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<h1 id="firstHeading" class="firstHeading mw-first-heading"><span class="mw-page-title-main">Hexene</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"><p><b>Hexene</b> (<i><a href="Singular" title="Singular">Singular</a>:</i> <b>Hexen</b>, <i><a href="Internationales_Phonetisches_Alphabet" title="Internationales Phonetisches Alphabet">IPA</a>:</i> [<style data-mw-deduplicate="TemplateStyles:r227981795">
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</style><span class="navigation-not-searchable"><span class="IPA"><a href="Liste_der_IPA-Zeichen" title="Liste der IPA-Zeichen"><span title="Aussprache im Internationalen Phonetischen Alphabet (IPA)" lang="zxx">hɛˈkseːn</span></a></span></span>], <span class="navigation-not-searchable" style="white-space:nowrap;"><span class="ext-phonos"><span data-nosnippet="" id="ooui-php-1" class="noexcerpt ext-phonos-PhonosButton oo-ui-widget oo-ui-widget-enabled oo-ui-buttonElement oo-ui-buttonElement-frameless oo-ui-iconElement oo-ui-labelElement oo-ui-buttonWidget" data-ooui="{&quot;_&quot;:&quot;mw.Phonos.PhonosButton&quot;,&quot;href&quot;:&quot;\/\/upload.wikimedia.org\/wikipedia\/commons\/transcoded\/b\/b3\/De-Hexen2.ogg\/De-Hexen2.ogg.mp3&quot;,&quot;rel&quot;:[&quot;nofollow&quot;],&quot;framed&quot;:false,&quot;icon&quot;:&quot;volumeUp&quot;,&quot;label&quot;:{&quot;html&quot;:&quot;<span style=\&quot;white-space:initial;\&quot;>anh\u00f6ren<\/span>&quot;},&quot;data&quot;:{&quot;ipa&quot;:&quot;&quot;,&quot;text&quot;:&quot;&quot;,&quot;lang&quot;:&quot;de&quot;,&quot;wikibase&quot;:&quot;&quot;,&quot;file&quot;:&quot;De-Hexen2.ogg&quot;},&quot;classes&quot;:[&quot;noexcerpt&quot;,&quot;ext-phonos-PhonosButton&quot;]}"><a role="button" tabindex="0" href="https://upload.wikimedia.org/wikipedia/commons/transcoded/b/b3/De-Hexen2.ogg/De-Hexen2.ogg.mp3" rel="nofollow" aria-label="Audio abspielen" title="Audio abspielen" class="oo-ui-buttonElement-button"><span class="oo-ui-iconElement-icon oo-ui-icon-volumeUp"></span><span class="oo-ui-labelElement-label"><span style="white-space:initial;">anhören</span></span><span class="oo-ui-indicatorElement-indicator oo-ui-indicatorElement-noIndicator"></span></a></span><sup class="ext-phonos-attribution noexcerpt navigation-not-searchable">ⓘ</sup></span></span>) sind <a href="Chemische_Verbindung" title="Chemische Verbindung">chemische Verbindungen</a> aus der Gruppe der <a href="Alkene" title="Alkene">Alkene</a> mit der Summenformel C<sub>6</sub>H<sub>12</sub>. Der Wortstamm <i>Hex</i> weist auf die sechs <a href="Kohlenstoff" title="Kohlenstoff">Kohlenstoffatome</a>, die Endung <i>en</i> auf die <a href="Doppelbindung" title="Doppelbindung">Doppelbindung</a> zwischen zwei der Kohlenstoffatome hin. Es existieren 13 <a href="Strukturisomer" class="mw-redirect" title="Strukturisomer">Strukturisomere</a>, die sich in der Position der Doppelbindung und dem Vorhandensein bzw. der Lage einer Verzweigung der Kohlenstoffkette unterscheiden.<sup id="cite_ref-1" class="reference"><a href="#cite_note-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup> Die in der Industrie am häufigsten eingesetzte Verbindung ist <a href="1-Hexen" title="1-Hexen">1-Hexen</a>, welche z.&nbsp;B. als <a href="Comonomer" class="mw-redirect" title="Comonomer">Comonomer</a> bei der Produktion von <a href="Polyethen" class="mw-redirect" title="Polyethen">Polyethen</a> eingesetzt wird.
