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Under this heading are placed tests that are frequently referred to in the Pharmacopeia for the identification of official articles. Before using any acid or base to modify the PH of the sample solution, make sure that the added substance will not interfere with the results of the test. [NOTE¡ªThe tests are not intended to be applicable to mixtures of substances unless so specified.]

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Acetate¡ªDissolve about 30mg of the substance to be examined in 3ml of the prescribed solution. Adjust the PH of the solution with sodium hydroxide to slightly alkaline. Add 0.25ml of lanthanum nitrate TS. If a white precipitate is formed, filter the solution. Add successively 0.1ml of iodine and potassium iodide TS 3 and 0.1ml of ammonia TS 2 to the solution. I f no blue color is observed, heat carefully to boiling. In the presence of acetates, a dark color develops or a blue precipitate is fprmed. With neureal solutions of acetates, ferric chloride TS produces a red color tha is destroyed by the addition of mineral acids. ´×ËáÑΣº½«30mg±»¼ìÎïÈÜÓÚ3mlµÄË®ÖУ¬»òÓÃ3mlµÄ¹æ¶¨ÈÜÒº¡£ÓÃÇâÑõ»¯ÄƵ÷½ÚPHÖÁÈõ¼î¡£¼ÓÈë0.25mlÏõËáïçÊÔÒº¡£Èç³öÏÖ°×É«³Áµí£¬¹ýÂËÈÜÒº¡£ÏȺó¼ÓÈë0.1mlµÄµâºÍµâ»¯¼ØÊÔÒº3ºÍ0.1mlµÄ°±ÊÔÒºÖÁÈÜÒºÖС£ÈçûµÃµ½À¶É«£¬Ð¡ÐļÓÈÈÖÁ·ÐÌÚ¡£ÈçÏõËáÑγöÏÖÉîÉ«»òÀ¶É«³ÁµíÎȡ´×ËáµÄÖÐÐÔÈÜÒº£¬¼ÓÈýÂÈ»¯ÌúÊÔÒº³öÏÖºìÉ«£¬¼ÓÎÞ»úËᣬºìÉ«ÆÆ»µ¡£Aluminum¡ª With 6 N ammonium hydroxide, solutions of aluminum salts yield a

gelatinous, white precipitate that is insoluble in an excess of 6 N ammonium hydroxide. 1 N sodium hydroxide or sodium sulfide TS produces the same precipitate, which dissolves in an excess of either of these reagents.

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indicator solution, prepared by mixing 1ml of 0.1M hydrochloric acid and 0.05ml of methyl red TS2. In the presence of ammonium, the color of the indicator solution is changed to yellow. After directing the gas into the indicator solution for a sufficient period of time, add 1ml of freshly prepared sodium cobaltinitrite TS to the indicator solution. Upon the addition of the sodium cobaltinitrite TS, a yellow precipitate is formed when ammonium is present. 泥ºÈÜÒºÖмÓÈë0.2gÑõ»¯Ã¾¡£»ìºÏÎï²úÉúÆøÌ壬°Ñ²úÉúµÄÆøÌåͨÈëָʾ¼ÁµÄÒºÃæÏ£¬£¨Ö¸Ê¾¼ÁÅäÖÆ£º1ml0.1MÑÎËáºÍ0.05mlµÄ¼×»ùºìÊÔÒº2.£©Ö¸Ê¾Òº±ä»ÆÉ«¡£ÆøÌåͨÈëָʾҺ³ä·Öºó£¬¼ÓÈë1mlÐÂÅäµÄÑÇÏõËáîÜÄÆÊÔÒº¡£ÓÉÓÚÑÇÏõËáîÜÄÆÊÔÒºµÄ¼ÓÈ룬炙á³öÏÖ»ÆÉ«³ÁµíÎï¡£ Antimony¡ª With hydrogen sulfide, solutions of antimony (III) compounds, strongly acidified with hydrochloric acid, yield an orange precipitate of antimony sulfide that is insoluble in 6 N ammonium hydroxide, but is soluble in ammonium sulfide TS.

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Barium¡ª Solutions of barium salts yield a white precipitate with 2N sulfuric acid. This precipitate is insoluble in hydrochloric acid and in nitric acid. Barium salts impart a yellowish-green color to a nonluminous flame that appears blue when viewed through green glass.

