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Postion:Product Catalog >Testosterone EP Impurity H
Testosterone EP Impurity H
  • Testosterone EP Impurity H
  • Testosterone EP Impurity H
  • Testosterone EP Impurity H
  • Testosterone EP Impurity H
  • Testosterone EP Impurity H

Testosterone EP Impurity H NEW

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Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-07-31

Product Details

Product Name: Testosterone EP Impurity H CAS No.: 162890-98-4
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/07/31
Molecular formula: C33H54O4

Testosterone EP Impurity H;162890-98-4

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

  • Product Number: T109002
    English Name: Testosterone Enantate EP Impurity H
    English Alias: (3S,8R,9S,10R,13S,14S,17S)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,17-diyl diheptanoate
    CAS Number: 162890-98-4
    Molecular Formula: C33H54O4
    Molecular Weight: 514.78

  • Product Advantages: Testosterone Enantate EP Impurity H has high purity and good chemical stability. As a reference substance, its structure is precise and its properties are uniform. It can maintain stable characteristics under different experimental environments and storage conditions, ensuring the accuracy and consistency of pharmaceutical impurity detection results, and providing a reliable basis for the quality research and quality control of testosterone enantate - based drugs.
    Application Fields: It is mainly applied in the quality control and research and development of testosterone enantate - related drugs. As an impurity reference standard, it is used to establish and validate the detection methods of impurities in testosterone enantate - based drugs, ensuring the sensitivity and accuracy of detection methods. During the drug production process, it is used to monitor the impurity content, assist in optimizing the production process, and prevent excessive impurities from affecting drug quality. In the study of drug stability, it analyzes the changes of this impurity during storage, providing key references for determining the shelf life and storage conditions of drugs.
    Background Description: Testosterone enantate is a synthetic androgen commonly used in the treatment of male hypogonadism and other diseases, and is widely used in clinical treatment. In the process of drug research and development, production and quality control, impurity research is of great significance. Impurities may affect the safety and effectiveness of drugs. As a related impurity of testosterone enantate, in - depth research on Testosterone Enantate EP Impurity H helps to comprehensively evaluate drug quality and ensure the safety of patients' medication and treatment effects.
    Research Status: Currently, research on Testosterone Enantate EP Impurity H continues to deepen. In terms of detection technology, advanced technologies 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 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 testosterone enantate drugs and its impact on drug efficacy and safety is also gradually carried out, aiming to improve the comprehensive understanding of the quality of testosterone enantate - 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


NEW IN STOCK!

The Molcoo Laboratory added drug impurity reference standards, including Baricitinib, Piperazine, Benzylpenicillin, Tranilast and multiple N-Nitroso drug impurities! Now available for immediate delivery! 





Company Profile Introduction

1. Drug standards and drug impurity reference substances: provide more than 20,000 kinds of spot impurity reference substances, with sufficient supply and same-day delivery. We have a professional R&D team and comprehensive quality control testing to ensure product quality and reliability. 2. Customized synthesis of impurities and new molecules: Quickly respond to the customized needs of CDE impurities, stably supply impurities that have established quality standards, and provide customized synthesis services for new compounds in the research and development of innovative drugs. 3. Preparation and separation of unknown impurities: With a professional impurity preparation and separation technical team and SFC preparation and separation instruments, we can solve the problems of impurity preparation in complex projects. 4. Process development of new drug intermediates: provide the supply of new drugs and new molecular impurities, process optimization services, as well as the screening and impurity analysis of commercialization routes. 5. Peptide synthesis: Provide customized peptide synthesis services, and cover all kinds of degradation impurities and process impurities generated in the research and development of peptide drugs. At the same time, it provides comprehensive structural confirmation data and customized testing services.

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