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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] The University of Hertfordshire maintains a database of the chemical and biological properties of these materials, [2] including their brand names and the countries and dates where and when they have been ...
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 ...
The product is used at application rates of 0.008–0.0155 pounds per acre (9.0–17.4 g/ha). [16] The estimated use in US agriculture is mapped by the US Geological Service and shows that from 1992 to 2017, the latest date for which figures are available, up to 120,000 pounds (54,000 kg) were applied each year.
Dimethyl tetrachloroterephthalate (DCPA, with the main trade name Dacthal) is an organic compound with the formula C 6 Cl 4 (CO 2 CH 3) 2. It is the di methyl ester of tetrachloro terephthalic acid , used as a preemergent herbicide with the ISO common name chlorthal-dimethyl .
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. It was widely used in the agricultural industry until being phased out, starting ...
A label is a legally binding document that mandates how the pesticide can and must be used and failure to follow the label as written when using the pesticide is a federal offence. [ 10 ] [ 11 ] The label includes use for removal of sedges and newly emerged broadleaf weeds including purple and yellow nutsedge , Kyllinga , plantain , clover ...
As described in the BASF patent, the key step in the preparation of saflufenacil involved the reaction between a substituted aniline and an oxazinone. 2-chloro-4-fluoro-5-aminobenzoic acid and 2-dimethylamino-4-(trifluoromethyl)-6H-1,3-oxazin-6-one were heated in acetic acid to form the ring systems of the herbicide in over 90% yield, with further standard chemical transformations to generate ...
Fomesafen is the ISO common name [2] for an organic compound used as an herbicide. It acts by inhibiting the enzyme protoporphyrinogen oxidase (PPO) [3] which is necessary for chlorophyll synthesis. Soybeans naturally have a high tolerance to fomesafen, [3] [4] via metabolic disposal by glutathione S-transferase.
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