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The Collaborative International Dictionary
borneol

Camphor \Cam"phor\ (k[a^]m"f[~e]r), n. [OE. camfere, F. camphre (cf. It. canfora, Sp. camfora, alcanfor, LL. canfora, camphora, NGr. kafoyra`), fr. Ar. k[=a]f[=u]r, prob. fr. Skr. karp[=u]ra.]

  1. A tough, white, aromatic resin, or gum, obtained from different species of the Laurus family, esp. from Cinnamomum camphara (the Laurus camphora of Linn[ae]us.). Camphor, C10H16O, is volatile and fragrant, and is used in medicine as a diaphoretic, a stimulant, or sedative.

  2. originally, a gum resembling ordinary camphor, obtained from a tree ( Dryobalanops aromatica formerly Dryobalanops camphora) growing in Sumatra and Borneo; now applied to its main constituent, a terpene alcohol obtainable as a white solid C10H18O, called also Borneo camphor, Malay camphor, Malayan camphor, camphor of Borneo, Sumatra camphor, bornyl alcohol, camphol, and borneol. The isomer from Dryobalanops is dextrorotatory; the levoratatory form is obtainable from other species of plants, and the racemic mixture may be obtained by reduction of camphor. It is used in perfumery, and for manufacture of its esters. See Borneol.

    Note: The name camphor is also applied to a number of bodies of similar appearance and properties, as cedar camphor, obtained from the red or pencil cedar ( Juniperus Virginiana), and peppermint camphor, or menthol, obtained from the oil of peppermint.

    Camphor oil (Chem.), name variously given to certain oil-like products, obtained especially from the camphor tree.

    Camphor tree, a large evergreen tree ( Cinnamomum Camphora) with lax, smooth branches and shining triple-nerved lanceolate leaves, probably native in China, but now cultivated in most warm countries. Camphor is collected by a process of steaming the chips of the wood and subliming the product.

Wiktionary
borneol

n. (context biochemistry English) A bicyclic organic compound and a terpene, easily oxidized to the ketone yielding camphor.

Wikipedia
Borneol

Borneol is a bicyclic organic compound and a terpene. The hydroxyl group in this compound is placed in an endo position. There are two different enantiomers of borneol. Both d-(+)-borneol and l-(–)-borneol are found in nature.