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<h1 id="firstHeading" class="firstHeading mw-first-heading"><span class="mw-page-title-main">Heptadecan</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>
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<th colspan="2" style="background:#FFDEAD; color:#202122;">Allgemeines
</th></tr>
<tr>
<td style="width:33%;">Name
</td>
<td>Heptadecan
</td></tr>
<tr>
<td><a href="Summenformel" title="Summenformel">Summenformel</a>
</td>
<td>C<sub>17</sub>H<sub>36</sub>
</td></tr>
<tr>
<td>Kurzbeschreibung
</td>
<td>
<p>farbloser Feststoff oder farblose Flüssigkeit<sup id="cite_ref-TCI_1-0" class="reference"><a href="#cite_note-TCI-1"><span class="cite-bracket">[</span>1<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><span title="Untervorlage eingebunden: CASRN"></span><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=629-78-7">629-78-7</a><span class="editoronly" style="display:none;"></span>
</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">211-108-4
</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/100.010.100">100.010.100</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/12398">12398</a>
</td></tr>
<tr>
<td><a href="ChemSpider" title="ChemSpider">ChemSpider</a>
</td>
<td colspan="2"><a rel="nofollow" class="external text" href="https://www.chemspider.com/Chemical-Structure.11892.html">11892</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/Q150888" class="extiw external" title="d:Q150888">Q150888</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>240,47 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>fest oder flüssig<sup id="cite_ref-TCI_1-1" class="reference"><a href="#cite_note-TCI-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup>
</p>
</td></tr>
<tr>
<td><a href="Dichte" title="Dichte">Dichte</a>
</td>
<td>
<p>0,778 g·cm<sup>−3</sup><sup id="cite_ref-Römpp_2-0" class="reference"><a href="#cite_note-Römpp-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>20–22 °C<sup id="cite_ref-Römpp_2-1" class="reference"><a href="#cite_note-Römpp-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup>
</p>
</td></tr>
<tr>
<td><a href="Siedepunkt" title="Siedepunkt">Siedepunkt</a>
</td>
<td>
<p>302 °C<sup id="cite_ref-Römpp_2-2" class="reference"><a href="#cite_note-Römpp-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>löslich in <a href="Ethanol" title="Ethanol">Ethanol</a> und <a href="Diethylether" title="Diethylether">Diethylether</a><sup id="cite_ref-Römpp_2-3" class="reference"><a href="#cite_note-Römpp-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup></li>
<li>kaum löslich in Wasser<sup id="cite_ref-Römpp_2-4" class="reference"><a href="#cite_note-Römpp-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup></li></ul>
</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-TCI_1-2" class="reference"><a href="#cite_note-TCI-1"><span class="cite-bracket">[</span>1<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><span typeof="mw:File"><a href="Global_harmonisiertes_System_zur_Einstufung_und_Kennzeichnung_von_Chemikalien#Übersicht:_EU-Gefahrensymbole,_UN/GHS-Gefahrenpiktogramme,_UN/ADR-Gefahrensymbole" title="08 – Gesundheitsgefährdend"></a></span>
</td></tr></tbody></table>
<p><b>Gefahr</b>
</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><a href="H-_und_P-S%C3%A4tze#H-Sätze" title="H- und P-Sätze"><span style="display:inline-block;"><span style="color:#ff5400; border-bottom:1px dotted #ff5400;" title="Kann bei Verschlucken und Eindringen in die Atemwege tödlich sein.">304</span></span></a>
</td></tr>
<tr>
<td style="border-top:1px #A7A7A7 dashed;">P: <span title="Untervorlage eingebunden: P-Sätze"></span><a href="H-_und_P-S%C3%A4tze#P-Sätze" title="H- und P-Sätze"><span style="display:inline-block;"><span style="color:#ff5400; border-bottom:1px dotted #ff5400;" title="Inhalt / Behälter … zuführen.
