Revision as of 11:58, 23 November 2011 editBeetstra (talk | contribs)Edit filter managers, Administrators172,031 edits Saving copy of the {{chembox}} taken from revid 400145489 of page Linoelaidic_acid for the Chem/Drugbox validation project (updated: 'ChEMBL', 'CASNo'). |
Latest revision as of 02:59, 4 February 2023 edit 109.241.162.167 (talk) the term 'geometric isomer' is obsolete and its usage is strongly discouraged by IUPAC |
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{{ambox | text = This page contains a copy of the infobox ({{tl|chembox}}) taken from revid of page ] with values updated to verified values.}} |
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{{chembox |
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{{chembox |
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| Verifiedfields = changed |
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| verifiedrevid = 400143251 |
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| verifiedrevid = 462091801 |
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| Reference=<ref> at Sigma-Aldrich</ref> |
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| Reference =<ref> at chemexper.com</ref><ref> at pubchem.ncbi.nlm.nih.gov</ref> |
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| ImageFile = Linoelaidic acid.png |
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| ImageFile = Linoelaidic acid.png |
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| ImageSize = 250px |
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| ImageSize = 250px |
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| Name = Linoelaidic acid |
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| Name = Linolelaidic acid |
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| IUPACName = (9''E'',12''E'')-octadeca-9,12-dienoic acid |
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| IUPACName = (9''E'',12''E'')-Octadeca-9,12-dienoic acid |
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| OtherNames = ''trans, trans''-9,12-octadecadienoic acid |
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| OtherNames = ''trans'',''trans''-9,12-Octadecadienoic acid, Linoelaidic acid |
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| Section1 = {{Chembox Identifiers |
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|Section1={{Chembox Identifiers |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID = 4445609 |
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| ChemSpiderID = 4445609 |
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| InChI = 1/C18H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h6-7,9-10H,2-5,8,11-17H2,1H3,(H,19,20)/b7-6+,10-9+ |
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| InChI = 1/C18H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h6-7,9-10H,2-5,8,11-17H2,1H3,(H,19,20)/b7-6+,10-9+ |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey = OYHQOLUKZRVURQ-AVQMFFATSA-N |
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| StdInChIKey = OYHQOLUKZRVURQ-AVQMFFATSA-N |
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| CASNo_Ref = {{cascite|correct|CAS}} |
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| CASNo = <!-- blanked - oldvalue: 506-21-8 --> |
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| ChEMBL = 93204 |
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| CASNo = 506-21-8 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| UNII = 7552P0K6PN |
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| ChEMBL_Ref = {{ebicite|correct|EBI}} |
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| ChEMBL = 93204 |
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| PubChem = 5282457 |
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| PubChem = 5282457 |
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| SMILES = O=C(O)CCCCCCC/C=C/C/C=C/CCCCC |
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| SMILES = O=C(O)CCCCCCC/C=C/C/C=C/CCCCC |
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}} |
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}} |
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| Section2 = {{Chembox Properties |
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|Section2={{Chembox Properties |
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| C=18 | H=32 | O=2 |
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| Formula = C<sub>18</sub>H<sub>32</sub>O<sub>2</sub> |
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| MolarMass = 280.45 g/mol |
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| MolarMass = 280.45 g/mol |
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| Density = |
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| Density = |
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| MeltingPt = −5 °C |
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| MeltingPtC = 28-29 |
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| MeltingPt_ref = <ref>{{Cite journal | doi = 10.1021/ja01874a022| title = The Elaidinization of Linoleic Acid| journal = Journal of the American Chemical Society| volume = 61| issue = 5| pages = 1062| year = 1939| last1 = Kass| first1 = J.P.| last2 = Burr| first2 = G.O.| bibcode = 1939JAChS..61.2492E}}</ref> |
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| BoilingPt = 229-230 °C at 16 mmHg |
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| BoilingPtC = 229 to 230 |
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| BoilingPt_notes = at 16 mmHg |
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'''Linolelaidic acid''' is an ] ] (TFA) and is a ] of ]. It is found in partially ] vegetable oils. It is a white (or colourless) viscous liquid. |
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TFAs are classified as conjugated and nonconjugated, corresponding usually to the structural elements {{chem2|\sCH\dCH\sCH\dCH\s}} and {{chem2|\sCH\dCH\sCH2\sCH\dCH\s}}, respectively. Nonconjugated TFAs are represented by ] and linolelaidic acid. Their presence is linked heart diseases. The TFA ], which is of animal origin, poses less of a health risk.<ref>Park, Yeonhwa "Conjugated linoleic acid (CLA): Good or bad trans fat?" Journal of Food Composition and Analysis 2009, vol. 22, S4-S12. {{doi|10.1016/j.jfca.2008.12.002}}</ref> |
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==References== |
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<references/> |
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{{Fatty acids}} |
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] |
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] |
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{{Organic-chem-stub}} |