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Azo compound - Wikipedia

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class="vector-toc-numb">3.1</span> <span>European regulation</span> </div> </a> <ul id="toc-European_regulation-sublist" class="vector-toc-list"> </ul> </li> </ul> </li> <li id="toc-See_also" class="vector-toc-list-item vector-toc-level-1 vector-toc-list-item-expanded"> <a class="vector-toc-link" href="#See_also"> <div class="vector-toc-text"> <span class="vector-toc-numb">4</span> <span>See also</span> </div> </a> <ul id="toc-See_also-sublist" class="vector-toc-list"> </ul> </li> <li id="toc-References" class="vector-toc-list-item vector-toc-level-1 vector-toc-list-item-expanded"> <a class="vector-toc-link" href="#References"> <div class="vector-toc-text"> <span class="vector-toc-numb">5</span> <span>References</span> </div> </a> <ul id="toc-References-sublist" class="vector-toc-list"> </ul> </li> </ul> </div> </div> </nav> </div> </div> <div class="mw-content-container"> <main id="content" class="mw-body"> <header class="mw-body-header vector-page-titlebar"> <nav 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class="firstHeading mw-first-heading"><span class="mw-page-title-main">Azo compound</span></h1> <div id="p-lang-btn" class="vector-dropdown mw-portlet mw-portlet-lang" > <input type="checkbox" id="p-lang-btn-checkbox" role="button" aria-haspopup="true" data-event-name="ui.dropdown-p-lang-btn" class="vector-dropdown-checkbox mw-interlanguage-selector" aria-label="Go to an article in another language. Available in 37 languages" > <label id="p-lang-btn-label" for="p-lang-btn-checkbox" class="vector-dropdown-label cdx-button cdx-button--fake-button cdx-button--fake-button--enabled cdx-button--weight-quiet cdx-button--action-progressive mw-portlet-lang-heading-37" aria-hidden="true" ><span class="vector-icon mw-ui-icon-language-progressive mw-ui-icon-wikimedia-language-progressive"></span> <span class="vector-dropdown-label-text">37 languages</span> </label> <div class="vector-dropdown-content"> <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li class="interlanguage-link interwiki-ar mw-list-item"><a href="https://ar.wikipedia.org/wiki/%D9%85%D8%B1%D9%83%D8%A8_%D8%A2%D8%B2%D9%88" title="مركب آزو – Arabic" lang="ar" hreflang="ar" data-title="مركب آزو" data-language-autonym="العربية" data-language-local-name="Arabic" class="interlanguage-link-target"><span>العربية</span></a></li><li class="interlanguage-link interwiki-ca mw-list-item"><a href="https://ca.wikipedia.org/wiki/Azocompost" title="Azocompost – Catalan" lang="ca" hreflang="ca" data-title="Azocompost" data-language-autonym="Català" data-language-local-name="Catalan" class="interlanguage-link-target"><span>Català</span></a></li><li class="interlanguage-link interwiki-cs mw-list-item"><a href="https://cs.wikipedia.org/wiki/Azoslou%C4%8Denina" title="Azosloučenina – Czech" lang="cs" hreflang="cs" data-title="Azosloučenina" data-language-autonym="Čeština" data-language-local-name="Czech" class="interlanguage-link-target"><span>Čeština</span></a></li><li class="interlanguage-link interwiki-da mw-list-item"><a href="https://da.wikipedia.org/wiki/Azoforbindelse" title="Azoforbindelse – Danish" lang="da" hreflang="da" data-title="Azoforbindelse" data-language-autonym="Dansk" data-language-local-name="Danish" class="interlanguage-link-target"><span>Dansk</span></a></li><li class="interlanguage-link interwiki-es mw-list-item"><a href="https://es.wikipedia.org/wiki/Azoderivado" title="Azoderivado – Spanish" lang="es" hreflang="es" data-title="Azoderivado" data-language-autonym="Español" data-language-local-name="Spanish" class="interlanguage-link-target"><span>Español</span></a></li><li class="interlanguage-link interwiki-eu mw-list-item"><a href="https://eu.wikipedia.org/wiki/Konposatu_azoiko" title="Konposatu azoiko – Basque" lang="eu" hreflang="eu" data-title="Konposatu azoiko" data-language-autonym="Euskara" data-language-local-name="Basque" class="interlanguage-link-target"><span>Euskara</span></a></li><li class="interlanguage-link interwiki-fa mw-list-item"><a href="https://fa.wikipedia.org/wiki/%D8%AA%D8%B1%DA%A9%DB%8C%D8%A8_%D8%A2%D8%B2%D9%88" title="ترکیب آزو – Persian" lang="fa" hreflang="fa" data-title="ترکیب آزو" data-language-autonym="فارسی" data-language-local-name="Persian" class="interlanguage-link-target"><span>فارسی</span></a></li><li class="interlanguage-link interwiki-fr mw-list-item"><a href="https://fr.wikipedia.org/wiki/Compos%C3%A9_azo%C3%AFque" title="Composé azoïque – French" lang="fr" hreflang="fr" data-title="Composé azoïque" data-language-autonym="Français" data-language-local-name="French" class="interlanguage-link-target"><span>Français</span></a></li><li class="interlanguage-link interwiki-ga mw-list-item"><a href="https://ga.wikipedia.org/wiki/As%C3%B3ruaim%C3%AD" title="Asóruaimí – Irish" lang="ga" hreflang="ga" data-title="Asóruaimí" data-language-autonym="Gaeilge" data-language-local-name="Irish" class="interlanguage-link-target"><span>Gaeilge</span></a></li><li class="interlanguage-link interwiki-gl mw-list-item"><a href="https://gl.wikipedia.org/wiki/Composto_azo" title="Composto azo – Galician" lang="gl" hreflang="gl" data-title="Composto azo" data-language-autonym="Galego" data-language-local-name="Galician" class="interlanguage-link-target"><span>Galego</span></a></li><li class="interlanguage-link interwiki-ko mw-list-item"><a href="https://ko.wikipedia.org/wiki/%EC%95%84%EC%A1%B0_%ED%99%94%ED%95%A9%EB%AC%BC" title="아조 화합물 – Korean" lang="ko" hreflang="ko" data-title="아조 화합물" data-language-autonym="한국어" data-language-local-name="Korean" class="interlanguage-link-target"><span>한국어</span></a></li><li class="interlanguage-link interwiki-hy mw-list-item"><a href="https://hy.wikipedia.org/wiki/%D4%B1%D5%A6%D5%B8%D5%B4%D5%AB%D5%A1%D6%81%D5%B8%D6%82%D5%A9%D5%B5%D5%B8%D6%82%D5%B6%D5%B6%D5%A5%D6%80" title="Ազոմիացություններ – Armenian" lang="hy" hreflang="hy" data-title="Ազոմիացություններ" data-language-autonym="Հայերեն" data-language-local-name="Armenian" class="interlanguage-link-target"><span>Հայերեն</span></a></li><li class="interlanguage-link interwiki-hi mw-list-item"><a href="https://hi.wikipedia.org/wiki/%E0%A4%90%E0%A4%9C%E0%A5%8B_%E0%A4%AF%E0%A5%8C%E0%A4%97%E0%A4%BF%E0%A4%95" title="ऐजो यौगिक – Hindi" lang="hi" hreflang="hi" data-title="ऐजो यौगिक" data-language-autonym="हिन्दी" data-language-local-name="Hindi" class="interlanguage-link-target"><span>हिन्दी</span></a></li><li class="interlanguage-link interwiki-id mw-list-item"><a href="https://id.wikipedia.org/wiki/Senyawa_azo" title="Senyawa azo – Indonesian" lang="id" hreflang="id" data-title="Senyawa azo" data-language-autonym="Bahasa Indonesia" data-language-local-name="Indonesian" class="interlanguage-link-target"><span>Bahasa