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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  Latest revision as of 02:59, 4 February 2023 edit 109.241.162.167 (talk) the term 'geometric isomer' is obsolete and its usage is strongly discouraged by IUPAC 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.}}
{{chembox {{chembox
| Verifiedfields = changed
| verifiedrevid = 400143251 | verifiedrevid = 462091801
| Reference=<ref> at Sigma-Aldrich</ref>
| Reference =<ref> at chemexper.com</ref><ref> at pubchem.ncbi.nlm.nih.gov</ref>
| ImageFile = Linoelaidic acid.png | ImageFile = Linoelaidic acid.png
| ImageSize = 250px | ImageSize = 250px
| Name = Linoelaidic acid | Name = Linolelaidic acid
| IUPACName = (9''E'',12''E'')-octadeca-9,12-dienoic acid | IUPACName = (9''E'',12''E'')-Octadeca-9,12-dienoic acid
| OtherNames = ''trans, trans''-9,12-octadecadienoic acid | OtherNames = ''trans'',''trans''-9,12-Octadecadienoic acid, Linoelaidic acid
| Section1 = {{Chembox Identifiers |Section1={{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 4445609 | ChemSpiderID = 4445609
| 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+ | 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}} | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = OYHQOLUKZRVURQ-AVQMFFATSA-N | StdInChIKey = OYHQOLUKZRVURQ-AVQMFFATSA-N
| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo = <!-- blanked - oldvalue: 506-21-8 -->
| ChEMBL = 93204 | CASNo = 506-21-8
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = 7552P0K6PN
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 93204
| PubChem = 5282457 | PubChem = 5282457
| SMILES = O=C(O)CCCCCCC/C=C/C/C=C/CCCCC | SMILES = O=C(O)CCCCCCC/C=C/C/C=C/CCCCC
}} }}
| Section2 = {{Chembox Properties |Section2={{Chembox Properties
| C=18 | H=32 | O=2
| Formula = C<sub>18</sub>H<sub>32</sub>O<sub>2</sub>
| MolarMass = 280.45 g/mol | MolarMass = 280.45 g/mol
| Density = | Density =
| MeltingPt = −5 °C | MeltingPtC = 28-29
| 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>
| BoilingPt = 229-230 °C at 16 mmHg
| BoilingPtC = 229 to 230
| BoilingPt_notes = at 16 mmHg
}} }}
}} }}

'''Linolelaidic acid''' is an ] ] (TFA) and is a ] of ]. It is found in partially ] vegetable oils. It is a white (or colourless) viscous liquid.

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>

==References==
<references/>

{{Fatty acids}}

]
]

{{Organic-chem-stub}}