Oil of turpentine in the context of Α-pinene


Oil of turpentine in the context of Α-pinene

⭐ Core Definition: Oil of turpentine

Turpentine (which is also called spirit of turpentine, oil of turpentine, terebenthine, terebenthene, terebinthine and, colloquially, turps) is a fluid obtainable by the distillation of resin harvested from living trees, mainly pines. Principally used as a specialized solvent, it is also a source of material for organic syntheses.

Turpentine is composed of terpenes, primarily the monoterpenes α-pinene and β-pinene, with lesser amounts of carene, camphene, limonene, and terpinolene. Nowadays, turpentine is rarely the product of distillation of pine resin, but is a byproduct of pulping. Pulping is achieved by two processes, the Kraft process and the sulfite process. The turpentines obtained from these two processes differ in their chemical compositions. The sulfite process gives a product that is rich in cymene, whereas the Kraft process gives a pinene-rich product.

↓ Menu
HINT:

In this Dossier

Oil of turpentine in the context of Oleoresin

Oleoresins are semi-solid extracts composed of resin and essential or fatty oil. They are obtained by evaporating relevant solvents. The oleoresin of conifers is known as crude turpentine or gum turpentine, which consists of oil of turpentine and rosin.

View the full Wikipedia page for Oleoresin
↑ Return to Menu

Oil of turpentine in the context of Camphor

Camphor (/ˈkæmfər/) is a waxy, colorless solid with a strong aroma. It is classified as a terpenoid and a cyclic ketone. It is found in the wood of the camphor laurel (Cinnamomum camphora), a large evergreen tree found in East Asia; and in the kapur tree (Dryobalanops sp.), a tall timber tree from South East Asia. It also occurs in some other related trees in the laurel family, notably Ocotea usambarensis. Rosemary leaves (Rosmarinus officinalis) contain 0.05 to 0.5% camphor, while camphorweed (Heterotheca) contains some 5%. A major source of camphor in Asia is camphor basil (the parent of African blue basil). Camphor can also be synthetically produced from oil of turpentine.

The compound is chiral, existing in two possible enantiomers as shown in the structural diagrams. The structure on the left is the naturally occurring (+)-camphor ((1R,4R)-bornan-2-one), while its mirror image shown on the right is the (−)-camphor ((1S,4S)-bornan-2-one). Camphor has few uses but is of historic significance as a compound that is readily purified from natural sources.

View the full Wikipedia page for Camphor
↑ Return to Menu