<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0">
<channel>
<title>Acetyl hexapeptide-3 (Argireline): an alternative to Botox or </title>
<link>http://www.duyp.net/</link>
        <image>
        <title>http://www.duyp.net/</title>
        <link>http://www.duyp.net/</link>
        <url>http://www.duyp.net/image/duyp.gif</url>
        </image>
<description>Dig yellowpages: Acetyl hexapeptide-3 (Argireline): an alternative to Botox or </description>
<lastBuildDate>Sat, 06 Sep 2008 04:38:16 +0800</lastBuildDate>
<docs>http://www.duyp.net/aa505900.htm</docs>
<generator>davekid2</generator>
<category>Dig yellowpages</category>
<language>UTF-8</language>

<item>
<title>Coenzyme A - Wikipedia, the free encyclopedia</title>
<link>http://www.duyp.net/digg/505899-acetyl_coenzyme_a.htm</link>
<description><![CDATA[Coenzyme A. Identifiers. CAS number, [85-61-0]. PubChem &amp;middot; 317 &amp;middot; MeSH &amp;middot; Coenzyme+A &amp;middot; SMILES, CC(C)(COP(=O)(O)OP(=O)(O)OCC1C (C(C(O1)N2C=NC3=C2N=CN=C3N)O) ...]]></description>
<pubDate>Wes, 30 Jan 2008 04:27:48 +0800</pubDate>
<guid>http://www.duyp.net/digg/505899-acetyl_coenzyme_a.htm</guid>
</item>

<item>
<title>L Tyrosine supplement : by Ray Sahelian, M.D., Benefits and Side </title>
<link>http://www.duyp.net/digg/505898-n_acetyl_l_tyrosine.htm</link>
<description><![CDATA[I also decided to experiment with my dopamine system, so I tried n-acetyl-l tyrosine. Immediately, I noticed an improved ability to perceive color. ...]]></description>
<pubDate>Wes, 30 Jan 2008 04:27:45 +0800</pubDate>
<guid>http://www.duyp.net/digg/505898-n_acetyl_l_tyrosine.htm</guid>
</item>

<item>
<title>Acetylcholine - Wikipedia, the free encyclopedia</title>
<link>http://www.duyp.net/digg/505897-acetyl_choline.htm</link>
<description><![CDATA[The chemical compound acetylcholine (often abbreviated ACh) is a neurotransmitter in both the peripheral nervous system (PNS) and central nervous system ...]]></description>
<pubDate>Wes, 30 Jan 2008 04:27:41 +0800</pubDate>
<guid>http://www.duyp.net/digg/505897-acetyl_choline.htm</guid>
</item>

<item>
<title>Acetyl - Wikipedia, the free encyclopedia</title>
<link>http://www.duyp.net/digg/505896-acetyl_group.htm</link>
<description><![CDATA[Chemical structure of an acetyl group bound to the remainder R of a molecule. ... The introduction of an acetyl group into a molecule is called acetylation ...]]></description>
<pubDate>Wes, 30 Jan 2008 04:27:39 +0800</pubDate>
<guid>http://www.duyp.net/digg/505896-acetyl_group.htm</guid>
</item>

<item>
<title>Cysteine - Wikipedia, the free encyclopedia</title>
<link>http://www.duyp.net/digg/505895-n_acetyl_l_cysteine.htm</link>
<description><![CDATA[N-acetyl-L-cysteine (NAC) is a derivative of cysteine wherein an acetyl group is attached to the nitrogen atom. This compound is sometimes considered as a ...]]></description>
<pubDate>Wes, 30 Jan 2008 04:27:33 +0800</pubDate>
<guid>http://www.duyp.net/digg/505895-n_acetyl_l_cysteine.htm</guid>
</item>

<item>
<title>Acetylcysteine - Wikipedia,  the free encyclopedia</title>
<link>http://www.duyp.net/digg/505894-n_acetyl_cysteine.htm</link>
<description><![CDATA[NAC is undergoing clinical trials in the United States for the treatment of obsessive-compulsive disorder. [1] It is thought to counteract the glutamate ...]]></description>
<pubDate>Wes, 30 Jan 2008 04:27:31 +0800</pubDate>
<guid>http://www.duyp.net/digg/505894-n_acetyl_cysteine.htm</guid>
</item>

