1.0 2010-04-08 22:12:07 UTC 2025-11-19 01:01:35 UTC FDB015894 delta-Carotene Found in carrots and tomatoes delta-Carotene e,y-Carotene Epsilon,psi-carotene C40H56 536.8726 536.438201792 6-[(1E,3Z,5E,7E,9E,11E,13E,15E,17E,19Z)-3,7,12,16,20,24-hexamethylpentacosa-1,3,5,7,9,11,13,15,17,19,23-undecaen-1-yl]-1,5,5-trimethylcyclohex-1-ene 6-[(1E,3Z,5E,7E,9E,11E,13E,15E,17E,19Z)-3,7,12,16,20,24-hexamethylpentacosa-1,3,5,7,9,11,13,15,17,19,23-undecaen-1-yl]-1,5,5-trimethylcyclohex-1-ene 472-92-4 CC(C)=CCC\C(C)=C/C=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(\C)/C=C/C=C(/C)\C=C\C1C(C)=CCCC1(C)C InChI=1S/C40H56/c1-32(2)18-13-21-35(5)24-15-26-36(6)25-14-22-33(3)19-11-12-20-34(4)23-16-27-37(7)29-30-39-38(8)28-17-31-40(39,9)10/h11-12,14-16,18-20,22-30,39H,13,17,21,31H2,1-10H3/b12-11+,22-14+,23-16+,26-15+,30-29+,33-19+,34-20+,35-24-,36-25+,37-27- WGIYGODPCLMGQH-KVLQZIEZSA-N belongs to the class of organic compounds known as carotenes. These are a type of unsaturated hydrocarbons containing eight consecutive isoprene units. They are characterized by the presence of two end-groups (mostly cyclohexene rings, but also cyclopentene rings or acyclic groups) linked by a long branched alkyl chain. Carotenes belonging form a subgroup of the carotenoids family. Carotenes Organic compounds Lipids and lipid-like molecules Prenol lipids Tetraterpenoids Aliphatic homomonocyclic compounds Branched unsaturated hydrocarbons Cycloalkenes Unsaturated aliphatic hydrocarbons Aliphatic homomonocyclic compound Branched unsaturated hydrocarbon Carotene Cyclic olefin Cycloalkene Hydrocarbon Olefin Unsaturated aliphatic hydrocarbon Unsaturated hydrocarbon logp 9.50 ALOGPS logs -6.20 ALOGPS solubility 3.39e-04 g/l ALOGPS melting_point Mp 172° logp 11.57 ChemAxon iupac 6-[(1E,3Z,5E,7E,9E,11E,13E,15E,17E,19Z)-3,7,12,16,20,24-hexamethylpentacosa-1,3,5,7,9,11,13,15,17,19,23-undecaen-1-yl]-1,5,5-trimethylcyclohex-1-ene ChemAxon average_mass 536.8726 ChemAxon mono_mass 536.438201792 ChemAxon smiles CC(C)=CCC\C(C)=C/C=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(\C)/C=C/C=C(/C)\C=C\C1C(C)=CCCC1(C)C ChemAxon formula C40H56 ChemAxon inchi InChI=1S/C40H56/c1-32(2)18-13-21-35(5)24-15-26-36(6)25-14-22-33(3)19-11-12-20-34(4)23-16-27-37(7)29-30-39-38(8)28-17-31-40(39,9)10/h11-12,14-16,18-20,22-30,39H,13,17,21,31H2,1-10H3/b12-11+,22-14+,23-16+,26-15+,30-29+,33-19+,34-20+,35-24-,36-25+,37-27- ChemAxon inchikey WGIYGODPCLMGQH-KVLQZIEZSA-N ChemAxon polar_surface_area 0 ChemAxon refractivity 194.98 ChemAxon polarizability 71.99 ChemAxon rotatable_bond_count 13 ChemAxon acceptor_count 0 ChemAxon donor_count 0 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 11019 Specdb::MsMs 90921 Specdb::MsMs 90922 Specdb::MsMs 90923 Specdb::MsMs 154200 Specdb::MsMs 154201 Specdb::MsMs 154202 HMDB36925 27705 #<Reference:0x00007f093c150b20> #<Reference:0x00007f093c150968> Asparagus Type 1 specific Asparagus officinalis 4686 Bitter gourd Type 1 specific Momordica charantia 3673 Carrot Type 1 specific Daucus carota ssp. sativus 79200 Garden tomato Type 1 specific Solanum lycopersicum 4081 Root vegetables Unknown generic Sea-buckthornberry Type 1 specific Hippophae rhamnoides 193516 Wild carrot Type 1 specific Daucus carota 4039 Colorant 826