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Postion:Product Catalog >Indobufen Impurity 71
Indobufen Impurity 71
  • Indobufen Impurity 71
  • Indobufen Impurity 71
  • Indobufen Impurity 71
  • Indobufen Impurity 71
  • Indobufen Impurity 71

Indobufen Impurity 71 NEW

Price Get Latest Price
Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-07-02

Product Details

Product Name: Indobufen Impurity 71 CAS No.: 1461705-59-8
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/07/02
Molecular formula: C12H13NO6

Indobufen Impurity 71;1461705-59-8

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


  • Product Information

  • Product Number: I036071

  • English Name: Indobufen Impurity 71

  • English Alias: 2-ethyl-2-(4-nitrobenzyl)malonic acid

  • CAS Number: 1461705-59-8

  • Molecular Formula: C??H??NO?

  • Molecular Weight: 267.23

  • Advantages

  • As an impurity reference standard for indobufen, this compound has the following advantages:

  • Well-defined structure and high stability, which can be used to analyze the by-product formation mechanism of nitro substitution and alkylation reactions in indobufen synthesis, optimizing processes to control benzyl impurity generation;

  • As a reference standard for polar compounds containing nitro and carboxyl groups, it provides a standard substance for detecting polar impurities in drugs, improving the quantitative accuracy of methods such as HPLC;

  • Helps study the impact of nitro structures on drug stability and toxicological properties (nitro compounds may have potential genotoxicity) to provide a scientific basis for impurity control strategies.

  • Applications

  • Drug Development: Used as an impurity reference standard to identify and quantify Impurity 71 in indobufen preparations, evaluating the purity of APIs and formulations;

  • Quality Control: Acting as a standard substance to validate the sensitivity of detection methods (e.g., HPLC or LC-MS), ensuring the impurity content meets pharmacopoeia requirements during production;

  • Toxicological Research: Assisting in evaluating the potential genotoxicity of nitro impurities to provide dat

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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