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	<id>https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=2%2C4%2C6-Tribromophenol</id>
	<title>2,4,6-Tribromophenol - Revision history</title>
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	<updated>2026-04-27T09:32:53Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://wikimd.org/index.php?title=2,4,6-Tribromophenol&amp;diff=6303009&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=2,4,6-Tribromophenol&amp;diff=6303009&amp;oldid=prev"/>
		<updated>2025-02-16T22:08:22Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 22:08, 16 February 2025&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l35&quot;&gt;Line 35:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 35:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Category:Phenols]]&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Category:Phenols]]&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Category:Flame retardants]]&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Category:Flame retardants]]&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;== 2,4,6-Tribromophenol ==&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;gallery&amp;gt;&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;File:2,4,6-Tribromphenol_Reaktionsschemata.svg&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;/gallery&amp;gt;&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Prab</name></author>
	</entry>
	<entry>
		<id>https://wikimd.org/index.php?title=2,4,6-Tribromophenol&amp;diff=6288451&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=2,4,6-Tribromophenol&amp;diff=6288451&amp;oldid=prev"/>
		<updated>2025-02-11T20:35:58Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;== 2,4,6-Tribromophenol ==&lt;br /&gt;
&lt;br /&gt;
[[File:2,4,6-Tribromphenol_Reaktionsschemata.svg|thumb|right|Chemical structure and reaction scheme of 2,4,6-Tribromophenol]]&lt;br /&gt;
&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;2,4,6-Tribromophenol&amp;#039;&amp;#039;&amp;#039; is a brominated derivative of [[phenol]], with the chemical formula C_H_Br_O. It is a white crystalline solid that is used in various industrial applications, including as a flame retardant and as an intermediate in the synthesis of other chemical compounds.&lt;br /&gt;
&lt;br /&gt;
== Chemical Properties ==&lt;br /&gt;
&lt;br /&gt;
2,4,6-Tribromophenol is characterized by the presence of three bromine atoms attached to the benzene ring of the phenol molecule. This substitution pattern significantly alters the chemical properties of the compound compared to [[phenol]]. The presence of bromine atoms increases the molecular weight and affects the compound&amp;#039;s reactivity and solubility.&lt;br /&gt;
&lt;br /&gt;
=== Synthesis ===&lt;br /&gt;
&lt;br /&gt;
2,4,6-Tribromophenol can be synthesized through the bromination of phenol. The reaction involves the substitution of hydrogen atoms on the aromatic ring with bromine atoms, typically using a brominating agent such as [[bromine]] or [[N-bromosuccinimide]] (NBS) in the presence of a catalyst.&lt;br /&gt;
&lt;br /&gt;
=== Reactivity ===&lt;br /&gt;
&lt;br /&gt;
The bromine atoms in 2,4,6-Tribromophenol make it more reactive than phenol. It can undergo further chemical reactions, such as [[nucleophilic substitution]] and [[oxidation]]. The compound is also known to form complexes with various metal ions, which can be utilized in different chemical processes.&lt;br /&gt;
&lt;br /&gt;
== Applications ==&lt;br /&gt;
&lt;br /&gt;
2,4,6-Tribromophenol is used in several industrial applications due to its flame-retardant properties. It is incorporated into [[polymers]] and [[plastics]] to reduce their flammability. Additionally, it serves as an intermediate in the synthesis of other brominated compounds, which are used in the production of [[pharmaceuticals]], [[pesticides]], and other specialty chemicals.&lt;br /&gt;
&lt;br /&gt;
== Safety and Environmental Impact ==&lt;br /&gt;
&lt;br /&gt;
Like many brominated compounds, 2,4,6-Tribromophenol is subject to scrutiny regarding its environmental impact and potential health effects. It is important to handle the compound with care, using appropriate safety measures to prevent exposure. The compound can persist in the environment and may contribute to [[brominated flame retardant]] pollution.&lt;br /&gt;
&lt;br /&gt;
== Related Pages ==&lt;br /&gt;
&lt;br /&gt;
* [[Phenol]]&lt;br /&gt;
* [[Bromine]]&lt;br /&gt;
* [[Flame retardant]]&lt;br /&gt;
* [[Brominated flame retardant]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Organobromides]]&lt;br /&gt;
[[Category:Phenols]]&lt;br /&gt;
[[Category:Flame retardants]]&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
	</entry>
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