Butyrate content

Basic investigations on conditions for coupling by use of butyric acid and dextran confirm that the imidazolide is formed within 2 h. The reaction at room temperature for 17 h results in butyrate content of 92% of the acid applied. Only 0.25% N is found in the product. The solvent has a pronounced influence for dextran the solvent of choice is the mixture formamide/DMF/CH2Cl2 [189]. 4-Pyrrolidinopyridine is used as catalyst in this process. 

Lopez Nl, Eloccaii ME, Garcia AE, Steinbiichel A, Mendez BS (1995) Effect of poly-3-hydroxy-butyrate content on the starvation survival of bacteria in natural waters. FEMS Microbiol Ecol 16 95-102... 

Diisodecyl adipate (DIDA) n. (-C2H4 COOCioH2i)2. a plasticizer for PVC in lower concentrations, e.g. up to 30 phr, at which it imparts low-temperature flexibility and resistance to lacquer marring. It is often used in combination with phthalate and phosphate plasticizers. DIDA is completely compatible with vinyl chloride-acetate copolymers, cellulose acetate-butyrate with high butyral content, cellulose nitrate, ethyl cellulose, and chlorinated rubber. In polystyrene, it may be used up to 25 phr. 

Ethylhexyl isodecyl phthalate (octyl iso-decyl phthalate) n, C8H17-OOCC6H4 COOC10H21. A mixed ester compatible with PVC, vinyl chloride-acetate copolymers, cellulose acetate-butyrates with higher butyrate contents, cellulose nitrate, and, in lower concentrations, with polyvinyl butyral. In vinyls, it is somewhat less volatile than dioctyl phthalate and has equivalent low-temperature properties. 

Poly(vinyl butyral) used in safety glass generally has 78—80% butyral content, 18-19% hydroxy content and less than 2% acetate content. For this application the polymer is plasticized with an ester such as dibutyl sebacate to the extent of about 30 parts of plasticizer per 100 parts of polymer the compound is then sheeted by calendering. To produce safety glass, the sheet is placed between two pieces of glass and the laminate is then bonded under heat and pressure. 

High butyrate content resins (45-53%) exhibit better general compatibility and when combined with lower molecular weights (15000-30000) result in products which are used mainly as flow additives. 

Fig. 5. Composition of cellulose acetate butyrate (propionate) as a function of butyryl (propionyl) content of esterification bath.

Cellulose acetate butyrates with high butyryl content and low viscosity are soluble in inexpensive lacquer solvents. They are widely used in lacquers for protective and decorative coatings appHed to automobiles and wood furniture. 

Acetylated polysaccharides form part of the structure of wood, the acetyl radical constituting some 2-5Vo by weight of the dry wood. Hydrolysis to free acetic acid occurs in the presence of moisture at a rate varying from one species to another a wood of lower acetyl content can liberate acetic acid much faster under given conditions than another wood of higher content Small quantities of formic, propionic and butyric acids are also formed but their effects can be neglected in comparison with those of acetic acid. There is a broad, but only a broad, correlation between the corrosivity of a wood and its acidity. The chemistry of acetyl linkage in wood and of its hydrolysis has been examined in some detail. ... 

As previously discussed, solvents that dissolve cellulose by derivatization may be employed for further functionahzation, e.g., esterification. Thus, cellulose has been dissolved in paraformaldehyde/DMSO and esterified, e.g., by acetic, butyric, and phthalic anhydride, as well as by unsaturated methacrylic and maleic anhydride, in the presence of pyridine, or an acetate catalyst. DS values from 0.2 to 2.0 were obtained, being higher, 2.5 for cellulose acetate. H and NMR spectroscopy have indicated that the hydroxyl group of the methy-lol chains are preferably esterified with the anhydrides. Treatment of celliflose with this solvent system, at 90 °C, with methylene diacetate or ethylene diacetate, in the presence of potassium acetate, led to cellulose acetate with a DS of 1.5. Interestingly, the reaction with acetyl chloride or activated acid is less convenient DMAc or DMF can be substituted for DMSO [215-219]. In another set of experiments, polymer with high o -celliflose content was esterified with trimethylacetic anhydride, 1,2,4-benzenetricarboylic anhydride, trimellitic anhydride, phthalic anhydride, and a pyridine catalyst. The esters were isolated after 8h of reaction at 80-100°C, or Ih at room temperature (trimellitic anhydride). These are versatile compounds with interesting elastomeric and thermoplastic properties, and can be cast as films and membranes [220]. 

