Amoxicillin EP Impurity I

Amoxicillin EP Impurity I is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard in quality control testing of Amoxicillin drug formulations. It is also used in research and development of new drugs, and in the development of analytical methods for the detection and quantification of Amoxicillin and its related compounds. Chemically, Amoxicillin EP Impurity I is a degradation product of Amoxicillin, which is an antibiotic in the penicillin group of drugs. It is a white to off-white powder that is soluble in water and ethanol. The chemical name of Amoxicillin EP Impurity I is (2S,5R,6R)-6-{[(2R)-2-Amino-2-(4-hydroxyphenyl)acetyl]amino}-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid. Amoxicillin EP Impurity I is used as a reference standard in the analysis of Amoxicillin drug formulations for purity, stability, and quality. It is also used in the development of analytical methods for the detection and quantification of Amoxicillin and its related compounds. The use of this reference standard ensures the accuracy and reliability of the analytical results obtained during quality control testing. In conclusion, Amoxicillin EP Impurity I is a vital chemical compound in the pharmaceutical industry, and its usage in quality control testing of Amoxicillin drug formulations plays a significant role in ensuring the safety and efficacy of the drug.