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Available in 30 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-30" 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">30 languages</span> </label> <div class="vector-dropdown-content"> <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li class="interlanguage-link interwiki-azb mw-list-item"><a href="https://azb.wikipedia.org/wiki/%D8%AF%DB%8C%D9%88%D9%85%D8%AA%DB%8C%D9%84_%D8%AC%DB%8C%D9%88%D9%87" title="دیومتیل جیوه – South Azerbaijani" lang="azb" hreflang="azb" data-title="دیومتیل جیوه" data-language-autonym="تۆرکجه" data-language-local-name="South Azerbaijani" class="interlanguage-link-target"><span>تۆرکجه</span></a></li><li class="interlanguage-link interwiki-bn mw-list-item"><a href="https://bn.wikipedia.org/wiki/%E0%A6%A1%E0%A6%BE%E0%A6%87%E0%A6%AE%E0%A6%BF%E0%A6%A5%E0%A6%BE%E0%A6%87%E0%A6%B2%E0%A6%AE%E0%A6%BE%E0%A6%B0%E0%A6%95%E0%A6%BE%E0%A6%B0%E0%A6%BF" title="ডাইমিথাইলমারকারি – Bangla" lang="bn" hreflang="bn" data-title="ডাইমিথাইলমারকারি" data-language-autonym="বাংলা" data-language-local-name="Bangla" class="interlanguage-link-target"><span>বাংলা</span></a></li><li class="interlanguage-link interwiki-bs mw-list-item"><a href="https://bs.wikipedia.org/wiki/Dimetil_%C5%BEiva" title="Dimetil živa – Bosnian" lang="bs" hreflang="bs" data-title="Dimetil živa" data-language-autonym="Bosanski" data-language-local-name="Bosnian" class="interlanguage-link-target"><span>Bosanski</span></a></li><li class="interlanguage-link interwiki-ca mw-list-item"><a href="https://ca.wikipedia.org/wiki/Dimetilmercuri" title="Dimetilmercuri – Catalan" lang="ca" hreflang="ca" data-title="Dimetilmercuri" 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/Dimethylrtu%C5%A5" title="Dimethylrtuť – Czech" lang="cs" hreflang="cs" data-title="Dimethylrtuť" data-language-autonym="Čeština" data-language-local-name="Czech" class="interlanguage-link-target"><span>Čeština</span></a></li><li class="interlanguage-link interwiki-de mw-list-item"><a href="https://de.wikipedia.org/wiki/Dimethylquecksilber" title="Dimethylquecksilber – German" lang="de" hreflang="de" data-title="Dimethylquecksilber" data-language-autonym="Deutsch" data-language-local-name="German" class="interlanguage-link-target"><span>Deutsch</span></a></li><li class="interlanguage-link interwiki-el mw-list-item"><a href="https://el.wikipedia.org/wiki/%CE%94%CE%B9%CE%BC%CE%B5%CE%B8%CF%85%CE%BB%CF%85%CE%B4%CF%81%CE%AC%CF%81%CE%B3%CF%85%CF%81%CE%BF%CF%82" title="Διμεθυλυδράργυρος – Greek" lang="el" hreflang="el" data-title="Διμεθυλυδράργυρος" data-language-autonym="Ελληνικά" data-language-local-name="Greek" class="interlanguage-link-target"><span>Ελληνικά</span></a></li><li class="interlanguage-link interwiki-es mw-list-item"><a href="https://es.wikipedia.org/wiki/Dimetilmercurio" title="Dimetilmercurio – Spanish" lang="es" hreflang="es" data-title="Dimetilmercurio" data-language-autonym="Español" data-language-local-name="Spanish" class="interlanguage-link-target"><span>Español</span></a></li><li class="interlanguage-link interwiki-fa mw-list-item"><a href="https://fa.wikipedia.org/wiki/%D8%AF%DB%8C%E2%80%8C%D9%85%D8%AA%DB%8C%D9%84_%D8%AC%DB%8C%D9%88%D9%87" title="دی‌متیل جیوه – Persian" lang="fa" hreflang="fa" data-title="دی‌متیل جیوه" 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/Dim%C3%A9thylmercure" title="Diméthylmercure – French" lang="fr" hreflang="fr" data-title="Diméthylmercure" data-language-autonym="Français" data-language-local-name="French" class="interlanguage-link-target"><span>Français</span></a></li><li class="interlanguage-link interwiki-ko mw-list-item"><a href="https://ko.wikipedia.org/wiki/%EB%8B%A4%EC%9D%B4%EB%A9%94%ED%8B%B8%EC%88%98%EC%9D%80" title="다이메틸수은 – Korean" lang="ko" hreflang="ko" data-title="다이메틸수은" data-language-autonym="한국어" data-language-local-name="Korean" class="interlanguage-link-target"><span>한국어</span></a></li><li class="interlanguage-link interwiki-hi mw-list-item"><a href="https://hi.wikipedia.org/wiki/%E0%A4%A1%E0%A4%BE%E0%A4%87%E0%A4%AE%E0%A4%BF%E0%A4%A5%E0%A4%BE%E0%A4%87%E0%A4%B2%E0%A4%AE%E0%A4%B0%E0%A5%8D%E0%A4%95%E0%A4%B0%E0%A5%80" title="डाइमिथाइलमर्करी – Hindi" lang="hi" hreflang="hi" data-title="डाइमिथाइलमर्करी" data-language-autonym="हिन्दी" data-language-local-name="Hindi" class="interlanguage-link-target"><span>हिन्दी</span></a></li><li class="interlanguage-link interwiki-is mw-list-item"><a href="https://is.wikipedia.org/wiki/D%C3%ADmet%C3%BDlkvikasilfur" title="Dímetýlkvikasilfur – Icelandic" lang="is" hreflang="is" data-title="Dímetýlkvikasilfur" data-language-autonym="Íslenska" data-language-local-name="Icelandic" class="interlanguage-link-target"><span>Íslenska</span></a></li><li class="interlanguage-link interwiki-it mw-list-item"><a href="https://it.wikipedia.org/wiki/Dimetilmercurio" title="Dimetilmercurio – Italian" lang="it" hreflang="it" data-title="Dimetilmercurio" data-language-autonym="Italiano" data-language-local-name="Italian" class="interlanguage-link-target"><span>Italiano</span></a></li><li class="interlanguage-link interwiki-hu mw-list-item"><a href="https://hu.wikipedia.org/wiki/Dimetil-higany" title="Dimetil-higany – Hungarian" lang="hu" hreflang="hu" data-title="Dimetil-higany" data-language-autonym="Magyar" data-language-local-name="Hungarian" class="interlanguage-link-target"><span>Magyar</span></a></li><li class="interlanguage-link interwiki-nl mw-list-item"><a href="https://nl.wikipedia.org/wiki/Dimethylkwik" title="Dimethylkwik – Dutch" lang="nl" hreflang="nl" data-title="Dimethylkwik" 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%B8%E3%83%A1%E3%83%81%E3%83%AB%E6%B0%B4%E9%8A%80" title="ジメチル水銀 – Japanese" lang="ja" hreflang="ja" data-title="ジメチル水銀" 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-pl mw-list-item"><a href="https://pl.wikipedia.org/wiki/Dimetylort%C4%99%C4%87" title="Dimetylortęć – Polish" lang="pl" hreflang="pl" data-title="Dimetylortęć" 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/Dimetil_merc%C3%BArio" title="Dimetil mercúrio – Portuguese" lang="pt" hreflang="pt" data-title="Dimetil mercúrio" 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/Dimetilmercur" title="Dimetilmercur – Romanian" lang="ro" hreflang="ro" data-title="Dimetilmercur" 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%94%D0%B8%D0%BC%D0%B5%D1%82%D0%B8%D0%BB%D1%80%D1%82%D1%83%D1%82%D1%8C" title="Диметилртуть – Russian" lang="ru" hreflang="ru" data-title="Диметилртуть" data-language-autonym="Русский" data-language-local-name="Russian" class="interlanguage-link-target"><span>Русский</span></a></li><li class="interlanguage-link interwiki-simple mw-list-item"><a href="https://simple.wikipedia.org/wiki/Dimethylmercury" title="Dimethylmercury – Simple English" lang="en-simple" hreflang="en-simple" data-title="Dimethylmercury" data-language-autonym="Simple English" data-language-local-name="Simple English" class="interlanguage-link-target"><span>Simple English</span></a></li><li class="interlanguage-link interwiki-sr mw-list-item"><a href="https://sr.wikipedia.org/wiki/Dimetil%C5%BEiva" title="Dimetilživa – Serbian" lang="sr" hreflang="sr" data-title="Dimetilživa" 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/Dimetil%C5%BEiva" title="Dimetilživa – Serbo-Croatian" lang="sh" hreflang="sh" data-title="Dimetilživa" 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/Dimetyylielohopea" title="Dimetyylielohopea – Finnish" lang="fi" hreflang="fi" data-title="Dimetyylielohopea" data-language-autonym="Suomi" data-language-local-name="Finnish" class="interlanguage-link-target"><span>Suomi</span></a></li><li class="interlanguage-link interwiki-th mw-list-item"><a href="https://th.wikipedia.org/wiki/%E0%B9%84%E0%B8%94%E0%B9%80%E0%B8%A1%E0%B8%97%E0%B8%B4%E0%B8%A5%E0%B9%80%E0%B8%A1%E0%B8%AD%E0%B8%A3%E0%B9%8C%E0%B8%84%E0%B8%B4%E0%B8%A7%E0%B8%A3%E0%B8%B5" title="ไดเมทิลเมอร์คิวรี – Thai" lang="th" hreflang="th" data-title="ไดเมทิลเมอร์คิวรี" data-language-autonym="ไทย" data-language-local-name="Thai" class="interlanguage-link-target"><span>ไทย</span></a></li><li class="interlanguage-link interwiki-tr mw-list-item"><a href="https://tr.wikipedia.org/wiki/Dimetilc%C4%B1va" title="Dimetilcıva – Turkish" lang="tr" hreflang="tr" data-title="Dimetilcıva" data-language-autonym="Türkçe" data-language-local-name="Turkish" class="interlanguage-link-target"><span>Türkçe</span></a></li><li class="interlanguage-link interwiki-uk mw-list-item"><a href="https://uk.wikipedia.org/wiki/%D0%94%D0%B8%D0%BC%D0%B5%D1%82%D0%B8%D0%BB%D1%80%D1%82%D1%83%D1%82%D1%8C" title="Диметилртуть – Ukrainian" lang="uk" hreflang="uk" data-title="Диметилртуть" data-language-autonym="Українська" data-language-local-name="Ukrainian" class="interlanguage-link-target"><span>Українська</span></a></li><li class="interlanguage-link interwiki-vi mw-list-item"><a href="https://vi.wikipedia.org/wiki/Dimethyl_th%E1%BB%A7y_ng%C3%A2n" title="Dimethyl thủy ngân – Vietnamese" lang="vi" hreflang="vi" data-title="Dimethyl thủy ngân" data-language-autonym="Tiếng Việt" data-language-local-name="Vietnamese" class="interlanguage-link-target"><span>Tiếng Việt</span></a></li><li class="interlanguage-link interwiki-zh mw-list-item"><a href="https://zh.wikipedia.org/wiki/%E4%BA%8C%E7%94%B2%E5%9F%BA%E6%B1%9E" title="二甲基汞 – Chinese" lang="zh" hreflang="zh" data-title="二甲基汞" 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/Q422087#sitelinks-wikipedia" title="Edit interlanguage links" class="wbc-editpage">Edit links</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="Namespaces"> <div id="p-associated-pages" class="vector-menu vector-menu-tabs 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.ib-chembox td,.mw-parser-output .ib-chembox th{border:1px solid #a2a9b1;width:40%}.mw-parser-output .ib-chembox td+td{width:60%}</style> <table class="infobox ib-chembox"> <caption>Dimethylmercury </caption> <tbody><tr> <td colspan="2" style="text-align:center; padding:2px;"><span typeof="mw:File"><a href="/wiki/File:Dimethylmercury_Structural_Formulae_V2.svg" class="mw-file-description" title="Skeletal formula of dimethylmercury with all hydrogens added"><img alt="Skeletal formula of dimethylmercury with all hydrogens added" src="//upload.wikimedia.org/wikipedia/commons/thumb/0/04/Dimethylmercury_Structural_Formulae_V2.svg/150px-Dimethylmercury_Structural_Formulae_V2.svg.png" decoding="async" width="150" height="29" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/04/Dimethylmercury_Structural_Formulae_V2.svg/225px-Dimethylmercury_Structural_Formulae_V2.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/04/Dimethylmercury_Structural_Formulae_V2.svg/300px-Dimethylmercury_Structural_Formulae_V2.svg.png 2x" data-file-width="179" data-file-height="35" /></a></span> </td></tr> <tr> <td colspan="2" style="text-align:center; padding:2px;"><span typeof="mw:File"><a href="/wiki/File:Dimethyl-mercury-3D-vdW.png" class="mw-file-description" title="Space-filling model of dimethylmercury"><img alt="Space-filling model of dimethylmercury" src="//upload.wikimedia.org/wikipedia/commons/thumb/2/2e/Dimethyl-mercury-3D-vdW.png/150px-Dimethyl-mercury-3D-vdW.png" decoding="async" width="150" height="90" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/2e/Dimethyl-mercury-3D-vdW.png/225px-Dimethyl-mercury-3D-vdW.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/2e/Dimethyl-mercury-3D-vdW.png/300px-Dimethyl-mercury-3D-vdW.png 2x" data-file-width="1100" data-file-height="660" /></a></span> </td></tr> <tr> <th colspan="2" style="background: #f8eaba; text-align: center;">Names </th></tr> <tr> <td colspan="2" style="text-align:left;"><a href="/wiki/Chemical_nomenclature" title="Chemical nomenclature">IUPAC name</a> <div style="max-width:22em; word-wrap:break-word; padding-left:1.7em;">Dimethylmercury<sup id="cite_ref-1" class="reference"><a href="#cite_note-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup></div> </td></tr> <tr> <td colspan="2" style="text-align:left;">Other names <div style="max-width:22em; word-wrap:break-word; padding-left:1.7em;">Mercury dimethanide</div> </td></tr> <tr> <th colspan="2" style="background: #f8eaba; text-align: center;">Identifiers </th></tr> <tr> <td><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/CAS_Registry_Number" title="CAS Registry Number">CAS Number</a></div> </td> <td><style data-mw-deduplicate="TemplateStyles:r1126788409">.mw-parser-output .plainlist ol,.mw-parser-output .plainlist ul{line-height:inherit;list-style:none;margin:0;padding:0}.mw-parser-output .plainlist ol li,.mw-parser-output .plainlist ul li{margin-bottom:0}</style><div class="plainlist"><ul><li><span title="commonchemistry.cas.org"><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=593-74-8">593-74-8</a></span><sup> <span typeof="mw:File"><span><img alt="☒" src="//upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/7px-X_mark.svg.png" decoding="async" width="7" height="8" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/11px-X_mark.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/14px-X_mark.svg.png 2x" data-file-width="525" data-file-height="600" /></span></span><span style="display:none">N</span></sup></li></ul></div> </td></tr> <tr> <td><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;">3D model (<a href="/wiki/JSmol" class="mw-redirect" title="JSmol">JSmol</a>)</div> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><span title="chemapps.stolaf.edu (3D interactive model)"><a rel="nofollow" class="external text" href="https://chemapps.stolaf.edu/jmol/jmol.php?model=C%5BHg%5DC">Interactive image</a></span></li></ul></div> </td></tr> <tr> <td><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/Beilstein_database" title="Beilstein database">Beilstein Reference</a></div> </td> <td>3600205 </td></tr> <tr> <td><a href="/wiki/ChEBI" title="ChEBI">ChEBI</a> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><span title="www.ebi.ac.uk"><a rel="nofollow" class="external text" href="https://www.ebi.ac.uk/chebi/searchId.do?chebiId=30786">CHEBI:30786</a></span><sup> <span typeof="mw:File"><span><img alt="check" src="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png" decoding="async" width="7" height="7" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/11px-Yes_check.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/14px-Yes_check.svg.png 2x" data-file-width="600" data-file-height="600" /></span></span><span style="display:none">Y</span></sup></li></ul></div> </td></tr> <tr> <td><a href="/wiki/ChemSpider" title="ChemSpider">ChemSpider</a> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><span title="www.chemspider.com"><a rel="nofollow" class="external text" href="https://www.chemspider.com/Chemical-Structure.11155.html">11155</a></span><sup> <span typeof="mw:File"><span><img alt="check" src="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png" decoding="async" width="7" height="7" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/11px-Yes_check.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/14px-Yes_check.svg.png 2x" data-file-width="600" data-file-height="600" /></span></span><span style="display:none">Y</span></sup></li></ul></div> </td></tr> <tr> <td><a href="/wiki/ECHA_InfoCard" class="mw-redirect" title="ECHA InfoCard"><span title="echa.europa.eu">ECHA InfoCard</span></a> </td> <td><a rel="nofollow" class="external text" href="https://echa.europa.eu/substance-information/-/substanceinfo/100.008.916">100.008.916</a> <span class="mw-valign-text-top noprint" typeof="mw:File/Frameless"><a href="https://www.wikidata.org/wiki/Q422087#P2566" title="Edit this at Wikidata"><img alt="Edit this at Wikidata" src="//upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/10px-OOjs_UI_icon_edit-ltr-progressive.svg.png" decoding="async" width="10" height="10" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/15px-OOjs_UI_icon_edit-ltr-progressive.