(Die vom Gesetzgeber offen gelassene Einfügung ist vom Inverkehrbringer zu ergänzen)">501</span></span></a>‐<a href="H-_und_P-S%C3%A4tze#P-Sätze" title="H- und P-Sätze"><span style="display:inline-block;"><span style="color:#ff5400; border-bottom:1px dotted #ff5400;" title="Kein Erbrechen herbeiführen.">331</span></span></a>‐<a href="H-_und_P-S%C3%A4tze#P-Sätze" title="H- und P-Sätze"><span style="display:inline-block;"><span style="color:#ff5400; border-bottom:1px dotted #ff5400;" title="Bei Verschlucken: Sofort Giftinformationszentrum, Arzt oder … anrufen.">301+310</span></span></a>‐<a href="H-_und_P-S%C3%A4tze#P-Sätze" title="H- und P-Sätze"><span style="display:inline-block;"><span style="color:#ff5400; border-bottom:1px dotted #ff5400;" title="Unter Verschluss aufbewahren.">405</span></span></a><sup id="cite_ref-TCI_1-3" class="reference"><a href="#cite_note-TCI-1"><span class="cite-bracket">[</span>1<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).
</td></tr></tbody></table><p><span class="editoronly" style="display:none;"></span>
</p><p><b>Heptadecan</b> ist ein langkettiges, lineares <a href="Alkane" title="Alkane">Alkan</a>. Es kommt in <a href="Erd%C3%B6l" title="Erdöl">Erdöl</a> vor sowie in daraus hergestellten Produkten wie <a href="Heiz%C3%B6l" title="Heizöl">Heizöl</a> und <a href="Schmier%C3%B6l" title="Schmieröl">Schmieröl</a>.
</p>
<div class="mw-heading mw-heading2"><h2 id="Vorkommen">Vorkommen</h2></div>
<p>Heptadecan ist Bestandteil von Erdöl.<sup id="cite_ref-:0_3-0" class="reference"><a href="#cite_note-:0-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup>
</p><p>Heptadecan kommt in den Ausscheidungen des <a href="Kaffeekirschenk%C3%A4fer" title="Kaffeekirschenkäfer">Kaffeekirschenkäfers</a> (<i>Hypothenemus hampei</i>) vor und wirkt als <a href="Kairomon" title="Kairomon">Kairomon</a>, das den <a href="Parasitismus" title="Parasitismus">Parasiten</a> <i>Prorops nasuta</i> (Ordnung <a href="Hautfl%C3%BCgler" title="Hautflügler">Hautflügler</a>) anlockt.<sup id="cite_ref-4" class="reference"><a href="#cite_note-4"><span class="cite-bracket">[</span>4<span class="cite-bracket">]</span></a></sup> Heptadecan wurde außerdem als Hauptkomponente des Sexualpheromons der <a href="Trauerm%C3%BCcken" title="Trauermücken">Trauermücke</a> <i>Lycoriella ingenua</i> postuliert, was jedoch später widerlegt wurde. In einer neueren Untersuchung konnten keine nennenswerten Mengen der Verbindung im Pheromon gefunden werden, außerdem erzeugte sie bei den Insekten auch keine einschlägige Reaktion. Die tatsächlich aktive Verbindung ist vermutlich ein <a href="Terpenoide" title="Terpenoide">Terpenoid</a> mit ähnlicher Molmasse.<sup id="cite_ref-5" class="reference"><a href="#cite_note-5"><span class="cite-bracket">[</span>5<span class="cite-bracket">]</span></a></sup> Pentadecan kommt in geringen Mengen in mehreren Arten der Gattung <i><a href="Vanille_(Orchideen)" title="Vanille (Orchideen)">Vanilla</a></i><sup id="cite_ref-6" class="reference"><a href="#cite_note-6"><span class="cite-bracket">[</span>6<span class="cite-bracket">]</span></a></sup> vor.
