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Postion:Product Catalog >Lobeline Impurity 14
Lobeline Impurity 14
  • Lobeline Impurity 14
  • Lobeline Impurity 14
  • Lobeline Impurity 14
  • Lobeline Impurity 14
  • Lobeline Impurity 14

Lobeline Impurity 14 NEW

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Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-07-01

Product Details

Product Name: Lobeline Impurity 14 CAS No.: 950194-40-8
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/07/01
Molecular formula: C??H??NO?

Lobeline Impurity 14;950194-40-8

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WhatsAPP: +86 17386083646
E-mail: anna@molcoo.com


  • Product Information

  • Product Number: L045014

  • English Name: Lobeline Impurity 14

  • English Alias: (S)-2-((2S,6R)-1-methyl-6-(2-oxo-2-phenylethyl)piperidin-2-yl)-1-phenylethyl propionate

  • CAS Number: 950194-40-8

  • Molecular Formula: C??H??NO?

  • Molecular Weight: 393.52

  • Advantages

  • As a key impurity of lobeline, the research on Lobeline Impurity 14 offers significant advantages. It helps to analyze the root causes of impurity generation during esterification, substitution, and other reaction steps in lobeline synthesis, optimizing the process to precisely control the formation of this impurity. As a reference standard with ester, piperidine, and benzene ring structures, it provides a reliable basis for detecting impurities with complex structures in drugs, improving the accuracy of impurity quantification. Additionally, it aids in exploring how its structure impacts drug stability, activity, and toxicological properties, laying a scientific foundation for formulating impurity control strategies.

  • Applications

  • It is mainly applied in the research, development, and quality control of lobeline-related drugs. In the R & D stage, as an impurity reference standard, it assists researchers in accurately identifying and quantifying Lobeline Impurity 14 in drugs, strictly evaluating the purity of active pharmaceutical ingredients and formulations. During the quality control process, it serves as a standard substance to validate the sensitivity and reliability of detection methods such as HPLC and LC - MS, ensuring that the content of this impurity throughout the production process meets pharmacopoeia standards. It also provides strong support for the improvement of drug quality standards.

  • Background Description

  • Lobeline is an important respiratory center stimulant, commonly used in the treatment of neonatal asphyxia, carbon monoxide poisoning, and other conditions. Due to its complex molecular structure, various impurities are likely to be generated during synthesis, affected by factors such as reaction conditions and raw material purity. Lobeline Impurity 14, as an impurity with a unique structure, its content directly affects drug quality and safety. With the increasing requirements for drug quality in the pharmaceutical industry, the study of this impurity has become a crucial part of the lobeline quality control system.

  • Research Status

  • Currently, research on Lobeline Impurity 14 is carried out in multiple aspects. In terms of synthesis, researchers are committed to developing efficient, stable, and high-purity synthesis routes to obtain sufficient impurities for subsequent studies. In detection technologies, advanced methods such as ultra-high-performance liquid chromatography-tandem mass spectrometry (UPLC - MS/MS) are continuously being explored to improve the sensitivity and resolution of impurity detection. In toxicological research, animal experiments and in vitro cell experiments are used to deeply evaluate the potential toxicity and action mechanisms of this impurity. At the same time, studies on its formation mechanisms and control strategies during lobeline production are also being continuously and deeply advanced, aiming to reduce impurity content from the source and ensure drug quality and safety

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



Company Profile Introduction

1. Drug standards and drug impurity reference substances: provide more than 20,000 kinds of spot impurity reference substances, with sufficient supply and same-day delivery. We have a professional R&D team and comprehensive quality control testing to ensure product quality and reliability. 2. Customized synthesis of impurities and new molecules: Quickly respond to the customized needs of CDE impurities, stably supply impurities that have established quality standards, and provide customized synthesis services for new compounds in the research and development of innovative drugs. 3. Preparation and separation of unknown impurities: With a professional impurity preparation and separation technical team and SFC preparation and separation instruments, we can solve the problems of impurity preparation in complex projects. 4. Process development of new drug intermediates: provide the supply of new drugs and new molecular impurities, process optimization services, as well as the screening and impurity analysis of commercialization routes. 5. Peptide synthesis: Provide customized peptide synthesis services, and cover all kinds of degradation impurities and process impurities generated in the research and development of peptide drugs. At the same time, it provides comprehensive structural confirmation data and customized testing services.

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