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/20px-OOjs_UI_icon_edit-ltr-progressive.svg.png 2x" data-file-width="20" data-file-height="20" /></a></span> </td></tr> <tr> <td><a href="/wiki/European_Community_number" title="European Community number"><span title="European Community number (chemical identifier)">EC Number</span></a> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li>209-805-3</li></ul></div> </td></tr> <tr> <td><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/Gmelin_database" title="Gmelin database">Gmelin Reference</a></div> </td> <td>25889 </td></tr> <tr> <td><a href="/wiki/Medical_Subject_Headings" title="Medical Subject Headings">MeSH</a> </td> <td><span title="www.nlm.nih.gov"><a rel="nofollow" class="external text" href="https://www.nlm.nih.gov/cgi/mesh/2014/MB_cgi?mode=&term=dimethyl+mercury">dimethyl+mercury</a></span> </td></tr> <tr> <td><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/PubChem" title="PubChem">PubChem</a> <abbr title="Compound ID">CID</abbr></div> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><span title="pubchem.ncbi.nlm.nih.gov"><a rel="nofollow" class="external text" href="https://pubchem.ncbi.nlm.nih.gov/compound/11645">11645</a></span></li></ul></div> </td></tr> <tr> <td><a href="/wiki/RTECS" class="mw-redirect" title="RTECS">RTECS number</a> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li>OW3010000</li></ul></div> </td></tr> <tr> <td><a href="/wiki/Unique_Ingredient_Identifier" title="Unique Ingredient Identifier">UNII</a> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><span title="precision.fda.gov"><a rel="nofollow" class="external text" href="https://precision.fda.gov/uniisearch/srs/unii/C60TQU15XY">C60TQU15XY</a></span><sup> <span typeof="mw:File"><span><img alt="check" src="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png" decoding="async" width="7" height="7" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/11px-Yes_check.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/14px-Yes_check.svg.png 2x" data-file-width="600" data-file-height="600" /></span></span><span style="display:none">Y</span></sup></li></ul></div> </td></tr> <tr> <td><a href="/wiki/UN_number" title="UN number">UN number</a> </td> <td>2929 </td></tr> <tr> <td><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/CompTox_Chemicals_Dashboard" title="CompTox Chemicals Dashboard">CompTox Dashboard</a> <span style="font-weight:normal">(<abbr title="U.S. Environmental Protection Agency">EPA</abbr>)</span></div> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><span title="comptox.epa.gov"><a rel="nofollow" class="external text" href="https://comptox.epa.gov/dashboard/chemical/details/DTXSID5047742">DTXSID5047742</a> <span class="mw-valign-text-top noprint" typeof="mw:File/Frameless"><a href="https://www.wikidata.org/wiki/Q422087#P3117" title="Edit this at Wikidata"><img alt="Edit this at Wikidata" src="//upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/10px-OOjs_UI_icon_edit-ltr-progressive.svg.png" decoding="async" width="10" height="10" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/15px-OOjs_UI_icon_edit-ltr-progressive.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/20px-OOjs_UI_icon_edit-ltr-progressive.svg.png 2x" data-file-width="20" data-file-height="20" /></a></span></span></li></ul></div> </td></tr> <tr> <td colspan="2"><div class="collapsible-list mw-collapsible mw-collapsed" style="text-align: left;"> <div style="line-height: 1.6em; font-weight: bold; text-align:left; font-weight:normal; background:transparent;"><div><a href="/wiki/International_Chemical_Identifier" title="International Chemical Identifier">InChI</a></div></div> <ul class="mw-collapsible-content" style="margin-top: 0; margin-bottom: 0; line-height: inherit; list-style: none; margin-left: 0; word-break:break-all;"><li style="line-height: inherit; margin: 0"><div style="border-top:1px solid #ccc; padding:0.2em 0 0.2em 1.5em; text-align:left;"><div style="word-wrap:break-word; text-indent:-1.5em; font-size:97%; line-height:120%;">InChI=1S/2CH3.Hg/h2*1H3;<sup> <span typeof="mw:File"><span><img alt="check" src="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png" decoding="async" width="7" height="7" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/11px-Yes_check.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/14px-Yes_check.svg.png 2x" data-file-width="600" data-file-height="600" /></span></span><span style="display:none">Y</span></sup></div><div style="word-wrap:break-word; text-indent:-1.5em; font-size:97%; line-height:120%;">Key: ATZBPOVXVPIOMR-UHFFFAOYSA-N<sup> <span typeof="mw:File"><span><img alt="check" src="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png" decoding="async" width="7" height="7" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/11px-Yes_check.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/14px-Yes_check.svg.png 2x" data-file-width="600" data-file-height="600" /></span></span><span style="display:none">Y</span></sup></div></div></li></ul> </div> </td></tr> <tr> <td colspan="2"><div class="collapsible-list mw-collapsible mw-collapsed" style="text-align: left;"> <div style="line-height: 1.6em; font-weight: bold; text-align:left; font-weight:normal; background:transparent;"><div><a href="/wiki/Simplified_molecular-input_line-entry_system" class="mw-redirect" title="Simplified molecular-input line-entry system">SMILES</a></div></div> <ul class="mw-collapsible-content" style="margin-top: 0; margin-bottom: 0; line-height: inherit; list-style: none; margin-left: 0; word-break:break-all;"><li style="line-height: inherit; margin: 0"><div style="border-top:1px solid #ccc; padding:0.2em 0 0.2em 1.6em; word-wrap:break-word; text-indent:-1.5em; text-align:left; font-size:97%; line-height:120%;">C[Hg]C</div></li></ul> </div> </td></tr> <tr> <th colspan="2" style="background: #f8eaba; text-align: center;">Properties </th></tr> <tr> <td><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/Chemical_formula" title="Chemical formula">Chemical formula</a></div> </td> <td><span class="chemf nowrap">C<span class="nowrap"><span style="display:inline-block;margin-bottom:-0.3em;vertical-align:-0.4em;line-height:1em;font-size:80%;text-align:left"><sup style="font-size:inherit;line-height:inherit;vertical-align:baseline"></sup><br /><sub style="font-size:inherit;line-height:inherit;vertical-align:baseline">2</sub></span></span>H<span class="nowrap"><span style="display:inline-block;margin-bottom:-0.3em;vertical-align:-0.4em;line-height:1em;font-size:80%;text-align:left"><sup style="font-size:inherit;line-height:inherit;vertical-align:baseline"></sup><br /><sub style="font-size:inherit;line-height:inherit;vertical-align:baseline">6</sub></span></span>Hg</span><br /><span class="chemf nowrap">(<span class="chemf nowrap">CH<span class="nowrap"><span style="display:inline-block;margin-bottom:-0.3em;vertical-align:-0.4em;line-height:1em;font-size:80%;text-align:left"><sup style="font-size:inherit;line-height:inherit;vertical-align:baseline"></sup><br /><sub style="font-size:inherit;line-height:inherit;vertical-align:baseline">3</sub></span></span></span>)<span class="nowrap"><span style="display:inline-block;margin-bottom:-0.3em;vertical-align:-0.4em;line-height:1em;font-size:80%;text-align:left"><sup style="font-size:inherit;line-height:inherit;vertical-align:baseline"></sup><br /><sub style="font-size:inherit;line-height:inherit;vertical-align:baseline">2</sub></span></span>Hg</span>  </td></tr> <tr> <td><a href="/wiki/Molar_mass" title="Molar mass">Molar mass</a> </td> <td>230.66 g mol<sup>−1</sup>    </td></tr> <tr> <td>Appearance </td> <td>Colorless liquid </td></tr> <tr> <td><a href="/wiki/Odor" title="Odor">Odor</a> </td> <td>Sweet </td></tr> <tr> <td><a href="/wiki/Density" title="Density">Density</a> </td> <td>2.961 g mL<sup>−1</sup> </td></tr> <tr> <td><a href="/wiki/Melting_point" title="Melting point">Melting point</a> </td> <td>−43 °C (−45 °F; 230 K) </td></tr> <tr> <td><a href="/wiki/Boiling_point" title="Boiling point">Boiling point</a> </td> <td>93 to 94 °C (199 to 201 °F; 366 to 367 K) </td></tr> <tr> <td><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/Refractive_index" title="Refractive index">Refractive index</a> (<i>n</i><sub>D</sub>)</div> </td> <td>1.543 </td></tr> <tr> <th colspan="2" style="background: #f8eaba; text-align: center;">Thermochemistry </th></tr> <tr> <td><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/Standard_enthalpy_change_of_formation" class="mw-redirect" title="Standard enthalpy change of formation">Std enthalpy of<br />formation</a> <span style="font-size:112%;">(Δ<sub>f</sub><i>H</i><sup>⦵</sup><sub>298</sub>)</span></div> </td> <td>57.9–65.7 kJ mol<sup>−1</sup> </td></tr> <tr> <th colspan="2" style="background: #f8eaba; text-align: center;">Hazards </th></tr> <tr> <td colspan="2" style="text-align:left; background-color:#eaeaea;"><b><a href="/wiki/Occupational_safety_and_health" title="Occupational safety and health">Occupational safety and health</a></b> (OHS/OSH): </td></tr> <tr> <td style="padding-left:1em;"><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;">Main hazards</div> </td> <td>Extremely flammable, extremely poisonous, persistent environmental pollutant </td></tr> <tr> <td colspan="2" style="text-align:left; background-color:#eaeaea;"><a href="/wiki/Globally_Harmonized_System_of_Classification_and_Labelling_of_Chemicals" title="Globally Harmonized System of Classification and Labelling of Chemicals"><b>GHS</b> labelling</a>: </td></tr> <tr> <td style="padding-left:1em;"><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/GHS_hazard_pictograms" title="GHS hazard pictograms">Pictograms</a></div> </td> <td><span typeof="mw:File"><a href="/wiki/File:GHS-pictogram-skull.svg" class="mw-file-description" title="GHS06: Toxic"><img alt="GHS06: Toxic" src="//upload.wikimedia.org/wikipedia/commons/thumb/5/58/GHS-pictogram-skull.svg/50px-GHS-pictogram-skull.svg.png" decoding="async" width="50" height="50" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/5/58/GHS-pictogram-skull.svg/75px-GHS-pictogram-skull.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/5/58/GHS-pictogram-skull.svg/100px-GHS-pictogram-skull.svg.png 2x" data-file-width="724" data-file-height="724" /></a></span><span typeof="mw:File"><a href="/wiki/File:GHS-pictogram-silhouette.svg" class="mw-file-description" title="GHS08: Health hazard"><img alt="GHS08: Health hazard" src="//upload.wikimedia.org/wikipedia/commons/thumb/2/21/GHS-pictogram-silhouette.svg/50px-GHS-pictogram-silhouette.svg.png" decoding="async" width="50" height="50" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/21/GHS-pictogram-silhouette.svg/75px-GHS-pictogram-silhouette.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/21/GHS-pictogram-silhouette.svg/100px-GHS-pictogram-silhouette.svg.png 2x" data-file-width="724" data-file-height="724" /></a></span><span typeof="mw:File"><a href="/wiki/File:GHS-pictogram-flamme.svg" class="mw-file-description" title="GHS02: Flammable"><img alt="GHS02: Flammable" src="//upload.wikimedia.org/wikipedia/commons/thumb/6/6d/GHS-pictogram-flamme.svg/50px-GHS-pictogram-flamme.svg.png" decoding="async" width="50" height="50" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/6d/GHS-pictogram-flamme.svg/75px-GHS-pictogram-flamme.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/6d/GHS-pictogram-flamme.svg/100px-GHS-pictogram-flamme.svg.png 2x" data-file-width="512" data-file-height="512" /></a></span><span typeof="mw:File"><a href="/wiki/File:GHS-pictogram-pollu.svg" class="mw-file-description" title="GHS09: Environmental hazard"><img alt="GHS09: Environmental hazard" src="//upload.wikimedia.org/wikipedia/commons/thumb/b/b9/GHS-pictogram-pollu.svg/50px-GHS-pictogram-pollu.svg.png" decoding="async" width="50" height="50" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/b/b9/GHS-pictogram-pollu.svg/75px-GHS-pictogram-pollu.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/b/b9/GHS-pictogram-pollu.svg/100px-GHS-pictogram-pollu.svg.png 2x" data-file-width="724" data-file-height="724" /></a></span> </td></tr> <tr> <td style="padding-left:1em;"><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/Globally_Harmonized_System_of_Classification_and_Labelling_of_Chemicals#Signal_word" title="Globally Harmonized System of Classification and Labelling of Chemicals">Signal word</a></div> </td> <td><b>Danger</b> </td></tr> <tr> <td style="padding-left:1em;"><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/GHS_hazard_statements" title="GHS hazard statements">Hazard statements</a></div> </td> <td><abbr class="abbr" title="H224: Extremely flammable liquid and vapour">H224</abbr>, <abbr class="abbr" title="H300+H310+H330: Fatal if swallowed, in contact with skin or if inhaled">H300+H310+H330</abbr>, <abbr class="abbr" title="H372: Causes damage to organs through prolonged or repeated exposure">H372</abbr>, <abbr class="abbr" title="H410: Very toxic to aquatic life with long lasting effects">H410</abbr> </td></tr> <tr> <td style="padding-left:1em;"><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/GHS_precautionary_statements" title="GHS precautionary statements">Precautionary statements</a></div> </td> <td><abbr class="abbr" title="P260: Do not breathe dust/fume/gas/mist/vapours/spray.">P260</abbr>, <abbr class="abbr" title="P264: Wash ... thoroughly after handling.">P264</abbr>, <abbr class="abbr" title="P273: Avoid release to the environment.">P273</abbr>, <abbr class="abbr" title="P280: Wear protective gloves/protective clothing/eye protection/face protection.">P280</abbr>, <abbr class="abbr" title="P284: Wear respiratory protection.">P284</abbr>, <abbr class="abbr" title="P301+P310: IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.">P301+P310</abbr> </td></tr> <tr> <td><a href="/wiki/NFPA_704" title="NFPA 704"><b>NFPA 704</b></a> (fire diamond) </td> <td><style data-mw-deduplicate="TemplateStyles:r1170367383">.mw-parser-output .nfpa-704-diamond-ref{float:right;padding:1px;text-align:right}.mw-parser-output .nfpa-704-diamond-container{width:82px;font-family:sans-serif;margin:0 auto}.mw-parser-output .nfpa-704-diamond-container-ref{float:left;margin-left:1em}.mw-parser-output .nfpa-704-diamond-images{float:left;font-size:20px;text-align:center;position:relative;height:80px;width:80px;padding:1px}.mw-parser-output .nfpa-704-diamond-map{position:absolute;height:80px;width:80px}.mw-parser-output .nfpa-704-diamond .noresize{margin:0 auto}.mw-parser-output .nfpa-704-diamond-code{line-height:1em;text-align:center;position:absolute}.mw-parser-output .nfpa-704-diamond-code>a{color:black}.mw-parser-output .nfpa-704-diamond-blue{width:13px;top:31px;left:15px}.mw-parser-output .nfpa-704-diamond-red{width:12px;top:12px;left:35px}.mw-parser-output .nfpa-704-diamond-yellow{width:13px;top:31px;left:54px}.mw-parser-output .nfpa-704-diamond-white-image{position:relative;top:51px;left:0}.mw-parser-output .nfpa-704-diamond-white-text{vertical-align:middle;text-align:center;line-height:80%;position:absolute;top:52px}.mw-parser-output .nfpa-704-diamond-white-text a>span{position:absolute;color:black}.mw-parser-output .nfpa-704-diamond-white-wors{font-size:15px;width:23px;left:29px}.mw-parser-output .nfpa-704-diamond-white-wox{font-size:15px;font-stretch:condensed;width:21px;line-height:80%;top:-4px;left:29px}.mw-parser-output .nfpa-704-diamond-white-abcp{font-size:13.5px;font-stretch:condensed;width:28px;left:26px}.mw-parser-output .nfpa-704-diamond-white-ac{font-size:10px;width:30px;left:25px}.mw-parser-output .nfpa-704-diamond-white-strike{text-decoration:line-through}</style><div class="nfpa-704-diamond notheme"><div class="nfpa-704-diamond-container"><div class="nfpa-704-diamond-images nounderlines"> <div class="nfpa-704-diamond-map"><figure class="noresize" typeof="mw:File"><span><img alt="NFPA 704 four-colored diamond" src="//upload.wikimedia.org/wikipedia/commons/thumb/6/6f/NFPA_704.svg/80px-NFPA_704.svg.png" decoding="async" width="80" height="80" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/6f/NFPA_704.svg/120px-NFPA_704.