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Iodomethane, also called methyl iodide, and commonly abbreviated "MeI", is the chemical compound with the formula CH 3 I. It is a dense, colorless, volatile liquid. In terms of chemical structure, it is related to methane by replacement of one hydrogen atom by an atom of iodine. It is naturally emitted in small amounts by rice plantations. [5]
[36] After the approval of methyl iodide's registration as a pesticide available in the United States, Arysta sold for $2.2 billion. [35] In 2006, the Japanese chemical giant Arysta presented it to the EPA as the perfect candidate to replace methyl bromide. The pitch: It works just as well on nematodes, but it doesn’t harm the ozone layer.
The pesticide manual provides much information on pesticides. [6] [7] Many of the insecticides in the list are not in use. The developer of a pesticide applies for a common name when they intend to sell it, but some nevertheless do not reach the market. Many insecticides have been banned or otherwise withdrawn from the market over the decades.
Industrially significant organoiodine compounds, often used as disinfectants or pesticides, are iodoform (CHI 3), methylene iodide (CH 2 I 2), and methyl iodide (CH 3 I). [4] Although methyl iodide is not an industrially important product, it is an important intermediate, being a transiently generated intermediate in the industrial production ...
Diiodomethane or methylene iodide, commonly abbreviated "MI", is an organoiodine compound. Diiodomethane is a very dense colorless liquid; however, it decomposes upon exposure to light liberating iodine, which colours samples brownish. It is slightly soluble in water, but soluble in organic solvents.
4-Hydroxyphenylpyruvate dioxygenase (HPPD) inhibitors (HPPD inhibitors) are a class of herbicides that prevent growth in plants by blocking 4-Hydroxyphenylpyruvate dioxygenase, an enzyme in plants that breaks down the amino acid tyrosine into molecules that are then used by plants to create other molecules that plants need.
Methyldichlorophosphine is produced by alkylation of phosphorus trichloride with methyl iodide followed by reduction of the resulting phosphonium salt with iron powder: [2] [3] CH 3 I + PCl 3 + AlCl 3 → [CH 3 PCl 3] + AlCl 3 I − [CH 3 PCl 3] + AlCl 3 I − + Fe → CH 3 PCl 2 + FeICl + AlCl 3
The product is formed as the iodide salt, and the reaction proceeds via an S N 2 pathway. [8] The industrial synthesis of MPP + for sale as the herbicide cyperquat used methyl chloride as the source of the methyl group.
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