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Disponible en 15 langues." > <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-15" 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">15 langues</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/4-%D8%A3%D9%85%D9%8A%D9%86%D9%88_%D8%AB%D9%86%D8%A7%D8%A6%D9%8A_%D8%A7%D9%84%D9%81%D9%8A%D9%86%D9%8A%D9%84" title="4-أمينو ثنائي الفينيل – arabe" lang="ar" hreflang="ar" data-title="4-أمينو ثنائي الفينيل" data-language-autonym="العربية" data-language-local-name="arabe" class="interlanguage-link-target"><span>العربية</span></a></li><li class="interlanguage-link interwiki-azb mw-list-item"><a href="https://azb.wikipedia.org/wiki/%DB%B4-%D8%A2%D9%85%DB%8C%D9%86%D9%88%D8%A8%DB%8C%E2%80%8C%D9%81%D9%86%DB%8C%D9%84" title="۴-آمینوبی‌فنیل – South Azerbaijani" lang="azb" hreflang="azb" data-title="۴-آمینوبی‌فنیل" data-language-autonym="تۆرکجه" data-language-local-name="South Azerbaijani" class="interlanguage-link-target"><span>تۆرکجه</span></a></li><li class="interlanguage-link interwiki-de mw-list-item"><a href="https://de.wikipedia.org/wiki/4-Aminobiphenyl" title="4-Aminobiphenyl – allemand" lang="de" hreflang="de" data-title="4-Aminobiphenyl" data-language-autonym="Deutsch" data-language-local-name="allemand" class="interlanguage-link-target"><span>Deutsch</span></a></li><li class="interlanguage-link interwiki-en mw-list-item"><a href="https://en.wikipedia.org/wiki/4-Aminobiphenyl" title="4-Aminobiphenyl – anglais" lang="en" hreflang="en" data-title="4-Aminobiphenyl" data-language-autonym="English" data-language-local-name="anglais" class="interlanguage-link-target"><span>English</span></a></li><li class="interlanguage-link interwiki-fa mw-list-item"><a href="https://fa.wikipedia.org/wiki/%DB%B4-%D8%A2%D9%85%DB%8C%D9%86%D9%88%D8%A8%DB%8C%E2%80%8C%D9%81%D9%86%DB%8C%D9%84" title="۴-آمینوبی‌فنیل – persan" lang="fa" hreflang="fa" data-title="۴-آمینوبی‌فنیل" data-language-autonym="فارسی" data-language-local-name="persan" class="interlanguage-link-target"><span>فارسی</span></a></li><li class="interlanguage-link interwiki-fi mw-list-item"><a href="https://fi.wikipedia.org/wiki/4-aminobifenyyli" title="4-aminobifenyyli – finnois" lang="fi" hreflang="fi" data-title="4-aminobifenyyli" data-language-autonym="Suomi" data-language-local-name="finnois" class="interlanguage-link-target"><span>Suomi</span></a></li><li class="interlanguage-link interwiki-hu mw-list-item"><a href="https://hu.wikipedia.org/wiki/4-Aminobifenil" title="4-Aminobifenil – hongrois" lang="hu" hreflang="hu" data-title="4-Aminobifenil" data-language-autonym="Magyar" data-language-local-name="hongrois" class="interlanguage-link-target"><span>Magyar</span></a></li><li class="interlanguage-link interwiki-it mw-list-item"><a href="https://it.wikipedia.org/wiki/Amminodifenile" title="Amminodifenile – italien" lang="it" hreflang="it" data-title="Amminodifenile" data-language-autonym="Italiano" data-language-local-name="italien" class="interlanguage-link-target"><span>Italiano</span></a></li><li class="interlanguage-link interwiki-ja mw-list-item"><a href="https://ja.wikipedia.org/wiki/4-%E3%82%A2%E3%83%9F%E3%83%8E%E3%83%93%E3%83%95%E3%82%A7%E3%83%8B%E3%83%AB" title="4-アミノビフェニル – japonais" lang="ja" hreflang="ja" data-title="4-アミノビフェニル" data-language-autonym="日本語" data-language-local-name="japonais" class="interlanguage-link-target"><span>日本語</span></a></li><li class="interlanguage-link interwiki-nl mw-list-item"><a href="https://nl.wikipedia.org/wiki/4-aminobifenyl" title="4-aminobifenyl – néerlandais" lang="nl" hreflang="nl" data-title="4-aminobifenyl" data-language-autonym="Nederlands" data-language-local-name="néerlandais" class="interlanguage-link-target"><span>Nederlands</span></a></li><li class="interlanguage-link interwiki-pt mw-list-item"><a href="https://pt.wikipedia.org/wiki/4-Aminobifenil" title="4-Aminobifenil – portugais" lang="pt" hreflang="pt" data-title="4-Aminobifenil" data-language-autonym="Português" data-language-local-name="portugais" class="interlanguage-link-target"><span>Português</span></a></li><li class="interlanguage-link interwiki-sh mw-list-item"><a href="https://sh.wikipedia.org/wiki/4-Aminobifenil" title="4-Aminobifenil – serbo-croate" lang="sh" hreflang="sh" data-title="4-Aminobifenil" data-language-autonym="Srpskohrvatski / српскохрватски" data-language-local-name="serbo-croate" class="interlanguage-link-target"><span>Srpskohrvatski / српскохрватски</span></a></li><li class="interlanguage-link interwiki-sr mw-list-item"><a href="https://sr.wikipedia.org/wiki/4-Aminobifenil" title="4-Aminobifenil – serbe" lang="sr" hreflang="sr" data-title="4-Aminobifenil" data-language-autonym="Српски / srpski" data-language-local-name="serbe" class="interlanguage-link-target"><span>Српски / srpski</span></a></li><li class="interlanguage-link interwiki-tr mw-list-item"><a href="https://tr.wikipedia.org/wiki/4-Aminobifenil" title="4-Aminobifenil – turc" lang="tr" hreflang="tr" data-title="4-Aminobifenil" data-language-autonym="Türkçe" data-language-local-name="turc" class="interlanguage-link-target"><span>Türkçe</span></a></li><li class="interlanguage-link interwiki-zh mw-list-item"><a href="https://zh.wikipedia.org/wiki/4-%E6%B0%A8%E5%9F%BA%E8%81%94%E8%8B%AF" title="4-氨基联苯 – chinois" lang="zh" hreflang="zh" data-title="4-氨基联苯" data-language-autonym="中文" data-language-local-name="chinois" 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/Q229922#sitelinks-wikipedia" title="Modifier les liens interlangues" class="wbc-editpage">Modifier les liens</a></span></div> </div> </div> </div> </header> <div class="vector-page-toolbar"> <div class="vector-page-toolbar-container"> <div id="left-navigation"> <nav aria-label="Espaces de noms"> <div id="p-associated-pages" class="vector-menu vector-menu-tabs mw-portlet mw-portlet-associated-pages" > <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li id="ca-nstab-main" class="selected vector-tab-noicon mw-list-item"><a href="/wiki/Amino-4-diph%C3%A9nyle" title="Voir le contenu de la page [c]" accesskey="c"><span>Article</span></a></li><li id="ca-talk" class="vector-tab-noicon mw-list-item"><a