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<h3>Overview</h3>
<p><strong>Salbutamol EP Impurity D</strong> (CAS 124670-56-2) is a critical reference standard for the quality control of salbutamol sulfate. Synthesized via specific oxidation pathways, its molecular formula is C<sub>13</sub>H<sub>21</sub>NO<sub>3</sub>. This impurity serves as an essential tool for validating analytical methods in pharmaceutical manufacturing.</p>
<h3>Application</h3>
<ul>
<li><strong>Quality Control:</strong> Used in HPLC and GC assays to detect trace levels during production.</li>
<li><strong>R&D:</strong> Supports stability testing and degradation pathway studies.</li>
<li><strong>Regulatory Compliance:</strong> Ensures adherence to EP and USP purity specifications.</li>
</ul>
<h3>Precautions</h3>
<p>Store at -20°C in airtight containers protected from light. Handle with appropriate PPE to avoid inhalation or skin contact, ensuring strict containment to prevent environmental release.</p>