| 词条 | Vanillyl alcohol |
| 释义 |
| Name =Vanillyl alcohol | ImageFile = Vanillylalkohol.svg | ImageSize = 150px | ImageAlt = | ImageName = | PIN = 4-(Hydroxymethyl)-2-methoxyphenol | OtherNames = 3-Methoxy-4-hydroxybenzyl alcohol 4-Hydroxy-3-methoxybenzenemethanol 4-Hydroxy-3-methoxybenzyl alcohol Vanillic alcohol Vanillin alcohol |Section1={{Chembox Identifiers | 3DMet = | Abbreviations = | Beilstein = | CASNo =498-00-0 | CASNo_Ref = {{cascite|correct|CAS}} | CASNoOther = | ChEBI = 18353 | ChemSpiderID =56139 | DrugBank = | EC_number = | EINECS = | Gmelin = | InChI =1S/C8H10O3/c1-11-8-4-6(5-9)2-3-7(8)10/h2-4,9-10H,5H2,1H3 | KEGG = | MeSHName = | PubChem =62348 | RTECS = | SMILES = | UNNumber = }} |Section2={{Chembox Properties | AtmosphericOHRateConstant = | Appearance =Crystalline white to off-white powder | BoilingPtC = 293 | BoilingPt_notes = | BoilingPt_ref = [1] | Density = | C=8 | H=10 | O=3 | HenryConstant = | LogP = | MeltingPtC = 113 | MeltingPt_notes = | MeltingPt_ref = [1] | pKa = 9.75[1] | pKb = | Solubility = | SolubleOther = | Solvent = | VaporPressure =}} |Section3={{Chembox Structure | Coordination = | CrystalStruct = | MolShape = }} |Section5={{Chembox Thermochemistry | DeltaHc = | DeltaHf = | Entropy = | HeatCapacity = }} |Section6={{Chembox Pharmacology | ATCvet = | ATCCode_prefix = | ATCCode_suffix = | ATC_Supplemental = | AdminRoutes = | Bioavail = | Excretion = | HalfLife = | Metabolism = | Legal_status = | Legal_US = | Legal_UK = | Legal_AU = | Legal_CA = | Pregnancy_category = | Pregnancy_AU = | Pregnancy_US = | ProteinBound = }} |Section4={{Chembox Explosive | DetonationV = | FrictionSens = | REFactor = | ShockSens = }} |Section7={{Chembox Hazards | AutoignitionPt = | EUClass = | ExploLimits = | ExternalSDS = | FlashPt = | LD50 = | MainHazards = | NFPA-H = | NFPA-F = | NFPA-R = | NFPA-S = | PEL = | RPhrases = | RSPhrases = | SPhrases = }} |Section8={{Chembox Related | OtherFunction_label =phenols | OtherAnions = | OtherCations = | OtherCompounds = | OtherFunction = vanillic acid, vanillin}} }}Vanillyl alcohol is derived from vanillin.[2] It is used to flavor food.[3] See also
References1. ^1 2 http://www.chemicalbook.com/ProductMSDSDetailCB8709532_EN.htm {{alcohol-stub}}2. ^{{cite web | url=https://docs.google.com/viewer?a=v&q=cache:lM7XCO6D92AJ:marian.edu/chemphys/greenchem/Vanillin.pdf+&hl=en&gl=us&pid=bl&srcid=ADGEEShIXdM7gLgZHKl28twxz7yjoxy03oEzgaZ7hiiIeyZuXktebV7j0Xv4FIIj4TYfXF6kdrreGox-X5Yjj8xJteuKEqxAA4U3HFwdcMGRsCbQzBqVwoSZ7bEje1Rensr6EeNxDUGe&sig=AHIEtbQMlIrBYCtUnj_k17MDOalfV_fw9g | title=Microsoft PowerPoint - Borohydride Reduction of Vanillin.ppt | date=2005 | accessdate=January 10, 2013}} 3. ^{{cite web | url=http://www.chemicalbook.com/ProductMSDSDetailCB8709532_EN.htm | title=Vanillyl alcohol(498-00-0) | publisher=Chemical Book | date=2008 | accessdate=January 10, 2013}} 3 : Aromatic alcohols|Phenols|Phenol ethers |
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