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<h1 id="firstHeading" class="firstHeading mw-first-heading"><span class="mw-page-title-main">Tribromethanol</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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<tr>
<th colspan="2" style="background:#FFDEAD; color:#202122;">Allgemeines
</th></tr>
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<td style="width:33%;">Name
</td>
<td>Tribromethanol
</td></tr>
<tr>
<td>Andere Namen
</td>
<td>
<ul><li>2,2,2-Tribromethanol (<a href="IUPAC-Nomenklatur" class="mw-redirect" title="IUPAC-Nomenklatur">IUPAC</a>)</li>
<li>Tribromethylalkohol</li>
<li>Bromethol</li>
<li>Ethobrom</li>
<li>Avertin (Lösung in <a href="2-Methyl-2-butanol" title="2-Methyl-2-butanol"><i>tert</i>-Amylalkohol</a>)</li></ul>
</td></tr>
<tr>
<td><a href="Summenformel" title="Summenformel">Summenformel</a>
</td>
<td>Br<sub>3</sub>CCH<sub>2</sub>OH
</td></tr>
<tr>
<td>Kurzbeschreibung
</td>
<td>
<p>beiger Feststoff<sup id="cite_ref-Sigma_1-0" class="reference"><a href="#cite_note-Sigma-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=75-80-9">75-80-9</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">200-903-1
</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/100.000.822">100.000.822</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/6400">6400</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.6160.html">6160</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/Q25105561" class="extiw external" title="d:Q25105561">Q25105561</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>282,76 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<sup id="cite_ref-Sigma_1-1" class="reference"><a href="#cite_note-Sigma-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup>
</p>
</td></tr>
<tr>
<td><a href="Schmelzpunkt" title="Schmelzpunkt">Schmelzpunkt</a>
</td>
<td>
<p>73–79 <a href="Grad_Celsius" title="Grad Celsius">°C</a><sup id="cite_ref-Sigma_1-2" class="reference"><a href="#cite_note-Sigma-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup>
</p>
</td></tr>
<tr>
<td><a href="Siedepunkt" title="Siedepunkt">Siedepunkt</a>
</td>
<td>
<p>92–93 °C (10 mmHg)<sup id="cite_ref-Sigma_1-3" class="reference"><a href="#cite_note-Sigma-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup>
</p>
</td></tr>
<tr>
<td><a href="L%C3%B6slichkeit" title="Löslichkeit">Löslichkeit</a>
</td>
<td>
<p>löslich in Wasser (25 g·l<sup>−1</sup> bei 40 °C)<sup id="cite_ref-GESTIS_2-0" class="reference"><a href="#cite_note-GESTIS-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;">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-GESTIS_2-1" class="reference"><a href="#cite_note-GESTIS-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><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="07 – Achtung"></a></span>
</td></tr></tbody></table>
<p><b>Achtung</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="Gesundheitsschädlich bei Verschlucken.">302</span></span></a>‐<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="Verursacht Hautreizungen.">315</span></span></a>‐<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="Verursacht schwere Augenreizung.">319</span></span></a>‐<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 die Atemwege reizen.">335</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="Einatmen von Staub / Rauch / Gas / Nebel / Dampf / Aerosol vermeiden.">261</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 Kontakt mit den Augen: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach Möglichkeit entfernen. Weiter spülen.
(Geänderter Text seit Inkraftreten der „8. Anpassung an den Technischen Fortschritt“ am 1. Februar 2018)">305+351+338</span></span></a><sup id="cite_ref-GESTIS_2-2" class="reference"><a href="#cite_note-GESTIS-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).
