Terpene hydrocarbon

C, b.p. 156 C. The most important of the terpene hydrocarbons. It is found in most essential oils derived from the Coniferae, and is the main constituent of turpentine oil. Contains two asymmetric carbon atoms. The (- -)-form is easily obtained in a pure state by fractionation of Greek turpentine oil, of which it constitutes 95%. Pinene may be separated from turpentine oil in the form of its crystalline nitrosochloride, CioHigClNO, from which the ( + )-form may be recovered by boiling with aniline in alcoholic solution. When heated under pressure at 250-270 C, a-pinene is converted into dipentene. It can be reduced by hydrogen in the presence of a catalyst to form... [Pg.314]

Terpene-based resins Terpene hydrocarbons Terpeneless lime oil Terp ene-phenolics Terpenes... [Pg.968]

Ma.nufa.cture. The preparation of sulfuryl chloride is carried out by feeding dry sulfur dioxide and chlorine into a water-cooled glass-lined steel vessel containing a catalyst, eg, activated charcoal. Alternatively, chlorine is passed into Hquefted sulfur dioxide at ca 0°C in the presence of a dissolved catalyst, eg, camphor, a terpene hydrocarbon, an ether, or an ester. The sulfuryl chloride is purified by distillation the commercial product is typically 99 wt % pure, as measured by ASTM distillation method D850. [Pg.143]

Trees, especially conifers, contain tall oils. Tall oil is not isolated dkecfly tall oil fatty acids are isolated from the soaps generated as a by-product of the sulfate pulping process for making paper. Refined tall oil fatty acids are obtained by acidification of the soaps, followed by fractional distillation to separate the fatty acids from the rosin acids and terpene hydrocarbons that also are present in the cmde tall oil fatty acids (see Carboxylic acids Fatty ACIDS FROMTALL OIL). [Pg.259]

Terpin hydrate [2451-01-6] (10), one of the most weU-known expectorants, is isolated from cmde pine rosin left after the distillation of volatile terpene hydrocarbons and alcohols. It is also manufactured from turpentine (a-pinene) by acid-cataly2ed hydration. Terpin hydrate may exist as cis and trans isomers, but only the cis isomer forms a stable, crystalline monohydrate. Terpin hydrate is available in the United States only in prescription products. [Pg.518]

Forests can act as sources of some of the trace gases in the atmosphere, such as hydrocarbons, hydrogen sulfide, NO, and NH3. Forests have been identified as emitters of terpene hydrocarbons. In 1960, Went (10) estimated that hydrocarbon releases to the atmosphere were on the order of 108 tons per year. Later work by Rasmussen (11) suggested that the release of terpenes from forest systems is 2 x 10 tons of reactive materials per year on a global basis. This is several times the anthropogenic input. Yet, it is important to remember that forest emissions are much more widely dispersed and less concentrated than anthropogenic emissions. Table 8-2 shows terpene emissions from different types of forest systems in the United States. [Pg.117]

Terpen-gruppe, /. terpene group, -kohlenwas-serstoff, m. terpene hydrocarbon. [Pg.443]

Dicarbonyls. A third area of uncertainty is the treatment of dicarbonyls formed from aromatic or terpene hydrocarbon oxidation. (The simplest is glyoxal, CHOCHO, but a large number have been identified, 47. The yields and subsequent reactions of these compounds represent a major area of uncertainty in urban air photochemistry (186) and since they may be a significant source of HOjj through photolysis, inaccuracies in their portrayal may result in errors in calculated values of HO. and HO2.. [Pg.97]

Longifolene is a tricyclic sesquiterpene. It is a typical terpene hydrocarbon in terms of the structural complexity. The synthetic challenge lies in construction of the bicyclic ring system. Schemes 13.24 through 13.33 describe nine separate syntheses of longifolene. We wish to particularly emphasize the methods for carbon-carbon bond formation used in these syntheses. There are four stereogenic centers in longifolene,... [Pg.1186]

Violent explosions which occurred at —100 to —180°C in ammonia synthesis gas units were traced to the formation of explosive addition products of dienes and oxides of nitrogen, produced from interaction of nitrogen oxide and oxygen. Laboratory experiments showed that the addition products from 1,3-butadiene or cyclopentadiene formed rapidly at about — 150°C, and ignited or exploded on warming to —35 to — 15°C. The unconjugated propadiene, and alkenes or acetylene reacted slowly and the products did not ignite until +30 to +50°C [1], This type of derivative ( pseudo-nitrosite ) was formerly used (Wallach) to characterise terpene hydrocarbons. Further comments were made later [2],... [Pg.1782]