href="/wiki/Discussion:Amino-4-diph%C3%A9nyle" rel="discussion" title="Discussion au sujet de cette page de contenu [t]" accesskey="t"><span>Discussion</span></a></li> </ul> </div> </div> <div id="vector-variants-dropdown" class="vector-dropdown emptyPortlet" > <input type="checkbox" id="vector-variants-dropdown-checkbox" role="button" aria-haspopup="true" data-event-name="ui.dropdown-vector-variants-dropdown" class="vector-dropdown-checkbox " aria-label="Modifier la variante de langue" > <label id="vector-variants-dropdown-label" for="vector-variants-dropdown-checkbox" class="vector-dropdown-label cdx-button cdx-button--fake-button cdx-button--fake-button--enabled cdx-button--weight-quiet" aria-hidden="true" ><span class="vector-dropdown-label-text">français</span> </label> <div class="vector-dropdown-content"> <div id="p-variants" class="vector-menu mw-portlet mw-portlet-variants emptyPortlet" > <div class="vector-menu-content"> <ul class="vector-menu-content-list"> </ul> </div> </div> </div> </div> </nav> </div> <div id="right-navigation" class="vector-collapsible"> <nav aria-label="Affichages"> <div id="p-views" class="vector-menu vector-menu-tabs mw-portlet mw-portlet-views" > <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li id="ca-view" class="selected vector-tab-noicon mw-list-item"><a href="/wiki/Amino-4-diph%C3%A9nyle"><span>Lire</span></a></li><li id="ca-ve-edit" class="vector-tab-noicon mw-list-item"><a href="/w/index.php?title=Amino-4-diph%C3%A9nyle&veaction=edit" title="Modifier cette page [v]" accesskey="v"><span>Modifier</span></a></li><li id="ca-edit" class="collapsible vector-tab-noicon mw-list-item"><a href="/w/index.php?title=Amino-4-diph%C3%A9nyle&action=edit" title="Modifier le wikicode de cette page [e]" accesskey="e"><span>Modifier le code</span></a></li><li id="ca-history" class="vector-tab-noicon mw-list-item"><a href="/w/index.php?title=Amino-4-diph%C3%A9nyle&action=history" title="Historique des versions de cette page [h]" accesskey="h"><span>Voir l’historique</span></a></li> </ul> </div> </div> </nav> <nav class="vector-page-tools-landmark" aria-label="Outils de la page"> <div id="vector-page-tools-dropdown" class="vector-dropdown vector-page-tools-dropdown" > <input type="checkbox" id="vector-page-tools-dropdown-checkbox" role="button" aria-haspopup="true" data-event-name="ui.dropdown-vector-page-tools-dropdown" class="vector-dropdown-checkbox " aria-label="Outils" > <label id="vector-page-tools-dropdown-label" for="vector-page-tools-dropdown-checkbox" class="vector-dropdown-label cdx-button cdx-button--fake-button cdx-button--fake-button--enabled cdx-button--weight-quiet" aria-hidden="true" ><span class="vector-dropdown-label-text">Outils</span> </label> <div class="vector-dropdown-content"> <div id="vector-page-tools-unpinned-container" class="vector-unpinned-container"> <div id="vector-page-tools" class="vector-page-tools vector-pinnable-element"> <div class="vector-pinnable-header vector-page-tools-pinnable-header vector-pinnable-header-unpinned" data-feature-name="page-tools-pinned" data-pinnable-element-id="vector-page-tools" data-pinned-container-id="vector-page-tools-pinned-container" data-unpinned-container-id="vector-page-tools-unpinned-container" > <div class="vector-pinnable-header-label">Outils</div> <button class="vector-pinnable-header-toggle-button vector-pinnable-header-pin-button" data-event-name="pinnable-header.vector-page-tools.pin">déplacer vers la barre latérale</button> <button class="vector-pinnable-header-toggle-button vector-pinnable-header-unpin-button" data-event-name="pinnable-header.vector-page-tools.unpin">masquer</button> </div> <div id="p-cactions" class="vector-menu mw-portlet mw-portlet-cactions emptyPortlet vector-has-collapsible-items" title="Plus d’options" > <div class="vector-menu-heading"> Actions </div> <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li id="ca-more-view" class="selected vector-more-collapsible-item mw-list-item"><a href="/wiki/Amino-4-diph%C3%A9nyle"><span>Lire</span></a></li><li id="ca-more-ve-edit" class="vector-more-collapsible-item mw-list-item"><a href="/w/index.php?title=Amino-4-diph%C3%A9nyle&veaction=edit" title="Modifier cette page [v]" accesskey="v"><span>Modifier</span></a></li><li id="ca-more-edit" class="collapsible vector-more-collapsible-item mw-list-item"><a href="/w/index.php?title=Amino-4-diph%C3%A9nyle&action=edit" title="Modifier le wikicode de cette page [e]" accesskey="e"><span>Modifier le code</span></a></li><li id="ca-more-history" class="vector-more-collapsible-item mw-list-item"><a href="/w/index.php?title=Amino-4-diph%C3%A9nyle&action=history"><span>Voir l’historique</span></a></li> </ul> </div> </div> <div id="p-tb" class="vector-menu mw-portlet mw-portlet-tb" > <div class="vector-menu-heading"> Général </div> <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li id="t-whatlinkshere" class="mw-list-item"><a href="/wiki/Sp%C3%A9cial:Pages_li%C3%A9es/Amino-4-diph%C3%A9nyle" title="Liste des pages liées qui pointent sur celle-ci [j]" accesskey="j"><span>Pages liées</span></a></li><li id="t-recentchangeslinked" class="mw-list-item"><a href="/wiki/Sp%C3%A9cial:Suivi_des_liens/Amino-4-diph%C3%A9nyle" rel="nofollow" title="Liste des modifications récentes des pages appelées par celle-ci [k]" accesskey="k"><span>Suivi des pages liées</span></a></li><li id="t-upload" class="mw-list-item"><a href="/wiki/Aide:Importer_un_fichier" title="Téléverser des fichiers [u]" accesskey="u"><span>Téléverser un fichier</span></a></li><li id="t-specialpages" class="mw-list-item"><a href="/wiki/Sp%C3%A9cial:Pages_sp%C3%A9ciales" title="Liste de toutes les pages spéciales [q]" accesskey="q"><span>Pages spéciales</span></a></li><li id="t-permalink" class="mw-list-item"><a href="/w/index.php?title=Amino-4-diph%C3%A9nyle&oldid=213636812" title="Adresse permanente de cette version de cette page"><span>Lien permanent</span></a></li><li id="t-info" class="mw-list-item"><a href="/w/index.php?title=Amino-4-diph%C3%A9nyle&action=info" title="Davantage d’informations sur cette page"><span>Informations sur la page</span></a></li><li id="t-cite" class="mw-list-item"><a