Loratadine Impurity NEW

Loratadine Impurity

• Product Number: L019055
• English Name: Loratadine Impurity 55
• English Alias: 5-(3-chlorophenethyl)picolinonitrile
• CAS Number: 31255-58-0
• Molecular Formula: C14H11ClN2
• Molecular Weight: 242.70
• Advantages: Loratadine Impurity 55 is synthesized using advanced technologies and strict purification processes, ensuring extremely high purity and excellent stability. Through precise analytical methods such as nuclear magnetic resonance (NMR) and high-resolution mass spectrometry (HRMS), comprehensive structural identification and accurate content determination are carried out on the product, guaranteeing an accurate chemical structure and uniform, stable composition. It can provide a reliable and precise reference substance for drug research, development, and quality testing, effectively reducing experimental errors and significantly enhancing the accuracy and credibility of data.
• Applications: It is mainly applied to the fields of impurity research, quality analysis, and control of Loratadine drugs. In the drug research and development stage, it can be used to accurately determine the content of this impurity in drugs and deeply evaluate its potential impact on drug safety and effectiveness. During the quality control of pharmaceutical production, as a key reference substance, it can accurately detect the presence of impurities in products, helping enterprises strictly control drug quality and ensure compliance with relevant domestic and international regulations and quality standards. In addition, it also plays an important role in drug stability research and the exploration of drug metabolism pathways.
• Background Description: With the continuous improvement of requirements for drug quality and safety in the pharmaceutical industry, the research on drug impurities has become a core part of ensuring drug quality. As an important drug widely used in anti-allergy treatment, the control of impurities in Loratadine is directly related to patient medication safety and treatment effects. Loratadine Impurity 55, as one of the possible impurities in the drug, in-depth research on its properties, sources, and impacts on the drug is the key to improving the drug quality control system and enhancing drug quality, which helps to reduce medication risks and protect patient health.
• Research Status: Currently, research on Loratadine Impurity 55 is continuously deepening. Researchers are actively exploring more sensitive and efficient detection technologies, such as ultra-high performance liquid chromatography - tandem mass spectrometry (UPLC - MS/MS) technology and high-resolution gas chromatography - mass spectrometry (HRGC - MS) technology, to achieve trace detection and precise quantification of this impurity. Meanwhile, studies on its generation mechanism during drug synthesis, its interaction mechanism with drug active ingredients, as well as its impact on drug stability and efficacy, are also actively being carried out, aiming to provide more comprehensive and scientific theoretical basis and technical support for the research, development, production, and quality control of Loratadine drugs.

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

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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!