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<h1 id="firstHeading" class="firstHeading mw-first-heading"><span class="mw-page-title-main">3-Nonanol</span></h1>
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<div id="mw-content-text" class="mw-body-content mw-content-ltr" lang="de" dir="ltr"><div class="mw-content-ltr mw-parser-output" lang="de" dir="ltr"><table class="wikitable infobox float-right" id="Vorlage_Infobox_Chemikalie" style="font-size:90%; margin-top:0; width:350px;" summary="Infobox Chemikalie">
<tbody><tr>
<th colspan="2" style="background:#FFDEAD; color:#202122;">Strukturformel
</th></tr>
<tr>
<td colspan="2" class="hintergrundfarbe-basis skin-invert-image" style="text-align:center;"><span typeof="mw:File"></span>
</td></tr>
<tr>
<td colspan="2" style="text-align:center; font-size:80%;">Vereinfachte Strukturformel ohne <a href="Stereochemie" title="Stereochemie">Stereochemie</a>
</td></tr>
<tr>
<th colspan="2" style="background:#FFDEAD; color:#202122;">Allgemeines
</th></tr>
<tr>
<td style="width:33%;">Name
</td>
<td>3-Nonanol
</td></tr>
<tr>
<td>Andere Namen
</td>
<td>
<ul><li>Nonan-3-ol</li>
<li>Ethylhexylcarbinol</li>
<li>Hexylethylcarbinol</li>
<li><small>NONAN-3-OL</small> (<a href="Internationale_Nomenklatur_f%C3%BCr_kosmetische_Inhaltsstoffe" title="Internationale Nomenklatur für kosmetische Inhaltsstoffe">INCI</a>)<sup id="cite_ref-CosIng_1-0" class="reference"><a href="#cite_note-CosIng-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup><span class="editoronly" style="display:none;"></span></li></ul>
</td></tr>
<tr>
<td><a href="Summenformel" title="Summenformel">Summenformel</a>
</td>
<td>C<sub>9</sub>H<sub>20</sub>O
</td></tr>
<tr>
<td>Kurzbeschreibung
</td>
<td>
<p>farblose Flüssigkeit<sup id="cite_ref-Alfa_2-0" class="reference"><a href="#cite_note-Alfa-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup>
</p>
</td></tr>
<tr>
<th colspan="2" style="background:#FFDEAD; color:#202122;">Externe Identifikatoren/Datenbanken
</th></tr>
<tr>
<td colspan="2" style="padding:0;">
<table class="mw-collapsible mw-collapsed wikitable" data-expandtext="+" data-collapsetext="−" style="border-top:none; margin:-1px; width:calc(100% + 2px);">
<tbody><tr>
<td style="width:33%;"><a href="CAS-Nummer" title="CAS-Nummer">CAS-Nummer</a>
</td>
<td>
<ul><li><span title="Untervorlage eingebunden: CASRN"></span><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=624-51-1">624-51-1</a><span class="editoronly" style="display:none;"></span></li>
<li><span title="Untervorlage eingebunden: CASRN"></span><span class="KeinCASLink" title="CAS-Nummer ohne Common-Chemistry-Eintrag">61925-50-6</span><span class="editoronly" style="display:none;"></span> [(<i>R</i>)-Form]</li>
<li><span title="Untervorlage eingebunden: CASRN"></span><span class="KeinCASLink" title="CAS-Nummer ohne Common-Chemistry-Eintrag">61925-49-3</span><span class="editoronly" style="display:none;"></span> [(<i>S</i>)-Form]</li></ul>
</td>
<td style="background:#FFDEAD; color:#202122; border-top:1px solid #FFDEAD; padding:0.2em 0; vertical-align:bottom; width:5%;">
</td></tr>
<tr>
<td><a href="EG-Nummer" title="EG-Nummer">EG-Nummer</a>
</td>
<td colspan="2">210-850-6
