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Complexometry Metal-Chelate Complexes Complexometry Metal-Chelate Complexes.

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Presentation on theme: "Complexometry Metal-Chelate Complexes Complexometry Metal-Chelate Complexes."— Presentation transcript:

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2 Complexometry

3 Metal-Chelate Complexes

4 Complexometry Metal-Chelate Complexes

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22 C: unidentatni ligand B: bidentatni ligand A: tetradentatni ligand

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24 EDTA: Acid-Base properties K 1 =1.02x10 -2 K 2 =2.14x10 -3 K 3 =6.92x10 -7 K 4 =5.5x10 -11

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34  Y -4 = [Y -4 ] [H 6 y +2 ]+[H 5 Y + ]+[H 4 Y]+[H 3 Y - ]+[H 2 Y -2 ]+ [HY -3 ]+[Y -4 ]  Y -4 = [Y -4 ] [EDTA]

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36 غلظت مولار Y 4- را در محلول M EDTA 02/0 که تا pH برابر 0/10 بافری شده است را محاسبه کنید.

37 [Y 4- ]=α 4 C T =(0.35)(0.02) = 7.0x10 -3 M

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40 K 1 =1.02x10 -2 K 2 =2.14x10 -3 K 3 =6.92x10 -7 K 4 =5.5x10 -11

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55 pH=6

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58 Indicators

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64 Eriochrome Black T is blue, but turns red in the presence of metals

65 کاربرد در داروسازی

66 Ph.Eu. 0.1 M Sodium edetate. Dissolve 37.5 g of sodium edetate R in 500 ml of water R, add 100 ml of 1 M sodium hydroxide and dilute to 1000.0 ml with water R. Standardisation. Dissolve 0.120 g of zinc RV in 4 ml of hydrochloric acid R1 and add 0.1 ml of bromine water R. Drive off the excess of bromine by boiling, add dilute sodium hydroxide solution R until the solution is weakly acid or neutral and carry out the assay of zinc by complexometry (2.5.11). 1 ml of 0.1 M sodium edetate is equivalent to 6.54 mg of Zn. Storage: in a polyethylene container.

67 Ph.Eu. 2. Methods of Analysis 2.5. Assays 2.5.11. Complexometric titrations ZINC Introduce the prescribed solution into a 500 ml conical flask and dilute to 200 ml with water R. Add about 50 mg of xylenol orange triturate R and hexamethylenetetramine R until the solution becomes violet-pink. Add 2 g of hexamethylenetetramine R in excess. Titrate with 0.1M sodium edetate until the violet-pink colour changes to yellow. 1 ml of 0.1M sodium edetate is equivalent to 6.54 mg of Zn.

68 CALCIUM Introduce the prescribed solution into a 500 ml conical flask, and dilute to 300 ml with water R. Add 6.0 ml of strong sodium hydroxide solution R and about 15 mg of calconecarboxylic acid triturate R. Titrate with 0.1M sodium edetate until the colour changes from violet to full blue. 1 ml of 0.1M sodium edetate is equivalent to 2.431 mg of Mg. MAGNESIUM Introduce the prescribed solution into a 500 ml conical flask and dilute to 300 ml with water R. Add 10 ml of ammonium chloride buffer solution pH 10.0 R and about 50 mg of mordant black 11 triturate R. Heat to about 40° then titrate at this temperature with 0.1M sodium edetate until the colour changes from violet to full blue. 1 ml of 0.1M sodium edetate is equivalent to 2.431 mg of Mg. 2. Methods of Analysis 2.5. Assays 2.5.11. Complexometric titrations