</p>

<div class="mw-heading mw-heading2"><h2 id="Isomere">Isomere</h2></div>
<div class="mw-heading mw-heading3"><h3 id="Ohne_Verzweigung">Ohne Verzweigung</h3></div>
<ul><li><a href="1-Hexen" title="1-Hexen">1-Hexen</a></li>
<li>2-Hexen (tritt in <i>cis</i>- und <i>trans</i>-Form auf)</li>
<li>3-Hexen (tritt in <i>cis</i>- und <i>trans</i>-Form auf)</li></ul>
<div class="mw-heading mw-heading3"><h3 id="Mit_einfacher_Verzweigung">Mit einfacher Verzweigung</h3></div>
<ul><li><a href="2-Methyl-1-penten" title="2-Methyl-1-penten">2-Methyl-1-penten</a></li>
<li>2-Methyl-2-penten</li>
<li>3-Methyl-1-penten (zwei <a href="Enantiomer" title="Enantiomer">Enantiomere</a>)</li>
<li>3-Methyl-2-penten (tritt in <i>cis</i>- und <i>trans</i>-Form auf)</li>
<li><a href="4-Methyl-1-penten" title="4-Methyl-1-penten">4-Methyl-1-penten</a></li>
<li>4-Methyl-2-penten (tritt in <i>cis</i>- und <i>trans</i>-Form auf)</li>
<li>2-Ethyl-1-buten</li></ul>
<div class="mw-heading mw-heading3"><h3 id="Mit_doppelter_Verzweigung">Mit doppelter Verzweigung</h3></div>
<ul><li>2,3-Dimethyl-1-buten</li>
<li><a href="2%2C3-Dimethyl-2-buten" title="2,3-Dimethyl-2-buten">2,3-Dimethyl-2-buten</a></li>
<li><a href="3%2C3-Dimethyl-1-buten" class="mw-redirect" title="3,3-Dimethyl-1-buten">3,3-Dimethyl-1-buten</a></li></ul>
<div class="mw-heading mw-heading2"><h2 id="Eigenschaften">Eigenschaften</h2></div>
<table class="wikitable sortable">

<tbody><tr>
<th>Name</th>
<th><a href="Strukturformel" title="Strukturformel">Strukturformel</a></th>
<th><a href="CAS-Nummer" title="CAS-Nummer">CAS-Nummer</a></th>
<th><a href="Schmelzpunkt" title="Schmelzpunkt">Schmelzpunkt</a><sup id="cite_ref-CRC90_3_1_523_2-0" class="reference"><a href="#cite_note-CRC90_3_1_523-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup><br>in °C</th>
<th><a href="Siedepunkt" title="Siedepunkt">Siedepunkt</a><sup id="cite_ref-CRC90_3_1_523_2-1" class="reference"><a href="#cite_note-CRC90_3_1_523-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup><br>in °C</th>
<th><a href="Dichte" title="Dichte">Dichte</a><sup id="cite_ref-CRC90_3_1_523_2-2" class="reference"><a href="#cite_note-CRC90_3_1_523-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup><br>in g/cm<sup>3</sup></th>
<th><a href="Brechungsindex" title="Brechungsindex">Brechungsindex</a><sup id="cite_ref-CRC90_3_1_523_2-3" class="reference"><a href="#cite_note-CRC90_3_1_523-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup><br>(589&nbsp;nm)
</th></tr>
<tr>
<td>1-Hexen</td>
<td><span class="mw-default-size" typeof="mw:File"></span></td>
<td><span title="Untervorlage eingebunden: CASRN"></span><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=592-41-6">592-41-6</a><span class="editoronly" style="display:none;"></span></td>
<td>−139,76</td>
<td>63,48</td>
<td>0,6685 (25&nbsp;°C)</td>
<td>1,3852 (25&nbsp;°C)
</td></tr>
<tr>
<td>(<i>E</i>)-2-Hexen</td>
<td><span class="mw-default-size" typeof="mw:File"></span></td>