Indonesia</span></a></li><li class="interlanguage-link interwiki-it mw-list-item"><a href="https://it.wikipedia.org/wiki/Azocomposti" title="Azocomposti – Italian" lang="it" hreflang="it" data-title="Azocomposti" data-language-autonym="Italiano" data-language-local-name="Italian" class="interlanguage-link-target"><span>Italiano</span></a></li><li class="interlanguage-link interwiki-he mw-list-item"><a href="https://he.wikipedia.org/wiki/%D7%90%D7%96%D7%95_(%D7%9B%D7%99%D7%9E%D7%99%D7%94)" title="אזו (כימיה) – Hebrew" lang="he" hreflang="he" data-title="אזו (כימיה)" data-language-autonym="עברית" data-language-local-name="Hebrew" class="interlanguage-link-target"><span>עברית</span></a></li><li class="interlanguage-link interwiki-kn mw-list-item"><a href="https://kn.wikipedia.org/wiki/%E0%B2%86%E0%B2%9C%E0%B3%8A%E0%B2%BC_%E0%B2%B8%E0%B2%82%E0%B2%AF%E0%B3%81%E0%B2%95%E0%B3%8D%E0%B2%A4%E0%B2%97%E0%B2%B3%E0%B3%81" title="ಆಜೊ಼ ಸಂಯುಕ್ತಗಳು – Kannada" lang="kn" hreflang="kn" data-title="ಆಜೊ಼ ಸಂಯುಕ್ತಗಳು" data-language-autonym="ಕನ್ನಡ" data-language-local-name="Kannada" class="interlanguage-link-target"><span>ಕನ್ನಡ</span></a></li><li class="interlanguage-link interwiki-kk mw-list-item"><a href="https://kk.wikipedia.org/wiki/%D0%90%D0%B7%D0%BE%D2%9B%D0%BE%D1%81%D1%8B%D0%BB%D1%8B%D1%81%D1%82%D0%B0%D1%80" title="Азоқосылыстар – Kazakh" lang="kk" hreflang="kk" data-title="Азоқосылыстар" data-language-autonym="Қазақша" data-language-local-name="Kazakh" class="interlanguage-link-target"><span>Қазақша</span></a></li><li class="interlanguage-link interwiki-lv mw-list-item"><a href="https://lv.wikipedia.org/wiki/Azokr%C4%81svielas" title="Azokrāsvielas – Latvian" lang="lv" hreflang="lv" data-title="Azokrāsvielas" data-language-autonym="Latviešu" data-language-local-name="Latvian" class="interlanguage-link-target"><span>Latviešu</span></a></li><li class="interlanguage-link interwiki-hu mw-list-item"><a href="https://hu.wikipedia.org/wiki/Azovegy%C3%BClet" title="Azovegyület – Hungarian" lang="hu" hreflang="hu" data-title="Azovegyület" data-language-autonym="Magyar" data-language-local-name="Hungarian" class="interlanguage-link-target"><span>Magyar</span></a></li><li class="interlanguage-link interwiki-mk mw-list-item"><a href="https://mk.wikipedia.org/wiki/%D0%90%D0%B7%D0%BE%D1%81%D0%BE%D0%B5%D0%B4%D0%B8%D0%BD%D0%B5%D0%BD%D0%B8%D0%B5" title="Азосоединение – Macedonian" lang="mk" hreflang="mk" data-title="Азосоединение" data-language-autonym="Македонски" data-language-local-name="Macedonian" class="interlanguage-link-target"><span>Македонски</span></a></li><li class="interlanguage-link interwiki-nl mw-list-item"><a href="https://nl.wikipedia.org/wiki/Azoverbinding" title="Azoverbinding – Dutch" lang="nl" hreflang="nl" data-title="Azoverbinding" data-language-autonym="Nederlands" data-language-local-name="Dutch" class="interlanguage-link-target"><span>Nederlands</span></a></li><li class="interlanguage-link interwiki-ja mw-list-item"><a href="https://ja.wikipedia.org/wiki/%E3%82%A2%E3%82%BE%E5%8C%96%E5%90%88%E7%89%A9" title="アゾ化合物 – Japanese" lang="ja" hreflang="ja" data-title="アゾ化合物" data-language-autonym="日本語" data-language-local-name="Japanese" class="interlanguage-link-target"><span>日本語</span></a></li><li class="interlanguage-link interwiki-no mw-list-item"><a href="https://no.wikipedia.org/wiki/Azoforbindelse" title="Azoforbindelse – Norwegian Bokmål" lang="nb" hreflang="nb" data-title="Azoforbindelse" data-language-autonym="Norsk bokmål" data-language-local-name="Norwegian Bokmål" class="interlanguage-link-target"><span>Norsk bokmål</span></a></li><li class="interlanguage-link interwiki-pl mw-list-item"><a href="https://pl.wikipedia.org/wiki/Azozwi%C4%85zki" title="Azozwiązki – Polish" lang="pl" hreflang="pl" data-title="Azozwiązki" data-language-autonym="Polski" data-language-local-name="Polish" class="interlanguage-link-target"><span>Polski</span></a></li><li class="interlanguage-link interwiki-pt mw-list-item"><a href="https://pt.wikipedia.org/wiki/Azocomposto" title="Azocomposto – Portuguese" lang="pt" hreflang="pt" data-title="Azocomposto" data-language-autonym="Português" data-language-local-name="Portuguese" class="interlanguage-link-target"><span>Português</span></a></li><li class="interlanguage-link interwiki-ro mw-list-item"><a href="https://ro.wikipedia.org/wiki/Azoderivat" title="Azoderivat – Romanian" lang="ro" hreflang="ro" data-title="Azoderivat" data-language-autonym="Română" data-language-local-name="Romanian" class="interlanguage-link-target"><span>Română</span></a></li><li class="interlanguage-link interwiki-ru mw-list-item"><a href="https://ru.wikipedia.org/wiki/%D0%90%D0%B7%D0%BE%D1%81%D0%BE%D0%B5%D0%B4%D0%B8%D0%BD%D0%B5%D0%BD%D0%B8%D1%8F" title="Азосоединения – Russian" lang="ru" hreflang="ru" data-title="Азосоединения" data-language-autonym="Русский" data-language-local-name="Russian" class="interlanguage-link-target"><span>Русский</span></a></li><li class="interlanguage-link interwiki-sk mw-list-item"><a href="https://sk.wikipedia.org/wiki/Azozl%C3%BA%C4%8Denina" title="Azozlúčenina – Slovak" lang="sk" hreflang="sk" data-title="Azozlúčenina" data-language-autonym="Slovenčina" data-language-local-name="Slovak" class="interlanguage-link-target"><span>Slovenčina</span></a></li><li class="interlanguage-link interwiki-sl mw-list-item"><a href="https://sl.wikipedia.org/wiki/Azo_spojina" title="Azo spojina – Slovenian" lang="sl" hreflang="sl" data-title="Azo spojina" data-language-autonym="Slovenščina" data-language-local-name="Slovenian" class="interlanguage-link-target"><span>Slovenščina</span></a></li><li class="interlanguage-link interwiki-sr mw-list-item"><a href="https://sr.wikipedia.org/wiki/Azo_jedinjenje" title="Azo jedinjenje – Serbian" lang="sr" hreflang="sr" data-title="Azo jedinjenje" data-language-autonym="Српски / srpski" data-language-local-name="Serbian" class="interlanguage-link-target"><span>Српски / srpski</span></a></li><li class="interlanguage-link interwiki-sh mw-list-item"><a href="https://sh.wikipedia.org/wiki/Azo_jedinjenje" title="Azo jedinjenje – Serbo-Croatian" lang="sh" hreflang="sh" data-title="Azo jedinjenje" data-language-autonym="Srpskohrvatski / српскохрватски" data-language-local-name="Serbo-Croatian" class="interlanguage-link-target"><span>Srpskohrvatski / српскохрватски</span></a></li><li class="interlanguage-link interwiki-fi mw-list-item"><a href="https://fi.wikipedia.org/wiki/Atsoyhdisteet" title="Atsoyhdisteet – Finnish" lang="fi" hreflang="fi" data-title="Atsoyhdisteet" data-language-autonym="Suomi" data-language-local-name="Finnish" class="interlanguage-link-target"><span>Suomi</span></a></li><li class="interlanguage-link interwiki-sv mw-list-item"><a href="https://sv.wikipedia.org/wiki/Azof%C3%B6rening" title="Azoförening – Swedish" lang="sv" hreflang="sv" data-title="Azoförening" data-language-autonym="Svenska" data-language-local-name="Swedish" class="interlanguage-link-target"><span>Svenska</span></a></li><li class="interlanguage-link interwiki-ta mw-list-item"><a href="https://ta.wikipedia.org/wiki/%E0%AE%85%E0%AE%9A%E0%AF%8B_%E0%AE%9A%E0%AF%87%E0%AE%B0%E0%AF%8D%E0%AE%AE%E0%AE%AE%E0%AF%8D" title="அசோ சேர்மம் – Tamil" lang="ta" hreflang="ta" data-title="அசோ சேர்மம்" data-language-autonym="தமிழ்" data-language-local-name="Tamil" class="interlanguage-link-target"><span>தமிழ்</span></a></li><li class="interlanguage-link interwiki-uk mw-list-item"><a href="https://uk.wikipedia.org/wiki/%D0%90%D0%B7%D0%BE%D1%81%D0%BF%D0%BE%D0%BB%D1%83%D0%BA%D0%B8" title="Азосполуки – Ukrainian" lang="uk" hreflang="uk" data-title="Азосполуки" data-language-autonym="Українська" data-language-local-name="Ukrainian" class="interlanguage-link-target"><span>Українська</span></a></li><li class="interlanguage-link interwiki-zh mw-list-item"><a href="https://zh.wikipedia.org/wiki/%E5%81%B6%E6%B0%AE%E5%8C%96%E7%89%A9" title="偶氮化物 – Chinese" lang="zh" hreflang="zh" data-title="偶氮化物" data-language-autonym="中文" data-language-local-name="Chinese" class="interlanguage-link-target"><span>中文</span></a></li> </ul> <div class="after-portlet after-portlet-lang"><span class="wb-langlinks-edit wb-langlinks-link"><a href="https://www.wikidata.org/wiki/Special:EntityPage/Q322251#sitelinks-wikipedia" title="Edit interlanguage links" class="wbc-editpage">Edit links</a></span></div> </div> </div> </div> </header> <div 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href="/wiki/File:Azo-group-2D-flat.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/f/fc/Azo-group-2D-flat.png/120px-Azo-group-2D-flat.png" decoding="async" width="120" height="104" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/fc/Azo-group-2D-flat.png/180px-Azo-group-2D-flat.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/fc/Azo-group-2D-flat.png/240px-Azo-group-2D-flat.png 2x" data-file-width="1100" data-file-height="956" /></a><figcaption>General chemical structure of azo compounds</figcaption></figure> <div class="shortdescription nomobile noexcerpt noprint searchaux" style="display:none">Organic compounds with a diazenyl group (–N=N–)</div> <style data-mw-deduplicate="TemplateStyles:r1236090951">.mw-parser-output .hatnote{font-style:italic}.mw-parser-output div.hatnote{padding-left:1.6em;margin-bottom:0.5em}.mw-parser-output .hatnote i{font-style:normal}.mw-parser-output .hatnote+link+.hatnote{margin-top:-0.5em}@media print{body.ns-0 .mw-parser-output .hatnote{display:none!important}}</style><div role="note" class="hatnote navigation-not-searchable">"Azene" redirects here. Not to be confused with the polycyclic hydrocarbons known as "<a href="/wiki/Acene" title="Acene">acenes</a>" or the acyclic saturated hydronitrogens known as "<a href="/wiki/Azane" title="Azane">azanes</a>".</div> <p><b>Azo compounds</b> are <a href="/wiki/Organic_compound" title="Organic compound">organic compounds</a> bearing the <a href="/wiki/Functional_group" title="Functional group">functional group</a> diazenyl (<style data-mw-deduplicate="TemplateStyles:r1123817410">.mw-parser-output .template-chem2-su{display:inline-block;font-size:80%;line-height:1;vertical-align:-0.35em}.mw-parser-output .template-chem2-su>span{display:block;text-align:left}.mw-parser-output sub.template-chem2-sub{font-size:80%;vertical-align:-0.35em}.mw-parser-output sup.template-chem2-sup{font-size:80%;vertical-align:0.65em}</style><span class="chemf nowrap">R−N=N−R′</span>, in which R and R′ can be either <a href="/wiki/Aryl" class="mw-redirect" title="Aryl">aryl</a> or <a href="/wiki/Alkyl" class="mw-redirect" title="Alkyl">alkyl</a> groups). </p><p><a href="/wiki/IUPAC" class="mw-redirect" title="IUPAC">IUPAC</a> defines azo compounds as: "Derivatives of <a href="/wiki/Diazene" class="mw-redirect" title="Diazene">diazene</a> (diimide), <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1123817410"><span class="chemf nowrap">HN=NH</span>, wherein both hydrogens are substituted by hydrocarbyl groups, e.g. <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1123817410"><span class="chemf nowrap">PhN=NPh</span> <a href="/wiki/Azobenzene" title="Azobenzene">azobenzene</a> or diphenyldiazene.", where Ph stands for <a href="/wiki/Phenyl" class="mw-redirect" title="Phenyl">phenyl</a> group.<sup id="cite_ref-Gold_1-0" class="reference"><a href="#cite_note-Gold-1"><span class="cite-bracket">&#91;</span>1<span class="cite-bracket">&#93;</span></a></sup> The more stable derivatives contain two aryl groups. The <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1123817410"><span class="chemf nowrap">N=N</span> group is called an <i>azo group</i> (from&#32;<a href="/wiki/French_language" title="French language">French</a>&#32;<i> azote</i>&#160;'<a href="/wiki/Nitrogen" title="Nitrogen">nitrogen</a>', from&#32;<a href="/wiki/Ancient_Greek_language" class="mw-redirect" title="Ancient Greek language">Ancient Greek</a>&#32;<i> </i>ἀ-<i> (a-)</i>&#160;'not'&#32;and&#32;<i> </i>ζωή<i> (zōē)</i>&#160;'life'). </p><p>Many <a href="/wiki/Textile" title="Textile">textile</a> and <a href="/wiki/Leather" title="Leather">leather</a> articles are dyed with <a href="/wiki/Azo_dye" title="Azo dye">azo dyes</a> and <a href="/wiki/Pigment" title="Pigment">pigments</a>.<sup id="cite_ref-TFL_2-0" class="reference"><a href="#cite_note-TFL-2"><span class="cite-bracket">&#91;</span>2<span class="cite-bracket">&#93;</span></a></sup> </p> <meta property="mw:PageProp/toc" /> <div class="mw-heading mw-heading2"><h2 id="Aryl_azo_compounds">Aryl azo compounds</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Azo_compound&amp;action=edit&amp;section=1" title="Edit section: Aryl azo compounds"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <figure class="mw-halign-right" typeof="mw:File/Thumb"><a href="/wiki/File:Phenazopyridine.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/6f/Phenazopyridine.svg/150px-Phenazopyridine.svg.png" decoding="async" width="150" height="119" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/6f/Phenazopyridine.svg/225px-Phenazopyridine.