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data-mw-deduplicate="TemplateStyles:r1084375498">.mw-parser-output .ib-chembox{border-collapse:collapse;text-align:left}.mw-parser-output .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>8,5′-Diferulic acid </caption> <tbody><tr> <td colspan="2" style="text-align:center; padding:2px;"><span typeof="mw:File"><a href="/wiki/File:8,5%27-diferulic_acid.svg" class="mw-file-description"><img alt="Chemical structure of 8,5′-diferulic acid." src="//upload.wikimedia.org/wikipedia/commons/thumb/1/19/8%2C5%27-diferulic_acid.svg/200px-8%2C5%27-diferulic_acid.svg.png" decoding="async" width="200" height="93" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/19/8%2C5%27-diferulic_acid.svg/300px-8%2C5%27-diferulic_acid.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/19/8%2C5%27-diferulic_acid.svg/400px-8%2C5%27-diferulic_acid.svg.png 2x" data-file-width="850" data-file-height="395" /></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/Preferred_IUPAC_name" title="Preferred IUPAC name">Preferred IUPAC name</a> <div style="max-width:22em; word-wrap:break-word; padding-left:1.7em;"><div style="display: inline-block; line-height: 1.2em; padding: .1em 0; max-width:22em;">(2<i>E</i>)-2-{5-[(<i>E</i>)-2-Carboxyethen-1-yl]-2-hydroxy-3-methoxyphenyl}-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoic acid</div></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;">8,5′-DiFA<br />Ferulic acid 8-5-dehydrodimer<br />8,5′-diFA (open form)<br />8,5-DiFA<br />5-8′-Dehydrodiferulic acid</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=180579-78-6">180579-78-6</a></span><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><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=O%3DC%28O%29%5CC%3DC%5Cc1cc%28OC%29c%28O%29c%28c1%29%2FC%28%3DC%5Cc2ccc%28O%29c%28OC%29c2%29C%28%3DO%29O">Interactive image</a></span></li></ul></div> </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=88363">CHEBI:88363</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.8560889.html">8560889</a></span></li></ul></div> </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/10385447">10385447</a></span></li></ul></div> </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/DTXSID201045390">DTXSID201045390</a> <span class="mw-valign-text-top noprint" typeof="mw:File/Frameless"><a href="https://www.wikidata.org/wiki/Q15410237#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/C20H18O8/c1-27-16-9-11(3-5-15(16)21)8-14(20(25)26)13-7-12(4-6-18(22)23)10-17(28-2)19(13)24/h3-10,21,24H,1-2H3,(H,22,23)(H,25,26)/b6-4+,14-8+</div><div style="word-wrap:break-word; text-indent:-1.5em; font-size:97%; line-height:120%;">Key: DEPVSDIYICBTJE-SITOFEAGSA-N</div></div></li><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=1/C20H18O8/c1-27-16-9-11(3-5-15(16)21)8-14(20(25)26)13-7-12(4-6-18(22)23)10-17(28-2)19(13)24/h3-10,21,24H,1-2H3,(H,22,23)(H,25,26)/b6-4+,14-8+</div><div style="word-wrap:break-word; text-indent:-1.5em; font-size:97%; line-height:120%;">Key: DEPVSDIYICBTJE-SITOFEAGBF</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%;">O=C(O)\C=C\c1cc(OC)c(O)c(c1)/C(=C\c2ccc(O)c(OC)c2)C(=O)O</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 title="Carbon">C</span><sub>20</sub><span title="Hydrogen">H</span><sub>18</sub><span title="Oxygen">O</span><sub>8</sub> </td></tr> <tr> <td><a href="/wiki/Molar_mass" title="Molar mass">Molar mass</a> </td> <td><span class="nowrap"><span data-sort-value="7002386356000000000♠"></span>386.356</span> g·mol<sup>−1</sup>   </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> <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>8,5′-Diferulic acid</b> is a non cyclic type of <a href="/wiki/Diferulic_acid" class="mw-redirect" title="Diferulic acid">diferulic acid</a>. It is the predominant diferulic acid in <a href="/wiki/Sugar_beet_pulp" class="mw-redirect" title="Sugar beet pulp">sugar beet pulp</a>.