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href="#Reaksi"> <div class="vector-toc-text"> <span class="vector-toc-numb">2</span> <span>Reaksi</span> </div> </a> <ul id="toc-Reaksi-sublist" class="vector-toc-list"> </ul> </li> <li id="toc-Kegunaan" class="vector-toc-list-item vector-toc-level-1 vector-toc-list-item-expanded"> <a class="vector-toc-link" href="#Kegunaan"> <div class="vector-toc-text"> <span class="vector-toc-numb">3</span> <span>Kegunaan</span> </div> </a> <ul id="toc-Kegunaan-sublist" class="vector-toc-list"> </ul> </li> <li id="toc-Toksisitas" class="vector-toc-list-item vector-toc-level-1 vector-toc-list-item-expanded"> <a class="vector-toc-link" href="#Toksisitas"> <div class="vector-toc-text"> <span class="vector-toc-numb">4</span> <span>Toksisitas</span> </div> </a> <ul id="toc-Toksisitas-sublist" class="vector-toc-list"> </ul> </li> <li id="toc-Lihat_pula" class="vector-toc-list-item vector-toc-level-1 vector-toc-list-item-expanded"> <a class="vector-toc-link" href="#Lihat_pula"> <div 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class="vector-dropdown-checkbox " aria-label="Gulingkan daftar isi" > <label id="vector-page-titlebar-toc-label" for="vector-page-titlebar-toc-checkbox" class="vector-dropdown-label cdx-button cdx-button--fake-button cdx-button--fake-button--enabled cdx-button--weight-quiet cdx-button--icon-only " aria-hidden="true" ><span class="vector-icon mw-ui-icon-listBullet mw-ui-icon-wikimedia-listBullet"></span> <span class="vector-dropdown-label-text">Gulingkan daftar isi</span> </label> <div class="vector-dropdown-content"> <div id="vector-page-titlebar-toc-unpinned-container" class="vector-unpinned-container"> </div> </div> </div> </nav> <h1 id="firstHeading" class="firstHeading mw-first-heading"><span class="mw-page-title-main">Tritioaseton</span></h1> <div id="p-lang-btn" class="vector-dropdown mw-portlet mw-portlet-lang" > <input type="checkbox" id="p-lang-btn-checkbox" role="button" aria-haspopup="true" data-event-name="ui.dropdown-p-lang-btn" class="vector-dropdown-checkbox 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title="Tritioacetona – Spanyol" lang="es" hreflang="es" data-title="Tritioacetona" data-language-autonym="Español" data-language-local-name="Spanyol" class="interlanguage-link-target"><span>Español</span></a></li><li class="interlanguage-link interwiki-ja mw-list-item"><a href="https://ja.wikipedia.org/wiki/%E3%83%88%E3%83%AA%E3%83%81%E3%82%AA%E3%82%A2%E3%82%BB%E3%83%88%E3%83%B3" title="トリチオアセトン – Jepang" lang="ja" hreflang="ja" data-title="トリチオアセトン" data-language-autonym="日本語" data-language-local-name="Jepang" class="interlanguage-link-target"><span>日本語</span></a></li><li class="interlanguage-link interwiki-uk mw-list-item"><a href="https://uk.wikipedia.org/wiki/%D0%A2%D1%80%D0%B8%D1%82%D1%96%D0%BE%D0%B0%D1%86%D0%B5%D1%82%D0%BE%D0%BD" title="Тритіоацетон – Ukraina" lang="uk" hreflang="uk" data-title="Тритіоацетон" data-language-autonym="Українська" data-language-local-name="Ukraina" class="interlanguage-link-target"><span>Українська</span></a></li><li class="interlanguage-link interwiki-zh mw-list-item"><a href="https://zh.wikipedia.org/wiki/%E4%B8%89%E7%A1%AB%E4%B8%99%E9%85%AE" title="三硫丙酮 – Tionghoa" lang="zh" hreflang="zh" data-title="三硫丙酮" data-language-autonym="中文" data-language-local-name="Tionghoa" 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/Q11321962#sitelinks-wikipedia" title="Sunting pranala interwiki" class="wbc-editpage">Sunting pranala</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="Ruang nama"> <div id="p-associated-pages" class="vector-menu vector-menu-tabs mw-portlet mw-portlet-associated-pages" > <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li id="ca-nstab-main" class="selected vector-tab-noicon mw-list-item"><a href="/wiki/Tritioaseton" title="Lihat halaman isi [c]" accesskey="c"><span>Halaman</span></a></li><li id="ca-talk" class="vector-tab-noicon mw-list-item"><a href="/wiki/Pembicaraan:Tritioaseton" rel="discussion" title="Pembicaraan halaman isi [t]" accesskey="t"><span>Pembicaraan</span></a></li> </ul> </div> </div> <div id="vector-variants-dropdown" class="vector-dropdown emptyPortlet" > <input type="checkbox" id="vector-variants-dropdown-checkbox" role="button" aria-haspopup="true" data-event-name="ui.dropdown-vector-variants-dropdown" class="vector-dropdown-checkbox " aria-label="Ubah varian bahasa" > <label id="vector-variants-dropdown-label" for="vector-variants-dropdown-checkbox" class="vector-dropdown-label cdx-button cdx-button--fake-button cdx-button--fake-button--enabled cdx-button--weight-quiet" aria-hidden="true" ><span class="vector-dropdown-label-text">Bahasa Indonesia</span> </label> <div class="vector-dropdown-content"> <div id="p-variants" class="vector-menu mw-portlet 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href="/w/index.php?title=Tritioaseton&action=history" title="Revisi sebelumnya dari halaman ini. [h]" accesskey="h"><span>Lihat riwayat</span></a></li> </ul> </div> </div> </nav> <nav class="vector-page-tools-landmark" aria-label="Peralatan halaman"> <div id="vector-page-tools-dropdown" class="vector-dropdown vector-page-tools-dropdown" > <input type="checkbox" id="vector-page-tools-dropdown-checkbox" role="button" aria-haspopup="true" data-event-name="ui.dropdown-vector-page-tools-dropdown" class="vector-dropdown-checkbox " aria-label="Perkakas" > <label id="vector-page-tools-dropdown-label" for="vector-page-tools-dropdown-checkbox" class="vector-dropdown-label cdx-button cdx-button--fake-button cdx-button--fake-button--enabled cdx-button--weight-quiet" aria-hidden="true" ><span class="vector-dropdown-label-text">Perkakas</span> </label> <div