</p><p>Unter den organischen Verbindungen des <a href="Murchison-Meteorit" class="mw-redirect" title="Murchison-Meteorit">Murchison-Meteoriten</a> wurden Alkane der Kettenlänge 12 bis 26 gefunden, darunter auch Heptadecan als eine der Hauptkomponenten.<sup id="cite_ref-7" class="reference"><a href="#cite_note-7"><span class="cite-bracket">[</span>7<span class="cite-bracket">]</span></a></sup>
</p>
<div class="mw-heading mw-heading2"><h2 id="Eigenschaften">Eigenschaften</h2></div>
<p>Heptadecan ist eine klare, hochsiedende Flüssigkeit. Es ist löslich in <a href="Ethanol" title="Ethanol">Ethanol</a> und <a href="Diethylether" title="Diethylether">Diethylether</a>, jedoch kaum löslich in Wasser. Der <a href="Flammpunkt" title="Flammpunkt">Flammpunkt</a> liegt bei 149 °C.<sup id="cite_ref-Römpp_2-5" class="reference"><a href="#cite_note-Römpp-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup>
</p>
<div class="mw-heading mw-heading2"><h2 id="Verwendung">Verwendung</h2></div>
<p><a href="Dieseltreibstoff" class="mw-redirect" title="Dieseltreibstoff">Dieseltreibstoff</a> enthält unter anderem <i>n</i>-Alkane, die im Allgemeinen eine Kettenlänge zwischen neun und 24 aufweisen, wozu auch Heptadecan gehört.<sup id="cite_ref-8" class="reference"><a href="#cite_note-8"><span class="cite-bracket">[</span>8<span class="cite-bracket">]</span></a></sup> Auch andere Produkte, die aus Erdöl hergestellt werden, enthalten Heptadecan, beispielsweise <a href="Heiz%C3%B6l" title="Heizöl">Heizöl</a> und <a href="Schmier%C3%B6l" title="Schmieröl">Schmieröle</a> auf Erdölbasis.<sup id="cite_ref-:0_3-1" class="reference"><a href="#cite_note-:0-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup>
</p><p>Heptadecan wird gelegentlich als <a href="Referenzstandard" class="mw-redirect" title="Referenzstandard">Referenzstandard</a> in der <a href="Gaschromatographie" title="Gaschromatographie">Gaschromatographie</a> verwendet.<sup id="cite_ref-Römpp_2-6" class="reference"><a href="#cite_note-Römpp-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup> Auch als <a href="Extraktionsl%C3%B6sungsmittel" class="mw-redirect" title="Extraktionslösungsmittel">Extraktionslösungsmittel</a> für die Analyse <a href="%C3%84therische_%C3%96le" title="Ätherische Öle">ätherischer Öle</a> wird es gelegentlich verwendet.<sup id="cite_ref-9" class="reference"><a href="#cite_note-9"><span class="cite-bracket">[</span>9<span class="cite-bracket">]</span></a></sup>
</p>
<div class="mw-heading mw-heading2"><h2 id="Weblinks">Weblinks</h2></div>
<div class="sisterproject" style="margin:0.1em 0 0 0;"><div class="noresize noviewer" style="display:inline-block; line-height:10px; min-width:1.6em; text-align:center;" aria-hidden="true" role="presentation"><span class="mw-default-size" typeof="mw:File"><span title="Commons"></span></span></div><b><span class=""><a class="external text" href="https://commons.wikimedia.org/wiki/Category:Heptadecane?uselang=de"><span lang="en">Commons</span>: Heptadecan</a></span></b> – Sammlung von Bildern, Videos und Audiodateien</div>
<div class="sisterproject" style="margin:0.1em 0 0 0;"><span class="noviewer" style="display:inline-block; line-height:10px; min-width:1.6em; text-align:center;" aria-hidden="true" role="presentation"><span class="mw-default-size" typeof="mw:File"><span title="Wiktionary"></span></span></span><b><a href="https://de.wiktionary.org/wiki/Heptadecan" class="extiw external" title="wikt:Heptadecan">Wiktionary: Heptadecan</a></b> – Bedeutungserklärungen, Wortherkunft, Synonyme, Übersetzungen</div>
<div class="mw-heading mw-heading2"><h2 id="Einzelnachweise">Einzelnachweise</h2></div>
<div class="mw-references-wrap"><ol class="references">