<sup id="cite_ref-2" class="reference"><a href="#cite_note-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup> It is also found in <a href="/wiki/Barley" title="Barley">barley</a>,<sup id="cite_ref-3" class="reference"><a href="#cite_note-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup> in <a href="/wiki/Maize_bran" class="mw-redirect" title="Maize bran">maize bran</a><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> and <a href="/wiki/Rye" title="Rye">rye</a>.<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> 8,5′-Diferulic acid has also been identified to be covalently linked to carbohydrate moieties of the arabinogalactan-protein fraction of <a href="/wiki/Gum_arabic" title="Gum arabic">gum arabic</a>.<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> </p> <div class="mw-heading mw-heading2"><h2 id="See_also">See also</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=8,5%27-Diferulic_acid&action=edit&section=1" title="Edit section: See also"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <ul><li><a href="/wiki/Decarboxylated_8,5%27-diferulic_acid" title="Decarboxylated 8,5'-diferulic acid">Decarboxylated 8,5'-diferulic acid</a></li></ul> <div class="mw-heading mw-heading2"><h2 id="References">References</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=8,5%27-Diferulic_acid&action=edit&section=2" title="Edit section: References"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <style data-mw-deduplicate="TemplateStyles:r1239543626">.mw-parser-output .reflist{margin-bottom:0.5em;list-style-type:decimal}@media screen{.mw-parser-output .reflist{font-size:90%}}.mw-parser-output .reflist .references{font-size:100%;margin-bottom:0;list-style-type:inherit}.mw-parser-output .reflist-columns-2{column-width:30em}.mw-parser-output .reflist-columns-3{column-width:25em}.mw-parser-output .reflist-columns{margin-top:0.3em}.mw-parser-output .reflist-columns ol{margin-top:0}.mw-parser-output .reflist-columns li{page-break-inside:avoid;break-inside:avoid-column}.mw-parser-output .reflist-upper-alpha{list-style-type:upper-alpha}.mw-parser-output .reflist-upper-roman{list-style-type:upper-roman}.mw-parser-output .reflist-lower-alpha{list-style-type:lower-alpha}.mw-parser-output .reflist-lower-greek{list-style-type:lower-greek}.mw-parser-output .reflist-lower-roman{list-style-type:lower-roman}</style><div class="reflist"> <div class="mw-references-wrap"><ol class="references"> <li id="cite_note-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://jglobal.jst.go.jp/en/detail?JGLOBAL_ID=200907097862177529">"8,5'-Diferulic acid | Chemical Substance Information | J-GLOBAL"</a>. <i>jglobal.jst.go.jp</i>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=unknown&rft.jtitle=jglobal.jst.go.jp&rft.atitle=8%2C5%27-Diferulic+acid+%7C+Chemical+Substance+Information+%7C+J-GLOBAL&rft_id=https%3A%2F%2Fjglobal.jst.go.jp%2Fen%2Fdetail%3FJGLOBAL_ID%3D200907097862177529&rfr_id=info%3Asid%2Fen.wikipedia.org%3A8%2C5%27-Diferulic+acid" class="Z3988"></span></span> </li> <li id="cite_note-2"><span class="mw-cite-backlink"><b><a href="#cite_ref-2">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFMicardGrabberRalphRenard1997" class="citation journal cs1">Micard, V.; Grabber, J.H.; Ralph, J.; Renard, C.M.G.C.; Thibault, J.-F. 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"Hydroxycinnamic acids and ferulic acid dehydrodimers in barley and processed barley". <i>Journal of Agricultural and Food Chemistry</i>. <b>49</b> (10): 4884–8. