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Postion:Product Catalog >Olopatadine Methyl Ester
Olopatadine Methyl Ester
  • Olopatadine Methyl Ester
  • Olopatadine Methyl Ester
  • Olopatadine Methyl Ester
  • Olopatadine Methyl Ester
  • Olopatadine Methyl Ester

Olopatadine Methyl Ester NEW

Price Get Latest Price
Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-07-31

Product Details

Product Name: Olopatadine Methyl Ester CAS No.: 113805-71-3
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/07/31

Olopatadine Methyl Ester; 113805-71-3

Article illustration


  • Product Information

  • Product No.:O021023

  • English Name:Olopatadine Methyl Ester

  • English Alias:(Z)-methyl 11-(3-(dimethylamino)propylidene)-6,11-dihydrodibenzo[b,e]oxepine-2-carboxylate

  • CAS No.:113805-71-3

  • Molecular Formula:C₂₁H₂₃NO₃

  • Molecular Weight:337.41

  • Advantages

  • High Purity:As an intermediate or impurity reference standard for pharmaceuticals, it features a well-defined chemical structure and stable physicochemical properties, meeting the requirements for high-purity standards in drug research, development, and quality control.

  • Structural Specificity:Its specific methyl ester structure makes it a key intermediate in synthetic pathways, enabling the preparation of target compounds or traceability analysis of impurities.

  • Applications

  • Drug Development:Serves as an important intermediate in the synthesis of Olopatadine, contributing to the construction of the target molecule and optimization of the synthesis process.

  • Quality Control:Acts as an impurity reference standard for quality research on Olopatadine and its formulations, such as qualitative and quantitative analysis of impurities and methodological validation.

  • Background Description

  • Olopatadine is a potent H1 receptor antagonist with mast cell stabilizing effects, clinically used for treating allergic rhinitis, urticaria, and other diseases. Its synthesis involves the preparation of ester intermediates. As a methyl ester derivative, Olopatadine Methyl Ester is a key precursor for synthesizing Olopatadine or its analogs. The structural design of this compound is closely related to the pharmacophore of Olopatadine, and studies on its synthesis and properties are of great significance for optimizing drug production processes.
  • Research Status

  • Current research on Olopatadine Methyl Ester mainly focuses on the field of drug synthesis. It is commonly reported as an intermediate for preparing Olopatadine and related derivatives in literature. Some studies focus on optimizing its synthesis methods (such as improving yield and reducing side reactions) and its application in impurity control. Additionally, in the field of pharmaceutical analysis, this compound is used as a reference standard for establishing analytical methods (e.g., HPLC, MS) to ensure the quality and safety of Olopatadine formulations.
  • 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! 




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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