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  2. Hydrogen cyanide - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_cyanide

    Hydrogen cyanide (formerly known as prussic acid) is a chemical compound with the formula HCN and structural formula H−C≡N.It is a highly toxic and flammable liquid that boils slightly above room temperature, at 25.6 °C (78.1 °F).

  3. Antifeedant - Wikipedia

    en.wikipedia.org/wiki/Antifeedant

    In addition to their role defending the plant, antifeedants often confer taste or odors, enhancing the flavor of certain plants. Examples are provided by cruciferous vegetables including mustard , cabbage , and horseradish , which release pungent oils containing glucosinolates when the plant material is chewed, cut, or otherwise damaged. [ 7 ]

  4. Cyanide - Wikipedia

    en.wikipedia.org/wiki/Cyanide

    The most hazardous compound is hydrogen cyanide, which is a gas and kills by inhalation. For this reason, working with hydrogen cyanide requires wearing an air respirator supplied by an external oxygen source. [11] Hydrogen cyanide is produced by adding acid to a solution containing a cyanide salt.

  5. Gaseous signaling molecules - Wikipedia

    en.wikipedia.org/wiki/Gaseous_signaling_molecules

    Gaseous signaling molecules are gaseous molecules that are either synthesized internally (endogenously) in the organism, tissue or cell or are received by the organism, tissue or cell from outside (say, from the atmosphere or hydrosphere, as in the case of oxygen) and that are used to transmit chemical signals which induce certain physiological or biochemical changes in the organism, tissue or ...

  6. Glycoside - Wikipedia

    en.wikipedia.org/wiki/Glycoside

    Plants that make cyanogenic glycosides store them in the vacuole, but, if the plant is attacked, they are released and become activated by enzymes in the cytoplasm. These remove the sugar part of the molecule, allowing the cyanohydrin structure to collapse and release toxic hydrogen cyanide. Storing them in inactive forms in the vacuole ...

  7. Hydrocyanation - Wikipedia

    en.wikipedia.org/wiki/Hydrocyanation

    In organic chemistry, hydrocyanation is a process for conversion of alkenes to nitriles. The reaction involves the addition of hydrogen cyanide and requires a catalyst. This conversion is conducted on an industrial scale for the production of precursors to nylon.

  8. Cyanohydrin reaction - Wikipedia

    en.wikipedia.org/wiki/Cyanohydrin_reaction

    The cyanide source can be potassium cyanide (KCN), sodium cyanide (NaCN) or trimethylsilyl cyanide ((CH 3) 3 SiCN). With aromatic aldehydes such as benzaldehyde, the benzoin condensation is a competing reaction. The reaction is used in carbohydrate chemistry as a chain extension method for example that of D-xylose.

  9. Cyanohydrin - Wikipedia

    en.wikipedia.org/wiki/Cyanohydrin

    In organic chemistry, a cyanohydrin or hydroxynitrile is a functional group found in organic compounds in which a cyano and a hydroxy group are attached to the same carbon atom. The general formula is R 2 C(OH)CN , where R is H, alkyl , or aryl .

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