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1021%2Fjf010530u">10.1021/jf010530u</a>. <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/11600039">11600039</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Journal+of+Agricultural+and+Food+Chemistry&rft.atitle=Hydroxycinnamic+acids+and+ferulic+acid+dehydrodimers+in+barley+and+processed+barley&rft.volume=49&rft.issue=10&rft.pages=4884-8&rft.date=2001&rft_id=info%3Adoi%2F10.1021%2Fjf010530u&rft_id=info%3Apmid%2F11600039&rft.aulast=Hernanz&rft.aufirst=D&rft.au=Nu%C3%B1ez%2C+V&rft.au=Sancho%2C+AI&rft.au=Faulds%2C+CB&rft.au=Williamson%2C+G&rft.au=Bartolom%C3%A9%2C+B&rft.au=G%C3%B3mez-Cordov%C3%A9s%2C+C&rfr_id=info%3Asid%2Fen.wikipedia.org%3A8%2C5%27-Diferulic+acid" class="Z3988"></span></span> </li> <li id="cite_note-4"><span class="mw-cite-backlink"><b><a href="#cite_ref-4">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFBunzelFunkSteinhart2004" class="citation journal cs1">Bunzel, M; Funk, C; Steinhart, H (2004). "Semipreparative isolation of dehydrodiferulic and dehydrotriferulic acids as standard substances from maize bran". <i>Journal of Separation Science</i>. <b>27</b> (13): 1080–6. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1002%2Fjssc.200301703">10.1002/jssc.200301703</a>. <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/15495409">15495409</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Journal+of+Separation+Science&rft.atitle=Semipreparative+isolation+of+dehydrodiferulic+and+dehydrotriferulic+acids+as+standard+substances+from+maize+bran&rft.volume=27&rft.issue=13&rft.pages=1080-6&rft.date=2004&rft_id=info%3Adoi%2F10.1002%2Fjssc.200301703&rft_id=info%3Apmid%2F15495409&rft.aulast=Bunzel&rft.aufirst=M&rft.au=Funk%2C+C&rft.au=Steinhart%2C+H&rfr_id=info%3Asid%2Fen.wikipedia.org%3A8%2C5%27-Diferulic+acid" 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="CITEREFAndreasenChristensenMeyerHansen2000" class="citation journal cs1">Andreasen, MF; Christensen, LP; Meyer, AS; Hansen, A (2000). "Content of phenolic acids and ferulic acid dehydrodimers in 17 rye (Secale cereale L.) varieties". <i>Journal of Agricultural and Food Chemistry</i>. <b>48</b> (7): 2837–42. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1021%2Fjf991266w">10.1021/jf991266w</a>. <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/11032481">11032481</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Journal+of+Agricultural+and+Food+Chemistry&rft.atitle=Content+of+phenolic+acids+and+ferulic+acid+dehydrodimers+in+17+rye+%28Secale+cereale+L.%29+varieties&rft.volume=48&rft.issue=7&rft.pages=2837-42&rft.date=2000&rft_id=info%3Adoi%2F10.1021%2Fjf991266w&rft_id=info%3Apmid%2F11032481&rft.aulast=Andreasen&rft.aufirst=MF&rft.au=Christensen%2C+LP&rft.au=Meyer%2C+AS&rft.au=Hansen%2C+A&rfr_id=info%3Asid%2Fen.wikipedia.org%3A8%2C5%27-Diferulic+acid" 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="CITEREFRenardLavenant-GourgeonRaletSanchez2006" class="citation journal cs1">Renard, D; Lavenant-Gourgeon, L; Ralet, MC; Sanchez, C (2006). "Acacia senegal gum: Continuum of molecular species differing by their protein to sugar ratio, molecular weight, and charges". <i>Biomacromolecules</i>. <b>7</b> (9): 2637–49. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1021%2Fbm060145j">10.1021/bm060145j</a>. <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/16961328">16961328</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Biomacromolecules&rft.atitle=Acacia+senegal+gum%3A+Continuum+of+molecular+species+differing+by+their+protein+to+sugar+ratio%2C+molecular+weight%2C+and+charges&rft.volume=7&rft.issue=9&rft.pages=2637-49&rft.date=2006&rft_id=info%3Adoi%2F10.1021%2Fbm060145j&rft_id=info%3Apmid%2F16961328&rft.aulast=Renard&rft.aufirst=D&rft.au=Lavenant-Gourgeon%2C+L&rft.au=Ralet%2C+MC&rft.au=Sanchez%2C+C&rfr_id=info%3Asid%2Fen.wikipedia.org%3A8%2C5%27-Diferulic+acid" 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=8,5%27-Diferulic_acid&action=edit&section=3" 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="http://www.phenol-explorer.eu/compounds/508">5-8'-Dehydrodiferulic acid at phenol-explorer.eu</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 .hlist.inline,.mw-parser-output .hlist.inline dl,.mw-parser-output .hlist.inline ol,.mw-parser-output .hlist.inline ul,.mw-parser-output .hlist dl dl,.mw-parser-output .hlist dl ol,.mw-parser-output .hlist dl ul,.mw-parser-output .hlist ol dl,.mw-parser-output .hlist ol ol,.mw-parser-output .hlist ol