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/6f/NFPA_704.svg/160px-NFPA_704.svg.png 2x" data-file-width="512" data-file-height="512" usemap="#ImageMap_235fd8be78b8119a" /></span><map name="ImageMap_235fd8be78b8119a"><area href="/wiki/NFPA_704#Blue" shape="poly" coords="23,23,47,47,23,70,0,47" alt="Health 4: Very short exposure could cause death or major residual injury. E.g. VX gas" title="Health 4: Very short exposure could cause death or major residual injury. E.g. VX gas" /><area href="/wiki/NFPA_704#Red" shape="poly" coords="47,0,70,23,47,47,23,23" alt="Flammability 4: Will rapidly or completely vaporize at normal atmospheric pressure and temperature, or is readily dispersed in air and will burn readily. Flash point below 23 °C (73 °F). E.g. propane" title="Flammability 4: Will rapidly or completely vaporize at normal atmospheric pressure and temperature, or is readily dispersed in air and will burn readily. Flash point below 23 °C (73 °F). E.g. propane" /><area href="/wiki/NFPA_704#Yellow" shape="poly" coords="70,23,94,47,70,70,47,47" alt="Instability 3: Capable of detonation or explosive decomposition but requires a strong initiating source, must be heated under confinement before initiation, reacts explosively with water, or will detonate if severely shocked. E.g. hydrogen peroxide" title="Instability 3: Capable of detonation or explosive decomposition but requires a strong initiating source, must be heated under confinement before initiation, reacts explosively with water, or will detonate if severely shocked. E.g. hydrogen peroxide" /><area href="/wiki/NFPA_704#White" shape="poly" coords="47,47,70,70,47,94,23,70" alt="Special hazards (white): no code" title="Special hazards (white): no code" /></map><figcaption></figcaption></figure></div><div class="nfpa-704-diamond-code nfpa-704-diamond-blue"> <a href="/wiki/NFPA_704#Blue" title="NFPA 704"><span title="Health 4: Very short exposure could cause death or major residual injury. E.g. VX gas" class="notheme mw-no-invert">4</span></a></div><div class="nfpa-704-diamond-code nfpa-704-diamond-red"> <a href="/wiki/NFPA_704#Red" title="NFPA 704"><span title="Flammability 4: Will rapidly or completely vaporize at normal atmospheric pressure and temperature, or is readily dispersed in air and will burn readily. Flash point below 23 °C (73 °F). E.g. propane" class="notheme mw-no-invert">4</span></a></div><div class="nfpa-704-diamond-code nfpa-704-diamond-yellow"> <a href="/wiki/NFPA_704#Yellow" title="NFPA 704"><span title="Instability 3: Capable of detonation or explosive decomposition but requires a strong initiating source, must be heated under confinement before initiation, reacts explosively with water, or will detonate if severely shocked. E.g. hydrogen peroxide" class="notheme mw-no-invert">3</span></a></div></div></div></div> </td></tr> <tr> <td><a href="/wiki/Flash_point" title="Flash point">Flash point</a> </td> <td>5 °C (41 °F; 278 K) </td></tr> <tr> <th colspan="2" style="background: #f8eaba; text-align: center;">Related compounds </th></tr> <tr> <td><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;">Other <a href="/wiki/Ion" title="Ion">anions</a></div> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><a href="/wiki/Diethylmercury" title="Diethylmercury">Diethylmercury</a></li><li><a href="/wiki/Diphenylmercury" title="Diphenylmercury">Diphenylmercury</a></li></ul></div> </td></tr> <tr> <td><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;">Other <a href="/wiki/Ion" title="Ion">cations</a></div> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><a href="/wiki/Dimethylzinc" title="Dimethylzinc">Dimethylzinc</a></li><li><a href="/wiki/Dimethylcadmium" title="Dimethylcadmium">Dimethylcadmium</a></li><li><a href="/wiki/Dimethylmagnesium" title="Dimethylmagnesium">Dimethylmagnesium</a></li></ul></div> </td></tr> <tr> <td colspan="2" style="text-align:left; background:#f8eaba; border:1px solid #a2a9b1;"><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;">Except where otherwise noted, data are given for materials in their <a href="/wiki/Standard_state" title="Standard state">standard state</a> (at 25 °C [77 °F], 100 kPa).</div> <div style="margin-top: 0.3em;"><div style="text-align:center;"><span typeof="mw:File"><span><img alt="☒" src="//upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/12px-X_mark.svg.png" decoding="async" width="12" height="14" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/18px-X_mark.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/24px-X_mark.svg.png 2x" data-file-width="525" data-file-height="600" /></span></span><span style="display:none">N</span> <span class="reflink plainlinks nourlexpansion"><a class="external text" href="https://en.wikipedia.org/w/index.php?title=Special:ComparePages&rev1=460790372&page2=Dimethylmercury">verify</a></span> (<a href="/wiki/Wikipedia:WikiProject_Chemicals/Chembox_validation" title="Wikipedia:WikiProject Chemicals/Chembox validation">what is</a> <sup><span typeof="mw:File"><span><img alt="check" src="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png" decoding="async" width="7" height="7" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/11px-Yes_check.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/14px-Yes_check.svg.png 2x" data-file-width="600" data-file-height="600" /></span></span><span style="display:none">Y</span><span typeof="mw:File"><span><img alt="☒" src="//upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/7px-X_mark.svg.png" decoding="async" width="7" height="8" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/11px-X_mark.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/14px-X_mark.svg.png 2x" data-file-width="525" data-file-height="600" /></span></span><span style="display:none">N</span></sup> ?) </div></div> <div style="margin-top: 0.3em; text-align: center;"><a href="/wiki/Wikipedia:Chemical_infobox#References" title="Wikipedia:Chemical infobox">Infobox references</a></div> </td></tr> </tbody></table><div class="shortdescription nomobile noexcerpt noprint searchaux" style="display:none">Chemical compound</div> <p><b>Dimethylmercury</b> is an extremely toxic <a href="/wiki/Organomercury_compound" class="mw-redirect" title="Organomercury compound">organomercury compound</a> with the formula (<a href="/wiki/Methyl" class="mw-redirect" title="Methyl">CH<sub>3</sub></a>)<sub>2</sub><a href="/wiki/Mercury_(element)" title="Mercury (element)">Hg</a>. A volatile, flammable, dense and colorless liquid, dimethylmercury is one of the strongest known <a href="/wiki/Neurotoxin" title="Neurotoxin">neurotoxins</a>. Less than 0.1 mL is capable of inducing severe <a href="/wiki/Mercury_poisoning" title="Mercury poisoning">mercury poisoning</a> resulting in death.<sup id="cite_ref-OSHA_2-0" class="reference"><a href="#cite_note-OSHA-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup> </p> <meta property="mw:PageProp/toc" /> <div class="mw-heading mw-heading2"><h2 id="Synthesis,_structure,_and_reactions"><span id="Synthesis.2C_structure.2C_and_reactions"></span>Synthesis, structure, and reactions</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Dimethylmercury&action=edit&section=1" title="Edit section: Synthesis, structure, and reactions"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>The compound was one of the earliest <a href="/wiki/Organometallic" class="mw-redirect" title="Organometallic">organometallics</a> reported, reflecting its considerable stability. The compound was first prepared by <a href="/wiki/George_Bowdler_Buckton" title="George Bowdler Buckton">George Buckton</a> in 1857 by a reaction of <a href="/wiki/Methylmercury" title="Methylmercury">methylmercury</a> <a href="/wiki/Iodide" title="Iodide">iodide</a> with <a href="/wiki/Potassium_cyanide" title="Potassium cyanide">potassium cyanide</a>:<sup id="cite_ref-:0_3-0" class="reference"><a href="#cite_note-:0-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup> </p> <dl><dd>2 CH<sub>3</sub>HgI + 2 KCN → Hg(CH<sub>3</sub>)<sub>2</sub> + 2 KI + (CN)<sub>2</sub> + Hg</dd></dl> <p>Later, <a href="/wiki/Edward_Frankland" title="Edward Frankland">Edward Frankland</a> discovered that it could be synthesized by treating <a href="/wiki/Sodium_amalgam" title="Sodium amalgam">sodium amalgam</a> with <a href="/wiki/Methyl" class="mw-redirect" title="Methyl">methyl</a> <a href="/wiki/Halide" title="Halide">halides</a>: </p> <dl><dd>Hg + 2 Na + 2 <a href="/wiki/Methyl_iodide" class="mw-redirect" title="Methyl iodide">CH<sub>3</sub>I</a> → Hg(CH<sub>3</sub>)<sub>2</sub> + 2 <a href="/wiki/Sodium_iodide" title="Sodium iodide">NaI</a></dd></dl> <p>It can also be obtained by <a href="/wiki/Alkylation" title="Alkylation">alkylation</a> of <a href="/wiki/Mercury(II)_chloride" title="Mercury(II) chloride">mercuric chloride</a> with <a href="/wiki/Methyllithium" title="Methyllithium">methyllithium</a>: </p> <dl><dd>HgCl<sub>2</sub> + 2 LiCH<sub>3</sub> → Hg(CH<sub>3</sub>)<sub>2</sub> + 2 <a href="/wiki/Lithium_chloride" title="Lithium chloride">LiCl</a></dd></dl> <p>The molecule adopts a linear structure with Hg–C bond lengths of 2.083 Å.<sup id="cite_ref-4" class="reference"><a href="#cite_note-4"><span class="cite-bracket">[</span>4<span class="cite-bracket">]</span></a></sup> </p> <div class="mw-heading mw-heading3"><h3 id="Reactivity_and_physical_properties">Reactivity and physical properties</h3><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Dimethylmercury&action=edit&section=2" title="Edit section: Reactivity and physical properties"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>Dimethylmercury is stable in water and reacts with mineral acids at a significant rate only at elevated temperatures,<sup id="cite_ref-5" class="reference"><a href="#cite_note-5"><span class="cite-bracket">[</span>5<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-6" class="reference"><a href="#cite_note-6"><span class="cite-bracket">[</span>6<span class="cite-bracket">]</span></a></sup> whereas the corresponding <a href="/wiki/Organocadmium" class="mw-redirect" title="Organocadmium">organocadmium</a> and <a href="/wiki/Organozinc" class="mw-redirect" title="Organozinc">organozinc</a> compounds (and most metal alkyls in general) hydrolyze rapidly. The difference reflects the high <a href="/wiki/Electronegativity" title="Electronegativity">electronegativity</a> of Hg (Pauling EN = 2.00) and the low affinity of Hg(II) for oxygen ligands. The compound undergoes a <a href="/wiki/Redistribution_(chemistry)" title="Redistribution (chemistry)">redistribution reaction</a> with mercuric chloride to give methylmercury chloride: </p> <dl><dd>(CH<sub>3</sub>)<sub>2</sub>Hg + HgCl<sub>2</sub> → 2 CH<sub>3</sub>HgCl</dd></dl> <p>Whereas dimethylmercury is a <a href="/wiki/Volatile_liquids" class="mw-redirect" title="Volatile liquids">volatile liquid</a>, <a href="/wiki/Methylmercury" title="Methylmercury">methylmercury chloride</a> is a <a href="/wiki/Crystalline_solid" class="mw-redirect" title="Crystalline solid">crystalline solid</a>.<sup id="cite_ref-7" class="reference"><a href="#cite_note-7"><span class="cite-bracket">[</span>7<span class="cite-bracket">]</span></a></sup> </p> <div class="mw-heading mw-heading2"><h2 id="Use">Use</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Dimethylmercury&action=edit&section=3" title="Edit section: Use"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>Dimethylmercury has few applications because of the risks involved. It has been studied for reactions involving bonding <a href="/wiki/Methylmercury" title="Methylmercury">methylmercury</a> cations to target molecules, forming potent bactericides, but methylmercury's <a href="/wiki/Bioaccumulation" title="Bioaccumulation">bioaccumulation</a> and ultimate toxicity has led to it being largely abandoned in favor of the less toxic <a href="/wiki/Ethylmercury" title="Ethylmercury">ethylmercury</a> and <a href="/wiki/Diethylmercury" title="Diethylmercury">diethylmercury</a> compounds, which perform a similar function without the bioaccumulation hazard. </p><p>In <a href="/wiki/Toxicology" title="Toxicology">toxicology</a>, it still finds limited use as a reference toxin. It is also used to calibrate <a href="/wiki/NMR_spectroscopy" class="mw-redirect" title="NMR spectroscopy">NMR</a> instruments for detection of mercury (δ 0 ppm for <sup>199</sup>Hg NMR), although diethylmercury and less toxic mercury salts are now preferred.<sup id="cite_ref-8" class="reference"><a href="#cite_note-8"><span class="cite-bracket">[</span>8<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-9" class="reference"><a href="#cite_note-9"><span class="cite-bracket">[</span>9<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-10" class="reference"><a href="#cite_note-10"><span class="cite-bracket">[</span>10<span class="cite-bracket">]</span></a></sup> </p><p>Around 1960, Phil Pomerantz, a man working at the <a href="/wiki/Bureau_of_Naval_Weapons" title="Bureau of Naval Weapons">Bureau of Naval Weapons</a>, suggested that dimethylmercury be used as a fuel mix with <a href="/wiki/Red_fuming_nitric_acid" title="Red fuming nitric acid">red fuming nitric acid</a>.<sup id="cite_ref-Ignition162_11-0" class="reference"><a href="#cite_note-Ignition162-11"><span class="cite-bracket">[</span>11<span class="cite-bracket">]</span></a></sup> This was never done although it did lead to testing a <a href="/wiki/Red_fuming_nitric_acid" title="Red fuming nitric acid">red fuming nitric acid</a>-<a href="/wiki/Unsymmetrical_dimethylhydrazine" title="Unsymmetrical dimethylhydrazine">Unsymmetrical dimethylhydrazine</a> rocket with elemental mercury being injected into the combustion chamber at the <a href="/wiki/Naval_Ordnance_Test_Station" class="mw-redirect" title="Naval Ordnance Test Station">Naval Ordnance Test Station</a>.<sup id="cite_ref-Ignition162_11-1" class="reference"><a href="#cite_note-Ignition162-11"><span class="cite-bracket">[</span>11<span class="cite-bracket">]</span></a></sup> </p> <div class="mw-heading mw-heading2"><h2 id="Safety">Safety</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Dimethylmercury&action=edit&section=4" title="Edit section: Safety"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>Dimethylmercury is extremely toxic and dangerous to handle. Absorption of doses as low as 0.1 <a href="/wiki/Millilitre" class="mw-redirect" title="Millilitre">mL</a> can result in severe mercury poisoning.<sup id="cite_ref-OSHA_2-1" class="reference"><a href="#cite_note-OSHA-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup> The risks are enhanced because of the compound's high <a href="/wiki/Vapor_pressure" title="Vapor pressure">vapor pressure</a>.<sup id="cite_ref-OSHA_2-2" class="reference"><a href="#cite_note-OSHA-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup> Since it is highly lipophilic, it absorbs through the skin and into body fat very easily and can permeate many materials, including many plastics and rubber compounds. </p><p>Permeation tests showed that several types of disposable latex or polyvinyl chloride gloves (typically, about 0.1 mm thick), commonly used in most <a href="/wiki/Laboratory" title="Laboratory">laboratories</a> and clinical settings, had high and maximal rates of permeation by dimethylmercury within 15 seconds.<sup id="cite_ref-nejm_12-0" class="reference"><a href="#cite_note-nejm-12"><span class="cite-bracket">[</span>12<span class="cite-bracket">]</span></a></sup> The American <a href="/wiki/Occupational_Safety_and_Health_Administration" title="Occupational Safety and Health Administration">Occupational Safety and Health Administration</a> advises handling dimethylmercury with highly resistant laminated gloves with an additional pair of abrasion-resistant gloves worn over the laminate pair, and also recommends using a face shield and working in a <a href="/wiki/Fume_hood" title="Fume hood">fume hood</a>.