AMO Pharmaceutical Standards Ltd. is an independent service company specializing in customized synthesis of drug reference standards for biomedical and pharmaceutical research. We provide reference standards for our customer base within our scope, including major biotechnology companies, pharmaceutical and diagnostic companies, clinical and various other research institutions.
Our company specializes in supplying drug impurity standard reference materials and provides customized impurity services. Please feel free to inquire and place an order.
158-128-17678 Manager Chen
Product Name: * Impurities
English name: Salbutamol EP Impurity
*Impurity A

*Impurity B

*Impurity C

*Impurity D

*Impurity E

*Impurity F

*Impurity G

*Impurity H

*Impurity I

*Impurity J

*Impurity K

*Impurity M

*Impurity N

Drug impurities
Impurity "refers to the synthetic impurity standards and known metabolites that have been re synthesized into high-purity raw materials, and provide complete analytical data to accurately identify and quantify foreign molecules that may be present in the drug. Impurities in active pharmaceutical ingredients (APIs) can significantly alter the properties of drugs, and the importance of impurity reference materials has become clear during the registration process. Accurate identification and quantification of impurities during the registration process are essential for document preparation. The more than 800 impurity reference standards we have collected come from over 300 types of active pharmaceutical ingredients, and after 10 years of development, they serve the pharmaceutical industry.