ul,.mw-parser-output .hlist ul dl,.mw-parser-output .hlist ul ol,.mw-parser-output .hlist ul ul{display:inline}.mw-parser-output .hlist .mw-empty-li{display:none}.mw-parser-output .hlist dt::after{content:": "}.mw-parser-output .hlist dd::after,.mw-parser-output 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.navbox-abovebelow{background-color:#e6e6ff}.mw-parser-output .navbox-even{background-color:#f7f7f7}.mw-parser-output .navbox-odd{background-color:transparent}.mw-parser-output .navbox .hlist td dl,.mw-parser-output .navbox .hlist td ol,.mw-parser-output .navbox .hlist td ul,.mw-parser-output .navbox td.hlist dl,.mw-parser-output .navbox td.hlist ol,.mw-parser-output .navbox td.hlist ul{padding:0.125em 0}.mw-parser-output .navbox .navbar{display:block;font-size:100%}.mw-parser-output .navbox-title .navbar{float:left;text-align:left;margin-right:0.5em}body.skin--responsive .mw-parser-output .navbox-image img{max-width:none!important}@media print{body.ns-0 .mw-parser-output .navbox{display:none!important}}</style></div><div role="navigation" class="navbox" aria-labelledby="Types_of_hydroxycinnamic_acids" style="padding:3px"><table class="nowraplinks 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"><style data-mw-deduplicate="TemplateStyles:r1239400231">.mw-parser-output .navbar{display:inline;font-size:88%;font-weight:normal}.mw-parser-output .navbar-collapse{float:left;text-align:left}.mw-parser-output .navbar-boxtext{word-spacing:0}.mw-parser-output .navbar ul{display:inline-block;white-space:nowrap;line-height:inherit}.mw-parser-output .navbar-brackets::before{margin-right:-0.125em;content:"[ "}.mw-parser-output .navbar-brackets::after{margin-left:-0.125em;content:" ]"}.mw-parser-output .navbar li{word-spacing:-0.125em}.mw-parser-output .navbar a>span,.mw-parser-output .navbar a>abbr{text-decoration:inherit}.mw-parser-output .navbar-mini abbr{font-variant:small-caps;border-bottom:none;text-decoration:none;cursor:inherit}.mw-parser-output .navbar-ct-full{font-size:114%;margin:0 7em}.mw-parser-output .navbar-ct-mini{font-size:114%;margin:0 4em}html.skin-theme-clientpref-night .mw-parser-output .navbar li a abbr{color:var(--color-base)!important}@media(prefers-color-scheme:dark){html.skin-theme-clientpref-os .mw-parser-output .navbar li a abbr{color:var(--color-base)!important}}@media print{.mw-parser-output .navbar{display:none!important}}</style><div class="navbar plainlinks hlist navbar-mini"><ul><li class="nv-view"><a href="/wiki/Template:Hydroxycinnamic_acid" title="Template:Hydroxycinnamic acid"><abbr title="View this template">v</abbr></a></li><li class="nv-talk"><a href="/wiki/Template_talk:Hydroxycinnamic_acid" title="Template talk:Hydroxycinnamic acid"><abbr title="Discuss this template">t</abbr></a></li><li class="nv-edit"><a href="/wiki/Special:EditPage/Template:Hydroxycinnamic_acid" title="Special:EditPage/Template:Hydroxycinnamic acid"><abbr title="Edit this template">e</abbr></a></li></ul></div><div id="Types_of_hydroxycinnamic_acids" style="font-size:114%;margin:0 4em">Types of <a href="/wiki/Hydroxycinnamic_acid" title="Hydroxycinnamic acid">hydroxycinnamic acids</a></div></th></tr><tr><th scope="row" class="navbox-group" style="width:1%">Aglycones</th><td class="navbox-list-with-group navbox-list navbox-odd hlist" 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%">Precursor</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/Cinnamic_acid" title="Cinnamic acid">Cinnamic acid</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Monohydroxycinnamic acids<br />(Coumaric acids)</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/P-Coumaric_acid" title="P-Coumaric acid"><i>p</i>-Coumaric acid</a></li> <li><a href="/wiki/O-Coumaric_acid" title="O-Coumaric acid"><i>o</i>-Coumaric acid</a></li> <li><a href="/wiki/M-Coumaric_acid" title="M-Coumaric acid"><i>m</i>-Coumaric acid</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Dihydroxycinnamic_acid" title="Dihydroxycinnamic