<sup id="cite_ref-OSHA_2-3" class="reference"><a href="#cite_note-OSHA-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-story_13-0" class="reference"><a href="#cite_note-story-13"><span class="cite-bracket">[</span>13<span class="cite-bracket">]</span></a></sup> </p><p>Dimethylmercury is metabolized after several days to <a href="/wiki/Methylmercury" title="Methylmercury">methylmercury</a>.<sup id="cite_ref-nejm_12-1" class="reference"><a href="#cite_note-nejm-12"><span class="cite-bracket">[</span>12<span class="cite-bracket">]</span></a></sup> Methylmercury crosses the <a href="/wiki/Blood%E2%80%93brain_barrier" title="Blood–brain barrier">blood–brain barrier</a> easily, probably owing to formation of a <a href="/wiki/Coordination_complex" title="Coordination complex">complex</a> with <a href="/wiki/Cysteine" title="Cysteine">cysteine</a>.<sup id="cite_ref-story_13-1" class="reference"><a href="#cite_note-story-13"><span class="cite-bracket">[</span>13<span class="cite-bracket">]</span></a></sup> It easily absorbs into the body, and has a tendency to <a href="/wiki/Bioaccumulation" title="Bioaccumulation">bioaccumulate</a>. The symptoms of <a href="/wiki/Mercury_poisoning" title="Mercury poisoning">poisoning</a> may be delayed by months, resulting in cases in which a diagnosis is ultimately discovered, but only at a point in which it is too late or almost too late for an effective treatment regimen to be successful.<sup id="cite_ref-story_13-2" class="reference"><a href="#cite_note-story-13"><span class="cite-bracket">[</span>13<span class="cite-bracket">]</span></a></sup> Methylmercury poisoning is also known as <a href="/wiki/Minamata_disease" title="Minamata disease">Minamata disease</a>. </p> <div class="mw-heading mw-heading2"><h2 id="Incidents">Incidents</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Dimethylmercury&action=edit&section=5" title="Edit section: Incidents"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <ul><li>As early as 1865, two workers in the laboratory of <a href="/wiki/Edward_Frankland" title="Edward Frankland">Edward Frankland</a> died after exhibiting progressive neurological symptoms following accidental exposure to the compound.<sup id="cite_ref-:0_3-1" class="reference"><a href="#cite_note-:0-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup></li></ul> <ul><li><a href="/wiki/Karen_Wetterhahn" title="Karen Wetterhahn">Karen Wetterhahn</a>, a professor of chemistry at <a href="/wiki/Dartmouth_College" title="Dartmouth College">Dartmouth College</a>, died in 1997, ten months after spilling only a few drops of dimethylmercury onto her latex gloves.<sup id="cite_ref-OSHA_2-4" class="reference"><a href="#cite_note-OSHA-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-14" class="reference"><a href="#cite_note-14"><span class="cite-bracket">[</span>14<span class="cite-bracket">]</span></a></sup> This incident resulted in improved awareness of the substance's extreme toxicity, and its ability to easily penetrate latex, compared to less porous materials such as <a href="/wiki/Nitrile_rubber" title="Nitrile rubber">nitrile</a>. New <a href="/wiki/OSHA" class="mw-redirect" title="OSHA">OSHA</a> material-handling guidelines were published, many institutions purged their supplies of the compound, and it became almost impossible to buy.<sup id="cite_ref-15" class="reference"><a href="#cite_note-15"><span class="cite-bracket">[</span>15<span class="cite-bracket">]</span></a></sup></li></ul> <ul><li><a href="/wiki/Death_of_Christoph_Bulwin" title="Death of Christoph Bulwin">Christoph Bulwin</a>, a 40-year-old German database administrator for <a href="/wiki/IG_Bergbau,_Chemie,_Energie" title="IG Bergbau, Chemie, Energie">IG Bergbau, Chemie, Energie</a>, claimed to have been attacked with a <a href="/wiki/Bulgarian_umbrella" title="Bulgarian umbrella">syringe-tipped umbrella</a> on 15 July 2011 in <a href="/wiki/Hanover" title="Hanover">Hanover</a>, Germany. Bulwin, who died a year later from <a href="/wiki/Mercury_poisoning" title="Mercury poisoning">mercury poisoning</a>, had said he confiscated the syringe, which was later found to contain dimethylmercury.<sup id="cite_ref-16" class="reference"><a href="#cite_note-16"><span class="cite-bracket">[</span>16<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-17" class="reference"><a href="#cite_note-17"><span class="cite-bracket">[</span>17<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-18" class="reference"><a href="#cite_note-18"><span class="cite-bracket">[</span>18<span class="cite-bracket">]</span></a></sup> According to a 2020 article in <i>Forensic Science, Medicine and Pathology,</i> police investigations revealed a syringe containing a typical mercury thallium compound in Bulwin's car, and mercury and thallium in thermometers at his workplace. Inconclusive antemortem and postmortem blood, urine, and tissue analysis cast doubts on the assault account. The absence of an identified assailant or motive, as well as the presence of different mercury compounds in Bulwin's car, led police to conclude that the intoxication was likely self-administered, thereby terminating the preliminary investigation.<sup id="cite_ref-19" class="reference"><a href="#cite_note-19"><span class="cite-bracket">[</span>19<span class="cite-bracket">]</span></a></sup> The <i>Forensic Science, Medicine and Pathology</i> account is contradicted by other reports, including the 2022 episode of the German TV program <a href="/wiki/Aktenzeichen_XY..._ungel%C3%B6st" title="Aktenzeichen XY... ungelöst">Aktenzeichen XY .. ungelöst</a> that was co-edited by the Hannover criminal police.<sup id="cite_ref-20" class="reference"><a href="#cite_note-20"><span class="cite-bracket">[</span>20<span class="cite-bracket">]</span></a></sup></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=Dimethylmercury&action=edit&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 mw-references-columns"><ol class="references"> <li id="cite_note-1"><span class="mw-cite-backlink"><b><a href="#cite_ref-1">^</a></b></span> <span class="reference-text"><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><cite class="citation web cs1"><a rel="nofollow" class="external text" href="https://pubchem.ncbi.nlm.nih.gov/compound/11645#x291">"dimethylmercury – Compound Summary"</a>. <i>PubChem Compound</i>. US: National Center for Biotechnology Information. 16 September 2004. Identification and Related Records<span class="reference-accessdate">. Retrieved <span class="nowrap">29 January</span> 2021</span>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=unknown&rft.jtitle=PubChem+Compound&rft.atitle=dimethylmercury+%E2%80%93+Compound+Summary&rft.pages=Identification+and+Related+Records&rft.date=2004-09-16&rft_id=https%3A%2F%2Fpubchem.ncbi.nlm.nih.gov%2Fcompound%2F11645%23x291&rfr_id=info%3Asid%2Fen.wikipedia.org%3ADimethylmercury" class="Z3988"></span></span> </li> <li id="cite_note-OSHA-2"><span class="mw-cite-backlink">^ <a href="#cite_ref-OSHA_2-0"><sup><i><b>a</b></i></sup></a> <a href="#cite_ref-OSHA_2-1"><sup><i><b>b</b></i></sup></a> <a href="#cite_ref-OSHA_2-2"><sup><i><b>c</b></i></sup></a> <a href="#cite_ref-OSHA_2-3"><sup><i><b>d</b></i></sup></a> <a href="#cite_ref-OSHA_2-4"><sup><i><b>e</b></i></sup></a></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation web cs1"><a rel="nofollow" class="external text" href="https://www.osha.gov/publications/hib19980309">"OSHA Hazard Information Bulletins – Dimethylmercury"</a>. <i>OSHA.gov</i><span class="reference-accessdate">. Retrieved <span class="nowrap">29 January</span> 2021</span>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=unknown&rft.jtitle=OSHA.gov&rft.atitle=OSHA+Hazard+Information+Bulletins+%E2%80%93+Dimethylmercury&rft_id=https%3A%2F%2Fwww.osha.gov%2Fpublications%2Fhib19980309&rfr_id=info%3Asid%2Fen.wikipedia.org%3ADimethylmercury" class="Z3988"></span></span> </li> <li id="cite_note-:0-3"><span class="mw-cite-backlink">^ <a href="#cite_ref-:0_3-0"><sup><i><b>a</b></i></sup></a> <a href="#cite_ref-:0_3-1"><sup><i><b>b</b></i></sup></a></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation book cs1"><a rel="nofollow" class="external text" href="https://www.worldcat.org/oclc/1057702183"><i>The Chemistry of mercury</i></a>. C. A. McAuliffe. London: Macmillan. 1977. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-1-349-02489-6" title="Special:BookSources/978-1-349-02489-6"><bdi>978-1-349-02489-6</bdi></a>. <a href="/wiki/OCLC_(identifier)" class="mw-redirect" title="OCLC (identifier)">OCLC</a> <a rel="nofollow" class="external text" href="https://search.worldcat.org/oclc/1057702183">1057702183</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=The+Chemistry+of+mercury&rft.place=London&rft.pub=Macmillan&rft.date=1977&rft_id=info%3Aoclcnum%2F1057702183&rft.isbn=978-1-349-02489-6&rft_id=https%3A%2F%2Fwww.worldcat.org%2Foclc%2F1057702183&rfr_id=info%3Asid%2Fen.wikipedia.org%3ADimethylmercury" class="Z3988"></span><span class="cs1-maint citation-comment"><code class="cs1-code">{{<a href="/wiki/Template:Cite_book" title="Template:Cite book">cite book</a>}}</code>: CS1 maint: others (<a href="/wiki/Category:CS1_maint:_others" title="Category:CS1 maint: others">link</a>)</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="CITEREFHollemanWibergWiberg2001" class="citation book cs1">Holleman, A. F.; Wiberg, Egon; Wiberg, Nils (2001). <i>Inorganic Chemistry</i>. San Diego: Academic Press. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/0-12-352651-5" title="Special:BookSources/0-12-352651-5"><bdi>0-12-352651-5</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Inorganic+Chemistry&rft.place=San+Diego&rft.pub=Academic+Press&rft.date=2001&rft.isbn=0-12-352651-5&rft.aulast=Holleman&rft.aufirst=A.+F.&rft.au=Wiberg%2C+Egon&rft.au=Wiberg%2C+Nils&rfr_id=info%3Asid%2Fen.wikipedia.org%3ADimethylmercury" class="Z3988"></span></span> </li> <li id="cite_note-5"><span class="mw-cite-backlink"><b><a href="#cite_ref-5">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFCrabtree2005" class="citation book cs1"><a href="/wiki/Robert_H._Crabtree" title="Robert H. Crabtree">Crabtree, Robert H.</a> (2005). <i>The Organometallic Chemistry of the Transition Metals</i> (4th ed.). Hoboken, N.J.: John Wiley. p. 424. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/0471662569" title="Special:BookSources/0471662569"><bdi>0471662569</bdi></a>. <a href="/wiki/OCLC_(identifier)" class="mw-redirect" title="OCLC (identifier)">OCLC</a> <a rel="nofollow" class="external text" href="https://search.worldcat.org/oclc/61520528">61520528</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=The+Organometallic+Chemistry+of+the+Transition+Metals&rft.place=Hoboken%2C+N.J.&rft.pages=424&rft.edition=4th&rft.pub=John+Wiley&rft.date=2005&rft_id=info%3Aoclcnum%2F61520528&rft.isbn=0471662569&rft.aulast=Crabtree&rft.aufirst=Robert+H.&rfr_id=info%3Asid%2Fen.wikipedia.org%3ADimethylmercury" class="Z3988"></span></span> </li> <li id="cite_note-6"><span class="mw-cite-backlink"><b><a href="#cite_ref-6">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFBaughmanGordonWolfeZepp1973" class="citation book cs1">Baughman, George L.; Gordon, John A.; Wolfe, N. Lee; Zepp, Richard G. (September 1973). <a rel="nofollow" class="external text" href="https://nepis.epa.gov/Exe/ZyPURL.cgi?Dockey=9100TLU0.TXT"><i>Chemistry of Organomercurials in Aquatic Systems</i></a>. <a href="/wiki/United_States_Environmental_Protection_Agency" title="United States Environmental Protection Agency">United States Environmental Protection Agency</a> Ecological Research Series. <a href="/wiki/U.S._Govt._Print._Off." class="mw-redirect" title="U.S. Govt. Print. Off.">U.S. Govt. Print. Off.</a> pp. 34–40<span class="reference-accessdate">. Retrieved <span class="nowrap">29 January</span> 2021</span>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Chemistry+of+Organomercurials+in+Aquatic+Systems&rft.series=United+States+Environmental+Protection+Agency+Ecological+Research+Series&rft.pages=34-40&rft.pub=U.S.+Govt.+Print.+Off.&rft.date=1973-09&rft.aulast=Baughman&rft.aufirst=George+L.&rft.au=Gordon%2C+John+A.&rft.au=Wolfe%2C+N.+Lee&rft.au=Zepp%2C+Richard+G.&rft_id=https%3A%2F%2Fnepis.epa.gov%2FExe%2FZyPURL.cgi%3FDockey%3D9100TLU0.TXT&rfr_id=info%3Asid%2Fen.wikipedia.org%3ADimethylmercury" class="Z3988"></span></span> </li> <li id="cite_note-7"><span class="mw-cite-backlink"><b><a href="#cite_ref-7">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation web cs1"><a rel="nofollow" class="external text" href="https://pubchem.ncbi.nlm.nih.gov/compound/Methylmercuric_chloride#section=Top">"Methylmercury chloride"</a>. <i><a href="/wiki/PubChem" title="PubChem">PubChem</a></i>. <a href="/wiki/National_Center_for_Biotechnology_Information" title="National Center for Biotechnology Information">National Center for Biotechnology Information</a>, United States <a href="/wiki/National_Institutes_of_Health" title="National Institutes of Health">National Institutes of Health</a><span class="reference-accessdate">. Retrieved <span class="nowrap">29 January</span> 2021</span>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=unknown&rft.jtitle=PubChem&rft.atitle=Methylmercury+chloride&rft_id=https%3A%2F%2Fpubchem.ncbi.nlm.nih.gov%2Fcompound%2FMethylmercuric_chloride%23section%3DTop&rfr_id=info%3Asid%2Fen.wikipedia.org%3ADimethylmercury" class="Z3988"></span></span> </li> <li id="cite_note-8"><span class="mw-cite-backlink"><b><a href="#cite_ref-8">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFO'HalloranSinger1998" class="citation web cs1">O'Halloran, T. V.; Singer, C. P. (10 March 1998). <a rel="nofollow" class="external text" href="https://web.archive.org/web/20050514072706/http://www.chem.northwestern.edu/~ohallo/HgNMRStandards/">"<sup>199</sup>Hg Standards"</a>. Northwestern University. Archived from <a rel="nofollow" class="external text" href="http://www.chem.northwestern.edu/~ohallo/HgNMRStandards/">the original</a> on 14 May 2005<span class="reference-accessdate">. Retrieved <span class="nowrap">20 January</span> 2021</span>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=unknown&rft.btitle=%3Csup%3E199%3C%2Fsup%3EHg+Standards&rft.pub=Northwestern+University&rft.date=1998-03-10&rft.aulast=O%27Halloran&rft.aufirst=T.+V.&rft.au=Singer%2C+C.+P.&rft_id=http%3A%2F%2Fwww.chem.northwestern.edu%2F~ohallo%2FHgNMRStandards%2F&rfr_id=info%3Asid%2Fen.wikipedia.org%3ADimethylmercury" class="Z3988"></span></span> </li> <li id="cite_note-9"><span class="mw-cite-backlink"><b><a href="#cite_ref-9">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFHoffman2011" class="citation web cs1">Hoffman, R. (1 August 2011). <a rel="nofollow" class="external text" href="http://chem.ch.huji.ac.il/nmr/techniques/1d/row6/hg.html">"(Hg) Mercury NMR"</a>. Jerusalem: The Hebrew University<span class="reference-accessdate">. Retrieved <span class="nowrap">29 January</span> 2021</span>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=unknown&rft.btitle=%28Hg%29+Mercury+NMR&rft.place=Jerusalem&rft.pub=The+Hebrew+University&rft.date=2011-08-01&rft.aulast=Hoffman&rft.aufirst=R.