69 Analiza in nadzor zdravil- vaje 2006/2007 ALUMINIUM Introduce 20 ml of the prescribed solution into a 500 ml conical flask, add 25.0 ml of 0.1M sodium edetate VS and 10 ml of a mixture of equal volumes of a 155 g/l solution of ammonium acetate R and dilute acetic acid R. Boil for 2 min, then cool. Add 50 ml of ethanol R and 3 ml of a freshly prepared 0.25 g/l solution of dithizone R in ethanol R. Titrate the excess of sodium edetate with 0.1M zinc sulphate until the colour changes from greenish-blue to reddish-violet. 1 ml of 0.1M sodium edetate is equivalent to 2.698 mg of Al. 2. Methods of Analysis 2.5. Assays 2.5.11. Complexometric titrations

70 CALCIUM GLUCONATE C 12 H 22 CaO 14,H 2 O Mr 448.4 Assay Dissolve 0.8000 g in 20 ml of hot water R, allow to cool and dilute to 300 ml with water R. Carry out the complexometric titration of calcium (2.5.11). 1 ml of 0.1M sodium edetate is equivalent to 44.84 mg of C 12 H 22 CaO 14,H 2 O.

71 MAGNESIUM STEARATE Definition Magnesium stearate is a mixture of magnesium salts of different fatty acids consisting mainly of stearic acid [(C 17 H 35 COO) 2 Mg; M r 591.3] and palmitic acid [(C 15 H 31 COO) 2 Mg; M r 535.1] with minor proportions of other fatty acids. It contains not less than 4.0 per cent and not more than 5.0 per cent of Mg (A r 24.30), calculated with reference to the dried substance. The fatty acid fraction contains not less than 40.0 per cent of stearic acid and the sum of stearic acid and palmitic acid is not less than 90.0 per cent. Assay Magnesium. To 0.500 g in a 250 ml conical flask add 50 ml of a mixture of equal volumes of butanol R and ethanol R, 5 ml of concentrated ammonia R, 3 ml of ammonium chloride buffer solution pH 10.0 R, 30.0 ml of 0.1M sodium edetate and 15 mg of mordant black 11 triturate R. Heat to 45-50°C until the solution is clear and titrate with 0.1M zinc sulphate until the colour changes from blue to violet. Carry out a blank titration. 1 ml of 0.1M sodium edetate is equivalent to 2.431 mg of Mg.

72 KANAMYCIN MONOSULPHATE C 18 H 38 N 4 O 15 S,H 2 O Mr 601 TESTS Sulphate 15.0 per cent to 17.0 per cent of sulphate (SO 4 ), calculated with reference to the dried substance. Dissolve 0.250 g in 100 ml of water R and adjust the solution to pH 11 using concentrated ammonia R. Add 10.0 ml of 0.1M barium chloride and about 0.5 mg of phthalein purple R. Titrate with 0.1M sodium edetate adding 50 ml of alcohol R when the colour of the solution begins to change and continue the titration until the violet-blue colour disappears. 1 ml of 0.1M barium chloride is equivalent to 9.606 mg of sulphate (SO 4 ).

73 Definition Compound Zinc Paste contains 25% w/w each of Zinc Oxide and Starch in a suitable hydrophobic basis. Extemporaneous preparation The following formula and directions apply. Zinc Oxide, 250 g Starch, 250 g White Soft Paraffin500 g Melt the White Soft Paraffin, incorporate the Zinc Oxide and the Starch and stir until cold. The paste complies with the requirements stated under Topical Semi-solid Preparations and with the following requirements. Content of zinc oxide, ZnO 23.5 to 26.5% w/w. Identification The residue obtained in the Assay is yellow when hot and white when cool. Compound Zinc Paste BP2003

74 Assay Heat 0.5 g of the paste gently in a porcelain dish over a small flame until the basis is completely volatilised or charred. Increase the heat until all the carbon is removed. Dissolve the residue in 10 ml of 2M acetic acid and add sufficient water to produce 50 ml. To the resulting solution add 50 mg of xylenol orange triturate and sufficient hexamine to produce a violet-pink colour. Add a further 2 g of hexamine and titrate with 0.1M disodium edetate VS until the solution becomes yellow. Each ml of 0.1M disodium edetate VS is equivalent to 8.138 mg of ZnO. Compound Zinc Paste BP2003

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