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1-Naphthylamine - Revision history
2026-04-27T00:12:19Z
Revision history for this page on the wiki
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https://wikimd.org/index.php?title=1-Naphthylamine&diff=6309000&oldid=prev
Prab: CSV import
2025-02-18T00:42:59Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 00:42, 18 February 2025</td>
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<tr><td class="diff-marker"></td><td style="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;"><div>File:1-Naphthylamine-3D-balls.png|1-Naphthylamine 3D balls</div></td><td class="diff-marker"></td><td style="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;"><div>File:1-Naphthylamine-3D-balls.png|1-Naphthylamine 3D balls</div></td></tr>
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<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="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;"><div><ins style="font-weight: bold; text-decoration: none;">== 1-Naphthylamine ==</ins></div></td></tr>
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Prab: CSV import
2025-02-17T01:54:55Z
<p>CSV import</p>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 01:54, 17 February 2025</td>
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2025-02-11T20:15:50Z
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<p><b>New page</b></p><div>= 1-Naphthylamine =<br />
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[[File:1-Naphthylamine.png|thumb|Chemical structure of 1-Naphthylamine]]<br />
[[File:1-Naphthylamine-3D-balls.png|thumb|3D model of 1-Naphthylamine]]<br />
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'''1-Naphthylamine''' is an organic compound with the formula C__H_NH_. It is one of the two isomeric naphthylamines, the other being [[2-Naphthylamine]]. 1-Naphthylamine is a derivative of [[naphthalene]], consisting of a naphthalene ring system with an amino group attached to the first carbon atom.<br />
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== Structure and Properties ==<br />
1-Naphthylamine is a crystalline solid that is typically colorless to pale yellow. It has a characteristic odor and is soluble in organic solvents. The compound exhibits basic properties due to the presence of the amino group, which can participate in hydrogen bonding and other interactions.<br />
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== Synthesis ==<br />
1-Naphthylamine can be synthesized through the reduction of 1-nitronaphthalene, which is itself derived from the nitration of [[naphthalene]]. The reduction process typically involves the use of iron and hydrochloric acid or other reducing agents.<br />
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== Applications ==<br />
1-Naphthylamine is used in the production of dyes, particularly azo dyes, where it serves as a precursor. It is also employed in the synthesis of various organic compounds and as an intermediate in the manufacture of [[pharmaceuticals]].<br />
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== Health and Safety ==<br />
1-Naphthylamine is considered a hazardous substance. It is classified as a potential [[carcinogen]], and exposure to it should be minimized. Proper safety measures, including the use of personal protective equipment and adequate ventilation, are essential when handling this compound.<br />
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== Environmental Impact ==<br />
Due to its potential health risks, the release of 1-naphthylamine into the environment is regulated. It can pose a threat to aquatic life and should be disposed of in accordance with environmental regulations.<br />
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== Related Compounds ==<br />
* [[2-Naphthylamine]]<br />
* [[Naphthalene]]<br />
* [[Aniline]]<br />
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== Related Pages ==<br />
* [[Aromatic amine]]<br />
* [[Azo dye]]<br />
* [[Carcinogen]]<br />
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== Gallery ==<br />
<gallery><br />
File:1-Naphthylamine.png|Chemical structure of 1-Naphthylamine<br />
File:1-Naphthylamine-3D-balls.png|3D model of 1-Naphthylamine<br />
</gallery><br />
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[[Category:Aromatic amines]]<br />
[[Category:Carcinogens]]<br />
[[Category:Chemical compounds]]</div>
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