<li id="cite_note-TCI-1"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-TCI_1-0">a</a></sup> <sup><a href="#cite_ref-TCI_1-1">b</a></sup> <sup><a href="#cite_ref-TCI_1-2">c</a></sup> <sup><a href="#cite_ref-TCI_1-3">d</a></sup></span> <span class="reference-text">Eintrag zu <span style="font-style:italic;"><a rel="nofollow" class="external text" href="https://www.tcichemicals.com/eshop/de/de/commodity/S0289">Heptadecane, >99.5%</a></span> bei TCI Europe, abgerufen am 22. April 2024.<span class="editoronly" style="display:none;"></span></span>
</li>
<li id="cite_note-Römpp-2"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-Römpp_2-0">a</a></sup> <sup><a href="#cite_ref-Römpp_2-1">b</a></sup> <sup><a href="#cite_ref-Römpp_2-2">c</a></sup> <sup><a href="#cite_ref-Römpp_2-3">d</a></sup> <sup><a href="#cite_ref-Römpp_2-4">e</a></sup> <sup><a href="#cite_ref-Römpp_2-5">f</a></sup> <sup><a href="#cite_ref-Römpp_2-6">g</a></sup></span> <span class="reference-text">Eintrag zu <a rel="nofollow" class="external text" href="https://roempp.thieme.de/lexicon/RD-08-00924"><i>Heptadecan</i></a>. In: <i><a href="R%C3%B6mpp_Online" class="mw-redirect" title="Römpp Online">Römpp Online</a>.</i> Georg Thieme Verlag, abgerufen am 21. April 2024.<span class="editoronly" style="display:none;"></span></span>
</li>
<li id="cite_note-:0-3"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-:0_3-0">a</a></sup> <sup><a href="#cite_ref-:0_3-1">b</a></sup></span> <span class="reference-text">Osei-Wusu Achaw, Eric Danso-Boateng: <cite style="font-style:italic">Chemical and Process Industries: With Examples of Industries in Ghana</cite>. Springer Nature, 2021, ISBN 978-3-03079139-1, <span style="white-space:nowrap">S.<span style="display:inline-block;width:.2em"> </span>240</span> (<a rel="nofollow" class="external text" href="https://www.google.de/books/edition/Chemical_and_Process_Industries/Org8EAAAQBAJ?hl=de&gbpv=1&dq=alkanes%20crude%20oil%20refinery&pg=PA240&printsec=frontcover">google.de</a> [abgerufen am 28. Dezember 2025]).<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:Heptadecan&rft.au=Osei-Wusu+Achaw%2C+Eric+Danso-Boateng&rft.btitle=Chemical+and+Process+Industries%3A+With+Examples+of+Industries+in+Ghana&rft.date=2021-08-09&rft.genre=book&rft.isbn=9783030791391&rft.pages=240&rft.pub=Springer+Nature" style="display:none"> </span></span>
</li>
<li id="cite_note-4"><span class="mw-cite-backlink"><a href="#cite_ref-4">↑</a></span> <span class="reference-text">Ariana K. Román-Ruíz, Edi A. Malo, Graciela Huerta, Alfredo Castillo, Juan F. Barrera, Julio C. Rojas: <cite style="font-style:italic">Identification and origin of host-associated volatiles attractive to Prorops nasuta, a parasitoid of the coffee berry borer</cite>. In: <cite style="font-style:italic">Arthropod-Plant Interactions</cite>. <span style="white-space:nowrap">Band<span style="display:inline-block;width:.2em"> </span>6</span>, <span style="white-space:nowrap">Nr.<span style="display:inline-block;width:.2em"> </span>4</span>, Dezember 2012, <span style="white-space:nowrap">S.<span style="display:inline-block;width:.2em"> </span>611–620</span>, <a href="Digital_Object_Identifier" title="Digital Object Identifier">doi</a>:<span class="uri-handle" style="white-space:nowrap"><a rel="nofollow" class="external text" href="https://doi.org/10.1007/s11829-012-9197-0">10.1007/s11829-012-9197-0</a></span>.<span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rfr_id=info:sid/de.wikipedia.org:Heptadecan&rft.atitle=Identification+and+origin+of+host-associated+volatiles+attractive+to+Prorops+nasuta%2C+a+parasitoid+of+the+coffee+berry+borer&rft.au=Ariana+K.+Rom%C3%A1n-Ru%C3%ADz%2C+Edi+A.+Malo%2C+Graciela+Huerta%2C+...&rft.date=2012-12&rft.doi=10.1007%2Fs11829-012-9197-0&rft.genre=journal&rft.issue=4&rft.jtitle=Arthropod-Plant+Interactions&rft.pages=611-620&rft.volume=6" style="display:none"> </span></span>
