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		<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;&amp;#039;&amp;#039;&amp;#039;Phenylhydroxylamine&amp;#039;&amp;#039;&amp;#039; is an [[organic compound]] with the formula C6H5NHOH. It is a white solid that is used in organic synthesis and as a reagent in the production of pharmaceuticals and agrochemicals. &lt;br /&gt;
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== Structure and properties ==&lt;br /&gt;
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Phenylhydroxylamine is a [[hydroxylamine]] derivative where the hydroxyl group is directly attached to a [[phenyl group]]. It is a weak [[base]] and can form salts with acids. The compound is stable under normal conditions, but it can decompose upon heating, releasing toxic fumes of nitrogen oxides.&lt;br /&gt;
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== Synthesis ==&lt;br /&gt;
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Phenylhydroxylamine can be synthesized from [[nitrobenzene]] by reduction with [[zinc]] and [[hydrochloric acid]]. The reaction proceeds via the intermediate formation of [[phenylhydroxylammonium chloride]], which is then neutralized with a base to give the free amine.&lt;br /&gt;
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== Applications ==&lt;br /&gt;
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Phenylhydroxylamine is used as a reagent in organic synthesis. It can be used to convert [[ketones]] and [[aldehydes]] into [[oximes]], which can then be reduced to amines. It is also used in the synthesis of pharmaceuticals and agrochemicals.&lt;br /&gt;
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== Safety ==&lt;br /&gt;
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Phenylhydroxylamine is harmful if swallowed, inhaled, or comes into contact with skin. It can cause burns and eye damage. Appropriate safety measures should be taken when handling this compound.&lt;br /&gt;
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[[File:Phenylhydroxylamine.png|thumb|right|200px|Structure of phenylhydroxylamine]]&lt;br /&gt;
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== See also ==&lt;br /&gt;
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* [[Hydroxylamine]]&lt;br /&gt;
* [[Nitrobenzene]]&lt;br /&gt;
* [[Phenyl group]]&lt;br /&gt;
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== References ==&lt;br /&gt;
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{{chemistry-stub}}&lt;br /&gt;
[[Category:Organic compounds]]&lt;br /&gt;
[[Category:Amines]]&lt;br /&gt;
[[Category:Phenyl compounds]]&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
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