class="vector-dropdown-content"> <div id="vector-page-tools-unpinned-container" class="vector-unpinned-container"> <div id="vector-page-tools" class="vector-page-tools vector-pinnable-element"> <div class="vector-pinnable-header vector-page-tools-pinnable-header vector-pinnable-header-unpinned" data-feature-name="page-tools-pinned" data-pinnable-element-id="vector-page-tools" data-pinned-container-id="vector-page-tools-pinned-container" data-unpinned-container-id="vector-page-tools-unpinned-container" > <div class="vector-pinnable-header-label">Perkakas</div> <button class="vector-pinnable-header-toggle-button vector-pinnable-header-pin-button" data-event-name="pinnable-header.vector-page-tools.pin">pindah ke bilah sisi</button> <button class="vector-pinnable-header-toggle-button vector-pinnable-header-unpin-button" data-event-name="pinnable-header.vector-page-tools.unpin">sembunyikan</button> </div> <div id="p-cactions" class="vector-menu mw-portlet mw-portlet-cactions emptyPortlet vector-has-collapsible-items" title="Opsi lainnya" > <div class="vector-menu-heading"> Tindakan </div> <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li id="ca-more-view" class="selected vector-more-collapsible-item mw-list-item"><a href="/wiki/Tritioaseton"><span>Baca</span></a></li><li id="ca-more-ve-edit" class="vector-more-collapsible-item mw-list-item"><a href="/w/index.php?title=Tritioaseton&veaction=edit" title="Sunting halaman ini [v]" accesskey="v"><span>Sunting</span></a></li><li id="ca-more-edit" class="collapsible vector-more-collapsible-item mw-list-item"><a href="/w/index.php?title=Tritioaseton&action=edit" title="Sunting kode sumber halaman ini [e]" accesskey="e"><span>Sunting sumber</span></a></li><li id="ca-more-history" class="vector-more-collapsible-item mw-list-item"><a href="/w/index.php?title=Tritioaseton&action=history"><span>Lihat riwayat</span></a></li> </ul> </div> </div> <div id="p-tb" class="vector-menu mw-portlet mw-portlet-tb" > <div class="vector-menu-heading"> Umum </div> <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li id="t-whatlinkshere" class="mw-list-item"><a href="/wiki/Istimewa:Pranala_balik/Tritioaseton" title="Daftar semua halaman wiki yang memiliki pranala ke halaman ini [j]" accesskey="j"><span>Pranala balik</span></a></li><li id="t-recentchangeslinked" class="mw-list-item"><a href="/wiki/Istimewa:Perubahan_terkait/Tritioaseton" rel="nofollow" title="Perubahan terbaru halaman-halaman yang memiliki pranala ke halaman ini [k]" accesskey="k"><span>Perubahan terkait</span></a></li><li id="t-specialpages" class="mw-list-item"><a href="/wiki/Istimewa:Halaman_istimewa" title="Daftar semua halaman istimewa [q]" accesskey="q"><span>Halaman istimewa</span></a></li><li id="t-permalink" class="mw-list-item"><a href="/w/index.php?title=Tritioaseton&oldid=23182885" title="Pranala permanen untuk revisi halaman ini"><span>Pranala permanen</span></a></li><li id="t-info" class="mw-list-item"><a href="/w/index.php?title=Tritioaseton&action=info" title="Informasi lanjut tentang halaman ini"><span>Informasi halaman</span></a></li><li id="t-cite" class="mw-list-item"><a href="/w/index.php?title=Istimewa:Kutip&page=Tritioaseton&id=23182885&wpFormIdentifier=titleform" title="Informasi tentang bagaimana mengutip halaman ini"><span>Kutip halaman ini</span></a></li><li id="t-urlshortener" class="mw-list-item"><a href="/w/index.php?title=Istimewa:UrlShortener&url=https%3A%2F%2Fid.wikipedia.org%2Fwiki%2FTritioaseton"><span>Lihat URL pendek</span></a></li><li id="t-urlshortener-qrcode" class="mw-list-item"><a href="/w/index.php?title=Istimewa:QrCode&url=https%3A%2F%2Fid.wikipedia.org%2Fwiki%2FTritioaseton"><span>Unduh kode QR</span></a></li> </ul> </div> </div> <div id="p-coll-print_export" class="vector-menu mw-portlet mw-portlet-coll-print_export" > <div class="vector-menu-heading"> Cetak/ekspor </div> <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li id="coll-create_a_book" class="mw-list-item"><a href="/w/index.php?title=Istimewa:Buku&bookcmd=book_creator&referer=Tritioaseton"><span>Buat buku</span></a></li><li id="coll-download-as-rl" class="mw-list-item"><a href="/w/index.php?title=Istimewa:DownloadAsPdf&page=Tritioaseton&action=show-download-screen"><span>Unduh versi PDF</span></a></li><li id="t-print" class="mw-list-item"><a href="/w/index.php?title=Tritioaseton&printable=yes" title="Versi cetak halaman ini [p]" accesskey="p"><span>Versi cetak</span></a></li> </ul> </div> </div> <div id="p-wikibase-otherprojects" class="vector-menu mw-portlet mw-portlet-wikibase-otherprojects" > <div class="vector-menu-heading"> Dalam proyek lain </div> <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li class="wb-otherproject-link wb-otherproject-commons mw-list-item"><a href="https://commons.wikimedia.org/wiki/Category:Hexamethyl-1,3,5-trithiane" hreflang="en"><span>Wikimedia Commons</span></a></li><li id="t-wikibase" class="wb-otherproject-link wb-otherproject-wikibase-dataitem mw-list-item"><a href="https://www.wikidata.org/wiki/Special:EntityPage/Q11321962" title="Pranala untuk menghubungkan butir pada ruang penyimpanan data [g]" accesskey="g"><span>Butir di Wikidata</span></a></li> </ul> </div> </div> </div> </div> </div> </div> </nav> </div> </div> </div> <div class="vector-column-end"> <div class="vector-sticky-pinned-container"> <nav class="vector-page-tools-landmark" aria-label="Peralatan halaman"> <div id="vector-page-tools-pinned-container" class="vector-pinned-container"> </div> </nav> <nav class="vector-appearance-landmark" aria-label="Tampilan"> <div id="vector-appearance-pinned-container" class="vector-pinned-container"> <div