</li>
<li id="cite_note-5"><span class="mw-cite-backlink"><a href="#cite_ref-5">↑</a></span> <span class="reference-text">Stefanos S. Andreadis, Kevin R. Cloonan, Andrew J. Myrick, Haibin Chen, Thomas C. Baker: <cite style="font-style:italic">Isolation of a Female-Emitted Sex Pheromone Component of the Fungus Gnat, Lycoriella ingenua, Attractive to Males</cite>. In: <cite style="font-style:italic">Journal of Chemical Ecology</cite>. <span style="white-space:nowrap">Band<span style="display:inline-block;width:.2em"> </span>41</span>, <span style="white-space:nowrap">Nr.<span style="display:inline-block;width:.2em"> </span>12</span>, Dezember 2015, <span style="white-space:nowrap">S.<span style="display:inline-block;width:.2em"> </span>1127–1136</span>, <a href="Digital_Object_Identifier" title="Digital Object Identifier">doi</a>:<span class="uri-handle" style="white-space:nowrap"><a rel="nofollow" class="external text" href="https://doi.org/10.1007/s10886-015-0650-2">10.1007/s10886-015-0650-2</a></span>.<span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rfr_id=info:sid/de.wikipedia.org:Heptadecan&rft.atitle=Isolation+of+a+Female-Emitted+Sex+Pheromone+Component+of+the+Fungus+Gnat%2C+Lycoriella+ingenua%2C+Attractive+to+Males&rft.au=Stefanos+S.+Andreadis%2C+Kevin+R.+Cloonan%2C+Andrew+J.+Myrick%2C+...&rft.date=2015-12&rft.doi=10.1007%2Fs10886-015-0650-2&rft.genre=journal&rft.issue=12&rft.jtitle=Journal+of+Chemical+Ecology&rft.pages=1127-1136&rft.volume=41" style="display:none"> </span></span>
</li>
<li id="cite_note-6"><span class="mw-cite-backlink"><a href="#cite_ref-6">↑</a></span> <span class="reference-text">Béatrice Ramaroson-Raonizafinimanana, Émile M. Gaydou, Isabelle Bombarda: <cite style="font-style:italic">Hydrocarbons from Three Vanilla Bean Species: V. fragrans , V. madagascariensis , and V. tahitensis</cite>. In: <cite style="font-style:italic">Journal of Agricultural and Food Chemistry</cite>. <span style="white-space:nowrap">Band<span style="display:inline-block;width:.2em"> </span>45</span>, <span style="white-space:nowrap">Nr.<span style="display:inline-block;width:.2em"> </span>7</span>, 1. Juli 1997, <span style="white-space:nowrap">S.<span style="display:inline-block;width:.2em"> </span>2542–2545</span>, <a href="Digital_Object_Identifier" title="Digital Object Identifier">doi</a>:<span class="uri-handle" style="white-space:nowrap"><a rel="nofollow" class="external text" href="https://doi.org/10.1021/jf960927b">10.1021/jf960927b</a></span>.<span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rfr_id=info:sid/de.wikipedia.org:Heptadecan&rft.atitle=Hydrocarbons+from+Three+Vanilla+Bean+Species%3A+V.+fragrans+%2C+V.+madagascariensis+%2C+and+V.+tahitensis&rft.au=B%C3%A9atrice+Ramaroson-Raonizafinimanana%2C+%C3%89mile+M.+Gaydou%2C+Isabelle+Bombarda&rft.date=1997-07-01&rft.doi=10.1021%2Fjf960927b&rft.genre=journal&rft.issue=7&rft.jtitle=Journal+of+Agricultural+and+Food+Chemistry&rft.pages=2542-2545&rft.volume=45" style="display:none"> </span></span>
</li>
<li id="cite_note-7"><span class="mw-cite-backlink"><a href="#cite_ref-7">↑</a></span> <span class="reference-text">J.R. Cronin: <cite style="font-style:italic">Origin of organic compounds in carbonaceous chondrites</cite>. In: <cite style="font-style:italic">Advances in Space Research</cite>. <span style="white-space:nowrap">Band<span style="display:inline-block;width:.2em"> </span>9</span>, <span style="white-space:nowrap">Nr.<span style="display:inline-block;width:.2em"> </span>2</span>, Januar 1989, <span style="white-space:nowrap">S.