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Glycerol selectivity

Figure 4. Oxidation of allyl alcohol in water at 65 °C conversion glycidol selectivity glycerol selectivity. Figure 4. Oxidation of allyl alcohol in water at 65 °C conversion glycidol selectivity glycerol selectivity.
Figure 5. Oxidation of allyl alcohol in methanol at 65 C conversion glycidol selectivity A ether diols glycerol selectivity. Figure 5. Oxidation of allyl alcohol in methanol at 65 C conversion glycidol selectivity A ether diols glycerol selectivity.
Other L-amino acids are manufactured much more economically ia thousands of tons per year ia Japan by simplified fermentations direcdy from glucose, ethanol, acetic acid, glycerol, or / -paraffin, by means of selected auxotrophic, regulatory, and analogue-resistant bacterial mutants (94,95). [Pg.314]

Alkyd resins are produced by reaction of a polybasic acid, such as phthaUc or maleic anhydride, with a polyhydric alcohol, such as glycerol, pentaerythritol, or glycol, in the presence of an oil or fatty acid. The resulting polymeric material can be further modified with other polymers and chemicals such as acryhcs, siUcones, and natural oils. On account of the broad selection of various polybasic acids, polyhydric alcohols, oils and fatty acids, and other modifying ingredients, many different types of alkyd resins can be produced that have a wide range of coating properties (see Alkyd resins). [Pg.541]

The newer HFC refrigerants are not soluble in or miscible with mineral oils or alkylbenzenes. The leading candidates for use with HFC refrigerants are polyol ester lubricants. These lubricants are derived from a reaction between an alcohol and a normal or branched carboxyflc acid. The most common alcohols used are pentaerythritol, trimethylolpropane, neopentjlglycol, and glycerol. The acids are usually selected to give the correct viscosity and fluidity at low temperatures. [Pg.69]

Selected physical and chemical properties of sodium nitrate are Hsted in Table 1. At room temperature, sodium nitrate is an ododess and colodess soHd, moderately hygroscopic, saline in taste, and very soluble in water, ammonia, and glycerol. Detailed physical and chemical properties are also available (3,4). [Pg.192]

Cocoa butter substitutes and equivalents differ greatly with respect to their method of manufacture, source of fats, and functionaHty they are produced by several physical and chemical processes (17,18). Cocoa butter substitutes are produced from lauric acid fats such as coconut, palm, and palm kernel oils by fractionation and hydrogenation from domestic fats such as soy, com, and cotton seed oils by selective hydrogenation or from palm kernel stearines by fractionation. Cocoa butter equivalents can be produced from palm kernel oil and other specialty fats such as shea and ilHpe by fractional crystallization from glycerol and selected fatty acids by direct chemical synthesis or from edible beef tallow by acetone crystallization. [Pg.93]

Fig. 2. Drying capacity of selected drying agents in liquid form. A represents lithium chloride B, calcium chloride C, sulfuric acid D, glycerol E, triethylene... Fig. 2. Drying capacity of selected drying agents in liquid form. A represents lithium chloride B, calcium chloride C, sulfuric acid D, glycerol E, triethylene...
Novel glycerol and formaldehyde selective sensors based on pEI-Sensitive Field Effect Transistors as transducers and Glycerol Dehydrogenase and Formaldehyde Dehydrogenase as biorecognition elements have been developed. The main analytical parameters of the sensors have been investigated and will be discussed. [Pg.303]

Eicosanoids, so named because they are all derived from 20-carbon fatty acids, are ubiquitous breakdown products of phospholipids. In response to appropriate stimuli, cells activate the breakdown of selected phospholipids (Figure 25.27). Phospholipase Ag (Chapter 8) selectively cleaves fatty acids from the C-2 position of phospholipids. Often these are unsaturated fatty acids, among which is arachidonic acid. Arachidonic acid may also be released from phospholipids by the combined actions of phospholipase C (which yields diacyl-glycerols) and diacylglycerol lipase (which releases fatty acids). [Pg.829]

Acetonide formation is the most commonly used protection for 1,2- and 1,3-diols. The acetonide has been used extensively in carbohydrate chemistry to mask selectively the hydroxyls of the many different sugars. In preparing ace-tonides of triols, the 1,2-derivative is generally favored over the 1,3-derivative which in turn is favored over the 1,4-derivative, but the extent to which the 1,2-acetonide is favored is dependent upon the structure of the triol. Note that the 1,2-selectivity for the ketal from 3-pentanone is better than that from acetone. Its greater lipophilicity also improves the isolation of the ketals of small alcohols such as glycerol. ... [Pg.207]

Furthermore, if the antibiotic passes membranes through a specific port of entry, its mutational loss leads to resistance. The lack of the outer membrane protein OprD in P. aeruginosa causes resistance to the (3-lactam antibiotic imipenem. Fosfomycin passes the cytoplasmic membrane via an L-a-glycerol phosphate permease. This transport system is not essential for bacterial growth and therefore mutants with a reduced expression are frequently selected under therapy. [Pg.772]

Importantly, there was a general marked selectivity for inhibition of influenza A over influenza B viral sialidases in the carboxamide series (e.g. as seen with 27) (Smith et al. 1996, 1998), determined from crystallographic and molecular modelling studies (Smith et al. 1996 Taylor et al. 1998) to be due to the relative abilities of each of the sialidases to absorb the structural changes required to accommodate the hydrophobic alkyl chains in the glycerol side-chain binding pocket. In influenza... [Pg.128]

The simultaneous analysis of orthophosphate, glycerol phosphates, and inositol phosphates has been achieved by spectrophotometric analysis of the molybdovanadate complexes. Also, a sensitive and selective chemiluminescent molecular emission method for the estimation of phosphorus and sulphur is described, which is based on passing solutions into a cool, reducing, nitrogen-hydrogen diffusion flame. For organic compounds it was usually necessary to prepare test solutions by an oxygen-flask combustion technique. [Pg.278]

Selective catal3ftic oxidation with air of glycerol and oxygenated derivatives on platinum metals... [Pg.161]

Figure 6. Selectivity for dihydroxyacetone vs. conversion of glycerol, on PtBi/C, for batch and continuous systems. Figure 6. Selectivity for dihydroxyacetone vs. conversion of glycerol, on PtBi/C, for batch and continuous systems.

See other pages where Glycerol selectivity is mentioned: [Pg.246]    [Pg.538]    [Pg.303]    [Pg.308]    [Pg.246]    [Pg.538]    [Pg.303]    [Pg.308]    [Pg.1008]    [Pg.179]    [Pg.70]    [Pg.73]    [Pg.259]    [Pg.156]    [Pg.159]    [Pg.352]    [Pg.118]    [Pg.150]    [Pg.150]    [Pg.1132]    [Pg.331]    [Pg.465]    [Pg.466]    [Pg.782]    [Pg.126]    [Pg.138]    [Pg.277]    [Pg.510]    [Pg.921]    [Pg.928]    [Pg.161]    [Pg.165]    [Pg.165]    [Pg.166]    [Pg.169]    [Pg.124]   
See also in sourсe #XX -- [ Pg.227 ]




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Glycerol selective oxidation

Selective oxidation of glycerol

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