id="vector-appearance" class="vector-appearance vector-pinnable-element"> <div class="vector-pinnable-header vector-appearance-pinnable-header vector-pinnable-header-pinned" data-feature-name="appearance-pinned" data-pinnable-element-id="vector-appearance" data-pinned-container-id="vector-appearance-pinned-container" data-unpinned-container-id="vector-appearance-unpinned-container" > <div class="vector-pinnable-header-label">Tampilan</div> <button class="vector-pinnable-header-toggle-button vector-pinnable-header-pin-button" data-event-name="pinnable-header.vector-appearance.pin">pindah ke bilah sisi</button> <button class="vector-pinnable-header-toggle-button vector-pinnable-header-unpin-button" data-event-name="pinnable-header.vector-appearance.unpin">sembunyikan</button> </div> </div> </div> </nav> </div> </div> <div id="bodyContent" class="vector-body" aria-labelledby="firstHeading" data-mw-ve-target-container> <div class="vector-body-before-content"> <div class="mw-indicators"> </div> <div id="siteSub" class="noprint">Dari Wikipedia bahasa Indonesia, ensiklopedia bebas</div> </div> <div id="contentSub"><div id="mw-content-subtitle"></div></div> <div id="mw-content-text" class="mw-body-content"><div class="mw-content-ltr mw-parser-output" lang="id" dir="ltr"><table class="infobox bordered" style="border-collapse:collapse; width:22em; text-align:left; ;"> <caption style="text-align:center;">Tritioaseton </caption> <tbody><tr> <td colspan="2" style="text-align:center; padding:2px;"><span typeof="mw:File"><a href="/wiki/Berkas:2,2,4,4,6,6-Hexamethyl-1,3,5-trithiane_flat.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/d/d1/2%2C2%2C4%2C4%2C6%2C6-Hexamethyl-1%2C3%2C5-trithiane_flat.png/220px-2%2C2%2C4%2C4%2C6%2C6-Hexamethyl-1%2C3%2C5-trithiane_flat.png" decoding="async" width="220" height="194" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/d/d1/2%2C2%2C4%2C4%2C6%2C6-Hexamethyl-1%2C3%2C5-trithiane_flat.png/330px-2%2C2%2C4%2C4%2C6%2C6-Hexamethyl-1%2C3%2C5-trithiane_flat.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/d/d1/2%2C2%2C4%2C4%2C6%2C6-Hexamethyl-1%2C3%2C5-trithiane_flat.png/440px-2%2C2%2C4%2C4%2C6%2C6-Hexamethyl-1%2C3%2C5-trithiane_flat.png 2x" data-file-width="578" data-file-height="510" /></a></span> </td></tr> <tr> <th colspan="2" style="background: #f8eaba; text-align: center;">Nama </th></tr> <tr> <td colspan="2" style="text-align:left;"><a href="/wiki/Tata_nama_senyawa_kimia" title="Tata nama senyawa kimia">Nama IUPAC (preferensi)</a> <div style="max-width:22em; word-wrap:break-word; padding-left:1.7em;"><div style="display:inline-block; padding:0.1em 0;line-height:1.2em;">Heksametil-1,3,5-tritiana</div></div> </td></tr> <tr> <td colspan="2" style="text-align:left;">Nama lain <div style="max-width:22em; word-wrap:break-word; padding-left:1.7em;">Tritioaseton<sup id="cite_ref-nih2020_1-0" class="reference"><a href="#cite_note-nih2020-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup></div> </td></tr> <tr> <th colspan="2" style="background: #f8eaba; text-align: center;">Penanda </th></tr> <tr> <td><div style="display:inline-block; padding:0.1em 0;line-height:1.2em;"><a href="/wiki/Nomor_CAS" title="Nomor CAS">Nomor CAS</a></div> </td> <td><style data-mw-deduplicate="TemplateStyles:r23782729">.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="www.commonchemistry.org"><a rel="nofollow" class="external text" href="http://www.commonchemistry.org/ChemicalDetail.aspx?ref=828-26-2">828-26-2</a></span></li></ul></div> </td></tr> <tr> <td><div style="display:inline-block; padding:0.1em 0;line-height:1.2em;">Model 3D (<a href="/wiki/Jmol" title="Jmol">JSmol</a>)</div> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r23782729"><div class="plainlist"><ul><li><span title="chemapps.stolaf.edu (model interaktif 3D)"><a rel="nofollow" class="external text" href="https://chemapps.stolaf.edu/jmol/jmol.php?model=C1%28SC%28SC%28S1%29%28C%29C%29%28C%29C%29%28C%29C">Gambar interaktif</a></span></li></ul></div> </td></tr> <tr> <td>3DMet </td> <td><span title="www.3dmet.dna.affrc.go.jp"><a rel="nofollow" class="external text" href="http://www.3dmet.dna.affrc.go.jp/cgi/show_data.php?acc={{{3DMet}}}">{{{3DMet}}}</a></span> </td></tr> <tr> <td><a href="/wiki/Basis_data_Beilstein" title="Basis data Beilstein">Referensi Beilstein</a> </td> <td>5-19-09-00119 </td></tr> <tr> <td><a href="/wiki/ChEMBL" title="ChEMBL">ChEMBL</a> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r23782729"><div class="plainlist"><ul><li><span title="www.ebi.ac.uk"><a rel="nofollow" class="external text" href="https://www.ebi.ac.uk/chembldb/index.php/compound/inspect/ChEMBL3187896">ChEMBL3187896</a></span></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:r23782729"><div class="plainlist"><ul><li><span title="www.chemspider.com"><a rel="nofollow" class="external text" href="http://www.chemspider.com/Chemical-Structure.12678.html">12678</a></span></li></ul></div> </td></tr> <tr> <td><a href="/wiki/Nomor_EC" title="Nomor EC"><span title="Nomor Masyarakat Eropa (penanda kimia)">Nomor EC</span></a> </td> <td> </td></tr> <tr> <td><div style="display:inline-block; padding:0.1em 0;line-height:1.2em;"><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:r23782729"><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/13233">13233</a></span></li></ul></div> </td></tr> <tr> <td><a href="/wiki/RTECS" title="RTECS">Nomor RTECS</a> </td> <td>{{{value}}} </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:r23782729"><div class="plainlist"><ul><li><span title="fdasis.nlm.nih.gov"><a rel="nofollow" class="external text" href="https://fdasis.nlm.nih.gov/srs/srsdirect.jsp?regno=L0ME5B2ZWY">L0ME5B2ZWY</a></span></li></ul></div> </td></tr> <tr> <td><div