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<h1 id="firstHeading" class="firstHeading mw-first-heading"><span class="mw-page-title-main">Butyraldehyde</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>Butyraldehyde</b> sind <a href="Aldehyde" title="Aldehyde">Aldehyde</a> mit vier Kohlenstoffatomen. Sie haben die allgemeine <a href="Summenformel" title="Summenformel">Summenformel</a> C<sub>4</sub>H<sub>8</sub>O und eine <a href="Molare_Masse" title="Molare Masse">molare Masse</a> von 72,11 g/mol. Es gibt nur zwei <a href="Isomer" class="mw-redirect" title="Isomer">Isomere</a>:<sup id="cite_ref-Römpp_1-0" class="reference"><a href="#cite_note-Römpp-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup>
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<td class="hintergrundfarbe6" align="center" colspan="3"><b>Butyraldehyde</b>
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<td class="hintergrundfarbe5" align="left">Name
</td>
<td><a href="Butanal" title="Butanal">Butyraldeyd</a></td>
<td><a href="Isobutanal" title="Isobutanal">Isobutyraldeyd</a>
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<td class="hintergrundfarbe5" align="left"><a href="IUPAC-Nomenklatur" class="mw-redirect" title="IUPAC-Nomenklatur">IUPAC-Nomenklatur</a>
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<td>Butanal</td>
<td>2-Methylpropanal
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<td class="hintergrundfarbe5" align="left"><a href="Strukturformel" title="Strukturformel">Strukturformel</a>
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<td><span class="mw-default-size" typeof="mw:File"></span></td>
<td><span class="mw-default-size" typeof="mw:File"></span>
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<tr>
<td class="hintergrundfarbe5" align="left"><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=123-72-8">123-72-8</a><span class="editoronly" style="display:none;"></span></td>
<td><span title="Untervorlage eingebunden: CASRN"></span><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=78-84-2">78-84-2</a><span class="editoronly" style="display:none;"></span>
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<td class="hintergrundfarbe5" align="left"><a href="PubChem" title="PubChem">PubChem</a>
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<td><a rel="nofollow" class="external text" href="https://pubchem.ncbi.nlm.nih.gov/compound/261">261</a></td>
<td><a rel="nofollow" class="external text" href="https://pubchem.ncbi.nlm.nih.gov/compound/6561">6561</a>
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<td class="hintergrundfarbe5" align="left"><a href="Summenformel" title="Summenformel">Summenformel</a>
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<td colspan="2">C<sub>4</sub>H<sub>8</sub>O
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<td class="hintergrundfarbe5" align="left"><a href="Molare_Masse" title="Molare Masse">Molare Masse</a>
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<td colspan="2">72,11 g·<a href="Mol" title="Mol">mol</a><sup>−1</sup>
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<td class="hintergrundfarbe5" align="left"><a href="Aggregatzustand" title="Aggregatzustand">Aggregatzustand</a>
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<td colspan="2">flüssig
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<td class="hintergrundfarbe5" align="left"><a href="Schmelzpunkt" title="Schmelzpunkt">Schmelzpunkt</a>
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<td>−91,7 <a href="Grad_Celsius" title="Grad Celsius">°C</a><sup id="cite_ref-GESTIS_n_2-0" class="reference"><a href="#cite_note-GESTIS_n-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup>
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<td>−65 <a href="Grad_Celsius" title="Grad Celsius">°C</a><sup id="cite_ref-GESTIS_iso_3-0" class="reference"><a href="#cite_note-GESTIS_iso-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup>
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<td class="hintergrundfarbe5" align="left"><a href="Siedepunkt" title="Siedepunkt">Siedepunkt</a>
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<td>75 °C<sup id="cite_ref-GESTIS_n_2-1" class="reference"><a href="#cite_note-GESTIS_n-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup>
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<td>64 °C<sup id="cite_ref-GESTIS_iso_3-1" class="reference"><a href="#cite_note-GESTIS_iso-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup>
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<p>Die gleiche Summenformel besitzen auch <a href="Crotylalkohol" title="Crotylalkohol">Crotylalkohol</a>, <a href="3-Buten-1-ol" title="3-Buten-1-ol">3-Buten-1-ol</a> und <a href="Butanon" title="Butanon">Butanon</a>.
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<div class="mw-heading mw-heading2"><h2 id="Einzelnachweise">Einzelnachweise</h2></div>
<ol class="references">
<li id="cite_note-Römpp-1"><span class="mw-cite-backlink"><a href="#cite_ref-Römpp_1-0">↑</a></span> <span class="reference-text">Eintrag zu <a rel="nofollow" class="external text" href="https://roempp.thieme.de/lexicon/RD-02-03217"><i>Butyraldehyde</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 16.&nbsp;August 2022.<span class="editoronly" style="display:none;"></span></span>
</li>
<li id="cite_note-GESTIS_n-2"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-GESTIS_n_2-0">a</a></sup> <sup><a href="#cite_ref-GESTIS_n_2-1">b</a></sup></span> <span class="reference-text">Eintrag zu <span style="font-style:italic;"><a rel="nofollow" class="external text" href="https://gestis.dguv.de/data?name=028130">Butyraldehyd</a></span> in der <a href="GESTIS-Stoffdatenbank" title="GESTIS-Stoffdatenbank">GESTIS-Stoffdatenbank</a> des <a href="Institut_f%C3%BCr_Arbeitsschutz_der_Deutschen_Gesetzlichen_Unfallversicherung" title="Institut für Arbeitsschutz der Deutschen Gesetzlichen Unfallversicherung">IFA</a>, abgerufen am 24.&nbsp;Mai 2016.<small class="noscript"><span></span> (JavaScript erforderlich)</small></span>
</li>
<li id="cite_note-GESTIS_iso-3"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-GESTIS_iso_3-0">a</a></sup> <sup><a href="#cite_ref-GESTIS_iso_3-1">b</a></sup></span> <span class="reference-text">Eintrag zu <span style="font-style:italic;"><a rel="nofollow" class="external text" href="https://gestis.dguv.de/data?name=017450">Isobutyraldehyd</a></span> in der <a href="GESTIS-Stoffdatenbank" title="GESTIS-Stoffdatenbank">GESTIS-Stoffdatenbank</a> des <a href="Institut_f%C3%BCr_Arbeitsschutz_der_Deutschen_Gesetzlichen_Unfallversicherung" title="Institut für Arbeitsschutz der Deutschen Gesetzlichen Unfallversicherung">IFA</a>, abgerufen am 24.&nbsp;Mai 2016.<small class="noscript"><span></span> (JavaScript erforderlich)</small></span>
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Dieser Artikel wurde von <a class="external text" title="Zuletzt bearbeitet am 2024-08-25" href="https://de.wikipedia.org/wiki/?title=Butyraldehyde&amp;oldid=248022988">Wikipedia</a> herausgegeben. Der Text ist unter <a class="external text" href="https://creativecommons.org/licenses/by-sa/4.0/deed.de">Creative Commons Attribution-Share Alike 4.0</a> verfügbar, sofern nicht anders angegeben. Für die Mediendateien können zusätzliche Bedingungen gelten.
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