Turpentine is a mixture of CioHie volatile terpenes (hydrocarbons made of isoprene units). There are actually four different types and methods of making turpentine, including steam distillation of wood. The two pinenes, a and P, are major components of turpentine. Other compounds found in abundant amounts are camphene, dipentene, terpinolene, and A -carene. Although it has been replaced by petroleum hydrocarbons as paint thinners (lower price, less odor), turpentine is still a good solvent and thinner in many specialty applications. The use pattern for turpentine is as follows synthetic... [Pg.412]

Hendriks, H., T. M. Malingre, S. Batterman and R. Bos. Mono- and sesqui-terpene hydrocarbons of the essential oil of Cannabis sativa. Phytochemistry 1975 14 814—815. Thorbum, M. J. Jamaican bushes and human chromosomes. Jamaica J 1975 8(4) 18. [Pg.95]

Terpenes. Hydrocarbon volatile oils, often with a strong smell. [Pg.576]

Cyclic terpene hydrocarbons occur in essential oils, sometimes in large amounts. They often serve as starting materials for the synthesis of fragrance and flavor materials. By themselves they generally contribute relatively little to fragrance and aroma. They are used mainly in household perfumery and for reconstitution of essential oils. [Pg.48]

Of the various types of monocyclic terpene hydrocarbons, those with the p-menthadiene structure are the most important. Examples are as follows ... [Pg.48]

Of the bicyclic terpene hydrocarbons, the pinenes are by far the most important industrially. Camphene and 3-carene are used as starting materials for fragrance substances. [Pg.49]

Pinenes are widespread, naturally occurring terpene hydrocarbons. The a- and /3-forms occur in varying ratios in essential oils. [Pg.50]

Hydrogenation of a-terpineol yields />-menthan-8-ol. Terpineol is readily dehydrated by acids, yielding a mixture of unsaturated cyclic terpene hydrocarbons. Under mildly acidic conditions, terpin hydrate is formed. The most important... [Pg.56]

Citrus peel oils are a special type of essential oil. They are isolated by pressing the peel to release the volatile substances stored in the pericarp in small oil glands. The resulting products are termed essential oils because they consist largely of highly volatile terpene hydrocarbons. However, they also contain small amounts of nonvolatile compounds, such as dyes, waxes, and furocoumarines. [Pg.169]

Grapefruit oil is produced mainly in the United States and its composition varies with the species. White grapefruit oil obtained from the varieties Marsh seedless and Duncan that are grown in Florida, contains more than 90% terpene hydrocarbons ((+)-limonene, 93.5-95%), 0.5% alcohols (mainly linalool), 1% aldehydes (mainly octanal and decanal), 0.05-0.8% nootkatone [371]. Worldwide production is ca. 200 t/yr. [Pg.186]

The oils have a high terpene hydrocarbon content (>90%, mainly (+)-limonene), but their content of oxygen-containing compounds differs and affects their quality. Important for aroma are aldehydes, mainly decanal and citral, and aliphatic and terpenoid esters. The sesquiterpene aldehydes a-sinensal [17909-77-2] and/3-sinensal [6066-88-8], which contribute particularly to the special sweet orange aroma, also occur in other citrus oils, although in lower concentration [369-370a, 370d, 394,421, 430-438]. [Pg.189]

After separation of neroli oil, the aqueous layer of the steam distillate, known as orange blossom water, is extracted with suitable solvents (e.g., petroleum ether). Evaporation gives orange flower water absolute (absolue de Teau de fleurs d oranger), which is a dark brown-red liquid. It contains less terpene hydrocarbons and correspondingly more polar compounds than neroli oil. [Pg.207]

Indonesian oils contain ca. 90% terpene hydrocarbons, mainly sabinene (14-29%) and a- (15-28%) and /3-pinene (13-18%). Major oxygen-containing constituents are l-terpinen-4-ol (2 6%) and phenol ether derivatives like myristicine (5-12%) [646-650cj. [Pg.208]

Labdanum Cistus ladaniferus L. Labdane diterpenes and mono-terpene hydrocarbons ... [Pg.83]

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