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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: 2025-12-16

Product Details

Product Name: Iloperidone Impurity 27 CAS No.: 84163-64-4
Min. Order: 10mg Purity: 95%+
Supply Ability: 10000 Release date: 2025/12/16
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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