acid">Dihydroxycinnamic acids</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/Caffeic_acid" title="Caffeic acid">Caffeic acid</a> (3,4-dihydroxycinnamic acid)</li> <li><a href="/wiki/Umbellic_acid" title="Umbellic acid">Umbellic acid</a> (2,4-dihydroxycinnamic acid)</li> <li><a href="/wiki/2,3-Dihydroxycinnamic_acid" title="2,3-Dihydroxycinnamic acid">2,3-Dihydroxycinnamic acid</a></li> <li><a href="/wiki/2,5-Dihydroxycinnamic_acid" title="2,5-Dihydroxycinnamic acid">2,5-Dihydroxycinnamic acid</a></li> <li><a href="/wiki/3,5-Dihydroxycinnamic_acid" title="3,5-Dihydroxycinnamic acid">3,5-Dihydroxycinnamic acid</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Trihydroxycinnamic acids</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/2,4,5-Trihydroxycinnamic_acid" title="2,4,5-Trihydroxycinnamic acid">2,4,5-Trihydroxycinnamic acid</a></li> <li><a href="/w/index.php?title=3,4,5-Trihydroxycinnamic_acid&action=edit&redlink=1" class="new" title="3,4,5-Trihydroxycinnamic acid (page does not exist)">3,4,5-Trihydroxycinnamic acid</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><i>O</i>-methylated forms</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/Ferulic_acid" title="Ferulic acid">Ferulic acid</a></li> <li><a href="/wiki/5-Hydroxyferulic_acid" title="5-Hydroxyferulic acid">5-Hydroxyferulic acid</a></li> <li><a href="/wiki/Isoferulic_acid" title="Isoferulic acid">Isoferulic acid</a></li> <li><a href="/wiki/Sinapinic_acid" title="Sinapinic acid">Sinapinic acid</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">others</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/Plicatin_A" title="Plicatin A">Plicatin A</a></li> <li><a href="/wiki/Plicatin_B" title="Plicatin B">Plicatin B</a></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Esters</th><td class="navbox-list-with-group navbox-list navbox-odd hlist" 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%">glycoside-likes</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%">Esters of<br />caffeic acid<br />with cyclitols</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%">esters of<br /><a href="/wiki/Quinic_acid" title="Quinic acid">quinic acid</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/Chlorogenic_acid" title="Chlorogenic acid">Chlorogenic acid</a> (3-caffeoylquinic acid)</li> <li><a href="/w/index.php?title=Cryptochlorogenic_acid&action=edit&redlink=1" class="new" title="Cryptochlorogenic acid (page does not exist)">Cryptochlorogenic acid</a> (4-<i>O</i>-caffeoylquinic acid)</li> <li><a href="/wiki/Neochlorogenic_acid" title="Neochlorogenic acid">Neochlorogenic acid</a> (5-<i>O</i>-Caffeoylquinic acid)</li> <li><a href="/wiki/Cynarine" title="Cynarine">Cynarine</a> (1,5-dicaffeoylquinic acid)</li> <li><a href="/w/index.php?title=3,4-dicaffeoylquinic_acid&action=edit&redlink=1" class="new" title="3,4-dicaffeoylquinic acid (page does not exist)">3,4-dicaffeoylquinic acid</a></li> <li><a href="/w/index.php?title=3,5-dicaffeoylquinic_acid&action=edit&redlink=1" class="new" title="3,5-dicaffeoylquinic acid (page does not exist)">3,5-dicaffeoylquinic acid</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">esters of<br /><a href="/wiki/Shikimic_acid" title="Shikimic acid">shikimic acid</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/Dactylifric_acid" title="Dactylifric acid">Dactylifric acid</a> (3-<i>O</i>-caffeoylshikimic acid)</li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Glycosides</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=Ferulic_acid_glucoside&action=edit&redlink=1" class="new" title="Ferulic acid glucoside (page does not exist)">Ferulic acid glucoside</a></li> <li><a href="/wiki/P-Coumaric_acid_glucoside" title="P-Coumaric acid glucoside"><i>p</i>-Coumaric acid glucoside</a></li> <li><a href="/w/index.php?title=1-Sinapoyl-D-glucose&action=edit&redlink=1" class="new" title="1-Sinapoyl-D-glucose (page does not exist)">1-Sinapoyl-<small>D</small>-glucose</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/Tartaric_acid" title="Tartaric