Media organic acids

Lomefloxacin was synthesized by Faba el ai (6) by the acidic hydrolysis of l-ethyl-6,8-difluoro-l,4-dihydro-7-(3-methyl-l-piperazinyl)-4-oxoquinoline-3-carbonitrile with sulfuric acid in a hydro-alcoholic medium. Methanol, ethanol or isopropanol may be used as the reaction solvent and the reaction temperature (75°C-125°C) depends on the composition of the medium. Organic acids or other... 

It is frequently advisable in the routine examination of an ester, and before any derivatives are considered, to determine the saponification equivalent of the ester. In order to ensure that complete hydrolysis takes place in a comparatively short time, the quantitative saponi fication is conducted with a standardised alcoholic solution of caustic alkali—preferably potassium hydroxide since the potassium salts of organic acids are usuaUy more soluble than the sodium salts. A knowledge of the b.p. and the saponification equivalent of the unknown ester would provide the basis for a fairly accurate approximation of the size of the ester molecule. It must, however, be borne in mind that certain structures may effect the values of the equivalent thus aliphatic halo genated esters may consume alkali because of hydrolysis of part of the halogen during the determination, nitro esters may be reduced by the alkaline hydrolysis medium, etc. 

To hydrolyse an ester of a phenol (e.g., phenyl acetate), proceed as above but cool the alkaline reaction mixture and treat it with carbon dioxide until saturated (sohd carbon dioxide may also be used). Whether a solid phenol separates or not, remove it by extraction with ether. Acidify the aqueous bicarbonate solution with dilute sulphuric acid and isolate the acid as detailed for the ester of an alcohol. An alternative method, which is not so time-consuming, may be employed. Cool the alkaline reaction mixture in ice water, and add dilute sulphuric acid with stirring until the solution is acidic to Congo red paper and the acid, if aromatic or otherwise insoluble in the medium, commences to separate as a faint but permanent precipitate. Now add 5 per cent, sodium carbonate solution with vigorous stirring until the solution is alkaline to litmus paper and the precipitate redissolves completely. Remove the phenol by extraction with ether. Acidify the residual aqueous solution and investigate the organic acid as above. 

Description of Method. Creatine is an organic acid found in muscle tissue that supplies energy for muscle contractions. One of its metabolic products is creatinine, which is excreted in urine. Because the concentration of creatinine in urine and serum is an important indication of renal function, rapid methods for its analysis are clinically important. In this method the rate of reaction between creatinine and picrate in an alkaline medium is used to determine the concentration of creatinine in urine. Under the conditions of the analysis, the reaction is first-order in picrate, creatinine, and hydroxide. 

Because of the insolubility of cellulose it is not possible to carry out uniform esterification with the lower organic acids (acetic acid, propionic acid etc.) and in those cases where incompletely substituted derivatives are required a two-stage reaction is employed. This involves total esterification in a medium in... 

Medium reactivity contaminants alcohols, ketones, organic acids, esters, alkyl-substituted aromatics, nitro-substituted aromatics, carbohydrates. 

In more detail the nutrient medium used may contain sources of carbon such as starch, hydrolyzed starch, sugars such as lactose, maltose, dextrose, sucrose, or sugar sources such as molasses alcohols, such as glycerol and mannitol organic acids, such as citric acid and acetic acid and various natural products which may contain other nutrient materials in addition to carbonaceous substances. 

Several supported metalhc catalysts were evalrrated for the selective hydrogenolysis of glycerol. Initially, the reactions were performed tmder acidic conditions in order to promote the formation of 1,3-PDO. Rutheniirm-based catalysts were found to be the most active catalysts but significant amount of tmdesired products resulted from C-C cleavages were detected. On the contrary, Rh/C catalysts were found selective to C-O cleavages. As far as the selectivity to 1,3-PDO was concerned, we previously reported that the addition of iron salts in the medium improved the l,3-PDO/l,2-PDO selectivity (11). A systematic study on the influence of additives was therefore carried out in the present investigation. Mineral and organic acids were evaluated for this purpose (Table 35.1). 

Increasing the water-wet surface area of a petroleum reservoir is one mechanism by which alkaline floods recover incremental oil(19). Under basic pH conditions, organic acids in acidic crudes produce natural surfactants which can alter the wettability of pore surfaces. Recovery of incremental oil by alkaline flooding is dependent on the pH and salinity of the brine (20), the acidity of the crude and the wettability of the porous medium(1,19,21,22). Thus, alkaline flooding is an oil and reservoir specific recovery process which can not be used in all reservoirs. The usefulness of alkaline flooding is also limited by the large volumes of caustic required to satisfy rock reactions(23). 

Vitreous humour organic acids in medium chain acyl-CoA dehydrogenase deficiency. 

Proteolysis. Proteolysis is the cleavage of amide bonds that comprise the backbone of proteins and peptides. The reaction can occur spontaneously in aqueous medium under acidic, neutral, or basic conditions. This process is accelerated by proteases, ubiquitous enzymes that catalyze peptide-bond hydrolysis at rates much higher than occur spontaneously. In humans, these enzymes only recognize sequences of L-amino acids but not d-amino acids. They are found in barrier tissues (nasal membranes, stomach and intestinal linings, vaginal and respiratory mucosa, ocular epithelium), blood, all internal solid organs, connective tissue, and fat. The same protease may be present in multiple sites in the body. 

Table 3.1.3 Pathologic acylglycine species detected by organic acid analysis. CoA coenzyme A, FAO fatty acid oxidation, ILE isoleucine, LEU Leucine, MCAD medium-chain acyl-CoA dehydrogenase, MET methionine,...

The treatment of cyanates with organic acids (oxalic acid, for example) in a non-aqueous medium, for instance by grinding the two together, does not result in the decomposition of cyanic acid, but in the formation of a trimer, cyamelide, to which the formula of the trioxymethylene derivative is attributed (I)... 

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