href="/w/index.php?title=Sp%C3%A9cial:Citer&page=Amino-4-diph%C3%A9nyle&id=213636812&wpFormIdentifier=titleform" title="Informations sur la manière de citer cette page"><span>Citer cette page</span></a></li><li id="t-urlshortener" class="mw-list-item"><a href="/w/index.php?title=Sp%C3%A9cial:UrlShortener&url=https%3A%2F%2Ffr.wikipedia.org%2Fwiki%2FAmino-4-diph%25C3%25A9nyle"><span>Obtenir l'URL raccourcie</span></a></li><li id="t-urlshortener-qrcode" class="mw-list-item"><a href="/w/index.php?title=Sp%C3%A9cial:QrCode&url=https%3A%2F%2Ffr.wikipedia.org%2Fwiki%2FAmino-4-diph%25C3%25A9nyle"><span>Télécharger le code QR</span></a></li> </ul> </div> </div> <div id="p-coll-print_export" class="vector-menu mw-portlet mw-portlet-coll-print_export" > <div class="vector-menu-heading"> Imprimer / exporter </div> <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li id="coll-create_a_book" class="mw-list-item"><a href="/w/index.php?title=Sp%C3%A9cial:Livre&bookcmd=book_creator&referer=Amino-4-diph%C3%A9nyle"><span>Créer un livre</span></a></li><li id="coll-download-as-rl" class="mw-list-item"><a href="/w/index.php?title=Sp%C3%A9cial:DownloadAsPdf&page=Amino-4-diph%C3%A9nyle&action=show-download-screen"><span>Télécharger comme PDF</span></a></li><li id="t-print" class="mw-list-item"><a href="/w/index.php?title=Amino-4-diph%C3%A9nyle&printable=yes" title="Version imprimable de cette page [p]" accesskey="p"><span>Version imprimable</span></a></li> </ul> </div> </div> <div id="p-wikibase-otherprojects" class="vector-menu mw-portlet mw-portlet-wikibase-otherprojects" > <div class="vector-menu-heading"> Dans d’autres projets </div> <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li id="t-wikibase" class="wb-otherproject-link wb-otherproject-wikibase-dataitem mw-list-item"><a href="https://www.wikidata.org/wiki/Special:EntityPage/Q229922" title="Lien vers l’élément dans le dépôt de données connecté [g]" accesskey="g"><span>Élément Wikidata</span></a></li> </ul> </div> </div> </div> </div> </div> </div> </nav> </div> </div> </div> <div class="vector-column-end"> <div class="vector-sticky-pinned-container"> <nav class="vector-page-tools-landmark" aria-label="Outils de la page"> <div id="vector-page-tools-pinned-container" class="vector-pinned-container"> </div> </nav> <nav class="vector-appearance-landmark" aria-label="Apparence"> <div id="vector-appearance-pinned-container" class="vector-pinned-container"> <div id="vector-appearance" class="vector-appearance vector-pinnable-element"> <div class="vector-pinnable-header vector-appearance-pinnable-header vector-pinnable-header-pinned" data-feature-name="appearance-pinned" data-pinnable-element-id="vector-appearance" data-pinned-container-id="vector-appearance-pinned-container" data-unpinned-container-id="vector-appearance-unpinned-container" > <div class="vector-pinnable-header-label">Apparence</div> <button class="vector-pinnable-header-toggle-button vector-pinnable-header-pin-button" data-event-name="pinnable-header.vector-appearance.pin">déplacer vers la barre latérale</button> <button class="vector-pinnable-header-toggle-button vector-pinnable-header-unpin-button" data-event-name="pinnable-header.vector-appearance.unpin">masquer</button> </div> </div> </div> </nav> </div> </div> <div id="bodyContent" class="vector-body" aria-labelledby="firstHeading" data-mw-ve-target-container> <div class="vector-body-before-content"> <div class="mw-indicators"> </div> <div id="siteSub" class="noprint">Un article de Wikipédia, l'encyclopédie libre.</div> </div> <div id="contentSub"><div id="mw-content-subtitle"></div></div> <div id="mw-content-text" class="mw-body-content"><div class="mw-content-ltr mw-parser-output" lang="fr" dir="ltr"><p class="mw-empty-elt"> </p> <table class="infobox_v2 infobox infobox--frwiki noarchive"> <tbody><tr> <td colspan="2" class="entete defaut" style="background-color:#FFDEAD;color:black;">Amino-4-diphényle </td></tr> <tr><td colspan="2" style="text-align:center; line-height: 1.5em;"><span typeof="mw:File/Frameless"><a href="/w/index.php?title=Fichier:4-Aminobiphenyl_structural_formula_V.1.svg&lang=fr" class="mw-file-description"><img alt="Image illustrative de l’article Amino-4-diphényle" src="//upload.wikimedia.org/wikipedia/commons/thumb/0/02/4-Aminobiphenyl_structural_formula_V.1.svg/langfr-200px-4-Aminobiphenyl_structural_formula_V.1.svg.png" decoding="async" width="200" height="54" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/02/4-Aminobiphenyl_structural_formula_V.1.svg/langfr-300px-4-Aminobiphenyl_structural_formula_V.1.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/02/4-Aminobiphenyl_structural_formula_V.1.svg/langfr-400px-4-Aminobiphenyl_structural_formula_V.1.svg.png 2x" data-file-width="438" data-file-height="119" /></a></span> </td></tr> <tr> <td colspan="2" style="text-align:center;">Structure chimique de l'amino-4-diphényle</td> </tr><tr> <th colspan="2" style="padding:4px; text-align:center; background-color:#FFDEAD; color:#000000">Identification</th></tr> <tr> <th scope="row"><a href="/wiki/Nomenclature_de_l%27UICPA" title="Nomenclature de l'UICPA">Nom UICPA</a> </th> <td><small>[1,1′-Biphenyl]-4-amine</small> </td> </tr> <tr> <th scope="row"><a href="/wiki/Synonymie" title="Synonymie">Synonymes</a> </th> <td> <p>biphényle-4-ylamine </p> </td> </tr> <tr> <th scope="row"><a href="/wiki/Num%C3%A9ro_CAS" title="Numéro CAS">N<sup>o</sup> CAS</a> </th> <td><span class="reflink plainlinksneverexpand"><span class="noarchive"><a class="external text" href="//tools.wmflabs.org/magnustools/cas.php?cas=92-67-1&language=fr&title=Amino-4-diphényle">92-67-1</a></span></span> </td> </tr> <tr> <th scope="row"> N<sup>o</sup> <a href="/wiki/Agence_europ%C3%A9enne_des_produits_chimiques" title="Agence européenne des produits chimiques">ECHA</a> </th> <td><span class="plainlinks"><span class="noarchive"><a rel="nofollow" class="external text" href="https://echa.europa.eu/substance-information/-/substanceinfo/100.001.980">100.001.980</a></span></span></td> </tr> <tr> <th scope="row"><a href="/wiki/Num%C3%A9ro_CE" title="Numéro CE">N<sup>o</sup> CE</a> </th> <td>202-177-1 </td> </tr> <tr> <th scope="row"><a href="/wiki/Simplified_Molecular_Input_Line_Entry_System" title="Simplified Molecular Input Line Entry System">SMILES</a> </th> <td><div class="NavFrame" title="[Afficher]/[Masquer]" style="border: none; padding: 0;"><div class="NavContent" style="display: none; text-align: left;">c1(c2ccccc2)ccc(N)cc1 <br /><span class="reflink plainlinksneverexpand"><a rel="nofollow" class="external text" href="http://pubchem.ncbi.nlm.nih.gov/search/?smarts=c1%28c2ccccc2%29ccc%28N%29cc1">PubChem</a></span>, <span class="reflink plainlinksneverexpand"><a rel="nofollow" class="external text" href="http://chemapps.stolaf.edu/jmol/jmol.php?title=Amino-4-diph%C3%A9nyle&model=c1%28c2ccccc2%29ccc%28N%29cc1">vue 3D</a></span></div></div> </td> </tr> <tr> <th scope="row"><a href="/wiki/International_Chemical_Identifier" title="International Chemical Identifier">InChI</a> </th> <td><div class="NavFrame" title="[Afficher]/[Masquer]" style="border: none; padding: 0;"><div class="NavContent" style="display: none; text-align: left;"><b>InChI :</b> <span class="reflink plainlinksneverexpand"><a rel="nofollow" class="external text" href="http://chemapps.stolaf.edu/jmol/jmol.php?title=Amino-4-diph%C3%A9nyle&model=InChI%3D1%2FC12H11N%2Fc13-12-8-6-11%287-9-12%2910-4-2-1-3-5-10%2Fh1-9H%2C13H2">vue 3D</a></span> <br />InChI=1/C12H11N/c13-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9H,13H2 <br /></div></div> </td> </tr> <tr> <th scope="row">Apparence </th> <td>Solide de formes variables, incolore, d'odeur caractéristique. Devient pourpre exposé à l'air<sup id="cite_ref-ICSC_1-0" class="reference"><a href="#cite_note-ICSC-1"><span class="cite_crochet">[</span>1<span class="cite_crochet">]</span></a></sup>. </td> </tr> <tr> <th colspan="2" style="padding:4px; text-align:center; background-color:#FFDEAD; color:#000000">Propriétés chimiques</th></tr> <tr> <th scope="row"><a href="/wiki/Formule_chimique" title="Formule chimique">Formule</a> </th> <td><a href="/wiki/Carbone" title="Carbone">C</a><sub>12</sub><a href="/wiki/Hydrog%C3%A8ne" title="Hydrogène">H</a><sub>11</sub><a href="/wiki/Azote" title="Azote">N</a>  <span class="page_h"><a href="/wiki/C12H11N" class="mw-disambig" title="C12H11N"><small>[Isomères]</small></a></span><br /> </td> </tr> <tr> <th scope="row"><a href="/wiki/Masse_molaire" title="Masse molaire">Masse molaire</a><sup id="cite_ref-3" class="reference"><a href="#cite_note-3"><span class="cite_crochet">[</span>3<span class="cite_crochet">]</span></a></sup> </th> <td>169,222 4 ± 0,010 6 <a href="/wiki/Gramme" title="Gramme">g</a>/<a href="/wiki/Mole_(unit%C3%A9)" title="Mole (unité)">mol</a> <br /><small>C 85,17 %,  H 6,55 %,  N 8,28 %,  </small> </td> </tr> <tr> <th scope="row"><a href="/wiki/Constante_d%27acidit%C3%A9" title="Constante d'acidité">p<i>K</i><sub>a</sub></a> </th> <td>4,35 à <span title="64,4 °F ou 291,2 K">18 </span><abbr class="abbr" title="degré Celsius">°C</abbr><sup id="cite_ref-chemidplus_2-0" class="reference"><a href="#cite_note-chemidplus-2"><span class="cite_crochet">[</span>2<span class="cite_crochet">]</span></a></sup> </td> </tr> <tr> <th colspan="2" style="padding:4px; text-align:center; background-color:#f7efa8; color:#000000">Propriétés physiques</th></tr> <tr> <th scope="row"><a href="/wiki/Point_de_fusion" title="Point de fusion"><abbr class="abbr" title="Température">T°</abbr> fusion</a> </th> <td><span title="128,3 °F ou 326,7 K">53,5 </span><abbr class="abbr" title="degré Celsius">°C</abbr><sup id="cite_ref-chemidplus_2-1" class="reference"><a href="#cite_note-chemidplus-2"><span class="cite_crochet">[</span>2<span class="cite_crochet">]</span></a></sup> </td> </tr> <tr> <th scope="row"><a href="/wiki/Point_d%27%C3%A9bullition" title="Point d'ébullition"><abbr class="abbr" title="Température">T°</abbr> ébullition</a> </th> <td><span title="575,6 °F ou 575,2 K">302 </span><abbr class="abbr" title="degré Celsius">°C</abbr><sup id="cite_ref-chemidplus_2-2" class="reference"><a href="#cite_note-chemidplus-2"><span class="cite_crochet">[</span>2<span class="cite_crochet">]</span></a></sup><br /><span title="375,8 °F ou 464,2 K">191 </span><abbr class="abbr" title="degré Celsius">°C</abbr> sous <span title="1 999,836 Pa ou 0,019 998 bar" style="cursor:help">15</span> <abbr class="abbr" title="millimètre de mercure"><a href="/wiki/Millim%C3%A8tre_de_mercure" title="Millimètre de mercure">mmHg</a></abbr> </td> </tr> <tr> <th scope="row"><a href="/wiki/Solubilit%C3%A9" title="Solubilité">Solubilité</a> </th> <td><span class="nowrap"><span title="">224</span> <span title="milligramme">mg</span>·<span title="Litre">l</span><sup>-1</sup></span> dans l'eau à <span title="77 °F ou 298,2 K">25 </span><abbr class="abbr" title="degré Celsius">°C</abbr><sup id="cite_ref-chemidplus_2-3" class="reference"><a href="#cite_note-chemidplus-2"><span class="cite_crochet">[</span>2<span class="cite_crochet">]</span></a></sup> </td> </tr> <tr> <th scope="row"><a href="/wiki/Masse_volumique" title="Masse volumique">Masse volumique</a> </th> <td><span class="nowrap"><span title="1 200 kg⋅m⁻³ ou 24,17 °Baumé">1,2</span> <span title="Gramme">g</span>·<span title="centimètre">cm</span><sup>-3</sup></span><sup id="cite_ref-ICSC_1-1" class="reference"><a href="#cite_note-ICSC-1"><span class="cite_crochet">[</span>1<span class="cite_crochet">]</span></a></sup> </td> </tr> <tr> <th scope="row"><a href="/wiki/Point_d%27auto-inflammation" title="Point d'auto-inflammation"><abbr class="abbr" title="Température">T°</abbr> d'auto-inflammation</a> </th> <td><span title="842 °F ou 723,2 K">450 </span><abbr class="abbr" title="degré Celsius">°C</abbr><sup id="cite_ref-ICSC_1-2" class="reference"><a href="#cite_note-ICSC-1"><span class="cite_crochet">[</span>1<span class="cite_crochet">]</span></a></sup> </td> </tr> <tr> <th scope="row"><a href="/wiki/Point_d%27%C3%A9clair" title="Point d'éclair">Point d’éclair</a> </th> <td><span title="307,4 °F ou 426,2 K">153 </span><abbr class="abbr" title="degré Celsius">°C</abbr> (coupelle fermée)<sup id="cite_ref-ICSC_1-3" class="reference"><a href="#cite_note-ICSC-1"><span