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	<title>Products &#8211; ChemiMart</title>
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	<link>https://www.chemimart.de</link>
	<description>Professional expertise in chemical research and preparation of complex organic compounds from Berlin-Adlershof. We do chemistry for you!</description>
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	<title>Products &#8211; ChemiMart</title>
	<link>https://www.chemimart.de</link>
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	<item>
		<title>R27 Dye</title>
		<link>https://www.chemimart.de/product/r27-dye/</link>
		
		<dc:creator><![CDATA[Dr. Patrick Durkin]]></dc:creator>
		<pubDate>Thu, 27 Nov 2025 10:12:35 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=1078</guid>

					<description><![CDATA[R27 is a light stable benzothiazolium/pyridinium-based dye which finds application in the detection of double stranded DNA. This offers a more stable alternative to SYBR Green I and LC Green Plus, displaying almost no degradation of fluorescence after prolonged exposure (over 6 h) at temperatures up to 95 °C when used in a LightCycler® system [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>R27 is a light stable benzothiazolium/pyridinium-based dye which finds application in the detection of double stranded DNA. This offers a more stable alternative to SYBR Green I and LC Green Plus, displaying almost no degradation of fluorescence after prolonged exposure (over 6 h) at temperatures up to 95 °C when used in a LightCycler® system for PCR.</p>
<p>λex 440 nm; λem 483-533 nm (dynamic mode)</p>
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		<title>Cyan 500 NHS Ester</title>
		<link>https://www.chemimart.de/product/cyan500-nhs-ester/</link>
		
		<dc:creator><![CDATA[Dr. Patrick Durkin]]></dc:creator>
		<pubDate>Thu, 25 Jan 2024 11:17:02 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=1038</guid>

					<description><![CDATA[Cyan 500 NHS Ester is a moderately hydrophilic amine-reactive fluorescent marker. This compound is used to label oligonucleotides, peptides, and other biomolecules bearing an amino-functionality, that can be detected when excited at 450 nm. λex 450 nm; λem 495 nm]]></description>
										<content:encoded><![CDATA[<p>Cyan 500 NHS Ester is a moderately hydrophilic amine-reactive fluorescent marker. This compound is used to label oligonucleotides, peptides, and other biomolecules bearing an amino-functionality, that can be detected when excited at 450 nm.</p>
<p>λex 450 nm; λem 495 nm</p>
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		<title>1-Undecanethiol</title>
		<link>https://www.chemimart.de/product/1-undecanethiol/</link>
		
		<dc:creator><![CDATA[Dr. Patrick Durkin]]></dc:creator>
		<pubDate>Tue, 17 May 2022 08:07:20 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=1011</guid>

					<description><![CDATA[1-Undecanethiol can be used to produce hydrophobic self-assembled monolayers, and also reduce non-specific protein adsorption mechanisms. Synonym(s): N-UNDECYL MERCAPTAN;UNDECANETHIOL;undecane-1-thiol;Undecyl mercaptan;1-UNDECANETHIOL;1-UNDECANETHIOL 95+%;1-Mercaptoundecane;1-Undecanethiol,1-UDT, 11-Mercapto-1-undecanol, Undecyl Mercaptan References: Simple and rapid mercury ion selective electrode based on 1-undecanethiol assembled Au substrate and its recognition mechanism. Li et al. Mater. Sci. Eng. C. Mater. Biol. Appl. 2017 Mar 1;72:26-33.]]></description>
										<content:encoded><![CDATA[<div>
<p>1-Undecanethiol can be used to produce hydrophobic self-assembled monolayers, and also reduce non-specific protein adsorption mechanisms.</p>
<div class="MuiTypography-root jss205 MuiTypography-caption"><strong>Synonym(s):</strong></div>
<div class="MuiTypography-root jss206 MuiTypography-body1">N-UNDECYL MERCAPTAN;UNDECANETHIOL;undecane-1-thiol;Undecyl mercaptan;1-UNDECANETHIOL;1-UNDECANETHIOL 95+%;1-Mercaptoundecane;1-Undecanethiol,1-UDT, 11-Mercapto-1-undecanol, Undecyl Mercaptan</div>
</div>
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<div><strong>References:</strong></div>
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<div id="peer-paper-title" class="MuiTypography-root jss343 jss344 MuiTypography-body1" data-testid="peer-paper-title">Simple and rapid mercury ion selective electrode based on 1-undecanethiol assembled Au substrate and its recognition mechanism.</div>
<div class="MuiTypography-root MuiTypography-caption">Li et al. Mater. Sci. Eng. C. Mater. Biol. Appl. 2017 Mar 1;72:26-33.</div>
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		<title>Bis(1-butylpentyl)decane-1,10-diyl diglutarate</title>
		<link>https://www.chemimart.de/product/bis1-butylpentyldecane-110-diyl-diglutarate/</link>
		
		<dc:creator><![CDATA[Dr. Patrick Durkin]]></dc:creator>
		<pubDate>Fri, 25 Mar 2022 10:41:22 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=994</guid>