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/6f/Phenazopyridine.svg/300px-Phenazopyridine.svg.png 2x" data-file-width="1209" data-file-height="960" /></a><figcaption><a href="/wiki/Phenazopyridine" title="Phenazopyridine">Phenazopyridine</a>, an aryl azo compound, is used to treat <a href="/wiki/Urinary_tract_infections" class="mw-redirect" title="Urinary tract infections">urinary tract infections</a></figcaption></figure> <p><a href="/wiki/Aryl" class="mw-redirect" title="Aryl">Aryl</a> azo compounds are usually stable, crystalline species. <a href="/wiki/Azobenzene" title="Azobenzene">Azobenzene</a> is the prototypical <a href="/wiki/Aromatic" class="mw-redirect" title="Aromatic">aromatic</a> azo compound. It exists mainly as the <a href="/wiki/Cis-trans_isomerism" class="mw-redirect" title="Cis-trans isomerism"><i>trans</i></a> <a href="/wiki/Isomer" title="Isomer">isomer</a>, but upon illumination, converts to the <a href="/wiki/Cis-trans_isomerism" class="mw-redirect" title="Cis-trans isomerism"><i>cis</i></a> isomer. </p><p>Aromatic azo compounds can be synthesized by <a href="/wiki/Azo_coupling" title="Azo coupling">azo coupling</a>, which entails an <a href="/wiki/Electrophilic_substitution_reaction" class="mw-redirect" title="Electrophilic substitution reaction">electrophilic substitution reaction</a> where an <a href="/wiki/Diazonium_salt" class="mw-redirect" title="Diazonium salt">aryl diazonium cation</a> is attacked by another aryl ring, especially those substituted with <a href="/wiki/Electron-donating_group" class="mw-redirect" title="Electron-donating group">electron-donating groups</a>:<sup id="cite_ref-3" class="reference"><a href="#cite_note-3"><span class="cite-bracket">&#91;</span>3<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-4" class="reference"><a href="#cite_note-4"><span class="cite-bracket">&#91;</span>4<span class="cite-bracket">&#93;</span></a></sup> </p> <dl><dd><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1123817410"><span class="chemf nowrap"><a href="/wiki/Aryl" class="mw-redirect" title="Aryl">Ar</a>N<span class="template-chem2-su"><span>+</span><span>2</span></span> + Ar'H → ArN=NAr' + H<sup class="template-chem2-sup">+</sup></span></dd></dl> <p>Since <a href="/wiki/Diazonium_salt" class="mw-redirect" title="Diazonium salt">diazonium salts</a> are often unstable near room temperature, the azo coupling reactions are typically conducted near 0&#160;°C. The <a href="/wiki/Oxidation" class="mw-redirect" title="Oxidation">oxidation</a> of <a href="/wiki/Hydrazines" title="Hydrazines">hydrazines</a> (<link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1123817410"><span class="chemf nowrap">R−NH−NH−R′</span>) also gives azo compounds.<sup id="cite_ref-5" class="reference"><a href="#cite_note-5"><span class="cite-bracket">&#91;</span>5<span class="cite-bracket">&#93;</span></a></sup> Azo dyes are also prepared by the <a href="/wiki/Condensation_reaction" title="Condensation reaction">condensation</a> of <a href="/wiki/Nitro_compound" title="Nitro compound">nitroaromatics</a> with <a href="/wiki/Aniline" title="Aniline">anilines</a> followed by <a href="/wiki/Redox" title="Redox">reduction</a> of the resulting <a href="/wiki/Azoxy" class="mw-redirect" title="Azoxy">azoxy</a> intermediate: </p> <dl><dd><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1123817410"><span class="chemf nowrap">ArNO<sub class="template-chem2-sub">2</sub> + Ar'NH<sub class="template-chem2-sub">2</sub> → ArN(O)=NAr' + H<sub class="template-chem2-sub">2</sub>O</span></dd> <dd><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1123817410"><span class="chemf nowrap">ArN(O)=NAr' + C<sub class="template-chem2-sub">6</sub>H<sub class="template-chem2-sub">12</sub>O<sub class="template-chem2-sub">6</sub> → ArN=NAr' + C<sub class="template-chem2-sub">6</sub>H<sub class="template-chem2-sub">10</sub>O<sub class="template-chem2-sub">6</sub> + H<sub class="template-chem2-sub">2</sub>O</span></dd></dl> <p>For textile dying, a typical <a href="/wiki/Nitro_compound" title="Nitro compound">nitro</a> <a href="/wiki/Cross-coupling_partner" title="Cross-coupling partner">coupling partner</a> would be <a href="/wiki/Disodium_4,4%27-dinitrostilbene-2,2%27-disulfonate" title="Disodium 4,4&#39;-dinitrostilbene-2,2&#39;-disulfonate">disodium 4,4′-dinitrostilbene-2,2′-disulfonate</a>. Typical aniline partners are shown below.<sup id="cite_ref-Azodye_6-0" class="reference"><a href="#cite_note-Azodye-6"><span class="cite-bracket">&#91;</span>6<span class="cite-bracket">&#93;</span></a></sup> </p> <figure typeof="mw:File/Thumb"><a href="/wiki/File:4-hydroxyphenylazobenzene.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/d/d0/4-hydroxyphenylazobenzene.png/200px-4-hydroxyphenylazobenzene.png" decoding="async" width="200" height="68" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/d/d0/4-hydroxyphenylazobenzene.png/300px-4-hydroxyphenylazobenzene.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/d/d0/4-hydroxyphenylazobenzene.png/400px-4-hydroxyphenylazobenzene.png 2x" data-file-width="2059" data-file-height="701" /></a><figcaption>An orange azo dye <a href="/wiki/Solvent_Yellow_7" title="Solvent Yellow 7">Solvent Yellow 7</a></figcaption></figure> <p>As a consequence of <a href="/wiki/Pi_bond" title="Pi bond"><i>π</i></a>-<a href="/wiki/Delocalization" class="mw-redirect" title="Delocalization">delocalization</a>, aryl azo compounds have vivid colors, especially reds, oranges, and yellows. Therefore, they are used as <a href="/wiki/Dye" title="Dye">dyes</a>, and are commonly known as <a href="/wiki/Azo_dye" title="Azo dye">azo dyes</a>, an example of which is <a href="/wiki/Disperse_Orange_1" title="Disperse Orange 1">Disperse Orange 1</a>. Some azo compounds, e.g., <a href="/wiki/Methyl_orange" title="Methyl orange">methyl orange</a>, are used as <a href="/wiki/PH_indicator" title="PH indicator">acid-base indicators</a> due to the different colors of their acid and salt forms. Most <a href="/wiki/DVD-R" class="mw-redirect" title="DVD-R">DVD-R</a>/<a href="/wiki/DVD%2BR" class="mw-redirect" title="DVD+R">+R</a> and some <a href="/wiki/CD-R" title="CD-R">CD-R</a> discs use blue azo dye as the recording layer. The commercial success of azo dyes motivated the development of azo compounds in general. </p> <div class="mw-heading mw-heading2"><h2 id="Alkyl_azo_compounds">Alkyl azo compounds</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Azo_compound&amp;action=edit&amp;section=2" title="Edit section: Alkyl azo compounds"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1236090951"><div role="note" class="hatnote navigation-not-searchable">See also: <a href="/wiki/Diazo_group" class="mw-redirect" title="Diazo group">Diazo group</a></div> <p><a href="/wiki/Aliphatic" class="mw-redirect" title="Aliphatic">Aliphatic</a> azo compounds (R and/or R′ = aliphatic) are less commonly encountered than the aryl azo compounds. A commercially important alkyl azo compound is <a href="/wiki/Azobisisobutyronitrile" title="Azobisisobutyronitrile">azobisisobutyronitrile</a> (AIBN), which is widely used as an initiator in <a href="/wiki/Free-radical_polymerization" class="mw-redirect" title="Free-radical polymerization">free-radical polymerizations</a> and other radical-induced reactions. It achieves this initiation by <a href="/wiki/Chemical_decomposition" title="Chemical decomposition">decomposition</a>, eliminating a molecule of <a href="/wiki/Nitrogen" title="Nitrogen">nitrogen</a> gas to form two 2-cyanoprop-2-yl radicals: </p> <dl><dd><span typeof="mw:File"><a href="/wiki/File:Formation_of_Radicals_from_AIBN.