<?xml version="1.0"?>
<feed xmlns="http://www.w3.org/2005/Atom" xml:lang="en">
	<id>https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=Allyl_mercaptan</id>
	<title>Allyl mercaptan - Revision history</title>
	<link rel="self" type="application/atom+xml" href="https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=Allyl_mercaptan"/>
	<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=Allyl_mercaptan&amp;action=history"/>
	<updated>2026-04-26T07:09:29Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
	<generator>MediaWiki 1.44.2</generator>
	<entry>
		<id>https://wikimd.org/index.php?title=Allyl_mercaptan&amp;diff=6294001&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=Allyl_mercaptan&amp;diff=6294001&amp;oldid=prev"/>
		<updated>2025-02-15T11:01:39Z</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;== Allyl Mercaptan ==&lt;br /&gt;
&lt;br /&gt;
[[File:allyl_mercaptan.svg|thumb|right|Chemical structure of allyl mercaptan]]&lt;br /&gt;
&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;Allyl mercaptan&amp;#039;&amp;#039;&amp;#039; is an organosulfur compound with the chemical formula C&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;6&amp;lt;/sub&amp;gt;S. It is a member of the [[thiol]] family, characterized by the presence of a [[sulfhydryl group]] (-SH) attached to an [[allyl group]]. This compound is known for its strong odor, reminiscent of [[garlic]], and is found naturally in [[Allium]] species such as [[garlic]] and [[onion]].&lt;br /&gt;
&lt;br /&gt;
== Chemical Properties ==&lt;br /&gt;
&lt;br /&gt;
Allyl mercaptan is a colorless liquid at room temperature. It is soluble in organic solvents and slightly soluble in water. The presence of the thiol group makes it reactive, particularly in forming [[disulfide]] bonds. This reactivity is utilized in various chemical synthesis processes.&lt;br /&gt;
&lt;br /&gt;
== Biological Significance ==&lt;br /&gt;
&lt;br /&gt;
In nature, allyl mercaptan is a breakdown product of [[allicin]], a compound found in garlic. It is believed to contribute to the health benefits associated with garlic consumption, including [[antimicrobial]] and [[antioxidant]] properties. Studies suggest that allyl mercaptan may play a role in [[cardiovascular health]] by influencing [[cholesterol]] metabolism and [[blood pressure]] regulation.&lt;br /&gt;
&lt;br /&gt;
== Industrial Applications ==&lt;br /&gt;
&lt;br /&gt;
Allyl mercaptan is used in the synthesis of [[polymers]] and as a flavoring agent in the food industry. Its strong odor is also utilized in [[odorant]] formulations to impart a garlic-like smell to products.&lt;br /&gt;
&lt;br /&gt;
== Safety and Handling ==&lt;br /&gt;
&lt;br /&gt;
Due to its strong odor and potential irritant properties, allyl mercaptan should be handled with care. It can cause irritation to the skin, eyes, and respiratory tract. Proper [[personal protective equipment]] (PPE) such as gloves and goggles should be worn when handling this chemical.&lt;br /&gt;
&lt;br /&gt;
== Related Pages ==&lt;br /&gt;
&lt;br /&gt;
* [[Thiol]]&lt;br /&gt;
* [[Allicin]]&lt;br /&gt;
* [[Organosulfur compound]]&lt;br /&gt;
* [[Garlic]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Organosulfur compounds]]&lt;br /&gt;
[[Category:Thiol chemistry]]&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
	</entry>
</feed>