfalfa, peanuts, soybeans, and other crops. Its active metabolite, 2,4-D, inhibits growth at the tips of stems and roots. It is classified in toxicity class III.
If 50- to 70-percent of your lawn area is covered with crabgrass, you should spray the entire lawn according to label instructions for the most efficient approach, says Waltz. Mow your grass.
The grass is medium to light green in color and has a coarse texture with short upright seedhead stems that grow to about 3-5 inches. Native to Southern China, it was introduced to the United States in 1916 [1] and has since become one of the common grasses in the Southeastern United States and Hawaii. It can also be considered a weed. [2]
Dicamba use in the US in 2019. Usage has substantially increased since dicamba was approved for use over dicamba-resistant GMO crops in 2016. Dicamba is a selective and systemic herbicide that kills annual and perennial broadleaf weeds. [10]
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.
2,4,5-Trichlorophenoxyacetic acid (also known as 2,4,5-T), a synthetic auxin, is a chlorophenoxy acetic acid herbicide used to defoliate broad-leafed plants. It was developed in the late 1940s, synthesized by reaction of 2,4,5-Trichlorophenol and chloroacetic acid.
Carbaryl is often inexpensively produced by direct reaction of methyl isocyanate with 1-naphthol. [5]C 10 H 7 OH + CH 3 NCO → C 10 H 7 OC(O)NHCH 3. Alternatively, 1-naphthol can be treated with excess phosgene to produce 1-naphthyl chloroformate, which is then converted to carbaryl by reaction with methylamine. [5]