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SCOPE Pharmachem plus LLP

Scope Pharmachem Plus LLP is a reliable contract research organization (CRO) specialized in the custom synthesis of pharmacopeial & non-pharmacopeial reference standards, working standards, drug metabolites, glucuronides, and nitrosamine impurities for global pharmaceutical quality assurance.

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Azelastine EP Impurity C (CAS 53242-76-5) | Scope Pharmachem Reference Standards
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Home/Pharmaceutical Reference Standards/Pharmaceutical Reference Standards/Azelastine EP Impurity C

Azelastine EP Impurity C

Azelastine EP Impurity C
CAT No:CL-A043004
CAS No:53242-76-5
Mol. F:C15H11ClO3
Mol. Wt.:274.7
Chemical Name:2-[2-(4-Chlorophenyl)acetyl]benzoic acid (as per EP) ; 2-[2-(4-Chlorophenyl)acetyl]benzoic acid (as per USP)
Purity:>99.0%
SMILES:O=C(CC1=CC=C(Cl)C=C1)C2=CC=CC=C2C(O)=O
Inventory Status:In Stock
Storage Conditions:Store at 2°C - 8°C
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Origin: India • Standard Dossier Available

This impurity is related to Azelastine EP Impurity C and is provided with comprehensive characterization data in accordance with international regulatory guidelines.

Suitable for analytical method development (AMD), analytical method validation (AMV), Quality Control (QC) release testing, Abbreviated New Drug Applications (ANDA), DMF filing, and commercial production batch release.

Standard Analytical Dossier Included:
  • Certified Certificate of Analysis (COA) with quantitative purity determination
  • High-Performance Liquid Chromatography (HPLC) chromatogram
  • Proton Nuclear Magnetic Resonance (1H-NMR) spectral confirmation
  • Mass Spectrometry (MS) molecular confirmation

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