Method of Analysis For Sodium Citrate: Pharmaguideline

Method of Analysis for Sodium Citrate : Pharmaguideline 20/12/22, 12:34

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Method of Analysis for Sodium Citrate

Procedure for analysis
Προβολήof της
Sodium Citrateσελίδας
τρέχουσας in pharmaceutical
σε: ΕλληνικάqualityΜετάφραση
control laboratory.
Απενεργοποίηση για τη γλώσσα: Αγγλικά Επιλογές ▼
1. Description
A white, crystalline powder or white, granular crystals, slightly deliquescent in moist air.
2. Solubility
Freely soluble in water, practically insoluble in alcohol.
3. Identification
Solution S
Dissolve 10.0 g sample in carbon dioxide-free water prepared from distilled water and dilute to 100 ml with the same solvent.
A. Reactions of Citrates
To 1 ml of solution S add 4 ml of water. To this solution add 0.5 ml of sulphuric acid and 1 ml of potassium permanganate solution and warm until the
color of the permanganate is discharged. Add 0.5 ml of a 10% w/v solution of sodium nitroprusside in 1M sulphuric acid and 4 g of sulphamic acid
and add 13.5M ammonia dropwise until all the sulphamic acid has dissolved. On addition of an excess of 13.5M ammonia, a violet color is produced
which changes to violet-blue.
B. Gives the reactions of Sodium Salt

To 1 ml of solution S add 2 ml of a 15% w/v solution of potassium carbonate and heat to boiling; no precipitate is produced. Add 4 ml of freshly
prepared potassium antimonate (V) solution and heat to boiling. Allow cooling in ice and if necessary scratching the inside of the tube with a glass
rod; a dense, white precipitate is produced.
4 Appearance of Solution
Limit: Solution S is clear and colorless
Clarity of the Solution
Sample Preparation: Solution S
Standard Preparation: Dissolve 1.0 g of hydrazine sulfate in sufficient water to produce 100.0 ml and allow standing for 4 to 6 hours. Add 25.0 ml of
this solution to a solution containing 2.5 g of hexamine in 25.0 ml of water mix well and allow standing for 24 hours. To prepare the standard of
opalescence, dilute 15.0 ml of the suspension to 1000.0 ml with water.
Into separate matched, flat-bottomed test tubes, 15 to 25 mm in internal diameter and of colorless, transparent, neutral glass, place sufficient of the
solution being examined and of the appropriate reference suspension, such that the test tubes are filled to a depth of 40 mm. Five minutes after
preparation of the reference suspension, compare the contents of the test tubes against a black background by viewing in diffused daylight down the
vertical axes of the tubes.
Color of Solution
Sample Preparation: Solution S
Using identical tubes of colorless, transparent, neutral glass 12 mm in external diameter compare 2.0 ml of the sample, with 2.0 ml of water in
another tube. Compare the colors in diffused daylight, viewing horizontally against a white background.
5. Acidity or alkalinity
Limit: Not more than 0.2 ml of 0.1 M hydrochloric acid or 0.1 M sodium hydroxide is required to change the color of the indicator.
Reagent required
Phenolphthalein solution.
0.1M Hydrochloride Acid
0.1M Sodium Hydroxide
Procedure: To 10 ml of solution S add 0.1 ml of phenolphthalein solution R. Not more than 0.2 ml of 0.1 M hydrochloric acid or 0.1 M sodium
hydroxide is required to change the color of the indicator.
6. Readily Carbonized Substances

