Nitrates crystalline

Amino-4 -methylthiazole slowly decomposes on storage to a red viscous mass. It can be stored as the nitrate, which is readily deposited as pink crystals when dilute nitric acid is added to a cold ethanolic solution of the thiazole. The nitrate can be recrystallised from ethanol, although a faint pink colour persists. Alternatively, water can be added dropwise to a boiling suspension of the nitrate in acetone until the solution is just clear charcoal is now added and the solution, when boiled for a short time, filtered and cooled, deposits the colourless crystalline nitrate, m.p. 192-194° (immersed at 185°). The thiazole can be regenerated by decomposing the nitrate with aqueous sodium hydroxide, and extracting the free base with ether as before. 

Determination of nitrate as nitron nitrate Discussion. The mono-acid base nitron, C20H16N4, forms a fairly insoluble crystalline nitrate, C20H 16N4,HN03 (solubility is 0.099 g L 1 at about 20 °C), which can be used for the quantitative determination of nitrates [see Section 11.11(E)]. The sulphate and acetate are soluble so that precipitation may be made in sulphuric or acetic (ethanoic) acid solution. Perchlorates (0.08 g), iodides (0.17 g), thiocyanates (0.4 g), chromates (0.6 g), chlorates (1.2g), nitrites (1.9 g), bromides (6.1 g), hexacyanoferrate(II), hexacyanoferrate(III), oxalates, and considerable quantities of chlorides interfere, and should be absent. The figures in parentheses are the approximate solubilities of the nitron salts in g L-1 at about 20 °C. 

During propionitrile manufacture by oxidative amination of propanol, nitric acid was used for neutralisation. This eventually led to concentration of nitrates, which exploded, at the bottom of the final distillation column [1], Many amines form highly crystalline nitrates, which are usually explosive once isolated. 

In contrast to other crystaUine nitrates, pentaerythrol tetranitrate (PETN C Hg(0N02)4) is a crystalline nitrate ester similar to NG and NC. Though PETN is one of the most powerful energetic materials used in explosives, no excess oxidizer fragments are formed when it decomposes. Thus, PETN is not used as an oxidizer of propellants. 

It is better to prepare the cobalt nitrate solution by dissolving 60g of cobalt carbonate in portions in 70ml of concentrated nitric acid and filtering the solution as the crystalline nitrate is deliquescent it may contain considerably more water than indicated by the 6-hydrate.]... 

No simple salts of 2,1 -benzisothiazole have been described in the literature, other than those of amino-substituted derivatives,101 in which the site of protonation is probably the cyclic nitrogen atom, at least in the 3-substituted compounds. The parent compound does, however, form a simple crystalline nitrate 114 which is not very stable. A number of complex salts with platinum, gold, lead, and mercury salts and with picric acid have been described.96,97,116 The picrate is highly crystalline and stable, and is useful for the isolation and characterization of 2,1-benzisothiazole. Many substituted 2,1-benzisothiazoles form similarly useful picrates.106... 

This interpretation is supported by structural studies on crystalline nitrate compounds all the N-0 bond distances are the same, and they are intermediate in length between the values expected for single and double bonds. 

The solubility of Sr(N03)2 is diminished by HNO3, but less so than with Ba. Aqueous Ba " yields a fairly coarse, crystalline nitrate when treated with HNO3, quite insoluble in concentrated HNO3. 

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