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Benzoate¡ª In neutral solutions, benzoates yield a salmon-colored precipitate with ferric chloride TS. In moderately concentrated solutions, benzoates yield a precipitate of benzoic acid upon acidification with 2N sulfuric acid. This precipitate is readily soluble in ethyl ether.

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Bismuth¡ª When dissolved in a slight excess of nitric acid or hydrochloric acid, bismuth salts yield a white precipitate upon dilution with water. This precipitate is colored brown by

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hydrogen sulfide, and the resulting compound dissolves in a warm mixture of equal parts of nitric acid and water.

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Borate¡ª To 1 mL of a borate solution, acidified with hydrochloric acid to litmus, add 3 or 4 drops of iodine TS and 3 or 4 drops of polyvinyl alcohol solution (1 in 50): an intense blue color is produced. When a borate is treated with sulfuric acid, methanol is added, and the mixture is ignited, it burns with a green-bordered flame.

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Bromide¡ª Solutions of bromides, upon the addition of chlorine TS, dropwise, liberate bromine, which is dissolved by shaking with chloroform, coloring the chloroform red to reddish brown. Silver nitrate TS produces in solutions of bromides a yellowish¨Cwhite precipitate that is insoluble in nitric acid and is slightly soluble in 6N ammonium hydroxide. ä廯Î1¡¢ä廯ÎïÈÜÒºÖðµÎ¼ÓÈëÂÈÊÔÒº£¬ÓÎÀë³öä壬ÓÃÂÈ·ÂÝÍÈ¡£¬Âȷ²ãӦΪºì×ØÉ«¡£2¡¢ä廯ÎïÈÜÒºÖмÓÈëÏõËáÒøÊÔÒº£¬Ó¦²úÉúdz»ÆÉ«ÐõÈé×´³Áµí£¬³Áµí²»ÈÜÓÚÏõËᣬ΢ÈÜÓÚ6NµÄ°±Ë®¡£

Calcium¡ª Solutions of calcium salts form insoluble oxalates when treated as follows. To a solution of the calcium salt (1 in 20) add 2 drops of methyl red TS, and neutralize with 6N ammonium hydroxide. Add 3N hydrochloric acid, dropwise, until the solution is acid to the indicator. Upon the addition of ammonium oxalate TS, a white precipitate is formed. This precipitate is insoluble in 6N acetic acid but dissolves in hydrochloric acid. Calcium salts moistened with hydrochloric acid impart a transient yellowish-red color to a nonluminous flame.

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Carbonate¡ª Carbonates and bicarbonates effervesce with acids, evolving a colorless gas that, when passed into calcium hydroxide TS, produces a white precipitate immediately. A cold solution (1 in 20) of a soluble carbonate is colored red by phenolphthalein TS, while a similar solution of a bicarbonate remains unchanged or is only slightly colored.

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Chlorate¡ª Solutions of chlorates yield no precipitate with silver nitrate TS. The addition of sulfurous acid to this mixture produces a white precipitate that is insoluble in nitric acid, but is soluble in 6N ammonium hydroxide. Upon ignition, chlorates yield chlorides, recognizable by appropriate tests. When sulfuric acid is added to a dry chlorate, decrepitation occurs, and a greenish yellow-gas is evolved. [Caution¡ªUse only a small amount of chlorate for this test, and exercise extreme caution in performing it. ]

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Chloride¡ª With silver nitrate TS, solutions of chlorides yield a white, curdy precipitate that is insoluble in nitric acid but is soluble in a slight excess of 6N ammonium hydroxide. When testing amine (including alkaloidal) hydrochlorides that do not respond to the above test, add one drop of diluted nitric acid and 0.5 mL of silver nitrate TS to a solution of the substance being examined containing, unless otherwise directed in the monograph, about 2mg of chloride ion in 2mL: a white, curdy precipitate is formed. Centrifuge the mixture without delay, and decant the supernatant layer. Wash the precipitate with three 1-mL portions of nitric acid solution (1 in 100), and discard the washings. Add ammonia TS dropwise to this precipitate. It dissolves readily. When a monograph specifies that an article responds to the test for dry chlorides, mix the solid to be tested with an equal weight of manganese dioxide, moisten with sulfuric acid, and gently heat the mixture: chlorine, which is recognizable by the production of a blue color with moistened starch iodide paper, is evolved.

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