<td><span title="Untervorlage eingebunden: CASRN"></span><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=4050-45-7">4050-45-7</a><span class="editoronly" style="display:none;"></span></td>
<td>−133</td>
<td>67,9</td>
<td>0,6733 (25&nbsp;°C)</td>
<td>1,3936 (20&nbsp;°C)
</td></tr>
<tr>
<td>(<i>Z</i>)-2-Hexen</td>
<td><span class="mw-default-size" typeof="mw:File"></span></td>
<td><span title="Untervorlage eingebunden: CASRN"></span><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=7688-21-3">7688-21-3</a><span class="editoronly" style="display:none;"></span></td>
<td>−141,11</td>
<td>68,8</td>
<td>0,6824 (25&nbsp;°C)</td>
<td>1,3979 (20&nbsp;°C)
</td></tr>
<tr>
<td>(<i>E</i>)-3-Hexen</td>
<td><span class="mw-default-size" typeof="mw:File"></span></td>
<td><span title="Untervorlage eingebunden: CASRN"></span><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=13269-52-8">13269-52-8</a><span class="editoronly" style="display:none;"></span></td>
<td>−115,4</td>
<td>67,1</td>
<td>0,6772 (20&nbsp;°C)</td>
<td>1,3943 (20&nbsp;°C)
</td></tr>
<tr>
<td>(<i>Z</i>)-3-Hexen</td>
<td><span class="mw-default-size" typeof="mw:File"></span></td>
<td><span title="Untervorlage eingebunden: CASRN"></span><span class="KeinCASLink" title="CAS-Nummer ohne Common-Chemistry-Eintrag">7642-09-3</span><span class="editoronly" style="display:none;"></span></td>
<td>−137,8</td>
<td>66,4</td>
<td>0,6778 (20&nbsp;°C)</td>
<td>1,3947 (20&nbsp;°C)
</td></tr>
<tr>
<td>2-Methyl-1-penten</td>
<td><span class="mw-default-size" typeof="mw:File"></span></td>
<td><span title="Untervorlage eingebunden: CASRN"></span><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=763-29-1">763-29-1</a><span class="editoronly" style="display:none;"></span></td>
<td>−135,7</td>
<td>62,1</td>
<td>0,6799 (20&nbsp;°C)</td>
<td>1,3920 (20&nbsp;°C)
</td></tr>
<tr>
<td>2-Methyl-2-penten</td>
<td><span class="mw-default-size" typeof="mw:File"></span></td>
<td><span title="Untervorlage eingebunden: CASRN"></span><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=625-27-4">625-27-4</a><span class="editoronly" style="display:none;"></span></td>
<td>−135</td>
<td>67,3</td>
<td>0,6863 (20&nbsp;°C)</td>
<td>1,4004 (20&nbsp;°C)
</td></tr>
<tr>
<td>3-Methyl-1-penten</td>
<td><span class="mw-default-size" typeof="mw:File"></span></td>
<td><span title="Untervorlage eingebunden: CASRN"></span><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=760-20-3">760-20-3</a><span class="editoronly" style="display:none;"></span></td>
<td>−153</td>
<td>54,2</td>
<td>0,6675 (20&nbsp;°C)</td>
<td>1,3841 (20&nbsp;°C)
</td></tr>
<tr>
<td>
<p>(<i>R</i>)-3-Methyl-1-penten
</p>
</td>
<td><span class="mw-default-size" typeof="mw:File"></span></td>
<td><span title="Untervorlage eingebunden: CASRN"></span><span class="KeinCASLink" title="CAS-Nummer ohne Common-Chemistry-Eintrag">39914-58-4</span><span class="editoronly" style="display:none;"></span></td>
<td></td>
<td></td>
<td></td>
<td>
</td></tr>
<tr>
<td>
<p>(<i>S</i>)-3-Methyl-1-penten
</p>
</td>
<td><span class="mw-default-size" typeof="mw:File"></span></td>
