Pharmaceutical Chemistry I (D. Pharm 1st Year)
Pharmaceutical Chemistry I (D. Pharm 1st Year)
Pharmaceutical Chemistry I (D. Pharm 1st Year)
S. No. EXPERIMENTS
1 To determine the strength of a given unknown solution of HCl by
titrating it against with the help of a known solution of NaOH using
phenolphthalein indicator.
2 To determine the strength of a given unknown solution of NaOH by
titrating it against with the help of a known solution of HCl using
methyl orange indicator.
3 Determination of the concentration (strong) of a given NaOH
solution by titrating it against a standard (M/20) solution of C2H2O4
using phenolphthalein indicator.
4 To perform the limit test of chloride in the given sample of tap water.
5 To perform the limit test for sulphate in the given sample of tap water.
6 To perform the limit test for chloride in the given sample of sodium
bicarbonate.
7 To perform the limit test for chloride in the given sample of sodium
hydroxide.
8 To perform the limit test for chloride in the given sample of sodium acetate.
9 To perform the limit test for sulphates in the given sample of sodium
bicarbonate.
10 To perform the limit test for sulphates in the given sample of sodium citrate.
11 To perform the limit test for sulphates in the given sample of sodium
dihydrogen phosphate dihydrate.
12 To perform the identification tests for the given sample of ammonium
chloride.
13 To perform the identification tests for the given sample of sodium
chloride.
14 To perform the identification tests for the given sample of sodium
bicarbonate.
15 To perform the identification tests for the given sample of magnesium
sulphate.
16 To perform the identification tests for the given sample of barium
sulphate.
17 To perform the identification tests for the given sample of iodine.
18 To perform the assay of iodine.
20 To perform the limit test for heavy metals in the given sample.
REFERENCE
1. Parle A., " Pharmaceutical Chemistry 1 Laboratory Manual", CBS Publishers and
Distributors Pvt. Ltd., Ed Ist, 2008, pp 59.
REQUIREMENTS: -
Chemical required: NaOH Solution, HCl solution, phenolphthalein indicator
Apparatus required: - burette, conical flask, and beaker
PROCEDURE:-
(a) Take a burette and wash it with distilled water.
(b) Rinse and fill the solution HCl N/10 with the help of a funnel and set the initial burette
reading as zero. Clamp it vertically to the burette stand.
(c) Rinse the pipette with water and then with the given NaOH solution.
(d) Pipette out 10ml of given NaOH (N/10) solution into a conical flask and add one or two
drops of methyl orange.
(e) Titrate it against the HCl (N/10) solution taken in the burette till the color of the solution in
the conical flask changes from a yellowish color to pink color
(f) Note down the final burette reading.
(g) Repeat the titration until concordant values are obtained.
OBSERVATION:
Calculation:
N1V1=N2V2
REFERENCE
Parle A., "Pharmaceutical Chemistry 1 Laboratory Manual", CBS Publishers and distributors
Pvt. Ltd., Ed Ist, 2008, pp 55.
REQUIREMENTS: -
Chemical required: NaOH Solution, HCl solution, methyl orange indicator
Apparatus required: - burette, conical flask, and beaker.
PROCEDURE:-
Take a burette and wash it with distilled water.
Rinse and fill the solution HCl N/10 with the help of a conical funnel and set the initial burette
reading as zero. Clamp it vertically to the burette stand. Rinse the pipette with water and then
with the given NaOH solution.
(a) Pipette out 10ml of given NaOH (N/10) solution into a conical flask and add
one or two drops of methyl orange.
(b) Titrate it against the HCl(N/10) solution taken in the burette till the color of the solution
in the conical flask changes from a yellowish color to pink color
Note down the final burette reading.
(c) Repeat the titration until concordant values are obtained.
OBSERVATION:
Calculation:
N1V1=N2V2
REFERENCE
Parle A. ,"Pharmaceutical Chemistry 1 Laboratory Manual", CBS Publishers and Distributors
Pvt. Ltd., Ed Ist, 2008, pp 59.
REQUIREMENTS: -
Chemical required: NaOH Solution, HCl solution, phenolphthalein indicator, C2H2O4
Apparatus required: - burette, conical flask, and beaker.
PROCEDURE:-
(a) Take a burette and wash it with distilled water.
(b) Rinse and fill the solution HCl N/10 with the help of a conical funnel and set the initial
burette reading as zero. Clamp it vertically to the burette stand.
(c) Rinse the pipette with water and then with the given NaOH solution.
(d) Pipette out 10ml of given NaOH (N/10) solution into a conical flask and add one or two
drops of methyl orange.
(e) Titrate it against the HCl(N/10) solution taken in the burette till the color of the solution in
the conical flask changes from a yellowish color to pink color
(f) Note down the final burette reading.
(g) Repeat the titration until concordant values are obtained.
