Диметиламин — Википедия

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Dimethylamine is an organic compound with the formula CH 3 2 NH. This secondary amine is a colorless, flammable gas with an ammonia -like odor. In , an estimated , tons were produced industrially, \\\\\\\\\\\\\[5\\\\\\\\\\\\\] but it is also found as a natural product. The molecule consists of a nitrogen atom with two methyl substituents and one proton. Dimethylamine reacts with acids to form salts, such as dimethylamine hydrochloride, an odorless white solid with a melting point of Dimethylamine is produced by catalytic reaction of methanol and ammonia at elevated temperatures and high pressure: Dimethylamine is a precursor to several industrially significant compounds. The solvents dimethylformamide and dimethylacetamide are derived from dimethylamine. It is raw material for the production of many agrichemicals and pharmaceuticals , such as dimefox and diphenhydramine , respectively. The chemical weapon tabun is derived from dimethylamine. The surfactant lauryl dimethylamine oxide is found in soaps and cleaning compounds. Unsymmetrical dimethylhydrazine , a rocket fuel, is prepared from dimethylamine. The German cockroach utilizes dimethylamine as a pheromone for communication. It is an attractant for boll weevils. Dimethylamine undergoes nitrosation under weak acid conditions to give dimethylnitrosamine. This animal carcinogen has been detected and quantified in human urine samples and it may also arise from nitrosation of dimethylamine by nitrogen oxides present in acid rain in highly industrialized countries. Deprotonation of dimethylamine can be effected with organolithium compounds. This lithium amide has been used to prepare volatile metal complexes such as tetrakis dimethylamido titanium and pentakis dimethylamido tantalum. Dimethylamine is not very toxic with the following LD 50 values: From Wikipedia, the free encyclopedia. Dimethyl amine The name dimethylamine is deprecated. LD 50 median dose. LC 50 median concentration. Trimethylamine Diethylamine Triethylamine Diisopropylamine Dimethylaminopropylamine Triisopropylamine. National Institute of Standards and Technology. Retrieved 21 October Immediately Dangerous to Life and Health. Retrieved from ' https: Alkylamines Insect pheromones Insect ecology. Views Read Edit View history. In other projects Wikimedia Commons. This page was last edited on 5 October , at By using this site, you agree to the Terms of Use and Privacy Policy. Other names Dimethyl amine The name dimethylamine is deprecated. Basicity p K b. Lethal dose or concentration LD , LC:.

MDMA в Луге