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	<title>Recent Additions &#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>Recent Additions &#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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		<item>
		<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>
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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>
</div>
<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>
<div></div>
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</div>
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<div class="jss342">
<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>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>

					<description><![CDATA[]]></description>
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		<title>Ethyl 2-((tert-butoxycarbonyl)amino)-3,3,3-trifluoro-2-hydroxypropanoate</title>
		<link>https://www.chemimart.de/product/ethyl-2-tert-butoxycarbonylamino-333-trifluoro-2-hydroxypropanoate/</link>
		
		<dc:creator><![CDATA[mzaug]]></dc:creator>
		<pubDate>Tue, 08 Dec 2020 17:26:55 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=453</guid>

					<description><![CDATA[This derivative can be used to synthesize CF3-bearing quaternary amino acids. Ref.: &#160; 1)  Synthesis of α-​(trifluoromethyl)​-​substituted α-​amino acids. 8. New synthetic pathways to 3,​3,​3-​trifluoroalanine, 2-​deutero-​3,​3,​3-​trifluoroalanine and their derivatives Burger, Klaus; Hoess, Eva; Gaa, Karl; Sewald, Norbert; Schierlinger, Christian Zeitschrift fuer Naturforschung, B:  Chemical Sciences, 1991, 46, 361-384 DOI: 10.1515/znb-1991-0316]]></description>
										<content:encoded><![CDATA[<p>This derivative can be used to synthesize CF3-bearing quaternary amino acids.</p>
<p><em>Ref.:</em></p>
<p>&nbsp;</p>
<p>1)  Synthesis of α-​(trifluoromethyl)​-​substituted α-​amino acids. 8. New synthetic pathways to 3,​3,​3-​trifluoroalanine, 2-​deutero-​3,​3,​3-​trifluoroalanine and their derivatives</p>
<p>Burger, Klaus; Hoess, Eva; Gaa, Karl; Sewald, Norbert; Schierlinger, Christian<br />
<em>Zeitschrift fuer Naturforschung, B:  Chemical Sciences</em>, <strong>1991</strong>, <em>46</em>, 361-384<br />
DOI: 10.1515/znb-1991-0316</p>
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		<item>
		<title>Ethyl (E)-2-((tert-butoxycarbonyl)imino)-3,3,3-trifluoropropanoate</title>
		<link>https://www.chemimart.de/product/ethyl-e-2-tert-butoxycarbonylimino-333-trifluoropropanoate/</link>
		
		<dc:creator><![CDATA[mzaug]]></dc:creator>
		<pubDate>Tue, 08 Dec 2020 17:24:58 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=448</guid>

					<description><![CDATA[Trifluoropyruvate ketimine derivative that can be used to synthesize CF3-bearing quaternary amino acids. Ref.: &#160; 1)  Enantioselective Organocatalytic Synthesis of Quaternary α-Amino Acids Bearing a CF3 Moiety Ralph Husmann, Erli Sugiono, Stefanie Mersmann, Gerhard Raabe, Magnus Rueping, and Carsten Bolm Organic Letters, 2011, 13, 1044-1047 DOI: 10.1021/ol103093r]]></description>
										<content:encoded><![CDATA[<p>Trifluoropyruvate ketimine derivative that can be used to synthesize CF3-bearing quaternary amino acids.</p>
<p><em>Ref.:</em></p>
<p>&nbsp;</p>
<p>1)  Enantioselective Organocatalytic Synthesis of Quaternary α-Amino Acids Bearing a CF3 Moiety</p>
<p>Ralph Husmann, Erli Sugiono, Stefanie Mersmann, Gerhard Raabe, Magnus Rueping, and Carsten Bolm<br />
<em>Organic Letters</em>, <strong>2011</strong>, <em>13</em>, 1044-1047<br />
DOI: 10.1021/ol103093r</p>
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