Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Phytosterols hydrolysis

Unsaponifiable matter. Oils and fats contain variable amounts of sterols, hydrocarbons, tocopherols, carotenoids, and other compounds, collectively referred to as unsaponifiable matter because they do not produce soaps upon hydrolysis (Table 6). The sterol and tocopherol composition of commodity oils is discussed in another chapter. Some of these minor components are removed during refining, and the resulting concentrates may be useful byproducts, for example, tocopherol antioxidants. Characteristic fingerprints of minor components, particularly phytosterols and tocopherols, are also used to authenticate oils and detect adulteration (18). [Pg.54]

In the DOD, phytosterols are present in both the free and esterified forms with fatty acids. Therefore, the first step in the extraction of phytosterols is conversion of phytosterol fatty esters into free phytosterols. This is achieved either by hydrolysis or trani-esterification. Hydrolysis could be carried out under strong basic conditions (saponification with further acidulation), under strong acidic conditions, or under chemical or enzyme (specific or nonspecific) catalyzation. Re-esterification of phytosterols occurs during methyl ester distillation as a result of the high temperatures involved therefore, a further trani-esterification step for free sterols is required. Esterification of phytosterols or trani-esterification of sterol fatty acid esters is the second step in this process. Methanol is the most commonly used alcohol, and it leads to methyl esters, which are characterized by a higher volatility, however, other Ci to C4 alcohols may also be used. Esterification and trans-esterification of fatty acids or phytosterols can be catalyzed by metal alcoholates, or hydroxide, by organic catalysts, or by enzymes (Table 7). [Pg.1969]

Wild cherry is a large tree, native to southern Canada. It is widespread in the United States and Europe. The bark, small branches, and twigs are used to prepare the fluid extract and tincture. The main constituent of wild cherry extract is the glucoside prunasin, which on enzymatic hydrolysis yields prussic acid, glucose, and benzaldehyde. Also present are coumarin, phytosterols, benzoic acid, and fatty acids (e.g., oleic, linoleic, and palmitic acids). It has a characteristic sweet, tart, cherry-like flavor. Wild cherry bark extract is commonly used at concentrations of approximately 50-800 ppm in foods and pharmaceuticals. [Pg.1764]


See other pages where Phytosterols hydrolysis is mentioned: [Pg.453]    [Pg.243]    [Pg.57]    [Pg.76]    [Pg.316]    [Pg.326]    [Pg.329]    [Pg.337]    [Pg.337]    [Pg.343]    [Pg.607]    [Pg.799]    [Pg.1685]    [Pg.1908]    [Pg.413]    [Pg.591]    [Pg.622]    [Pg.181]    [Pg.67]    [Pg.564]   
See also in sourсe #XX -- [ Pg.333 ]




SEARCH



Phytosterol

Phytosterols

© 2024 chempedia.info