acid">Tartaric acid</a> esters</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/Caftaric_acid" title="Caftaric acid">Caftaric acid</a></li> <li><a href="/wiki/Chicoric_acid" title="Chicoric acid">Chicoric acid</a> (dicaffeoyltartaric acid)</li> <li><a href="/wiki/Coutaric_acid" title="Coutaric acid">Coutaric acid</a></li> <li><a href="/wiki/Fertaric_acid" title="Fertaric acid">Fertaric acid</a></li> <li><a href="/wiki/Grape_reaction_product" title="Grape reaction product">Grape reaction product</a> (caftaric acid conjugated with glutathione)</li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Other esters<br />with caffeic acid</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/Caffeoylmalic_acid" title="Caffeoylmalic acid">Caffeoylmalic acid</a></li> <li><a href="/wiki/Ethyl_caffeate" title="Ethyl caffeate">Ethyl caffeate</a></li> <li><a href="/wiki/Methyl_caffeate" title="Methyl caffeate">Methyl caffeate</a></li> <li><a href="/wiki/Caffeic_acid_phenethyl_ester" title="Caffeic acid phenethyl ester">Caffeic acid phenethyl ester</a> (CAPE)</li> <li><a href="/wiki/Rosmarinic_acid" title="Rosmarinic acid">Rosmarinic acid</a> (ester with 3,4-dihydroxyphenyllactic acid)</li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Caffeoyl phenylethanoid<br /> glycoside (CPG)</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/Echinacoside" title="Echinacoside">Echinacoside</a></li> <li><a href="/w/index.php?title=Calceolarioside_A&action=edit&redlink=1" class="new" title="Calceolarioside A (page does not exist)">Calceolarioside A</a>, <a href="/w/index.php?title=Calceolarioside_B&action=edit&redlink=1" class="new" title="Calceolarioside B (page does not exist)">B</a>, <a href="/w/index.php?title=Calceolarioside_C&action=edit&redlink=1" class="new" title="Calceolarioside C (page does not exist)">C</a>, <a href="/w/index.php?title=Calceolarioside_F&action=edit&redlink=1" class="new" title="Calceolarioside F (page does not exist)">F</a></li> <li><a href="/w/index.php?title=Chiritoside_A&action=edit&redlink=1" class="new" title="Chiritoside A (page does not exist)">Chiritoside A</a>, <a href="/w/index.php?title=Chiritoside_B&action=edit&redlink=1" class="new" title="Chiritoside B (page does not exist)">B</a>, <a href="/w/index.php?title=Chiritoside_C&action=edit&redlink=1" class="new" title="Chiritoside C (page does not exist)">C</a></li> <li><a href="/w/index.php?title=Cistanoside_A&action=edit&redlink=1" class="new" title="Cistanoside A (page does not exist)">Cistanoside A</a>, <a href="/w/index.php?title=Cistanoside_B&action=edit&redlink=1" class="new" title="Cistanoside B (page does not exist)">B</a>, <a href="/w/index.php?title=Cistanoside_C&action=edit&redlink=1" class="new" title="Cistanoside C (page does not exist)">C</a>, <a href="/w/index.php?title=Cistanoside_D&action=edit&redlink=1" class="new" title="Cistanoside D (page does not exist)">D</a>, <a href="/w/index.php?title=Cistanoside_E&action=edit&redlink=1" class="new" title="Cistanoside E (page does not exist)">E</a>, <a href="/w/index.php?title=Cistanoside_F&action=edit&redlink=1" class="new" title="Cistanoside F (page does not exist)">F</a>, <a href="/w/index.php?title=Cistanoside_G&action=edit&redlink=1" class="new" title="Cistanoside G (page does not exist)">G</a>, <a href="/w/index.php?title=Cistanoside_H&action=edit&redlink=1" class="new" title="Cistanoside H (page does not exist)">H</a></li> <li><a href="/w/index.php?title=Conandroside&action=edit&redlink=1" class="new" title="Conandroside (page does not exist)">Conandroside</a></li> <li><a href="/w/index.php?title=Myconoside&action=edit&redlink=1" class="new" title="Myconoside (page does not exist)">Myconoside</a></li> <li><a href="/w/index.php?title=Pauoifloside&action=edit&redlink=1" class="new" title="Pauoifloside (page does not exist)">Pauoifloside</a></li> <li><a href="/w/index.php?title=Plantainoside_A&action=edit&redlink=1" class="new" title="Plantainoside