Silver chloride salicylate

Ethanol has also received considerable attention as a solvent over a long period of time. Data on this solvent, however, are rather few compared to methanol and very few systematic studies exist. Several solubility studies have been made since the publication of Seidell and Linke. Thomas has reported solubilities for the alkali metal iodides at 20 and 25°C, and observed a decrease in solubility with an increase in ionic radius of the cation. Deno and Berkheimer have reported the solubilities of several tetraalkylammonium perchlorates. In every case the solid phase was the pure salt. Solubilities for several rare earth compounds have been reported.Since all of these salts form solvates in the solid phase, the results cannot be used in thermodynamic calculations without the corresponding thermodynamic values for the solid phases. Solubilities of silver chloride, caesium chloride, silver benzoate, silver salicylate and caesium nitrate have been measured in ethanol, using radioactive tracer techniques. Burgaud has measured the solubility of LiCl from 10.2 to 57.6°C and observed that there is a transition from the four-solvated solid phase to the non-solvated phase at 20.4°C. 

Potassium propionate Potassium propylparaben Potassium salicylate Potassium sorbate Potassium sulfite Propionic acid Propyl benzoate Propylparaben Quatemium-15 Salicylic acid Silver borosilicate Silver chloride Silver magnesium aluminum phosphate Sodium benzoate Sodium bisulfite Sodium butylparaben Sodium dehydroacetate Sodium ethylparaben Sodium formate Sodium hydroxymethylglycinate Sodium iodate Sodium metabisulfite Sodium methylparaben Sodium paraben Sodium o-phenylphenate... 

Quinoline Salicylic acid Silicon Dinitrogen tetroxide, linseed oil, maleic anhydride, thionyl chloride Iodine, iron salts, lead acetate Alkali carbonates, calcium, chlorine, cobalt(II) fluoride, manganese trifluoride, oxidants, silver fluoride, sodium-potassium alloy... 

Oxidation of saligenin with chromic acid or silver oxide yields salicyladehyde as the first product. Further oxidation results in the formation of salicylic acid, which is also obtained when saligenin is heated with sodium hydroxide at 200—240°C. Chlorination of an aqueous solution of the alcohol gives 2,4,6-trichlorophenol, and bromination in an alkaline medium yields 2,4,6-tribromophenol and tribromosaligenin. When saligenin is heated with one mole of resorcinol in the presence of anhydrous zinc chloride, 3-hydroxyxanthene forms. 

Part 13 of ISO 787 determines water-soluble sulfates, chlorides and nitrates. The sample extract can be prepared by either cold or hot extraction method described in Section 4.28. The sulfates in the extract are determined by precipitation with barium chloride, the chlorides are determined by titration with silver nitrate, and the nitrates are determined by a colorimetric method using Nessler reagent." Part 19 gives an alternative method of determination of nitrates by a salicylic acid method. 

IODINE (7553-56-2) A powerful oxidizer. Material or vapors react violently with reducing agents, combustible materials, alkali metals, acetylene, acetaldehyde, antimony, boron, bromine pentafluoride, bromine trifluoride, calcium hydride, cesium, cesium oxide, chlorine trifluoride, copper hydride, dipropylmercury, fluoride, francium, lithium, metal acetylides, metal carbides, nickel monoxide, nitryl fluoride, perchloryl perchlorate, polyacetylene, powdered metals, rubidium, phosphorus, sodium, sodium phosphinate, sulfur, sulfur trioxide, tetraamine, trioxygen difluoride. Forms heat- or shock-sensitive compounds with ammonia, silver azide, potassium, sodium, oxygen difluoride. Incompatible with aluminum-titanium alloy, barium acetylide, ethanol, formamide, halogens, mercmic oxide, mercurous chloride, oxygen, pyridine, pyrogallic acid, salicylic acid sodium hydride, sodium salicylate, sulfides, and other materials. 

NITRIC ACID, SILVER(I) SALT (7761-88-8) A powerful oxidizer. Forms friction- and shock-sensitive compounds with many materials, including acetylene, anhydrous ammonia (produces compounds that are explosive when dry), 1,3-butadiyne, buten-3-yne, calcium carbide, dicopper acetylide. Contact with hydrogen peroxide causes violent decomposition to oxygen gas. Violent reaction with chlorine trifluoride, metal powders, nitrous acid, phospho-nium iodide, red or yellow phosphorus, sulfur. Incompatible with acetylides, acrylonitrile, alcohols, alkalis, ammonium hydroxide, arsenic, arsenites, bromides, carbonates, carbon materials, chlorides, chlorosulfonic acid, cocaine chloride, hypophosphites, iodides, iodoform, magnesium, methyl acetylene, phosphates, phosphine, salts of antimony or iron, sodium salicylate, tannic acid, tartrates, thiocyanates. Attacks chemically active metals and some plastics, rubber, and coatings. 

SODIUM IODIDE (7681-82-5) Reacts violently with bromotrifluoride, perchloric acid, perchloryl fluoride, oxidants, chlorine trifluoride, fluorine, hydrazine. Incompatible with acrolein, isopropyl chlorocarbonate, mercuric salicylate, mercurous chloride, nitrosyl perchlorate, paraldehyde, peroxyfuroic acid, phosphorus pentoxide, silver nitrate, sodium acetylide, sodium borohydride. May sensitize organie azides, hydrazinium perchlorate. 

Picric acid Potassium bromide, 30% Salicylic acid Silver bromide, 10% Sodium carbonate Sodium chloride 300 149... 

---