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	<title>Residual Solvent Testing Archives - Chemetrix</title>
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		<title>Residual Solvent Analysis of Pharmaceutical Products</title>
		<link>https://chemetrix.co.za/residual-solvent-analysis-of-pharmaceutical-products/</link>
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		<dc:creator><![CDATA[Francois]]></dc:creator>
		<pubDate>Wed, 01 Mar 2023 08:59:16 +0000</pubDate>
				<category><![CDATA[Article]]></category>
		<category><![CDATA[Upcoming and New Events]]></category>
		<category><![CDATA[article]]></category>
		<category><![CDATA[Columns]]></category>
		<category><![CDATA[Gas Chromatography]]></category>
		<category><![CDATA[pharma]]></category>
		<category><![CDATA[Pharmaceutical]]></category>
		<category><![CDATA[Residual Solvent Testing]]></category>
		<guid isPermaLink="false">https://chemetrix.co.za/?p=4854</guid>

					<description><![CDATA[Organic solvents constitute a major fraction in the synthesis of pharmaceutical products. The manufacturing process for active pharmaceutical ingredients (APIs) may contribute to residual solvents remaining in the final product. Producers need to monitor and control the levels of residual solvents for several reasons—including safety, effect on crystalline form, solubility, bio-availability, and stability. Therefore, all &#8230; <a href="https://chemetrix.co.za/residual-solvent-analysis-of-pharmaceutical-products/" class="more-link">Continue reading<span class="screen-reader-text"> "Residual Solvent Analysis of Pharmaceutical Products"</span></a>]]></description>
										<content:encoded><![CDATA[<p>Organic solvents constitute a major fraction in the synthesis of pharmaceutical products. The manufacturing process for active pharmaceutical ingredients (APIs) may contribute to residual solvents remaining in the final product. Producers need to monitor and control the levels of residual solvents for several reasons—including safety, effect on crystalline form, solubility, bio-availability, and stability.</p>
<p>Therefore, all products must be tested to assess whether the solvents used during the manufacturing processes are within the accepted limits. Quality assurance laboratories routinely use the United States Pharmacopeia (USP) Method &lt;467&gt;.</p>
<p>&nbsp;</p>
<h3>Procedures for identification and quantification</h3>
<p>The USP &lt;467&gt; monograph specifies the different classes of solvents per their toxicity, sets the concentration limits according to their health hazard, and describes the assay procedure for the solvents. A complete list of all the solvents that may be used in manufacturing processes is not mentioned under these classes. Therefore, the final products should be screened according to the solvents used during their specific manufacturing process.</p>
<p>The method is composed of three analytical procedures for identification and quantification.</p>
<ul>
<li>Procedure A: Identification and limit testing. Uses a G43 phase (624-type column).</li>
<li>Procedure B: Confirms whether or not an identified solvent is above the regulated limits. Uses a G16 phase (WAX-type column).</li>
<li>Procedure C: Quantitative test using a G43 phase or G16 phase, depending on which produced fewer coelutions.</li>
</ul>
<p>&nbsp;</p>
<p><img decoding="async" fetchpriority="high" class="alignnone wp-image-4856" src="https://chemetrix.co.za/wp-content/uploads/2023/03/Screenshot-2023-03-01-at-08.56.43.png" alt="" width="600" height="422" srcset="https://chemetrix.co.za/wp-content/uploads/2023/03/Screenshot-2023-03-01-at-08.56.43.png 992w, https://chemetrix.co.za/wp-content/uploads/2023/03/Screenshot-2023-03-01-at-08.56.43-300x211.png 300w, https://chemetrix.co.za/wp-content/uploads/2023/03/Screenshot-2023-03-01-at-08.56.43-768x540.png 768w" sizes="(max-width: 709px) 85vw, (max-width: 909px) 67vw, (max-width: 984px) 61vw, (max-width: 1362px) 45vw, 600px" /></p>
<p class="p1"><em>USP &lt;467&gt; analytical flowchart for residual solvent analysis.</em></p>
<p>&nbsp;</p>
<h3>Columns for excellent performance</h3>
<p>Agilent J&amp;W DB-Select 624 UI columns have shown excellent performance for residual solvent analysis according to USP &lt;467&gt; Procedure A. Repeatability was generally better than 2.5% RSD for Class 1, Class 2A, and Class 2B solvents. Once a residual solvent was identified above the permitted daily exposure (PDE) limit, Procedure B is performed to confirm analyte identity. The Agilent J&amp;W DB-WAX UI GC column has been successfully used as a confirmation column, because it yields an alternate selectivity compared to that of a G43 column.</p>