&rft_id=http%3A%2F%2Fchem.ch.huji.ac.il%2Fnmr%2Ftechniques%2F1d%2Frow6%2Fhg.html&rfr_id=info%3Asid%2Fen.wikipedia.org%3ADimethylmercury" class="Z3988"></span></span> </li> <li id="cite_note-10"><span class="mw-cite-backlink"><b><a href="#cite_ref-10">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation web cs1"><a rel="nofollow" class="external text" href="https://web.archive.org/web/20120423091321/http://orise.orau.gov/files/reacts/aoo-course-handouts/Module-6-Terrorism-by-Fear-and-Uncertainty-Delayed-Toxic-Syndromes.pdf">"Delayed Toxic Syndromes"</a> <span class="cs1-format">(PDF)</span>. <i>Terrorism by Fear and Uncertainty</i>. <a href="/wiki/Oak_Ridge_Associated_Universities" title="Oak Ridge Associated Universities">ORAU</a>. Archived from <a rel="nofollow" class="external text" href="http://orise.orau.gov/files/reacts/aoo-course-handouts/Module-6-Terrorism-by-Fear-and-Uncertainty-Delayed-Toxic-Syndromes.pdf">the original</a> <span class="cs1-format">(PDF)</span> on 23 April 2012<span class="reference-accessdate">. Retrieved <span class="nowrap">29 January</span> 2021</span>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=unknown&rft.jtitle=Terrorism+by+Fear+and+Uncertainty&rft.atitle=Delayed+Toxic+Syndromes&rft_id=http%3A%2F%2Forise.orau.gov%2Ffiles%2Freacts%2Faoo-course-handouts%2FModule-6-Terrorism-by-Fear-and-Uncertainty-Delayed-Toxic-Syndromes.pdf&rfr_id=info%3Asid%2Fen.wikipedia.org%3ADimethylmercury" class="Z3988"></span></span> </li> <li id="cite_note-Ignition162-11"><span class="mw-cite-backlink">^ <a href="#cite_ref-Ignition162_11-0"><sup><i><b>a</b></i></sup></a> <a href="#cite_ref-Ignition162_11-1"><sup><i><b>b</b></i></sup></a></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFClark2018" class="citation book cs1">Clark, John Drury (23 May 2018). <i>Ignition!</i>. New Brunswick: Rutgers University Press Classics. pp. 162–164. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-0-8135-9583-2" title="Special:BookSources/978-0-8135-9583-2"><bdi>978-0-8135-9583-2</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Ignition%21&rft.place=New+Brunswick&rft.pages=162-164&rft.pub=Rutgers+University+Press+Classics&rft.date=2018-05-23&rft.isbn=978-0-8135-9583-2&rft.aulast=Clark&rft.aufirst=John+Drury&rfr_id=info%3Asid%2Fen.wikipedia.org%3ADimethylmercury" class="Z3988"></span></span> </li> <li id="cite_note-nejm-12"><span class="mw-cite-backlink">^ <a href="#cite_ref-nejm_12-0"><sup><i><b>a</b></i></sup></a> <a href="#cite_ref-nejm_12-1"><sup><i><b>b</b></i></sup></a></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFNierenbergNordgrenChangSiegler1998" class="citation journal cs1">Nierenberg, David W.; Nordgren, Richard E.; Chang, Morris B.; Siegler, Richard W.; Blayney, Michael B.; Hochberg, Fred; Toribara, Taft Y.; Cernichiari, Elsa; Clarkson, Thomas (1998). <a rel="nofollow" class="external text" href="https://doi.org/10.1056%2FNEJM199806043382305">"Delayed Cerebellar Disease and Death after Accidental Exposure to Dimethylmercury"</a>. <i><a href="/wiki/New_England_Journal_of_Medicine" class="mw-redirect" title="New England Journal of Medicine">New England Journal of Medicine</a></i>. <b>338</b> (23): 1672–1676. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<span class="id-lock-free" title="Freely accessible"><a rel="nofollow" class="external text" href="https://doi.org/10.1056%2FNEJM199806043382305">10.1056/NEJM199806043382305</a></span>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/9614258">9614258</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=New+England+Journal+of+Medicine&rft.atitle=Delayed+Cerebellar+Disease+and+Death+after+Accidental+Exposure+to+Dimethylmercury&rft.volume=338&rft.issue=23&rft.pages=1672-1676&rft.date=1998&rft_id=info%3Adoi%2F10.1056%2FNEJM199806043382305&rft_id=info%3Apmid%2F9614258&rft.aulast=Nierenberg&rft.aufirst=David+W.&rft.au=Nordgren%2C+Richard+E.&rft.au=Chang%2C+Morris+B.&rft.au=Siegler%2C+Richard+W.&rft.au=Blayney%2C+Michael+B.&rft.au=Hochberg%2C+Fred&rft.au=Toribara%2C+Taft+Y.&rft.au=Cernichiari%2C+Elsa&rft.au=Clarkson%2C+Thomas&rft_id=https%3A%2F%2Fdoi.org%2F10.1056%252FNEJM199806043382305&rfr_id=info%3Asid%2Fen.wikipedia.org%3ADimethylmercury" class="Z3988"></span></span> </li> <li id="cite_note-story-13"><span class="mw-cite-backlink">^ <a href="#cite_ref-story_13-0"><sup><i><b>a</b></i></sup></a> <a href="#cite_ref-story_13-1"><sup><i><b>b</b></i></sup></a> <a href="#cite_ref-story_13-2"><sup><i><b>c</b></i></sup></a></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFCotton2003" class="citation journal cs1">Cotton, Simon (October 2003). <a rel="nofollow" class="external text" href="http://www.chm.bris.ac.uk/motm/dimethylmercury/dmmh.htm">"Dimethylmercury and Mercury Poisoning: The Karen Wetterhahn story"</a>. <i>Molecule of the Month</i>. <a href="/wiki/Bristol_University" class="mw-redirect" title="Bristol University">Bristol University</a> School of Chemistry. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.6084%2Fm9.figshare.5245807">10.6084/m9.figshare.5245807</a><span class="reference-accessdate">. Retrieved <span class="nowrap">29 January</span> 2021</span>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Molecule+of+the+Month&rft.atitle=Dimethylmercury+and+Mercury+Poisoning%3A+The+Karen+Wetterhahn+story&rft.date=2003-10&rft_id=info%3Adoi%2F10.6084%2Fm9.figshare.5245807&rft.aulast=Cotton&rft.aufirst=Simon&rft_id=http%3A%2F%2Fwww.chm.bris.ac.uk%2Fmotm%2Fdimethylmercury%2Fdmmh.htm&rfr_id=info%3Asid%2Fen.wikipedia.org%3ADimethylmercury" class="Z3988"></span></span> </li> <li id="cite_note-14"><span class="mw-cite-backlink"><b><a href="#cite_ref-14">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation web cs1"><a rel="nofollow" class="external text" href="http://www.chm.bris.ac.uk/motm/dimethylmercury/dmmh.htm">"DimethylMercury and Mercury poisoning"</a>. <i>Molecule of the Month www.chm.bris.ac.uk</i>. October 2003<span class="reference-accessdate">. Retrieved <span class="nowrap">25 August</span> 2022</span>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=unknown&rft.jtitle=Molecule+of+the+Month+www.chm.bris.ac.uk&rft.atitle=DimethylMercury+and+Mercury+poisoning&rft.date=2003-10&rft_id=http%3A%2F%2Fwww.chm.bris.ac.uk%2Fmotm%2Fdimethylmercury%2Fdmmh.htm&rfr_id=info%3Asid%2Fen.wikipedia.org%3ADimethylmercury" class="Z3988"></span></span> </li> <li id="cite_note-15"><span class="mw-cite-backlink"><b><a href="#cite_ref-15">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFCavanaugh2019" class="citation magazine cs1">Cavanaugh, Ray (19 February 2019). <a rel="nofollow" class="external text" href="https://www.chemistryworld.com/opinion/the-dangers-of-dimethylmercury-/3010064.article">"The dangers of dimethylmercury"</a>. <i><a href="/wiki/Chemistry_World" title="Chemistry World">Chemistry World</a></i>. <a href="/wiki/Royal_Society_of_Chemistry" title="Royal Society of Chemistry">Royal Society of Chemistry</a><span class="reference-accessdate">. Retrieved <span class="nowrap">29 January</span> 2021</span>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Chemistry+World&rft.atitle=The+dangers+of+dimethylmercury&rft.date=2019-02-19&rft.aulast=Cavanaugh&rft.aufirst=Ray&rft_id=https%3A%2F%2Fwww.chemistryworld.com%2Fopinion%2Fthe-dangers-of-dimethylmercury-%2F3010064.article&rfr_id=info%3Asid%2Fen.wikipedia.org%3ADimethylmercury" class="Z3988"></span></span> </li> <li id="cite_note-16"><span class="mw-cite-backlink"><b><a href="#cite_ref-16">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFAlbersGiesRaatschenKlintschar2020" class="citation journal cs1">Albers, Anne; Gies, Ursula; Raatschen, Hans-Jurgen; Klintschar, Michael (1 September 2020). <a rel="nofollow" class="external text" href="https://doi.org/10.1007/s12024-020-00247-y">"Another umbrella murder? – A rare case of Minamata disease"</a>. <i>Forensic Science, Medicine and Pathology</i>. <b>16</b> (3): 504–509. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1007%2Fs12024-020-00247-y">10.1007/s12024-020-00247-y</a>. <a href="/wiki/ISSN_(identifier)" class="mw-redirect" title="ISSN (identifier)">ISSN</a> <a rel="nofollow" class="external text" href="https://search.worldcat.org/issn/1556-2891">1556-2891</a>. <a href="/wiki/PMC_(identifier)" class="mw-redirect" title="PMC (identifier)">PMC</a> <span class="id-lock-free" title="Freely accessible"><a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7449996">7449996</a></span>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/32323188">32323188</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Forensic+Science%2C+Medicine+and+Pathology&rft.atitle=Another+umbrella+murder%3F+%E2%80%93+A+rare+case+of+Minamata+disease&rft.volume=16&rft.issue=3&rft.pages=504-509&rft.date=2020-09-01&rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC7449996%23id-name%3DPMC&rft.issn=1556-2891&rft_id=info%3Apmid%2F32323188&rft_id=info%3Adoi%2F10.1007%2Fs12024-020-00247-y&rft.aulast=Albers&rft.aufirst=Anne&rft.au=Gies%2C+Ursula&rft.au=Raatschen%2C+Hans-Jurgen&rft.au=Klintschar%2C+Michael&rft_id=https%3A%2F%2Fdoi.org%2F10.1007%2Fs12024-020-00247-y&rfr_id=info%3Asid%2Fen.wikipedia.org%3ADimethylmercury" class="Z3988"></span></span> </li> <li id="cite_note-17"><span class="mw-cite-backlink"><b><a href="#cite_ref-17">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation news cs1"><a rel="nofollow" class="external text" href="https://www.thelocal.de/20120511/42495/">"Umbrella stab victim dies of mercury poisoning"</a>. <i>www.thelocal.de</i>. 11 May 2012<span class="reference-accessdate">. Retrieved <span class="nowrap">13 June</span> 2022</span>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=www.thelocal.de&rft.atitle=Umbrella+stab+victim+dies+of+mercury+poisoning&rft.date=2012-05-11&rft_id=https%3A%2F%2Fwww.thelocal.de%2F20120511%2F42495%2F&rfr_id=info%3Asid%2Fen.wikipedia.org%3ADimethylmercury" class="Z3988"></span></span> </li> <li id="cite_note-18"><span class="mw-cite-backlink"><b><a href="#cite_ref-18">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation magazine cs1 cs1-prop-foreign-lang-source"><a rel="nofollow" class="external text" href="https://www.spiegel.de/panorama/justiz/quecksilbervergiftung-mann-stirbt-nach-angrif-mit-spritze-in-hannover-a-832677.html">"Quecksilbervergiftung"</a> [Mercury poisoning]. <i><a href="/wiki/Der_Spiegel" title="Der Spiegel">Der Spiegel</a></i> (in German). 11 May 2012<span class="reference-accessdate">. Retrieved <span class="nowrap">3 September</span> 2020</span>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Der+Spiegel&rft.atitle=Quecksilbervergiftung&rft.date=2012-05-11&rft_id=https%3A%2F%2Fwww.spiegel.de%2Fpanorama%2Fjustiz%2Fquecksilbervergiftung-mann-stirbt-nach-angrif-mit-spritze-in-hannover-a-832677.html&rfr_id=info%3Asid%2Fen.wikipedia.org%3ADimethylmercury" class="Z3988"></span></span> </li> <li id="cite_note-19"><span class="mw-cite-backlink"><b><a href="#cite_ref-19">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFAlbersGiesRaatschenKlintschar2020" class="citation journal cs1">Albers, Anne; Gies, Ursula; Raatschen, Hans-Jurgen; Klintschar, Michael (1 September 2020). <a rel="nofollow" class="external text" href="https://doi.org/10.1007/s12024-020-00247-y">"Another umbrella murder? – A rare case of Minamata disease"</a>. <i>Forensic Science, Medicine and Pathology</i>. <b>16</b> (3): 504–509. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1007%2Fs12024-020-00247-y">10.1007/s12024-020-00247-y</a>. <a href="/wiki/ISSN_(identifier)" class="mw-redirect" title="ISSN (identifier)">ISSN</a> <a rel="nofollow" class="external text" href="https://search.worldcat.org/issn/1556-2891">1556-2891</a>. <a href="/wiki/PMC_(identifier)" class="mw-redirect" title="PMC (identifier)">PMC</a> <span class="id-lock-free" title="Freely accessible"><a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7449996">7449996</a></span>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/32323188">32323188</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Forensic+Science%2C+Medicine+and+Pathology&rft.atitle=Another+umbrella+murder%3F+%E2%80%93+A+rare+case+of+Minamata+disease&rft.volume=16&rft.issue=3&rft.pages=504-509&rft.date=2020-09-01&rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC7449996%23id-name%3DPMC&rft.issn=1556-2891&rft_id=info%3Apmid%2F32323188&rft_id=info%3Adoi%2F10.1007%2Fs12024-020-00247-y&rft.aulast=Albers&rft.aufirst=Anne&rft.au=Gies%2C+Ursula&rft.au=Raatschen%2C+Hans-Jurgen&rft.au=Klintschar%2C+Michael&rft_id=https%3A%2F%2Fdoi.org%2F10.1007%2Fs12024-020-00247-y&rfr_id=info%3Asid%2Fen.wikipedia.org%3ADimethylmercury" class="Z3988"></span></span> </li> <li id="cite_note-20"><span class="mw-cite-backlink"><b><a href="#cite_ref-20">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation web cs1"><a rel="nofollow" class="external text" href="https://web.archive.org/web/20220830210717/https://www.zdf.de/gesellschaft/aktenzeichen-xy-ungeloest/xy581-fall1-heimtueckischer-mord-100.html">"Heimtückischer Mord - Familienvater stirbt nach Spritzenattacke - ZDFmediathek"</a>. 30 August 2022. Archived from <a rel="nofollow" class="external text" href="https://www.zdf.de/gesellschaft/aktenzeichen-xy-ungeloest/xy581-fall1-heimtueckischer-mord-100.html">the original</a> on 30 August 2022<span class="reference-accessdate">. Retrieved <span class="nowrap">27 October</span> 2024</span>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=unknown&rft.btitle=Heimt%C3%BCckischer+Mord+-+Familienvater+stirbt+nach+Spritzenattacke+-+ZDFmediathek&rft.date=2022-08-30&rft_id=https%3A%2F%2Fwww.zdf.de%2Fgesellschaft%2Faktenzeichen-xy-ungeloest%2Fxy581-fall1-heimtueckischer-mord-100.html&rfr_id=info%3Asid%2Fen.wikipedia.org%3ADimethylmercury" class="Z3988"></span></span> </li> </ol></div></div> <div class="mw-heading mw-heading2"><h2 id="External_links">External links</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Dimethylmercury&action=edit&section=7" title="Edit section: External links"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <ul><li><a rel="nofollow" class="external text" href="https://www.atsdr.cdc.gov/toxfaqs/TF.asp?id=113&tid=24">ATSDR – ToxFAQs: Mercury</a></li> <li><a rel="nofollow" class="external text" href="https://www.atsdr.cdc.gov/PHS/PHS.asp?id=112&tid=24">ATSDR – Public Health Statement: Mercury</a></li> <li><a rel="nofollow" class="external text" href="https://www.atsdr.cdc.gov/MMG/MMG.asp?id=106&tid=24">ATSDR – MMG: Mercury</a></li> <li><a rel="nofollow" class="external text" href="https://www.atsdr.cdc.gov/toxprofiles/TP.asp?id=115&tid=24">ATSDR – Toxicological Profile: Mercury</a></li> <li><a rel="nofollow" class="external text" href="https://web.archive.org/web/20060425193836/http://www.npi.gov.au/database/substance-info/profiles/53.html">National Pollutant Inventory – Mercury and compounds Fact Sheet</a></li></ul> <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 dt,.mw-parser-output .hlist li{margin:0;display:inline}.mw-parser-output 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style="width:1%"><a href="/wiki/Blister_agent" title="Blister agent">Blister agents</a></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/Arsenical" title="Arsenical">Arsenicals</a></th><td class="navbox-list-with-group navbox-list navbox-even" style="width:100%;padding:0"><div style="padding:0 0.25em"> <li><a href="/wiki/Ethyldichloroarsine" title="Ethyldichloroarsine">Ethyldichloroarsine</a> (ED)</li> <li><a href="/wiki/Methyldichloroarsine" title="Methyldichloroarsine">Methyldichloroarsine</a> (MD)</li> <li><a href="/wiki/Phenyldichloroarsine" title="Phenyldichloroarsine">Phenyldichloroarsine</a> (PD)</li> <li><a href="/wiki/Lewisite" title="Lewisite">Lewisite</a> (L)</li> <li><a href="/wiki/Lewisite_2" title="Lewisite 2">Lewisite 2</a> (L2)</li> <li><a href="/wiki/Lewisite_3" title="Lewisite 3">Lewisite 3</a> (L3)</li> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Sulfur_mustard" class="mw-redirect" title="Sulfur mustard">Sulfur mustards</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/Mustard_gas" title="Mustard gas">Levinstein mustard</a> (EA-229)</li> <li><a href="/wiki/O-Mustard" class="mw-redirect" title="O-Mustard">T</a></li> <li><a href="/wiki/Sesquimustard" title="Sesquimustard">Q</a></li> <li><a href="/wiki/2-Chloroethyl_ethyl_sulfide" title="2-Chloroethyl ethyl sulfide">CEES</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Nitrogen_mustard" title="Nitrogen mustard">Nitrogen mustards</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/HN1_(nitrogen_mustard)" title="HN1 (nitrogen mustard)">HN1</a></li> <li><a href="/wiki/Chlormethine" title="Chlormethine">HN2</a></li> <li><a href="/wiki/HN3_(nitrogen_mustard)" title="HN3 (nitrogen mustard)">HN3</a></li> <li><a href="/wiki/TL-301" title="TL-301">TL-301</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Nettle_agent" title="Nettle