Диметиламин гидрохлорид Ч

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Диметиламин гидрохлорид Ч

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. An estimated , tons were produced in 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: \\\\\\\\\\\\[6\\\\\\\\\\\\]. 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. 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. From Wikipedia, the free encyclopedia. CAS Number. Interactive image. Beilstein Reference. Gmelin Reference. PubChem CID. Chemical formula. Solubility in water. GHS hazard statements. GHS precautionary statements. Autoignition temperature. LD 50 median dose. LC 50 median concentration. PEL Permissible. REL Recommended. IDLH Immediate danger. Trimethylamine Diethylamine Triethylamine Diisopropylamine Dimethylaminopropylamine Triisopropylamine. Unsymmetrical dimethylhydrazine. Retrieved 21 October Sigma-Aldrich Co. Catalysis Today. Food and Cosmetics Toxicology. Categories : Alkylamines Insect pheromones Insect ecology. Namespaces Article Talk. Views Read Edit View history. In other projects Wikimedia Commons. By using this site, you agree to the Terms of Use and Privacy Policy. Other names Dimethyl amine. EC Number. Basicity p K b. GHS Signal word. Explosive limits. Lethal dose or concentration LD, LC :.

Диметиламин гидрохлорид Ч

Диметиламин гидрохлорид, 99%

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. An estimated , tons were produced in 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: \\\\\\\\\\\\\\[6\\\\\\\\\\\\\\]. 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. 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. From Wikipedia, the free encyclopedia. CAS Number. Interactive image. Beilstein Reference. Gmelin Reference. PubChem CID. Chemical formula. Solubility in water. GHS hazard statements. GHS precautionary statements. Autoignition temperature. LD 50 median dose. LC 50 median concentration. PEL Permissible. REL Recommended. IDLH Immediate danger. Trimethylamine Diethylamine Triethylamine Diisopropylamine Dimethylaminopropylamine Triisopropylamine. Unsymmetrical dimethylhydrazine. Retrieved 21 October Sigma-Aldrich Co. Catalysis Today. Food and Cosmetics Toxicology. Categories : Alkylamines Insect pheromones Insect ecology. Namespaces Article Talk. Views Read Edit View history. In other projects Wikimedia Commons. By using this site, you agree to the Terms of Use and Privacy Policy. Other names Dimethyl amine. EC Number. Basicity p K b. GHS Signal word. Explosive limits. Lethal dose or concentration LD, LC :.

Dimethylamine

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Диметиламин гидрохлорид Ч

Диметиламин гидрохлорид, 99%

Dimethylamine

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