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Analysis fruit

Anthocyaiuns are widely distribnted in nature, occurring in most higher plants and found in all parts of the plants, being most important in flowers and fruits. Analysis of anthocyanins in fmits has revealed that the profile of the anthocyanin content varies among different species, and even within one species. Thus, differentiation of different grape species (species of Vitis vinifera) has been possible through the study of the anthocyanin composition. In general,... [Pg.286]

Based on their respective domain organizations, factors V, VIII, and ceruloplasmin likely constitute a gene family that has arisen from a common primordial gene. A fruitful analysis of the nature of this proposed relationship awaits characterization of the gene organizations of factor V and ceruloplasmin. [Pg.292]

Modern Methods of Plant Analysis, Vol. 18 Fruit Analysis... [Pg.3]

With this equipment many small molecules are detectable (Table 1). Some of them are particularly important in fruit analysis. Water vapour detection allows one to monitor respiration processes ethanol and especially acetaldehyde measurements permit one to follow the onset of fermentation (Bijnen 1995) ethane is taken as an indicator of cell membrane damage. It should be noted that periodic release of methane by cockroaches is investigated in detail with this setup (Bijnen 1995). [Pg.17]

The logical application of retrosynthetic analysis depends on the use of higher level strategies to guide the selection of effective transforms. Chapters 2-5 which follow describe the general strategies which speed the discovery of fruitful retrosynthetic pathways. In brief these strategies may be summarized as follows. [Pg.16]

The introduction of synthetic materials into natural products, often described as adulteration , is a common occurrence in food processing. The types of compounds introduced, however, are often chiral in nature, e.g. the addition of terpenes into fruit juices. The degree to which a synthetic terpene has been added to a natural product may be subsequently determined if chiral quantitation of the target species is enabled, since synthetic terpenes are manufactured as racemates. Two-dimensional GC has a long history as the methodology of choice for this particular aspect of organic analysis (38). [Pg.65]

Figure 3.7 shows some early examples of this type of analysis (39), illustrating the GC determination of the stereoisomeric composition of lactones in (a) a fruit drink (where the ratio is racemic, and the lactone is added artificially) and (b) a yoghurt, where the non-racemic ratio indicates no adulteration. Technically, this separation was enabled on a short 10 m slightly polar primary column coupled to a chiral selective cyclodextrin secondary column. Both columns were independently temperature controlled and the transfer cut performed by using a Deans switch, with a backflush of the primary column following the heart-cut. [Pg.65]

Figure 10.2 MDGC-MS differentiation between the enantiomers of theaspiranes in an aglycone fraction from puiple passion fruit DB5 pre-column (25 m X 0.25 mm i.d., 0.25 p.m film thickness canier gas He, 0.66 ml/min oven temperature, 60-300 °C at 10 °C/min with a final hold of 25 min) permethylated /3-cyclodextrin column (25 m X 0.25 mm i.d., 0.25 p.m film thickness canier gas He, 1.96 ml/min 80 °C isothermal for 20 min and then programmed to 220 °C at 2 °C/min). Reprinted from Journal of High Resolution Chromatography, 16, G. Full et al., MDGC- MS a powerful tool for enantioselective flavor analysis , pp. 642-644, 1993, with permission from Wiley-VCH. Figure 10.2 MDGC-MS differentiation between the enantiomers of theaspiranes in an aglycone fraction from puiple passion fruit DB5 pre-column (25 m X 0.25 mm i.d., 0.25 p.m film thickness canier gas He, 0.66 ml/min oven temperature, 60-300 °C at 10 °C/min with a final hold of 25 min) permethylated /3-cyclodextrin column (25 m X 0.25 mm i.d., 0.25 p.m film thickness canier gas He, 1.96 ml/min 80 °C isothermal for 20 min and then programmed to 220 °C at 2 °C/min). Reprinted from Journal of High Resolution Chromatography, 16, G. Full et al., MDGC- MS a powerful tool for enantioselective flavor analysis , pp. 642-644, 1993, with permission from Wiley-VCH.
From the practical point of view, the principal variation of environment which is definitely under the control of the cultivator, is, of course, the alteration in the composition of the soil, which is brought about by scientific manuring, llie analysis of fruits and vegetables will give the ordinary agriculturist much information as to the necessary mineral ingredients to be added to the soil but in the case of essential oils, the conditions are entirely different. The various parts of the plant tissue are affected in different ways by the same mineral salts, and successful development of the fruit or any other given part of the plant may have little or no relationship with the quantity or quality of essential oil produced. So that it is only by actual distillations of the plant, or portion of the plant, coupled with an exhaustive examination of the essential oil, that informative results can be obtained. [Pg.3]

Much valuable research has been devoted to developing the basic principles for the production of frozen fruits and vegetables of high and uniform quality. If this knowledge could be applied to its fullest extent, there would be little need for concern over the quality of such foods. Before this can be done, those responsible for quality control must be provided with suitable standards of quality and condition, and objective methods of analysis which will clearly indicate conformance or nonconformance to the standards. Responsibility for this resides with the research food technologist or chemist. It constitutes a rich field for profitable and practical research. [Pg.35]

Abscisin II is a plant hormone which accelerates (in interaction with other factors) the abscission of young fruit of cotton. It can accelerate leaf senescence and abscission, inhibit flowering, and induce dormancy. It has no activity as an auxin or a gibberellin but counteracts the action of these hormones. Abscisin II was isolated from the acid fraction of an acetone extract by chromatographic procedures guided by an abscission bioassay. Its structure was determined from elemental analysis, mass spectrum, and infrared, ultraviolet, and nuclear magnetic resonance spectra. Comparisons of these with relevant spectra of isophorone and sorbic acid derivatives confirmed that abscisin II is 3-methyl-5-(1-hydroxy-4-oxo-2, 6, 6-trimethyl-2-cyclohexen-l-yl)-c s, trans-2, 4-pen-tadienoic acid. This carbon skeleton is shown to be unique among the known sesquiterpenes. [Pg.101]

Although the absorption of a gas in a gas-liquid disperser is governed by basic mass-transfer phenomena, our knowledge of bubble dynamics and of the fluid dynamic conditions in the vessel are insufficient to permit the calculation of mass-transfer rates from first principles. One approach that is sometimes fruitful under conditions where our knowledge is insufficient to completely define the system is that of dimensional analysis. [Pg.324]

The two examples of sample preparation of solids containing low concentrations of the substances of interest will be the analysis of aflatoxins in corn meal (7) and the determination of the fungicide thiabendazole in citrus fruits. It should be pointed out that the applications chosen in this section attempt to reflect a range of analyses that the analyst is likely to meet in both research and industrial laboratories. [Pg.217]

A method has been reported for the quantification of five fungicides (shown in Figure 5.39) used to control post-harvest decay in citrus fruits to ensure that unacceptable levels of these are not present in fruit entering the food chain [26]. A survey of the literature showed that previously [27] APCl and electrospray ionization (ESI) had been compared for the analysis of ten pesticides, including two of the five of interest, i.e. carbendazim and thiabendazole, and since it was found that APCl was more sensitive for some of these and had direct flow rate compatibility with the HPLC system being used, APCl was chosen as the basis for method development. [Pg.246]

Sheridan RS, Meola JR. 1999. Analysis of pesticide residues in fruits, vegetables, and milk by gas chromatography/tandem mass spectrometry. J AOAC Int 82(4) 982-990. [Pg.230]


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See also in sourсe #XX -- [ Pg.856 , Pg.857 , Pg.858 ]




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