agent">Nettle agents</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/Phosgene_oxime" title="Phosgene oxime">Phosgene oxime</a> (CX)</li></ul> </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/KB-16" title="KB-16">KB-16</a></li> <li><a href="/wiki/Dibutylchloromethyltin_chloride" title="Dibutylchloromethyltin chloride">Dibutylchloromethyltin chloride</a></li> <li><a href="/wiki/Selenium_oxychloride" class="mw-redirect" title="Selenium oxychloride">Selenium oxychloride</a></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Nerve_agent" title="Nerve agent">Nerve agents</a></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/Nerve_agent#G-Series" title="Nerve agent">G-agents</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/Tabun_(nerve_agent)" title="Tabun (nerve agent)">Tabun</a> (GA)</li> <li><a href="/wiki/Sarin" title="Sarin">Sarin (GB)</a></li> <li><a href="/wiki/Chlorosarin" title="Chlorosarin">Chlorosarin</a> (ClGB)</li> <li><a href="/wiki/Thiosarin" title="Thiosarin">Thiosarin</a> (SGB)</li> <li><a href="/wiki/Soman" title="Soman">Soman</a> (GD)</li> <li><a href="/wiki/Chlorosoman" title="Chlorosoman">Chlorosoman</a> (ClGD)</li> <li><a href="/wiki/Ethylsarin" title="Ethylsarin">Ethylsarin</a> (GE)</li> <li><a href="/wiki/GH_(nerve_agent)" title="GH (nerve agent)">GH</a></li> <li><a href="/wiki/Cyclosarin" title="Cyclosarin">Cyclosarin</a> (GF)</li> <li><a href="/wiki/GP_(nerve_agent)" title="GP (nerve agent)">GP</a></li> <li><a href="/wiki/Fluorotabun" title="Fluorotabun">Fluorotabun</a></li> <li><a href="/wiki/EA-1356" title="EA-1356">EA-1356</a></li> <li><a href="/wiki/EA-4352" title="EA-4352">EA-4352</a></li> <li><a href="/wiki/Crotylsarin" title="Crotylsarin">Crotylsarin</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Nerve_agent#V-Series" title="Nerve agent">V-agents</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/EA-2192" title="EA-2192">EA-2192</a></li> <li><a href="/wiki/EA-3148" title="EA-3148">EA-3148</a></li> <li><a href="/wiki/VE_(nerve_agent)" title="VE (nerve agent)">VE</a></li> <li><a href="/wiki/VG_(nerve_agent)" title="VG (nerve agent)">VG</a></li> <li><a href="/wiki/VM_(nerve_agent)" title="VM (nerve agent)">VM</a></li> <li><a href="/wiki/3,3,5-Trimethylcyclohexyl_3-pyridyl_methylphosphonate" title="3,3,5-Trimethylcyclohexyl 3-pyridyl methylphosphonate">VP</a></li> <li><a href="/wiki/VR_(nerve_agent)" title="VR (nerve agent)">VR</a></li> <li><a href="/wiki/VS_(nerve_agent)" title="VS (nerve agent)">VS</a></li> <li><a href="/wiki/VX_(nerve_agent)" title="VX (nerve agent)">VX</a></li> <li><a href="/wiki/EA-1763" title="EA-1763">EA-1763</a></li> <li><a href="/wiki/Chinese_VX" title="Chinese VX">Chinese VX</a></li> <li><a href="/wiki/V-sub_x" title="V-sub x">V-sub x (GD-7)</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">GV agents</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/GV_(nerve_agent)" title="GV (nerve agent)">GV (EA-5365)</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Novichok_agent" class="mw-redirect" title="Novichok agent">Novichok agents</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/VR_(nerve_agent)" title="VR (nerve agent)">A-208</a></li> <li><a href="/wiki/A-232" title="A-232">A-232</a></li> <li><a href="/wiki/A-234_(nerve_agent)" title="A-234 (nerve agent)">A-234</a></li> <li><a href="/wiki/A-242" title="A-242">A-242</a></li> <li><a href="/wiki/A-262" title="A-262">A-262</a></li> <li><a href="/wiki/C01-A035" title="C01-A035">C01-A035</a></li> <li><a href="/wiki/C01-A039" title="C01-A039">C01-A039</a></li> <li><a href="/wiki/C01-A042" title="C01-A042">C01-A042</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Carbamate" title="Carbamate">Carbamates</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/Dimethylcarbamoyl_fluoride" title="Dimethylcarbamoyl fluoride">Dimethylcarbamoyl fluoride</a></li> <li><a href="/wiki/EA-3887" title="EA-3887">EA-3887</a></li> <li><a href="/wiki/EA-3887A" class="mw-redirect" title="EA-3887A">EA-3887A</a></li> <li><a href="/wiki/EA-3966" title="EA-3966">EA-3966</a></li> <li><a href="/wiki/EA-3990" title="EA-3990">EA-3990</a></li> <li><a href="/wiki/EA-4056" title="EA-4056">EA-4056</a></li> <li><a href="/wiki/T-1123" title="T-1123">T-1123</a></li> <li><a href="/wiki/T-1152" title="T-1152">T-1152</a></li> <li><a href="/wiki/T-1194" title="T-1194">T-1194</a></li> <li><a href="/wiki/Octamethylene-bis(5-dimethylcarbamoxyisoquinolinium_bromide)" title="Octamethylene-bis(5-dimethylcarbamoxyisoquinolinium bromide)">Octamethylene-bis(5-dimethylcarbamoxyisoquinolinium bromide)</a></li> <li><a href="/wiki/TL-599" title="TL-599">TL-599</a></li> <li><a href="/wiki/TL-1238" title="TL-1238">TL-1238</a></li> <li><a href="/wiki/TL-1299" class="mw-redirect" title="TL-1299">TL-1299</a></li> <li><a href="/wiki/TL-1317" class="mw-redirect" title="TL-1317">TL-1317</a></li> <li><a href="/wiki/Miotine" title="Miotine">Miotine (AR-28/T-1843)</a></li> <li><a href="/wiki/3152_CT" title="3152 CT">3152 CT</a></li> <li><a href="/wiki/4-686-293-01" title="4-686-293-01">4-686-293-01 (Agent 1-10)</a></li></ul> </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/Diisopropyl_fluorophosphate" title="Diisopropyl fluorophosphate">Diisopropyl fluorophosphate</a></li> <li><a href="/wiki/Dicyclohexyl_phosphorofluoridate" title="Dicyclohexyl phosphorofluoridate">Dicyclohexyl phosphorofluoridate</a></li> <li><a href="/wiki/EA-2012" title="EA-2012">EA-2012</a></li> <li><a href="/wiki/EA-2054" title="EA-2054">EA-2054</a></li> <li><a href="/wiki/EA-2098" title="EA-2098">EA-2098</a></li> <li><a href="/wiki/EA-2613" title="EA-2613">EA-2613</a></li> <li><a href="/wiki/2-Ethoxycarbonyl-1-methylvinyl_cyclohexyl_methylphosphonate" title="2-Ethoxycarbonyl-1-methylvinyl cyclohexyl methylphosphonate">2-Ethoxycarbonyl-1-methylvinyl cyclohexyl methylphosphonate</a></li> <li><a href="/wiki/Neopentylene_fluorophosphate" title="Neopentylene fluorophosphate">Neopentylene fluorophosphate</a></li> <li><a href="/wiki/Selenophos" title="Selenophos">Selenophos</a></li> <li><a href="/wiki/Phospholine" class="mw-redirect" title="Phospholine">Phospholine</a></li> <li><a href="/wiki/R-16661" title="R-16661">R-16661</a></li> <li><a href="/wiki/Ro_3-0422" title="Ro 3-0422">Ro 3-0422</a></li> <li><a href="/wiki/Methanesulfonyl_fluoride" title="Methanesulfonyl fluoride">Methanesulfonyl fluoride</a></li> <li><a href="/wiki/Dimefox" title="Dimefox">Dimefox (TL-792)</a></li> <li><a href="/wiki/MSPI_(nerve_agent)" title="MSPI (nerve agent)">MSPI</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Precursors</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/Acetonitrile" title="Acetonitrile">Acetonitrile</a></li> <li><a href="/wiki/Arsenic_trichloride" title="Arsenic trichloride">AT</a></li> <li><a href="/wiki/Arsenic_trioxide" title="Arsenic trioxide">ATO</a></li> <li><a href="/wiki/Aluminium_phosphide" title="Aluminium phosphide">AlP</a></li> <li><a href="/wiki/Kinnear%E2%80%93Perren_reaction" title="Kinnear–Perren reaction">A.P.C. complex</a></li> <li><a href="/wiki/Chlorosarin" title="Chlorosarin">Chlorosarin</a></li> <li><a href="/wiki/Chlorosoman" title="Chlorosoman">Chlorosoman</a></li> <li><a href="/wiki/Cyclohexanol" title="Cyclohexanol">Cyclohexanol</a></li> <li><a href="/wiki/1,8-Dibromooctane" title="1,8-Dibromooctane">1,8-Dibromooctane</a></li> <li><a href="/wiki/N,N-Diisopropylaminoethanol" title="N,N-Diisopropylaminoethanol">N,N-Diisopropylaminoethanol</a> (KB)</li> <li><a href="/wiki/Diisopropyl_methylphosphonate" title="Diisopropyl methylphosphonate">EA-1250</a></li> <li><a href="/wiki/Diisopropylphosphite" title="Diisopropylphosphite">DIHP</a></li> <li><a href="/wiki/Ethanol" title="Ethanol">ZS</a></li> <li><a href="/wiki/Diethylphosphite" title="Diethylphosphite">DEHP</a></li> <li><a href="/wiki/Dimethyl_methylphosphonate" title="Dimethyl methylphosphonate">EA-1224</a></li> <li><a href="/wiki/Dimethylamidophosphoric_dichloride" title="Dimethylamidophosphoric dichloride">Dimethylamidophosphoric dichloride</a></li> <li><a href="/wiki/Dimethylamidophosphoric_dicyanide" title="Dimethylamidophosphoric dicyanide">Dimethylamidophosphoric dicyanide</a></li> <li><a href="/wiki/Dimethylphosphite" title="Dimethylphosphite">DMHP</a></li> <li><a href="/wiki/Ethylphosphonoselenoic_dichloride" title="Ethylphosphonoselenoic dichloride">Ethylphosphonoselenoic dichloride</a></li> <li><a href="/wiki/Formaldoxime" title="Formaldoxime">Formaldoxime</a></li> <li><a href="/wiki/Fulminic_acid" title="Fulminic acid">Nital</a></li> <li><a href="/wiki/4-Hydroxycoumarin" title="4-Hydroxycoumarin">4-Hydroxycoumarin</a></li> <li><a href="/wiki/Isopropyl_alcohol" title="Isopropyl alcohol">Isopropyl alcohol</a> (TB)</li> <li><a href="/wiki/Methyldichlorophosphine" title="Methyldichlorophosphine">Methyldichlorophosphine</a> (SW)</li> <li><a href="/wiki/Methylphosphonyl_difluoride" title="Methylphosphonyl difluoride">Methylphosphonyl difluoride (difluoro)</a> (DF)</li> <li><a href="/wiki/Methylphosphonyl_dichloride" title="Methylphosphonyl dichloride">Methylphosphonyl dichloride (dichloro)</a></li> <li><a href="/wiki/Nitromethane" title="Nitromethane">Nitromethane</a></li> <li><a href="/wiki/OPA_mixture" title="OPA mixture">OPA mixture</a></li> <li><a href="/wiki/Phosphoryl_chloride" title="Phosphoryl chloride">Phosphoryl chloride</a></li> <li><a href="/wiki/Phosphorus_pentachloride" title="Phosphorus pentachloride">Phosphorus pentachloride</a></li> <li><a href="/wiki/Phosphorus_trichloride" title="Phosphorus trichloride">Phosphorus trichloride</a> (TH)</li> <li><a href="/wiki/Pinacolone" title="Pinacolone">Pinacolone</a></li> <li><a href="/wiki/Pinacolyl_alcohol" title="Pinacolyl alcohol">Pinacolyl alcohol</a></li> <li><a href="/wiki/Phenacyl_chloride" title="Phenacyl chloride">Phenacyl chloride</a></li> <li><a href="/wiki/QL_(chemical)" title="QL (chemical)">QL</a></li> <li><a href="/wiki/2,4,5-Trichlorophenol" title="2,4,5-Trichlorophenol">2,4,5-Trichlorophenol</a></li> <li><a href="/wiki/3,3,5-Trimethylcyclohexanol" title="3,3,5-Trimethylcyclohexanol">3,3,5-Trimethylcyclohexanol</a></li> <li><a href="/wiki/Triethyl_phosphite" title="Triethyl phosphite">Triethyl phosphite</a></li> <li><a href="/wiki/Trimethyl_phosphite" title="Trimethyl phosphite">Trimethyl phosphite</a></li> <li><a href="/wiki/Thionyl_chloride" title="Thionyl chloride">TC</a></li> <li><a href="/wiki/Thiodiglycol" title="Thiodiglycol">TG</a></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Neurotoxin" title="Neurotoxin">Neurotoxins</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/Anatoxin-a" title="Anatoxin-a">Anatoxin-a</a></li> <li><a href="/wiki/Saxitoxin" title="Saxitoxin">Saxitoxin</a> (TZ)</li> <li><a href="/wiki/Bungarotoxin" title="Bungarotoxin">Bungarotoxin</a></li> <li><a href="/wiki/Botulinum_toxin" title="Botulinum toxin">Botulinum toxin</a> (BTX)</li> <li><a href="/wiki/Tetanospasmin" class="mw-redirect" title="Tetanospasmin">Tetanospasmin</a> (TeNT)</li> <li><a href="/wiki/Ryanodine" title="Ryanodine">Ryanodine</a></li> <li><a href="/wiki/Ciguatoxin" title="Ciguatoxin">Ciguatoxin</a> (CTX)</li> <li><a href="/wiki/Guanitoxin" title="Guanitoxin">Guanitoxin</a> (GTX)</li> <li><a href="/wiki/Chlorophenylsilatrane" title="Chlorophenylsilatrane">Chlorophenylsilatrane</a></li> <li><a href="/wiki/Palytoxin" title="Palytoxin">Palytoxin</a> (PTX)</li> <li><a href="/wiki/Maitotoxin" title="Maitotoxin">Maitotoxin</a> (MTX)</li> <li><a href="/wiki/Tetrodotoxin" title="Tetrodotoxin">Tetrodotoxin</a></li> <li><a href="/wiki/Aconitine" title="Aconitine">Aconitine</a></li> <li><a href="/wiki/Brevetoxin" title="Brevetoxin">Brevetoxin</a> (PbTX)</li> <li><a href="/wiki/Strychnine" title="Strychnine">Strychnine</a></li> <li><a href="/wiki/Antillatoxin" title="Antillatoxin">Antillatoxin</a> (ATX)</li> <li><a href="/wiki/Tetraethyllead" title="Tetraethyllead">Tetraethyllead</a></li> <li><a class="mw-selflink selflink">Dimethylmercury</a></li> <li><a href="/wiki/HN1_(nitrogen_mustard)" title="HN1 (nitrogen mustard)">HN1 hydrochloride</a></li> <li><a href="/wiki/HN2" class="mw-redirect" title="HN2">HN2 hydrochloride</a></li> <li><a href="/wiki/Tris(2-chloroethyl)amine" class="mw-redirect" title="Tris(2-chloroethyl)amine">HN3 hydrochloride</a></li> <li><a href="/wiki/IDPN_(chemical)" title="IDPN (chemical)">A-8564</a></li> <li><a href="/wiki/Picrotoxin" title="Picrotoxin">Picrotoxin</a></li> <li><a href="/wiki/Sulfuryl_fluoride" title="Sulfuryl fluoride">Sulfuryl fluoride</a></li> <li><a href="/wiki/Tremorine" title="Tremorine">Tremorine</a></li> <li><a href="/wiki/Oxotremorine" title="Oxotremorine">Oxotremorine</a></li> <li><a href="/wiki/Batrachotoxin" title="Batrachotoxin">Batrachotoxin</a></li> <li><a href="/wiki/Tetramethylenedisulfotetramine" title="Tetramethylenedisulfotetramine">Tetramethylenedisulfotetramine (TETS)</a></li> <li><a href="/wiki/Bicyclic_phosphate" title="Bicyclic phosphate">Bicyclic phosphates</a> <ul><li><a href="/wiki/IPTBO" title="IPTBO">IPTBO</a></li> <li><a href="/wiki/TBPO" title="TBPO">TBPO</a></li> <li><a href="/wiki/TBPS" title="TBPS">TBPS</a></li></ul></li> <li><a href="/wiki/Cloflubicyne" title="Cloflubicyne">Cloflubicyne</a></li> <li><a href="/wiki/Trimethylolpropane_phosphite" title="Trimethylolpropane phosphite">Trimethylolpropane phosphite</a></li> <li><a href="/wiki/Domoic_acid" title="Domoic acid">Domoic acid</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Pulmonary_agent" title="Pulmonary agent">Pulmonary/<br />choking agents</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/Chlorine" title="Chlorine">Chlorine</a></li> <li><a href="/wiki/Bromine" title="Bromine">Bromine</a></li> <li><a href="/wiki/Phosgene" title="Phosgene">Phosgene</a> (CG)</li> <li><a href="/wiki/Fluorine" title="Fluorine">Fluorine</a></li> <li><a href="/wiki/Perfluoroisobutene" title="Perfluoroisobutene">Perfluoroisobutene</a></li> <li><a href="/wiki/Chloropicrin" title="Chloropicrin">Chloropicrin</a> (PS)</li> <li><a href="/wiki/Dimethyl(trifluoromethylthio)arsine" title="Dimethyl(trifluoromethylthio)arsine">Dimethyl(trifluoromethylthio)arsine</a></li> <li><a href="/wiki/Diphosgene" title="Diphosgene">Diphosgene</a> (DP)</li> <li><a href="/wiki/Disulfur_decafluoride" title="Disulfur decafluoride">Disulfur decafluoride</a> (Z)</li> <li><a href="/wiki/Acrolein" title="Acrolein">Acrolein</a></li> <li><a href="/wiki/Ethyl_bromoacetate" title="Ethyl bromoacetate">Ethyl bromoacetate</a></li> <li><a href="/wiki/Perchloromethyl_mercaptan" title="Perchloromethyl mercaptan">Perchloromethyl mercaptan</a></li> <li><a href="/wiki/Phenylcarbylamine_chloride" title="Phenylcarbylamine chloride">Phenylcarbylamine chloride</a></li> <li><a href="/wiki/Tetranitromethane" title="Tetranitromethane">Tetranitromethane</a></li> <li><a href="/wiki/Tetrachlorodinitroethane" title="Tetrachlorodinitroethane">Tetrachlorodinitroethane</a></li> <li><a href="/wiki/Chlorine_trifluoride" title="Chlorine trifluoride">Chlorine trifluoride</a></li> <li><a href="/wiki/Perchloryl_fluoride" title="Perchloryl fluoride">Perchloryl fluoride</a></li> <li><a href="/wiki/Cadmium_oxide" title="Cadmium oxide">Cadmium oxide</a></li> <li><a href="/wiki/Cadmium_chloride" title="Cadmium chloride">Cadmium chloride</a></li> <li><a href="/wiki/Mercury(II)_chloride" title="Mercury(II) chloride">Mercuric chloride</a></li> <li><a href="/wiki/Selenium_dioxide" title="Selenium dioxide">Selenium dioxide</a></li> <li><a href="/wiki/Selenoyl_fluoride" title="Selenoyl fluoride">Selenoyl fluoride</a></li> <li><a href="/wiki/Trifluoronitrosomethane" title="Trifluoronitrosomethane">Trifluoronitrosomethane</a></li> <li><a href="/wiki/Trichloronitrosomethane" title="Trichloronitrosomethane">Trichloronitrosomethane</a></li> <li><a href="/wiki/Nitric_oxide" title="Nitric oxide">Nitric oxide</a></li> <li><a href="/wiki/Nitrogen_dioxide" title="Nitrogen dioxide">Nitrogen dioxide</a></li> <li><a href="/wiki/Dinitrogen_tetroxide" title="Dinitrogen tetroxide">Dinitrogen