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	<title>Homobifunctional Carboxyl Reactive Monoprotected &#8211; VectorLabs</title>
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	<title>Homobifunctional Carboxyl Reactive Monoprotected &#8211; VectorLabs</title>
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		<title>t-boc-N-EDA</title>
		<link>https://staging.vectorlabs.com/products/t-boc-n-eda/</link>
		
		<dc:creator><![CDATA[Vector Laboratories R&D]]></dc:creator>
		<pubDate>Sat, 24 Feb 2024 02:07:24 +0000</pubDate>
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					<description><![CDATA[<p>t-boc-N-EDA, product number QBD-10226, CAS number 57260-73-8, is the boc-protected form of ethylenediamine. It is not a dPEG® product. However, it can be useful in bioconjugation reactions where an exceptionally short, monoprotected, homobifunctional crosslinker is needed. The free primary amine reacts with activated esters of carboxylic acids (for example, the N-hydroxysuccinimidyl ester, also known as NHS) to form amide bonds. Treatment of the resulting conjugate with acid (for example, TFA) removes the boc protecting group from the protected amine, leaving a primary amine that is free to react.</p>
<h3>Specifications</h3>
<table id="product-attribute-specs-table" class="data table additional-attributes" width="585">
<tbody>
<tr>
<th class="col label" scope="row">Unit Size</th>
<td class="col data" data-th="Unit Size">1000 mg</td>
</tr>
<tr>
<th class="col label" scope="row">Molecular Weight</th>
<td class="col data" data-th="Applications">160.21; single compound</td>
</tr>
<tr>
<th class="col label" scope="row">Chemical formula</th>
<td class="col data chemicalStructure">C₁₅H₃₂N₂O₅</td>
</tr>
<tr>
<th class="col label" scope="row">CAS</th>
<td class="col data" data-th="Target Species">57260-73-8</td>
</tr>
<tr>
<th class="col label" scope="row">Purity</th>
<td class="col data" data-th="Target Species">&#62; 98%</td>
</tr>
<tr>
<th class="col label" scope="row">Spacers</th>
<td class="col data" data-th="Target Species">dPEG® Spacer is 4 atoms and 3.8 Å</td>
</tr>
<tr>
<th class="col label" scope="row">Shipping</th>
<td class="col data" data-th="Target Species">Ambient</td>
</tr>
<tr>
<th class="col label" scope="row">Typical solubility properties (for additional information contact Customer Support)</th>
<td class="col data">Methylene chloride, DMAC or DMSO.</td>
</tr>
<tr>
<th class="col label" scope="row">Storage and handling</th>
<td class="col data">-20°C; Always let come to room temperature before opening; be careful to limit exposure to moisture and restore under an inert atmosphere; stock solutions can be prepared with dry solvent and kept for several days (freeze when not in use). dPEG® pegylation compounds are generally hygroscopic and should be treated as such. This will be less noticeable with liquids, but the solids will become tacky and difficult to manipulate, if care is not taken to minimize air exposure.</td>
</tr>
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<p>The post <a rel="nofollow" href="https://staging.vectorlabs.com/products/t-boc-n-eda/">t-boc-N-EDA</a> appeared first on <a rel="nofollow" href="https://staging.vectorlabs.com">VectorLabs</a>.</p>
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                                                            <h2 class="eael-tab-title title-after-icon" >Description</h2>                                                    </li>
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                                                            <h2 class="eael-tab-title title-after-icon" >Specifications</h2>                                                    </li>
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                                                            <h2 class="eael-tab-title title-after-icon" >Documents</h2>                                                    </li>
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                                                            <h2 class="eael-tab-title title-after-icon" >References</h2>                                                    </li>
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				        <h3>Description</h3><p>t-boc-N-EDA, product number QBD-10226, CAS number 57260-73-8, is the boc-protected form of ethylenediamine. It is not a dPEG® product. However, it can be useful in bioconjugation reactions where an exceptionally short, monoprotected, homobifunctional crosslinker is needed. The free primary amine reacts with activated esters of carboxylic acids (for example, the N-hydroxysuccinimidyl ester, also known as NHS) to form amide bonds. Treatment of the resulting conjugate with acid (for example, TFA) removes the boc protecting group from the protected amine, leaving a primary amine that is free to react.</p>                    </div>
		        
