1.02010-04-08 22:12:18 UTC2019-11-26 03:12:53 UTCFDB016221cis-beta-TerpineolTerpineol is a naturally occurring monoterpene alcohol that has been isolated from a variety of sources such as cajuput oil, pine oil, and petitgrain oil. There are three isomers, alpha-, beta-, and gamma-terpineol, the last two differing only by the location of the double bond. Terpineol is usually a mixture of these isomers with alpha-terpineol as the major constituent. cis-beta-Terpineol is found in caraway, rosemary, and common sage.(Z)-β-Terpineol(Z)-beta-Terpineolcis-β-Tterpineolcis-beta-Tterpineolcis-p-Menth-8-en-1-olp-Menth-8-en-1-ol; cis-formTerpineol, cis-β-C10H18O154.2493154.135765198(1r,4r)-1-methyl-4-(prop-1-en-2-yl)cyclohexan-1-ol(1r,4r)-1-methyl-4-(prop-1-en-2-yl)cyclohexan-1-ol7299-41-4CC(=C)[C@H]1CC[C@](C)(O)CC1InChI=1S/C10H18O/c1-8(2)9-4-6-10(3,11)7-5-9/h9,11H,1,4-7H2,2-3H3/t9-,10-RUJPNZNXGCHGID-MGCOHNPYSA-N belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes.Menthane monoterpenoidsOrganic compoundsLipids and lipid-like moleculesPrenol lipidsMonoterpenoidsAliphatic homomonocyclic compoundsCyclic alcohols and derivativesCyclohexanolsHydrocarbon derivativesMonocyclic monoterpenoidsTertiary alcoholsAlcoholAliphatic homomonocyclic compoundCyclic alcoholCyclohexanolHydrocarbon derivativeMonocyclic monoterpenoidOrganic oxygen compoundOrganooxygen compoundP-menthane monoterpenoidTertiary alcohollogp2.73logs-2.19solubility9.90e-01 g/lmelting_pointMp 36°logp2.23pka_strongest_acidic19pka_strongest_basic-1iupac(1r,4r)-1-methyl-4-(prop-1-en-2-yl)cyclohexan-1-olaverage_mass154.2493mono_mass154.135765198smilesCC(=C)[C@H]1CC[C@](C)(O)CC1formulaC10H18OinchiInChI=1S/C10H18O/c1-8(2)9-4-6-10(3,11)7-5-9/h9,11H,1,4-7H2,2-3H3/t9-,10-inchikeyRUJPNZNXGCHGID-MGCOHNPYSA-Npolar_surface_area20.23refractivity47.39polarizability18.8rotatable_bond_count1acceptor_count1donor_count1physiological_charge0formal_charge0Specdb::MsIr7467Specdb::MsIr7468Specdb::MsIr7469Specdb::MsMs52290Specdb::MsMs52291Specdb::MsMs52292Specdb::MsMs168744Specdb::MsMs168745Specdb::MsMs168746Specdb::MsMs2273955Specdb::MsMs2273956Specdb::MsMs2273957Specdb::MsMs2373144Specdb::MsMs2373145Specdb::MsMs2373146Specdb::CMs22715Specdb::CMs45268Specdb::CMs134128Specdb::CMs141862Specdb::CMs170689HMDB37214#<Reference:0x0000555675d97ad0>CarawayType 1specificCarum carvi48032Common sageType 1specificSalvia officinalis388683.33.33.3mg/100 gRosemaryType 1specificRosmarinus officinalis393675.755.755.75mg/100 g