Tim Steinbuchel (1990) studied the mechanisms of Alcaligenes spp. and Rhodospirillum rubrum for PHB synthesis by using butyric acid. Later, Steinbuchel (1991) confirmed the results for the potential of PHAs production and the compositions of PHAs. Under various microbial strains used, different contents of PHAs were obtained. 

In the reaction, it was essential to use an IL as a co-solvent. Lozano, Iborra and co-workers recently reported an interesting stabilizing effect of two types of water-immiscible ILs ([emim][TFSI] and [BuMe3N][TFSI]) for CAL-B-catalyzed transesterification of vinyl butyrate. The synthetic activity and the stability of the enzyme in these IL solvent systems were markedly enhanced as compared to those in hexane. CAL-B maintained its activity higher than 75% after 4 days of incubation in [emim][TFSI] solvent, while it showed an activity of only 25% when incubated in both water and hexane media at 50°C. Comparison of the ratio of a-helix and (3-sheet by CD spectra showed the activity was closely related with a-helix content which reduced to 31% immediately after lipase was added to hexane and had reached only 2% after 4 days in hexane. On the contrary, no significant reduction of a-helix content was... 

Ulberth F (1998) A rapid headspace gas chromatographic method for the determination of the butyric acid content in edible fats. Z Lebensm Unters Forsch 2o6A 305-3oy. 

In the liver, the ketone bodies suffer no transformation, and are excreted into the blood. The normal contents of ketone bodies (as acetoacetate or P-hydroxy-butyrate) amount to mere 0.1-0.6 mmol/ litre). Other tissues and organs (heart, lung, kidney, muscle, and nervous tissue), as distinct from the liver, utilize the ketone bodies as energy substrates. In the cells of these tissues, acetoacetate and 1-hydroxybutyrate enter ultimately the Krebs cycle and burn down to C02 and H,0 to release energy. 

Figure 3. Changes of D,L- malate and D-p-hydroxy butyric acid contents in...

Table VI compares results from air, dust and slurry investigations on VFA and phenolic/indolic compounds in piggeries. Relative values are used. When comparing the results derived from investigations on dust, air or slurry it is necessary to use relative values because of the different dimensions, for experience shows that in spite of large quantitative differences between two samples within the group of carboxylic acids and within the group of phenolic/indolic compounds the proportions of the components remain rather stable (36). In the group of VFA acetic acid is the main component in air, dust, and slurry followed by propionic and butyric acid. The other three acids amount to less than 25%. In the group of phenols/ indoles p-cresol is the main component in the four cited investigations. However, it seems that straw bedding can reduce the p-cresol content in this case phenol is the main component, instead (37).

Kraft mill that had used elemental chlorine historically Microbial community and diatom species in lake sediments sampled from 2-8 cm depths Drop in the ATP content, depressed butyrate-esterase activity indicating toxicity to microorganisms, and reduction in diatom species richness Mika et al., 1999 [31]... 

Crystals Obtained by Acid Addition. Figure 4 shows the effect of initial solution composition on the impurity content of crystals obtained by acid addition. Clearly, this corresponds to the definition of an ideal system as presented above. These data show the order followed in impurity incorporation in the L-Ile crystals is L-Val > L-Leu > L-a-ABA, although there is only one data point on a-amino butyric acid. Also, the value of purification factors for all impurities is less than one. This means that purification by crystallization was indeed occurring. 

Storage conditions and preservation treatments also can affect the free amino acid content. Some authors [242] reported changes in the concentration of free amino acids of broccoli florets stored in air or in controlled atmospheres. Arginine concentration varied greatly during air storage, while y-amino butyric acid, alanine and an unidentified amino acid accumulated in response to low O2 and/or high CO2 treatment. 

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