Revision as of 14:13, 24 November 2011 editBeetstra (talk | contribs)Edit filter managers, Administrators172,031 edits Saving copy of the {{chembox}} taken from revid 444029078 of page Nonadecylic_acid for the Chem/Drugbox validation project (updated: 'ChEMBL'). |
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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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| Watchedfields = changed |
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| verifiedrevid = 444027847 |
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| verifiedrevid = 462262462 |
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| Name = Nonadecylic acid |
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| Name = Nonadecylic acid |
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| ImageFile = Nonadecylic acid.png |
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| ImageFile = Nonadecylic acid.svg |
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| ImageSize = 250px |
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| ImageSize = 250px |
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| ImageFile1 = Nonadecylic-acid-3D-balls.png |
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| ImageAlt = |
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| ImageName = |
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| ImageSize1 = 250px |
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| IUPACName = Nonadecanoic acid |
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| SystematicName = |
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| ImageName = |
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| IUPACName = Nonadecanoic acid |
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| OtherNames = |
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| SystematicName = |
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| Section1 = {{Chembox Identifiers |
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| Abbreviations = |
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| OtherNames = |
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|Section1={{Chembox Identifiers |
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| CASNo = 646-30-0 |
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| CASNo_Ref = |
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| Abbreviations = |
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| CASNo = 646-30-0 |
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| CASNos = |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| CASNo_Ref = {{cascite|correct|CAS}} |
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| Beilstein = 1786261 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| UNII = H6M3VYC62P |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID = 12071 |
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| ChemSpiderID = 12071 |
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| DrugBank_Ref = {{drugbankcite|correct|drugbank}} |
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| DrugBank_Ref = {{drugbankcite|correct|drugbank}} |
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| DrugBank = |
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| DrugBank = |
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| EC-number = 211-472-4 |
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| EC_number = 211-472-4 |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey = ISYWECDDZWTKFF-UHFFFAOYSA-N |
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| StdInChIKey = ISYWECDDZWTKFF-UHFFFAOYSA-N |
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| ChEMBL_Ref = {{ebicite|correct|EBI}} |
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| ChEMBL = 1169674 |
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| ChEMBL = 1169674 |
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| PubChem = 12591 |
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| PubChem = 12591 |
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| ChEBI_Ref = {{ebicite|correct|EBI}} |
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| ChEBI_Ref = {{ebicite|correct|EBI}} |
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| ChEBI = 39246 |
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| ChEBI = 39246 |
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| SMILES = O=C(O)CCCCCCCCCCCCCCCCCC |
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| SMILES = O=C(O)CCCCCCCCCCCCCCCCCC |
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| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChI = 1S/C19H38O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21/h2-18H2,1H3,(H,20,21) |
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| StdInChI = 1S/C19H38O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21/h2-18H2,1H3,(H,20,21) |
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| Section2 = {{Chembox Properties |
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|Section2={{Chembox Properties |
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| Appearance = White flakes or powder |
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| Appearance = White flakes or powder |
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| BoilingPtC = 236 |
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| BoilingPt = 236°C (10 mmHg) </br> 297°C (100 mmHg) |
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| BoilingPt_notes = (10 mmHg) <br> 297 °C (100 mmHg) |
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| Density = |
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| Density = |
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| Formula = CH<sub>3</sub>(CH<sub>2</sub>)<sub>18</sub>COOH |
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| Formula = {{chem2|CH3(CH2)17COOH}} |
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| MolarMass = 298.50382 g/mol |
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| MolarMass = 298.50382 g/mol |
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| MeltingPt = 68-70°C |
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| MeltingPtC = 68 to 70 |
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| Solubility = Insoluble |
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| Solvent = }} |
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| Solubility = Insoluble |
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| Section7 = {{Chembox Hazards |
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| ExternalMSDS = |
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| Solvent = }} |
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|Section7={{Chembox Hazards |
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| FlashPt = |
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| MainHazards = Irritant ('''Xi''') |
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| GHS_ref=<ref>{{cite web |title=Nonadecanoic acid |url=https://pubchem.ncbi.nlm.nih.gov/compound/12591#section=Safety-and-Hazards |website=pubchem.ncbi.nlm.nih.gov |language=en}}</ref> |
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| RPhrases = {{R36/37/38}} |
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| SPhrases = {{S26}} |
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| GHSPictograms = {{GHS07}} |
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| GHSSignalWord = Warning |
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| HPhrases = {{H-phrases|315|319|335}} |
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| PPhrases = {{P-phrases|261|264|271|280|302+352|304+340|305+351+338|312|321|332+313|337+313|362|403+233|405|501}} |
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| Section8 = {{Chembox Related |
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|Section8={{Chembox Related |
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| Function = |
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'''Nonadecylic acid''', or '''nonadecanoic acid''', is a 19-] ] with the ] {{chem2|CH3(CH2)17COOH}}. It forms salts called ''nonadecylates''. Nonadecylic acid can be found in ]s and ]s, although it is rare.{{cn|date=April 2023}} |
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It is also present in the world of ]s as the major constituent of the substance secreted by soldiers of the ] '']'' for defence purposes.{{r|Blum}} |
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Nonadecanoic acid has found applications in the field of metal ].{{r|Smith}} |
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The compound can be prepared by permanganate oxidation of ].{{r|OS}} |
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==See also== |
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*] |
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==References== |
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{{reflist|refs= |
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<ref name = "Blum">{{cite journal | vauthors = Blum MS, Jones TH, Howard DF, Overal W | title = Biochemistry of termite defenses: Coptotermes, Rhinotermes and Cornitermes species | date = 1982 | journal = Comparative Biochemistry and Physiology Part B: Comparative Biochemistry | volume = 71 | number = 4 | pages = 731–733 | doi = 10.1016/0305-0491(82)90489-8}}</ref> |
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<ref name = "Smith">{{cite journal|title=The Adsorption of n-Nonadecanoic Acid on Mechanically Activated Metal Surfaces|journal=The Journal of Physical Chemistry|volume=61|issue=8|pages=1025–1036|doi=10.1021/j150554a001|year=1957|last1=Smith|first1=Hilton A.|last2=McGill|first2=Robert M.}}</ref> |
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<ref name=OS>{{cite journal|doi=10.15227/orgsyn.060.0011|doi-access=free|first1=Donald G.|last1=Lee|first2=Shannon E. |last2=Lamb|first3=Victor S.|last3=Chang|title=Carboxylic Acids from the Oxidation of Terminal Alkenes by Permanganate: Nonadecanoic Acid|journal=Organic Syntheses|year=1981|volume=60|page=11}}</ref> |
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}} |
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{{Fatty acids}} |
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] |
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] |
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{{organic-compound-stub}} |