                    <div id="specifications-tab" class="clearfix eael-tab-content-item inactive" data-title-link="specifications-tab">
				        <h3>Specifications</h3><table id="product-attribute-specs-table" class="data table additional-attributes" style="height: 186px;" width="585"><tbody><tr><th class="col label" scope="row">Unit Size</th><td class="col data" data-th="Unit Size">1000 mg</td></tr><tr><th class="col label" scope="row">Molecular Weight</th><td class="col data" data-th="Applications">160.21; single compound</td></tr><tr><th class="col label" scope="row">Chemical formula</th><td class="col data chemicalStructure">C₁₅H₃₂N₂O₅</td></tr><tr><th class="col label" scope="row">CAS</th><td class="col data" data-th="Target Species">57260-73-8</td></tr><tr><th class="col label" scope="row">Purity</th><td class="col data" data-th="Target Species">&gt; 98%</td></tr><tr><th class="col label" scope="row">Spacers</th><td class="col data" data-th="Target Species">dPEG® Spacer is 4 atoms and 3.8 Å</td></tr><tr><th class="col label" scope="row">Shipping</th><td class="col data" data-th="Target Species">Ambient</td></tr><tr><th class="col label" scope="row">Typical solubility properties (for additional information contact Customer Support)</th><td class="col data">Methylene chloride, DMAC or DMSO.</td></tr><tr><th class="col label" scope="row">Storage and handling</th><td class="col data">-20°C; Always let come to room temperature before opening; be careful to limit exposure to moisture and restore under an inert atmosphere; stock solutions can be prepared with dry solvent and kept for several days (freeze when not in use). dPEG® pegylation compounds are generally hygroscopic and should be treated as such. This will be less noticeable with liquids, but the solids will become tacky and difficult to manipulate, if care is not taken to minimize air exposure.</td></tr></tbody></table>                    </div>
		        
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				        <h3>Documents</h3><div class="explorer_section applications container documentSection catalog-product-document"><ul class="document_list"><li class="documentContainer documentItem"><a href="https://staging.vectorlabs.com/productattachments/sds/VL_QBD-10226_sds.pdf" target="_blank" rel="noopener">Safety Data Sheet</a></li><li><a class="woocommerce-print-products-pdf-link" href="https://staging.vectorlabs.com/products/t-boc-n-eda/?print-products=pdf" target="_blank">Datasheet</a></li></ul></div>                    </div>
		        
                    <div id="references-tab" class="clearfix eael-tab-content-item inactive" data-title-link="references-tab">
				        <h3>References</h3><ol><li>Greg T. Hermanson, Bioconjugate Techniques, 3rd Edition, Elsevier, Waltham, MA 02451, 2013, ISBN 978-0-12-382239-0; See Chapter 18, Discrete PEG Reagents, pp. 787-821, for a full overview of the dPEG® products.</li><li>DEVD-NucView 488: a novel class of enzyme substrates for real-time detection of caspase-3 activity in live cells. Hui Cen, Fei Mao, Ida Aronchik, Rholinelle Joy Fuentes, and Gary L. Firestone. The FASEB Journal. 2008, (22), pp 2243-2252. July 2010. DOI: 10.1096/fj.07-099234.</li></ol>                    </div>
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		<p>The post <a rel="nofollow" href="https://staging.vectorlabs.com/products/t-boc-n-eda/">t-boc-N-EDA</a> appeared first on <a rel="nofollow" href="https://staging.vectorlabs.com">VectorLabs</a>.</p>
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