Limit: The solution is not more intensely colored than reference solution Y2 or GY2.
Procedure:
Sample Solution: To 0.20 g of the powdered substance to be examined add 10 ml of sulphuric acid R and heat in a water-bath at 90°C ±1°C for 60
min. Cool rapidly.
Reference Solution Y2: Take 24ml of yellow primary standard solution, 6ml of the red primary solution in a 100 ml volumetric flask and make up the
volume with 1% w/v of HCl. Take 75ml of this solution in a 100 ml volumetric flask and make up the volume with 1% w/v of HCl.
Reference Solution GY2: Take 96 ml of yellow primary standard solution, 2 ml of red primary solution, 2 ml blue primary solution in a 100 ml
volumetric flask and make up the volume with 1% w/v of HCl. Take 15 ml of this solution in a 100 ml volumetric flask and make up the volume with
1% w/v of HCl.
https://www.pharmaguideline.com/2008/07/method-of-analysis-for-sodium-citrate.html Page 1 of 3
Using identical tubes of colorless, transparent, neutral glass with a flat base and an internal diameter of 15 to 25 mm compare a 40-mm layer of the
liquid being examined with a 40-mm layer of methanol Examine the columns of liquid in diffused daylight by viewing down the vertical axes of the
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7. Chlorides
Limit: Not more than 50 ppm
Procedure:
Sample Solution: Dilute 10 ml of solution S to 15 ml with water.
To 15 ml of sample solution add 1 ml of 2M nitric acid, pour the mixture as a single addition into 1 ml of silver nitrate solution and allow standing for 5
minutes protected from light. When viewed transversely against a black background any opalescence produced is not more intense than that
obtained by treating a mixture of 10 ml of chloride standard solution (5 ppm Cl) and 5 ml of water in the same manner.
8. Oxalate
Limit: Not more than 300 ppm.
Procedure: Dissolve 0.50 g sample in 4 ml of water, add 3 ml of hydrochloric acid and 1 g of granulated zinc and heat on a water-bath for 1 min.
Allow to stand for 2 min, decant the liquid into a test-tube containing 0.25 ml of a 10 g/l solution of phenylhydrazine hydrochloride and heat to boiling.
Cool rapidly, transfer to a graduated cylinder and add an equal volume of hydrochloric acid and 0.25 ml of potassium ferricyanide solution. Shake
and allow standing for 30 min. Any pink color in the solution is not more intense than that in a standard prepared at the same time, in the same
manner, using 4 ml of a 50 mg/l solution of oxalic acid.
9. Sulfate
Limit: Not more than 150 ppm.
Procedure: Sample Solution: To 10 ml of solution S add 2 ml of hydrochloric acid and dilute to 15 ml with distilled water.
Add 3 ml of a 250 g/l solution of barium chloride to 4.5 ml of sulfate standard solution (10 ppm SO4). Shake and allow standing for 1 min. To 2.5 ml of
this solution, add 15 ml of the sample solution and 0.5 ml of acetic acid. Prepare a standard, in the same manner, using 15 ml of sulfate standard
solution (10 ppm SO4 ) instead of the solution to be examined.
10. Heavy metals
Limit: Not more than 10 ppm,
Reagent required
Acetate buffer pH 3.5
Thioacetamide reagent
Lead standard solution (1 ppm)
To 12 ml of the solution S add 2 ml of acetate buffer pH 3.5, mix, add to 1.2 ml of Thioacetamide reagent, mix immediately and allow standing for 2
minutes. Any brown color produced is not more intense than that obtained by treating, in the same manner, a mixture of 10 ml of lead standard
solution (1 ppm Pb), and 2 ml of the solution being examined. The standard solution exhibits a slightly brown color when compared to a solution
prepared by treating, in the same manner, a mixture of 10 ml of water and 2 ml of the solution being examined.
11. Water
Limit: 11.0 to 13.0 %
Procedure: Transfer 35 to 40 ml of methanol to the titration vessel, and titrate with K.F. reagent, standardized earlier, to the electrometric endpoint to
consume any moisture that may be present. Quickly and accurately add 300 mg substance, after adding the substance to be examined, stir for 15
min before titrating, and again titrate with the reagent to the electrometric end-point. Calculate the % of water using the formula:
Calculation
V x F x 100
Water (% w/w) = -----------------
W
Where,
V= Volume of K.F. reagent consumed (ml)
F= Water equivalence factor of reagent in mg/ml
W= Weight of substances in mg
12. Assay
Limit: Not less than 99.0 % and Not more than 100.5 % on the anhydrous basis
Reagent required
Anhydrous glacial acetic acid,
Naphtholbenzene solution
Perchloric acid 0.1M
Procedure: Dissolve 0.150 g in 20 ml of anhydrous acetic acid R, heating to about 50°C. Allow cooling. Using 0.25 ml of naphtholbenzein solution R
as an indicator, titrate with 0.1 M perchloric acid until a green color is obtained. 1 ml of 0.1 M perchloric acid is equivalent to 8.602 mg of
C6H5Na3O7.
Calculation
V x M x F x 100 100
% Assay on dried basis = ----------------------- x -------------------
0.1 x W (100 – Water)
Where,
V= Consumed volume of 0.1 M Perchloric Acid
M= Molarity of 0.1 M Perchloric Acid
F= Factor
W= Weight of substance.
13. Arsenic
Limit: Not more than 2 ppm
Procedure: Dissolve 5 g sample in 50 ml of water and add 15 ml of stannated hydrochloric acid AsT.
Into the bottle or conical flask introduce the test solution; add 5 ml of 1M potassium iodide and 10 g of zinc AsT. Immediately assemble the apparatus
and immerse the flask in a water bath at a temperature such that a uniform evolution of gas is maintained. After 40 minutes any stain produced on
the mercuric chloride paper is not more intense than that obtained by treating in the same manner 1.0 ml of arsenic standard solution (10 ppm As)
diluted to 50 ml with water.
14. Tartrate
Limit: No crystalline precipitate is formed.
Procedure: To a solution of 1 g in 2 ml of water in a test-tube, add 1 ml of a 10% w/v solution of potassium acetate and 1 ml of 6M acetic acid.
Scratch the walls of the test-tube with a glass rod; no crystalline precipitate is formed.
Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of pharmaguideline.com, a widely-read pharmaceutical
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Method of Analysis for Sodium Citrate : Pharmaguideline 20/12/22, 12:34

Method of Analysis for Sodium Citrate

B. Gives the reactions of Sodium Salt

6. Readily Carbonized Substances

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