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Postion:Product Catalog >Ibrutinib Impurity 64
Ibrutinib Impurity 64
  • Ibrutinib Impurity 64
  • Ibrutinib Impurity 64
  • Ibrutinib Impurity 64
  • Ibrutinib Impurity 64
  • Ibrutinib Impurity 64

Ibrutinib Impurity 64 NEW

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

Product Details

Product Name: Ibrutinib Impurity 64 CAS No.: 2213398-77-5
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/07/01
Molecular formula: C21H21N5O

Ibrutinib Impurity 64;2213398-77-5

Article illustration

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

  • Product Information

  • Product No.:I021064

  • English Name:Ibrutinib Impurity 64

  • English Alias:1-butyl-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

  • CAS No.:2213398-77-5

  • Molecular Formula:C??H??N?O

  • Molecular Weight:359.42

  • Advantages

  • As an impurity reference standard for Ibrutinib, it features high purity and structural confirmation, which is applicable for the qualitative and quantitative analysis of impurities in drug research and development, as well as quality control, ensuring the safety and effectiveness of pharmaceuticals.
  • Applications

  • Mainly used in the research and development of Ibrutinib-related drugs, quality control during production (such as impurity limit detection and analytical method validation), and can also be applied to the study of drug stability and identification of degradation products.
  • Background Description

  • Ibrutinib is a Bruton's tyrosine kinase (BTK) inhibitor widely used in the treatment of B-cell malignancies (such as chronic lymphocytic leukemia, mantle cell lymphoma, etc.). In drug research, development, and production, the control of impurities is a key link to ensure drug quality. Therefore, the research and application of Ibrutinib impurity reference standards are of great significance for drug quality evaluation.
  • Research Status

  • At present, studies on Ibrutinib impurities mainly focus on the synthesis, structural characterization of impurities, and their impact on drug safety. As a specific impurity, Ibrutinib Impurity 64 has become an important part of drug quality research in terms of its preparation method and residual control in drugs. Relevant researches aim to further improve the quality standards and production processes of Ibrutinib

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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