| Revision as of 16:43, 16 February 2012 editBeetstra (talk | contribs)Edit filter managers, Administrators172,031 edits Saving copy of the {{chembox}} taken from revid 470849359 of page 1-Nonanol for the Chem/Drugbox validation project (updated: ''). |
Latest revision as of 23:56, 3 April 2024 edit Smokefoot (talk | contribs)Autopatrolled, Extended confirmed users, Pending changes reviewers, Rollbackers74,550 edits improved ref and improved context |
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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 = 443646289 |
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| verifiedrevid = 477208308 |
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| Name = 1-Nonanol |
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| ImageFile = 1-Nonanol.png |
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| Name = 1-Nonanol |
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| ImageFile = 1-Nonanol.png |
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| ImageName = Skeletal formula |
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| ImageSize = 200px |
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| ImageFile1 = 1-Nonanol-3D-vdW.png |
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| ImageName = Skeletal formula |
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| ImageName1 = Space-filling model |
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| ImageFile1 = 1-Nonanol-3D-vdW.png |
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| PIN = Nonan-1-ol |
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| ImageName1 = Space-filling model |
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| OtherNames = 1-Nonanol<br />Pelargonic alcohol<br />Nonyl alcohol<br />''n''-Nonyl alcohol |
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| IUPACName = 1-Nonanol |
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|Section1={{Chembox Identifiers |
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| OtherNames = Pelargonic alcohol; Nonyl alcohol; ''n''-Nonyl alcohol |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| Section1 = {{Chembox Identifiers |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChEBI_Ref = {{ebicite|correct|EBI}} |
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| ChEBI_Ref = {{ebicite|correct|EBI}} |
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| ChEBI = 35986 |
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| ChEBI = 35986 |
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| CASNo_Ref = {{cascite|correct|CAS}} |
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| CASNo_Ref = {{cascite|correct|CAS}} |
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| CASNo = 143-08-8 |
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| CASNo = 143-08-8 |
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| DrugBank_Ref = {{drugbankcite|correct|drugbank}} |
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| DrugBank_Ref = {{drugbankcite|correct|drugbank}} |
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| DrugBank = DB03143 |
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| DrugBank = DB03143 |
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| SMILES = OCCCCCCCCC |
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| SMILES = OCCCCCCCCC |
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| PubChem = 8914 |
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| PubChem = 8914 |
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}} |
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| Section2 = {{Chembox Properties |
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|Section2={{Chembox Properties |
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| C=9|H=20|O=1 |
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| C=9 | H=20 | O=1 |
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| Appearance = Colorless liquid |
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| Appearance = Colorless liquid |
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| Density = 0.83 g/cm<sup>3</sup><ref name=GESTIS>{{GESTIS|ZVG=490177}}</ref> |
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| Density = 0.83 g/cm<sup>3</sup><ref name=GESTIS>{{GESTIS|ZVG=490177}}</ref> |
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| MeltingPtC = -6 |
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| MeltingPtC = -6 |
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| Melting_notes = <ref name=GESTIS/> |
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| MeltingPt_ref = <ref name=GESTIS/> |
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| BoilingPtC = 214 |
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| BoilingPtC = 214 |
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| Boiling_notes = <ref name=GESTIS/> |
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| BoilingPt_ref = <ref name=GESTIS/> |
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| Solubility = 1 g/L<ref name=GESTIS/>}} |
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| Solubility = 0.13 g/L<ref name=GESTIS/>}} |
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| Section3 = {{Chembox Hazards |
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|Section3={{Chembox Hazards |
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| MainHazards = |
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| MainHazards = |
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| NFPA-H = 1 |
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| FlashPt = {{convert|96|C|F}} |
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| Autoignition = |
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| NFPA-F = 2 |
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| NFPA-R = 0 |
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| LD50 = 3560 mg/kg (oral, rat)<ref name=FCT>{{cite journal | journal = Food and Cosmetics Toxicology | volume = 11 | pages= 95–115 | year = 1973 | doi = 10.1016/0015-6264(73)90065-5 | pmid = 4716134 | last1 = Opdyke | first1 = DL | title = Monographs on fragrance raw materials | issue = 1}}</ref><br>4680 mg/kg (dermal, rabbit)<ref name=FCT/>}} |
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| FlashPtC = 96 |
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| Section8 = {{Chembox Related |
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| AutoignitionPtC = |
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| OtherFunctn = ] |
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| LD50 = 3560 mg/kg (oral, rat)<ref name=FCT>{{cite journal | journal = ] | volume = 11 | pages= 95–115 | year = 1973 | doi = 10.1016/0015-6264(73)90065-5 | pmid = 4716134 | last1 = Opdyke | first1 = DL | title = Monographs on fragrance raw materials | issue = 1}}</ref><br>4680 mg/kg (dermal, rabbit)<ref name=FCT/>}} |
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| Function = ]s |
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|Section8={{Chembox Related |
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| OtherCpds = |
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| OtherFunction = ] |
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| OtherFunction_label = ]s |
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| OtherCompounds = |
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'''1-Nonanol'''{{IPAc-en|ˈ|n|oʊ|n|ə|n|ɒ|l}} is a straight chain ] with nine ] ]s and the molecular formula CH<sub>3</sub>(CH<sub>2</sub>)<sub>8</sub>OH. It is a colorless oily liquid with a citrus odor similar to ]. |
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Nonanol occurs naturally in ]. The primary use of nonanol is in the manufacture of artificial lemon oil. Various esters of nonanol, such as ], are used in perfumery and flavors. |
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==Nonanols== |
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More common than 1-nonanol are its many isomers, including ], which are typically produced by ] of ]s. Isomeric octenes are produced by dimerization of ]s. These alcohol mixtures are used as solvents in paints and as precursors to ]s.<ref name=Ullmann>{{cite book |doi=10.1002/14356007.a01_279.pub2 |chapter=Alcohols, Aliphatic |title=Ullmann's Encyclopedia of Industrial Chemistry |date=2013 |last1=Falbe |first1=Jürgen |last2=Bahrmann |first2=Helmut |last3=Lipps |first3=Wolfgang |last4=Mayer |first4=Dieter |last5=Frey |first5=Guido D. |isbn=978-3-527-30385-4 }}</ref> |
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==Toxicity== |
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The ] (oral, rats) is about 2.98 g/kg.<ref name=Ullmann/> |
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==References== |
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{{reflist}} |
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{{Alcohols}} |
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{{DEFAULTSORT:Nonanol, 1-}} |
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] |
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] |
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] |