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📅 Last Updated: June 16, 2026
This article is about the SOP for Preparation and Standardization of 0.1M Ethanolic Sodium hydroxide solution. It includes apparatus, reagents, preparation of the thymolphthalein indicator, preparation of sodium hydroxide solution, standardization procedure of benzoic acid, formula to calculate the molarity, storage conditions and reference as per IP norms.
1.0 Scope:
This procedure can be used to prepare and standardize 0.1 Molar Ethanolic sodium hydroxide solution.
2.0 Apparatus:
- 1000 ml volumetric flask
- 250 ml glass-stoppered conical flask
- 100 ml graduated burette
- 100 ml volumetric flask
3.0 Reagents:
- Sodium hydroxide AR grade
- Benzoic acid AR grade
- Thymolphthalein solution
- Ethanol (95%v/v)
Preparation of Reagents:
Thymolphthalein solution:
Dissolve approximately 0.1g of Thymolphthalein in ethanol (95%v/v) and make to 100ml. and store in a clear glass stoppered bottle.
4.0 Preparation of 0.1M Ethanolic Sodium Hydroxide Solution:
- Dissolve approximately 4.2 g of sodium hydroxide in 5 ml of purified water and add enough aldehyde-free ethanol to make up to 1000 ml.
- Allow the solution to stand in a tightly-stoppered bottle for 24 hours.
- Then quickly pour off the clear liquid into a cleaned and dried plastic bottle.
5.0 Standardization of 0.1M Ethanolic Sodium Hydroxide:
- Transfer about 0.6 g (accurately weighed) of the powdered and dried Benzoic acid (Dried at about 120 °C for 2 hours) to a 250 ml glass stoppered conical flask, dissolve in a mixture of 30 ml ethanol (95%) and 6 ml purified water.
- Take 0.2 ml of thymolphthalein solution as indicator and titrate with the ethanolic sodium hydroxide solution (0.1 M) until a permanent pink colour is obtained.
Each ml of 0.1M ethanolic sodium hydroxide is equivalent to 0.01221 g of C7H6O2.

6.0 Molarity Calculation:

Where:
M = molarity of 0.1M ethanolic sodium hydroxide
W = weight of benzoic acid in g
V = volume of 0.1M ethanolic sodium hydroxide in ml
7.0 Storage:
Store in a transparent glass stoppered bottle
8.0 Reference:
As per IP –1996
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Reviewed by: Pankaj Sharma — Quality Control Specialist
Pankaj Sharma is a pharmaceutical QC professional who reviews our technical content for GMP accuracy, laboratory practices, and regulatory relevance.