<?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=Azine</id>
	<title>Azine - Revision history</title>
	<link rel="self" type="application/atom+xml" href="https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=Azine"/>
	<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=Azine&amp;action=history"/>
	<updated>2026-04-26T09:47:15Z</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=Azine&amp;diff=6416835&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=Azine&amp;diff=6416835&amp;oldid=prev"/>
		<updated>2025-03-03T05:37:53Z</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;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;tr class=&quot;diff-title&quot; lang=&quot;en&quot;&gt;
				&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 05:37, 3 March 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-l34&quot;&gt;Line 34:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 34:&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:Chemical compounds]]&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:Chemical compounds]]&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;{{Chemistry-stub}}&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;{{Chemistry-stub}}&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;== Azine gallery ==&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:Azine.png|Azine&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:Pechiney-Ugine-Kuhlmann process.png|Pechiney-Ugine-Kuhlmann process&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:Lasri condensation reaction.svg|Lasri condensation reaction&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:Acetone azine chem.png|Acetone azine chem&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;!-- diff cache key wikimd4:diff:1.41:old-5484475:rev-6416835:php=table --&gt;
&lt;/table&gt;</summary>
		<author><name>Prab</name></author>
	</entry>
	<entry>
		<id>https://wikimd.org/index.php?title=Azine&amp;diff=5484475&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=Azine&amp;diff=5484475&amp;oldid=prev"/>
		<updated>2024-04-03T01:54:24Z</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;{{png-image}}&amp;#039;&amp;#039;&amp;#039;Azine&amp;#039;&amp;#039;&amp;#039; refers to a class of organic compounds characterized by the presence of a nitrogen (N) double bond within a six-membered aromatic ring. The term is often used in the context of various chemical compounds, including those found in pharmaceuticals, dyes, and agricultural chemicals. Azines play a crucial role in the field of [[organic chemistry]] and have applications in [[synthetic chemistry]], [[pharmaceuticals]], and [[material science]].&lt;br /&gt;
&lt;br /&gt;
==Structure and Classification==&lt;br /&gt;
Azines are characterized by their core structure, which includes a six-membered aromatic ring containing one or more nitrogen atoms double-bonded to carbon atoms within the ring. This structure is a common motif in many organic compounds and can be classified based on the number of nitrogen atoms present in the ring. The most common types of azines include:&lt;br /&gt;
&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;Pyridine&amp;#039;&amp;#039;&amp;#039;: A basic structure with one nitrogen atom.&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;Pyrazine&amp;#039;&amp;#039;&amp;#039;: Contains two nitrogen atoms at the 1,4-positions.&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;Pyrimidine&amp;#039;&amp;#039;&amp;#039;: Features two nitrogen atoms at the 1,3-positions.&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;Pyridazine&amp;#039;&amp;#039;&amp;#039;: Has two nitrogen atoms at the 1,2-positions.&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;Triazines&amp;#039;&amp;#039;&amp;#039;: Contain three nitrogen atoms, with s-triazine being the most common, where the nitrogen atoms are at the 1,3,5-positions.&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
The synthesis of azines typically involves methods that allow for the introduction of nitrogen atoms into carbon-rich frameworks. Common approaches include:&lt;br /&gt;
&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;Condensation reactions&amp;#039;&amp;#039;&amp;#039;: Where carbon-nitrogen bonds are formed through the reaction of carbonyl compounds with ammonia or amines.&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;Cyclization reactions&amp;#039;&amp;#039;&amp;#039;: Involving the formation of a ring structure from linear or branched precursors containing the necessary carbon and nitrogen atoms.&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;Substitution reactions&amp;#039;&amp;#039;&amp;#039;: Where a nitrogen-containing group replaces a functional group in a pre-existing aromatic compound.&lt;br /&gt;
&lt;br /&gt;
==Applications==&lt;br /&gt;
Azines find a wide range of applications across various industries due to their unique chemical properties:&lt;br /&gt;
&lt;br /&gt;
* In [[pharmaceuticals]], azines are part of the structure of many drugs, contributing to their therapeutic effects.&lt;br /&gt;
* In [[agrochemicals]], certain azine derivatives serve as active ingredients in pesticides and herbicides.&lt;br /&gt;
* In [[dye industry|dyes]] and pigments, azines are used to impart color to textiles and other materials.&lt;br /&gt;
* In [[material science]], azine compounds are explored for their potential in creating new materials with specific electronic, optical, or mechanical properties.&lt;br /&gt;
&lt;br /&gt;
==Environmental and Health Aspects==&lt;br /&gt;
While azines are valuable in many applications, their environmental and health impacts depend on the specific compound and its use. Some azine derivatives may be toxic or hazardous, necessitating careful handling and disposal. Regulatory bodies oversee the use of these compounds to ensure safety and environmental protection.&lt;br /&gt;
&lt;br /&gt;
==Conclusion==&lt;br /&gt;
Azines represent a significant and versatile class of organic compounds with wide-ranging applications in modern science and industry. Their synthesis, structure, and functionalization continue to be areas of active research, driving advancements in various fields.&lt;br /&gt;
&lt;br /&gt;
[[Category:Organic compounds]]&lt;br /&gt;
[[Category:Chemical compounds]]&lt;br /&gt;
{{Chemistry-stub}}&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
	</entry>
</feed>