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  2. Benzylamine - Wikipedia

    en.wikipedia.org/wiki/Benzylamine

    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 .

  3. Solubility table - Wikipedia

    en.wikipedia.org/wiki/Solubility_table

    The tables below provides information on the variation of solubility of different substances (mostly inorganic compounds) in water with temperature, at one atmosphere pressure. Units of solubility are given in grams of substance per 100 millilitres of water (g/100 ml), unless shown otherwise. The substances are listed in alphabetical order.

  4. Free base - Wikipedia

    en.wikipedia.org/wiki/Free_base

    The free base form of cocaine is prepared from cocaine hydrochloride by extracting the cocaine with an alkaline solution (sodium hydroxide or ammonia) and adding a non-polar solvent such as diethyl ether or benzene. The mixture separates into two layers, the top solvent layer containing the dissolved cocaine.

  5. 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).

  6. Pargyline - Wikipedia

    en.wikipedia.org/wiki/Pargyline

    Pargyline is an derivative of benzylamine and is also known as N-methyl-N-propargylbenzylamine. [13] [49] It is used pharmaceutically as the hydrochloride salt. [4] [5] [13] Pargyline is a lipophilic compound, with a predicted log P of about 2.1. [49] [26]

  7. 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.

  8. Solubility equilibrium - Wikipedia

    en.wikipedia.org/wiki/Solubility_equilibrium

    A solubility equilibrium exists when a chemical compound in the solid state is in chemical equilibrium with a solution containing the compound. This type of equilibrium is an example of dynamic equilibrium in that some individual molecules migrate between the solid and solution phases such that the rates of dissolution and precipitation are equal to one another.

  9. Butenafine - Wikipedia

    en.wikipedia.org/wiki/Butenafine

    Butenafine hydrochloride is an odorless white crystalline powder that is freely soluble in methanol, ethanol, and chloroform, yet is only slightly soluble in water. Synthesis [ edit ]