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  2. Benzylamine - Wikipedia

    en.wikipedia.org/wiki/Benzylamine

    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]

  3. Dibenzylamine - Wikipedia

    en.wikipedia.org/wiki/Dibenzylamine

    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.

  4. Solubility table - Wikipedia

    en.wikipedia.org/wiki/Solubility_table

    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 ...

  5. Dimethylbenzylamine - Wikipedia

    en.wikipedia.org/wiki/Dimethylbenzylamine

    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.

  6. Isopropylbenzylamine - Wikipedia

    en.wikipedia.org/wiki/Isopropylbenzylamine

    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.

  7. Acid–base extraction - Wikipedia

    en.wikipedia.org/wiki/Acid–base_extraction

    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.

  8. PRL-8-53 - Wikipedia

    en.wikipedia.org/wiki/PRL-8-53

    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.

  9. Tribenzylamine - Wikipedia

    en.wikipedia.org/wiki/Tribenzylamine

    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]