style="display:inline-block; padding:0.1em 0;line-height:1.2em;"><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:r23782729"><div class="plainlist"><ul><li><span title="comptox.epa.gov"><a rel="nofollow" class="external text" href="https://comptox.epa.gov/dashboard/DTXSID2047723">DTXSID2047723</a></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:11px; line-height:120%;">InChI=1S/C9H18S3/c1-7(2)10-8(3,4)12-9(5,6)11-7/h1-6H3</div><div style="word-wrap:break-word; text-indent:-1.5em; font-size:11px; line-height:120%;">Key: NBNWHQAWKFYFKI-UHFFFAOYSA-N</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/SMILES" title="SMILES">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:11px; line-height:120%;">C1(SC(SC(S1)(C)C)(C)C)(C)C</div></li></ul> </div> </td></tr> <tr> <th colspan="2" style="background: #f8eaba; text-align: center;">Sifat </th></tr> <tr> <td><div style="display:inline-block; padding:0.1em 0;line-height:1.2em;"><a href="/wiki/Rumus_kimia" title="Rumus kimia">Rumus kimia</a></div> </td> <td><span title="Carbon">C</span><sub>9</sub><span title="Hydrogen">H</span><sub>18</sub><span title="Sulfur">S</span><sub>3</sub> </td></tr> <tr> <td><a href="/wiki/Massa_molar" title="Massa molar">Massa molar</a> </td> <td>222,42 g·mol<sup>−1</sup>   </td></tr> <tr> <td><a href="/wiki/Massa_jenis" title="Massa jenis">Densitas</a> </td> <td>1,0660 hingga 1,0700 g/mL<sup id="cite_ref-tcicat_2-0" class="reference"><a href="#cite_note-tcicat-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup> </td></tr> <tr> <td><a href="/wiki/Titik_lebur" title="Titik lebur">Titik lebur</a> </td> <td>21,8°C<sup id="cite_ref-pubchem_3-0" class="reference"><a href="#cite_note-pubchem-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup>   </td></tr> <tr> <td><a href="/wiki/Titik_didih" title="Titik didih">Titik didih</a> </td> <td>107°C/10mmHg<sup id="cite_ref-tcicat_2-1" class="reference"><a href="#cite_note-tcicat-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup>   </td></tr> <tr> <td><a href="/wiki/Indeks_bias" title="Indeks bias">Indeks bias</a> (<i>n</i><sub>D</sub>) </td> <td>1,5390 hingga 1,5430<sup id="cite_ref-tcicat_2-2" class="reference"><a href="#cite_note-tcicat-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup> </td></tr> <tr> <th colspan="2" style="background: #f8eaba; text-align: center;">Bahaya </th></tr> <tr> <td><a href="/wiki/Piktogram_bahaya_GHS" title="Piktogram bahaya GHS">Piktogram GHS</a> </td> <td><span typeof="mw:File"><a href="/wiki/Berkas:GHS-pictogram-exclam.svg" class="mw-file-description" title="GHS07: Tanda Seru"><img alt="GHS07: Tanda Seru" src="//upload.wikimedia.org/wikipedia/commons/thumb/c/c3/GHS-pictogram-exclam.svg/50px-GHS-pictogram-exclam.svg.png" decoding="async" width="50" height="50" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/c3/GHS-pictogram-exclam.svg/75px-GHS-pictogram-exclam.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/c3/GHS-pictogram-exclam.svg/100px-GHS-pictogram-exclam.svg.png 2x" data-file-width="512" data-file-height="512" /></a></span> </td></tr> <tr> <td><a href="/wiki/Sistem_Harmonisasi_Global_Klasifikasi_dan_Label_pada_Bahan_Kimia" title="Sistem Harmonisasi Global Klasifikasi dan Label pada Bahan Kimia">Keterangan bahaya GHS</a> </td> <td>{{{value}}} </td></tr> <tr> <td><div style="display:inline-block; padding:0.1em 0;line-height:1.2em;"><a href="/wiki/Pernyataan_bahaya_GHS" title="Pernyataan bahaya GHS">Pernyataan bahaya GHS</a></div> </td> <td><abbr class="abbr" title="Causes skin irritation">H315</abbr>, <abbr class="abbr" title="Causes serious eye irritation">H319</abbr>, <abbr class="abbr" title="May cause respiratory irritation">H335</abbr> </td></tr> <tr> <td><div style="display:inline-block; padding:0.1em 0;line-height:1.2em;"><a href="/wiki/Langkah_perlindungan_GHS" title="Langkah perlindungan GHS">Langkah perlindungan GHS</a></div> </td> <td><abbr class="abbr" title="Avoid breathing dust/fume/gas/mist/vapours/spray">P261</abbr>, <abbr class="abbr" title="Wash … thoroughly after handling">P264</abbr>, <abbr class="abbr" title="Use only outdoors or in a well-ventilated area">P271</abbr>, <abbr class="abbr" title="Wear protective gloves/protective clothing/eye protection/face protection">P280</abbr>, <abbr class="abbr" title="IF ON SKIN: Wash with soap and water">P302+352</abbr>, <abbr class="abbr" title="IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing">P304+340</abbr>, <abbr class="abbr" title="IF IN EYES: Rinse continuously with water for several minutes. Remove contact lenses if present and easy to do – continue rinsing">P305+351+338</abbr>, <abbr class="abbr" title="Call a POISON CENTER or doctor/physician if you feel unwell">P312</abbr>, <abbr class="abbr" title="Specific treatment (see … on this label)">P321</abbr>, <abbr class="abbr" title="If skin irritation occurs: Get medical advice/attention">P332+313</abbr>, <abbr class="abbr" title="Get medical advice/attention">P337+313</abbr>, <abbr class="abbr" title="Take off contaminated clothing and wash before reuse">P362</abbr>, <abbr class="abbr" title="Store in a well ventilated place. Keep container tightly closed">P403+233</abbr>, <abbr class="abbr" title="Store locked up">P405</abbr>, <abbr class="abbr" title="Dispose of contents/container to …">P501</abbr> </td></tr> <tr> <td colspan="2" style="text-align:left; background:#f8eaba;"><div style="margin:0 auto; text-align:left;"><div style="display:inline-block; padding:0.1em 0;line-height:1.2em;">Kecuali dinyatakan lain, data di atas berlaku pada <a href="/wiki/Temperatur_dan_tekanan_standar" title="Temperatur dan tekanan standar">suhu dan tekanan standar</a> (25 °C [77 °F], 100 kPa).