1.0 2010-04-08 22:12:06 UTC 2019-11-26 03:12:22 UTC FDB015878 Triphasiaxanthin Constituent of fruit of Triphasia trifolia (limeberry). Triphasiaxanthin is found in fruits. 3-Hydroxysemi-b-carotenone 3'-Hydroxy-5,6-seco-b,b-carotene-5,6-dione C40H56O3 584.8708 584.422945658 (8E,10E,12E,14E,16E,18E,20E,22Z,24E)-25-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-6,6,10,14,19,23-hexamethylpentacosa-8,10,12,14,16,18,20,22,24-nonaene-2,7-dione (8E,10E,12E,14E,16E,18E,20E,22Z,24E)-25-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-6,6,10,14,19,23-hexamethylpentacosa-8,10,12,14,16,18,20,22,24-nonaene-2,7-dione 23939-69-7 CC(=O)CCCC(C)(C)C(=O)\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CC(O)CC1(C)C InChI=1S/C40H56O3/c1-30(18-13-20-32(3)23-25-37-34(5)28-36(42)29-40(37,9)10)16-11-12-17-31(2)19-14-21-33(4)24-26-38(43)39(7,8)27-15-22-35(6)41/h11-14,16-21,23-26,36,42H,15,22,27-29H2,1-10H3/b12-11+,18-13+,19-14+,25-23+,26-24+,30-16+,31-17+,32-20-,33-21+ DSSJLYAIYPLGLX-BEWVHMHCSA-N belongs to the class of organic compounds known as sesquaterpenoids. These are terpenoids with at least 7 consecutive isoprene units. Sesquaterpenoids Organic compounds Lipids and lipid-like molecules Prenol lipids Sesquaterpenoids Aliphatic homomonocyclic compounds Acryloyl compounds Enones Hydrocarbon derivatives Ketones Organic oxides Secondary alcohols Acryloyl-group Alcohol Aliphatic homomonocyclic compound Alpha,beta-unsaturated ketone Carbonyl group Enone Hydrocarbon derivative Ketone Organic oxide Organic oxygen compound Organooxygen compound Secondary alcohol Sesquaterpenoid logp 8.44 ALOGPS logs -6.08 ALOGPS solubility 4.83e-04 g/l ALOGPS melting_point Mp 95-97° logp 9.22 ChemAxon pka_strongest_acidic 18.91 ChemAxon pka_strongest_basic -1.1 ChemAxon iupac (8E,10E,12E,14E,16E,18E,20E,22Z,24E)-25-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-6,6,10,14,19,23-hexamethylpentacosa-8,10,12,14,16,18,20,22,24-nonaene-2,7-dione ChemAxon average_mass 584.8708 ChemAxon mono_mass 584.422945658 ChemAxon smiles CC(=O)CCCC(C)(C)C(=O)\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CC(O)CC1(C)C ChemAxon formula C40H56O3 ChemAxon inchi InChI=1S/C40H56O3/c1-30(18-13-20-32(3)23-25-37-34(5)28-36(42)29-40(37,9)10)16-11-12-17-31(2)19-14-21-33(4)24-26-38(43)39(7,8)27-15-22-35(6)41/h11-14,16-21,23-26,36,42H,15,22,27-29H2,1-10H3/b12-11+,18-13+,19-14+,25-23+,26-24+,30-16+,31-17+,32-20-,33-21+ ChemAxon inchikey DSSJLYAIYPLGLX-BEWVHMHCSA-N ChemAxon polar_surface_area 54.37 ChemAxon refractivity 195.89 ChemAxon polarizability 74.54 ChemAxon rotatable_bond_count 15 ChemAxon acceptor_count 3 ChemAxon donor_count 1 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 80139 Specdb::MsMs 80140 Specdb::MsMs 80141 Specdb::MsMs 140922 Specdb::MsMs 140923 Specdb::MsMs 140924 Specdb::MsMs 2827227 Specdb::MsMs 2827228 Specdb::MsMs 2827229 Specdb::MsMs 2851606 Specdb::MsMs 2851607 Specdb::MsMs 2851608 Specdb::CMs 23731 Specdb::CMs 45123 Specdb::CMs 282754 Specdb::CMs 407915 Specdb::CMs 407916 Specdb::CMs 407917 Specdb::CMs 407918 Specdb::CMs 407919 HMDB36914 #<Reference:0x000055ce3322d5d8> Fruits Unknown generic