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	<id>https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=Benzyl_bromide</id>
	<title>Benzyl bromide - Revision history</title>
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	<updated>2026-04-25T22:33:15Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>https://wikimd.org/index.php?title=Benzyl_bromide&amp;diff=5604848&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
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		<updated>2024-04-15T01:56:46Z</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;[[File:Darstellung_Benzylbromid.svg|thumb]] &amp;#039;&amp;#039;&amp;#039;Benzyl bromide&amp;#039;&amp;#039;&amp;#039; is a [[chemical compound]] with the formula C&amp;lt;sub&amp;gt;6&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;CH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;Br. This [[organic compound]] is a colorless liquid, although older samples can appear yellowish. The compound is often used as a [[reagent]] in [[organic synthesis]], particularly in the introduction of benzyl groups to various substrates. Benzyl bromide is known for its lachrymatory properties, making it a potent irritant to the eyes and respiratory system.&lt;br /&gt;
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==Properties==&lt;br /&gt;
Benzyl bromide has a boiling point of 198-199 °C and a density of 1.439 g/cm&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;. It is slightly soluble in [[water]], but it is highly soluble in organic solvents such as [[ethanol]], [[diethyl ether]], and [[chloroform]]. Due to its reactive bromide ion, benzyl bromide is a versatile building block in organic chemistry.&lt;br /&gt;
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==Synthesis==&lt;br /&gt;
Benzyl bromide is typically synthesized through the [[bromination]] of [[toluene]] with [[bromine]] in the presence of a [[Lewis acid]] catalyst such as [[ferric bromide]]. The reaction involves the free radical substitution of a hydrogen atom on the methyl group of toluene, resulting in the formation of benzyl bromide.&lt;br /&gt;
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==Applications==&lt;br /&gt;
In [[organic chemistry]], benzyl bromide is used primarily for the benzyl protection of alcohols and amines. The benzyl group (Bn) serves as a protective group that can be removed under specific conditions, allowing for further functionalization of the molecule without affecting the protected site. This compound is also employed in the synthesis of other benzyl derivatives and in the preparation of [[pharmaceuticals]], [[agrochemicals]], and [[fragrances]].&lt;br /&gt;
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==Safety==&lt;br /&gt;
Benzyl bromide is a highly toxic and corrosive substance. It is a strong irritant to the skin, eyes, and respiratory system. Proper safety precautions must be taken when handling this chemical, including the use of personal protective equipment (PPE) such as gloves, goggles, and respiratory protection. It should be used only in well-ventilated areas or under a chemical fume hood.&lt;br /&gt;
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==Environmental Impact==&lt;br /&gt;
Like many brominated organic compounds, benzyl bromide poses risks to the environment. It should be disposed of properly to prevent contamination of water sources and harm to aquatic life. Regulations may vary by region, but generally, disposal should be handled by qualified waste management services.&lt;br /&gt;
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[[Category:Organic compounds]]&lt;br /&gt;
[[Category:Bromides]]&lt;br /&gt;
[[Category:Chemical reagents]]&lt;br /&gt;
[[Category:Toxicology]]&lt;br /&gt;
{{Chem-stub}}&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
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