</div></div> </td></tr> <tr style="background:#f8eaba; border-top:2px solid transparent;"> <td colspan="2" style="text-align:center;"><a href="https://en.wikipedia.org/wiki/Wikipedia:Chemical_infobox#References" class="extiw" title="en:Wikipedia:Chemical infobox">Referensi</a> </td></tr> <tr style="background:#f8eaba;"> <td style="width:40%; max-height:1px; border-top:2px solid transparent; border-right:1px solid transparent;"> </td> <td style="width:60%; max-height:1px; border-top:2px solid transparent; border-left:1px solid transparent;"> </td></tr> </tbody></table> <p><b>Tritioaseton</b> (<b>2,2,4,4,6,6-heksametil-1,3,5-tritiana</b>) sebuah <a href="/wiki/Senyawa_organik" title="Senyawa organik">bahan kimia organik</a> dengan <a href="/wiki/Rumus_kimia" title="Rumus kimia">rumus</a> <span class="chemf nowrap">C<sub>9</sub>H<sub>18</sub>S<sub>3</sub></span>. Struktur <a href="/wiki/Ikatan_kovalen" title="Ikatan kovalen">kovalennya</a> adalah <span class="chemf nowrap">[–C(CH<sub>3</sub>)<sub>2</sub>–S–]<sub>3</sub></span>, yaitu cincin beranggota enam dari atom <a href="/wiki/Karbon" title="Karbon">karbon</a> dan <a href="/wiki/Belerang" title="Belerang">belerang</a> yang berselang-seling, dengan dua <a href="/wiki/Gugus_metil" title="Gugus metil">gugus metil</a> yang terikat pada setiap karbon.<sup id="cite_ref-tcicat_2-3" class="reference"><a href="#cite_note-tcicat-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-bres2009_4-0" class="reference"><a href="#cite_note-bres2009-4"><span class="cite-bracket">[</span>4<span class="cite-bracket">]</span></a></sup> Ia dapat dilihat sebagai turunan dari <a href="/w/index.php?title=1,3,5-Tritiana&action=edit&redlink=1" class="new" title="1,3,5-Tritiana (halaman belum tersedia)">1,3,5-tritiana</a>, dengan <a href="/wiki/Substituen" title="Substituen">substituen</a> gugus metil untuk semua atom hidrogen dalam struktur induknya. </p><p>Senyawa tritioaseton adalah trimer <a href="/wiki/Senyawa_siklik" title="Senyawa siklik">siklik</a> stabil dari <a href="/wiki/Tioaseton" title="Tioaseton">tioaseton</a> (propana-2-tiona), yang dengan sendirinya merupakan senyawa yang tak stabil.<sup id="cite_ref-lips1970_5-0" class="reference"><a href="#cite_note-lips1970-5"><span class="cite-bracket">[</span>5<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-shar1979_6-0" class="reference"><a href="#cite_note-shar1979-6"><span class="cite-bracket">[</span>6<span class="cite-bracket">]</span></a></sup> Sebaliknya, senyawa <a href="/w/index.php?title=1,3,5-trioksana&action=edit&redlink=1" class="new" title="1,3,5-trioksana (halaman belum tersedia)">trioksana</a> analog, <a href="/w/index.php?title=2,2,4,4,6,6-heksametil-1,3,5-trioksana&action=edit&redlink=1" class="new" title="2,2,4,4,6,6-heksametil-1,3,5-trioksana (halaman belum tersedia)">2,2,4,4,6,6-heksametil-1,3,5-trioksana</a> (<a href="/w/index.php?title=Triaseton&action=edit&redlink=1" class="new" title="Triaseton (halaman belum tersedia)">triaseton</a>), dengan atom <a href="/wiki/Oksigen" title="Oksigen">oksigen</a> menggantikan atom belerang, tampaknya tidak stabil, sedangkan <a href="/wiki/Aseton" title="Aseton">aseton</a> monomer yang sesuai (2-propanon) stabil. </p> <meta property="mw:PageProp/toc" /> <div class="mw-heading mw-heading2"><h2 id="Sintesis">Sintesis</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Tritioaseton&veaction=edit&section=1" title="Sunting bagian: Sintesis" class="mw-editsection-visualeditor"><span>sunting</span></a><span class="mw-editsection-divider"> | </span><a href="/w/index.php?title=Tritioaseton&action=edit&section=1" title="Sunting kode sumber bagian: Sintesis"><span>sunting sumber</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>Tritioaseton pertama kali dibuat pada tahun 1889 oleh Baumann dan Fromm, melalui reaksi <a href="/wiki/Hidrogen_sulfida" title="Hidrogen sulfida">hidrogen sulfida</a> dengan aseton.<sup id="cite_ref-shar1979_6-1" class="reference"><a href="#cite_note-shar1979-6"><span class="cite-bracket">[</span>6<span class="cite-bracket">]</span></a></sup> Dengan adanya katalis <span class="chemf nowrap">ZnCl<sub>2</sub></span> yang diasamkan pada suhu 25 °C, diperoleh produk yang terdiri dari 60–70% tritioaseton, 30–40% 2,2-propanaditiol, dan sejumlah kecil dua pengotor isomer, <a href="/w/index.php?title=3,3,5,5,6,6-heksametil_1,2,4-tritiana&action=edit&redlink=1" class="new" title="3,3,5,5,6,6-heksametil 1,2,4-tritiana (halaman belum tersedia)">3,3,5,5,6,6-heksametil 1,2,4-tritiana</a> dan <a href="/w/index.php?title=4-merkapto-2,2,4,6,6-pentametil-1,3-ditiana&action=edit&redlink=1" class="new" title="4-merkapto-2,2,4,6,6-pentametil-1,3-ditiana (halaman belum tersedia)">4-merkapto-2,2,4,6,6-pentametil-1,3-ditiana</a>.<sup id="cite_ref-shar1979_6-2" class="reference"><a href="#cite_note-shar1979-6"><span class="cite-bracket">[</span>6<span class="cite-bracket">]</span></a></sup> Produk tersebut juga dapat diperoleh dengan <a href="/wiki/Pirolisis" title="Pirolisis">pirolisis</a> <a href="/w/index.php?title=Alil_isopropil_sulfida&action=edit&redlink=1" class="new" title="Alil isopropil sulfida (halaman belum tersedia)">alil isopropil sulfida</a>.