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Benzylamine, also known as phenylmethylamine, is an organic chemical compound with the condensed structural formula C 6 H 5 CH 2 NH 2 (sometimes abbreviated as PhCH 2 NH 2 or BnNH 2).It consists of a benzyl group, C 6 H 5 CH 2, attached to an amine functional group, NH 2.
Names Preferred IUPAC name. N,N-Dimethyl-1-phenylmethanamine. Other names ... Chemical formula. C 9 H 13 N: Molar mass: 135.210 g·mol −1 Appearance colourless liquid
The Incompleat Chymist: Being an Essay on the Eighteenth-Century Chemist in His Laboratory, with a Dictionary of Obsolete Chemical Terms of the Period (Smithsonian Studies in History and Technology, Number 33). Smithsonian Institution Press. Giunta, Carmen. Glossary of Archaic Chemical Terms: Introduction and Part I (A-B). Classic Chemistry.
His first video was uploaded on March 24, 2014, and many of his early videos were recordings of his projects as a laboratory technician or at his parents' garage, with them later being filmed at his industrial-grade laboratory. [3] Braun wanted his channel name, NileRed, to be related to chemistry, but not too chemical-sounding.
Xylamine is a monoaminergic neurotoxin and benzylamine derivative that is closely related to DSP-4. [1] [2] It is a relatively selective noradrenergic neurotoxin, which is attributed to its high affinity for the norepinephrine transporter (NET). [1]
Chemical nomenclature is a set of rules to generate systematic names for chemical compounds. The nomenclature used most frequently worldwide is the one created and developed by the International Union of Pure and Applied Chemistry (IUPAC). IUPAC Nomenclature ensures that each compound (and its various isomers) have only one formally accepted ...
IUPAC nomenclature is used for the naming of chemical compounds, based on their chemical composition and their structure. [1] For example, one can deduce that 1-chloropropane has a Chlorine atom on the first carbon in the 3-carbon propane chain.
Fatty amines are commonly prepared from fatty acids; which are themselves obtained from natural sources, typically seed-oils.The overall reaction is sometimes referred to as the Nitrile Process [3] and begins with a reaction between the fatty acid and ammonia at high temperature (>250 °C) and in the presence of a metal oxide catalyst (e.g., alumina or zinc oxide) to give the fatty nitrile.