</td></tr>
<tr>
<td><a href="Europ%C3%A4ische_Chemikalienagentur" title="Europäische Chemikalienagentur">ECHA</a>-InfoCard
</td>
<td colspan="2"><a rel="nofollow" class="external text" href="https://www.echa.europa.eu/de/substance-information/-/substanceinfo/100.009.864">100.009.864</a>
</td></tr>
<tr>
<td><a href="PubChem" title="PubChem">PubChem</a>
</td>
<td colspan="2"><a rel="nofollow" class="external text" href="https://pubchem.ncbi.nlm.nih.gov/compound/12216">12216</a>
</td></tr>
<tr>
<td style="border-right:1px solid #a2a9b1;"><a href="Wikidata" title="Wikidata">Wikidata</a>
</td>
<td colspan="2"><a href="https://www.wikidata.org/wiki/Q22668733" class="extiw external" title="d:Q22668733">Q22668733</a>
</td></tr></tbody></table>
</td></tr>
<tr>
<th colspan="2" style="background:#FFDEAD; color:#202122;">Eigenschaften
</th></tr>
<tr>
<td><a href="Molare_Masse" title="Molare Masse">Molare Masse</a>
</td>
<td>144,26 g·<a href="Mol" title="Mol">mol</a><sup>−1</sup>
</td></tr>
<tr>
<td><a href="Aggregatzustand" title="Aggregatzustand">Aggregatzustand</a>
</td>
<td>
<p>flüssig<sup id="cite_ref-Alfa_2-1" class="reference"><a href="#cite_note-Alfa-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup>
</p>
</td></tr>
<tr>
<td><a href="Dichte" title="Dichte">Dichte</a>
</td>
<td>
<p>0,824 g·cm<sup>−3</sup><sup id="cite_ref-Alfa_2-2" class="reference"><a href="#cite_note-Alfa-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup>
</p>
</td></tr>
<tr>
<td><a href="Schmelzpunkt" title="Schmelzpunkt">Schmelzpunkt</a>
</td>
<td>
<p>22 <a href="Grad_Celsius" title="Grad Celsius">°C</a><sup id="cite_ref-William_M._Haynes_3-0" class="reference"><a href="#cite_note-William_M._Haynes-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup>
</p>
</td></tr>
<tr>
<td><a href="Siedepunkt" title="Siedepunkt">Siedepunkt</a>
</td>
<td>
<p>192–194 °C<sup id="cite_ref-Alfa_2-3" class="reference"><a href="#cite_note-Alfa-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup>
</p>
</td></tr>
<tr>
<td><a href="L%C3%B6slichkeit" title="Löslichkeit">Löslichkeit</a>
</td>
<td>
<ul><li>praktisch unlöslich in Wasser<sup id="cite_ref-William_M._Haynes_3-1" class="reference"><a href="#cite_note-William_M._Haynes-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup></li>
<li>löslich in Ethanol<sup id="cite_ref-William_M._Haynes_3-2" class="reference"><a href="#cite_note-William_M._Haynes-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup></li></ul>
</td></tr>
<tr>
<td><a href="Brechungsindex" title="Brechungsindex">Brechungsindex</a>
</td>
<td>
<p>1,4289 (20 °C)<sup id="cite_ref-William_M._Haynes_3-3" class="reference"><a href="#cite_note-William_M._Haynes-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup>
</p>
</td></tr>
<tr>
<th colspan="2" style="background:#FFDEAD; color:#202122;">Sicherheitshinweise
</th></tr>
<tr>
<td colspan="2">
<table cellspacing="0" cellpadding="2" style="width:100%;">
<tbody><tr>
<td colspan="2" style="text-align:center"><b><a href="Global_harmonisiertes_System_zur_Einstufung_und_Kennzeichnung_von_Chemikalien" title="Global harmonisiertes System zur Einstufung und Kennzeichnung von Chemikalien">GHS-Gefahrstoffkennzeichnung</a></b><sup id="cite_ref-Alfa_2-4" class="reference"><a href="#cite_note-Alfa-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup>