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/5/56/Formation_of_Radicals_from_AIBN.png/380px-Formation_of_Radicals_from_AIBN.png" decoding="async" width="380" height="87" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/5/56/Formation_of_Radicals_from_AIBN.png/570px-Formation_of_Radicals_from_AIBN.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/5/56/Formation_of_Radicals_from_AIBN.png/760px-Formation_of_Radicals_from_AIBN.png 2x" data-file-width="4409" data-file-height="1008" /></a></span></dd></dl> <p>For instance a mixture of <a href="/wiki/Styrene" title="Styrene">styrene</a> and <a href="/wiki/Maleic_anhydride" title="Maleic anhydride">maleic anhydride</a> in <a href="/wiki/Toluene" title="Toluene">toluene</a> will react if heated, forming the <a href="/wiki/Copolymer" title="Copolymer">copolymer</a> upon addition of AIBN. </p><p>A simple dialkyl diazo compound is diethyldiazene, <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1123817410"><span class="chemf nowrap">CH<sub class="template-chem2-sub">3</sub>CH<sub class="template-chem2-sub">2</sub>−N=N−CH<sub class="template-chem2-sub">2</sub>CH<sub class="template-chem2-sub">3</sub></span>, which can be synthesized through a variant of the <a href="/wiki/Ramberg%E2%80%93B%C3%A4cklund_reaction" title="Ramberg–Bäcklund reaction">Ramberg–Bäcklund reaction</a>.<sup id="cite_ref-7" class="reference"><a href="#cite_note-7"><span class="cite-bracket">&#91;</span>7<span class="cite-bracket">&#93;</span></a></sup> Because of their instability, aliphatic azo compounds pose the risk of <a href="/wiki/Explosion" title="Explosion">explosion</a>. </p><p>AIBN is produced by converting <a href="/wiki/Acetone_cyanohydrin" title="Acetone cyanohydrin">acetone cyanohydrin</a> to the <a href="/wiki/Hydrazine" title="Hydrazine">hydrazine</a> derivative followed by oxidation:<sup id="cite_ref-Ullmann_8-0" class="reference"><a href="#cite_note-Ullmann-8"><span class="cite-bracket">&#91;</span>8<span class="cite-bracket">&#93;</span></a></sup> </p> <dl><dd><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1123817410"><span class="chemf nowrap">2 (CH<sub class="template-chem2-sub">3</sub>)<sub class="template-chem2-sub">2</sub>C(CN)OH + N<sub class="template-chem2-sub">2</sub>H<sub class="template-chem2-sub">4</sub> → &#91;(CH<sub class="template-chem2-sub">3</sub>)<sub class="template-chem2-sub">2</sub>C(CN)]<sub class="template-chem2-sub">2</sub>N<sub class="template-chem2-sub">2</sub>H<sub class="template-chem2-sub">2</sub> + 2 H<sub class="template-chem2-sub">2</sub>O</span></dd> <dd><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1123817410"><span class="chemf nowrap">&#91;(CH<sub class="template-chem2-sub">3</sub>)<sub class="template-chem2-sub">2</sub>C(CN)]<sub class="template-chem2-sub">2</sub>N<sub class="template-chem2-sub">2</sub>H<sub class="template-chem2-sub">2</sub> + Cl<sub class="template-chem2-sub">2</sub> → &#91;(CH<sub class="template-chem2-sub">3</sub>)<sub class="template-chem2-sub">2</sub>C(CN)]<sub class="template-chem2-sub">2</sub>N<sub class="template-chem2-sub">2</sub> + 2 HCl</span></dd></dl> <div class="mw-heading mw-heading2"><h2 id="Safety_and_regulation">Safety and regulation</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Azo_compound&amp;action=edit&amp;section=3" title="Edit section: Safety and regulation"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>Many azo pigments are non-toxic, although some, such as <a href="/wiki/Dinitroaniline" title="Dinitroaniline">dinitroaniline</a> orange, <a href="/w/index.php?title=Ortho-nitroaniline_orange&amp;action=edit&amp;redlink=1" class="new" title="Ortho-nitroaniline orange (page does not exist)">ortho-nitroaniline orange</a>, or pigment orange 1, 2, and 5 have been found to be <a href="/wiki/Mutagen" title="Mutagen">mutagenic</a>.<sup id="cite_ref-9" class="reference"><a href="#cite_note-9"><span class="cite-bracket">&#91;</span>9<span class="cite-bracket">&#93;</span></a></sup> Likewise, several case studies have linked azo pigments with <a href="/wiki/Basal_cell_carcinoma" class="mw-redirect" title="Basal cell carcinoma">basal cell carcinoma</a>.<sup id="cite_ref-10" class="reference"><a href="#cite_note-10"><span class="cite-bracket">&#91;</span>10<span class="cite-bracket">&#93;</span></a></sup> </p> <div class="mw-heading mw-heading3"><h3 id="European_regulation">European regulation</h3><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Azo_compound&amp;action=edit&amp;section=4" title="Edit section: European regulation"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>Certain azo dyes can break down under reductive conditions to release any of a group of defined <a href="/wiki/Aromatic_amine" title="Aromatic amine">aromatic amines</a>. Consumer goods which contain listed aromatic amines originating from azo dyes were prohibited from manufacture and sale in <a href="/wiki/European_Union" title="European Union">European Union</a> countries in September 2003. As only a small number of dyes contained an equally small number of amines, relatively few products were affected.<sup id="cite_ref-TFL_2-1" class="reference"><a href="#cite_note-TFL-2"><span class="cite-bracket">&#91;</span>2<span class="cite-bracket">&#93;</span></a></sup> </p> <div class="mw-heading mw-heading2"><h2 id="See_also">See also</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Azo_compound&amp;action=edit&amp;section=5" title="Edit section: See also"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <ul><li><a href="/wiki/Azo_coupling" title="Azo coupling">Azo coupling</a></li></ul> <div class="mw-heading mw-heading2"><h2 id="References">References</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Azo_compound&amp;action=edit&amp;section=6" title="Edit section: References"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <style data-mw-deduplicate="TemplateStyles:r1239543626">.mw-parser-output .reflist{margin-bottom:0.5em;list-style-type:decimal}@media screen{.mw-parser-output .reflist{font-size:90%}}.mw-parser-output .reflist .references{font-size:100%;margin-bottom:0;list-style-type:inherit}.mw-parser-output .reflist-columns-2{column-width:30em}.mw-parser-output .reflist-columns-3{column-width:25em}.mw-parser-output .reflist-columns{margin-top:0.3em}.mw-parser-output .reflist-columns ol{margin-top:0}.mw-parser-output .reflist-columns li{page-break-inside:avoid;break-inside:avoid-column}.mw-parser-output .reflist-upper-alpha{list-style-type:upper-alpha}.mw-parser-output .reflist-upper-roman{list-style-type:upper-roman}.mw-parser-output .reflist-lower-alpha{list-style-type:lower-alpha}.mw-parser-output .reflist-lower-greek{list-style-type:lower-greek}.mw-parser-output .reflist-lower-roman{list-style-type:lower-roman}</style><div class="reflist"> <div class="mw-references-wrap"><ol class="references"> <li id="cite_note-Gold-1"><span class="mw-cite-backlink"><b><a href="#cite_ref-Gold_1-0">^</a></b></span> <span class="reference-text"><a href="/wiki/International_Union_of_Pure_and_Applied_Chemistry" title="International Union of Pure and Applied Chemistry">IUPAC</a>, <i><a href="/wiki/IUPAC_books#Gold_Book" class="mw-redirect" title="IUPAC books">Compendium of Chemical Terminology</a></i>, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006&#8211;) "<a rel="nofollow" class="external text" href="https://goldbook.iupac.org/terms/view/A00560.html">azo compounds</a>". <style data-mw-deduplicate="TemplateStyles:r1238218222">.mw-parser-output cite.citation{font-style:inherit;word-wrap:break-word}.mw-parser-output .citation q{quotes:"\"""\"""'""'"}.mw-parser-output .citation:target{background-color:rgba(0,127,255,0.133)}.mw-parser-output .id-lock-free.id-lock-free a{background:url("//upload.wikimedia.org/wikipedia/commons/6/65/Lock-green.svg")right 0.1em center/9px no-repeat}.mw-parser-output .id-lock-limited.id-lock-limited a,.mw-parser-output .id-lock-registration.id-lock-registration a{background:url("//upload.wikimedia.org/wikipedia/commons/d/d6/Lock-gray-alt-2.svg")right 0.1em center/9px no-repeat}.mw-parser-output .id-lock-subscription.id-lock-subscription a{background:url("//upload.wikimedia.org/wikipedia/commons/a/aa/Lock-red-alt-2.svg")right 0.1em center/9px no-repeat}.mw-parser-output .cs1-ws-icon a{background:url("//upload.wikimedia.org/wikipedia/commons/4/4c/Wikisource-logo.svg")right 0.1em center/12px no-repeat}body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .id-lock-free a,body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .id-lock-limited a,body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .id-lock-registration a,body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .id-lock-subscription a,body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .cs1-ws-icon a{background-size:contain;padding:0 1em 0 0}.mw-parser-output .cs1-code{color:inherit;background:inherit;border:none;padding:inherit}.mw-parser-output .cs1-hidden-error{display:none;color:var(--color-error,#d33)}.mw-parser-output .cs1-visible-error{color:var(--color-error,#d33)}.mw-parser-output .cs1-maint{display:none;color:#085;margin-left:0.3em}.mw-parser-output .cs1-kern-left{padding-left:0.2em}.mw-parser-output .cs1-kern-right{padding-right:0.2em}.mw-parser-output .citation .mw-selflink{font-weight:inherit}@media screen{.mw-parser-output .cs1-format{font-size:95%}html.skin-theme-clientpref-night .mw-parser-output .cs1-maint{color:#18911f}}@media screen and (prefers-color-scheme:dark){html.skin-theme-clientpref-os .mw-parser-output .cs1-maint{color:#18911f}}</style><a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1351%2Fgoldbook.A00560">10.1351/goldbook.A00560</a></span> </li> <li id="cite_note-TFL-2"><span class="mw-cite-backlink">^ <a href="#cite_ref-TFL_2-0"><sup><i><b>a</b></i></sup></a> <a href="#cite_ref-TFL_2-1"><sup><i><b>b</b></i></sup></a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.tfl.com/web/files/eubanazodyes.pdf">European Ban on Certain Azo Dyes</a> <a rel="nofollow" class="external text" href="https://web.archive.org/web/20120813054055/http://www.tfl.com/web/files/eubanazodyes.pdf">Archived</a> 2012-08-13 at the <a href="/wiki/Wayback_Machine" title="Wayback Machine">Wayback Machine</a>, Dr. A. Püntener and Dr. C. Page, Quality and Environment, TFL</span> </li> <li id="cite_note-3"><span class="mw-cite-backlink"><b><a href="#cite_ref-3">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFGrossman2003" class="citation book cs1">Grossman, Robert&#160;B. (2003). <i>The Art of Writing Reasonable Organic Reaction Mechanisms</i> (2nd&#160;ed.). New York: Springer. pp.&#160;130–131. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a>&#160;<a href="/wiki/Special:BookSources/0-387-95468-6" title="Special:BookSources/0-387-95468-6"><bdi>0-387-95468-6</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&amp;rft.genre=book&amp;rft.btitle=The+Art+of+Writing+Reasonable+Organic+Reaction+Mechanisms&amp;rft.place=New+York&amp;rft.pages=130-131&amp;rft.edition=2nd&amp;rft.pub=Springer&amp;rft.date=2003&amp;rft.isbn=0-387-95468-6&amp;rft.aulast=Grossman&amp;rft.aufirst=Robert+B.&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3AAzo+compound" class="Z3988"></span></span> </li> <li id="cite_note-4"><span class="mw-cite-backlink"><b><a href="#cite_ref-4">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFH._T._ClarkeW._R._Kirner1941" class="citation journal cs1">H. T. 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"Azo Pigments and a Basal Cell Carcinoma at the Thumb". <i>Dermatology</i>. <b>216</b> (1): 76–80. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1159%2F000109363">10.1159/000109363</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/18032904">18032904</a>. <a href="/wiki/S2CID_(identifier)" class="mw-redirect" title="S2CID (identifier)">S2CID</a>&#160;<a rel="nofollow" class="external text" href="https://api.semanticscholar.org/CorpusID:34959909">34959909</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Dermatology&amp;rft.atitle=Azo+Pigments+and+a+Basal+Cell+Carcinoma+at+the+Thumb&amp;rft.volume=216&amp;rft.issue=1&amp;rft.pages=76-80&amp;rft.date=2008&amp;rft_id=https%3A%2F%2Fapi.semanticscholar.org%2FCorpusID%3A34959909%23id-name%3DS2CID&amp;rft_id=info%3Apmid%2F18032904&amp;rft_id=info%3Adoi%2F10.1159%2F000109363&amp;rft.au=Eva+Engel&amp;rft.au=Heidi+Ulrich&amp;rft.au=Rudolf+Vasold&amp;rft.au=Burkhard+K%C3%B6nig&amp;rft.au=Michael+Landthaler&amp;rft.au=Rudolf+S%C3%BCttinger&amp;rft.au=Wolfgang+B%C3%A4umler&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3AAzo+compound" class="Z3988"></span></span> </li> </ol></div></div> <div class="navbox-styles"><style data-mw-deduplicate="TemplateStyles:r1129693374">.mw-parser-output .hlist dl,.mw-parser-output .hlist ol,.mw-parser-output .hlist ul{margin:0;padding:0}.mw-parser-output .hlist dd,.mw-parser-output .hlist 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li a abbr{color:var(--color-base)!important}@media(prefers-color-scheme:dark){html.skin-theme-clientpref-os .mw-parser-output .navbar li a abbr{color:var(--color-base)!important}}@media print{.mw-parser-output .navbar{display:none!important}}</style><div class="navbar plainlinks hlist navbar-mini"><ul><li class="nv-view"><a href="/wiki/Template:Functional_groups" title="Template:Functional groups"><abbr title="View this template">v</abbr></a></li><li class="nv-talk"><a