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  2. Piperidine - Wikipedia

    en.wikipedia.org/wiki/Piperidine

    Unlike cyclohexane, piperidine has two distinguishable chair conformations: one with the N–H bond in an axial position, and the other in an equatorial position. 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]

  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. Leaching (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Leaching_(chemistry)

    Biological substances can experience leaching themselves, [2] as well as be used for leaching as part of the solvent substance to recover heavy metals. [6] Many plants experience leaching of phenolics, carbohydrates, and amino acids, and can experience as much as 30% mass loss from leaching, [5] just from sources of water such as rain, dew, mist, and fog. [2]

  5. Piperidine alkaloids - Wikipedia

    en.wikipedia.org/wiki/Piperidine_alkaloids

    Piperidine, the parent compound of piperidine alkaloids Piperidine alkaloids are naturally occurring chemical compounds from the group of alkaloids , which are chemically derived from piperidine . Alkaloids with a piperidine building block are widespread and are usually further subdivided according to their occurrence and biogenetic origin.

  6. Hexane - Wikipedia

    en.wikipedia.org/wiki/Hexane

    Hexane (/ ˈ h ɛ k s eɪ n /) or n-hexane is an organic compound, a straight-chain alkane with six carbon atoms and the molecular formula C 6 H 14. [ 7 ] Hexane is a colorless liquid, odorless when pure, and with a boiling point of approximately 69 °C (156 °F).

  7. Solvent - Wikipedia

    en.wikipedia.org/wiki/Solvent

    Strongly polar compounds like sugars (e.g. sucrose) or ionic compounds, like inorganic salts (e.g. table salt) dissolve only in very polar solvents like water, while strongly non-polar compounds like oils or waxes dissolve only in very non-polar organic solvents like hexane. Similarly, water and hexane (or vinegar and vegetable oil) are not ...

  8. Alkaloid - Wikipedia

    en.wikipedia.org/wiki/Alkaloid

    Alkaloids and acids form salts of various strengths. These salts are usually freely soluble in water and ethanol and poorly soluble in most organic solvents. Exceptions include scopolamine hydrobromide, which is soluble in organic solvents, and the water-soluble quinine sulfate. [161] Most alkaloids have a bitter taste or are poisonous when ...

  9. Pyridine - Wikipedia

    en.wikipedia.org/wiki/Pyridine

    It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish-like smell. Pyridine is colorless, but older or impure samples can appear yellow, due to the formation of extended, unsaturated polymeric chains, which show significant electrical conductivity .