Testosterone EP Impurity L;2398-99-4

WhatsAPP: +86 17386083646
E-mail: anna@molcoo.com

• Product Number: T109001
  English Name: Testosterone EP Impurity L
  English Alias: (8S,10S,13S,14S,17S)-17-hydroxy-10,13-dimethyl-6,7,8,10,12,13,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3(2H)-one
  CAS Number: 2398-99-4
  Molecular Formula: C19H26O2
  Molecular Weight: 286.41
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• Product Advantages: Testosterone EP Impurity L has extremely high purity and good chemical stability. As a reference substance, its structure is clear and its properties are uniform. It can maintain stable characteristics under different experimental conditions, effectively ensuring the accuracy and reliability of pharmaceutical impurity detection results, and providing an accurate reference standard for pharmaceutical quality research and quality control.
  Application Fields: It is mainly applied in the quality control and research and development of testosterone - related drugs. As an impurity reference standard, it is used to establish and validate the detection methods of impurities in testosterone - based drugs, ensuring the sensitivity and specificity of detection methods. During the drug production process, it is used to monitor the impurity content, assist in optimizing the production process, and prevent the impact on drug quality due to excessive impurities. In the study of drug stability, it analyzes the changes of this impurity during storage, providing important basis for determining the shelf life and storage conditions of drugs.
  Background Description: Testosterone is an important steroid hormone that participates in various physiological processes in the human body. Related drugs are widely used in clinical treatment, such as for the treatment of hypogonadism, muscle atrophy and other diseases. During the research, development, production and quality control of testosterone - based drugs, impurity research is of great importance. The presence of impurities may affect the safety and effectiveness of drugs. As a related impurity of testosterone, in - depth research on Testosterone EP Impurity L helps to comprehensively evaluate the quality of testosterone - based drugs and ensure the safety of patients' medication and treatment effects.
  Research Status: Currently, research on Testosterone EP Impurity L continues to advance. In terms of detection technology, more advanced analytical methods are constantly being explored and optimized, such as Ultra - Performance Liquid Chromatography - Mass Spectrometry (UPLC - MS) technology and high - resolution mass spectrometry technology, 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 the drug synthesis process and storage environment, providing theoretical support for controlling impurities from the source. At the same time, research on the interaction between this impurity and testosterone drugs and its impact on drug efficacy and safety is also gradually carried out, aiming to further improve the comprehensive understanding of the quality of testosterone - based 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!