<p><img decoding="async" class="alignnone wp-image-4860 size-medium" src="https://chemetrix.co.za/wp-content/uploads/2023/03/JW-300x206.jpg" alt="" width="300" height="206" srcset="https://chemetrix.co.za/wp-content/uploads/2023/03/JW-300x206.jpg 300w, https://chemetrix.co.za/wp-content/uploads/2023/03/JW.jpg 606w" sizes="(max-width: 300px) 85vw, 300px" /></p>
<p><a href="https://chemetrix.co.za/product/gc-columns/"><em>Agilent J&amp;W DB-Select 624 UI columns</em></a></p>
<p>&nbsp;</p>
<h3>Recommended instruments</h3>
<p>For this method, Chemetrix can recommend state-of-the-art analytical instruments. With best-in-class technology and powerful software, the Agilent 7697A headspace sampler is packed with the latest productivity-boosting features.  It&#8217;s unique sampling design allows you to use hydrogen as a carrier gas, delivering optimal chromatography and helping to future-proof your lab.</p>
<p><img decoding="async" class="alignnone wp-image-4862" src="https://chemetrix.co.za/wp-content/uploads/2023/03/8860-7697HCU-1600px_zoom-1024x679.jpg" alt="" width="600" height="398" srcset="https://chemetrix.co.za/wp-content/uploads/2023/03/8860-7697HCU-1600px_zoom-1024x679.jpg 1024w, https://chemetrix.co.za/wp-content/uploads/2023/03/8860-7697HCU-1600px_zoom-300x199.jpg 300w, https://chemetrix.co.za/wp-content/uploads/2023/03/8860-7697HCU-1600px_zoom-768x509.jpg 768w, https://chemetrix.co.za/wp-content/uploads/2023/03/8860-7697HCU-1600px_zoom-1536x1019.jpg 1536w, https://chemetrix.co.za/wp-content/uploads/2023/03/8860-7697HCU-1600px_zoom-1200x796.jpg 1200w, https://chemetrix.co.za/wp-content/uploads/2023/03/8860-7697HCU-1600px_zoom.jpg 1600w" sizes="(max-width: 709px) 85vw, (max-width: 909px) 67vw, (max-width: 984px) 61vw, (max-width: 1362px) 45vw, 600px" /></p>
<p><a href="https://chemetrix.co.za/product/agilent-7697a-headspace/"><em>Agilent 7697A Headspace Sampler</em></a></p>
<p>&nbsp;</p>
<p>Based on the Agilent Intuvo 9000 GC system, Agilent Residual Solvent Analyzers are factory pretested and preconfigured to deliver results, fast, while saving precious startup time. What’s more, their analytical precision exceeds USP method requirements for the three classes of residual solvents. It&#8217;s chemically tested to ensure optimal analysis of class 1 and class 2A/B solvents and labs can begin system calibration and validation immediately following installation.</p>
<p><img decoding="async" class="alignnone wp-image-4864" src="https://chemetrix.co.za/wp-content/uploads/2023/03/5991-8659EN_gc_residual_analysis_brochure_LR_1.jpg" alt="" width="413" height="400" srcset="https://chemetrix.co.za/wp-content/uploads/2023/03/5991-8659EN_gc_residual_analysis_brochure_LR_1.jpg 741w, https://chemetrix.co.za/wp-content/uploads/2023/03/5991-8659EN_gc_residual_analysis_brochure_LR_1-300x290.jpg 300w" sizes="(max-width: 413px) 85vw, 413px" /></p>
<p><a href="https://chemetrix.co.za/product/agilent-intuvo-9000/"><em>Agilent Intuvo 9000 GC</em></a></p>
<p>&nbsp;</p>
<h3>A critical process</h3>
<p>Residual Solvent Analysis is a must in any manufacturing environment where solvents form part of the production process. Because this process is so critical, using the correct instruments suited for the lab requirements can save time and boost accuracy.</p>
<p>&nbsp;</p>
<h3>Quality control at the heart of it all</h3>
<p>At every stage of the quality control process, Chemetrix can assist labs with full end-to-end solutions for your residual solvent analysis. Our team of qualified professionals can share a comprehensive portfolio of solutions, including different instrument models, software and consumables, that work together to provide accurate and reproducible results.</p>
<p>&nbsp;</p>
<h4><a href="https://chemetrix.co.za/analytical-strategies-for-usp-residual-solvents-analysis/">Looking for more information on Residual Solvent Analyis? Watch our webinar &gt;</a></h4>
<p>&nbsp;</p>
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			</item>
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		<title>Analytical Strategies for USP Residual Solvents Analysis</title>
		<link>https://chemetrix.co.za/analytical-strategies-for-usp-residual-solvents-analysis/</link>
					<comments>https://chemetrix.co.za/analytical-strategies-for-usp-residual-solvents-analysis/#respond</comments>
		