<sup id="cite_ref-bail1965_7-0" class="reference"><a href="#cite_note-bail1965-7"><span class="cite-bracket">[</span>7<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-bohme1942_8-0" class="reference"><a href="#cite_note-bohme1942-8"><span class="cite-bracket">[</span>8<span class="cite-bracket">]</span></a></sup> </p> <div class="mw-heading mw-heading2"><h2 id="Reaksi">Reaksi</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Tritioaseton&veaction=edit&section=2" title="Sunting bagian: Reaksi" class="mw-editsection-visualeditor"><span>sunting</span></a><span class="mw-editsection-divider"> | </span><a href="/w/index.php?title=Tritioaseton&action=edit&section=2" title="Sunting kode sumber bagian: Reaksi"><span>sunting sumber</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>Pirolisis tritioaseton pada suhu 500–650 °C dan 5–20 <a href="/wiki/Milimeter_air_raksa" title="Milimeter air raksa">mmHg</a> menghasilkan tioaseton, yang dapat dikumpulkan dengan perangkap dingin pada suhu −78 °C. </p> <figure class="mw-halign-center" typeof="mw:File"><a href="/wiki/Berkas:ThioacetoneTrimer.svg" class="mw-file-description" title="Pirolisis/polimerisasi antara tritioaseton (kiri) dan tioaseton (kanan)."><img alt="Pirolisis/polimerisasi antara tritioaseton (kiri) dan tioaseton (kanan)." src="//upload.wikimedia.org/wikipedia/commons/thumb/f/f5/ThioacetoneTrimer.svg/300px-ThioacetoneTrimer.svg.png" decoding="async" width="300" height="89" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/f5/ThioacetoneTrimer.svg/450px-ThioacetoneTrimer.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/f5/ThioacetoneTrimer.svg/600px-ThioacetoneTrimer.svg.png 2x" data-file-width="2150" data-file-height="636" /></a><figcaption>Pirolisis/polimerisasi antara tritioaseton (kiri) dan tioaseton (kanan).</figcaption></figure> <div class="mw-heading mw-heading2"><h2 id="Kegunaan">Kegunaan</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Tritioaseton&veaction=edit&section=3" title="Sunting bagian: Kegunaan" class="mw-editsection-visualeditor"><span>sunting</span></a><span class="mw-editsection-divider"> | </span><a href="/w/index.php?title=Tritioaseton&action=edit&section=3" title="Sunting kode sumber bagian: Kegunaan"><span>sunting sumber</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>Tritioaseton ditemukan pada beberapa <a href="/wiki/Perisa" title="Perisa">agen penyedap</a>. Nomor <a href="/w/index.php?title=Asosiasi_Produsen_Rasa_dan_Ekstrak&action=edit&redlink=1" class="new" title="Asosiasi Produsen Rasa dan Ekstrak (halaman belum tersedia)">FEMA</a>-nya adalah 3475.<sup id="cite_ref-mora1980_9-0" class="reference"><a href="#cite_note-mora1980-9"><span class="cite-bracket">[</span>9<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-who_10-0" class="reference"><a href="#cite_note-who-10"><span class="cite-bracket">[</span>10<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-ohlo1979_11-0" class="reference"><a href="#cite_note-ohlo1979-11"><span class="cite-bracket">[</span>11<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-euro2012_12-0" class="reference"><a href="#cite_note-euro2012-12"><span class="cite-bracket">[</span>12<span class="cite-bracket">]</span></a></sup> </p> <div class="mw-heading mw-heading2"><h2 id="Toksisitas">Toksisitas</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Tritioaseton&veaction=edit&section=4" title="Sunting bagian: Toksisitas" class="mw-editsection-visualeditor"><span>sunting</span></a><span class="mw-editsection-divider"> | </span><a href="/w/index.php?title=Tritioaseton&action=edit&section=4" title="Sunting kode sumber bagian: Toksisitas"><span>sunting sumber</span></a><span class="mw-editsection-bracket">]</span></span></div> <p><a href="/wiki/Dosis_letal" title="Dosis letal">LD<sub>50</sub></a> (oral) pada tikus adalah 2,4 g/kg.<sup id="cite_ref-pubchem_3-1" class="reference"><a href="#cite_note-pubchem-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-mora1980_9-1" class="reference"><a href="#cite_note-mora1980-9"><span class="cite-bracket">[</span>9<span class="cite-bracket">]</span></a></sup> </p> <div class="mw-heading mw-heading2"><h2 id="Lihat_pula">Lihat pula</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Tritioaseton&veaction=edit&section=5" title="Sunting bagian: Lihat pula" class="mw-editsection-visualeditor"><span>sunting</span></a><span class="mw-editsection-divider"> | </span><a href="/w/index.php?title=Tritioaseton&action=edit&section=5" title="Sunting kode sumber bagian: Lihat pula"><span>sunting sumber</span></a><span class="mw-editsection-bracket">]</span></span></div> <ul><li><a href="/w/index.php?title=2,4,6-trimetil-1,3,5-tritiana&action=edit&redlink=1" class="new" title="2,4,6-trimetil-1,3,5-tritiana (halaman belum tersedia)">2,4,6-trimetil-1,3,5-tritiana</a></li> <li><a href="/w/index.php?title=Heksametilsiklotrisiloksana&action=edit&redlink=1" class="new" title="Heksametilsiklotrisiloksana (halaman belum tersedia)">Heksametilsiklotrisiloksana</a>, analog dengan cincin <a href="/wiki/Silikon" title="Silikon">silikon</a>−oksigen, bukan cincin karbon−belerang.</li> <li><a href="/w/index.php?title=Heksametilsiklotrisilazana&action=edit&redlink=1" class="new" title="Heksametilsiklotrisilazana (halaman belum tersedia)">Heksametilsiklotrisilazana</a>, dengan cincin silikon−<a href="/wiki/Nitrogen" title="Nitrogen">nitrogen</a>.<sup id="cite_ref-brew1948_13-0" class="reference"><a href="#cite_note-brew1948-13"><span class="cite-bracket">[</span>13<span class="cite-bracket">]</span></a></sup></li> <li><a href="/w/index.php?title=2,2,4,4,6,6-heksametil-1,3,5-triselena-2,4,6-tristanasikloheksana&action=edit&redlink=1" class="new" title="2,2,4,4,6,6-heksametil-1,3,5-triselena-2,4,6-tristanasikloheksana (halaman belum tersedia)">2,2,4,4,6,6-heksametil-1,3,5-triselena-2,4,6-tristanasikloheksana</a>, dengan cincin <a href="/wiki/Timah" title="Timah">timah</a>−<a href="/wiki/Selenium" title="Selenium">selenium</a>.