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Flavors molecule

Figure 10.1 Analysis of racemic 2,5-dimethyl-4-hydroxy-3[2H]-furanone (1) obtained from a strawbeny tea, flavoured with the synthetic racemate of 1 (natural component), using an MDGC procedure (a) dichloromethane extract of the flavoured strawbeny tea, analysed on a Carbowax 20M pre-column (60 m, 0.32 mm i.d., 0.25 p.m film thickness earner gas H2, 1.95 bar 170 °C isothermal) (b) chirospecific analysis of (1) from the sti awbeny tea exti act, ti ansfened foi stereoanalysis by using a pemiethylated /3-cyclodextrin column (47 m X 0.23 mm i.d. canier gas H2, 1.70 bar 110 °C isothemial). Reprinted from Journal of High Resolution Chromatography, 13, A. Mosandl et al., Stereoisomeric flavor compounds. XLIV enantioselective analysis of some important flavor molecules , pp. 660-662, 1990, with permission from Wiley-VCH. Figure 10.1 Analysis of racemic 2,5-dimethyl-4-hydroxy-3[2H]-furanone (1) obtained from a strawbeny tea, flavoured with the synthetic racemate of 1 (natural component), using an MDGC procedure (a) dichloromethane extract of the flavoured strawbeny tea, analysed on a Carbowax 20M pre-column (60 m, 0.32 mm i.d., 0.25 p.m film thickness earner gas H2, 1.95 bar 170 °C isothermal) (b) chirospecific analysis of (1) from the sti awbeny tea exti act, ti ansfened foi stereoanalysis by using a pemiethylated /3-cyclodextrin column (47 m X 0.23 mm i.d. canier gas H2, 1.70 bar 110 °C isothemial). Reprinted from Journal of High Resolution Chromatography, 13, A. Mosandl et al., Stereoisomeric flavor compounds. XLIV enantioselective analysis of some important flavor molecules , pp. 660-662, 1990, with permission from Wiley-VCH.
A. Mosandl, G. Bmche, C. Askaii and H.-G. SclimaiT, Stereoisomeric flavor compounds. XLIV enantioselective analysis of some important flavor molecules , ]. High Resolut. Chromatogr. 13 660-662 (1990). [Pg.246]

Once the lactic add and alcohol fermentation is complete, the moromi is aged until its moldy odor has disappeared. During this portion of the aging period other flavor molecules, particularly 4-ethylguaiacol and 4-ethylphenol are added to the moromi by Candida versatilis (4), These compounds are the major components contributing to the flavor of soy sauce. The entire moromi process is completed in about six months. [Pg.202]

Sensory information obtained from the interaction of fragrance and flavor molecules with olfactory and taste receptors is processed in defined cerebral areas, resulting in perception. During the past 10 years much research has been done concerning sensory perception and results have been published in, e.g., [2 4b]. [Pg.3]

Mosandl A, Bruche G, Askari C, Schmarr H-G (1990) Steroisomeric flavor compoimds XLIV Enantioselective analysis of some important flavor molecules. J High Resolut Chromatogr... [Pg.404]

QSAR studies of flavor molecules require two types of data... [Pg.33]

These examples are merely modest beginnings at relating geometrical maps that represent similarities in odor quality with physicochemical parameters. It is now necessary to expand these mathematical techniques to more data sets with extensive use of the non-covalent bonding parameters shown in Table 1. Ultimately reliable design of flavor molecules by computer will be feasible as ve explore a wider range of molecular types, especially isomers, with the techniques described in this paper. [Pg.50]

Previous work has shown that flavor retention increases with increasing inlet air temperature until internal steam is formed in the drying droplet (12). The higher inlet air temperatures produce a more rapid drying which thereby results in a shorter time until the formation of a high solids "skin" around the drying droplet. This "skin" acts as a semipermeable membrane which retains the larger (relative to water) flavor molecules. [Pg.82]

The components of mixtures can be separated from one another by taking advantage of differences in the components physical properties. A mixture of solids and liquids, for example, can be separated using filter paper through which the liquids pass but the solids do not. This is how coffee is often made the caffeine and flavor molecules in the hot water pass through the filter and into the coffee pot while the solid coffee grounds remain behind. This method of separating a solid-liquid mixture is called filtration and is a common technique used by chemists. [Pg.53]