		<dc:creator><![CDATA[Francois]]></dc:creator>
		<pubDate>Mon, 27 Feb 2023 15:15:37 +0000</pubDate>
				<category><![CDATA[Upcoming and New Events]]></category>
		<category><![CDATA[Webinar]]></category>
		<category><![CDATA[Analysis]]></category>
		<category><![CDATA[Drugs of abuse]]></category>
		<category><![CDATA[Gas Chromatography]]></category>
		<category><![CDATA[Residual Solvent Testing]]></category>
		<category><![CDATA[webinar]]></category>
		<guid isPermaLink="false">https://chemetrix.co.za/?p=4846</guid>

					<description><![CDATA[In this presentation, we will present the relevant GC/FID and GC/FID/MS based analytical strategies to confidently detect and quantify Class 1, 2, and 3 as well as unknown solvents in drug products. Learn how taking advantage of dual channel configuration and Agilent’s Smart, Connected, and Self-Aware systems can help you successfully meet your requirements for &#8230; <a href="https://chemetrix.co.za/analytical-strategies-for-usp-residual-solvents-analysis/" class="more-link">Continue reading<span class="screen-reader-text"> "Analytical Strategies for USP Residual Solvents Analysis"</span></a>]]></description>
										<content:encoded><![CDATA[<p class="p1">In this presentation, we will present the relevant GC/FID and GC/FID/MS based analytical strategies to confidently detect and quantify Class 1, 2, and 3 as well as unknown solvents in drug products. Learn how taking advantage of dual channel configuration and Agilent’s Smart, Connected, and Self-Aware systems can help you successfully meet your requirements for residual solvent analysis and ensure your testing is right first time and every time.</p>
<p>&nbsp;</p>
<h3>What will you learn</h3>
<ul>
<li>Understand what residual solvent impurities are and why it’s important to characterise and quantify them, even when present in trace amounts</li>
<li>Understand the current regulatory guidelines for residual solvent analysis in drug substance and product</li>
<li>Learn about the approaches for the confident identification and quantification of residual solvents</li>
</ul>
<p>&nbsp;</p>
<h3>Who should attend this webinar</h3>
<ul>
<li>Laboratory managers</li>
<li>Chromatographers</li>
<li>Analytical chemists and scientists</li>
<li>New product developers</li>
<li>Pharma quality control managers</li>
</ul>
<h3></h3>
<p>&nbsp;</p>
<h3 class="section-header js-header data-section-label">Speaker</h3>
<div class="speaker-fields-container">
<div class="section">
<div class="sp-begin">
<h4><strong>Ian Eisele</strong><br />
Applications Chemist,<br />
Gas Phase Separation Division,<br />
Agilent Technologies</h4>
<p>&nbsp;</p>
</div>
<h4><strong>Youjuan Zhang</strong><br />
Applications Chemist,<br />
Gas Phase Separation Division,<br />
Agilent Technologies</h4>
<div class="sp-end">
<p>&nbsp;</p>
</div>
</div>
<h4><a href="https://www.agilent.com/en/training-events/eseminars/residual-solvents">Register and watch on demand &gt;</a></h4>
<p>&nbsp;</p>
</div>
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			</item>
		<item>
		<title>Quality Control &#124; Residual Solvent Testing</title>
		<link>https://chemetrix.co.za/quality-control-residual-solvent-testing/</link>
					<comments>https://chemetrix.co.za/quality-control-residual-solvent-testing/#respond</comments>
		
		<dc:creator><![CDATA[Ryno Swanepoel]]></dc:creator>
		<pubDate>Tue, 27 Jul 2021 12:37:50 +0000</pubDate>
				<category><![CDATA[Solution]]></category>
		<category><![CDATA[Quality Control]]></category>
		<category><![CDATA[Residual Solvent Testing]]></category>
		<guid isPermaLink="false">http://chemetrix.co.za/?p=4067</guid>

