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Postion:Product Catalog >Loxoprofen Impurity 80
Loxoprofen Impurity 80
  • Loxoprofen Impurity 80
  • Loxoprofen Impurity 80
  • Loxoprofen Impurity 80
  • Loxoprofen Impurity 80
  • Loxoprofen Impurity 80

Loxoprofen Impurity 80 NEW

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

Product Details

Product Name: Loxoprofen Impurity 80 CAS No.: 57964-61-1
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/07/31

Loxoprofen Impurity 57964-61-1
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WhatsAPP: +86 17320513646
E-mail: anna@molcoo.com






Loxoprofen, a prodrug-type nonsteroidal anti-inflammatory drug (NSAID), exerts analgesic, anti-inflammatory, and antipyretic effects via metabolic conversion to its active trans-OH form. In pharmaceutical R&D and quality control, impurity reference standards are critical for ensuring drug safety and efficacy. This documentation provides high-purity Loxoprofen impurity reference standards, covering major degradation products and process-related impurities (e.g., Impurity A, B, C), suitable for forced degradation studies, analytical method validation, and ICH Q3A/Q3B compliance.

Technical Specifications


ParameterDetails
Purity≥98.0% (HPLC area normalization), single impurity ≤0.1%
Structural Confirmation¹H-NMR, ¹³C-NMR, MS, and HPLC spectra provided for structural elucidation
Packaging10mg/vial (customizable to 25mg, 50mg)
StabilityInert gas packaging, stored at -20°C (dark), shelf life ≥3 years
ComplianceAligned with ChP, USP, EP pharmacopoeias; includes CoA and DSC support


Applications

  1. Forced Degradation Studies: Simulate degradation under light, heat, and acid/base conditions to establish impurity profiles.

  2. Method Validation: Support HPLC/UPLC method development for specificity, linearity, and LOQ/LOD studies.

  3. Genotoxic Impurity Screening: Assess mutagenic potential per ICH M7 guidelines.

  4. Drug Metabolism Research: Track metabolic pathways of Loxoprofen in vivo.

Representative Impurities


Impurity CodeChemical NameCAS No.Molecular FormulaMolecular WeightKey Properties
Impurity ALoxoprofen Acid (Active Metabolite)68767-14-6C₁₅H₁₈O₃246.30Trans-OH configuration, core anti-inflammatory structure
Impurity BLoxoprofen Ethyl Ester (Process Impurity)81623-55-0C₁₇H₂₂O₄290.35Prodrug ester, less stable than parent drug
Impurity CLoxoprofen Epoxide (Degradation Impurity)112853-53-5C₁₅H₁₆O₃244.28Potential genotoxic impurity, strict control required
Impurity DLoxoprofen Amide (Synthetic Intermediate)157293-95-3C₁₄H₁₇NO₂231.29Used for synthetic route optimization


Quality Assurance

  • Full Traceability: Multi-step QC (ID, LC-MS, KF) for each batch.

  • Spectral Library: Electronic spectra package with retention time and peak annotations.

  • Custom Synthesis: Isotope-labeled (e.g., ¹³C, D₃) or positional isomers available upon request.

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    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! 



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