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Postion:Product Catalog >Iloperidone Impurity 27
Iloperidone Impurity 27
  • Iloperidone Impurity 27
  • Iloperidone Impurity 27
  • Iloperidone Impurity 27

Iloperidone Impurity 27 NEW

Price Get Latest Price
Package 10mg 30mg 100mg
Min. Order: 10mg
Supply Ability: 10000
Update Time: 2025-04-29

Product Details

Product Name: Iloperidone Impurity 27 CAS No.: 84163-64-4
Min. Order: 10mg Purity: 95%+
Supply Ability: 10000 Release date: 2025/04/29
Iloperidone Impurity 84163-64-4
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Product Name: Iloperidone Impurity Reference Standard
CAS No.: Including 133454-47-4 (Iloperidone API), 129938-20-1 (Impurity A), 531524-17-1 (Impurity 13), etc.
Molecular Formula & MW: Varies by impurity type (e.g., C12H13F2NO for HC102-201801, MW 225.23; C24H27FN2O4 for Impurity A, MW 426.4806).
Storage Conditions: 2-8°C (some impurities require -20°C storage).
Purity: ≥95% (some ≥98%).


Product Category: Pharmaceutical Impurity Reference Standard.
Applications: Quality control, stability studies, method development, and regulatory filing for Iloperidone API and formulations.

Key Features

  1. Multiple Specifications: Available in 10mg, 25mg, 50mg, and 100mg packages.

  2. Structural Confirmation: Includes COA, HPLC, NMR, and MS spectra for impurity identification.

  3. Regulatory Compliance: Meets ICH, FDA, and NMPA requirements for drug development.

  4. Custom Synthesis: Tailored impurity production for specific research needs.

Applications

  • Method Development: Validates HPLC and LC-MS methods for impurity separation.

  • Stability Studies: Evaluates degradation products under various conditions.

  • Impurity Profiling: Identifies impurity sources to optimize manufacturing processes.

  • Regulatory Filings: Supports pharmacopeial method validation and impurity limit setting.

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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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