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<h1 id="firstHeading" class="firstHeading mw-first-heading"><span class="mw-page-title-main">QDX</span></h1>
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<table class="wikitable infobox float-right" id="Vorlage_Infobox_Chemikalie" style="font-size:90%; margin-top:0; width:350px;" summary="Infobox Chemikalie">
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<th colspan="2" style="background:#FFDEAD; color:#202122;">Strukturformel
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<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
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<td style="width:33%;">Name
</td>
<td>QDX
</td></tr>
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<td>Andere Namen
</td>
<td>
<ul><li>1-(3,5,7-Trinitro-1,3,5,7-tetrazocan-1-yl)ethanon</li>
<li>1-Acetyl-3,5,7-trinitro-1,3,5,7-octahydrotetrazocin</li>
<li>SEX</li>
<li>Solex</li></ul>
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<tr>
<td><a href="Summenformel" title="Summenformel">Summenformel</a>
</td>
<td>C<sub>6</sub>H<sub>11</sub>N<sub>7</sub>O<sub>7</sub>
</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=13980-00-2">13980-00-2</a><span class="editoronly" style="display:none;"></span>
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<td style="background:#FFDEAD; color:#202122; border-top:1px solid #FFDEAD; padding:0.2em 0; vertical-align:bottom; width:5%;">
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<td><a href="EG-Nummer" title="EG-Nummer">EG-Nummer</a>
</td>
<td colspan="2">237-765-7
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<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/100.034.318">100.034.318</a>
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<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/26367">26367</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.24565.html">24565</a>
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<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/Q2121168" class="extiw external" title="d:Q2121168">Q2121168</a>
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</td></tr>
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<th colspan="2" style="background:#FFDEAD; color:#202122;">Eigenschaften
</th></tr>
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<td><a href="Molare_Masse" title="Molare Masse">Molare Masse</a>
</td>
<td>293,2 g·<a href="Mol" title="Mol">mol</a><sup>−1</sup>
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<tr>
<td><a href="Aggregatzustand" title="Aggregatzustand">Aggregatzustand</a>
</td>
<td>
<p>fest<sup id="cite_ref-Fedoroff_1-0" class="reference"><a href="#cite_note-Fedoroff-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup>
</p>
</td></tr>
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<td><a href="Schmelzpunkt" title="Schmelzpunkt">Schmelzpunkt</a>
</td>
<td>
<p>224 °C<sup id="cite_ref-Fedoroff_1-1" class="reference"><a href="#cite_note-Fedoroff-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup>
</p>
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<th colspan="2" style="background:#FFDEAD; color:#202122;">Sicherheitshinweise
</th></tr>
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<td colspan="2">
<table cellspacing="0" cellpadding="2" style="width:100%;">
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<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><br><i>keine Einstufung verfügbar</i><sup id="cite_ref-NV_2-0" class="reference"><a href="#cite_note-NV-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup>
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</td></tr>
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<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>QDX</b> ist ein <a href="Sprengstoff" title="Sprengstoff">Sprengstoff</a> aus der Gruppe der <a href="Nitramine" title="Nitramine">Nitramine</a>, der strukturell mit <a href="Oktogen" title="Oktogen">Oktogen</a> verwandt ist. Bei der Herstellung von Oktogen fällt QDX als Nebenprodukt an.<sup id="cite_ref-3" class="reference"><a href="#cite_note-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup>
