1.0 2010-04-08 22:14:29 UTC 2025-11-19 02:23:00 UTC FDB019653 (1S,2R,4R,8S)-p-Menthane-2,8,9-triol 9-glucoside Constituent of fruit of Carum carvi (caraway). (1S,2R,4R,8S)-p-Menthane-2,8,9-triol 9-glucoside is found in fats and oils and herbs and spices. (1S,2R,4R,8S)-p-Menthane-2,8,9-triol 9-glucoside (1S,2R,4R,8S)-p-Menthane-2,8,9-triol 9-O-b-D-glucopyranoside (1S,2R,4R,8S)-p-Menthane-2,8,9-triol 9-O-b-D-glucoside C16H30O8 350.4046 350.194067936 2-[2-hydroxy-2-(3-hydroxy-4-methylcyclohexyl)propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 2-[2-hydroxy-2-(3-hydroxy-4-methylcyclohexyl)propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 378254-08-1 CC1CCC(CC1O)C(C)(O)COC1OC(CO)C(O)C(O)C1O InChI=1S/C16H30O8/c1-8-3-4-9(5-10(8)18)16(2,22)7-23-15-14(21)13(20)12(19)11(6-17)24-15/h8-15,17-22H,3-7H2,1-2H3 KRTKKVIKRTZKGY-UHFFFAOYSA-N belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone. Terpene glycosides Organic compounds Lipids and lipid-like molecules Prenol lipids Terpene glycosides Aliphatic heteromonocyclic compounds Acetals Cyclic alcohols and derivatives Cyclohexanols Hexoses Hydrocarbon derivatives Menthane monoterpenoids Monocyclic monoterpenoids O-glycosyl compounds Oxacyclic compounds Oxanes Polyols Primary alcohols Tertiary alcohols Acetal Alcohol Aliphatic heteromonocyclic compound Cyclic alcohol Cyclohexanol Glycosyl compound Hexose monosaccharide Hydrocarbon derivative Monocyclic monoterpenoid Monosaccharide Monoterpenoid O-glycosyl compound Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Oxane P-menthane monoterpenoid Polyol Primary alcohol Secondary alcohol Terpene glycoside Tertiary alcohol logp -1.36 ALOGPS logs -1.09 ALOGPS solubility 2.83e+01 g/l ALOGPS logp -1.5 ChemAxon pka_strongest_acidic 12.2 ChemAxon pka_strongest_basic -2.8 ChemAxon iupac 2-[2-hydroxy-2-(3-hydroxy-4-methylcyclohexyl)propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol ChemAxon average_mass 350.4046 ChemAxon mono_mass 350.194067936 ChemAxon smiles CC1CCC(CC1O)C(C)(O)COC1OC(CO)C(O)C(O)C1O ChemAxon formula C16H30O8 ChemAxon inchi InChI=1S/C16H30O8/c1-8-3-4-9(5-10(8)18)16(2,22)7-23-15-14(21)13(20)12(19)11(6-17)24-15/h8-15,17-22H,3-7H2,1-2H3 ChemAxon inchikey KRTKKVIKRTZKGY-UHFFFAOYSA-N ChemAxon polar_surface_area 139.84 ChemAxon refractivity 83.16 ChemAxon polarizability 36.56 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 8 ChemAxon donor_count 6 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 24435 Specdb::CMs 46670 Specdb::CMs 162611 Specdb::MsMs 320065 Specdb::MsMs 320066 Specdb::MsMs 320067 Specdb::MsMs 367375 Specdb::MsMs 367376 Specdb::MsMs 367377 Specdb::MsMs 2764356 Specdb::MsMs 2764357 Specdb::MsMs 2764358 Specdb::MsMs 2941489 Specdb::MsMs 2941490 Specdb::MsMs 2941491 Specdb::NmrOneD 37502 Specdb::NmrOneD 37503 Specdb::NmrOneD 37504 Specdb::NmrOneD 37505 Specdb::NmrOneD 37506 Specdb::NmrOneD 37507 Specdb::NmrOneD 37508 Specdb::NmrOneD 37509 Specdb::NmrOneD 37510 Specdb::NmrOneD 37511 Specdb::NmrOneD 37512 Specdb::NmrOneD 37513 Specdb::NmrOneD 37514 Specdb::NmrOneD 37515 Specdb::NmrOneD 37516 Specdb::NmrOneD 37517 Specdb::NmrOneD 37518 Specdb::NmrOneD 37519 Specdb::NmrOneD 37520 Specdb::NmrOneD 37521 HMDB39978 #<Reference:0x000055ce317cd828> Fats and oils Unknown generic Herbs and Spices Unknown generic