Many aldehydes are particularly fragrant. A number of flowers, for example, owe their pleasant odor to the presence of simple aldehydes. The smells of lemons, cinnamon, and almonds are due to the aldehydes citral, cinnamalde-hyde, and benzaldehyde, respectively. The structures of these three aldehydes are shown in Figure 12.21. The aldehyde vanillin, introduced at the beginning of this chapter, is the key flavoring molecule derived from the vanilla orchid. You may have noticed that vanilla seed pods and vanilla extract are fairly expensive. Imitation vanilla flavoring is less expensive because it is merely a solution of the compound vanillin, which is economically synthesized from the waste chemicals of the wood pulp industry. Imitation vanilla does not taste the same as natural vanilla extract, however, because in addition to vanillin many other flavorful molecules contribute to the complex taste of natural vanilla. Many books made in the days before acid-free paper smell of vanilla because of the vanillin formed and released as the paper ages, a process that is accelerated by the acids the paper contains. [Pg.408]

Vinegar made from apples contains the molecules that give apples their flavor and color. These flavor molecules usually cannot be smelled in the vinegar because the acetic acid has a stronger smell. The flavor molecules of apples can, however, be isolated from apple cider vinegar. [Pg.35]

When the acetic acid and the water molecules evaporate, some of the apple flavor molecules are left. The apple flavor molecules are in the brown, sticky substance in the bottom of the cup that contained the apple cider vinegar. This brown, sticky substance is called a residue. It is expected that there will not be a residue in the cup that contained the distilled white vinegar. The flavor molecules from the grain are... [Pg.35]

Can you isolate the flavor molecules from tea Make a cup of tea and let it sit in a warm place until all the water is gone. What does the residue smell like ... [Pg.36]

Recycled materials may contain absorbed odorous or flavorful molecules from earlier use that, when introduced into a new packaging material, may cause taint (Franz and Welle, 2003 Kilcast, 1996). Analytical detection... [Pg.46]

Flavor Partitioning The perception of a flavor depends on the precise location of the flavor molecules within an emulsion. The aroma is determined by the presence of volatile molecules in the vapor phase above an emulsion (122, 126). Most flavors are perceived more intensely when they are present in the aqueous phase, rather than in the oil phase (127, 128). Certain flavor molecules may associate with the interfacial region, which alters their concentration in the vapor and aqueous phases (129). It is therefore important to establish the factors that determine the partitioning of flavor molecules within an emulsion. An emulsion system can be conveniently divided into four phases between which the flavor molecules distribute themselves the interior of the droplets, the continuous phase, the oil-water interfacial region, and the vapor phase above the emulsion. The relative concentration of the flavor molecules in each of these regions depends on their molecular structure and the properties of each of the phases (130, 131). [Pg.1853]

Flavor partition coefficients. The equilibrium distribution of a particular flavor molecule between two phases (e.g., oil-water, air-water, or air-oil) is characterized by an equilibrium partition function. These partition coefficients determine the distribution of the flavor molecules between the oil, water, and head space phases of an emulsion. [Pg.1853]

Surface activity. Many flavor molecules are amphiphilic in character, having both nonpolar and polar regions. These molecules will tend to accumulate at an oil-water interface. [Pg.1853]

Droplet concentration. The concentration of flavor molecules in the headspace of an emulsion depends on the disperse phase volume fraction, i.e., the ratio of oil to water. Previous studies have shown that there is a decrease in the fraction of a nonpolar flavor in the vapor phase as the oil content increases, whereas the amount of a polar flavor is relatively unaffected. Thus, nonpolar flavors in an emulsion become more odorous as the fat content is decreased, whereas the polar flavors remain relatively unchanged. This has important consequences when deciding the type and concentration of flavors to use in low-fat analogs of existing emulsion-based food products. [Pg.1853]

Flavor Binding. Many proteins and carbohydrates are capable of binding flavor molecules, and therefore altering their distribution within an emulsion (131-135). [Pg.1853]