<sup id="cite_ref-mikh2008_14-0" class="reference"><a href="#cite_note-mikh2008-14"><span class="cite-bracket">[</span>14<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-draeg1978_15-0" class="reference"><a href="#cite_note-draeg1978-15"><span class="cite-bracket">[</span>15<span class="cite-bracket">]</span></a></sup></li></ul> <div class="mw-heading mw-heading2"><h2 id="Referensi">Referensi</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Tritioaseton&veaction=edit&section=6" title="Sunting bagian: Referensi" class="mw-editsection-visualeditor"><span>sunting</span></a><span class="mw-editsection-divider"> | </span><a href="/w/index.php?title=Tritioaseton&action=edit&section=6" title="Sunting kode sumber bagian: Referensi"><span>sunting sumber</span></a><span class="mw-editsection-bracket">]</span></span></div> <ol class="references"> <li id="cite_note-nih2020-1"><span class="mw-cite-backlink"><b><a href="#cite_ref-nih2020_1-0">^</a></b></span> <span class="reference-text">"<a rel="nofollow" class="external text" href="https://chem.nlm.nih.gov/chemidplus/rn/828-26-2">Trithioacetone</a>". Lembar data kimia daring, diakses tanggal 22 Maret 2023.</span> </li> <li id="cite_note-tcicat-2"><span class="mw-cite-backlink">^ <a href="#cite_ref-tcicat_2-0"><sup><i><b>a</b></i></sup></a> <a href="#cite_ref-tcicat_2-1"><sup><i><b>b</b></i></sup></a> <a href="#cite_ref-tcicat_2-2"><sup><i><b>c</b></i></sup></a> <a href="#cite_ref-tcicat_2-3"><sup><i><b>d</b></i></sup></a></span> <span class="reference-text">TCI America (2020): "<a rel="nofollow" class="external text" href="https://www.tcichemicals.com/eshop/en/us/commodity/H1278/">Product H1278: 2,2,4,4,6,6-Hexamethyl-1,3,5-trithiane</a>". Halaman katalog daring, diakses tanggal 22 Maret 2023.</span> </li> <li id="cite_note-pubchem-3"><span class="mw-cite-backlink">^ <a href="#cite_ref-pubchem_3-0"><sup><i><b>a</b></i></sup></a> <a href="#cite_ref-pubchem_3-1"><sup><i><b>b</b></i></sup></a></span> <span class="reference-text">NCBI PubChem (2010): "<a rel="nofollow" class="external text" href="https://pubchem.ncbi.nlm.nih.gov/compound/13233">2,2,4,4,6,6-Hexamethyl-1,3,5-trithiane</a>". Lembar data kimia daring, diakses tanggal 22 Maret 2023.</span> </li> <li id="cite_note-bres2009-4"><span class="mw-cite-backlink"><b><a href="#cite_ref-bres2009_4-0">^</a></b></span> <span class="reference-text">David S. Breslow, Herman S. Award (2009): <i>Multi-Sulfur and Sulfur and Oxygen Five- and Six-Membered Heterocycles</i>, Bagian 2; halaman 712. Volume 68 dari <i>Chemistry of Heterocyclic Compounds</i>. <a href="/wiki/International_Standard_Book_Number" class="mw-redirect" title="International Standard Book Number">ISBN</a> <a href="/wiki/Istimewa:Sumber_buku/9780470188330" title="Istimewa:Sumber buku/9780470188330">9780470188330</a></span> </li> <li id="cite_note-lips1970-5"><span class="mw-cite-backlink"><b><a href="#cite_ref-lips1970_5-0">^</a></b></span> <span class="reference-text">R. D. Lipscomb dan W. H. Sharkey (1970): "Characterization and polymerization of thioacetone". <i>Journal of Polymer Science – Part A: Polymer Chemistry</i>, volume 8, terbitan 8, halaman 2187–2196. <a href="/wiki/Pengenal_objek_digital" title="Pengenal objek digital">DOI</a>:<a rel="nofollow" class="external text" href="https://dx.doi.org/10.1002/pol.1970.150080826">10.1002/pol.1970.150080826</a></span> </li> <li id="cite_note-shar1979-6"><span class="mw-cite-backlink">^ <a href="#cite_ref-shar1979_6-0"><sup><i><b>a</b></i></sup></a> <a href="#cite_ref-shar1979_6-1"><sup><i><b>b</b></i></sup></a> <a href="#cite_ref-shar1979_6-2"><sup><i><b>c</b></i></sup></a></span> <span class="reference-text">William H. Sharkey (1979): "Polymerization through the carbon-sulfur double bond". <i>Polymerization</i>, seri <i>Advances in Polymer Science</i>, volume 17, halaman 73–103. <a href="/wiki/Pengenal_objek_digital" title="Pengenal objek digital">DOI</a>:<a rel="nofollow" class="external text" href="https://dx.doi.org/10.1007/3-540-07111-3_2">10.1007/3-540-07111-3_2</a></span> </li> <li id="cite_note-bail1965-7"><span class="mw-cite-backlink"><b><a href="#cite_ref-bail1965_7-0">^</a></b></span> <span class="reference-text">William J. Bailey dan Hilda Chu (1965): "Synthesis of polythioacetone". <i>ACS Polymer Preprints</i>, volume 6, halaman 145–155</span> </li> <li id="cite_note-bohme1942-8"><span class="mw-cite-backlink"><b><a href="#cite_ref-bohme1942_8-0">^</a></b></span> <span class="reference-text">Horst Bohme, Hans Pfeifer, dan Erich Schneider (1942): "Dimeric thioketones". <i>Berichte der Deutschen Chemischen Gesellschaft</i>, volume 75B, terbitan 7, halaman 900–909. <a href="/wiki/Pengenal_objek_digital" title="Pengenal objek digital">DOI</a>:<a rel="nofollow" class="external text" href="https://dx.doi.org/10.1002/cber.19420750722">10.1002/cber.19420750722</a> Catatan: Laporan awal ini salah mengira trimer sebagai monomer.</span> </li> <li id="cite_note-mora1980-9"><span class="mw-cite-backlink">^ <a href="#cite_ref-mora1980_9-0"><sup><i><b>a</b></i></sup></a> <a href="#cite_ref-mora1980_9-1"><sup><i><b>b</b></i></sup></a></span> <span class="reference-text">E. J. Moran, O. D. Easterday, dan B. L. Oser (1980): "Acute oral toxicity of selected flavor chemicals". <i>Drug and Chemical Toxicology</i>, volume 3, terbitan 3, halaman 249–258.