Methylprednisolone Acetate EP Impurity G;1625-11-2
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E-mail: anna@molcoo.com
Product Number: M038017
English Name: Methylprednisolone Acetate EP Impurity G
English Alias: 2-((6S,8S,9S,10R,11S,13S,14S,17R)-11,17-dihydroxy-6,10,13-trimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl acetate
CAS Number: 1625-11-2
Molecular Formula: C24H34O6
Molecular Weight: 418.52
Product Advantages: Methylprednisolone Acetate EP Impurity G has high purity and excellent chemical stability. With a clear structure and uniform properties, it remains stable under different experimental environments and storage conditions. As a reference substance, it can be accurately applied to the impurity analysis of Methylprednisolone Acetate, ensuring that the detection results are highly accurate and repeatable, and providing a reliable foundation for pharmaceutical quality research and quality control.
Application Fields: It is mainly applied in the quality control and research and development of Methylprednisolone Acetate-related drugs. As an impurity reference standard, it is used to establish and validate the detection methods of Methylprednisolone Acetate impurities, ensuring the sensitivity and specificity of detection methods. During the drug production process, it monitors the content of this impurity in real - time to assist in optimizing the production process and prevent excessive impurities from affecting drug quality. In the study of drug stability, it analyzes its change rules during storage, providing key basis for determining the shelf life and suitable storage conditions of drugs.
Background Description: Methylprednisolone Acetate is a widely used glucocorticoid drug in clinical practice, often used for anti - inflammatory and immunosuppressive treatments. In its research, development, production and quality control, impurity research is related to drug safety and effectiveness. As a related impurity of Methylprednisolone Acetate, the presence of Methylprednisolone Acetate EP Impurity G may change the pharmacological properties of the drug and cause adverse reactions. Therefore, the study of this impurity is an important part of ensuring drug quality and clinical medication safety.
Research Status: Currently, research on Methylprednisolone Acetate EP Impurity G continues to deepen. In terms of detection technology, researchers are constantly exploring advanced technologies such as Ultra - Performance Liquid Chromatography - Mass Spectrometry (UPLC - MS) and high - resolution mass spectrometry to achieve precise determination of trace impurities. In the study of impurity generation mechanisms, the formation causes and influencing factors are deeply explored by simulating the drug synthesis route and storage environment, providing theoretical support for controlling impurities from the source. At the same time, research on the interaction between this impurity and Methylprednisolone Acetate and its impact on drug efficacy and safety is also gradually advancing, aiming to comprehensively improve the understanding of the quality of Methylprednisolone Acetate drugs.
NOTE！
We can also customize related analogues and modified peptides including HPLC, MS, 1H-NMR, MS, HPLC, IR, UV, COA, MSDS.
This product is intended for laboratory use only!
WhatsAPP: +86 17386083646
E-mail: anna@molcoo.com
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