1.0 2010-04-08 22:12:18 UTC 2019-11-26 03:12:53 UTC FDB016221 cis-beta-Terpineol Terpineol 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)-&beta;-Terpineol (Z)-beta-Terpineol cis-&beta;-Tterpineol cis-beta-Tterpineol cis-p-Menth-8-en-1-ol p-Menth-8-en-1-ol; cis-form Terpineol, cis-&beta;- C10H18O 154.2493 154.135765198 (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-ol 7299-41-4 CC(=C)[C@H]1CC[C@](C)(O)CC1 InChI=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 monoterpenoids Organic compounds Lipids and lipid-like molecules Prenol lipids Monoterpenoids Aliphatic homomonocyclic compounds Cyclic alcohols and derivatives Cyclohexanols Hydrocarbon derivatives Monocyclic monoterpenoids Tertiary alcohols Alcohol Aliphatic homomonocyclic compound Cyclic alcohol Cyclohexanol Hydrocarbon derivative Monocyclic monoterpenoid Organic oxygen compound Organooxygen compound P-menthane monoterpenoid Tertiary alcohol logp 2.73 ALOGPS logs -2.19 ALOGPS solubility 9.90e-01 g/l ALOGPS melting_point Mp 36° logp 2.23 ChemAxon pka_strongest_acidic 19 ChemAxon pka_strongest_basic -1 ChemAxon iupac (1r,4r)-1-methyl-4-(prop-1-en-2-yl)cyclohexan-1-ol ChemAxon average_mass 154.2493 ChemAxon mono_mass 154.135765198 ChemAxon smiles CC(=C)[C@H]1CC[C@](C)(O)CC1 ChemAxon formula C10H18O ChemAxon inchi InChI=1S/C10H18O/c1-8(2)9-4-6-10(3,11)7-5-9/h9,11H,1,4-7H2,2-3H3/t9-,10- ChemAxon inchikey RUJPNZNXGCHGID-MGCOHNPYSA-N ChemAxon polar_surface_area 20.23 ChemAxon refractivity 47.39 ChemAxon polarizability 18.8 ChemAxon rotatable_bond_count 1 ChemAxon acceptor_count 1 ChemAxon donor_count 1 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::MsIr 7467 Specdb::MsIr 7468 Specdb::MsIr 7469 Specdb::CMs 22715 Specdb::CMs 45268 Specdb::CMs 134128 Specdb::CMs 141862 Specdb::CMs 170689 Specdb::MsMs 52290 Specdb::MsMs 52291 Specdb::MsMs 52292 Specdb::MsMs 168744 Specdb::MsMs 168745 Specdb::MsMs 168746 Specdb::MsMs 2273955 Specdb::MsMs 2273956 Specdb::MsMs 2273957 Specdb::MsMs 2373144 Specdb::MsMs 2373145 Specdb::MsMs 2373146 HMDB37214 #<Reference:0x000055ce31e90c28> Caraway Type 1 specific Carum carvi 48032 Common sage Type 1 specific Salvia officinalis 38868 3.3 3.3 3.3 mg/100 g Rosemary Type 1 specific Rosmarinus officinalis 39367 5.75 5.75 5.75 mg/100 g