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2,4,5-Trichlorophenol (TCP) is an organochloride with the molecular formula C 6 H 3 Cl 3 O.It has been used as a fungicide and herbicide. [2] Precursor chemical used in the production of 2,4,5-Trichlorophenoxyacetic acid (2,4,5-T) and hexachlorophene involves the intermediate production of 2,4,5-trichlorophenol (TCP) and the formation of 2,3,7,8-Tetrachlorodibenzodioxin (TCDD, commonly ...
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 ...
2,4,6-Trichlorophenol, also known as TCP, phenaclor, Dowicide 2S, Dowcide 2S, omal, is a chlorinated phenol that has been used as a fungicide, herbicide, insecticide, antiseptic, [3] defoliant, and glue preservative. [4] It is a clear to yellowish crystalline solid with a strong, phenolic odor.
Indian toxicity label system Toxicity symbol for European toxicity class I and class II. Toxicity class refers to a classification system for pesticides that has been created by a national or international government-related or -sponsored organization.
Didecyldimethylammonium chloride (DDAC) is a quaternary ammonium compound used as antiseptic/disinfectant.It causes the disruption of intermolecular interactions and the dissociation of lipid bilayers.
[4] [5] [6] Its major uses include: Seed treatment – Imidacloprid is a popular seed treatment insecticide in the world [ 8 ] Agriculture – Control of aphids , cane beetles , thrips , [ 16 ] stink bugs , locusts , and a variety of other insects that damage crops
p-Cresol is a major component in pig odor. [11] Temporal glands secretion examination showed the presence of phenol and p-cresol during musth in male elephants. [12] [13] It is one of the very few compounds to attract the orchid bee Euglossa cyanura and has been used to capture and study the species.
The Dow Chemical Company also developed Chlorpyrifos methyl in 1966, which had a lower acute toxicity (WHO class III), but this appears to be no longer in commercial use. The molecule is similar to Chlorpyrifos ethyl, but with a O,O dimethyl chain.
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