<span style="display:inline-block;width:.2em"> </span>59–64</span>, <a href="Digital_Object_Identifier" title="Digital Object Identifier">doi</a>:<span class="uri-handle" style="white-space:nowrap"><a rel="nofollow" class="external text" href="https://doi.org/10.1016/0273-1177%2889%2990364-5">10.1016/0273-1177(89)90364-5</a></span>.<span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rfr_id=info:sid/de.wikipedia.org:Heptadecan&rft.atitle=Origin+of+organic+compounds+in+carbonaceous+chondrites&rft.au=J.R.+Cronin&rft.date=1989-01&rft.doi=10.1016%2F0273-1177%2889%2990364-5&rft.genre=journal&rft.issue=2&rft.jtitle=Advances+in+Space+Research&rft.pages=59-64&rft.volume=9" style="display:none"> </span></span>
</li>
<li id="cite_note-8"><span class="mw-cite-backlink"><a href="#cite_ref-8">↑</a></span> <span class="reference-text">L. V. Ivanova, V. N. Koshelev, E. A. Burov: <cite style="font-style:italic">Influence of the hydrocarbon composition of diesel fuels on their performance characteristics</cite>. In: <cite style="font-style:italic"><a href="Petroleum_Chemistry" title="Petroleum Chemistry">Petroleum Chemistry</a></cite>. <span style="white-space:nowrap">Band<span style="display:inline-block;width:.2em"> </span>54</span>, <span style="white-space:nowrap">Nr.<span style="display:inline-block;width:.2em"> </span>6</span>, November 2014, <span style="white-space:nowrap">S.<span style="display:inline-block;width:.2em"> </span>466–472</span>, <a href="Digital_Object_Identifier" title="Digital Object Identifier">doi</a>:<span class="uri-handle" style="white-space:nowrap"><a rel="nofollow" class="external text" href="https://doi.org/10.1134/S0965544114060061">10.1134/S0965544114060061</a></span>.<span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rfr_id=info:sid/de.wikipedia.org:Heptadecan&rft.atitle=Influence+of+the+hydrocarbon+composition+of+diesel+fuels+on+their+performance+characteristics&rft.au=L.+V.+Ivanova%2C+V.+N.+Koshelev%2C+E.+A.+Burov&rft.date=2014-11&rft.doi=10.1134%2FS0965544114060061&rft.genre=journal&rft.issue=6&rft.jtitle=Petroleum+Chemistry&rft.pages=466-472&rft.volume=54" style="display:none"> </span></span>
</li>
<li id="cite_note-9"><span class="mw-cite-backlink"><a href="#cite_ref-9">↑</a></span> <span class="reference-text">Peyman Salehi, Ali Reza Fakhari, Samad Nejad Ebrahimi, Rouhollah Heydari: <cite style="font-style:italic">Rapid essential oil screening of Rosmarinus officinalis L. by hydrodistillation–headspace solvent microextraction</cite>. In: <cite style="font-style:italic"><a href="Flavour_and_Fragrance_Journal" title="Flavour and Fragrance Journal">Flavour and Fragrance Journal</a></cite>. <span style="white-space:nowrap">Band<span style="display:inline-block;width:.2em"> </span>22</span>, <span style="white-space:nowrap">Nr.<span style="display:inline-block;width:.2em"> </span>4</span>, Juli 2007, <span style="white-space:nowrap">S.<span style="display:inline-block;width:.2em"> </span>280–285</span>, <a href="Digital_Object_Identifier" title="Digital Object Identifier">doi</a>:<span class="uri-handle" style="white-space:nowrap"><a rel="nofollow" class="external text" href="https://doi.org/10.1002/ffj.1793">10.1002/ffj.1793</a></span>.<span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rfr_id=info:sid/de.wikipedia.org:Heptadecan&rft.atitle=Rapid+essential+oil+screening+of+Rosmarinus+officinalis+L.+by+hydrodistillation-headspace+solvent+microextraction&rft.au=Peyman+Salehi%2C+Ali+Reza+Fakhari%2C+Samad+Nejad+Ebrahimi%2C+...&rft.date=2007-07&rft.doi=10.1002%2Fffj.1793&rft.genre=journal&rft.issue=4&rft.jtitle=Flavour+and+Fragrance+Journal&rft.pages=280-285&rft.volume=22" style="display:none"> </span></span>
</li>
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