<table class="hintergrundfarbe-neutral" style="text-align:center; margin-left:auto; margin-right:auto; display:flex; justify-content:center;">
<tbody><tr>
<td><i>keine GHS-Piktogramme</i>
</td></tr></tbody></table>
<p>
</p>
</td></tr>
<tr>
<td rowspan="2" width="33%" style="border-top:1px #A7A7A7 dashed; border-right:1px #A7A7A7 dashed;"><a href="H-_und_P-S%C3%A4tze" title="H- und P-Sätze">H- und P-Sätze</a>
</td>
<td style="border-top:1px #A7A7A7 dashed;">H: <span title="Untervorlage eingebunden: H-Sätze"></span><i>keine H-Sätze</i>
</td></tr>
<tr>
<td style="border-top:1px #A7A7A7 dashed;">P: <span title="Untervorlage eingebunden: P-Sätze"></span><i>keine P-Sätze</i><sup id="cite_ref-Alfa_2-5" class="reference"><a href="#cite_note-Alfa-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup>
</td></tr>
</tbody></table>
</td></tr>
<tr>
<td colspan="2" style="background:#FFDEAD; color:#202122; font-size:80%; text-align:center; line-height:150%; padding:.25em;">Wenn nicht anders vermerkt, gelten die angegebenen Daten bei <a href="Standardbedingungen" title="Standardbedingungen">Standardbedingungen</a> (0 °C, 1000 hPa). Brechungsindex: <a href="Natrium-D-Linie" title="Natrium-D-Linie">Na-D-Linie</a>, 20 °C
</td></tr></tbody></table><p><span class="editoronly" style="display:none;"></span>
</p><p><b>3-Nonanol</b> ist eine <a href="Chemische_Verbindung" title="Chemische Verbindung">chemische Verbindung</a> aus der Stoffgruppe der <a href="Alkohole" title="Alkohole">aliphatischen Alkohole</a>. Neben dem 3-Nonanol existieren weitere <a href="Isomere" class="mw-redirect" title="Isomere">Isomere</a>, zum Beispiel das <a href="1-Nonanol" title="1-Nonanol">1-Nonanol</a>, <a href="2-Nonanol" title="2-Nonanol">2-Nonanol</a>, <a href="4-Nonanol" title="4-Nonanol">4-Nonanol</a> und <a href="5-Nonanol" title="5-Nonanol">5-Nonanol</a>.
</p>
<div class="mw-heading mw-heading2"><h2 id="Vorkommen">Vorkommen</h2></div>
<p>3-Nonanol kommt natürlich in der Cypressengarbe (<i>Achillea fragrantissima</i>),<sup id="cite_ref-Frank_D._Gunstone,_John_L._Harwood,_Fred_B._Padley_4-0" class="reference"><a href="#cite_note-Frank_D._Gunstone,_John_L._Harwood,_Fred_B._Padley-4"><span class="cite-bracket">[</span>4<span class="cite-bracket">]</span></a></sup> <a href="Gr%C3%BCne_Minze" title="Grüne Minze">Grüner Minze</a> (<i>Mentha spicata</i>)<sup id="cite_ref-Dr._Dukes_5-0" class="reference"><a href="#cite_note-Dr._Dukes-5"><span class="cite-bracket">[</span>5<span class="cite-bracket">]</span></a></sup> <a href="Spearmint" class="mw-redirect" title="Spearmint">Spearmint Öl</a><sup id="cite_ref-Brian_M._Lawrence_6-0" class="reference"><a href="#cite_note-Brian_M._Lawrence-6"><span class="cite-bracket">[</span>6<span class="cite-bracket">]</span></a></sup> und der <a href="Trockenrasen-Knotenameise" title="Trockenrasen-Knotenameise">Trockenrasen-Knotenameise</a> (<i>Myrmica scabrinodis</i>)<sup id="cite_ref-E._David_Morgan_7-0" class="reference"><a href="#cite_note-E._David_Morgan-7"><span class="cite-bracket">[</span>7<span class="cite-bracket">]</span></a></sup> vor.