</td></tr></tbody></table><p><span class="editoronly" style="display:none;"></span>
</p><p><b>Tribromethanol</b> (älter <i>Tribromäthanol</i>) ist eine <a href="Chemische_Verbindung" title="Chemische Verbindung">chemische Verbindung</a> aus der Gruppe der <a href="Alkohole" title="Alkohole">Alkohole</a>. Es wird in der Veterinärmedizin als <a href="Sedativ" class="mw-redirect" title="Sedativ">Sedativ</a> zur <a href="Intraperitoneal" title="Intraperitoneal">intraperitonealen</a> <a href="Narkose" title="Narkose">Injektionsnarkose</a> von <a href="Nagetiere" title="Nagetiere">Nagetieren</a> verwendet.<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><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>
</p><p>Tribromethanol wurde 1917 von <a href="Richard_Willst%C3%A4tter" title="Richard Willstätter">Richard Willstätter</a> entdeckt und als <i><b>Avertin</b></i> 1926/1927 von <a href="Fritz_Eichholtz" title="Fritz Eichholtz">Fritz Eichholtz</a> und <a href="Otto_Butzengeiger" title="Otto Butzengeiger">Otto Butzengeiger</a> zum ersten Mal klinisch, als rektales Narkotikum, angewendet. <a href="Martin_Kirschner_(Mediziner%2C_1879)" title="Martin Kirschner (Mediziner, 1879)">Martin Kirschner</a> benutzte es 1929 erfolgreich zur intravenösen Narkose.<sup id="cite_ref-Diepgen_5-0" class="reference"><a href="#cite_note-Diepgen-5"><span class="cite-bracket">[</span>5<span class="cite-bracket">]</span></a></sup><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>
</p>
<div class="mw-heading mw-heading2"><h2 id="Synthese">Synthese</h2></div>
<p>2,2,2-Tribromethanol wird durch <a href="Chemische_Reaktion" title="Chemische Reaktion">Reaktion</a> von <a href="Aluminiumethoxid" class="mw-redirect" title="Aluminiumethoxid">Aluminiumethoxid</a> und <a href="Chemisches_Element" title="Chemisches Element">elementarem</a> Brom hergestellt.<sup id="cite_ref-Kar_7-0" class="reference"><a href="#cite_note-Kar-7"><span class="cite-bracket">[</span>7<span class="cite-bracket">]</span></a></sup>
</p>
<div class="mw-heading mw-heading2"><h2 id="Anwendungen">Anwendungen</h2></div>
<p>Tribromethanol wird als <a href="Konzentrat" title="Konzentrat">Konzentrat</a> in einer Massenkonzentration von 55 % in <a href="2-Methyl-2-butanol" title="2-Methyl-2-butanol">tertiärem Amylalkohol</a> unter dem Namen <i>Avertin</i> zur als Injektionsnarkose durchgeführten <b>Avertinnarkose</b><sup id="cite_ref-Diepgen_5-1" class="reference"><a href="#cite_note-Diepgen-5"><span class="cite-bracket">[</span>5<span class="cite-bracket">]</span></a></sup> verwendet;<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> dieses wird als 1,2–2,5 % Lösung in <a href="Physiologische_Kochsalzl%C3%B6sung" class="mw-redirect" title="Physiologische Kochsalzlösung">physiologischer Kochsalzlösung</a> appliziert.<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><sup id="cite_ref-10" class="reference"><a href="#cite_note-10"><span class="cite-bracket">[</span>10<span class="cite-bracket">]</span></a></sup> Alternativ werden Tribromethanol mit <a href="Buprenorphin" title="Buprenorphin">Buprenorphin</a> oder <a href="Ketamin" title="Ketamin">Ketamin</a> mit <a href="Xylazin" title="Xylazin">Xylazin</a> verwendet. Während die <a href="Toxizit%C3%A4t" title="Toxizität">Toxizität</a> gering und der <a href="Therapeutischer_Index" class="mw-redirect" title="Therapeutischer Index">therapeutische Index</a> groß ist, wurde die narkotische Wirkung als variabel beschrieben.