OBSERVATION:
Calculation:
N1V1=N2V2
OBJECT: - To perform the limit test for chloride in a given sample of tap water.
REQUIREMENTS: -
Chemical required: Silver nitrate, dilute nitric acid, sodium chloride, etc.
Apparatus required: - Measuring cylinder, glass rod, and Nessler’s cylinder.
THEORY
Limit tests are quantitative or semi-quantitative test designed to identify and control a small
number of impurities which are likely to be present in the substance. This test involves the
reaction of silver nitrate with soluble chloride to form the ppt. of silver chloride which is
insoluble in dilute HNO3. The extent of the precipitation depends upon the amount of silver
chloride formed i.e. on the number of chloride ions present in the substance. The opalescence
produced in the test solution is compared with a reference/standard solution under the same
experimental conditions.
Cl- + AgNO3 → AgCl ↓ + NO3-
ppt.
NaCl + AgNO3 → AgCl ↓ + NaNO3
ppt.
PROCEDURE
STANDARD - 1mL of 0.05845% w/v solution of NaCl is taken in Nessler’s cylinder Add 10 mL of
Dil. HNO3 Make up the volume up to 50 ml with distilled water. Now add 1mL of silver nitrate to this
solution. Stirrer the solution with glass road and allow to stand for 5 minutes.
TEST
Dissolve a specified quantity of substances as per I.P. monograph in10mL of distilled water.
Add 10 mL of Dil. Nitric acid. Makeup the volume up to 50 mL with tap water. Now add 1mL
of silver nitrate to this solution. Stirrer the solution with glass road and allow to stand for 5
minutes.
OBSERVATION
The opalescence of the test solution is less/more than the standard solution. If the opalescence of
the test solution has been less than the standard opalescence, the sample will pass the limit test.
RESULT
A limit test for chloride was performed.
PHARMACEUTICAL CHEMISTRY
EXPERIMENT NO -5
OBJECT: To perform a limit test for sulphate in a given sample of tap water.
REFERENCES:
Parle A., "Pharmaceutical Chemistry 1 Laboratory Manual”, CBS Publishers and Distributors
Pvt. Ltd.,Ed Ist, 2008, pp 59
REQUIREMENTS
Chemical required: Hydrochloric acid, Barium sulphate, and Barium chloride
Apparatus required: Measuring cylinder, glass rod, pipette and Nessler’s cylinder, etc.
THEORY
Limit tests are quantitative or semi-quantitative test designed to identify and control a small
number of impurities which are likely to be present in the substance. This test involves the
reaction of Barium chloride with soluble sulphate to form the precipitate of Barium sulphate
which is insoluble in dilute hydrochloric acid. The Barium sulphate precipitate is white in
color.
REACTION - SO4-- + BaCl2 → BaSO4 + Cl-
(White ppt.)
Na2 SO4 + BaCl2 → BaSO4 + NaCl
(White ppt.)
PROCEDURE
STANDARD - Take 1mL of 0.1089 w/v of Na2SO4 or K2SO4 as per I.P. in Nessler cylinder. Add 2 mL
of dilute Hydrochloric acid. Makeup the volume up to 45 ml with distilled water. Add in this solution of
5 mL of Barium sulphate reagent. Stirrer the solution with a glass rod and allow to stand for 5 minutes.
TEST
Dissolve the specific quantity of test substances in 10 mL of tap water. Add 2 mL of dilute
Hydrochloric acid. Makeup the volume up to 45 ml with distilled water. Add in this solution of
5 mL of Barium sulphate reagent Stirrer the solution with a glass rod and allow to stand for 5
minutes.
OBSERVATION
The opalescence of the test solution is less/more than the standard solution. If the opalescence of
the test solution has been less than the standard opalescence, the sample will pass the limit test.
RESULT
Limit test for sulphate was performed
8
PHARMACEUTICAL CHEMISTRY
EXPERIMENT NO- 6
OBJECT: - To perform the limit test for chloride in a given sample of sodium bicarbonate.
REFERENCE
Parle A., "Pharmaceutical Chemistry 1 Laboratory Manual", CBS Publishers and Distributors
Pvt. Ltd., Ed Ist, 2008, pp 59
REQUIREMENTS: -
Chemical required: sodium bicarbonate, dilute nitric acid, 0.1 M silver nitrate solution, etc.
Apparatus required: - Measuring cylinder, glass rod, and Nessler’s cylinder, Beaker.
THEORY
Limit tests are quantitative or semi-quantitative test designed to identify and control a small
number of impurities which are likely to be present in the substance. This test involves the
reaction of silver nitrate with soluble chloride to form the ppt. of silver chloride which is
insoluble in dilute HNO3. The extent of the precipitation depends upon the amount of silver
chloride formed i.e. on the number of chloride ions present in the substance. The opalescence
produced in the test solution is compared with a reference/standard solution under the same
experimental conditions.
