On Glycolic Acid United States Pharmacopoeia Monograph Related
Glycolic acid, in the pharmaceutical application field, has unique properties and uses. The United States Pharmacopoeia Monograph regulates it in detail, related to quality, traits, identification, inspection and other items.

As far as quality is concerned, it specializes in its purity standard, which must reach the corresponding value, and it can be used for medicinal purposes. In terms of properties, it is important to describe its appearance, whether it is a colorless and transparent liquid, or other specific physical forms, and has corresponding odor characteristics.

The method of identification is delicately designed in the monograph. Or according to the chemical characteristics of the reaction, so that glycolic acid and specific reagents, observe the phenomenon, to prove that it is true; or use instrumental analysis techniques, such as spectroscopy, chromatography, etc., to accurately identify from the molecular structure characteristics to ensure that it is correct.

Inspection process, carefully review key indicators such as impurities and moisture. Impurity content must be strictly controlled, because it is related to efficacy and safety. The amount of moisture is also fixed, too much or too little can affect the stability and application effect of glycolic acid.

United States Pharmacopoeia monographs, such as the beacon of navigation, are for the standardized application of glycolic acid in the pharmaceutical industry, guiding the direction to ensure high-quality, safe and effective drugs.