Methylprednisolone Acetate EP Impurity E NEW

Methylprednisolone Acetate EP Impurity E;52-21-1

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E-mail: anna@molcoo.com

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• Product Number: M038016
  English Name: Methylprednisolone Acetate EP Impurity E
  English Alias: 2-((8S,9S,10R,11S,13S,17R)-11,17-dihydroxy-10,13-dimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl acetate
  CAS Number: 52-21-1
  Molecular Formula: C₂₃H₃₀O₆
  Molecular Weight: 402.48
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• Product Advantages: Methylprednisolone Acetate EP Impurity E has high purity and good chemical stability. With a clear structure and uniform properties, it remains stable under different experimental conditions and can be used as a reliable reference substance for Methylprednisolone Acetate impurity analysis. Its precise characteristics can ensure the accuracy and repeatability of detection results, providing a solid basis for pharmaceutical quality research and quality control.
  Application Fields: It is mainly applied in the quality control and research and development process 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 is used to monitor the content of this impurity, assist in optimizing the production process, and prevent excessive impurities from affecting drug quality. In the study of drug stability, it analyzes its changes during storage, providing important references for determining the shelf life and storage conditions of drugs.
  Background Description: Methylprednisolone Acetate is a commonly used glucocorticoid drug. In its research, development, production and quality control, impurity research is of great significance. The presence of impurities may affect the safety, effectiveness and stability of drugs. As a related impurity of Methylprednisolone Acetate, in-depth research on Methylprednisolone Acetate EP Impurity E helps to comprehensively evaluate the quality of Methylprednisolone Acetate drugs and ensure the safety and effectiveness of clinical medication.
  Research Status: Currently, research on Methylprednisolone Acetate EP Impurity E continues to advance. In terms of detection technology, advanced methods such as Ultra-Performance Liquid Chromatography-Mass Spectrometry (UPLC-MS) and high-resolution mass spectrometry are constantly being explored to achieve accurate detection of trace impurities. In the study of impurity generation mechanisms, the formation causes and influencing factors are deeply analyzed by simulating drug synthesis reactions and storage environments, 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 carried out, aiming to improve the comprehensive 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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The Molcoo Laboratory added drug impurity reference standards, including Baricitinib, Piperazine, Benzylpenicillin, Tranilast and multiple N-Nitroso drug impurities! Now available for immediate delivery!