class="cite_crochet">[</span>1<span class="cite_crochet">]</span></a></sup> </td> </tr> <tr> <th scope="row"><a href="/wiki/Pression_de_vapeur_saturante" title="Pression de vapeur saturante">Pression de vapeur saturante</a> </th> <td><span class="nowrap"><span title="2 000 Pa">20</span> <span title="millibar">mbar</span></span> à <span title="375,8 °F ou 464,2 K">191 </span><abbr class="abbr" title="degré Celsius">°C</abbr> </td> </tr> <tr> <th colspan="2" style="padding:4px; text-align:center; background-color:#FFDEAD; color:#000000">Thermochimie</th></tr> <tr> <th scope="row"><a href="/wiki/Capacit%C3%A9_thermique" title="Capacité thermique">C<sub>p</sub></a> </th> <td><div class="NavFrame" title="[+]/[-]" style="border:none; padding: 0;"><div class="NavContent" style="display:none; text-align:left;"><hr /> <p>équation<sup id="cite_ref-Yaws_4-0" class="reference"><a href="#cite_note-Yaws-4"><span class="cite_crochet">[</span>4<span class="cite_crochet">]</span></a></sup> : <span class="mwe-math-element"><span class="mwe-math-mathml-inline mwe-math-mathml-a11y" style="display: none;"><math xmlns="http://www.w3.org/1998/Math/MathML" alttext="{\displaystyle C_{P}=(-95.528)+(1.2611)\times T+(-1.1955E-3)\times T^{2}+(5.8242E-7)\times T^{3}+(-1.1477E-10)\times T^{4}}"> <semantics> <mrow class="MJX-TeXAtom-ORD"> <mstyle displaystyle="true" scriptlevel="0"> <msub> <mi>C</mi> <mrow class="MJX-TeXAtom-ORD"> <mi>P</mi> </mrow> </msub> <mo>=</mo> <mo stretchy="false">(</mo> <mo>−</mo> <mn>95.528</mn> <mo stretchy="false">)</mo> <mo>+</mo> <mo stretchy="false">(</mo> <mn>1.2611</mn> <mo stretchy="false">)</mo> <mo>×</mo> <mi>T</mi> <mo>+</mo> <mo stretchy="false">(</mo> <mo>−</mo> <mn>1.1955</mn> <mi>E</mi> <mo>−</mo> <mn>3</mn> <mo stretchy="false">)</mo> <mo>×</mo> <msup> <mi>T</mi> <mrow class="MJX-TeXAtom-ORD"> <mn>2</mn> </mrow> </msup> <mo>+</mo> <mo stretchy="false">(</mo> <mn>5.8242</mn> <mi>E</mi> <mo>−</mo> <mn>7</mn> <mo stretchy="false">)</mo> <mo>×</mo> <msup> <mi>T</mi> <mrow class="MJX-TeXAtom-ORD"> <mn>3</mn> </mrow> </msup> <mo>+</mo> <mo stretchy="false">(</mo> <mo>−</mo> <mn>1.1477</mn> <mi>E</mi> <mo>−</mo> <mn>10</mn> <mo stretchy="false">)</mo> <mo>×</mo> <msup> <mi>T</mi> <mrow class="MJX-TeXAtom-ORD"> <mn>4</mn> </mrow> </msup> </mstyle> </mrow> <annotation encoding="application/x-tex">{\displaystyle C_{P}=(-95.528)+(1.2611)\times T+(-1.1955E-3)\times T^{2}+(5.8242E-7)\times T^{3}+(-1.1477E-10)\times T^{4}}</annotation> </semantics> </math></span><img src="https://wikimedia.org/api/rest_v1/media/math/render/svg/4479656729f662fe0324fb3d46611be23e9a489e" class="mwe-math-fallback-image-inline mw-invert skin-invert" aria-hidden="true" style="vertical-align: -0.838ex; width:104.173ex; height:3.176ex;" alt="{\displaystyle C_{P}=(-95.528)+(1.2611)\times T+(-1.1955E-3)\times T^{2}+(5.8242E-7)\times T^{3}+(-1.1477E-10)\times T^{4}}"></span><br /> Capacité thermique du gaz en J·mol<sup>-1</sup>·K<sup>-1</sup> et température en kelvins, de 298 à 1 500 K.<br /> Valeurs calculées : <br />188,726 J·mol<sup>-1</sup>·K<sup>-1</sup> à 25 °C. </p> <table><tbody><tr><td> <table class="wikitable"> <tbody><tr><th>T<br />(K)</th> <th>T<br />(°C)</th> <th>C<sub>p</sub><br /><span class="mwe-math-element"><span class="mwe-math-mathml-inline mwe-math-mathml-a11y" style="display: none;"><math xmlns="http://www.w3.org/1998/Math/MathML" alttext="{\displaystyle ({\tfrac {J}{kmol\times K}})}"> <semantics> <mrow class="MJX-TeXAtom-ORD"> <mstyle displaystyle="true" scriptlevel="0"> <mo stretchy="false">(</mo> <mrow class="MJX-TeXAtom-ORD"> <mstyle displaystyle="false" scriptlevel="0"> <mfrac> <mi>J</mi> <mrow> <mi>k</mi> <mi>m</mi> <mi>o</mi> <mi>l</mi> <mo>×</mo> <mi>K</mi> </mrow> </mfrac> </mstyle> </mrow> <mo stretchy="false">)</mo> </mstyle> </mrow> <annotation encoding="application/x-tex">{\displaystyle ({\tfrac {J}{kmol\times K}})}</annotation> </semantics> </math></span><img src="https://wikimedia.org/api/rest_v1/media/math/render/svg/0284c56a605f091ad5194cf9ad3de996f5d757b2" class="mwe-math-fallback-image-inline mw-invert skin-invert" aria-hidden="true" style="vertical-align: -1.338ex; width:8.972ex; height:3.843ex;" alt="{\displaystyle ({\tfrac {J}{kmol\times K}})}"></span></th> <th>C<sub>p</sub><br /><span class="mwe-math-element"><span class="mwe-math-mathml-inline mwe-math-mathml-a11y" style="display: none;"><math xmlns="http://www.w3.org/1998/Math/MathML" alttext="{\displaystyle ({\tfrac {J}{kg\times K}})}"> <semantics> <mrow class="MJX-TeXAtom-ORD"> <mstyle displaystyle="true" scriptlevel="0"> <mo stretchy="false">(</mo> <mrow class="MJX-TeXAtom-ORD"> <mstyle displaystyle="false" scriptlevel="0"> <mfrac> <mi>J</mi> <mrow> <mi>k</mi> <mi>g</mi> <mo>×</mo> <mi>K</mi> </mrow> </mfrac> </mstyle> </mrow> <mo stretchy="false">)</mo> </mstyle> </mrow> <annotation encoding="application/x-tex">{\displaystyle ({\tfrac {J}{kg\times K}})}</annotation> </semantics> </math></span><img src="https://wikimedia.org/api/rest_v1/media/math/render/svg/e2ffae996ebf9a4ddfe360b8b7aa9f0f89711fa4" class="mwe-math-fallback-image-inline mw-invert skin-invert" aria-hidden="true" style="vertical-align: -1.671ex; width:7.03ex; height:4.176ex;" alt="{\displaystyle ({\tfrac {J}{kg\times K}})}"></span></th></tr> <tr><td>298</td> <td>24,85</td> <td>188 622</td> <td>1 115</td></tr> <tr><td>378</td> <td>104,85</td> <td>239 463</td> <td>1 415</td></tr> <tr><td>418</td> <td>144,85</td> <td>261 762</td> <td>1 547</td></tr> <tr><td>458</td> <td>184,85</td> <td>282 187</td> <td>1 668</td></tr> <tr><td>498</td> <td>224,85</td> <td>300 884</td> <td>1 778</td></tr> <tr><td>538</td> <td>264,85</td> <td>317 993</td> <td>1 879</td></tr> <tr><td>578</td> <td>304,85</td> <td>333 646</td> <td>1 972</td></tr> <tr><td>618</td> <td>344,85</td> <td>347 969</td> <td>2 056</td></tr> <tr><td>658</td> <td>384,85</td> <td>361 079</td> <td>2 134</td></tr> <tr><td>698</td> <td>424,85</td> <td>373 087</td> <td>2 205</td></tr> <tr><td>738</td> <td>464,85</td> <td>384 099</td> <td>2 270</td></tr> <tr><td>778</td> <td>504,85</td> <td>394 211</td> <td>2 330</td></tr> <tr><td>818</td> <td>544,85</td> <td>403 512</td> <td>2 