Chloroprocaine Impurity NEW

Chloroprocaine Impurity 

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

• Product Information

• Product Number: C081015

• English Name: Chloroprocaine Impurity 15

• English Alias: 2 - chloro - 4 - ((3 - chloro - 4 - ((2 - (diethylamino)ethoxy)carbonyl)phenyl)diazenyl)benzoic acid

• CAS Number: None

• Molecular Formula: C20H21Cl2N3O4

• Molecular Weight: 438.30

• Advantages: As a reference standard for Chloroprocaine Impurity 15, it has a clear and precise chemical structure, and has undergone strict purity testing and quality control, with good stability, which can maintain stable properties under different environmental conditions for a long time. It can provide a reliable reference standard for the quality inspection of Chloroprocaine-related products, ensure the accuracy and repeatability of impurity analysis results, and help researchers and pharmaceutical companies effectively control drug quality.

• Applications: It is mainly used in the quality research, impurity analysis, and quality control of Chloroprocaine 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). In the research and development process of Chloroprocaine, it is used to study the source and formation mechanism of impurities, and optimize the synthesis process to reduce impurity generation. In the production process, it is used to monitor the content of this impurity 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 Chloroprocaine drugs during storage and transportation, providing support for the stability research of drugs.

• Background Description: Chloroprocaine is a commonly used local anesthetic widely applied in the field of clinical anesthesia. In its production and research and development process, the presence of impurities may affect the safety, effectiveness, and stability of the drug. To ensure the safety of patients' medication and drug quality, it is crucial to conduct strict research and control on the impurities in Chloroprocaine. As one of the impurities of Chloroprocaine, in-depth research on Chloroprocaine Impurity 15 helps to improve the quality standards of Chloroprocaine, enhance drug quality, and meet the requirements of drug regulatory authorities.

• Research Status: Currently, the research on Chloroprocaine Impurity 15 mainly focuses on the optimization and improvement of impurity analysis methods, aiming to improve the sensitivity and accuracy of detection 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 Chloroprocaine, and reducing impurity generation by improving process conditions. In addition, the research on the potential impact of this impurity on the performance and safety of Chloroprocaine drugs is also gradually underway, aiming to provide a more comprehensive scientific basis for the overall evaluation of Chloroprocaine quality.

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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!