Cl- + AgNO3 → AgCl ↓ + NO3-
ppt.
NaCl + AgNO3 → AgCl ↓ + NaNO3
ppt.
PROCEDURE STANDARD - 10 ml of chloride standard solution is taken in Nessler’s cylinder. Mix
it with 5 ml of water. Add 10 mL of Dil. HNO3 Make up the volume up to 50 ml with distilled water.
Now add 1mL of silver nitrate to this solution. Stirrer the solution with glass road and allow to stand for
5 minutes.
TEST
Dissolve a specified quantity of substances as per I.P. monograph in10mL of distilled water.
Add 10 mL of Dil. Nitric acid. Makeup the volume up to 50 mL with tap water. Now add 1mL
of silver nitrate to this solution. Stirrer the solution with glass road and allow to stand for 5
minutes.
OBSERVATION
The opalescence of the test solution is less/more than the standard solution. If the opalescence of
the test solution has been less than the standard opalescence, the sample will pass the limit test.
RESULT
Limit test for chloride was performed
9
PHARMACEUTICAL CHEMISTRY
EXPERIMENT NO- 7
OBJECT: - To perform a limit test for chloride in a given sample of sodium hydroxide.
REFERENCE
Parle A., "Pharmaceutical Chemistry 1 Laboratory Manual", CBS Publishers and distributors
Pvt. Ltd., Ed Ist, 2008, pp 59
REQUIREMENTS: -
Chemical required: sodium hydroxide, dilute nitric acid, 0.1 M silver nitrate solution, etc.
Apparatus required: - Measuring cylinder, glass rod, and Nessler’s cylinder, Beaker.
THEORY
A limit test is a quantitative or semi-quantitative test designed to identify and control a small
number of impurities which are likely to be present in the substance. This test involves the
reaction of silver nitrate with soluble chloride to form the ppt. of silver chloride which is
insoluble in dilute HNO3. The extent of the precipitation depends upon the amount of silver
chloride formed i.e. on the number of chloride ions present in the substance. The opalescence
produced in the test solution is compared with a reference/standard solution under the same
experimental conditions.
Cl- + AgNO3 → AgCl ↓ + NO3-
ppt.
NaCl + AgNO3 → AgCl ↓ + NaNO3
ppt.
PROCEDURE
STANDARD -10 ml of chloride standard solution is taken in Nessler’s cylinder. Mix it with 5 ml of
water. Add 10 mL of Dil. HNO3 Make up the volume up to 50 ml with distilled water. Now add 1mL of
silver nitrate to this solution. Stirrer the solution with glass road and allow to stand for 5 minutes.
TEST - Dissolve a specified quantity of substances as per I.P. monograph in10mL of distilled
water. Add 10 mL of Dil. Nitric acid. Makeup the volume up to 50 mL with tap water. Now add
1mL of silver nitrate to this solution. Stirrer the solution with glass road and allow to stand for 5
minutes.
OBSERVATION
The opalescence of the test solution is less/more than the standard solution. If the opalescence of
the test solution has been less than the standard opalescence, the sample will pass the limit test.
RESULT
A limit test for chloride was performed.
10
PHARMACEUTICAL CHEMISTRY
EXPERIMENT NO- 8
OBJECT: - To perform the limit test for chloride in a given sample of sodium acetate.
REFERENCE
Parle A., "Pharmaceutical Chemistry 1 Laboratory Manual", CBS Publishers and Distributors
Pvt. Ltd., Ed Ist, 2008, pp 59
REQUIREMENTS: -
Chemical required: sodium acetate, dilute nitric acid, 0.1 M silver nitrate solution, etc.
Apparatus required: - Measuring cylinder, glass rod, and Nessler’s cylinder, Beaker.
THEORY
Limit tests are quantitative or semi-quantitative test designed to identify and control a small
number of impurities which are likely to be present in the substance. This test involves the
reaction of silver nitrate with soluble chloride to form the ppt. of silver chloride which is
insoluble in dilute HNO3. The extent of the precipitation depends upon the amount of silver
chloride formed i.e. on the number of chloride ions present in the substance. The opalescence
produced in the test solution is compared with a reference/standard solution under the same
experimental conditions.
Cl- + AgNO3 → AgCl ↓ + NO3-
ppt.
PROCEDURE
STANDARD - 10 ml of chloride standard solution is taken in Nessler’s cylinder. Mix it with 5 ml of
water. Add 10 mL of Dil. HNO3 Make up the volume up to 50 ml with distilled water. Now add 1mL of
silver nitrate to this solution. Stirrer the solution with glass road and allow to stand for 5 minutes.
TEST
Dissolve a specified quantity of substances as per I.P. monograph in10mL of distilled water.
Add 10 mL of Dil. Nitric acid. Makeup the volume up to 50 mL with tap water. Now add 1mL
of silver nitrate to this solution. Stirrer the solution with glass road and allow to stand for 5
minutes.