<a href="/wiki/PMID" class="mw-redirect" title="PMID">PMID</a> <a rel="nofollow" class="external text" href="//pubmed.ncbi.nlm.nih.gov/7449655">7449655</a> <a href="/wiki/Pengenal_objek_digital" title="Pengenal objek digital">DOI</a>:<a rel="nofollow" class="external text" href="https://dx.doi.org/10.3109/01480548009002221">10.3109/01480548009002221</a></span> </li> <li id="cite_note-who-10"><span class="mw-cite-backlink"><b><a href="#cite_ref-who_10-0">^</a></b></span> <span class="reference-text">World Health Organization (1999): "<a rel="nofollow" class="external text" href="https://who.int/food-additives-contaminants-jecfa-database/chemical.aspx?chemID=2916">Trithioacetone</a><sup class="noprint Inline-Template"><span style="white-space: nowrap;">[<i><a href="/wiki/Wikipedia:Pranala_mati" title="Wikipedia:Pranala mati"><span title=" pranala nonaktif sejak Desember 2021">pranala nonaktif</span></a></i>]</span></sup>". Lembar data daring di <i>Evaluation of the Joint FAO/WHO Expert Committee on Food Additives (JECFA)</i>. Diakses tanggal 22 Maret 2023.</span> </li> <li id="cite_note-ohlo1979-11"><span class="mw-cite-backlink"><b><a href="#cite_ref-ohlo1979_11-0">^</a></b></span> <span class="reference-text">G. Ohloff dan I. Flament (1979): "The Role of Heteroatomic Substances in the Aroma Compounds of Foodstuffs". Dalam <i>Fortschritte der Chemie Organischer Naturstoffe</i> (<i>Kemajuan dalam Kimia Produk Alami Organik</i>), volume 36, halaman 231–283. <a href="/wiki/Pengenal_objek_digital" title="Pengenal objek digital">DOI</a>:<a rel="nofollow" class="external text" href="https://dx.doi.org/10.1007/978-3-7091-3265-4_2">10.1007/978-3-7091-3265-4_2</a></span> </li> <li id="cite_note-euro2012-12"><span class="mw-cite-backlink"><b><a href="#cite_ref-euro2012_12-0">^</a></b></span> <span class="reference-text">EUR-Lex (2012): "<a rel="nofollow" class="external text" href="https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:32012R0872">Table entry 15.009: Trithioacetone</a>". Dalam <i>EU Regulation No. 872/2012</i>, Dokumen 32012R0872, <i>Official Journal of the EU – Series L</i>, volume 267, halaman 1–161.</span> </li> <li id="cite_note-brew1948-13"><span class="mw-cite-backlink"><b><a href="#cite_ref-brew1948_13-0">^</a></b></span> <span class="reference-text">Stuart D. Brewer dan Charles P. Haber (1948): "Alkylsilazanes and Some Related Compounds". <i>Journal of the American Chemical Society</i>, volume 70, terbitan 11, halaman 3888–3891. <a href="/wiki/Pengenal_objek_digital" title="Pengenal objek digital">DOI</a>:<a rel="nofollow" class="external text" href="https://dx.doi.org/10.1021/ja01191a106">10.1021/ja01191a106</a></span> </li> <li id="cite_note-mikh2008-14"><span class="mw-cite-backlink"><b><a href="#cite_ref-mikh2008_14-0">^</a></b></span> <span class="reference-text">B. M. Mikhova (2008), "NMR Data for Carbon-13 – C6H18Se3Sn3" dalam <i>Landolt-Börnstein – Group III Condensed Matter</i>, volume 35 <i>Nuclear Magnetic Resonance Data</i>, subvolume D5, <i>Organometallic Compounds</i>. <a href="/wiki/Pengenal_objek_digital" title="Pengenal objek digital">DOI</a>:<a rel="nofollow" class="external text" href="https://dx.doi.org/10.1007/978-3-540-74189-3_1362">10.1007/978-3-540-74189-3_1362</a></span> </li> <li id="cite_note-draeg1978-15"><span class="mw-cite-backlink"><b><a href="#cite_ref-draeg1978_15-0">^</a></b></span> <span class="reference-text">Martin Dräger, Axel Blecher, Hans-Jürgen Jacobsen, Bernt Krebs (1978): "Molekül- und kristallstruktur von hexamethylcyclo-tristannaselenan <span class="chemf nowrap">[(CH<sub>3</sub>)<sub>2</sub>SnSe]<sub>3</sub></span>". <i>Journal of Organometallic Chemistry</i>, volume 161, terbitan 3, halaman 319–325. <a href="/wiki/Pengenal_objek_digital" title="Pengenal objek digital">DOI</a>:<a rel="nofollow" class="external text" href="https://dx.doi.org/10.1016/S0022-328X(00)92243-5">10.1016/S0022-328X(00)92243-5</a></span> </li> </ol>    </div><noscript><img src="https://login.wikimedia.org/wiki/Special:CentralAutoLogin/start?type=1x1&useformat=desktop" alt="" width="1" height="1" style="border: none; position: absolute;"></noscript> <div class="printfooter" data-nosnippet="">Diperoleh dari "<a dir="ltr" href="https://id.wikipedia.org/w/index.php?title=Tritioaseton&oldid=23182885">https://id.wikipedia.org/w/index.php?title=Tritioaseton&oldid=23182885</a>"</div></div> <div id="catlinks" class="catlinks" data-mw="interface"><div id="mw-normal-catlinks" class="mw-normal-catlinks"><a href="/wiki/Istimewa:Daftar_kategori" title="Istimewa:Daftar kategori">Kategori</a>: <ul><li><a href="/w/index.php?title=Kategori:Heterosiklus_belerang&action=edit&redlink=1" class="new" title="Kategori:Heterosiklus belerang (halaman belum tersedia)">Heterosiklus belerang</a></li></ul></div><div id="mw-hidden-catlinks" class="mw-hidden-catlinks mw-hidden-cats-hidden">Kategori tersembunyi: <ul><li><a href="/wiki/Kategori:Artikel_dengan_pranala_luar_nonaktif" title="Kategori:Artikel dengan pranala luar nonaktif">Artikel dengan pranala luar nonaktif</a></li><li><a href="/wiki/Kategori:Articles_without_InChI_source" title="Kategori:Articles without InChI source">Articles without InChI source</a></li><li><a href="/wiki/Kategori:Articles_without_KEGG_source" title="Kategori:Articles without KEGG source">Articles without KEGG source</a></li><li><a href="/wiki/Kategori:Chembox_having_GHS_data" title="Kategori:Chembox having GHS data">Chembox having GHS data</a></li><li><a href="/wiki/Kategori:Articles_containing_unverified_chemical_infoboxes" title="Kategori:Articles containing unverified chemical infoboxes">Articles containing unverified chemical infoboxes</a></li></ul></div></div> </div> </main> </div> <div class="mw-footer-container"> <footer id="footer" class="mw-footer" > <ul id="footer-info"> <li id="footer-info-lastmod"> Halaman ini terakhir diubah pada 28 Maret 2023, pukul 08.12.</li> <li id="footer-info-copyright">Teks tersedia di bawah <a rel="nofollow" class="external text" href="https://creativecommons.org/licenses/by-sa/4.0/deed.en">Lisensi Atribusi-BerbagiSerupa Creative Commons</a>; ketentuan tambahan mungkin berlaku. 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