</p>
<div class="mw-heading mw-heading2"><h2 id="Eigenschaften">Eigenschaften</h2></div>
<p>3-Nonanol ist eine farblose Flüssigkeit,<sup id="cite_ref-Alfa_2-6" class="reference"><a href="#cite_note-Alfa-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup> die praktisch unlöslich in Wasser ist.<sup id="cite_ref-William_M._Haynes_3-4" class="reference"><a href="#cite_note-William_M._Haynes-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup>
</p>
<div class="mw-heading mw-heading2"><h2 id="Verwendung">Verwendung</h2></div>
<p>3-Nonanol kann als Geruchsstoff für erdige Düfte verwendet werden.<sup id="cite_ref-H._Panda_8-0" class="reference"><a href="#cite_note-H._Panda-8"><span class="cite-bracket">[</span>8<span class="cite-bracket">]</span></a></sup>
</p>
<div class="mw-heading mw-heading2"><h2 id="Einzelnachweise">Einzelnachweise</h2></div>
<ol class="references">
<li id="cite_note-CosIng-1"><span class="mw-cite-backlink"><a href="#cite_ref-CosIng_1-0">↑</a></span> <span class="reference-text">Eintrag zu <a rel="nofollow" class="external text" href="https://ec.europa.eu/growth/tools-databases/cosing/details/40910"><i><small>NONAN-3-OL</small></i></a> in der <a href="CosIng-Datenbank" title="CosIng-Datenbank">CosIng-Datenbank</a> der EU-Kommission, abgerufen am 17. September 2021.</span>
</li>
<li id="cite_note-Alfa-2"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-Alfa_2-0">a</a></sup> <sup><a href="#cite_ref-Alfa_2-1">b</a></sup> <sup><a href="#cite_ref-Alfa_2-2">c</a></sup> <sup><a href="#cite_ref-Alfa_2-3">d</a></sup> <sup><a href="#cite_ref-Alfa_2-4">e</a></sup> <sup><a href="#cite_ref-Alfa_2-5">f</a></sup> <sup><a href="#cite_ref-Alfa_2-6">g</a></sup></span> <span class="reference-text">Datenblatt <span style="font-style:italic;"><a rel="nofollow" class="external text" href="https://www.alfa.com/de/catalog/A19120">3-Nonanol, 98%</a></span> bei <a href="Alfa_Aesar" title="Alfa Aesar">Alfa Aesar</a>, abgerufen am 10. Januar 2016 <small>(Seite nicht mehr abrufbar)</small>.<span class="editoronly" style="display:none;"></span></span>
</li>
<li id="cite_note-William_M._Haynes-3"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-William_M._Haynes_3-0">a</a></sup> <sup><a href="#cite_ref-William_M._Haynes_3-1">b</a></sup> <sup><a href="#cite_ref-William_M._Haynes_3-2">c</a></sup> <sup><a href="#cite_ref-William_M._Haynes_3-3">d</a></sup> <sup><a href="#cite_ref-William_M._Haynes_3-4">e</a></sup></span> <span class="reference-text">William M. Haynes: <cite style="font-style:italic">CRC Handbook of Chemistry and Physics, 96th Edition</cite>. CRC Press, 2015, ISBN 978-1-4822-6097-7, <span style="white-space:nowrap">S.<span style="display:inline-block;width:.2em"> </span>420</span> (<a rel="nofollow" class="external text" href="https://books.google.de/books?id=RpLYCQAAQBAJ&pg=RA3-PA420#v=onepage">eingeschränkte Vorschau</a> in der Google-Buchsuche).<span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rfr_id=info:sid/de.wikipedia.org:3-Nonanol&rft.au=William+M.+Haynes&rft.btitle=CRC+Handbook+of+Chemistry+and+Physics%2C+96th+Edition&rft.date=2015&rft.genre=book&rft.isbn=9781482260977&rft.pages=420&rft.pub=CRC+Press" style="display:none"> </span></span>
</li>
