Paclitaxel Impurity; 409319-62-6
WhatsAPP: +86 17386083646
E-mail: anna@molcoo.com
Product Number: P027050
English Name: Paclitaxel Impurity 50
English Alias: (2aR,4S,4aR,6R,9S,11S,12S,12aR,12bS)-9-(((2R,3S)-3-benzamido-2-hydroxy-3-phenylpropanoyl)oxy)-12-(benzoyloxy)-4,11-dihydroxy-4a-(hydroxymethyl)-8,13,13-trimethyl-5-oxo-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-1H-7,11-methanocyclodeca[3,4]benzo[1,2-b]oxete-6,12b-diyl diacetate
CAS Number: 409319-62-6
Molecular Formula: C47H51NO15
Molecular Weight: 869.91
Product Advantages: Paclitaxel Impurity 50 has extremely high purity and stable chemical properties. With a clear structure and uniform properties, it remains stable under different experimental conditions and can be used as a reliable reference substance for Paclitaxel impurity analysis. Its precise characteristics ensure the accuracy and repeatability of detection results, providing a solid guarantee for Paclitaxel drug quality research and quality control.
Application Fields: It is mainly applied in the quality control and research and development of Paclitaxel-related drugs. As an impurity reference standard, it is used to establish and validate the detection methods of Paclitaxel impurities, ensuring the sensitivity and specificity of detection methods. During the drug production process, it monitors the content of this impurity, assists in optimizing the production process, and prevents excessive impurities from affecting drug quality. In the study of drug stability, it analyzes its changes during storage, providing important basis for determining the shelf life and storage conditions of drugs.
Background Description: Paclitaxel is an important drug widely used in cancer treatment. During the process of its research, development, production and quality control, impurity research is of great importance. The presence of impurities may affect the safety and effectiveness of drugs. As a related impurity of Paclitaxel, in - depth research on Paclitaxel Impurity 50 helps to comprehensively evaluate the quality of Paclitaxel drugs and ensure the safety of clinical medication and treatment effects.
Research Status: Currently, research on Paclitaxel Impurity 50 continues to advance. In terms of detection technology, advanced methods 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 deeply 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 Paclitaxel and its impact on drug efficacy and safety is also gradually carried out, aiming to improve the comprehensive understanding of the quality of Paclitaxel 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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