Levofloxacin Impurity(Hydrochloride) NEW

Levofloxacin Impurity A(Hydrochloride)

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

Product Information

• Product Information

• Product Number: L004001A

• English Name: Levofloxacin Impurity A(Hydrochloride)

• English Alias: (S)-9-fluoro-3-methyl-7-oxo-10-(piperazin-1-yl)-3,7-dihydro-2H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid hydrochloride

• CAS Number: 2254176-11-7

• Molecular Formula: C17H18FN3O4.HCl

• Molecular Weight: 383.8

• Advantages: As a reference standard for Levofloxacin Impurity A (hydrochloride), it has a clear chemical structure and has undergone strict purity testing and quality control, with good stability and uniformity. In drug quality testing, it can serve as a reliable reference substance, ensuring the accuracy and repeatability of impurity detection results for levofloxacin bulk drugs and formulations, providing strong support for quality control in the drug research and production process, and meeting the strict requirements of drug regulation.

• Applications: It is mainly used in the quality research, impurity analysis, and quality control of levofloxacin bulk drugs and formulations. It can be used to establish and validate impurity detection methods such as high-performance liquid chromatography (HPLC) and liquid chromatography - mass spectrometry (LC - MS). During the research and development of levofloxacin, 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 A (hydrochloride) in products in real time to ensure that drug quality meets relevant standards and regulatory requirements. It can also be used to evaluate the changes of impurities in levofloxacin drugs during storage and transportation, providing data support for drug stability research.

• Background Description: Levofloxacin is a widely used quinolone antibiotic that plays an important role in clinical anti-infective treatment. In the process of its production and research and development, the presence of impurities may affect the safety, effectiveness, and stability of the drug. To ensure the safety of patients' medication and meet the requirements of drug regulation, strict research and precise control of impurities in levofloxacin are essential. As one of the impurities of levofloxacin, in-depth research on Levofloxacin Impurity A(Hydrochloride) helps to improve the quality standard system of levofloxacin and enhance drug quality.

• Research Status: Currently, the research on Levofloxacin Impurity A(Hydrochloride) 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 actively exploring the source and change rules of this impurity during the synthesis and storage of levofloxacin, 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 levofloxacin drugs is also gradually underway, aiming to provide a more comprehensive scientific basis for the overall evaluation of levofloxacin 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!