</p>
<div class="mw-heading mw-heading2"><h2 id="Gewinnung_und_Darstellung">Gewinnung und Darstellung</h2></div>
<p>QDX kann durch Nitrolyse von <a href="Hexamin" class="mw-redirect" title="Hexamin">Hexamin</a> oder durch <a href="Oxidation" title="Oxidation">Oxidation</a> von 1-Aceto-3,7-dinitro-5-nitroso-1,3,5,7-tetrazacyclooctan mit <a href="Salpeters%C3%A4ure" title="Salpetersäure">Salpetersäure</a> oder einer Mischung aus Salpetersäure und <a href="Wasserstoffperoxid" title="Wasserstoffperoxid">Wasserstoffperoxid</a> gewonnen werden.<sup id="cite_ref-Fedoroff_1-2" class="reference"><a href="#cite_note-Fedoroff-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup>
</p>
<div class="mw-heading mw-heading2"><h2 id="Toxikologie">Toxikologie</h2></div>
<p>Der Stoff kann sowohl oral, als auch über die Haut aufgenommen werden. Im Tierversuch erzeugte QDX bei Kaninchen und Ratten Schädigungen der Leber, <a href="Hypermotilit%C3%A4t" class="mw-redirect" title="Hypermotilität">Hypermotilität</a> des <a href="Magen-Darm-Trakt" class="mw-redirect" title="Magen-Darm-Trakt">Gastrointestinaltrakts</a> und Durchfall.<sup id="cite_ref-Chem_SIS_4-0" class="reference"><a href="#cite_note-Chem_SIS-4"><span class="cite-bracket">[</span>4<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-Fedoroff-1"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-Fedoroff_1-0">a</a></sup> <sup><a href="#cite_ref-Fedoroff_1-1">b</a></sup> <sup><a href="#cite_ref-Fedoroff_1-2">c</a></sup></span> <span class="reference-text">Basil Timothy Fedoroff: <cite style="font-style:italic">Encyclopedia of Explosives and Related Items</cite>. Picatinny Arsenal, 1960 (<a rel="nofollow" class="external text" href="https://books.google.de/books?id=-sNTAAAAMAAJ&pg=SL1-PA49&lpg=SL1-PA49">books.google.de</a>).<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:QDX&rft.au=Basil+Timothy+Fedoroff&rft.btitle=Encyclopedia+of+Explosives+and+Related+Items&rft.date=1960&rft.genre=book&rft.pub=Picatinny+Arsenal" style="display:none"> </span></span>
</li>
<li id="cite_note-NV-2"><span class="mw-cite-backlink"><a href="#cite_ref-NV_2-0">↑</a></span> <span class="reference-text">Dieser Stoff wurde in Bezug auf seine Gefährlichkeit entweder noch nicht eingestuft oder eine verlässliche und zitierfähige Quelle hierzu wurde noch nicht gefunden.</span>
</li>
<li id="cite_note-3"><span class="mw-cite-backlink"><a href="#cite_ref-3">↑</a></span> <span class="reference-text">Elizabeth P. Burrows, Ernst E. Brueggemann: <i>Reversed-phase gradient high-performance liquid chromatography of nitramine munitions and characterization of munitions process samples by gas chromatography-mass spectrometry</i>. Journal of Chromatography, Volume 329, 1985, S. 285–289, <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/S0021-9673%2801%2981932-4">10.1016/S0021-9673(01)81932-4</a></span>.</span>
</li>
<li id="cite_note-Chem_SIS-4"><span class="mw-cite-backlink"><a href="#cite_ref-Chem_SIS_4-0">↑</a></span> <span class="reference-text">Eintrag zu <span style="font-style:italic;"><a rel="nofollow" class="external text" href="https://chem.nlm.nih.gov/chemidplus/rn/13980-00-2">1,3,5,7-Tetrazocine, octahydro-1-acetyl-3,5,7-trinitro-</a></span> in der <a href="ChemIDplus" title="ChemIDplus">ChemIDplus</a>-Datenbank der <a href="United_States_National_Library_of_Medicine" title="United States National Library of Medicine">United States National Library of Medicine</a> (NLM) <small>(Seite nicht mehr abrufbar<span style="display:none;" class="editoronly">, Inhalt nun verfügbar via PubChem ID <span class="wikidata-content"><a rel="nofollow" class="external text" href="https://pubchem.ncbi.nlm.nih.gov/compound/26367">26367</a></span></span>)</small><span class="editoronly" style="display:none;"></span></span>
</li>
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