<td><span title="Untervorlage eingebunden: CASRN"></span><span class="KeinCASLink" title="CAS-Nummer ohne Common-Chemistry-Eintrag">5026-95-9</span><span class="editoronly" style="display:none;"></span></td>
<td></td>
<td></td>
<td></td>
<td>
</td></tr>
<tr>
<td>(<i>E</i>)-3-Methyl-2-penten</td>
<td><span class="mw-default-size" typeof="mw:File"></span></td>
<td><span title="Untervorlage eingebunden: CASRN"></span><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=616-12-6">616-12-6</a><span class="editoronly" style="display:none;"></span></td>
<td>−138,5</td>
<td>70,4</td>
<td>0,6930 (25&nbsp;°C)</td>
<td>1,4045 (20&nbsp;°C)
</td></tr>
<tr>
<td>(<i>Z</i>)-3-Methyl-2-penten</td>
<td><span class="mw-default-size" typeof="mw:File"></span></td>
<td><span title="Untervorlage eingebunden: CASRN"></span><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=922-62-3">922-62-3</a><span class="editoronly" style="display:none;"></span></td>
<td>−134,8</td>
<td>67,7</td>
<td>0,6886 (25&nbsp;°C)</td>
<td>1,4016 (20&nbsp;°C)
</td></tr>
<tr>
<td>4-Methyl-1-penten</td>
<td><span class="mw-default-size" typeof="mw:File"></span></td>
<td><span title="Untervorlage eingebunden: CASRN"></span><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=691-37-2">691-37-2</a><span class="editoronly" style="display:none;"></span></td>
<td>−153,6</td>
<td>53,9</td>
<td>0,6642 (20&nbsp;°C)</td>
<td>1,3828 (20&nbsp;°C)
</td></tr>
<tr>
<td>(<i>E</i>)-4-Methyl-2-penten</td>
<td><span class="mw-default-size" typeof="mw:File"></span></td>
<td><span title="Untervorlage eingebunden: CASRN"></span><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=674-76-0">674-76-0</a><span class="editoronly" style="display:none;"></span></td>
<td>−140,8</td>
<td>58,6</td>
<td>0,6686 (20&nbsp;°C)</td>
<td>1,3889 (20&nbsp;°C)
</td></tr>
<tr>
<td>(<i>Z</i>)-4-Methyl-2-penten</td>
<td><span class="mw-default-size" typeof="mw:File"></span></td>
<td><span title="Untervorlage eingebunden: CASRN"></span><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=691-38-3">691-38-3</a><span class="editoronly" style="display:none;"></span></td>
<td>−134,8</td>
<td>56,3</td>
<td>0,6690 (20&nbsp;°C)</td>
<td>1,3800 (20&nbsp;°C)
</td></tr>
<tr>
<td>3-Methylidenpentan</td>
<td><span class="mw-default-size" typeof="mw:File"></span></td>
<td><span title="Untervorlage eingebunden: CASRN"></span><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=760-21-4">760-21-4</a><span class="editoronly" style="display:none;"></span></td>
<td>−131,5</td>
<td>64,7</td>
<td>0,6894 (20&nbsp;°C)</td>
<td>1,3969 (20&nbsp;°C)
</td></tr>
<tr>
<td>2,3-Dimethyl-1-buten</td>
<td><span class="mw-default-size" typeof="mw:File"></span></td>
<td><span title="Untervorlage eingebunden: CASRN"></span><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=563-78-0">563-78-0</a><span class="editoronly" style="display:none;"></span></td>
<td>−157,3</td>
<td>55,6</td>
<td>0,6803 (20&nbsp;°C)</td>
<td>1,3995 (20&nbsp;°C)
</td></tr>
<tr>
<td>2,3-Dimethyl-2-buten</td>
<td><span class="mw-default-size" typeof="mw:File"></span></td>
