*The following content is generated by AI and is for reference only.
<h3>Overview</h3>
<p>Rivaroxaban Impurity 12 is a critical reference standard for the pharmaceutical industry, utilized to monitor synthetic pathways and ensure purity compliance. Its core synthesis involves specific coupling reactions within the anticoagulant production chain. The compound is defined by molecular formula <strong>C28H37ClN4O5S</strong> and CAS number <strong>1496605-33-8</strong>.</p>
<h3>Application</h3>
<ul>
<li><strong>Quality Control:</strong> Used in HPLC analysis to identify and quantify trace impurities in active pharmaceutical ingredients.</li>
<li><strong>R&D Development:</strong> Serves as a structural analog for method validation during drug formulation studies.</li>
<li><strong>Regulatory Compliance:</strong> Essential for generating stability-indicating data required by FDA and EMA guidelines.</li>
</ul>
<h3>Precautions</h3>
<p>Strictly store at -20°C in a desiccated environment to prevent degradation. Handling requires appropriate PPE due to potential sensitization risks. Not intended for direct clinical administration or therapeutic use.</p>