Product Number: E041013
English Name: Ebastine Impurity 13
English Alias: 4-chloro-1-(4-(tert-pentyl)phenyl)butan-1-one
CAS Number: 1974707-25-9
Molecular Formula: C15H21ClO
Molecular Weight: 252.78
Advantages: Ebastine Impurity 13 is synthesized through high-precision processes and strict purification procedures, featuring high purity, strong stability, and good batch consistency. Structural confirmation and content determination are carried out by various analytical methods such as nuclear magnetic resonance (NMR) and high-performance liquid chromatography (HPLC), ensuring accurate chemical structure and uniform composition. It can provide a reliable reference substance for drug research, development, and quality control, effectively ensuring the accuracy and reproducibility of experimental data.
Applications: It is mainly applied to the fields of impurity research, quality analysis, and control of Ebastine drugs. During the drug research and development process, it can be used to determine the content of this impurity in drugs and evaluate its potential impact on drug safety and effectiveness. In the quality control of pharmaceutical production, as a key reference substance, it can accurately detect the presence of impurities in products, helping enterprises ensure that drug quality meets relevant domestic and international regulations and standards. It can also be used for drug degradation pathway research and stability investigation.
Background Description: With the increasingly stringent requirements for drug quality and safety in the pharmaceutical industry, the research on drug impurities has become an important part of ensuring drug safety and efficacy. As a commonly used clinical anti-allergic drug, the control of impurities in Ebastine is directly related to patient medication safety and treatment effects. The study of Ebastine Impurity 13, as one of the possible impurities in the drug, is a key content to improve the drug quality control system and help enhance the overall quality of drugs.
Research Status: Currently, research on Ebastine Impurity 13 is gradually deepening. Researchers are committed to developing more sensitive and efficient detection methods, such as ultra-high performance liquid chromatography-mass spectrometry (UPLC-MS) technology, to achieve trace detection and precise quantification of this impurity. At the same time, studies on its generation mechanism during drug synthesis, its interaction with drug active ingredients, as well as its impact on drug stability and efficacy are also actively carried out, aiming to provide more comprehensive theoretical support and technical guidance for the research, development, production, and quality control of Ebastine drugs.
WhatsAPP: +86 17320513646
E-mail: anna@molcoo.com
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
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