tetroxide</a></li> <li><a href="/wiki/Sulfur_dioxide" title="Sulfur dioxide">Sulfur dioxide</a></li> <li><a href="/wiki/Phosphorus_trichloride" title="Phosphorus trichloride">Phosphorus trichloride</a></li> <li><a href="/wiki/Methyl_isocyanate" title="Methyl isocyanate">Methyl isocyanate</a></li> <li><a href="/wiki/Ethenone" title="Ethenone">Ethenone</a></li> <li><a href="/wiki/Methyl_vinyl_ketone" title="Methyl vinyl ketone">Methyl vinyl ketone</a></li> <li><a href="/wiki/Trifluoroacetyl_chloride" title="Trifluoroacetyl chloride">Trifluoroacetyl chloride</a></li> <li><a href="/wiki/Salcomine" title="Salcomine">Salcomine</a></li> <li><a href="/wiki/Fluomine" title="Fluomine">Fluomine</a></li> <li><a href="/wiki/Uranium_hexafluoride" title="Uranium hexafluoride">Uranium hexafluoride</a></li> <li><a href="/wiki/Diborane" title="Diborane">Diborane</a></li> <li><a href="/wiki/Green_Cross_(chemical_warfare)" title="Green Cross (chemical warfare)">Green Cross</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Vomiting_agent" title="Vomiting agent">Vomiting agents</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/Adamsite" title="Adamsite">Adamsite</a> (DM)</li> <li><a href="/wiki/Chloropicrin" title="Chloropicrin">Chloropicrin</a></li> <li><a href="/wiki/Litharge" title="Litharge">Litharge</a>-<a href="/wiki/Glycerine" class="mw-redirect" title="Glycerine">glycerine</a></li> <li><a href="/wiki/Diphenylchlorarsine" title="Diphenylchlorarsine">Diphenylchlorarsine</a></li> <li><a href="/wiki/Diphenylcyanoarsine" title="Diphenylcyanoarsine">Diphenylcyanoarsine</a></li> <li><a href="/wiki/Cacodyl_cyanide" title="Cacodyl cyanide">Cacodyl cyanide</a></li> <li><a href="/wiki/O-Dianisidine" title="O-Dianisidine">o-Dianisidine</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Incapacitating_agent" title="Incapacitating agent">Incapacitating<br />agents</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/3-Quinuclidinyl_benzilate" title="3-Quinuclidinyl benzilate">BZ</a> (CS-4030)</li> <li><a href="/wiki/Apomorphine" title="Apomorphine">Apomorphine</a></li> <li><a href="/wiki/Butyrophenone" title="Butyrophenone">Butyrophenone</a></li> <li><a href="/wiki/Etonitazene" title="Etonitazene">EA-4941</a> (CS-4640)</li> <li><a href="/wiki/Etorphine" title="Etorphine">Etorphine</a></li> <li><a href="/wiki/Benactyzine" title="Benactyzine">EA-2092</a></li> <li><a href="/wiki/Ditran" title="Ditran">CS-4297</a></li> <li><a href="/wiki/Etoxadrol" title="Etoxadrol">Etoxadrol</a></li> <li><a href="/wiki/Dimethylheptylpyran" title="Dimethylheptylpyran">Dimethylheptylpyran</a> (DMHP)</li> <li><a href="/wiki/Phencyclidine" title="Phencyclidine">EA-2148</a></li> <li><a href="/wiki/EA-3167" title="EA-3167">EA-3167</a></li> <li><a href="/wiki/EA-3443" title="EA-3443">EA-3443</a></li> <li><a href="/wiki/Pethidine" title="Pethidine">Pethidine</a></li> <li><a href="/wiki/EA-3580" title="EA-3580">EA-3580</a></li> <li><a href="/wiki/Ibogaine" title="Ibogaine">Ibogaine</a></li> <li><a href="/wiki/EA-3834" title="EA-3834">EA-3834</a></li> <li><a href="/wiki/Kolokol-1" title="Kolokol-1">Kolokol-1</a></li> <li><a href="/wiki/LSD" title="LSD">LSD-25</a></li> <li><a href="/wiki/PAVA_spray" title="PAVA spray">PAVA spray</a></li> <li><a href="/wiki/Psilocybin" title="Psilocybin">Psilocybin</a></li> <li><a href="/wiki/Incapacitating_agent#Sleeping_gas" title="Incapacitating agent">Sleeping gas</a></li> <li><a href="/wiki/Carfentanil" title="Carfentanil">Carfentanil</a></li> <li><a href="/wiki/N-Ethyl-3-piperidyl_benzilate" title="N-Ethyl-3-piperidyl benzilate">JB-318</a></li> <li><a href="/wiki/N-Methyl-3-piperidyl_benzilate" title="N-Methyl-3-piperidyl benzilate">JB-336</a></li> <li><a href="/wiki/CS-27349" title="CS-27349">CS-27349</a></li> <li><a href="/wiki/CAR-226,086" title="CAR-226,086">CAR-226,086</a></li> <li><a href="/wiki/CAR-301,060" title="CAR-301,060">CAR-301,060</a></li> <li><a href="/wiki/CAR-302,196" title="CAR-302,196">CAR-302,196</a></li> <li><a href="/wiki/CAR-302,282" title="CAR-302,282">CAR-302,282</a></li> <li><a href="/wiki/CAR-302,668" title="CAR-302,668">CAR-302,668</a></li> <li><a href="/wiki/Benperidol" title="Benperidol">Benperidol</a></li> <li><a href="/wiki/Desflurane" title="Desflurane">Desflurane</a></li> <li><a href="/wiki/Enflurane" title="Enflurane">Enflurane</a></li> <li><a href="/wiki/Bufotenin" title="Bufotenin">Bufotenin</a></li> <li><a href="/wiki/Isoflurane" title="Isoflurane">Isoflurane</a></li> <li><a href="/wiki/Halothane" title="Halothane">Halothane</a></li> <li><a href="/wiki/Sevoflurane" title="Sevoflurane">Sevoflurane</a></li> <li><a href="/wiki/Pentazocine" title="Pentazocine">Pentazocine</a></li> <li><a href="/wiki/Procarbazine" title="Procarbazine">Procarbazine</a></li> <li><a href="/wiki/Fluphenazine" title="Fluphenazine">Fluphenazine</a></li> <li><a href="/wiki/Chlorpromazine" title="Chlorpromazine">Chlorpromazine</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Tear_gas" title="Tear gas">Lachrymatory<br />agents</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/Xylyl_bromide" title="Xylyl bromide">Xylyl bromide</a></li> <li><a href="/wiki/Pepper_spray" title="Pepper spray">Pepper spray</a> (OC)</li> <li><a href="/wiki/Mace_(spray)" title="Mace (spray)">Mace (spray)</a></li> <li><a href="/wiki/Phenacyl_chloride" title="Phenacyl chloride">CN</a></li> <li><a href="/wiki/CS_gas" title="CS gas">CS</a></li> <li><a href="/wiki/CR_gas" title="CR gas">CR</a></li> <li><a href="/wiki/CNS_(chemical_weapon)" title="CNS (chemical weapon)">CNS</a></li> <li><a href="/wiki/Benzyl_chloride" title="Benzyl chloride">Benzyl chloride</a></li> <li><a href="/wiki/Benzyl_bromide" title="Benzyl bromide">Benzyl bromide</a></li> <li><a href="/wiki/Benzyl_iodide" title="Benzyl iodide">Benzyl iodide</a></li> <li><a href="/wiki/Bromobenzyl_cyanide" title="Bromobenzyl cyanide">Bromobenzyl cyanide</a></li> <li><a href="/wiki/Thiophosgene" title="Thiophosgene">Thiophosgene</a></li> <li><a href="/wiki/Chloroacetone" title="Chloroacetone">Chloroacetone</a></li> <li><a href="/wiki/Bromoacetone" title="Bromoacetone">Bromoacetone</a></li> <li><a href="/wiki/Bromomethyl_ethyl_ketone" title="Bromomethyl ethyl ketone">Bromomethyl ethyl ketone</a></li> <li><a href="/wiki/Acrolein" title="Acrolein">Acrolein</a></li> <li><a href="/wiki/Phenacyl_bromide" title="Phenacyl bromide">Phenacyl bromide</a></li> <li><a href="/wiki/Chloroacetophenone_oxime" title="Chloroacetophenone oxime">Chloroacetophenone oxime</a></li> <li><a href="/wiki/Ethyl_bromoacetate" title="Ethyl bromoacetate">Ethyl bromoacetate</a></li> <li><a href="/wiki/Ethyl_iodoacetate" title="Ethyl iodoacetate">Ethyl iodoacetate</a></li> <li><a href="/wiki/Iodoacetone" title="Iodoacetone">Iodoacetone</a></li> <li><a href="/wiki/Allyl_isothiocyanate" title="Allyl isothiocyanate">Allyl isothiocyanate</a></li> <li><a href="/wiki/Hexamethylene_diisocyanate" title="Hexamethylene diisocyanate">Hexamethylene diisocyanate</a></li> <li><a href="/wiki/Crotonaldehyde" title="Crotonaldehyde">Crotonaldehyde</a></li> <li><a href="/wiki/DRC-5593" title="DRC-5593">DRC-5593</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Malodorant" title="Malodorant">Malodorant</a> agents</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/Thioacetone" title="Thioacetone">Thioacetone</a></li> <li><a href="/wiki/Allicin" title="Allicin">Allicin</a></li> <li><a href="/wiki/Skatole" title="Skatole">Skatole</a></li> <li><a href="/wiki/Cadaverine" title="Cadaverine">Cadaverine</a></li> <li><a href="/wiki/Putrescine" title="Putrescine">Putrescine</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Cornea-clouding agents</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/Lewisite" title="Lewisite">Lewisite</a></li> <li><a href="/wiki/Phosgene_oxime" title="Phosgene oxime">CX</a></li> <li><a href="/wiki/KB-16" title="KB-16">KB-16</a></li> <li><a href="/wiki/Methyl_cyanoacrylate" title="Methyl cyanoacrylate">Methyl cyanoacrylate</a></li> <li><a href="/wiki/N-Methylmorpholine" title="N-Methylmorpholine">N-Methylmorpholine</a></li> <li><a href="/wiki/Allyl_alcohol" title="Allyl alcohol">Allyl alcohol</a></li> <li><a href="/wiki/Osmium_tetroxide" title="Osmium tetroxide">Osmium tetroxide</a></li> <li><a href="/wiki/Acrolein" title="Acrolein">Acrolein</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Biological toxins</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/Abrin" title="Abrin">Abrin</a></li> <li><a href="/wiki/Aconitine" title="Aconitine">Aconitine</a></li> <li><a href="/wiki/Cyclopiazonic_acid" title="Cyclopiazonic acid">Cyclopiazonic acid</a></li> <li><a href="/wiki/Histrionicotoxins" title="Histrionicotoxins">Histrionicotoxins</a></li> <li><a href="/wiki/Aflatoxins" class="mw-redirect" title="Aflatoxins">Aflatoxins</a></li> <li><a href="/wiki/Anatoxin-a" title="Anatoxin-a">Anatoxin-a</a></li> <li><a href="/wiki/Batrachotoxin" title="Batrachotoxin">Batrachotoxin</a></li> <li><a href="/wiki/Botulinum_toxin" title="Botulinum toxin">Botulinum toxin</a></li> <li><a href="/wiki/Brevetoxin" title="Brevetoxin">Brevetoxin</a></li> <li><a href="/wiki/Ciguatoxin" title="Ciguatoxin">Ciguatoxin</a></li> <li><a href="/wiki/Domoic_acid" title="Domoic acid">Domoic acid</a></li> <li><a href="/wiki/Enterotoxin_type_B" title="Enterotoxin type B">Enterotoxin type B</a></li> <li><a href="/wiki/Grayanotoxin" title="Grayanotoxin">Grayanotoxin</a></li> <li><a href="/wiki/Guanitoxin" title="Guanitoxin">Guanitoxin</a></li> <li><a href="/wiki/Maitotoxin" title="Maitotoxin">Maitotoxin</a></li> <li><a href="/wiki/Modeccin" title="Modeccin">Modeccin</a></li> <li><a href="/wiki/Palytoxin" title="Palytoxin">Palytoxin</a></li> <li><a href="/wiki/Ricin" title="Ricin">Ricin</a></li> <li><a href="/wiki/Saxitoxin" title="Saxitoxin">Saxitoxin</a></li> <li><a href="/wiki/Shiga_toxin" title="Shiga toxin">Shiga toxin</a></li> <li><a href="/wiki/T-2_mycotoxin" title="T-2 mycotoxin">T-2 mycotoxin</a></li> <li><a href="/wiki/Tetanospasmin" class="mw-redirect" title="Tetanospasmin">Tetanospasmin</a></li> <li><a href="/wiki/Tetrodotoxin" title="Tetrodotoxin">Tetrodotoxin</a></li> <li><a href="/wiki/Volkensin" title="Volkensin">Volkensin</a></li> <li><a href="/wiki/Veratridine" title="Veratridine">Veratridine</a></li></ul> </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/Methyl_fluoroacetate" title="Methyl fluoroacetate">Methyl fluoroacetate</a></li> <li><a href="/wiki/Napalm" title="Napalm">Napalm</a> (variants and mixtures)</li> <li><a href="/wiki/Fluoroethyl_fluoroacetate" title="Fluoroethyl fluoroacetate">Fluoroethyl fluoroacetate</a></li> <li><a href="/wiki/Depleted_uranium" title="Depleted uranium">Depleted uranium</a> <ul><li>post-combustion <a href="/wiki/Uranium_oxide" title="Uranium oxide">uranium oxides</a></li></ul></li> <li><a href="/wiki/Plutonium" title="Plutonium">Plutonium</a> and <a href="/wiki/Plutonium_compounds" title="Plutonium compounds">its compounds</a></li> <li><a href="/wiki/Polonium" title="Polonium">Polonium</a></li> <li><a href="/wiki/White_phosphorus_munitions" class="mw-redirect" title="White phosphorus munitions">White phosphorus</a></li></ul> </div></td></tr><tr><td class="navbox-abovebelow" colspan="2"><div> <ul><li><a href="/wiki/List_of_chemical_warfare_agents" title="List of chemical warfare agents">List of chemical warfare agents</a></li> <li><a href="/wiki/CB_military_symbol" title="CB military symbol">CB military symbol</a></li></ul> </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: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><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1123817410"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1123817410"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1123817410"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1123817410"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1123817410"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1123817410"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1123817410"></div><div role="navigation" class="navbox" aria-labelledby="Mercury_compounds" style="padding:3px"><table class="nowraplinks mw-collapsible mw-collapsed navbox-inner" style="border-spacing:0;background:transparent;color:inherit"><tbody><tr><th scope="col" class="navbox-title" colspan="2"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1129693374"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1239400231"><div class="navbar plainlinks hlist navbar-mini"><ul><li class="nv-view"><a href="/wiki/Template:Mercury_compounds" title="Template:Mercury compounds"><abbr title="View this template">v</abbr></a></li><li class="nv-talk"><a href="/wiki/Template_talk:Mercury_compounds" title="Template talk:Mercury compounds"><abbr title="Discuss this template">t</abbr></a></li><li class="nv-edit"><a href="/wiki/Special:EditPage/Template:Mercury_compounds" title="Special:EditPage/Template:Mercury compounds"><abbr title="Edit this template">e</abbr></a></li></ul></div><div id="Mercury_compounds" style="font-size:114%;margin:0 4em"><a href="/wiki/Mercury_compounds" class="mw-redirect" title="Mercury compounds">Mercury compounds</a></div></th></tr><tr><th scope="row" class="navbox-group" style="width:1%">Mercury(I)</th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Mercury(I)_hydride" title="Mercury(I) hydride">HgH</a></li> <li><a href="/wiki/Mercury(I)_hydride" title="Mercury(I) hydride">Hg<sub>2</sub>H<sub>2</sub></a></li> <li><a href="/wiki/Mercury(I)_bromide" title="Mercury(I) bromide">Hg<sub>2</sub>Br<sub>2</sub></a></li> <li><a href="/wiki/Mercury(I)_chloride" title="Mercury(I) chloride">Hg<sub>2</sub>Cl<sub>2</sub></a></li> <li><a href="/wiki/Mercury(I)_fluoride" title="Mercury(I) fluoride">Hg<sub>2</sub>F<sub>2</sub></a></li> <li><a href="/wiki/Mercury(I)_iodide" title="Mercury(I) iodide">Hg<sub>2</sub>I<sub>2</sub></a></li> <li><a href="/wiki/Mercury(I)_nitrate" title="Mercury(I) nitrate">Hg<sub>2</sub>(NO<sub>3</sub>)<sub>2</sub></a></li> <li><a href="/wiki/Mercury(I)_oxide" title="Mercury(I) oxide">Hg<sub>2</sub>O</a></li> <li><a href="/wiki/Mercury(I)_carbonate" class="mw-redirect" title="Mercury(I) carbonate">Hg<sub>2</sub>CO<sub>3</sub></a></li> <li><a href="/wiki/Mercury(I)_sulfate" title="Mercury(I) sulfate">Hg<sub>2</sub>SO<sub>4</sub></a></li> <li><a href="/wiki/Mercury(I)_sulfide" title="Mercury(I) sulfide">Hg<sub>2</sub>S</a> (<i>hypothetical</i>)</li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Mercury(II)</th><td class="navbox-list-with-group navbox-list navbox-even hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Mercury(II)_hydride" title="Mercury(II) hydride">HgH<sub>2</sub></a></li> <li><a href="/wiki/Mercuric_amidochloride" title="Mercuric amidochloride">HgNH<sub>2</sub>Cl</a></li> <li><a href="/wiki/Mercury_selenide" title="Mercury selenide">HgSe</a></li> <li><a href="/wiki/Mercury_sulfide" title="Mercury sulfide">HgS</a></li> <li><a href="/wiki/Mercury_telluride" title="Mercury telluride">HgTe</a></li> <li><a href="/wiki/Mercury(II)_acetate" title="Mercury(II) acetate">Hg(O<sub>2</sub>CCH<sub>3</sub>)<sub>2</sub></a></li> <li><a href="/wiki/Mercury(II)_bromide" title="Mercury(II) bromide">HgBr<sub>2</sub></a></li> <li><a href="/wiki/Mercury(II)_chloride" title="Mercury(II) chloride">HgCl<sub>2</sub></a></li> <li><a href="/wiki/Mercury(II)_cyanide" title="Mercury(II) cyanide">Hg(CN)<sub>2</sub></a></li> <li><a href="/wiki/Mercury(II)_fluoride" title="Mercury(II) fluoride">HgF<sub>2</sub></a></li> <li><a href="/wiki/Mercury(II)_hydroxide" title="Mercury(II) hydroxide">Hg(OH)<sub>2</sub></a></li> <li><a href="/wiki/Mercury(II)_iodide" title="Mercury(II) iodide">HgI<sub>2</sub></a></li> <li><a href="/wiki/Mercury(II)_nitrate" title="Mercury(II) nitrate">Hg(NO<sub>3</sub>)<sub>2</sub></a></li> <li><a href="/wiki/Mercury(II)_oxide" title="Mercury(II) oxide">HgO</a></li> <li><a href="/wiki/Mercury(II)_sulfate" title="Mercury(II) sulfate">HgSO<sub>4</sub></a></li> <li><a