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A terpene is a naturally occurring hydrocarbon based on combinations of the isoprene unit. Terpenoids are compounds related to terpenes, which may include some oxygen functionality or some rearrangement, however the two terms are often used interchangeably.
The terpene alpha-pinene is a major component of the common solvent, turpentine. The one terpene that has major applications is natural rubber (i.e., polyisoprene). The possibility that other terpenes could be used as precursors to produce synthetic polymers has been investigated. Many terpenes have been shown to have pharmacological effects.
Turpentine is composed of terpenes, primarily the monoterpenes alpha-and beta-pinene, with lesser amounts of carene, camphene, limonene, and terpinolene. [ 3 ] Substitutes include white spirit or other petroleum distillates – although the constituent chemicals are very different.
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]
Monoterpenes are a class of terpenes that consist of two isoprene units and have the molecular formula C 10 H 16. Monoterpenes may be linear (acyclic) or contain rings (monocyclic and bicyclic). Modified terpenes, such as those containing oxygen functionality or missing a methyl group, are called monoterpenoids. Monoterpenes and monoterpenoids ...
Thymol (also known as 2-isopropyl-5-methylphenol, IPMP), C 10 H 14 O, is a natural monoterpenoid phenol derivative of p-Cymene, isomeric with carvacrol.It occurs naturally in the oil of thyme, and it is extracted from Thymus vulgaris (common thyme), ajwain, [4] and various other plants as a white crystalline substance of a pleasant aromatic odor and strong antiseptic properties.
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