href="/wiki/Template_talk:Functional_groups" title="Template talk:Functional groups"><abbr title="Discuss this template">t</abbr></a></li><li class="nv-edit"><a href="/wiki/Special:EditPage/Template:Functional_groups" title="Special:EditPage/Template:Functional groups"><abbr title="Edit this template">e</abbr></a></li></ul></div><div id="Functional_groups" style="font-size:114%;margin:0 4em"><a href="/wiki/Functional_group" title="Functional group">Functional groups</a></div></th></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Hydrocarbon" title="Hydrocarbon">Hydrocarbons</a> <br /><span class="nobold">(only C and H)</span></th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Alkyl" class="mw-redirect" title="Alkyl">Alkyl</a> <ul><li><a href="/wiki/Methyl_group" title="Methyl group">Methyl</a></li> <li><a href="/wiki/Ethyl_group" title="Ethyl group">Ethyl</a></li> <li><a href="/wiki/Propyl_group" title="Propyl group">Propyl</a></li> <li><a href="/wiki/Cyclopropyl" class="mw-redirect" title="Cyclopropyl">Cyclopropyl</a></li> <li><a href="/wiki/Butyl_group" title="Butyl group">Butyl</a></li> <li><a href="/wiki/Pentyl_group" title="Pentyl group">Pentyl</a></li></ul></li> <li><a href="/wiki/Methylene_group" title="Methylene group">Methylene</a> <ul><li><a href="/wiki/Methylene_bridge" title="Methylene bridge">Bridge</a></li> <li><a href="/wiki/Methine_group" title="Methine group">Methine</a></li></ul></li> <li><a href="/wiki/Alkene" title="Alkene">Alkene</a> <ul><li><a href="/wiki/Vinyl_group" title="Vinyl group">Vinyl</a></li> <li><a href="/wiki/Allyl_group" title="Allyl group">Allyl</a></li> <li><a href="/wiki/Propenyl" title="Propenyl">1-Propenyl</a></li> <li><a href="/wiki/Crotyl_group" title="Crotyl group">Crotyl</a></li> <li><a href="/wiki/Allenes" title="Allenes">Allene</a></li> <li><a href="/wiki/Cumulene" title="Cumulene">Cumulene</a></li></ul></li> <li><a href="/wiki/Aryl" class="mw-redirect" title="Aryl">Aryl</a> <ul><li><a href="/wiki/Phenyl_group" title="Phenyl group">Phenyl</a></li> <li><a href="/wiki/Benzyl_group" title="Benzyl group">Benzyl</a></li></ul></li> <li><a href="/wiki/Alkyne" title="Alkyne">Alkyne</a></li> <li><a href="/wiki/Carbene" title="Carbene">Carbene</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Only <a href="/wiki/Carbon" title="Carbon">carbon</a>, <br /><a href="/wiki/Hydrogen" title="Hydrogen">hydrogen</a>, <br />and <a href="/wiki/Oxygen" title="Oxygen">oxygen</a> <br /><span class="nobold">(only C, H and O)</span></th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"></div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th scope="row" class="navbox-group" style="width:1%">R-O-R</th><td class="navbox-list-with-group navbox-list navbox-even" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Acetal" title="Acetal">Acetal</a></li> <li><a href="/wiki/Alcohol_(chemistry)" title="Alcohol (chemistry)">Alcohol</a></li> <li><a href="/wiki/Alkoxy_group" title="Alkoxy group">Alkoxy</a> <ul><li><a href="/wiki/Methoxy_group" title="Methoxy group">Methoxy</a></li></ul></li> <li><a href="/wiki/Ether" title="Ether">Ether</a> <ul><li><a href="/wiki/Enol_ether" title="Enol ether">Enol ether</a></li> <li><a href="/wiki/Epoxide" title="Epoxide">Epoxide</a></li></ul></li> <li><a href="/wiki/Organic_peroxides" title="Organic peroxides">Peroxy</a> <ul><li><a href="/wiki/Hydroperoxide" title="Hydroperoxide">Hydroperoxy</a></li> <li><a href="/wiki/Dioxirane" title="Dioxirane">Dioxiranes</a></li></ul></li> <li><a href="/wiki/Ethylenedioxy" title="Ethylenedioxy">Ethylenedioxy</a></li> <li><a href="/wiki/Methylenedioxy" title="Methylenedioxy">Methylenedioxy</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Carbonyl_group" title="Carbonyl group">carbonyl</a></th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Acyl_group" title="Acyl group">Acyl</a> <ul><li><a href="/wiki/Acetyl_group" title="Acetyl group">Acetyl</a></li> <li><a href="/wiki/Acryloyl_group" class="mw-redirect" title="Acryloyl group">Acryloyl</a></li> <li><a href="/wiki/Benzoyl_group" title="Benzoyl group">Benzoyl</a></li></ul></li> <li><a href="/wiki/Aldehyde" title="Aldehyde">Aldehyde</a> <ul><li><a href="/wiki/Ketene" title="Ketene">Ketene</a></li></ul></li> <li><a href="/wiki/Ketone" title="Ketone">Ketone</a></li> <li><a href="/wiki/Ynone" title="Ynone">Ynone</a></li> <li><a href="/wiki/Reductone" title="Reductone">Reductone</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">carboxy</th><td class="navbox-list-with-group navbox-list navbox-even" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Carboxylic_acid" title="Carboxylic acid">Carboxyl</a> <ul><li><a href="/wiki/Acetoxy_group" title="Acetoxy group">Acetoxy</a></li> <li><a href="/wiki/Carboxylic_anhydride" class="mw-redirect" title="Carboxylic anhydride">Anhydride</a></li></ul></li> <li><a href="/wiki/Ester" title="Ester">Ester</a> <ul><li><a href="/wiki/Orthoester" class="mw-redirect" title="Orthoester">Orthoester</a></li></ul></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Only one <br />element, <br />not being <br />carbon, <br />hydrogen, <br />or oxygen <br /><span class="nobold">(one element, <br />not C,&#160;H or O)</span></th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"></div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Nitrogen" title="Nitrogen">Nitrogen</a></th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Amine" title="Amine">Amine</a> <ul><li><a href="/wiki/Enamine" title="Enamine">Enamine</a></li> <li><a href="/wiki/Quaternary_ammonium_cation" title="Quaternary ammonium cation">Ammonium</a></li></ul></li> <li><a href="/wiki/Hydrazines" title="Hydrazines">Hydrazo</a></li> <li><a href="/wiki/Nitrene" title="Nitrene">Nitrene</a></li> <li><a href="/wiki/Imine" title="Imine">Imine</a></li> <li><a href="/wiki/Oxime" title="Oxime">Oxime</a></li> <li><a href="/wiki/Hydrazone" title="Hydrazone">Hydrazone</a></li> <li><a class="mw-selflink selflink">Azo</a></li> <li><a href="/wiki/Amide_(functional_group)" title="Amide (functional group)">Amide</a></li> <li><a href="/wiki/Imidate" class="mw-redirect" title="Imidate">Imidate</a></li> <li><a href="/wiki/Amidine" title="Amidine">Amidine</a></li> <li><a href="/wiki/Carbamate" title="Carbamate">Carbamate</a></li> <li><a href="/wiki/Imide" title="Imide">Imide</a></li> <li><a href="/wiki/Nitrile" title="Nitrile">Nitrile</a></li> <li><a href="/wiki/Isocyanide" title="Isocyanide">Isonitrile</a></li> <li><a href="/wiki/Cyanate_ester" title="Cyanate ester">Cyanate</a></li> <li><a href="/wiki/Isocyanate" title="Isocyanate">Isocyanate</a></li> <li><a href="/wiki/Nitrate_ester" title="Nitrate ester">Nitrate</a></li> <li><a href="/wiki/Nitrite_ester" class="mw-redirect" title="Nitrite ester">Nitrite</a></li> <li><a href="/wiki/Nitro_compound" title="Nitro compound">Nitro</a></li> <li><a