					<description><![CDATA[Residual solvent impurities in pharmaceuticals are trace amounts of volatile organic compounds used in drug production that remain in the final drug product. Strict regulations require close monitoring on the presence of residual solvent, as even trace amounts can impact drug safety and efficacy. &#160; Resources Satisfy Requirements for Residual Solvent Analysis Brochure Residual Solvents &#8230; <a href="https://chemetrix.co.za/quality-control-residual-solvent-testing/" class="more-link">Continue reading<span class="screen-reader-text"> "Quality Control &#124; Residual Solvent Testing"</span></a>]]></description>
										<content:encoded><![CDATA[<p>Residual solvent impurities in pharmaceuticals are trace amounts of volatile organic compounds used in drug production that remain in the final drug product. Strict regulations require close monitoring on the presence of residual solvent, as even trace amounts can impact drug safety and efficacy.</p>
<p>&nbsp;</p>
<h2>Resources</h2>
<h4><strong>Satisfy Requirements for Residual Solvent Analysis</strong></h4>
<p><strong><a href="http://chemetrix.co.za/wp-content/uploads/2021/07/5991-8659EN_gc_residual_analysis_brochure_LR-1.pdf" target="_blank" rel="noopener">Brochure</a></strong></p>
<h4><strong>Residual Solvents Analysis Using an Agilent Intuvo 9000 GC with 8697 Headspace Sampler</strong></h4>
<p><strong><a href="http://chemetrix.co.za/wp-content/uploads/2021/07/application-residual-solvents-intuvo-9000-8697-headspace-5994-3075en-agilent.pdf" target="_blank" rel="noopener">Application Note</a></strong></p>
<h4><strong>Analysis of USP Method &lt;467&gt; </strong></h4>
<p><strong><a href="http://chemetrix.co.za/wp-content/uploads/2021/07/application-residual-solvents-8890-GC-5994-0442en-agilent.pdf" target="_blank" rel="noopener">Application Note</a></strong></p>
]]></content:encoded>
					
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		<item>
		<title>Testing Solutions &#124; Residual Solvent Testing</title>
		<link>https://chemetrix.co.za/testing-solutions-residual-solvent-testing/</link>
					<comments>https://chemetrix.co.za/testing-solutions-residual-solvent-testing/#respond</comments>
		
		<dc:creator><![CDATA[Francois]]></dc:creator>
		<pubDate>Mon, 26 Jul 2021 20:01:28 +0000</pubDate>
				<category><![CDATA[Solution]]></category>
		<category><![CDATA[Residual Solvent Testing]]></category>
		<category><![CDATA[Testing solutions]]></category>
		<guid isPermaLink="false">http://chemetrix.co.za/?p=3812</guid>

					<description><![CDATA[Residual solvents are by-products found in processed cannabis. Producers need to incorporate stringent protocols to ensure acceptable levels for their cannabis concentrates, distillates and extracts. Chemetrix can offer testing solutions to help meet regulatory mandates. &#160; Resources Novel Residual Solvents Analysis of Cannabinoid Products with the Agilent Headspace-GC/MS System Application Note]]></description>
										<content:encoded><![CDATA[<p><span data-sheets-value="{&quot;1&quot;:2,&quot;2&quot;:&quot;Residual solvents are by-products found in processed cannabis. Producers need to incorporate stringent protocols to ensure acceptable levels for their cannabis concentrates, distillates and extracts. Chemetrix can offer testing solutions to help meet regulatory mandates.&quot;}" data-sheets-userformat="{&quot;2&quot;:6528,&quot;10&quot;:0,&quot;11&quot;:4,&quot;14&quot;:[null,2,0],&quot;15&quot;:&quot;Arial&quot;}">Residual solvents are by-products found in processed cannabis. Producers need to incorporate stringent protocols to ensure acceptable levels for their cannabis concentrates, distillates and extracts. Chemetrix can offer testing solutions to help meet regulatory mandates.</span></p>
<p>&nbsp;</p>
<h2>Resources</h2>
<h4><strong>Novel Residual Solvents Analysis of Cannabinoid Products with the Agilent Headspace-GC/MS System<br />
</strong></h4>
<p><strong><a href="http://chemetrix.co.za/wp-content/uploads/2021/07/application-cannabis-testing-agilent-headspace-gcms-5994-1926en-agilent.pdf" target="_blank" rel="noopener">Application Note</a></strong></p>
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