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The chemical structure of cryptoxanthin, a yellow tetraterpenoid of the xanthophyll type.. Tetraterpenes are terpenes consisting of eight isoprene units and have the molecular formula C 40 H 64. [1]
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The term terpene was coined in 1866 by the German chemist August Kekulé to denote all hydrocarbons having the empirical formula C 10 H 16, of which camphene was one. Previously, many hydrocarbons having the empirical formula C 10 H 16 had been called "camphene", but many other hydrocarbons of the same composition had different names.
While sometimes used interchangeably with "terpenes", terpenoids contain additional functional groups, usually containing oxygen. [1] When combined with the hydrocarbon terpenes, terpenoids comprise about 80,000 compounds. [2] They are the largest class of plant secondary metabolites, representing about 60% of known natural products. [3]
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Terpineol is any of four isomeric monoterpenoids.Terpenoids are terpene that are modified by the addition of a functional group, in this case, an alcohol.Terpineols have been isolated from a variety of sources such as cardamom, cajuput oil, pine oil, and petitgrain oil. [2]
Biosynthetic pathway to alpha-terpinene from geranyl pyrophosphate. [2]The biosynthesis of α-terpinene and other terpenoids starts with the isomerization of geranyl pyrophosphate to linalyl pyrophosphate (LPP).
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