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	<title>4-tert-Butylbenzoesäure Archives | Comedol-Chemie</title>
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	<title>4-tert-Butylbenzoesäure Archives | Comedol-Chemie</title>
	<link>https://comedol.de/produkt-schlagwort/4-tert-butylbenzoesaeure/</link>
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	<item>
		<title>para-tert. Butylbenzoesäure</title>
		<link>https://comedol.de/produkt/basis-chemie/chemie-von-a-z/chemikalien-p-t/chemikalien-mit-p/para-tert-butylbenzoesaeure/</link>
		
		<dc:creator><![CDATA[Praktiker]]></dc:creator>
		<pubDate>Tue, 27 Jun 2023 09:40:48 +0000</pubDate>
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					<description><![CDATA[<p>Para-tertiäre Butylbenzoesäure (PTBBA) zählt zu den organischen Verbindungen und wird den Derivaten der Benzoesäure zugeordnet. Sie findet vor allem Anwendung in der Kunststoffherstellung. PTBBA entsteht durch die Oxidation von flüssigem 4-tert-Butyltoluol an der Luft. Bei der großtechnischen Produktion wird ein optimiertes Verfahren angewendet, bei dem diese Reaktion mithilfe eines Katalysators wie Cobalt(II)-acetat gefördert wird.</p>
<p>&#160;</p>
<p>The post <a href="https://comedol.de/produkt/basis-chemie/chemie-von-a-z/chemikalien-p-t/chemikalien-mit-p/para-tert-butylbenzoesaeure/">para-tert. Butylbenzoesäure</a> appeared first on <a href="https://comedol.de">Comedol-Chemie</a>.</p>
]]></description>
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				<h4><strong>Sicherheitshinweise:</strong></h4>
<p>GHS-Gefahrstoffkennzeichnung aus Verordnung (EG) Nr. 1272/2008 (CLP), ggf. erweitert</p>

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				<h4>Andere Namen:</h4>
<p>4-T-BUTYLBENZOIC ACID<br />
TBBA<br />
p-TBBA<br />
4-tert-Butylbenzoesäure</p>

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				<h4>Eigenschaften:</h4>
<p>Para-tertiäre Butylbenzoesäure (PTBBA) gehört zur Gruppe der organischen Verbindungen und ist ein Derivat der Benzoesäure. Sie wird hauptsächlich in der Kunststoffherstellung eingesetzt. PTBBA entsteht durch die Oxidation von flüssigem 4-tert-Butyltoluol in Gegenwart von Luft.</p>

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				<h4>Löslichkeit:</h4>
<p>schwerlöslich in Wasser (0,3 g·l−1 bei 20 °C)<br />
löslich in Wasser (12,6 g·l−1 bei 20 °C (pH 7)<br />
löslich in Methanol, Ethanol, Aceton, Chloroform, Benzol, Toluol</p>

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				<h4>Dichte</h4>
<p>0,6 g·cm−3 bei 20 °C<br />
1,142 g·cm−3 bei 20 °C</p>

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				<h4>H- und P-Sätze:</h4>
<p>H: 302​‐​360F​‐​372​‐​412<br />
P: 201​‐​202​‐​273​‐​260​‐​301+312​‐​308+313</p>

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				<h4>Toxikologische Daten:</h4>
<p>473 mg·kg−1 (LD50, Ratte, oral)<br />
&gt;900mg· kg−1 (LD50, Kaninchen, transdermal)<br />
&gt;1,9 mg·l−1·4h−1 (LD50, Ratte, inh.)</p>

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				<h4>MAK:</h4>
<p>Schweiz: 2 mg·m−3 (gemessen als einatembarer Staub)</p>

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				<h4>Summenformel:</h4>
<p>C<sub>11</sub>H<sub>14</sub>O<sub>2</sub></p>

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				<h4>CAS-Nummer:</h4>
<p>98-73-7</p>

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				<h4>PubChem</h4>
<p>7403</p>

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				<h4>Kurzbeschreibung:</h4>
<p>weiße Flocken, weiße Schuppen, weißes-fast weißes Kristallpulver</p>

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				<h4>Molare Masse:</h4>
<p>178,23 g·mol−1</p>

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				<h4>Aggregatzustand:</h4>
<p>fest</p>

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				<h4>Schmelzpunkt:</h4>
<p>161–165 °C<br />
165–167 °C<br />
167 °C</p>

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				<h4>Siedepunkt:</h4>
<p>280 °C unter Zersetzung</p>

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				<h4>Dampfdruck:</h4>
<p>0,057 Pa bei 20 °C</p>

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			<h2>Andere Chemikalien aus dieser <span> Stoffgruppe </span></h2>
<p class="underscore"><p>
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</div><p>The post <a href="https://comedol.de/produkt/basis-chemie/chemie-von-a-z/chemikalien-p-t/chemikalien-mit-p/para-tert-butylbenzoesaeure/">para-tert. Butylbenzoesäure</a> appeared first on <a href="https://comedol.de">Comedol-Chemie</a>.</p>
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