<sup id="cite_ref-11" class="reference"><a href="#cite_note-11"><span class="cite-bracket">[</span>11<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-Sigma-1"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-Sigma_1-0">a</a></sup> <sup><a href="#cite_ref-Sigma_1-1">b</a></sup> <sup><a href="#cite_ref-Sigma_1-2">c</a></sup> <sup><a href="#cite_ref-Sigma_1-3">d</a></sup></span> <span class="reference-text">Datenblatt <span style="font-style:italic;"><a rel="nofollow" class="external text" href="https://www.sigmaaldrich.com/catalog/product/ALDRICH/T48402">2,2,2-Tribromoethanol, 97%</a></span> bei <a href="Sigma-Aldrich" title="Sigma-Aldrich">Sigma-Aldrich</a>, abgerufen am 2. April 2017 (<a rel="nofollow" class="external text" href="https://www.sigmaaldrich.com/DE/de/sds/ALDRICH/T48402?userType=anonymous">PDF</a>).<span class="editoronly" style="display:none;"></span></span>
</li>
<li id="cite_note-GESTIS-2"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-GESTIS_2-0">a</a></sup> <sup><a href="#cite_ref-GESTIS_2-1">b</a></sup> <sup><a href="#cite_ref-GESTIS_2-2">c</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=492393">2,2,2-Tribromethanol</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 20. November 2022.<small class="noscript"><span></span> (JavaScript erforderlich)</small></span>
</li>
<li id="cite_note-3"><span class="mw-cite-backlink"><a href="#cite_ref-3">↑</a></span> <span class="reference-text"><span class="cite"><a rel="nofollow" class="external text" href="https://cshprotocols.cshlp.org/content/2006/1/pdb.rec701.full?text_only=true"><i>Tribromoethanol (Avertin).</i></a> In: <i>Cold Spring Harbor Protocols.</i> <a href="Cold_Spring_Harbor_Laboratory" title="Cold Spring Harbor Laboratory">Cold Spring Harbor Laboratory</a><span style="display:none">;</span><span class="Abrufdatum" style="display:none"> abgerufen im 1. Januar 1</span> (englisch).</span><span style="display: none;" class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&rfr_id=info%3Asid%2Fde.wikipedia.org%3ATribromethanol&rft.title=Tribromoethanol+%28Avertin%29&rft.description=Tribromoethanol+%28Avertin%29&rft.identifier=&rft.publisher=%5B%5BCold+Spring+Harbor+Laboratory%5D%5D&rft.date=&rft.language=en"> </span></span>
</li>
<li id="cite_note-4"><span class="mw-cite-backlink"><a href="#cite_ref-4">↑</a></span> <span class="reference-text">R. E. Meyer, R. E. Fish: <i>A review of tribromoethanol anesthesia for production of genetically engineered mice and rats.</i> In: <i>Lab animal.</i> Band 34, Nummer 10, November 2005, S. 47–52, <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/10.1038/laban1105-47">10.1038/laban1105-47</a></span>, <a class="external mw-magiclink-pmid" rel="nofollow" href="https://www.ncbi.nlm.nih.gov/pubmed/16261153?dopt=Abstract">PMID 16261153</a>.</span>
</li>
<li id="cite_note-Diepgen-5"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-Diepgen_5-0">a</a></sup> <sup><a href="#cite_ref-Diepgen_5-1">b</a></sup></span> <span class="reference-text"><a href="Paul_Diepgen" title="Paul Diepgen">Paul Diepgen</a>, <a href="Heinz_Goerke" title="Heinz Goerke">Heinz Goerke</a>: <i>Aschoff/Diepgen/Goerke: Kurze Übersichtstabelle zur Geschichte der Medizin.</i> 1960, S. 66.</span>
</li>
<li id="cite_note-6"><span class="mw-cite-backlink"><a href="#cite_ref-6">↑</a></span> <span class="reference-text">H. Orth, I. Kis: <i>Schmerzbekämpfung und Narkose.</i> In: Franz Xaver Sailer, Friedrich Wilhelm Gierhake (Hrsg.): <i>Chirurgie historisch gesehen. Anfang – Entwicklung – Differenzierung.</i> Dustri-Verlag, Deisenhofen bei München 1973, ISBN 3-87185-021-7, S. 1–32, hier: S. 16 und 26.</span>
</li>
