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The hydrochloride salt of benzylamine, C 6 H 5 CH 2 NH 3 Cl or C 6 H 5 CH 2 NH 2 ·HCl, [24] is prepared by reacting benzylamine with hydrochloric acid, and can be used in treating motion sickness. NASA astronaut John Glenn was issued with benzylamine hydrochloride for this purpose for the Mercury-Atlas 6 mission. [25]
Dibenzylamine is an organic compound with the formula (C 6 H 5 CH 2) 2 NH. It is classified as a secondary amine, being the middle member of the series that includes the primary amine benzylamine (C 6 H 5 CH 2 NH 2) and the tertiary amine tribenzylamine ((C 6 H 5 CH 2) 3 N). It is a colorless oily substance with a faint ammonia-like odor.
Download as PDF; Printable version; In other projects Wikidata item; ... Units of solubility are given in grams of substance per 100 millilitres of water (g/100 ml ...
Dimethylbenzylamine is the organic compound with the formula C 6 H 5 CH 2 N(CH 3) 2. The molecule consists of a benzyl group, C 6 H 5 CH 2, attached to a dimethylamino functional group. It is a colorless liquid. It is used as a catalyst for the formation of polyurethane foams and epoxy resins.
N-isopropylbenzylamine is a compound that has appeared in chemical literature often playing an intermediary role in applications of experimental synthesis and novel organic transformations.
Acid–base extraction is a subclass of liquid–liquid extractions and involves the separation of chemical species from other acidic or basic compounds. [1] It is typically performed during the work-up step following a chemical synthesis to purify crude compounds [2] and results in the product being largely free of acidic or basic impurities.
The terms of the agreement guaranteed Dr. Hansl access to his laboratory facilities and office space at the university for a period of 2 years. [4] Upon returning from a 4-month absence. Hansl found that the refrigerator he had used to store various experimental compounds had been unplugged, purportedly rendering the compounds unusable.
Tribenzylamine is an organic compound with the formula N(CH 2 C 6 H 5) 3. It is a symmetrical tertiary amine. It is of some historic interest as one of the first compounds produced by the Leuckart reaction. [1] The compound is a common target in the development of new synthetic methods, e.g. from benzyl alcohol. [2] [3]