1.0 2016-09-30 22:31:22 UTC 2020-03-13 16:21:30 UTC BMDB0000480 BMDB00480 7,10-Hexadecadienoic acid 7,10-Hexadecadienoate C16H28O2 252.398 252.208930142 (7E,10E)-hexadeca-7,10-dienoic acid 7,10-hexadecadienoic acid [H]\C(CCCCC)=C(\[H])C\C([H])=C(/[H])CCCCCC(O)=O InChI=1S/C16H28O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h6-7,9-10H,2-5,8,11-15H2,1H3,(H,17,18)/b7-6+,10-9+ WPJGPAAPSBVXNU-AVQMFFATSA-N belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms. Organic compounds Lipids and lipid-like molecules Fatty Acyls Fatty acids and conjugates Long-chain fatty acids Carbonyl compounds Carboxylic acids Hydrocarbon derivatives Monocarboxylic acids and derivatives Organic oxides Straight chain fatty acids Unsaturated fatty acids Aliphatic acyclic compound Carbonyl group Carboxylic acid Carboxylic acid derivative Hydrocarbon derivative Long-chain fatty acid Monocarboxylic acid or derivatives Organic oxide Organic oxygen compound Organooxygen compound Straight chain fatty acid Unsaturated fatty acid Aliphatic acyclic compounds Unsaturated fatty acids Solid logp 6.23 ALOGPS logs -5.58 ALOGPS logp 5.53 ChemAxon pka_strongest_acidic 4.96 ChemAxon iupac (7E,10E)-hexadeca-7,10-dienoic acid ChemAxon average_mass 252.398 ChemAxon mono_mass 252.208930142 ChemAxon smiles [H]\C(CCCCC)=C(\[H])C\C([H])=C(/[H])CCCCCC(O)=O ChemAxon formula C16H28O2 ChemAxon inchi InChI=1S/C16H28O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h6-7,9-10H,2-5,8,11-15H2,1H3,(H,17,18)/b7-6+,10-9+ ChemAxon inchikey WPJGPAAPSBVXNU-AVQMFFATSA-N ChemAxon polar_surface_area 37.3 ChemAxon refractivity 79.32 ChemAxon polarizability 31.24 ChemAxon rotatable_bond_count 12 ChemAxon acceptor_count 2 ChemAxon donor_count 1 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon number_of_rings 0 ChemAxon bioavailability 0 ChemAxon rule_of_five Yes ChemAxon ghose_filter Yes ChemAxon veber_rule Yes ChemAxon mddr_like_rule Yes ChemAxon Specdb::MsMs 1297693 Specdb::MsMs 1297694 Specdb::MsMs 1297695 Specdb::MsMs 1412314 Specdb::MsMs 1412315 Specdb::MsMs 1412316 13932171 Myagkova, G. I.; Novozhilov, A. V.; Bainova, M. S.; Bazilevskaya, G. I.; Yakimenko, S. M.; Preobrazhenskii, N. A. Synthesis of aliphatic acids. XXIII. New process for synthesizing linoleic acid and substituted linoleic acids. Biol. Aktiv. Soedin. (1968), 3-6.