385</td></tr> <tr><td>858</td> <td>584,85</td> <td>412 087</td> <td>2 435</td></tr> <tr><td>899</td> <td>625,85</td> <td>420 201</td> <td>2 483</td></tr> </tbody></table> </td><td> <table class="wikitable"> <tbody><tr><th>T<br />(K)</th> <th>T<br />(°C)</th> <th>C<sub>p</sub><br /><span class="mwe-math-element"><span class="mwe-math-mathml-inline mwe-math-mathml-a11y" style="display: none;"><math xmlns="http://www.w3.org/1998/Math/MathML" alttext="{\displaystyle ({\tfrac {J}{kmol\times K}})}"> <semantics> <mrow class="MJX-TeXAtom-ORD"> <mstyle displaystyle="true" scriptlevel="0"> <mo stretchy="false">(</mo> <mrow class="MJX-TeXAtom-ORD"> <mstyle displaystyle="false" scriptlevel="0"> <mfrac> <mi>J</mi> <mrow> <mi>k</mi> <mi>m</mi> <mi>o</mi> <mi>l</mi> <mo>×</mo> <mi>K</mi> </mrow> </mfrac> </mstyle> </mrow> <mo stretchy="false">)</mo> </mstyle> </mrow> <annotation encoding="application/x-tex">{\displaystyle ({\tfrac {J}{kmol\times K}})}</annotation> </semantics> </math></span><img src="https://wikimedia.org/api/rest_v1/media/math/render/svg/0284c56a605f091ad5194cf9ad3de996f5d757b2" class="mwe-math-fallback-image-inline mw-invert skin-invert" aria-hidden="true" style="vertical-align: -1.338ex; width:8.972ex; height:3.843ex;" alt="{\displaystyle ({\tfrac {J}{kmol\times K}})}"></span></th> <th>C<sub>p</sub><br /><span class="mwe-math-element"><span class="mwe-math-mathml-inline mwe-math-mathml-a11y" style="display: none;"><math xmlns="http://www.w3.org/1998/Math/MathML" alttext="{\displaystyle ({\tfrac {J}{kg\times K}})}"> <semantics> <mrow class="MJX-TeXAtom-ORD"> <mstyle displaystyle="true" scriptlevel="0"> <mo stretchy="false">(</mo> <mrow class="MJX-TeXAtom-ORD"> <mstyle displaystyle="false" scriptlevel="0"> <mfrac> <mi>J</mi> <mrow> <mi>k</mi> <mi>g</mi> <mo>×</mo> <mi>K</mi> </mrow> </mfrac> </mstyle> </mrow> <mo stretchy="false">)</mo> </mstyle> </mrow> <annotation encoding="application/x-tex">{\displaystyle ({\tfrac {J}{kg\times K}})}</annotation> </semantics> </math></span><img src="https://wikimedia.org/api/rest_v1/media/math/render/svg/e2ffae996ebf9a4ddfe360b8b7aa9f0f89711fa4" class="mwe-math-fallback-image-inline mw-invert skin-invert" aria-hidden="true" style="vertical-align: -1.671ex; width:7.03ex; height:4.176ex;" alt="{\displaystyle ({\tfrac {J}{kg\times K}})}"></span></th></tr> <tr><td>939</td> <td>665,85</td> <td>427 528</td> <td>2 526</td></tr> <tr><td>979</td> <td>705,85</td> <td>434 337</td> <td>2 567</td></tr> <tr><td>1 019</td> <td>745,85</td> <td>440 681</td> <td>2 604</td></tr> <tr><td>1 059</td> <td>785,85</td> <td>446 608</td> <td>2 639</td></tr> <tr><td>1 099</td> <td>825,85</td> <td>452 159</td> <td>2 672</td></tr> <tr><td>1 139</td> <td>865,85</td> <td>457 367</td> <td>2 703</td></tr> <tr><td>1 179</td> <td>905,85</td> <td>462 259</td> <td>2 732</td></tr> <tr><td>1 219</td> <td>945,85</td> <td>466 853</td> <td>2 759</td></tr> <tr><td>1 259</td> <td>985,85</td> <td>471 162</td> <td>2 784</td></tr> <tr><td>1 299</td> <td>1 025,85</td> <td>475 192</td> <td>2 808</td></tr> <tr><td>1 339</td> <td>1 065,85</td> <td>478 940</td> <td>2 830</td></tr> <tr><td>1 379</td> <td>1 105,85</td> <td>482 398</td> <td>2 851</td></tr> <tr><td>1 419</td> <td>1 145,85</td> <td>485 550</td> <td>2 869</td></tr> <tr><td>1 459</td> <td>1 185,85</td> <td>488 372</td> <td>2 886</td></tr> <tr><td>1 500</td> <td>1 226,85</td> <td>490 891</td> <td>2 901</td></tr> </tbody></table> </td></tr></tbody></table> </div></div> </td> </tr> <tr> <th colspan="2" style="padding:4px; text-align:center; background-color:#ffb4b4; color:#000000">Précautions</th></tr> <tr> <th colspan="2" style="padding:4px; text-align:center; background-color:#eeeeee; color:#000000"><a href="/wiki/Syst%C3%A8me_g%C3%A9n%C3%A9ral_harmonis%C3%A9_de_classification_et_d%27%C3%A9tiquetage_des_produits_chimiques" title="Système général harmonisé de classification et d'étiquetage des produits chimiques">SGH</a><sup id="cite_ref-SGH_7-0" class="reference"><a href="#cite_note-SGH-7"><span class="cite_crochet">[</span>7<span class="cite_crochet">]</span></a></sup></th></tr> <tr> <td colspan="2" style="text-align:center;"><div style="text-align: center;"><span typeof="mw:File"><a href="/wiki/Fichier:GHS-pictogram-exclam.svg" class="mw-file-description" title="SGH07 : Toxique, irritant, sensibilisant, narcotique"><img alt="SGH07 : Toxique, irritant, sensibilisant, narcotique" src="//upload.wikimedia.org/wikipedia/commons/thumb/c/c3/GHS-pictogram-exclam.svg/60px-GHS-pictogram-exclam.svg.png" decoding="async" width="60" height="60" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/c3/GHS-pictogram-exclam.svg/90px-GHS-pictogram-exclam.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/c3/GHS-pictogram-exclam.svg/120px-GHS-pictogram-exclam.svg.png 2x" data-file-width="512" data-file-height="512" /></a></span><span typeof="mw:File"><a href="/wiki/Fichier:GHS-pictogram-silhouette.svg" class="mw-file-description" title="SGH08 : Sensibilisant, mutagène, cancérogène, reprotoxique"><img alt="SGH08 : Sensibilisant, mutagène, cancérogène, reprotoxique" src="//upload.wikimedia.org/wikipedia/commons/thumb/2/21/GHS-pictogram-silhouette.svg/60px-GHS-pictogram-silhouette.svg.png" decoding="async" width="60" height="60" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/21/GHS-pictogram-silhouette.svg/90px-GHS-pictogram-silhouette.