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It has a fishy odor and is miscible with water. Like other amines, it is a weak base , compared to strong bases such as NaOH , but it is a stronger base than its aromatic analog, aniline . It is a useful intermediate in the production of many other organic compounds (e.g. cyclamate )
Methylhexanamine (also known as methylhexamine, 1,3-dimethylamylamine, 1,3-DMAA, dimethylamylamine, and DMAA; trade names Forthane and Geranamine) is an indirect sympathomimetic drug invented and developed by Eli Lilly and Company and marketed as an inhaled nasal decongestant from 1948 until it was voluntarily withdrawn from the market in the 1980s.
Hexylamine or n-hexylamine is a chemical compound with the formula CH 3 CH 2 CH 2 CH 2 CH 2 CH 2 NH 2. This colorless liquid is one of the isomeric amines of hexane. At standard temperature and pressure, it has the ammonia/bleach odor common to amines and is soluble in almost all organic solvents.
Chloramines refer to derivatives of ammonia and organic amines wherein one or more N−H bonds have been replaced by N−Cl bonds. [1] [2] Two classes of compounds are considered: inorganic chloramines and organic chloramines. Chloramines are the most widely used members of the halamines. [3]
Bis(2-chloroethyl)ethylamine is the organic compound with the formula C 2 H 5 N(CH 2 CH 2 Cl) 2. Often abbreviated HN1, it is a powerful vesicant and a nitrogen mustard gas. HN1 was developed in the 1920s and 1930s to remove warts and later as a military agent.
DMEA, when dissolved water, decomposes into a highly reactive aziridinium ion, N,N-dimethyl-2-phenylaziridinium (DPA). DPA binds to the anionic site of acetylcholinesterase, where it alkylates and irreversibly inhibits the enzyme. [2] [3] DMEA has been compared to N,N-dimethyl-2-chloro-2-phenyl-1-methylethyl-amine (M-DMEA) and the results show ...
Venenivibrio stagnispumantis gains energy by oxidizing hydrogen gas.. In biochemistry, chemosynthesis is the biological conversion of one or more carbon-containing molecules (usually carbon dioxide or methane) and nutrients into organic matter using the oxidation of inorganic compounds (e.g., hydrogen gas, hydrogen sulfide) or ferrous ions as a source of energy, rather than sunlight, as in ...
CH 3 CHO + NH 3 + H 2 → CH 3 CH 2 NH 2 + H 2 O. Ethylamine can be prepared by several other routes, but these are not economical. Ethylene and ammonia combine to give ethylamine in the presence of a sodium amide or related basic catalysts. [5] H 2 C=CH 2 + NH 3 → CH 3 CH 2 NH 2. Hydrogenation of acetonitrile, acetamide, and nitroethane ...