*The following content is generated by AI and is for reference only.
<h3>Overview</h3>
<p>Ozagrel Impurity 13 is a critical reference standard used in the quality control of the antiplatelet agent Ozagrel. It serves as an identification and quantification tool for process-related impurities during pharmaceutical manufacturing. The molecular formula is C<sub>17</sub>H<sub>15</sub>NO<sub>2</sub>, with CAS No. 147696-89-7.</p>
<h3>Application</h3>
<ul>
<li><strong>Pharmaceutical QC:</strong> Used for HPLC method validation to ensure product purity.</li>
<li><strong>R&D:</strong> Serves as a structural analog in degradation studies and stability testing.</li>
<li><strong>Regulatory Compliance:</strong> Supports ICH guidelines for impurity profiling in drug registration.</li>
</ul>
<h3>Precautions</h3>
<p>Store at -20°C in a dry, inert atmosphere to prevent hydrolysis. Handle with appropriate PPE; avoid direct contact as it may cause skin irritation. Not intended for clinical administration or therapeutic use.</p>