href="/wiki/Mercury(II)_thiocyanate" title="Mercury(II) thiocyanate">Hg(SCN)<sub>2</sub></a></li> <li><a href="/wiki/Mercury(II)_fulminate" title="Mercury(II) fulminate">Hg(CNO)<sub>2</sub></a></li> <li><a href="/wiki/Mercury_nitride" title="Mercury nitride">Hg<sub>3</sub>N<sub>2</sub></a></li> <li><a href="/wiki/Bis(trimethylsilyl)mercury" title="Bis(trimethylsilyl)mercury">Hg(Si(CH<sub>3</sub>)<sub>3</sub>)<sub>2</sub></a></li> <li><a href="/wiki/Potassium_tetraiodomercurate(II)" title="Potassium tetraiodomercurate(II)">K<sub>2</sub>HgI<sub>4</sub></a></li></ul> </div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th id="Organomercury_compounds" scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Organomercury" class="mw-redirect" title="Organomercury">Organomercury</a><br /> compounds</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 class="mw-selflink selflink">Hg(CH<sub>3</sub>)<sub>2</sub></a></li> <li><a href="/wiki/Diethylmercury" title="Diethylmercury">Hg(C<sub>2</sub>H<sub>5</sub>)<sub>2</sub></a></li> <li><a href="/wiki/Diphenylmercury" title="Diphenylmercury">Hg(C<sub>6</sub>H<sub>5</sub>)<sub>2</sub></a></li> <li><a href="/wiki/Phenylmercury_acetate" title="Phenylmercury acetate">HgC<sub>6</sub>H<sub>5</sub>CH<sub>3</sub>CO<sub>2</sub></a></li> <li><a href="/wiki/Phenylmercuric_borate" title="Phenylmercuric borate">HgC<sub>6</sub>H<sub>5</sub>OB(OH)<sub>2</sub></a></li> <li><a href="/wiki/Phenylmercuric_nitrate" title="Phenylmercuric nitrate">HgC<sub>6</sub>H<sub>5</sub>NO<sub>3</sub></a></li> <li><a href="/wiki/Phenyl(trichloromethyl)mercury" title="Phenyl(trichloromethyl)mercury">HgC<sub>6</sub>H<sub>5</sub>CCl<sub>3</sub></a></li> <li><a href="/wiki/4-Chloromercuribenzoic_acid" title="4-Chloromercuribenzoic acid">HgClC<sub>6</sub>H<sub>4</sub>CO<sub>2</sub>H</a></li> <li><a href="/wiki/Meralluride" title="Meralluride">HgOHCH<sub>2</sub>CHOCH<sub>3</sub>CH<sub>2</sub>(NHCO)</a></li> <li><a href="/wiki/Mercury(II)_stearate" title="Mercury(II) stearate"><span class="chemf nowrap">C<span class="nowrap"><span style="display:inline-block;margin-bottom:-0.3em;vertical-align:-0.4em;line-height:1em;font-size:80%;text-align:left"><sup style="font-size:inherit;line-height:inherit;vertical-align:baseline"></sup><br /><sub style="font-size:inherit;line-height:inherit;vertical-align:baseline">36</sub></span></span>H<span class="nowrap"><span style="display:inline-block;margin-bottom:-0.3em;vertical-align:-0.4em;line-height:1em;font-size:80%;text-align:left"><sup style="font-size:inherit;line-height:inherit;vertical-align:baseline"></sup><br /><sub style="font-size:inherit;line-height:inherit;vertical-align:baseline">70</sub></span></span>HgO<span class="nowrap"><span style="display:inline-block;margin-bottom:-0.3em;vertical-align:-0.4em;line-height:1em;font-size:80%;text-align:left"><sup style="font-size:inherit;line-height:inherit;vertical-align:baseline"></sup><br /><sub style="font-size:inherit;line-height:inherit;vertical-align:baseline">4</sub></span></span></span></a></li> <li><a href="/wiki/Mersalyl" title="Mersalyl">HgOHCH<sub>2</sub>CHOCH<sub>3</sub>CH<sub>2</sub>NHCOC<sub>6</sub>H<sub>4</sub>OCH<sub>2</sub>CO<sub>2</sub>H</a></li> <li><a href="/wiki/Merbromin" title="Merbromin">Na<sub>2</sub>HgOHC<sub>6</sub>HOBrC<sub>6</sub>H<sub>2</sub>OBrOCHC<sub>6</sub>H<sub>4</sub>CO<sub>2</sub></a></li> <li><a href="/wiki/Nitromersol" title="Nitromersol">HgOC<sub>6</sub>H<sub>2</sub>CH<sub>3</sub>NO<sub>2</sub></a></li> <li><a href="/wiki/Thiomersal" title="Thiomersal">NaHgC<sub>2</sub>H<sub>5</sub>SC<sub>6</sub>H<sub>4</sub>CO<sub>2</sub></a></li></ul> </div></td></tr></tbody></table><div> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Mercury(IV)</th><td class="navbox-list-with-group navbox-list navbox-even hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Mercury(IV)_fluoride" title="Mercury(IV) fluoride">HgF<sub>4</sub></a> (<i>hypothetical</i>)</li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Amalgam_(chemistry)" title="Amalgam (chemistry)">Amalgams</a></th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Sodium_amalgam" title="Sodium amalgam">Na(Hg)</a></li> <li><a href="/wiki/Aluminium_amalgam" title="Aluminium amalgam">Al(Hg)</a></li> <li><a href="/wiki/Amalgam_(chemistry)#Potassium_amalgam" title="Amalgam (chemistry)">K(Hg)</a></li> <li><a href="/wiki/Amalgam_(chemistry)#Gold_amalgam" title="Amalgam (chemistry)">Au(Hg)</a></li> <li><a href="/wiki/Amalgam_(chemistry)#Thallium_amalgam" title="Amalgam (chemistry)">Tl(Hg)</a></li> <li><a href="/wiki/Amalgam_(chemistry)#Tin_amalgam" title="Amalgam (chemistry)">Sn(Hg)</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Mercury_polycations" title="Mercury polycations">Mercury cations</a></th><td class="navbox-list-with-group navbox-list navbox-even hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Mercury_(element)#Compounds_of_mercury(II)" title="Mercury (element)"><span class="chemf nowrap">Hg<sup>2+</sup></span></a></li> <li><a href="/wiki/Mercury_(element)#Compounds_of_mercury(I)" title="Mercury (element)"><span class="chemf nowrap">Hg<span class="template-chem2-su"><span>2+</span><span>2</span></span></span></a></li> <li><a href="/wiki/Mercury_polycations#Linear_trimercury_and_tetramercury_cations" title="Mercury polycations"><span class="chemf nowrap">Hg<span class="template-chem2-su"><span>2+</span><span>3</span></span></span></a></li> <li><a href="/wiki/Mercury_polycations#Linear_trimercury_and_tetramercury_cations" title="Mercury polycations"><span class="chemf nowrap">Hg<span class="template-chem2-su"><span>2+</span><span>4</span></span></span></a></li> <li><a href="/wiki/Mercury_polycations#Cyclic_mercury_cations" title="Mercury polycations"><span class="chemf nowrap">Hg<span class="template-chem2-su"><span>4+</span><span>3</span></span></span></a></li> <li><a href="/wiki/Methylmercury" title="Methylmercury"><span class="chemf nowrap">HgCH<span class="template-chem2-su"><span>+</span><span>3</span></span></span></a></li> <li><a href="/wiki/Ethylmercury" title="Ethylmercury"><span class="chemf nowrap">HgC<sub class="template-chem2-sub">2</sub>H<span class="template-chem2-su"><span>+</span><span>5</span></span></span></a></li> <li><a href="/wiki/Phenylmercury_acetate" title="Phenylmercury acetate"><span class="chemf nowrap">HgC<sub class="template-chem2-sub">6</sub>H<span class="template-chem2-su"><span>+</span><span>5</span></span></span></a></li></ul> </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"></div><div role="navigation" class="navbox" aria-labelledby="Neurotoxins" style="padding:3px"><table class="nowraplinks hlist mw-collapsible autocollapse navbox-inner" style="border-spacing:0;background:transparent;color:inherit"><tbody><tr><th scope="col" class="navbox-title" colspan="2"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1129693374"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1239400231"><div class="navbar plainlinks hlist navbar-mini"><ul><li class="nv-view"><a href="/wiki/Template:Neurotoxins" title="Template:Neurotoxins"><abbr title="View this template">v</abbr></a></li><li class="nv-talk"><a href="/wiki/Template_talk:Neurotoxins" title="Template talk:Neurotoxins"><abbr title="Discuss this template">t</abbr></a></li><li class="nv-edit"><a href="/wiki/Special:EditPage/Template:Neurotoxins" title="Special:EditPage/Template:Neurotoxins"><abbr title="Edit this template">e</abbr></a></li></ul></div><div id="Neurotoxins" style="font-size:114%;margin:0 4em"><a href="/wiki/Neurotoxin" title="Neurotoxin">Neurotoxins</a></div></th></tr><tr><th scope="row" class="navbox-group" style="width:1%">Animal toxins</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/Batrachotoxin" title="Batrachotoxin">Batrachotoxin</a></li> <li><a href="/wiki/Bestoxin" title="Bestoxin">Bestoxin</a></li> <li><a href="/wiki/Birtoxin" title="Birtoxin">Birtoxin</a></li> <li><a href="/wiki/Bungarotoxin" title="Bungarotoxin">Bungarotoxin</a></li> <li><a href="/wiki/Charybdotoxin" title="Charybdotoxin">Charybdotoxin</a></li> <li><a href="/wiki/Conotoxin" title="Conotoxin">Conotoxin</a></li> <li><a href="/wiki/Fasciculin" title="Fasciculin">Fasciculin</a></li> <li><a href="/wiki/Huwentoxin" title="Huwentoxin">Huwentoxin</a></li> <li><a href="/wiki/Poneratoxin" title="Poneratoxin">Poneratoxin</a></li> <li><a href="/wiki/Saxitoxin" title="Saxitoxin">Saxitoxin</a></li> <li><a href="/wiki/Tetrodotoxin" title="Tetrodotoxin">Tetrodotoxin</a></li> <li><a href="/wiki/Vanillotoxin" title="Vanillotoxin">Vanillotoxin</a></li> <li><a href="/wiki/Ssm_spooky_toxin" title="Ssm spooky toxin">Spooky toxin (SsTx)</a></li> <li><a href="/wiki/Epibatidine" title="Epibatidine">Epibatidine</a></li> <li><a href="/wiki/Zetekitoxin_AB" title="Zetekitoxin AB">Zetekitoxin AB</a></li> <li><a href="/wiki/Dendrotoxin" title="Dendrotoxin">Dendrotoxin</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Bacterial_toxin" class="mw-redirect" title="Bacterial toxin">Bacterial</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/Botulinum_toxin" title="Botulinum toxin">Botulinum toxin</a></li> <li><a href="/wiki/Tetanospasmin" class="mw-redirect" title="Tetanospasmin">Tetanospasmin</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Cyanotoxin" title="Cyanotoxin">Cyanotoxins</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/Anatoxin-a" title="Anatoxin-a">Anatoxin-a</a></li> <li><a href="/wiki/Guanitoxin" title="Guanitoxin">Guanitoxin</a></li> <li><a href="/wiki/Beta-Methylamino-L-alanine" class="mw-redirect" title="Beta-Methylamino-L-alanine">BMAA</a></li> <li><a href="/wiki/Saxitoxin" title="Saxitoxin">Saxitoxin</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Plant_toxin" class="mw-redirect" title="Plant toxin">Plant toxins</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/Aconitine" title="Aconitine">Aconitine</a></li> <li><a href="/wiki/Bicuculline" title="Bicuculline">Bicuculline</a></li> <li><a href="/wiki/Penitrem_A" title="Penitrem A">Penitrem A</a></li> <li><a href="/wiki/Picrotoxin" title="Picrotoxin">Picrotoxin</a></li> <li><a href="/wiki/Strychnine" title="Strychnine">Strychnine</a></li> <li><a href="/wiki/Tutin_(toxin)" title="Tutin (toxin)">Tutin</a></li> <li><a href="/wiki/Rotenone" title="Rotenone">Rotenone</a></li> <li><a href="/wiki/Ginkgotoxin" title="Ginkgotoxin">Ginkgotoxin</a></li> <li><a href="/wiki/Cicutoxin" title="Cicutoxin">Cicutoxin</a></li> <li><a href="/wiki/Oenanthotoxin" title="Oenanthotoxin">Oenanthotoxin</a></li> <li><a href="/wiki/Thujone" title="Thujone">Thujone</a></li> <li><a href="/wiki/Volkensin" title="Volkensin">Volkensin</a></li> <li><a href="/wiki/Veratridine" title="Veratridine">Veratridine</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Mycotoxin" title="Mycotoxin">Mycotoxins</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/Ibotenic_acid" title="Ibotenic acid">Ibotenic acid</a></li> <li><a href="/wiki/Muscarine" title="Muscarine">Muscarine</a></li> <li><a href="/wiki/Muscimol" title="Muscimol">Muscimol</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Pesticide" title="Pesticide">Pesticides</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/Fenpropathrin" title="Fenpropathrin">Fenpropathrin</a></li> <li><a href="/wiki/Tetramethylenedisulfotetramine" title="Tetramethylenedisulfotetramine">Tetramethylenedisulfotetramine</a></li> <li><a href="/wiki/Bromethalin" title="Bromethalin">Bromethalin</a></li> <li><a href="/wiki/Crimidine" title="Crimidine">Crimidine</a></li> <li><a href="/wiki/Methamidophos" title="Methamidophos">Methamidophos</a></li> <li><a href="/wiki/Endosulfan" title="Endosulfan">Endosulfan</a></li> <li><a href="/wiki/Fipronil" title="Fipronil">Fipronil</a></li> <li><a href="/wiki/Phenylsilatrane" title="Phenylsilatrane">Phenylsilatrane</a></li> <li><a href="/wiki/Chlorophenylsilatrane" title="Chlorophenylsilatrane">Chlorophenylsilatrane</a></li> <li><a href="/wiki/Sulfuryl_fluoride" title="Sulfuryl fluoride">Sulfuryl fluoride</a></li> <li><a href="/wiki/Mipafox" title="Mipafox">Mipafox</a></li> <li><a href="/wiki/Schradan" title="Schradan">Schradan</a></li> <li><a href="/wiki/Dimefox" title="Dimefox">Dimefox</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Nerve_agent" title="Nerve agent">Nerve agents</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/Cyclosarin" title="Cyclosarin">Cyclosarin</a></li> <li><a href="/wiki/EA-3148" title="EA-3148">EA-3148</a></li> <li><a href="/wiki/Novichok_agent" class="mw-redirect" title="Novichok agent">Novichok agent</a></li> <li><a href="/wiki/Sarin" title="Sarin">Sarin</a></li> <li><a href="/wiki/Soman" title="Soman">Soman</a></li> <li><a href="/wiki/Tabun_(nerve_agent)" title="Tabun (nerve agent)">Tabun</a></li> <li><a href="/wiki/VE_(nerve_agent)" title="VE (nerve agent)">VE</a></li> <li><a href="/wiki/VG_(nerve_agent)" title="VG (nerve agent)">VG</a></li> <li><a href="/wiki/VM_(nerve_agent)" title="VM (nerve agent)">VM</a></li> <li><a href="/wiki/VP_(nerve_agent)" class="mw-redirect" title="VP (nerve agent)">VP</a></li> <li><a href="/wiki/VR_(nerve_agent)" title="VR (nerve agent)">VR</a></li> <li><a href="/wiki/VX_(nerve_agent)" title="VX (nerve agent)">VX</a></li> <li><a href="/wiki/GV_(nerve_agent)" title="GV (nerve agent)">GV</a></li> <li><a href="/wiki/EA-3990" title="EA-3990">EA-3990</a></li> <li><a href="/wiki/EA-4056" title="EA-4056">EA-4056</a></li> <li><a href="/wiki/T-1123" title="T-1123">T-1123</a></li> <li><a href="/wiki/Octamethylene-bis(5-dimethylcarbamoxyisoquinolinium_bromide)" title="Octamethylene-bis(5-dimethylcarbamoxyisoquinolinium bromide)">Octamethylene-bis(5-dimethylcarbamoxyisoquinolinium bromide)</a></li> <li><a href="/wiki/Fluorotabun" title="Fluorotabun">Fluorotabun</a></li> <li><a href="/wiki/Chinese_VX" title="Chinese VX">Chinese VX</a></li> <li><a href="/wiki/EA-2192" title="EA-2192">EA-2192</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Bicyclic_phosphate" title="Bicyclic phosphate">Bicyclic phosphates</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/TBPS" title="TBPS">TBPS</a></li> <li><a href="/wiki/TBPO" title="TBPO">TBPO</a></li> <li><a href="/wiki/IPTBO" title="IPTBO">IPTBO</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Cholinergic neurotoxins</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="/w/index.php?title=Acetylcholine_mustard&action=edit&redlink=1" class="new" title="Acetylcholine mustard (page does not exist)">Acetylcholine mustard</a></li> <li><a href="/w/index.php?title=Catecholine&action=edit&redlink=1" class="new" title="Catecholine (page does not exist)">Catecholine</a></li> <li><a href="/w/index.php?title=Choline_mustard&action=edit&redlink=1" class="new" title="Choline mustard (page does not exist)">Choline mustard</a></li> <li><a href="/wiki/Ethylcholine_mustard" title="Ethylcholine mustard">Ethylcholine mustard</a></li> <li><a href="/w/index.php?title=Hemicholinium_mustard&action=edit&redlink=1" class="new" title="Hemicholinium mustard (page does not exist)">Hemicholinium mustard</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Psychoactive_drug" title="Psychoactive drug">Psychoactive drugs</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/Alcohol_(drug)" title="Alcohol (drug)">Alcohol</a></li> <li><a href="/wiki/Nitrous_oxide" title="Nitrous oxide">Nitrous oxide</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Other</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/Dimethylcadmium" title="Dimethylcadmium">Dimethylcadmium</a></li> <li><a class="mw-selflink selflink">Dimethylmercury</a></li> <li><a href="/wiki/Toxopyrimidine" title="Toxopyrimidine">Toxopyrimidine</a></li> <li><a href="/wiki/IDPN_(chemical)" title="IDPN (chemical)">IDPN</a></li> <li><a href="/wiki/Tetraethyllead" title="Tetraethyllead">Tetraethyllead</a></li></ul> </div></td></tr></tbody></table></div> <p class="mw-empty-elt"> </p>    </div><noscript><img src="https://login.wikimedia.org/wiki/Special:CentralAutoLogin/start?type=1x1" alt="" 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