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/21/GHS-pictogram-silhouette.svg/120px-GHS-pictogram-silhouette.svg.png 2x" data-file-width="724" data-file-height="724" /></a></span><br />Danger</div><span title="Nocif en cas d'ingestion">H302</span> et <span title="Peut provoquer le cancer (indiquer la voie d'exposition s'il est formellement prouvé qu'aucune autre voie d'exposition ne conduit au même danger)">H350</span><div class="NavFrame" title="[+]/[–]" style="border:none; padding : 0;"><div class="NavContent" style="display:none; text-align:left;"><b>H302</b> : Nocif en cas d'ingestion<br /><b>H350</b> : Peut provoquer le cancer <span style="color: gray;">(indiquer la voie d'exposition s'il est formellement prouvé qu'aucune autre voie d'exposition ne conduit au même danger)</span><br /></div></div></td> </tr><tr> <th colspan="2" style="padding:4px; text-align:center; background-color:#eeeeee; color:#000000">Classification du <a href="/wiki/Centre_international_de_recherche_sur_le_cancer" title="Centre international de recherche sur le cancer">CIRC</a></th></tr> <tr> <td colspan="2" style="text-align:left;">Groupe 1 : Cancérogène pour l'homme<sup id="cite_ref-6" class="reference"><a href="#cite_note-6"><span class="cite_crochet">[</span>6<span class="cite_crochet">]</span></a></sup></td> </tr><tr> <th colspan="2" style="padding:4px; text-align:center; background-color:#ffb4b4; color:#000000"><a href="/wiki/%C3%89cotoxicologie" title="Écotoxicologie">Écotoxicologie</a></th></tr> <tr> <th scope="row"><a href="/wiki/Dose_l%C3%A9tale_m%C3%A9diane" title="Dose létale médiane">DL<small style="line-height: 1.5em; font-size: 80%;"><sub>50</sub></small></a> </th> <td><span class="nowrap"><span title="">500</span> <span title="milligramme">mg</span>·<span title="Kilogramme">kg</span><sup>-1</sup></span> (rat, oral)<sup id="cite_ref-chemidplus_2-4" class="reference"><a href="#cite_note-chemidplus-2"><span class="cite_crochet">[</span>2<span class="cite_crochet">]</span></a></sup> </td> </tr> <tr> <th scope="row"><a href="/wiki/LogP" title="LogP">LogP</a> </th> <td>2,8<sup id="cite_ref-ICSC_1-4" class="reference"><a href="#cite_note-ICSC-1"><span class="cite_crochet">[</span>1<span class="cite_crochet">]</span></a></sup> </td> </tr> <tr> <td colspan="2"><hr style="height:2px; background-color:#FFDEAD;" /></td></tr> <tr> <td colspan="2" style="text-align:center;">Unités du <a href="/wiki/Syst%C3%A8me_international_d%27unit%C3%A9s" title="Système international d'unités">SI</a> et <a href="/wiki/Conditions_normales_de_temp%C3%A9rature_et_de_pression" title="Conditions normales de température et de pression"><abbr title="conditions normales de température et de pression">CNTP</abbr></a>, sauf indication contraire.</td> </tr><tr> <td class="navigation-only" colspan="2" style="border-top: 2px #FFDEAD solid; font-size: 80%; background:inherit; color: inherit; text-align: right;"><span class="plainlinks" style="float:left;"><a class="external text" href="https://fr.wikipedia.org/w/index.php?title=Amino-4-diph%C3%A9nyle&action=edit&section=0"><span class="infodoc">modifier</span></a></span> <span typeof="mw:File"><a href="/wiki/Mod%C3%A8le:Infobox_Chimie" title="Consultez la documentation du modèle"><img alt="" src="//upload.wikimedia.org/wikipedia/commons/thumb/3/38/Info_Simple.svg/12px-Info_Simple.svg.png" decoding="async" width="12" height="12" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/3/38/Info_Simple.svg/18px-Info_Simple.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/3/38/Info_Simple.svg/24px-Info_Simple.svg.png 2x" data-file-width="512" data-file-height="512" /></a></span></td> </tr> </tbody></table> <p>L'<b>amino-4-diphényle</b> est un dérivé du <a href="/wiki/Biph%C3%A9nyle" title="Biphényle">biphényle</a> similaire à la <a href="/wiki/Benzidine" title="Benzidine">benzidine</a>. Il est utilisé pour la fabrication de <a href="/wiki/Colorant_azo%C3%AFque" title="Colorant azoïque">colorants azoïques</a>. Il est connu comme étant <a href="/wiki/Canc%C3%A9rog%C3%A8ne" title="Cancérogène">cancérogène</a> certain pour l'homme et il a été en grande partie remplacé par des substances moins toxiques. </p> <div class="mw-heading mw-heading2"><h2 id="Références"><span id="R.C3.A9f.C3.A9rences"></span>Références</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Amino-4-diph%C3%A9nyle&veaction=edit&section=1" title="Modifier la section : Références" class="mw-editsection-visualeditor"><span>modifier</span></a><span class="mw-editsection-divider"> | </span><a href="/w/index.php?title=Amino-4-diph%C3%A9nyle&action=edit&section=1" title="Modifier le code source de la section : Références"><span>modifier le code</span></a><span class="mw-editsection-bracket">]</span></span></div> <div class="mw-references-wrap"><ol class="references"> <li id="cite_note-ICSC-1"><span class="mw-cite-backlink noprint">↑ <sup><a href="#cite_ref-ICSC_1-0">a</a> <a href="#cite_ref-ICSC_1-1">b</a> <a href="#cite_ref-ICSC_1-2">c</a> <a href="#cite_ref-ICSC_1-3">d</a> et <a href="#cite_ref-ICSC_1-4">e</a></sup> </span><span class="reference-text"><a rel="nofollow" class="external text" href="https://www.ilo.org/dyn/icsc/showcard.display?p_lang=fr&p_card_id=0759">4 - AMINOBIPHENYLE</a>, <a href="/wiki/Fiches_internationales_de_s%C3%A9curit%C3%A9_chimique" title="Fiches internationales de sécurité chimique">Fiches internationales de sécurité chimique</a> </span> </li> <li id="cite_note-chemidplus-2"><span class="mw-cite-backlink noprint">↑ <sup><a href="#cite_ref-chemidplus_2-0">a</a> <a href="#cite_ref-chemidplus_2-1">b</a> <a href="#cite_ref-chemidplus_2-2">c</a> <a href="#cite_ref-chemidplus_2-3">d</a> et <a href="#cite_ref-chemidplus_2-4">e</a></sup> </span><span class="reference-text"><a rel="nofollow" class="external free" href="https://archive.wikiwix.com/cache/20110223160333/http://chem.sis.nlm.nih.gov/chemidplus/direct.jsp?result=advanced&regno=000092671">https://archive.wikiwix.com/cache/20110223160333/http://chem.sis.nlm.nih.gov/chemidplus/direct.jsp?result=advanced&regno=000092671</a>.</span> </li> <li id="cite_note-3"><span class="mw-cite-backlink noprint"><a href="#cite_ref-3">↑</a> </span><span class="reference-text">Masse molaire calculée d’après <span class="ouvrage">« <a rel="nofollow" class="external text" href="http://www.chem.qmul.ac.uk/iupac/AtWt/"><cite style="font-style:normal;"><span class="lang-en" lang="en">Atomic weights of the elements 2007</span></cite></a> », sur <span class="italique">www.chem.qmul.ac.uk</span></span>.</span> </li> <li id="cite_note-Yaws-4"><span class="mw-cite-backlink noprint"><a href="#cite_ref-Yaws_4-0">↑</a> </span><span class="reference-text"><span class="ouvrage" id="Yaws1996"><span class="ouvrage" id="Carl_L._Yaws1996"><abbr class="abbr indicateur-langue" title="Langue : anglais">(en)</abbr> Carl L. Yaws, <cite class="italique" lang="en">Handbook of Thermodynamic Diagrams : Organic Compounds C8 to C28</cite>, <abbr class="abbr" title="volume">vol.