OBSERVATION
The opalescence of the test solution is less/more than the standard solution. If the opalescence of
the test solution has been less than the standard opalescence, the sample will pass the limit test.
RESULT
The limit test for chloride was performed.
11
PHARMACEUTICAL CHEMISTRY
EXPERIMENT NO -9
OBJECT: To perform a limit test for sulphate in a given sample of sodium bicarbonate.
REFERENCES
Parle A., "Pharmaceutical Chemistry 1 Laboratory Manual", CBS Publishers and distributors
Pvt. Ltd., Ed Ist, 2008, pp 59.
REQUIREMENTS
Chemical required: sodium bicarbonate, ethanol, potassium sulphate, 5M acetic acid, HCl,
and Barium chloride
Apparatus required: Measuring cylinder, glass rod, pipette and Nessler’s cylinder, etc.
THEORY
Limit tests are quantitative or semi-quantitative test designed to identify and control the small
number of impurities which are likely to be present in the substance. This test involves the
reaction of Barium chloride with soluble sulphate to form the precipitate of Barium sulphate
which is insoluble in dilute hydrochloric acid. The Barium sulphate precipitate is white in
color.
TEST
Dissolve the specific quantity of test substances in 10 mL of tap water. Add 2 mL of dilute
Hydrochloric acid. Makeup the volume up to 45 ml with distilled water. Add in this solution of
5 mL of Barium sulphate reagent Stirrer the solution with a glass rod and allow to stand for 5
minutes.
OBSERVATION - The opalescence of the test solution is less/more than the standard solution.
If the opalescence of the test solution has been less than the standard opalescence, the sample
will pass the limit test.
RESULT - Limit test for sulphate was performed
12
PHARMACEUTICAL CHEMISTRY
EXPERIMENT NO -10
OBJECT: To perform a limit test for sulphate in a given sample of sodium citrate.
REFERENCES
Singh H.R., Kapoor V.K. “Practical Pharmaceutical chemistry”, Vallabh Prakashan, Ed Ist,
2008, pp 57.
REQUIREMENTS
Chemical required: sodium citrate, ethanol, potassium sulphate, 5M acetic acid, HCl, and
Barium chloride
Apparatus required: Measuring cylinder, glass rod, pipette and Nessler’s cylinder, etc.
THEORY
Limit test is a quantitative or semi-quantitative test designed to identify and control a small
quantity of impurities which are likely to be present in the substance This test involves the
reaction of Barium chloride with soluble sulphate to form the precipitate of Barium sulphate
which is insoluble in dilute hydrochloric acid. The Barium sulphate precipitate is white in
color.
PROCEDURE
STANDARD - Take 1mL of 0.1089 w/v of Na2SO4 or K2SO4 as per I.P. in Nessler cylinder. Add 2 ml
of dilute Hydrochloric acid. Makeup the volume up to 45 ml with distilled water. Add in this solution of
5 mL of Barium sulphate reagent. Stirrer the solution with a glass rod and allow to stand for 5 minutes.
TEST
Dissolve the specific quantity of test substances in 10 mL of tap water. Add 2 mL of dilute
Hydrochloric acid. Makeup the volume up to 45 ml with distilled water. Add in this solution of
5 mL of Barium sulphate reagent. Stirrer the solution with a glass rod and allow to stand for 5
minutes.
OBSERVATION
The opalescence of the test solution is less/more than the standard solution. If the opalescence of
the test solution has been less than the standard opalescence, the sample will pass the limit test.
EXPERIMENT NO 11
OBJECT: To perform a limit test for sulphate in a given sample of sodium dihydrogen
phosphate dihydrate.
REFERENCES
Singh H.R., Kapoor V.K. “Practical Pharmaceutical chemistry”, Vallabh Prakashan, Ed Ist,
2008, pp 57.
REQUIREMENTS
Chemical required: sodium dihydrogen phosphate dihydrate, ethanol, potassium sulphate, 5M
acetic acid, HCl, and Barium chloride
Apparatus required: Measuring cylinder, glass rod, pipette and Nessler’s cylinder, etc.
THEORY
Limit test are quantitative or semi-quantitative test designed to identify and control the small
quantity of impurities which are likely to be present in the substance
This test involves the reaction of Barium chloride with soluble sulphate to form the precipitate
of Barium sulphate which is insoluble in dilute hydrochloric acid. The Barium sulphate
precipitate is white in color.
REACTION
14
PHARMACEUTICAL CHEMISTRY
OBSERVATION
The opalescence of the test solution is less/more than the standard solution. If the opalescence of
the test solution has been less than the standard opalescence, the sample will pass the limit test.
RESULT
A limit test for sulphate was performed.
15
PHARMACEUTICAL CHEMISTRY
EXPERIMENT NO -12
OBJECT: To perform the identification tests for the given sample of ammonium chloride.
