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P-Terpineol

Synthetic pine oil is produced by the acid-catalyzed hydration of a-pinene (Fig. 1). Mineral acids, usually phosphoric acid, are used in concentrations of 20—40 wt % and at temperatures varying from 30—100°C. Depending on the conditions used, alcohols, chiefly a-terpineol (9), are produced along with /)-menthadienes and cineoles, mainly limonene, terpinolene, and 1,4- and 1,8-cineole (46—48). Various grades of pine oil can be produced by fractionation of the cmde products. Formation of terpin hydrate (10) from a-terpineol gives P-terpineol (11) and y-terpineol (12) as a consequence of the reversible... [Pg.411]

Principal terpene alcohol components of pine oils are a-terpineol, y-terpineol, p-terpineol, a-fenchol, bomeol, terpinen-l-ol, and terpinen-4-ol. The ethers, 1,4- and 1,8-cineole, are also formed by cydization of the y>-menthane-1,4- and 1,8-diols. The bicydic alcohols, a-fenchol [512-13-0] (61) and bomeol (62), are also formed by the Wagner-Meerwein rearrangement of the pinanyl carbonium ion and subsequent hydration. Bomeol is t / i7< -l,7,7-trimethylbicydo[2.2.1]heptan-2-ol [507-70-0]. Many other components of pine oils are also found, depending on the source of the turpentine used and the method of production. [Pg.419]

Limonene is the major monoterpene in orange oil. This is a colorless and odorless compound at high purity. However, it rapidly oxidizes to carveol and carvone in the presence of air. Under acidic conditions, a-terpineol, P-terpineol, and y-terpineol are also produced. Many of the impurities present in limonene have much higher odor potencies. These odor potent compounds can be perceived as limonene odor . [Pg.1048]

Terpineol is mainly isolated from plants of the Eucalyptus species and is a mixture of a-terpineol, P-terpineol, 4-terpineol, and 1,4- and 1,8-terpindiols. Both enantiomers of a-terpineol are commercially produced through hydration of a-pinenes.37... [Pg.65]

The steam-distilled oil derived from the galls of Pistacia integerrima was analyzed by chromatography and spectral techniques. The oil was found to be rich in a-pinene (13) (21.8%), P-pinene (14) (16.2%), a-phellandrene (15) (15.5%), and A3-carene (16) (11.1%). The other main constituents characterized were P-phellandrene (17), y-terpinene (18), a-terpineol (19), and P-terpineol (20) as well as a-ocimene (21) and P-ocimene (22). This steam-distilled oil was shown to possess CNS-depressant activity [75]. [Pg.582]

Spectrum Quality Prods. http //www.spectrumchemical.com T R Chem. Toyotama Perfumery P-Terpineol CAS 138-87-4 FEMA 3564... [Pg.4338]

Rhodinyl propionate Safrol Salicylaldehyde Santalol Santalyl acetate Santalyl phenylacetate Skatole Sorbitan stearate Styrene Sucrose octaacetate a-Terpinene y-Terpinene a-Terpineol Terpineol anhyd. P-Terpineol Terpinolene Terpinyl acetate Terpinyl anthranilate Terpinyl butyrate Terpinyl cinnamate... [Pg.5286]

Yomogi alcohol, aitemlsia alcohol, davanone, lyratol + lyratyl acetate, chrysanthenol, carveol, carvone, dihydrocarvone, terpinene-4-ol, y-campholenol, myrtenol, p terpineol, 4-thujene-2-a-yl-acetate, carveyl acetate, fkcubebene, juniper camphor, thymol, P-terpenyl acetate, linalool Sabinene, germacrene D... [Pg.94]

Polyoxyethylated tri-methylolpropane triacrylate Monohydroxy polycaproUactone monoacrylate, Mw 458 P-Terpineol (l-methyl-l-(4-methyl-4-hydroxycyclohexyl)ethane... [Pg.309]


See other pages where P-Terpineol is mentioned: [Pg.413]    [Pg.1062]    [Pg.1065]    [Pg.1066]    [Pg.1066]    [Pg.174]    [Pg.63]    [Pg.64]    [Pg.152]    [Pg.175]    [Pg.247]    [Pg.315]    [Pg.315]    [Pg.32]    [Pg.88]    [Pg.372]    [Pg.482]    [Pg.474]    [Pg.1120]    [Pg.2521]    [Pg.136]    [Pg.311]    [Pg.108]    [Pg.95]    [Pg.236]    [Pg.1134]    [Pg.461]    [Pg.523]    [Pg.716]    [Pg.518]    [Pg.315]    [Pg.511]    [Pg.491]    [Pg.522]    [Pg.715]    [Pg.474]   
See also in sourсe #XX -- [ Pg.297 ]

See also in sourсe #XX -- [ Pg.88 , Pg.90 ]

See also in sourсe #XX -- [ Pg.370 , Pg.372 ]




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