Solubilization. Surfactants are normally used to physically stabilize emulsion droplets against aggregation by providing a protective membrane around the droplet. Nevertheless, there is often enough free surfactant present in an aqueous phase to form surfactant micelles. These surfactant micelles are capable of solubilizing the nonpolar molecules in their hydrophobic interior, which increases the affinity of nonpolar flavors for the aqueous phase. By a similar argument, reverse micelles in an oil phase are capable of solubilizing polar flavor molecules. [Pg.1854]

Flavor Release Flavor release is the process whereby flavor molecules move out of a food and into the surrounding saliva or vapor phase during mastication (126, 127). The release of flavors from a food material occurs under extremely complex and dynamic conditions (136). A food usually spends a relatively short period (typically 1 to 30 seconds) in the mouth before being swallowed. During this period, it is diluted with saliva, experiences temperature changes, and is subjected to a variety of mechanical forces. Mastication may therefore cause dramatic changes in the structural characteristics of a food emulsion. [Pg.1854]

During mastication, nonvolatile flavor molecules must move from within the food, through the saliva to the taste receptors on the tongue, and the inside of the mouth, whereas volatile flavor molecules must move from the food, through the saliva and into the gas phase, where they are carried to the aroma receptors in the nasal cavity. The two major factors that determine the rate at which these processes occur are the equilibrium partition coefficient (because this determines the initial flavor concentration gradients at the various boundaries) and the mass transfer coefficient (because this determines the speed at which the molecules move from one location to another). A variety of mathematical models have been developed to describe the release of flavor molecules from oil-in-water emulsions. [Pg.1854]

Osmosis is the tendency for solvent to flow into salty solutions to dilute them. Osmosis is responsible for the revival of wilted celery when soaked in pure water water flows into the celery to dilute the salty cells. Osmosis is responsible for pickles pickling water flows out of the pickles in an attempt to dilute the salty brine. How does the taste get into the pickle Osmosis is also striving for equilibrium, and equilibrium situations in chemistry are dynamic. At equilibrium, the flavorful molecules will be redistributed between pickle and brine. Recall the demonstration with the paper towel and the food dye the paper towel was allowed to take on its equilibrium load of water from a puddle, and then food dye was added to the puddle. Because equilibrium is dynamic, some food dye eventually found its way into the towel. At equilibrium there will be more water outside the pickle cell than inside, but the flavoring in the brine will have found its way into the pickle. [Pg.239]

The oxidation of mercaptans can be useful to prepare other flavor molecules. Furfuryl Mercaptan and Methyl Mercaptan can be oxidized together to give Methyl Furfuryl Disulfide, a potent material useful for bread, pork and other meat products. It is also the third most active flavor material in fresh brewed coffee, being present at 0.38 ppm or 9,623 times its flavor threshold (0.04 ppb) (equation 11). [Pg.102]

Taste receptor cells within taste buds in different areas of the tongue respond to the sweet, sour, bitter, or salty flavor molecules. One soporous unit of fructose (C(,H]20, the sweetest kind of sugor, forms hydrogen bonds with the receptor site on the sweet toste buds. Saccharin contains a similar soporous unit (shaded area) and therefore evokes an equivalent response from the sweet taste receptor cells. [Pg.557]

The human tongue is studded with small conical bumps, or papillae, which house the taste buds. Each taste bud consists of receptor cells, and extending from each receptor cell are taste hairs with receptor sites for flavor molecules. The receptor cells can distinguish only four general flavors sweet, salty, bitter, and sour. The areas of response to these tastes are located on specific parts of the tongue. [Pg.557]


See other pages where Flavors molecule is mentioned: [Pg.298]    [Pg.336]    [Pg.486]    [Pg.492]    [Pg.14]    [Pg.406]    [Pg.55]    [Pg.57]    [Pg.58]    [Pg.54]    [Pg.173]    [Pg.144]    [Pg.169]    [Pg.70]    [Pg.70]    [Pg.48]    [Pg.48]    [Pg.2]    [Pg.206]    [Pg.1823]    [Pg.1853]    [Pg.250]   
See also in sourсe #XX -- [ Pg.84 ]




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