<li id="cite_note-Kar-7"><span class="mw-cite-backlink"><a href="#cite_ref-Kar_7-0">↑</a></span> <span class="reference-text">A. Kar: <i>Medicinal Chemistry</i>, Verlag New Age International, 2005, S. 66, ISBN 9788122415650. (<a rel="nofollow" class="external text" href="https://books.google.de/books?id=07g30rxCA0EC&pg=PA66#v=onepage">eingeschränkte Vorschau</a> in der Google-Buchsuche).</span>
</li>
<li id="cite_note-8"><span class="mw-cite-backlink"><a href="#cite_ref-8">↑</a></span> <span class="reference-text">F. Butzengeiger, A. Jüttemann: <i>Zur Geschichte des 1927 eingeführten Narkotikums Avertin.</i> In: <i>Anästh Intensivmed.</i> 58, 2017, S. 268–273.</span>
</li>
<li id="cite_note-9"><span class="mw-cite-backlink"><a href="#cite_ref-9">↑</a></span> <span class="reference-text"><span class="cite"><a rel="nofollow" class="external text" href="https://web.archive.org/web/20170126114843/https://ncifrederick.cancer.gov/Lasp/Acuc/Frederick/Media/Documents/ACUC32.pdf"><i>Guidelines for the Use of Tribromoethanol/Avertin Anesthesia.</i></a> <a href="National_Cancer_Institute" title="National Cancer Institute">National Cancer Institute</a>, archiviert vom <style data-mw-deduplicate="TemplateStyles:r250917974">
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</style><span class="dewiki-iconexternal"><a class="external text" href="https://redirecter.toolforge.org/?url=https%3A%2F%2Fncifrederick.cancer.gov%2Flasp%2Facuc%2Ffrederick%2FMedia%2FDocuments%2FACUC32.pdf">Original</a></span> am <span style="white-space:nowrap;">26. Januar 2017</span><span>;</span><span class="Abrufdatum"> abgerufen am 2. April 2017</span> (englisch).</span><span style="display: none;" class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&rfr_id=info%3Asid%2Fde.wikipedia.org%3ATribromethanol&rft.title=Guidelines+for+the+Use+of+Tribromoethanol%2FAvertin+Anesthesia&rft.description=Guidelines+for+the+Use+of+Tribromoethanol%2FAvertin+Anesthesia&rft.identifier=https%3A%2F%2Fweb.archive.org%2Fweb%2F20170126114843%2Fhttps%3A%2F%2Fncifrederick.cancer.gov%2FLasp%2FAcuc%2FFrederick%2FMedia%2FDocuments%2FACUC32.pdf&rft.publisher=%5B%5BNational+Cancer+Institute%5D%5D&rft.date=&rft.source=https://ncifrederick.cancer.gov/lasp/acuc/frederick/Media/Documents/ACUC32.pdf&rft.language=en"> </span></span>
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<li id="cite_note-10"><span class="mw-cite-backlink"><a href="#cite_ref-10">↑</a></span> <span class="reference-text">J. Weiss, F. Zimmermann: <a rel="nofollow" class="external text" href="http://journals.sagepub.com/doi/pdf/10.1258/002367799780578417"><i>Tribromoethanol (Avertin) as an anaesthetic in mice.</i></a> In: <i>Laboratory animals.</i> Band 33, Nummer 2, April 1999, S. 192–193, <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/10.1258/002367799780578417">10.1258/002367799780578417</a></span>, <a class="external mw-magiclink-pmid" rel="nofollow" href="https://www.ncbi.nlm.nih.gov/pubmed/10780824?dopt=Abstract">PMID 10780824</a>.</span>
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<li id="cite_note-11"><span class="mw-cite-backlink"><a href="#cite_ref-11">↑</a></span> <span class="reference-text">W. A. Hill, J. T. Tubbs, C. L. Carter, J. A. Czarra, K. M. Newkirk, T. E. Sparer, B. Rohrbach, C. M. Egger: <i>Repeated administration of tribromoethanol in C57BL/6NHsd mice.</i> In: <i>Journal of the American Association for Laboratory Animal Science : JAALAS.</i> Band 52, Nummer 2, März 2013, S. 176–179, <a class="external mw-magiclink-pmid" rel="nofollow" href="https://www.ncbi.nlm.nih.gov/pubmed/23562101?dopt=Abstract">PMID 23562101</a>, <a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3624786/">PMC 3624786</a> (freier Volltext).</span>
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