Magnesium ammonium nitrate iodide

Ammonium nitrate, Diesel fuel TNT, Dioxane, Hydrogen sulfide gas. Ammonia, Hydrochloric acid. Potassium iodide, Sulfuric acid, Paraformaldehyde, Methylene chloride, Nitric acid, Magnesium sulfate. Chloroform, Methanol Ammonium nitrate. Sulfur... 

Sodium chloride Sodium bromide Sodium iodide Sodium sulphate Sodium silicate Potassium sulphate Lithium chloride Calcium carbonate Calcium sulphate Magnesium sulphate Manganous carbonate Ferrous carbonate. Aluminium phosphate Ammonium nitrate Organic matter... 

A good number of alternative methods are also available in literature for the synthesis of 1,5-benzodiazepine derivatives involving the use of a variety of catalysts such magnesium oxide/ phosphorus oxychloride (MOPO) [1], ionic liquid (1,3-di-n-butylimidazolium bromide) [2], silica gel-supported cerium(lll) chloride/sodium iodide [3], Sc(OTf)3 [4], InCls [5], InBr3 [6], ceric ammonium nitrate (CAN) [7], 2,4,6-trichloro-l,3,5-triazine (TCT) [8,9], GaCl3 [10], and Zr0C2-8H20 [11] in the presence or absence of solvent(s) at room temperature. 

Anhydrous hydrazine dssolves many salts, thus, 100 parts of solvent at 12-5°-13° dissolve 12-2 parts of sodium chloride 8 5, of potassium chloride 56-4, of potassium bromide 135-7, of potassium iodide 26-6, of sodium nitrate 21-7, of potassium nitrate and 814, of barium nitrate. The hydrazine seemed to unite with sodium chloride with a warm soln. of ammonium chloride, ammonia is evolved, and in the cold, there seems to be a state of equilibrium a complex salt seems to be formed with lead nitrate. An aq. soln. of hydrazine hydrate also dissolves a number of salts, potassium bromide and iodide, ammonium sulphate, potassium cyanide, barium nitrate, magnesium sulphate, etc. According to T. W. B. Welsh and H. J. Broderson, the solubility of the metal haloids seems to... 

An alternative method for the elimination of arsenate is the following. Acidify the soda extract with dilute hydrochloric acid and then add about one-quarter of the volume of concentrated hydrochloric acid (the total volume should be about 10 ml). Add 0-5 ml of 10 per cent ammonium iodide solution, heat to boiling, and pass hydrogen sulphide into the boiling solution until precipitation is complete (5-10 minutes). Filter off the arsenic(III) sulphide, and boil off the hydrogen sulphide from the filtrate. Add ammonia solution until alkaline, and excess of the magnesium nitrate reagent. A white precipitate indicates the presence of a phosphate. 

NITRATE d ARGENT (French) (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 acetyUdes, 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. 

Ammonium carbonate 233-788-1 Barium chloride 233-789-7 Benzyl valerate 233-792-3 Bismuth nitrate 233-814-1 Camphorquinone 233-822-5 Lithium iodide 233-826-3 Magnesium nitrate 233-826-7... 

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