REFERENCES
Parle A., "Pharmaceutical Chemistry 1 Laboratory Manual", CBS Publishers and Distributors
Pvt. Ltd., Ed Ist, 2008, pp 59.
REQUIREMENTS
Chemical required: Ammonium chloride, sodium hydroxide, red litmus paper, sodium cobalt
nitrite, nitric acid, silver nitrate solution, dilute ammonia solution, potassium dichromate,
sulphuric acid, diphenyl carbazide solution.
Apparatus required: test tubes, test tube stands, test tube holders, glass rod.
THEORY
Any process that can provide a qualitative determination of the ions present in a simple
inorganic compound is based upon knowledge of acid/base chemistry, redox chemistry, and
solubility. In this regard, the identification of a single pure compound is therefore very much
simpler than the identification of a mixture. This experiment deals only with the identification
of simple compounds, ie those that contain only one cation and one anion.
CEDURE
STANDARD Take 1mL of 0.1089 w/v of Na2SO4 or K2SO4 as per I.P. in Nessler cylinder. Add 2 mL
of dilute Hydrochloric acid. Make up the volume up to 45 ml with distilled water. Add in this solution
of 5 mL of Barium sulphate reagent. Stirrer the solution with a glass rod and allow to stand for 5
minutes.
TEST
Dissolve the specific quantity of test substances in 10 mL of tap water. Add 2 ml of dilute
Hydrochloric acid. Makeup the volume up to 45 ml with distilled water. Add in this solution of
5 mL of Barium sulphate reagent. Stirrer the solution with a glass rod and allow to stand for 5
minutes.
OBSERVATION
The opalescence of the test solution is less/more than the standard solution. If the opalescence of
the test solution has been less than the standard opalescence, the sample will pass the limit test.
RESULT
Limit test for sulphate was performed
16
PHARMACEUTICAL CHEMISTRY
EXPERIMENT NO -13
THEORY
Any process that can provide a qualitative determination of the ions present in a simple
inorganic compound is based upon knowledge of acid/base chemistry, redox chemistry, and
solubility. In this regard, the identification of a single pure compound is therefore very much
simpler than the identification of a mixture. This experiment deals only with the identification of
simple compounds, ie those that contain only one cation and one anion.
PROCEDURE
REACTION 0F CHLORIDES
S. NO TEST OBSERVATION INFERENCE
1 Dissolve 2mg of sample in 2ml of
water. Acidify with dilute nitric acid.
Add 0.5 ml of silver nitrate solution.
Shake and allow to stand add
ammonia + nitric acid.
17
PHARMACEUTICAL CHEMISTRY
18
PHARMACEUTICAL CHEMISTRY
EXPERIMENT NO -14
REFERENCE
1. Singh H.R., Kapoor V.K. “Practical Pharmaceutical chemistry”, Vallabh Prakashan,
Ed Ist, 2008, pp 19-20.
2. Chatwal GR, “Pharmaceutical chemistry inorganic” Himalaya publishing house, Ed 5 th,
2010, pp 256-257
REQUIREMENTS
Chemical required: Sodium chloride, Potassium carbonate, potassium antimonite solution,
acetic acid, magnesium uranyl acetate solution, nitric acid, silver nitrate solution, dilute
ammonia solution, potassium dichromate, sulphuric acid, etc
Apparatus required: Volumetric flask, conical flask, Burette, Pipette, Glass rod.
THEORY
Any process that can provide a qualitative determination of the ions present in a simple
inorganic compound is based upon knowledge of acid/base chemistry, redox chemistry, and
solubility. In this regard, the identification of a single pure compound is therefore very much
simpler than the identification of a mixture. This experiment deals only with the identification of
simple compounds, ie those that contain only one cation and one anion.
PROCEDURE
REACTIONS OF SODIUM IONS
19
PHARMACEUTICAL CHEMISTRY
REACTION 0F CHLORIDES
RESULT:
An identification test of sodium chloride was performed.
20
PHARMACEUTICAL CHEMISTRY
EXPERIMENT NO -15
REFERENCE
3. Singh H.R., Kapoor V.K. “Practical Pharmaceutical chemistry”, Vallabh Prakashan,
Ed Ist, 2008, pp 19-20.
4. Chatwal GR, “Pharmaceutical chemistry inorganic” Himalaya publishing house, Ed 5 th,
2010, pp 256-257
REQUIREMENTS
Chemical required: Sodium bicarbonate, Potassium carbonate, potassium antimonite solution,
acetic acid, magnesium uranyl acetate solution, nitric acid, silver nitrate solution, dilute
ammonia solution, potassium dichromate, sulphuric acid, etc
Apparatus required: Volumetric flask, conical flask, Burette, Pipette, Glass rod.