</abbr> 3, Huston, Texas, Gulf Pub. Co., <time>1996</time>, 396 <abbr class="abbr" title="pages">p.</abbr> <small style="line-height:1em;">(<a href="/wiki/International_Standard_Book_Number" title="International Standard Book Number">ISBN</a> <a href="/wiki/Sp%C3%A9cial:Ouvrages_de_r%C3%A9f%C3%A9rence/0-88415-859-4" title="Spécial:Ouvrages de référence/0-88415-859-4"><span class="nowrap">0-88415-859-4</span></a>)</small><span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Handbook+of+Thermodynamic+Diagrams&rft.place=Huston%2C+Texas&rft.pub=Gulf+Pub.+Co.&rft.stitle=Organic+Compounds+C8+to+C28&rft.aulast=Yaws&rft.aufirst=Carl+L.&rft.date=1996&rft.volume=3&rft.tpages=396&rft.isbn=0-88415-859-4&rfr_id=info%3Asid%2Ffr.wikipedia.org%3AAmino-4-diph%C3%A9nyle"></span></span></span></span> </li> <li id="cite_note-ESIS-5"><span class="mw-cite-backlink noprint"><a href="#cite_ref-ESIS_5-0">↑</a> </span><span class="reference-text"><span class="ouvrage">« <a rel="nofollow" class="external text" href="https://archive.wikiwix.com/cache/20100428143316/http://ecb.jrc.ec.europa.eu/esis/index.php?GENRE=CASNO&ENTREE=92-67-1"><cite style="font-style:normal;">ESIS (European chemical Substances Information System).</cite></a> », sur <span class="italique">europa.eu via <a href="/wiki/Wikiwix" title="Wikiwix">Wikiwix</a></span> <small style="line-height:1em;">(consulté le <time class="nowrap" datetime="2023-10-12" data-sort-value="2023-10-12">12 octobre 2023</time>)</small></span>.</span> </li> <li id="cite_note-6"><span class="mw-cite-backlink noprint"><a href="#cite_ref-6">↑</a> </span><span class="reference-text"><span class="ouvrage" id="Working_Group_on_the_Evaluation_of_Carcinogenic_Risks_to_Humans2009"><span class="ouvrage" id="IARC_Working_Group_on_the_Evaluation_of_Carcinogenic_Risks_to_Humans2009">IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, <span class="noarchive">« <a rel="nofollow" class="external text" href="http://monographs.iarc.fr/FR/Classification/crthgr01list.php"><cite style="font-style:normal; color:var(--color-link-red, #d73333);">Evaluations Globales de la Cancérogénicité pour l'Homme, Groupe 1 : Cancérogènes pour l'homme</cite></a> »<sup class="plainlinks">(<a rel="nofollow" class="external text" href="https://web.archive.org/web/*/http://monographs.iarc.fr/FR/Classification/crthgr01list.php">Archive.org</a> • <a rel="nofollow" class="external text" href="https://archive.wikiwix.com/cache/?url=http://monographs.iarc.fr/FR/Classification/crthgr01list.php">Wikiwix</a> • <a rel="nofollow" class="external text" href="https://archive.is/http://monographs.iarc.fr/FR/Classification/crthgr01list.php">Archive.is</a> • <a rel="nofollow" class="external text" href="https://webcache.googleusercontent.com/search?hl=fr&q=cache:http://monographs.iarc.fr/FR/Classification/crthgr01list.php">Google</a> • <a href="/wiki/Projet:Correction_des_liens_externes#J'ai_trouvé_un_lien_mort,_que_faire_?" title="Projet:Correction des liens externes">Que faire ?</a>)</sup></span>, sur <span class="italique">monographs.iarc.fr</span>, CIRC, <time class="nowrap" datetime="2009-01-16" data-sort-value="2009-01-16">16 janvier 2009</time> <small style="line-height:1em;">(consulté le <time class="nowrap" datetime="2009-08-22" data-sort-value="2009-08-22">22 août 2009</time>)</small></span></span>.</span> </li> <li id="cite_note-SGH-7"><span class="mw-cite-backlink noprint"><a href="#cite_ref-SGH_7-0">↑</a> </span><span class="reference-text">Numéro index <span class="reflink plainlinksneverexpand"><span class="noarchive"><a rel="nofollow" class="external text" href="http://apps.kemi.se/klassificeringslistan/amne.cfm?id=612-072-00-6"><span title="4-aminobiphényle; 4-biphénylylamine">612-072-00-6</span></a></span></span> dans le tableau 3.1 de l'annexe VI du <a rel="nofollow" class="external text" href="http://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=OJ:L:2008:353:0001:1355:FR:PDF">règlement CE <abbr class="abbr" title="numéro">n<sup>o</sup></abbr> 1272/2008</a> (16 décembre 2008)</span> </li> </ol></div> <div class="mw-heading mw-heading2"><h2 id="Articles_connexes">Articles connexes</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Amino-4-diph%C3%A9nyle&veaction=edit&section=2" title="Modifier la section : Articles connexes" class="mw-editsection-visualeditor"><span>modifier</span></a><span class="mw-editsection-divider"> | </span><a href="/w/index.php?title=Amino-4-diph%C3%A9nyle&action=edit&section=2" title="Modifier le code source de la section : Articles connexes"><span>modifier le code</span></a><span class="mw-editsection-bracket">]</span></span></div> <ul><li><a href="/wiki/Naphtal%C3%A8ne" title="Naphtalène">Naphtalène</a></li> <li><a href="/wiki/Naphtol" title="Naphtol">Naphtol</a></li> <li><a href="/wiki/B%C3%AAta-Naphtylamine" title="Bêta-Naphtylamine">β-Naphtylamine</a></li> <li><a href="/wiki/Benzidine" title="Benzidine">Benzidine</a></li> <li><a href="/wiki/Amine_aromatique" title="Amine aromatique">Amine aromatique</a></li></ul> <ul id="bandeau-portail" class="bandeau-portail"><li><span class="bandeau-portail-element"><span class="bandeau-portail-icone"><span class="noviewer" typeof="mw:File"><a href="/wiki/Portail:Chimie" title="Portail de la chimie"><img alt="icône décorative" src="//upload.wikimedia.org/wikipedia/commons/thumb/5/59/Nuvola_apps_edu_science.svg/24px-Nuvola_apps_edu_science.svg.png" decoding="async" width="24" height="24" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/5/59/Nuvola_apps_edu_science.svg/36px-Nuvola_apps_edu_science.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/5/59/Nuvola_apps_edu_science.svg/48px-Nuvola_apps_edu_science.svg.png 2x" data-file-width="128" data-file-height="128" /></a></span></span> <span class="bandeau-portail-texte"><a href="/wiki/Portail:Chimie" title="Portail:Chimie">Portail de la chimie</a></span> </span></li> </ul>    </div><noscript><img src="https://login.wikimedia.org/wiki/Special:CentralAutoLogin/start?type=1x1&useformat=desktop" alt="" width="1" height="1" style="border: none; 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