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Degradation compounds

Stabihty studies ate developed to assure a desirable shelf-life period. These also estabhsh limits of acceptabiUty for impurities and degradation compounds, when present, and determine acceptable storage conditions for raw materials and the manufactured products. Stabihty studies are thus important to the deterrnination of expiration dates for dmg products. [Pg.225]

Ozone can be used to completely oxidize low concentrations of organics in aqueous streams or partially degrade compounds that are refractory or difficult to treat by other methods. Compounds that can be treated with ozone include alkanes, alcohols, ketones, aldehydes, phenols, benzene and its derivatives, and cyanide. Ozone readHy oxidizes cyanide to cyanate, however, further oxidation of the cyanate by ozone proceeds rather slowly and may require other oxidation treatment like alkaline chlorination to complete the degradation process. [Pg.163]

Vertical stratification, where the most easily degraded compounds are metabohzed first upon entering the filter bed. The more difficult-to-metabolize compounds pass through the lower region of the bed and are metabolized in the upper levels. [Pg.2193]

In order to ameliorate the problem of solvolytic degradation, compound 109 was treated with TIPSOTf, to provide silyl ether 113 in 72% yield (Scheme 19). The acetonides were removed with PPTS in warm MeOH to provide a mixture of compounds in which the TBS groups were also partially removed. Exposure of this mixture to HF-pyridine successfully generated filipin III (114), in 39 % overall yield from 113. [Pg.72]

Traditionally, dried or powdered plant material is used and extracts can be obtained by mixing the material with food-grade solvents like dichloromethane or acetone followed by washing, concentration, and solvent removal. The result is an oily product that may contain variable amounts of pheophytins and other chlorophyll degradation compounds usually accompanied by lipid-soluble substances like carotenoids (mainly lutein), carotenes, fats, waxes, and phospholipids, depending on the raw material and extraction techniques employed. This product is usually marketed as pheophytin after standardization with vegetable oils. [Pg.204]

It is experimentally difficult to obtain numerical estimates of the total number of bacteria present in seawater, and the contribution of ultramicroorganisms that have a small cell volume and low concentrations of DNA may be seriously underestimated. Although it is possible to evaluate their contribution to the uptake and mineralization of readily degraded compounds such as amino acids and carbohydrates, it is more difficult to estimate then-potential for degrading xenobiotics at realistic concentrations. [Pg.59]

Zepka, L. Q. and A. Z. Mercadante. 2009. Degradation compounds of carotenoids formed during heating of a simulated cashew apple juice. Food Chem. 117 28-34. [Pg.253]

Most of the methods in which the paper is treated with a chelating agent are capable of showing a separation of some of the tetracycline drugs from each other and from their respective epimeric forms. They are also capable of revealing the presence of common degradation compounds of these drugs. [Pg.125]

The mobility of very slowly degradable compounds or persistent metabolites present in surface water or bank filtration-enriched ground water is of particular interest for the production of potable water. In common with many other compounds, certain surfactants, and especially their polar metabolites, have the potential to bypass the technical purification units used, which may include flocculation (active charcoal) filtration, ozonation or chlorination, and thus can be found ultimately in drinking water destined for human consumption (see Chapter 6.4). [Pg.68]

Location of the contaminants in the subsurface. Degradable compounds must be dissolved in groundwater or adsorbed onto more permeable matrix materials within the saturated zone. [Pg.278]

ChemicaPPhysical Hwang et al. (2003) studied the chemical oxidation of mancozeb (100 ppm) in aqueous solution using ozone (continuously supplied at a concentration of 3 ppm) and chlorine dioxide (20 ppm). Ozonation of the solution for 60 min yielded several degradation compounds including ethylene thiourea as the major product. Degradation of mancozeb by chlorine dioxide also yielded ethylene thiourea. After 60 min of treatment, mancozeb was still detected suggesting that chlorine dioxide was less effective as an oxidant than ozone. However, the investigators... [Pg.1590]

Soil. Harvey and Pease (1973) reported that methomyl dissipated rapidly in fine sand and loamy sand soils. One month following application to a Delaware soil, 1.8% of the applied dosage was recovered and after 1 yr, methomyl was not detected. The hydrolysis product (5-methyl A/ hydroxythioacetimidate) and a trace mixture of very polar compounds were the intermediate degradation compounds before forming the principal end product, carbon dioxide. [Pg.1593]

Chiba, M. and Veres, D.F. Fate of benomyl and its degradation compound methyl 2-benzimidazolecarbamate on apple foliage, J. Agric. Food Chem., 29(3) 588-590,1981. [Pg.1643]

Category n — Analytical methods for determination of impurities in bulk drug substances or degradation compounds in finished pharmaceutical products. These methods include quantitative assays and limit tests. [Pg.451]

Exceptions exist to this tendency for ready incorporation of the initial transformation products of xenobiotic compounds into a common pathway. First, occasionally a product is formed which is unreactive in subsequent steps in a particular microorganism. Such partially degraded compounds have been referred to as dead-end metabolites (Knackmuss, 1981). An example of this is the 5-chloro-2-hydroxy-muconic acid semialdehyde produced by the meta cleavage of 4-chlorocatechol by a particular pseudomonad species ... [Pg.700]


See other pages where Degradation compounds is mentioned: [Pg.27]    [Pg.38]    [Pg.169]    [Pg.170]    [Pg.225]    [Pg.218]    [Pg.34]    [Pg.410]    [Pg.129]    [Pg.247]    [Pg.209]    [Pg.241]    [Pg.288]    [Pg.924]    [Pg.1148]    [Pg.26]    [Pg.556]    [Pg.191]    [Pg.374]    [Pg.183]    [Pg.1582]    [Pg.216]    [Pg.145]    [Pg.170]    [Pg.924]    [Pg.1148]    [Pg.147]    [Pg.437]    [Pg.4]    [Pg.253]    [Pg.27]    [Pg.38]   
See also in sourсe #XX -- [ Pg.22 , Pg.73 ]




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