*The following content is generated by AI and is for reference only.
<h3>Overview</h3>
<p><strong>Doxycycline EP Impurity C</strong> is a critical degradation product of Doxycycline used in pharmaceutical quality control. It serves as a reference standard for validating HPLC methods and ensuring compliance with European Pharmacopoeia specifications. The compound features the molecular formula <strong>C22H24N2O8</strong> and carries CAS No. 10592-16-6, synthesized via controlled oxidation pathways during active ingredient manufacturing.</p>
<h3>Application</h3>
<ul>
<li><strong>Quality Assurance:</strong> Used to calibrate analytical instruments for impurity profiling.</li>
<li><strong>Regulatory Compliance:</strong> Essential for batch release testing under ICH guidelines.</li>
<li><strong>R&D Development:</strong> Supports stability-indicating method development studies.</li>
</ul>
<h3>Precautions</h3>
<p>Store at <strong>-20°C</strong> in a dry, dark environment to prevent hydrolysis. Personnel must wear appropriate PPE including gloves and masks due to potential sensitization risks. This material is strictly for laboratory research and cannot be administered clinically.</p>