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This page was last edited on 18 November 2024, at 00:50 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
The page provides a comprehensive list of isomers of dodecane, including their chemical structures and properties.
Triphenylmethane was first synthesized in 1872 by the German chemist August Kekulé and his Dutch student Antoine Paul Nicolas Franchimont (1844–1919) by heating diphenylmercury (Hg(C 6 H 5) 2, Quecksilberdiphenyl) with benzal chloride (C 6 H 5 CHCl 2, Benzylenchlorid).
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Tuinal was the brand name of a discontinued combination drug composed of two barbiturate sodium salts (secobarbital and amobarbital) in equal proportions.. Tuinal was introduced as a sedative-hypnotic (sleeping pill) medication in the late 1940s by Eli Lilly.
114.232 g·mol −1 Appearance Colourless liquid Odor: Odourless Density: 705 mg mL −1: Melting point: −122 to −120 °C; −188 to −184 °F; 151 to 153 K Boiling point: 118 to 120 °C; 244 to 248 °F; 391 to 393 K Vapor pressure: 5.0 kPa (at 37.7 °C)
5.1 Tetramethyl. 5.2 Dimethyl+ethyl. ... 4-Ethyl-2-methylhexane; 3-Ethyl-3-methylhexane; 3-Ethyl-4-methylhexane; Pentane. Isomers where pentane is the longest chain
4-Methyl-α-ethyltryptamine (4-Me-αET) is a putative stimulant, psychedelic, and entactogen drug of the tryptamine class. [1] It is a designer drug and is sold online as a " research chemical ". [ 2 ]