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Ammonium Salts and Salts of Volatile Bases

Acetates

 

 A. Heat the substance to be examined with an equal quantity of oxalic acid R. Acid vapours with the characteristic odour of acetic acid are liberated, showing an acid reaction (2.2.4).

 

 B. Dissolve about 30 mg of the substance to be examined in 3 ml of water R or use 3 ml of the prescribed solution. Add successively 0.25 ml of lanthanum nitrate solution R, 0.1 ml of 0.05 M iodine and 0.05 ml of dilute ammonia R2. Heat carefully to boiling. Within a few minutes a blue precipitate is formed or a dark blue colour develops.

 

Acetyl Groups

 

In a test-tube about 180 mm long and 18 mm in external diameter, place about 15 mg of the substance to be examined, or the prescribed quantity, and 0.15 ml of phosphoric acid R. Close the tube with a stopper through which passes a small test-tube about 100 mm long and 10 mm in external diameter containing water R to act as a condenser. On the outside of the smaller tube, hang a drop of lanthanum nitrate solution R. Except for substances hydrolysable only with difficulty, place the apparatus in a water-bath for 5 min, then take out the smaller tube. Remove the drop and mix it with 0.05 ml of 0.01 M iodine on a tile. Add at the edge 0.05 ml of dilute ammonia R2. After 1 min to 2 min, a blue colour develops at the junction of the two drops; the colour intensifies and persists for a short time.

 

For substances hydrolysable only with difficulty heat the mixture slowly to boiling over an open flame and then proceed as prescribed above.

 

Alkaloids

 

Dissolve a few milligrams of the substance to be examined, or the prescribed quantity, in 5 ml of water R, add dilute hydrochloric acid R until an acid reaction occurs (2.2.4), then 1 ml of potassium iodobismuthate solution R. An orange or orange-red precipitate is formed immediately.

 

Aluminium Salts

 

Dissolve about 15 mg of the substance to be examined in 2 ml of water R or use 2 ml of the prescribed solution. Add about 0.5 ml of dilute hydrochloric acid R and about 0.5 ml of thioacetamide reagent R. No precipitate is formed. Add dropwise dilute sodium hydroxide solution R. A gelatinous white precipitate is formed which dissolves on further addition of dilute sodium hydroxide solution R. Gradually add ammonium chloride solution R. The gelatinous white precipitate is re-formed.

 

Amines, Primary Aromatic

 

Acidify the prescribed solution with dilute hydrochloric acid R and add 0.2 ml of sodium nitrite solution R. After 1 min to 2 min, add 1 ml of b-naphthol solution R. An intense orange or red colour and usually a precipitate of the same colour are produced.

 

Ammonium Salts

 

To the prescribed solution add 0.2 g of magnesium oxide R. Pass a current of air through the mixture and direct the gas that escapes just beneath the surface of a mixture of 1 ml of 0.1 M hydrochloric acid and 0.05 ml of methyl red solution R. The colour of the indicator changes to yellow. On addition of 1 ml of a freshly prepared 100 g/l solution of sodium cobaltinitrite R a yellow precipitate is formed.



 

Ammonium Salts and Salts of Volatile Bases

 

Dissolve about 20 mg of the substance to be examined in 2 ml of water R or use 2 ml of the prescribed solution. Add 2 ml of dilute sodium hydroxide solution R. On heating, the solution gives off vapour that can be identified by its odour and by its alkaline reaction (2.2.4).

 

Antimony Compounds

 

Dissolve with gentle heating about 10 mg of the substance to be examined in a solution of 0.5 g of sodium potassium tartrate R in 10 ml of water R and allow to cool: to 2 ml of this solution, or to 2 ml of the prescribed solution, add sodium sulphide solution R dropwise; an orange-red precipitate is formed which dissolves on addition of dilute sodium hydroxide solution R.

 

Arsenic Compounds

 

Heat 5 ml of the prescribed solution on a water-bath with an equal volume of hypophosphorous reagent R. A brown precipitate is formed.

 


Date: 2015-12-24; view: 917


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