THEORY
Any process that can provide a qualitative determination of the ions present in a simple
inorganic compound is based upon knowledge of acid/base chemistry, redox chemistry, and
solubility. In this regard, the identification of a single pure compound is therefore very much
simpler than the identification of a mixture. This experiment deals only with the identification of
simple compounds, ie those that contain only one cation and one anion.
PROCEDURE
21
PHARMACEUTICAL CHEMISTRY
REACTION 0F BICARBONATES
RESULT:
An identification test of sodium bicarbonate was performed.
22
PHARMACEUTICAL CHEMISTRY
EXPERIMENT NO -15
REFERENCE
1. Singh H.R., Kapoor V.K. “Practical Pharmaceutical chemistry”, Vallabh Prakashan,
Ed Ist, 2008, pp 19-20.
2. Chatwal GR, “Pharmaceutical chemistry inorganic” Himalaya publishing house, Ed 5th,
2010, pp 256-257
REQUIREMENTS
Chemical required: Magnesium sulphate, 2 M ammonium chloride, 0.25 M disodium
hydrogen phosphate, dilute ammonia solution lead acetate solution, ammonium acetate solution,
potassium dichromate, dilute hydrochloric acid, etc
Apparatus required: Volumetric flask, conical flask, Burette, Pipette, Glass rod.
THEORY
Any process that can provide a qualitative determination of the ions present in a simple
inorganic compound is based upon knowledge of acid/base chemistry, redox chemistry, and
solubility. In this regard, the identification of a single pure compound is therefore very much
simpler than the identification of a mixture. This experiment deals only with the identification of
simple compounds, ie those that contain only one cation and one anion.
PROCEDURE
REACTIONS OF MAGNESIUM IONS
1 Dissolve 15 mg of sample in 2 ml of
water. Add 1 ml of dilute ammonia
solution.
23
PHARMACEUTICAL CHEMISTRY
REACTION 0F SULPHATE
RESULT:
An identification test of magnesium sulphate was performed.
24
PHARMACEUTICAL CHEMISTRY
EXPERIMENT NO -16
REFERENCE
1. Singh H.R., Kapoor V.K. “Practical Pharmaceutical chemistry”, Vallabh Prakashan, Ed Ist,
2008, pp 19-20.
2. Chatwal GR, “Pharmaceutical chemistry inorganic” Himalaya publishing house, Ed 5 th,
2010, pp 256-257
REQUIREMENTS
Chemical required: Barium sulphate, barium chloride solution, dilute hydrochloric acid,
silver nitrate solution,dilute ammonia solution, potassium dichromate,sulphuric acid, etc
Apparatus required: Test tube, test tube stand, test tube holder, Pipette, Glass rod.
THEORY
Any process that can provide a qualitative determination of the ions present in a simple
inorganic compound is based upon knowledge of acid/base chemistry, redox chemistry and
solubility. In this regard, the identification of a single pure compound is therefore very much
simpler than the identification of a mixture. This experiment deals only with the identification of
simple compounds, ie those that contain only one cation and one anion.
PROCEDURE
REACTIONS OF BARIUM IONS
25
PHARMACEUTICAL CHEMISTRY
RESULT:
An identification test of barium sulphate was performed.
26
PHARMACEUTICAL CHEMISTRY
EXPERIMENT NO -17
REFERENCE
Singh H.R., Kapoor V.K. “Practical Pharmaceutical chemistry”, Vallabh Prakashan, Ed Ist,
2008, pp 19-20.
Chatwal GR, “Pharmaceutical chemistry inorganic” Himalaya publishing house, Ed 5 th, 2010,
pp 256-257
REQUIREMENTS
Chemical required: Iodine, starch solution
Apparatus required: Volumetric flask, conical flask, Burette, Pipette, Glass rod.
THEORY
Any process that can provide a qualitative determination of the ions present in a simple
inorganic compound is based upon knowledge of acid/base chemistry, redox chemistry, and
solubility. In this regard, the identification of a single pure compound is therefore very much
simpler than the identification of a mixture. This experiment deals only with the identification of
simple compounds, i.e. those that contain only one cation and one anion.
PROCEDURE
RESULT:
Identification test of iodine was performed.
27
PHARMACEUTICAL CHEMISTRY
EXPERIMENT NO -18
REFERENCE
1. Singh H.R., Kapoor V.K. “Practical Pharmaceutical chemistry”, Vallabh Prakashan, Ed Ist,
2008, pp 19-20.
2. Chatwal GR, “Pharmaceutical chemistry inorganic” Himalaya publishing house, Ed 5 th,
2010, pp 256-257
STANDARDS
Iodine contains nlt 99.5% and nmt 100.5% of I.
REQUIREMENTS
Chemical required: Iodine , potassium iodide, 2 M acetic acid, 0.1 M sodium
thiosulphate solution,starch solution
RESULT:
The percentage purity of I in the given sample of iodine is % w/w.
