Ammonium chloride Subject

Inorganic salt solutions Molybdenum has excellent resistance to 3% sodium chloride, 10% aluminium chloride and 10% ammonium chloride at temperatures up to 100°C. It is severely corroded by 20% solutions of ferric and cupric chlorides at 35°C and is subject to pinhole-type pitting in mercuric chloride solutions (Table 5.5). 

The chemistry of indium metal is the subject of current investigation, especially since the reactions induced by it can be performed in aqueous solution.15 The selective reductions of ethyl 4-nitrobenzoate (entry 1), 2-nitrobenzyl alcohol (entry 2), l-bromo-4-nitrobenzene (entry 3), 4-nitrocinnamyl alcohol (entry 4), 4-nitrobenzonitrile (entry 5), 4-nitrobenzamide (entry 6), 4-nitroanisole (entry 7), and 2-nitrofluorenone (entry 8) with indium metal in the presence of ammonium chloride using aqueous ethanol were performed and the corresponding amines were produced in good yield. These results indicate a useful selectivity in the reduction procedure. For example, ester, nitrile, bromo, amide, benzylic ketone, benzylic alcohol, aromatic ether, and unsaturated bonds remained unaffected during this transformation. Many of the previous methods produce a mixture of compounds. Other metals like zinc, tin, and iron usually require acid-catalysts for the activation process, with resultant problems of waste disposal. 

Soil sample is extracted with a mixture of methanol and 0.1 M ammonium chloride. Acetamiprid, IM-1-2 and IM-1-4 residues are extracted with dichloromethane under alkaline conditions. After adding diethylene glycol, dichloromethane in the extract is removed by rotary evaporation, and the residue is subjected to a cleanup procedure using Florisil PR column chromatography and then with a packed Extrelut 20 column. 

In a study with human subjects, whose urine pH was controlled with sodium bicarbonate and ammonium chloride, it was found that 10-25% of the administered pseudoephedrine hydrochloride was metabolized to norpseudoephedrine and the elimination of pseudoephedrine and norpseudoephedrine was related to urine pH. As the urine pH increased, the serum half-life of pseudoephedrine and norpseudoephedrine increased.15 In another similar study it was found that a decrease... 

Acidosis induced by salt feeding to humans influenced urinary calcium loss as effectively as feeding whole foods. Martin and Jones (25), for example, fed adult subjects a diet supplemented with ammonium chloride which resulted in marked hypercalciuria and an acidified urine. In a follow-up trial, feeding alkali as sodium bicarbonate, they also demonstrated that human hypercalciuria could be prevented by adding an alkaline supplement to the diet. 

This phenomenon also had been reported in human subjects fed acid ash foods. Farquharson, et al. (33) fed a high-protein (200 g) diet to human subjects who promptly excreted more urinary acid and calcium. This occurred whether the protein level was raised to 200 g, or an equivalent amount of ammonium chloride was fed. If, on the other hand, the acid ash in the protein were neutralized with sodium bicarbonate, the hypercalciuria did not occur. 

Mixed with NaOH solution and distilled distillate analyzed for ammonia by titration, colorimetry, or electrode method (see Ammonia and Ammonium chloride). Bromide portion of NH4Br in aqueous solution may be analyzed by ion chromatography, or by the colorimetry method in which red to violet color is produced upon treatment with chloramine-T, and phenol red at pH 4.5. The colorimetry test for bromide is subject to interference from oxidizing and reducing agents, chloride, and bicarbonate. NH4Br may then be determined stoichiometrically. 

Venus is completely covered with dense clouds. The composition of the clouds has been the subject of much speculation for many years. It includes ice, carbon suboxide, sulfuric acid, hydrocarbons, mercuric chloride, ammonium chloride, and hydrated ferrous chloride. Recently, Young (1066a) has proposed, based on refractive index measurement, that the clouds are composed most probably of droplets of 75% H2S04. 

The ammonia-radicle theory.—The oldest hypothesis concerning the nature of the ammonia-compounds, and that adopted by A. L. Lavoisier, supposed ammonia to be an independent base or radicle, saturating acids, and forming salts. This theory has been likened to the etherin theory of J. B. A. Dumas and P. F. G. Boullay. The radicle is NHS sal-ammoniac is NH3+HCI etc. The theory makes no attempt to explain the nature of the other classes of ammonia-compounds nor does it explain the relation of ammonia to ordinary bases, which are metallic oxides, nor the differences between the ammoniacal salts from metallic sails of the same acid. Later on, the theory became associated with the mol. compound theory, so that sal ammoniac was represented by F. A. Kekule as an associated complex of ammonia and hydrogen chloride, in which the ammonia remained tervalent. These compounds were considered to be analogous to double salts, and to substances with water of crystallization. This view was supported by the ready dissociation of sal ammoniac by heat—a subject discussed in connection with ammonium chloride (2. 20, 16). H. Rose also emphasized the analogy between compounds of ammonia and of water in various salts as exemplified by the use of the term ammonia of crystallization. 

AuC13OH], etc.—the linkage between the metal and the acid radicle is not broken and virtually no gold ions are formed. If auric tetramminonitrate, [Au(NH3)4](N03)3, be treated with potassium chloride, auric tetramminochloride, [Au(NH3)4]C13, is probably first formed and, owing to the affinity between the outer sphere and the complex itself, ammonia is displaced and the series of auric amines, [AuCl(NH3)s]Cl2, [AuC12(NH3)2]C1, and [AuC13NH3], is produced. As a matter of fact, some of the combined chlorine passes out with the ammonia as ammonium chloride, and hydroxyl remains in the complex. This subject has been studied by F. Ephraim, A. Pieroni, E. Weitz, etc. 

Cao and Zeng [52] used of an oscillopolarographic method for the determination and the electrochemical behavior of omeprazole. Portions of standard omeprazole solution were treated with 1 ml 1 M ammonia/ ammonium chloride at pH 8.9 and the solution was diluted with water to 10 ml. The diluted solution was subjected to single sweep oscillopolaro-graphy with measurement of the derivative reduction peak at —1.105 V versus saturated calomel electrode. The calibration graph was linear from 0.5 to 10 /iM omeprazole with a detection limit of 0.2 fiM. The method was applied to the analysis of omeprazole in capsules with recoveries of 100-118.6% and RSD of 6.78%. The electrochemical behavior of omeprazole at the mercury electrode was also investigated. 

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