<li id="cite_note-Frank_D._Gunstone,_John_L._Harwood,_Fred_B._Padley-4"><span class="mw-cite-backlink"><a href="#cite_ref-Frank_D._Gunstone,_John_L._Harwood,_Fred_B._Padley_4-0">↑</a></span> <span class="reference-text">Frank D. Gunstone, John L. Harwood, Fred B. Padley: <cite style="font-style:italic">The Lipid Handbook, Second Edition</cite>. CRC Press, 1994, ISBN 978-0-412-43320-7, <span style="white-space:nowrap">S.<span style="display:inline-block;width:.2em"> </span>291</span> (<a rel="nofollow" class="external text" href="https://books.google.de/books?id=m9J9pTDZEGEC&pg=PA291#v=onepage">eingeschränkte Vorschau</a> in der Google-Buchsuche).<span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rfr_id=info:sid/de.wikipedia.org:3-Nonanol&rft.au=Frank+D.+Gunstone%2C+John+L.+Harwood%2C+Fred+B.+Padley&rft.btitle=The+Lipid+Handbook%2C+Second+Edition&rft.date=1994&rft.genre=book&rft.isbn=9780412433207&rft.pages=291&rft.pub=CRC+Press" style="display:none"> </span></span>
</li>
<li id="cite_note-Dr._Dukes-5"><span class="mw-cite-backlink"><a href="#cite_ref-Dr._Dukes_5-0">↑</a></span> <span class="reference-text"><span style="font-style:italic;"><a rel="nofollow" class="external text" href="https://phytochem.nal.usda.gov/phytochem/chemicals/show/59021">NONAN-3-OL</a></span> (englisch). In: <i>Dr. Duke's Phytochemical and Ethnobotanical Database</i>, Hrsg. <a href="Landwirtschaftsministerium_der_Vereinigten_Staaten" title="Landwirtschaftsministerium der Vereinigten Staaten">U.S. Department of Agriculture</a>, abgerufen am 12. September 2021.<span class="editoronly" style="display:none;"></span></span>
</li>
<li id="cite_note-Brian_M._Lawrence-6"><span class="mw-cite-backlink"><a href="#cite_ref-Brian_M._Lawrence_6-0">↑</a></span> <span class="reference-text">Brian M. Lawrence: <cite style="font-style:italic">Mint The Genus Mentha</cite>. CRC Press, 2006, ISBN 0-8493-0798-8, <span style="white-space:nowrap">S.<span style="display:inline-block;width:.2em"> </span>292</span> (<a rel="nofollow" class="external text" href="https://books.google.de/books?id=BYPPEjWMOOQC&pg=PA292#v=onepage">eingeschränkte Vorschau</a> in der Google-Buchsuche).<span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rfr_id=info:sid/de.wikipedia.org:3-Nonanol&rft.au=Brian+M.+Lawrence&rft.btitle=Mint+The+Genus+Mentha&rft.date=2006&rft.genre=book&rft.isbn=0849307988&rft.pages=292&rft.pub=CRC+Press" style="display:none"> </span></span>
</li>
<li id="cite_note-E._David_Morgan-7"><span class="mw-cite-backlink"><a href="#cite_ref-E._David_Morgan_7-0">↑</a></span> <span class="reference-text">E. David Morgan: <cite style="font-style:italic">Biosynthesis in Insects</cite>. Royal Society of Chemistry, 2004, ISBN 0-85404-691-7, <span style="white-space:nowrap">S.<span style="display:inline-block;width:.2em"> </span>61</span> (<a rel="nofollow" class="external text" href="https://books.google.de/books?id=AbXid2E-17YC&pg=PA61#v=onepage">eingeschränkte Vorschau</a> in der Google-Buchsuche).<span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rfr_id=info:sid/de.wikipedia.org:3-Nonanol&rft.au=E.+David+Morgan&rft.btitle=Biosynthesis+in+Insects&rft.date=2004&rft.genre=book&rft.isbn=0854046917&rft.pages=61&rft.pub=Royal+Society+of+Chemistry" style="display:none"> </span></span>
</li>
<li id="cite_note-H._Panda-8"><span class="mw-cite-backlink"><a href="#cite_ref-H._Panda_8-0">↑</a></span> <span class="reference-text">H. Panda: <cite style="font-style:italic">The Complete Technology Book on Herbal Perfumes & Cosmetics</cite>. 2003, ISBN 81-86623-62-0, <span style="white-space:nowrap">S.<span style="display:inline-block;width:.2em"> </span>303</span>.<span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rfr_id=info:sid/de.wikipedia.org:3-Nonanol&rft.au=H.+Panda&rft.btitle=The+Complete+Technology+Book+on+Herbal+Perfumes+%26+Cosmetics&rft.date=2003&rft.genre=book&rft.isbn=8186623620&rft.pages=303" style="display:none"> </span></span>
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