1.0 2010-04-08 22:09:20 UTC 2015-07-20 22:35:58 UTC FDB010859 all-trans-Carophyll yellow Colour additive for foods, e.g. egg yolks 8'-Apo-beta, psi-carotenoid acid, ethyl ester all-trans Carophyll yellow beta-Apo-8'-carotenoic acid, ethyl ester C.I. Food Orange 7 Ethyl 8'-apo-beta-caroten-8'-oate Ethyl 8'-apo-beta, psi-carotenoate Food orange 7 C32H44O2 460.6906 460.334130652 ethyl (2E,4E,6E,8E,10E,12E,14Z,16E)-2,6,11,15-tetramethyl-17-(2,6,6-trimethylcyclohex-1-en-1-yl)heptadeca-2,4,6,8,10,12,14,16-octaenoate ethyl (2E,4E,6E,8E,10E,12E,14Z,16E)-2,6,11,15-tetramethyl-17-(2,6,6-trimethylcyclohex-1-en-1-yl)heptadeca-2,4,6,8,10,12,14,16-octaenoate 1109-11-1 CCOC(=O)C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C InChI=1S/C32H44O2/c1-9-34-31(33)29(6)20-13-19-26(3)16-11-10-15-25(2)17-12-18-27(4)22-23-30-28(5)21-14-24-32(30,7)8/h10-13,15-20,22-23H,9,14,21,24H2,1-8H3/b11-10+,17-12+,19-13+,23-22+,25-15+,26-16+,27-18-,29-20+ GIRXTOSJOKKBHO-GUCZFGIOSA-N belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Triterpenoids Organic compounds Lipids and lipid-like molecules Prenol lipids Triterpenoids Aliphatic homomonocyclic compounds Carbonyl compounds Enoate esters Fatty acid esters Hydrocarbon derivatives Monocarboxylic acids and derivatives Organic oxides Aliphatic homomonocyclic compound Alpha,beta-unsaturated carboxylic ester Carbonyl group Carboxylic acid derivative Carboxylic acid ester Enoate ester Fatty acid ester Fatty acyl Hydrocarbon derivative Monocarboxylic acid or derivatives Organic oxide Organic oxygen compound Organooxygen compound Triterpenoid logp 8.35 ALOGPS logs -5.87 ALOGPS solubility 6.18e-04 g/l ALOGPS melting_point Mp 137-138° logp 8.5 ChemAxon pka_strongest_basic -6.9 ChemAxon iupac ethyl (2E,4E,6E,8E,10E,12E,14Z,16E)-2,6,11,15-tetramethyl-17-(2,6,6-trimethylcyclohex-1-en-1-yl)heptadeca-2,4,6,8,10,12,14,16-octaenoate ChemAxon average_mass 460.6906 ChemAxon mono_mass 460.334130652 ChemAxon smiles CCOC(=O)C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C ChemAxon formula C32H44O2 ChemAxon inchi InChI=1S/C32H44O2/c1-9-34-31(33)29(6)20-13-19-26(3)16-11-10-15-25(2)17-12-18-27(4)22-23-30-28(5)21-14-24-32(30,7)8/h10-13,15-20,22-23H,9,14,21,24H2,1-8H3/b11-10+,17-12+,19-13+,23-22+,25-15+,26-16+,27-18-,29-20+ ChemAxon inchikey GIRXTOSJOKKBHO-GUCZFGIOSA-N ChemAxon polar_surface_area 26.3 ChemAxon refractivity 157.22 ChemAxon polarizability 59.15 ChemAxon rotatable_bond_count 11 ChemAxon acceptor_count 1 ChemAxon donor_count 0 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 14477 Specdb::CMs 132018 Specdb::CMs 139752 Specdb::MsMs 66246 Specdb::MsMs 66247 Specdb::MsMs 66248 Specdb::MsMs 123759 Specdb::MsMs 123760 Specdb::MsMs 123761 Specdb::MsMs 2837766 Specdb::MsMs 2837767 Specdb::MsMs 2837768 Specdb::MsMs 2868690 Specdb::MsMs 2868691 Specdb::MsMs 2868692 HMDB32879 #<Reference:0x000055ce30530670>