href="/wiki/Nitroso" title="Nitroso">Nitroso</a></li> <li><a href="/wiki/NONOate" title="NONOate">NONOate</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Phosphorus" title="Phosphorus">Phosphorus</a></th><td class="navbox-list-with-group navbox-list navbox-even" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Organophosphate" title="Organophosphate">Phosphate</a> <ul><li><a href="/wiki/Phosphodiester" class="mw-redirect" title="Phosphodiester">Phosphodiester</a></li></ul></li> <li><a href="/wiki/Phosphonate" title="Phosphonate">Phosphonate</a> <ul><li><a href="/wiki/Phosphite_ester" title="Phosphite ester">Phosphite</a></li></ul></li> <li><a href="/wiki/Phosphonite" title="Phosphonite">Phosphonous</a></li> <li><a href="/wiki/Phosphinate" title="Phosphinate">Phosphinate</a></li> <li><a href="/wiki/Phosphine_oxide" title="Phosphine oxide">Phosphine oxide</a></li> <li><a href="/wiki/Organophosphine" title="Organophosphine">Phosphine</a> <ul><li><a href="/wiki/Phosphonium" title="Phosphonium">Phosphonium</a></li></ul></li> <li><a href="/wiki/Phosphaalkene" title="Phosphaalkene">Phosphaalkene</a></li> <li><a href="/wiki/Phosphaalkyne" title="Phosphaalkyne">Phosphaalkyne</a></li> <li><a href="/wiki/1-Phosphaallenes" title="1-Phosphaallenes">Phosphaallene</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Sulfur" title="Sulfur">Sulfur</a></th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Thiol" title="Thiol">Thiol</a></li> <li><a href="/wiki/Sulfide_(organic)" class="mw-redirect" title="Sulfide (organic)">Sulfide</a> <ul><li><a href="/wiki/Sulfonium" title="Sulfonium">Sulfonium</a></li></ul></li> <li><a href="/wiki/Persulfide" title="Persulfide">Persulfide</a></li> <li><a href="/wiki/Disulfide" title="Disulfide">Disulfide</a></li> <li><a href="/wiki/Sulfenic_acid" title="Sulfenic acid">Sulfenic acid</a></li> <li><a href="/wiki/Thiosulfinate" title="Thiosulfinate">Thiosulfinate</a></li> <li><a href="/wiki/Sulfoxide" title="Sulfoxide">Sulfoxide</a></li> <li><a href="/wiki/Thiosulfonate" title="Thiosulfonate">Thiosulfonate</a></li> <li><a href="/wiki/Sulfinic_acid" title="Sulfinic acid">Sulfinic acid</a></li> <li><a href="/wiki/Sulfone" title="Sulfone">Sulfone</a></li> <li><a href="/wiki/Sulfonic_acid" title="Sulfonic acid">Sulfonic acid</a></li> <li><a href="/wiki/Thioketone" title="Thioketone">Thioketone</a></li> <li><a href="/wiki/Thial" title="Thial">Thial</a></li> <li><a href="/wiki/Thioester" title="Thioester">Thioester</a></li> <li><a href="/wiki/Thionoester" class="mw-redirect" title="Thionoester">Thionoester</a></li> <li><a href="/wiki/Thioxanthate" title="Thioxanthate">Thioxanthate</a></li> <li><a href="/wiki/Xanthate" title="Xanthate">Xanthate</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Boron" title="Boron">Boron</a></th><td class="navbox-list-with-group navbox-list navbox-even" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Boronic_acid" title="Boronic acid">Boronic acid</a></li> <li><a href="/wiki/Borinic_acid" title="Borinic acid">Borinic acid</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Selenium" title="Selenium">Selenium</a></th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Selenol" title="Selenol">Selenol</a></li> <li><a href="/wiki/Selenonic_acid" title="Selenonic acid">Selenonic acid</a></li> <li><a href="/wiki/Seleninic_acid" title="Seleninic acid">Seleninic acid</a></li> <li><a href="/wiki/Selenenic_acid" title="Selenenic acid">Selenenic acid</a></li> <li><a href="/wiki/Selone" title="Selone">Selone</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Tellurium" title="Tellurium">Tellurium</a></th><td class="navbox-list-with-group navbox-list navbox-even" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Tellurol" title="Tellurol">Tellurol</a></li> <li><a href="/wiki/Telluroketone" title="Telluroketone">Telluroketone</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><i><a href="/wiki/Halocarbon" title="Halocarbon">Halo</a></i></th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Haloalkane" title="Haloalkane">Haloalkane</a> <ul><li><a href="/wiki/Fluoroethyl" title="Fluoroethyl">Fluoroethyl</a></li> <li><a href="/wiki/Trifluoromethyl" class="mw-redirect" title="Trifluoromethyl">Trifluoromethyl</a></li> <li><a href="/wiki/Trichloromethyl_group" title="Trichloromethyl group">Trichloromethyl</a></li> <li><a href="/wiki/Trifluoromethoxy_group" title="Trifluoromethoxy group">Trifluoromethoxy</a></li> <li><a href="/wiki/Iodane" class="mw-redirect" title="Iodane">Hypervalent iodine</a></li></ul></li> <li><a href="/wiki/Vinyl_halide" title="Vinyl halide">Vinyl halide</a> <ul><li><a href="/wiki/Vinyl_iodide_functional_group" title="Vinyl iodide functional group">Iodide</a></li></ul></li> <li><a href="/wiki/Acyl_halide" title="Acyl halide">Acyl halide</a> <ul><li><a href="/wiki/Acyl_chloride" title="Acyl chloride">Chloride</a></li></ul></li> <li><a href="/wiki/Perchlorate_ester" class="mw-redirect" title="Perchlorate ester">Perchlorate</a></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Other</th><td class="navbox-list-with-group navbox-list navbox-even" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Isothiocyanate" title="Isothiocyanate">Isothiocyanate</a></li> <li><a href="/wiki/Phosphoramides" title="Phosphoramides">Phosphoramides</a></li> <li><a href="/wiki/Sulfenyl_chloride" title="Sulfenyl chloride">Sulfenyl chloride</a></li> <li><a href="/wiki/Sulfonamide" title="Sulfonamide">Sulfonamide</a></li> <li><a href="/wiki/Organic_thiocyanates" title="Organic thiocyanates">Thiocyanate</a></li> <li><a href="/wiki/Sulfinylamine" title="Sulfinylamine">Sulfinylamines</a></li></ul> </div></td></tr><tr><td class="navbox-abovebelow" colspan="2"><div> <dl><dt><span class="nobold">See also</span></dt> <dd><i><a href="/wiki/Chemical_classification" class="mw-redirect" title="Chemical classification">chemical classification</a></i></dd> <dd><i><a href="/wiki/Chemical_nomenclature" title="Chemical nomenclature">chemical nomenclature</a></i> <dl><dd><a href="/wiki/IUPAC_nomenclature_of_inorganic_chemistry" title="IUPAC nomenclature of inorganic chemistry">inorganic</a></dd> <dd><a href="/wiki/IUPAC_nomenclature_of_organic_chemistry" title="IUPAC nomenclature of organic chemistry">organic</a></dd></dl></dd></dl> </div></td></tr></tbody></table></div> <div class="navbox-styles"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1129693374"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1236075235"><style data-mw-deduplicate="TemplateStyles:r1038841319">.mw-parser-output .tooltip-dotted{border-bottom:1px dotted;cursor:help}</style><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1038841319"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1038841319"><link rel="mw-deduplicated-inline-style" 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