					<description><![CDATA[Bis(1-butylpentyl)decane-1,10-diyl diglutarate is a neutral ionophore that can be used to prepare sodium optode membranes. These can be used to measure total sodium concentration in human blood plasma. This can also be used as a nitrite-selective membrane electrode, for the determination of NAD(P)H coenzymes. Synonym(s): 5,30-Dibutyl-6,12,23,29-tetraoxatetratriacontane-7,11,24,28-tetrane, ETH 469 References: Ion-selective electrodes and their clinical application [&#8230;]]]></description>
										<content:encoded><![CDATA[<div>
<p>Bis(1-butylpentyl)decane-1,10-diyl diglutarate is a neutral ionophore that can be used to prepare sodium optode membranes. These can be used to measure total sodium concentration in human blood plasma. This can also be used as a nitrite-selective membrane electrode, for the determination of NAD(P)H coenzymes.</p>
<div class="MuiTypography-root jss205 MuiTypography-caption"><strong>Synonym(s):</strong></div>
<div class="MuiTypography-root jss206 MuiTypography-body1">5,30-Dibutyl-6,12,23,29-tetraoxatetratriacontane-7,11,24,28-tetrane, ETH 469</div>
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<div></div>
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<div></div>
<div><strong>References:</strong></div>
<div>
<div class="jss341">
<div class="jss342">
<div id="peer-paper-title" class="MuiTypography-root jss343 jss344 MuiTypography-body1" data-testid="peer-paper-title">Ion-selective electrodes and their clinical application in the continuous ion monitoring.</div>
<div class="MuiTypography-root MuiTypography-caption">W Simon et al. Annals of the New York Academy of Sciences, 428, 279-285 (1984-01-01)</div>
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</div>
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<div id="peer-paper-title" class="MuiTypography-root jss343 jss344 MuiTypography-body1" data-testid="peer-paper-title">Potentiometric Determination of NAD(P)H Coenzymes Using a Nitrite-Selective Membrane Electrode and a Nitrate Reductase Enzyme and the Application to Glucose Assay in Human Serum, Katsu, T., et al. Analytical Sciences, 15, 135-139 (1999)</div>
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		<item>
		<title>Acridine Orange Hydrochloride Salt, extra pure</title>
		<link>https://www.chemimart.de/product/acridine-orange-hydrochloride-salt-extra-pure/</link>
		
		<dc:creator><![CDATA[Dr. Patrick Durkin]]></dc:creator>
		<pubDate>Wed, 12 Jan 2022 09:53:54 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=983</guid>

					<description><![CDATA[Acirdine Orange is a cell permeable staining dye that intercalates with DNA. λex 460  nm; λem 650 nm]]></description>
										<content:encoded><![CDATA[<p>Acirdine Orange is a cell permeable staining dye that intercalates with DNA.</p>
<p>λex 460  nm; λem 650 nm</p>
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		<item>
		<title>Sodium 4-(adamantan-1-ylamino)-4-oxobutane-1-sulfonate</title>
		<link>https://www.chemimart.de/product/sodium-4-adamantan-1-ylamino-4-oxobutane-1-sulfonate/</link>
		
		<dc:creator><![CDATA[mzaug]]></dc:creator>
		<pubDate>Wed, 09 Dec 2020 16:06:47 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=832</guid>

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		<title>2-(2-Cyclooctyn-1-yloxy)acetic acid</title>
		<link>https://www.chemimart.de/product/2-2-cyclooctyn-1-yloxyacetic-acid/</link>
		
		<dc:creator><![CDATA[mzaug]]></dc:creator>
		<pubDate>Wed, 09 Dec 2020 15:47:16 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=810</guid>

					<description><![CDATA[Building block for the strain-promoted copper-free click chemistry ligation techniques. Can be attached to the protein, peptide or small molecule via amide or ester bond. Ref.: 1) Enabling the Multigram Synthesis of (2-Cyclooctyn-1-yloxy)acetic Acid. M. Burk, S. Rothstein, P. Dubé, Org. Process Res. Dev. 2018, 22, 108-110. DOI: 10.1021/acs.oprd.7b00275]]></description>
										<content:encoded><![CDATA[<p>Building block for the strain-promoted copper-free click chemistry ligation techniques. Can be attached to the protein, peptide or small molecule via amide or ester bond.</p>
<p><em>Ref.:</em></p>
<p>1) Enabling the Multigram Synthesis of (2-Cyclooctyn-1-yloxy)acetic Acid.</p>
<p>M. Burk, S. Rothstein, P. Dubé, <em>Org. Process Res. Dev.</em> <strong>2018</strong>, <em>22</em>, 108-110.</p>
<p>DOI: 10.1021/acs.oprd.7b00275</p>
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		<title>endo-BCN-OH</title>
		<link>https://www.chemimart.de/product/endo-bcn-oh/</link>
		
		<dc:creator><![CDATA[mzaug]]></dc:creator>
		<pubDate>Wed, 09 Dec 2020 15:44:25 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=803</guid>