A (page does not exist)">Plantainoside A</a></li> <li><a href="/w/index.php?title=Plantamajoside&action=edit&redlink=1" class="new" title="Plantamajoside (page does not exist)">Plantamajoside</a></li> <li><a href="/w/index.php?title=Tubuloside_B&action=edit&redlink=1" class="new" title="Tubuloside B (page does not exist)">Tubuloside B</a></li> <li><a href="/wiki/Verbascoside" title="Verbascoside">Verbascoside</a> (<a href="/w/index.php?title=Isoverbascoside&action=edit&redlink=1" class="new" title="Isoverbascoside (page does not exist)">Isoverbascoside</a>, <a href="/w/index.php?title=2%27-Acetylverbascoside&action=edit&redlink=1" class="new" title="2'-Acetylverbascoside (page does not exist)">2′-Acetylverbascoside</a>)</li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Oligomeric forms</th><td class="navbox-list-with-group navbox-list navbox-odd hlist" 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%">Dimers</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/Diferulic_acids" title="Diferulic acids">Diferulic acids</a> (DiFA) : <a href="/w/index.php?title=5,5%27-Diferulic_acid&action=edit&redlink=1" class="new" title="5,5'-Diferulic acid (page does not exist)">5,5′-Diferulic acid</a>, <a href="/w/index.php?title=8-O-4%27-Diferulic_acid&action=edit&redlink=1" class="new" title="8-O-4'-Diferulic acid (page does not exist)">8-<i>O</i>-4′-Diferulic acid</a>, <a class="mw-selflink selflink">8,5′-Diferulic acid</a>, <a href="/wiki/8,5%27-DiFA_(DC)" class="mw-redirect" title="8,5'-DiFA (DC)">8,5′-DiFA (DC)</a>, <a href="/w/index.php?title=8,5%27-DiFA_(BF)&action=edit&redlink=1" class="new" title="8,5'-DiFA (BF) (page does not exist)">8,5′-DiFA (BF)</a>, <a href="/w/index.php?title=8,8%27-Diferulic_acid&action=edit&redlink=1" class="new" title="8,8'-Diferulic acid (page does not exist)">8,8′-Diferulic acid</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Trimers</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/Triferulic_acid" title="Triferulic acid">Triferulic acids</a> : <a href="/w/index.php?title=5-5%27,8%27-O-4%22-Triferulic_acid&action=edit&redlink=1" class="new" title="5-5',8'-O-4"-Triferulic acid (page does not exist)">5-5′,8′-<i>O</i>-4″-Triferulic acid</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Tetramers</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=Tetraferulic_acid&action=edit&redlink=1" class="new" title="Tetraferulic acid (page does not exist)">Tetraferulic acids</a></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Conjugates with<br /><a href="/wiki/Coenzyme_A" title="Coenzyme A">coenzyme A</a> (CoA)</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="/w/index.php?title=Caffeoyl-CoA&action=edit&redlink=1" class="new" title="Caffeoyl-CoA (page does not exist)">Caffeoyl-CoA</a></li> <li><a href="/wiki/Cinnamoyl-CoA" title="Cinnamoyl-CoA">Cinnamoyl-CoA</a></li> <li><a href="/wiki/Coumaroyl-CoA" title="Coumaroyl-CoA">Coumaroyl-CoA</a></li></ul> </div></td></tr></tbody></table></div>    </div><noscript><img src="https://login.wikimedia.org/wiki/Special:CentralAutoLogin/start?type=1x1" alt="" width="1" height="1" style="border: none; position: absolute;"></noscript> <div class="printfooter" data-nosnippet="">Retrieved from "<a dir="ltr" href="https://en.wikipedia.org/w/index.php?title=8,5%27-Diferulic_acid&oldid=1196420039">https://en.wikipedia.org/w/index.php?title=8,5%27-Diferulic_acid&oldid=1196420039</a>"</div></div> <div id="catlinks" class="catlinks" data-mw="interface"><div id="mw-normal-catlinks" class="mw-normal-catlinks"><a href="/wiki/Help:Category" title="Help:Category">Categories</a>: <ul><li><a href="/wiki/Category:O-methylated_hydroxycinnamic_acids" title="Category:O-methylated hydroxycinnamic acids">O-methylated hydroxycinnamic acids</a></li><li><a href="/wiki/Category:Hydroxycinnamic_acid_dimers" title="Category:Hydroxycinnamic acid dimers">Hydroxycinnamic acid 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