Salicylic Acid Collodion
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This article is compiled based on the United States Pharmacopeia (USP) – 2025 Edition
Issued and maintained by the United States Pharmacopeial Convention (USP)
1 DEFINITION
Salicylic Acid Collodion contains NLT 9.5% and NMT 11.5% of salicylic acid (C7H6O3).
Salicylic Acid Collodion is prepared as follows.
| Salicylic Acid | 100 g |
| Flexible Collodion, a sufficient quantity to make | 1000 mL |
Dissolve the Salicylic Acid in about 750 mL of Flexible Collodion. Add a sufficient quantity of the Flexible Collodion to bring the preparation to final volume, and mix.
2 ASSAY
2.1 Procedure
Sample: 5 mL
Solution A: Ether and alcohol (3:1) neutralized to bromothymol blue TS
Titrimetric system
Mode: Direct titration
Titrant: 0.1 N sodium hydroxide VS
Endpoint detection: Visual
Analysis: Transfer the Sample to a 400-mL beaker, rinse the measuring device with three 10-mL portions of Solution A, and add the rinsings to the beaker. Add, with stirring, 5 mL of 100 mg/mL sodium lauryl sulfate solution that was previously neutralized with 0.1 N hydrochloric acid to the distinct yellow color of bromothymol blue TS, and add 20 mL of water. Mix, add 5 drops of bromothymol blue TS, and titrate with the Titrant. Each mL of Titrant is equivalent to 13.81 mg of salicylic acid (C7H6O3).
Acceptance criteria: 9.5%–11.5%
3 ADDITIONAL REQUIREMENTS
Packaging and Storage: Package in tight containers. Store at controlled room temperature, remote from fire.