<td><span title="Untervorlage eingebunden: CASRN"></span><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=563-79-1">563-79-1</a><span class="editoronly" style="display:none;"></span></td>
<td><span style="visibility:hidden;">0</span>−74,19</td>
<td>73,3</td>
<td>0,7080 (20&nbsp;°C)</td>
<td>1,4122 (20&nbsp;°C)
</td></tr>
<tr>
<td>3,3-Dimethyl-1-buten</td>
<td><span class="mw-default-size" typeof="mw:File"></span></td>
<td><span title="Untervorlage eingebunden: CASRN"></span><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=558-37-2">558-37-2</a><span class="editoronly" style="display:none;"></span></td>
<td>−115,2</td>
<td>41,2</td>
<td>0,6529 (20&nbsp;°C)</td>
<td>1,3763 (20&nbsp;°C)
</td></tr></tbody></table>
<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:Hexenes?uselang=de"><span lang="en">Commons</span>: Hexene</a></span></b>&nbsp;– Sammlung von Bildern 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/Hexen" class="extiw external" title="wikt:Hexen">Wiktionary: Hexen</a></b>&nbsp;– Bedeutungserklärungen, Wortherkunft, Synonyme, Übersetzungen</div>
<div class="mw-heading mw-heading2"><h2 id="Einzelnachweise">Einzelnachweise</h2></div>
<ol class="references">
<li id="cite_note-1"><span class="mw-cite-backlink"><a href="#cite_ref-1">↑</a></span> <span class="reference-text"><span class="cite"><a rel="nofollow" class="external text" href="https://oeis.org/A000631"><i>Number of ethylene derivatives with n carbon atoms.</i></a> In: <i>The On-Line Encyclopedia of Integer Sequences.</i><span class="Abrufdatum"> Abgerufen am 10.&nbsp;September 2021</span>.</span><span style="display: none;" class="Z3988" title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&amp;rfr_id=info%3Asid%2Fde.wikipedia.org%3AHexene&amp;rft.title=Number+of+ethylene+derivatives+with+n+carbon+atoms&amp;rft.description=Number+of+ethylene+derivatives+with+n+carbon+atoms&amp;rft.identifier=https%3A%2F%2Foeis.org%2FA000631">&nbsp;</span></span>
</li>
<li id="cite_note-CRC90_3_1_523-2"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-CRC90_3_1_523_2-0">a</a></sup> <sup><a href="#cite_ref-CRC90_3_1_523_2-1">b</a></sup> <sup><a href="#cite_ref-CRC90_3_1_523_2-2">c</a></sup> <sup><a href="#cite_ref-CRC90_3_1_523_2-3">d</a></sup></span> <span class="reference-text">David R. Lide (Hrsg.): <i><a href="CRC_Handbook_of_Chemistry_and_Physics" title="CRC Handbook of Chemistry and Physics">CRC Handbook of Chemistry and Physics</a></i>. 90.&nbsp;Auflage. (Internet-Version: 2010), CRC Press&nbsp;/ Taylor and Francis, Boca Raton FL, <i>Physical Constants of Organic Compounds</i>, S.&nbsp;3-1 – 3-523.<span class="editoronly" style="display:none;"></span></span>
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Normdaten&nbsp;(Sachbegriff): <a href="Gemeinsame_Normdatei" title="Gemeinsame Normdatei">GND</a>: <span class="-print"><a rel="nofollow" class="external text" href="https://d-nb.info/gnd/4159814-3">4159814-3</a></span> </div>
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