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  2. Piperidine - Wikipedia

    en.wikipedia.org/wiki/Piperidine

    After much controversy during the 1950s–1970s, the equatorial conformation was found to be more stable by 0.72 kcal/mol in the gas phase. [20] In nonpolar solvents , a range between 0.2 and 0.6 kcal/mol has been estimated, but in polar solvents the axial conformer may be more stable. [ 21 ]

  3. Piperine - Wikipedia

    en.wikipedia.org/wiki/Piperine

    Piperidine, a cyclic six-membered amine that results from hydrolysis of piperine; Piperic acid, the carboxylic acid also derived from hydrolysis of piperine; Capsaicin, the active piquant chemical in chili peppers; Allyl isothiocyanate, the active piquant chemical in mustard, radishes, horseradish, and wasabi

  4. Hexane - Wikipedia

    en.wikipedia.org/wiki/Hexane

    Hexane and other volatile hydrocarbons (petroleum ether) present an aspiration risk. [26] n-Hexane is sometimes used as a denaturant for alcohol, and as a cleaning agent in the textile, furniture, and leather industries. It is slowly being replaced with other solvents. [27] Like gasoline, hexane is highly volatile and is an explosion risk.

  5. Piperonal - Wikipedia

    en.wikipedia.org/wiki/Piperonal

    Piperonal can be prepared by the oxidative cleavage of isosafrole or by using a multistep sequence from catechol or 1,2-methylenedioxybenzene.Synthesis from the latter chemical is accomplished through a condensation reaction with glyoxylic acid followed by cleaving the resulting α-hydroxy acid with an oxidizing agent.

  6. Hildebrand solubility parameter - Wikipedia

    en.wikipedia.org/wiki/Hildebrand_solubility...

    The cohesive energy density is the amount of energy needed to completely remove a unit volume of molecules from their neighbours to infinite separation (an ideal gas). This is equal to the heat of vaporization of the compound divided by its molar volume in the condensed phase. In order for a material to dissolve, these same interactions need to ...

  7. Pyridine - Wikipedia

    en.wikipedia.org/wiki/Pyridine

    This difference is partly related to the lower symmetry of the individual pyridine molecule (C 2v vs D 6h for benzene). A tri hydrate (pyridine·3H 2 O) is known; it also crystallizes in an orthorhombic system in the space group Pbca , lattice parameters a = 1244 pm, b = 1783 pm, c = 679 pm and eight formula units per unit cell (measured at 223 K).

  8. Hydrophobic effect - Wikipedia

    en.wikipedia.org/wiki/Hydrophobic_effect

    [1] [2] The word hydrophobic literally means "water-fearing", and it describes the segregation of water and nonpolar substances, which maximizes the entropy of water and minimizes the area of contact between water and nonpolar molecules. In terms of thermodynamics, the hydrophobic effect is the free energy change of water surrounding a solute. [3]

  9. Lobeline - Wikipedia

    en.wikipedia.org/wiki/Lobeline

    Lobeline is a piperidine alkaloid found in a variety of plants, particularly those in the genus Lobelia, including Indian tobacco (Lobelia inflata), Devil's tobacco (Lobelia tupa), great lobelia (Lobelia siphilitica), Lobelia chinensis, and Hippobroma longiflora. In its pure form, it is a white amorphous powder which is freely soluble in water.