Clenbuterol Impurity B(Hydrobromide) NEW

Levofloxacin Impurity A(Hydrochloride)

WhatsAPP: +86 17320513646
E-mail: anna@molcoo.com

Product Information

• Product Information

• Product Number: C062004B

• English Name: Clenbuterol Impurity B(Hydrobromide)

• English Alias: 1-(4-amino-3,5-dichlorophenyl)-2-(tert-butylamino)ethanone hydrobromide

• CAS Number: None

• Molecular Formula: C12H16Cl2N2O.HBr

• Molecular Weight: 356.08

• Advantages: As a reference standard for Clenbuterol Impurity B (hydrobromide), it has a clear chemical structure, and its purity has been strictly verified. It has good stability and can maintain stable properties under different storage conditions. It can be used as a reliable reference substance for the impurity detection of clenbuterol bulk drugs and formulations, ensuring the accuracy and repeatability of detection results. It provides strong support for drug quality control and research and development, meeting the strict requirements of drug regulation for impurity research.

• Applications: It is mainly used in the quality research, impurity analysis, and quality control of clenbuterol bulk drugs and formulations. It is used to establish and validate impurity detection methods such as high-performance liquid chromatography (HPLC) and liquid chromatography - mass spectrometry (LC - MS). In the research and development process of clenbuterol, it is used to study the source and formation mechanism of this impurity, and optimize the synthesis process to reduce impurity generation. In the production process, it is used to monitor the content of Impurity B (hydrobromide) in products to ensure that drug quality meets relevant standards and regulatory requirements. It can also be used to evaluate the changes of impurities in clenbuterol drugs during storage and transportation, providing data support for drug stability research.

• Background Description: Clenbuterol is a β-agonist that was illegally used in animal husbandry to increase the lean meat rate of animals, posing serious risks to human health. In the research, development, and production of clenbuterol drugs, the control of impurities is related to the safety and effectiveness of drugs. As one of the impurities of clenbuterol, in-depth research and strict control of Clenbuterol Impurity B(Hydrobromide) help to improve the quality standard system of clenbuterol, ensure drug quality, and also comply with relevant regulations on drug impurity management, avoiding medication risks caused by impurity problems.

• Research Status: Currently, the research on Clenbuterol Impurity B(Hydrobromide) mainly focuses on the optimization and improvement of impurity analysis methods. By using more advanced detection technologies and instruments, the sensitivity and accuracy of detecting this impurity are improved to achieve precise determination of trace impurities. At the same time, researchers are also exploring the source and change rules of this impurity during the synthesis and storage of clenbuterol, and reducing the generation and accumulation of impurities by improving process conditions and optimizing the storage environment. In addition, the research on the potential impact of this impurity on the performance and safety of clenbuterol drugs is also gradually underway, aiming to provide a more comprehensive scientific basis for the overall evaluation of clenbuterol quality.

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 17320513646
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!