28
PHARMACEUTICAL CHEMISTRY
EXPERIMENT NO -19
REFERENCE:-
Singh H.R., Kapoor V.K. “Practical Pharmaceutical chemistry”, Vallabh Prakashan, Ed Ist, 2008,
pp 58.
REQUIREMENTS
Chemical required: Thioglycolic acid, citric acid, Ammonia solution, ferric ammonium
sulphate.
Apparatus required: Measuring cylinder, glass rod, pipette and Nessler’s cylinder.
THEORY
Limit test are quantitative or semi-quantitative test designed to identify and control small
quatity of impurities which are likely to be present in the substance.
The limit test of iron is based on the reaction between iron and thioglycolic acid in the
presence of citric acid in a ammonical solution. Citric acid prevents precipitation of iron with
Ammonia. A deep reddish purple colour is formed.
Ferrous thioglycolate is colourless in acidic medium but in alkaline medium it gives purple
colour.
2HSCH2COOH + Fe3+ → Fe (HSCH2COO) 2 + 2H+
PROCEDURE
STANDARD
Take standard 1.5 ml of Iron solution. Add 1.5 ml of iron free citric acid to this solution and 1.5
ml of thioglycollic acid and make the solution alkaline. Volume make up to 50 ml. Stare the
solution allow to stand for 5 minutes.
TEST
Dissolve specific quantity of substances being examined dissolved in water. Add 1.5 ml of iron
free citric acid to this solution and 1.5 ml of thioglycollic acid and make the solution alkaline.
Volume make up to 50 ml. Stare the solution allow to stand for 5 minutes
RESULT
Limit test for Iron was performed.
29
PHARMACEUTICAL CHEMISTRY
EXPERIMENT NO -20
OBJECT: To perform limit test of heavy metals in given sample of sodium chloride.
REFERENCE:-
Singh H.R., Kapoor V.K. “Practical Pharmaceutical chemistry”, Vallabh
Prakashan, Ed Ist, 2008, pp 58.
REQUIREMENTS
Chemical required: Thioglycolic acid, citric acid, Ammonia solution, ferric ammonium
sulphate.
Apparatus required: Measuring cylinder, glass rod, pipette and Nessler’s cylinder.
THEORY
Limit test of heavy metals is based on the reaction of metallic impurities with hydrogen
sulfide in acidic medium to form brownish colour solution. Metals that response to this test
are lead, mercury, bismuth, arsenic, antimony, tin, cadmium, silver, copper, and molybdenum.
The metallic impurities in substances are expressed as parts of lead per million parts of the
substance. The usual limit as per Indian Pharmacopoeia is 20
PROCEDURE STANDARD
Take 2 ml of standard lead solution and dilute to 25 ml with water. Adjust the pH between 3 to 4
by adding dilute acetic acid ‘Sp’ or dilute ammonia solution ‘Sp. Dilute with water to 35 ml.
Add freshly prepared 10 ml of hydrogen sulphide solution and dilute with water to 50 ml. Allow
to stand for five minutes, view downwards over a white surface.
TEST
Weigh specific quantity of test substance, moisten with sulphuric acid and ignite on a low flame
till completely charred. Add few drops of nitric acid and heat it. Allow to cool and add 4 ml of
hydrochloric acid and evaporate to dryness. Moisten the residue with 10 ml of hydrochloric acid
and digest for two minutes Neutralize with ammonia solution and make just acid with acetic
acid. Adjust the pH between 3 to 4 and filter if necessary. Dilute with water to 35 ml. Add
freshly prepared 10 ml of hydrogen sulphide solution. Dilute with water to 50 ml. Allow to stand
for five minutes. View downwards over a white surface.
RESULT
Limit test for heavy metals was performed. The color produce in sample solution should not be
greater than standard solution. If color produces in sample solution is less than the standard
solution, the sample will pass the limit test of heavy metals and vice versa.
30
PHARMACEUTICAL CHEMISTRY
EXPERIMENT NO -21
REFERENCE
Parle A., “Pharmaceutical chemistry I Laboratory Mannual”, CBS Publishers and distributors
Pvt. Ltd, Ed Ist, 2008, pp 109-110.
STANDARDS
Hydrogen peroxide solution (20 vol.) contains not less than 5% w/v and nmt 7% w/v of H2O2
corresponding to about 20 times its volume of available oxygen.
REQUIREMENTS
Chemical required: H2O2 , potassium iodide, 1 M sulphuric acid, 0.02 M potassium
permaganate.
THEORY
This is an oxidation-reduction titration of permanganometery.
2 KMnO4+ 3 H2SO4 → K2SO4 +
2MnSO4+3H2O+5[O]
5[H2O2]+ [O]→ H2O + O2
2 KMnO4+ 3 H2SO4+ 5 H2O2 →
K2SO4 + 2MnSO4+8H2O+5[O]2
PROCEDURE
Rinse the pipette with the dil. Hydrogen peroxide solution. Using pipette transfer 1 ml of
dil. Hydrogen peroxide solution to dry and clean conical flask. Add 20 ml of 1 M
sulphuric acid. Rinse the burette with 0.002 M potassium permagnetane and fill it with
this on up to zero mark. Titrate it with potassium permagnete solution until the solution
become pink. Note the burette reading.