<item>
<title>Acetylcarnitine - Wikipedia, the free encyclopedia</title>
<link>http://www.duyp.net/digg/505893-acetyl_l_carnitine.htm</link>
<description><![CDATA[Acetyl-L-carnitine or ALCAR, is an acetylated form of L-carnitine. ... Advocates of acetyl-L-carnitine market it as a life extension supplement. ...]]></description>
<pubDate>Wes, 30 Jan 2008 04:27:29 +0800</pubDate>
<guid>http://www.duyp.net/digg/505893-acetyl_l_carnitine.htm</guid>
</item>

<item>
<title>Design of instrumentation for probing changes in electrospray </title>
<link>http://www.duyp.net/digg/505892-acetonitrile_evaporation.htm</link>
<description><![CDATA[This suggests that the initial concentration of TMPD  may affect the rate of acetonitrile evaporation. Perhaps TMPD increases hydrogen bonding or van der ...]]></description>
<pubDate>Wes, 30 Jan 2008 04:27:25 +0800</pubDate>
<guid>http://www.duyp.net/digg/505892-acetonitrile_evaporation.htm</guid>
</item>

<item>
<title>Purification and recovery of acetonitrile from waste solvent </title>
<link>http://www.duyp.net/digg/505891-acetonitrile_water_azeotrope.htm</link>
<description><![CDATA[A first acetonitrile/water azeotrope containing about 70% acetonitrile, less than 30% ... A third acetonitrile/water azeotrope is withdrawn from the top of ...]]></description>
<pubDate>Wes, 30 Jan 2008 04:27:19 +0800</pubDate>
<guid>http://www.duyp.net/digg/505891-acetonitrile_water_azeotrope.htm</guid>
</item>

<item>
<title>Catalytic Synthesis of Acetonitrile by Ammonolysis of Acetic Acid</title>
<link>http://www.duyp.net/digg/505890-acetonitrile_synthesis.htm</link>
<description><![CDATA[In this work it has been demonstrated that initial temperatures of 360-380Â°C are optimum to effectively carry out the process of acetonitrile synthesis. ...]]></description>
<pubDate>Wes, 30 Jan 2008 04:27:16 +0800</pubDate>
<guid>http://www.duyp.net/digg/505890-acetonitrile_synthesis.htm</guid>
</item>

<item>
<title>N-(3-trifluoromethyl-phenyl)-N-propargyl-piperazine and salts </title>
<link>http://www.duyp.net/digg/505889-acetonitrile_melting_point.htm</link>
<description><![CDATA[Even small quantities of dihydrochloride influence the melting point. White crystals from acetonitrile, melting point 218Â°-219Â° C. (decomposition). ...]]></description>
<pubDate>Wes, 30 Jan 2008 04:27:15 +0800</pubDate>
<guid>http://www.duyp.net/digg/505889-acetonitrile_melting_point.htm</guid>
</item>

<item>
<title>[PDF] Trypsin, recombinant, proteomics grade</title>
<link>http://www.duyp.net/digg/505888-acetonitrile_mw.htm</link>
<description><![CDATA[File Format: PDF/Adobe Acrobat - View as HTML]]></description>
<pubDate>Wes, 30 Jan 2008 04:27:13 +0800</pubDate>
<guid>http://www.duyp.net/digg/505888-acetonitrile_mw.htm</guid>
</item>

<item>
<title>Journal of Chromatography A : Temperature-dependent refractive </title>
<link>http://www.duyp.net/digg/505887-refractive_index_of_acetonitrile.htm</link>
<description><![CDATA[Refractive index of acetonitrileâ€“water vs. % acetonitrile. â™? 25Â°C; â–? 30Â°C; up triangle, filled , 35Â°C; â€? 40Â°C; Ã—, 45Â°C; â€? 50Â°C. ...]]></description>
<pubDate>Wes, 30 Jan 2008 04:27:10 +0800</pubDate>
<guid>http://www.duyp.net/digg/505887-refractive_index_of_acetonitrile.htm</guid>
</item>

<item>
<title>ACETONITRILE -- Safety Assessment Data</title>
<link>http://www.duyp.net/digg/505886-acetonitrile_safety.htm</link>
<description><![CDATA[Copyright Â© 2005 Green Media Toolshed and GetActive Software All Rights Reserved. Powered by GetActive Software. Questions or Comments? Email: ...]]></description>
<pubDate>Wes, 30 Jan 2008 04:27:09 +0800</pubDate>
<guid>http://www.duyp.net/digg/505886-acetonitrile_safety.htm</guid>
</item>

</channel>
</rss>