					<description><![CDATA[Other names: (1α,8α,9β)-Bicyclo[6.1.0]non-4-yne-9-methanol. &#160; Building block for the strain-promoted copper-free click chemistry ligation techniques. Can be attached to the protein, peptide or small molecule via ether or ester bond. The hydroxyl functionality can also be used as a leaving group in nucleophilic substitution reactions. &#160; Ref.: 1) Bicyclononynes: New Ring-Strained Alkynes for Bioorthogonal Labeling. J. Dommerholt, S. [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>Other names: (1α,8α,9β)-Bicyclo[6.1.0]non-4-yne-9-methanol.</p>
<p>&nbsp;</p>
<p>Building block for the strain-promoted copper-free click chemistry ligation techniques. Can be attached to the protein, peptide or small molecule via ether or ester bond. The hydroxyl functionality can also be used as a leaving group in nucleophilic substitution reactions.</p>
<p>&nbsp;</p>
<p><em>Ref.:</em></p>
<p>1) Bicyclononynes: New Ring-Strained Alkynes for Bioorthogonal Labeling.</p>
<p>J. Dommerholt, S. Schmidt, R. Temming, L. J. A. Hendriks, F. P. J. T. Rutjes, J. C. M. van Hest, D. J. Lefeber, P. Friedl, F. L. van Delft, <em>Synfacts</em> <strong>2011</strong>, <em>2</em>, 0157-0157.</p>
<p>DOI: 10.1055/s-0030-1259250</p>
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		<title>5,6-Dihydro-11,12-didehydrodibenzo[a,e]cyclo-octen-5-ol</title>
		<link>https://www.chemimart.de/product/56-dihydro-1112-didehydrodibenzoaecyclo-octen-5-ol/</link>
		
		<dc:creator><![CDATA[mzaug]]></dc:creator>
		<pubDate>Wed, 09 Dec 2020 15:42:09 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=796</guid>

					<description><![CDATA[Other name: 3-Hydroxy-1,2:5,6-dibenzocyclooct-7-yne. &#160; Building block for the strain-promoted copper-free click chemistry ligation techniques. Can be attached to the protein, peptide or small molecule via ether or ester bond. &#160; Ref.: 1) The one-pot nonhydrolysis Staudinger reaction and Staudinger or SPAAC ligation. L. Cheng, X. Kang, D. Wang, Y. Gao, L. Yi,  Z. Xi, Org. Biomol. Chem. 2019, 17, [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>Other name: 3-Hydroxy-1,2:5,6-dibenzocyclooct-7-yne.</p>
<p>&nbsp;</p>
<p>Building block for the strain-promoted copper-free click chemistry ligation techniques. Can be attached to the protein, peptide or small molecule via ether or ester bond.</p>
<p>&nbsp;</p>
<p><em>Ref.:</em></p>
<p>1) The one-pot nonhydrolysis Staudinger reaction and Staudinger or SPAAC ligation.</p>
<p>L. Cheng, X. Kang, D. Wang, Y. Gao, L. Yi,  Z. Xi, Org. Biomol. Chem. <strong>2019</strong>, <em>17</em>, 5675-5679.</p>
<p>DOI: 10.1039/C9OB00528E</p>
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		<title>Biotin-PEG-COOH</title>
		<link>https://www.chemimart.de/product/biotin-peg-cooh/</link>
		
		<dc:creator><![CDATA[mzaug]]></dc:creator>
		<pubDate>Wed, 09 Dec 2020 15:37:54 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=790</guid>

					<description><![CDATA[Other names: Biotin-PEG6-COOH. Biotin-PEG6-CO2H. Biotin-PEG6-carboxylic acid. 21-[D-(+)-Biotinylamino]-4,7,10,13,16,19-hexaoxaheneicosanoic acid. &#160; Biotin-PEG-linker with end-carboxylic acid functionalty that is suitable for coupling to variuous amine functionalities, e.g. proteins, peptides or API molecules bearing free amino group. The biotin motif is a popular linker used in biotechnology to conjugate proteins for biochemical assays. Both streptavidin and avidin bind with [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>Other names: Biotin-PEG6-COOH. Biotin-PEG6-CO<sub>2</sub>H. Biotin-PEG6-carboxylic acid. 21-[D-(+)-Biotinylamino]-4,7,10,13,16,19-hexaoxaheneicosanoic acid.</p>
<p>&nbsp;</p>
<p>Biotin-PEG-linker with end-carboxylic acid functionalty that is suitable for coupling to variuous amine functionalities, e.g. proteins, peptides or API molecules bearing free amino group.</p>
<p>The biotin motif is a popular linker used in biotechnology to conjugate proteins for biochemical assays. Both streptavidin and avidin bind with biotin with high affinity and specificity, thus allowing target fishing in biological objects.</p>
<p>&nbsp;</p>
<p><em>Ref.:</em></p>
<p>1) Biotin-conjugated PEGylated porphyrin self-assembled nanoparticles co-targeting mitochondria and lysosomes for advanced chemo-photodynamic combination therapy.</p>
<p>B. Purushothaman, J. Choi, S. Park, J. Lee, A.A. Suganya Samson, S. Honga, J.M. Song, <em>J. Mater. Chem. B</em> <strong>2019</strong>, <em>7</em>, 65-79.</p>
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