RESULT:
The percentage purity of H2O2 in the given sample of iodine is % w/v.
31
PHARMACEUTICAL CHEMISTRY
EXPERIMENT NO -22
REFERENCE
Parle A., “Pharmaceutical chemistry I Laboratory Mannual”, CBS Publishers and
distributors Pvt. Ltd, Ed Ist, 2008, pp 86-87.
STANDARDS
Ammonium Chloride contains not less than 99.00% and not more than 100.5% of NH4Cl
.
REQUIREMENTS
Chemical required: Ammonium chloride ,formaldehyde solution, potassium iodide,
0.1 M sodium hydroxide solution.
RESULT:
The percentage purity of ammonium chloride in the given sample is % w/w.
32
PHARMACEUTICAL CHEMISTRY
EXPERIMENT NO -23
REFERENCE
Parle A., “Pharmaceutical chemistry I Laboratory Mannual”, CBS Publishers and distributors
Pvt. Ltd, Ed Ist, 2008, pp 117-118.
REQUIREMENTS
Chemical required: Silver nitrate, sodium chloride, acetic acid ,methanol, eosin solution.
THEORY
Mohr method of determination of chlorides by titration with silver nitrate is one of the oldest
titration methods still in use - it was researched and published by Karl Friedrich Mohr in 1856.
The idea behind is very simple - chlorides are titrated with the silver nitrate solution in the
presence of chromate anions. End point is signalled by the appearance of the red silver
chromate. Intense yellow colour of chromate may make detection of first signs of formation of
red silver chromate precipitation difficult. As some excess of silver must be added before
precipitate starts to form, if concentration of titrant is below 0.1M, we may expect singificant
positive error. To correct for this error we can determine a blank, titrating a solution of the
indicator potassium chromate with standard silver nitrate solution. To make result more realistic
we can add small amount of chloride free calcium carbonate to the solution to imitate the white
silver precipitate.
PROCEDURE
Dissolve 2.75 g of ceric ammonium nitrate in 1 N nitric acid to obtain 100 ml of solution, and filter.
Standardize the solution as follows.
RESULT:
The exact molarity of the prepared silver nitrate solution is M.
33
PHARMACEUTICAL CHEMISTRY
EXPERIMENT NO -24
REFERENCE
Parle A., “Pharmaceutical chemistry I Laboratory Mannual”, CBS Publishers and distributors
Pvt. Ltd, Ed Ist, 2008, pp 139-140.
STANDARDS
Magnesium sulphate contains not less than 99.00% and not more than 100.5% of MgSO4.
REQUIREMENTS
Chemical required: Ammonium chloride ,strong ammonia, ammonium chloride solution.
Your unknown for this experiment is a solution. When you obtain your unknown, you need to
quantitatively transfer it to a 100 mL volumetric flask and dilute it to the mark, resulting in the
"prepared" unknown solution. You are to report the results of this "prepared" unknown.
Transfer exactly 10 mL of the prepared unknown solution into 3 or 4 Erlenmeyer flasks. Add
approximately 15 mL of pH 10 buffer in the hood and 20 or 25 mL of distilled, deionized water
to each flask. Add a few crystals of Eriochrome Black T indicator -- it is crucial that you only
add enough indicator to produce a light, wine-red color. Titrate each solution with your
standardized EDTA solution to a clear blue color. .Report your results as percent magnesium (%
w/v) in your “prepared” unknown sample. Also report the 95% confidence interval.
RESULT:
The percentage purity of magnesium sulphate in the given sample is % w/w.
34
PHARMACEUTICAL CHEMISTRY
EXPERIMENT NO -25
REFERENCE
Parle A., “Pharmaceutical chemistry I Laboratory Mannual”, CBS Publishers and distributors
Pvt. Ltd, Ed Ist, 2008, pp 143-144.
STANDARDS
Calcium gluconate contains not less than 98.5% and not more than 102.0% of C12H22CaO4.H2O.
REQUIREMENTS
PROCEDURE
Weigh accurately about 0.5 g of the dried sample and dissolve in 5 ml of dilute hydrochloric
acid. Add 50 ml of water, 25 ml of sodium hydroxide TS and about 0.1 g of 2-hydroxy-1-(2'-
hydroxy-4'-sulfo-1'-naphthylazo)-3-naphthoic acid. Titrate with 0.05 M EDTA immediately. At
the end-point, the red colour changes completely to blue. Each ml of 0.05 M EDTA is equivalent
to 22.42 mg of C12H22CaO14 · H2O.
RESULT:
The percentage purity of magnesium sulphate in the given sample is % w/w.
35