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	<title>AOAO-12 - Revision history</title>
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	<updated>2026-10-18T03:30:00Z</updated>
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	<entry>
		<id>https://eln.excellgen.com/index.php?title=AOAO-12&amp;diff=2160&amp;oldid=prev</id>
		<title>Paul.xu at 17:43, 4 November 2011</title>
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		<updated>2011-11-04T17:43:56Z</updated>

		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;[[Image:Aoao 12.jpg|600px|Aoao 12.jpg]] &lt;br /&gt;
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For real-time PCR &lt;br /&gt;
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The dye (76 mg) was synthesized by using the procedure to make AOAO-2 from 10-(5-carboxypentyl)acridine orange chloride salt (147 mg, 0.35 mmol) and 2,2â² oxybis(ethyl-amine) dihydrochloride (25 mg, 0.14 mmol). &amp;lt;br&amp;gt;&lt;br /&gt;
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Preparation of AOAO-2 (Dye No. 7 of Table 1)&lt;br /&gt;
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Et&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;N (0.15 mL, 1.05 mmol) and TSTU (320 mg, 1.05 mmol) were added to a suspension of 10-(5-carboxypentyl)acridine orange chloride salt (438 mg, 1.03 mmol) in DMF (5 mL) at room temperature. The mixture was stirred at room temperature for 15 minutes, followed by the addition of Et&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;N (0.1 mL) and 3,3â²-diamino-N-methyldipropylamine (50 mg, 0.344 mmol). After the mixture was stirred at room temperature overnight, EtOAc (20 mL) was added to precipitate the product. The crude product was re-dissolved in DMF and precipitated out again with EtOAc. The solid (250 mg) was separated by centrifugation. &amp;lt;br&amp;gt;&lt;br /&gt;
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[[Category:Compounds_Synthesis]] [[Category:Paul]]&lt;/div&gt;</summary>
		<author><name>Paul.xu</name></author>
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