Cefixime EP Impurity C

Cefixime EP Impurity C is a chemical compound that is often used in the pharmaceutical industry as a reference standard for quality control purposes. It is a synthetic intermediate in the production of Cefixime, a third-generation cephalosporin antibiotic that is commonly used to treat bacterial infections such as pneumonia, bronchitis, and urinary tract infections. Chemically, Cefixime EP Impurity C is also known as 7-[2-(2-amino-1,3-thiazol-4-yl)-2-(carboxymethoxyimino)acetamido]-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid. This complex chemical structure contributes to its unique properties, including its ability to act as a reference standard for the identification and quantification of impurities in cefixime formulations. The usage of Cefixime EP Impurity C is not limited to quality control applications. It can also be used in research settings to investigate the mechanisms of action of cefixime and other cephalosporin antibiotics. Additionally, it can be used as a starting material for the synthesis of other bioactive compounds. In terms of safety, Cefixime EP Impurity C should be handled with care and stored in a cool, dry place away from heat and moisture. It is important to follow all relevant safety guidelines and regulations when working with this compound to ensure the safety of laboratory workers and the environment.