{"ymdb_id":"YMDB16026","created_at":"2016-08-03T23:52:03.000Z","updated_at":"2016-09-11T18:50:57.000Z","name":"Isobutyl butanoate","cas":null,"state":null,"melting_point":null,"description":"Isobutyl butanoate belongs to the class of chemical entities known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid.","experimental_water_solubility":null,"experimental_logp_hydrophobicity":null,"location":null,"synthesis_reference":null,"chebi_id":null,"hmdb_id":null,"kegg_id":null,"pubchem_id":null,"cs_id":null,"foodb_id":null,"wikipedia_link":null,"biocyc_id":null,"iupac":"2-methylpropyl butanoate","traditional_iupac":"2-methylpropyl butanoate","logp":"2.311956029666666","pka":null,"alogps_solubility":"1.72e+00 g/l","alogps_logp":"2.65","alogps_logs":"-1.92","acceptor_count":"1","donor_count":"0","rotatable_bond_count":"5","polar_surface_area":"26.3","refractivity":"40.38490000000001","polarizability":"17.06426819150894","formal_charge":"0","physiological_charge":"0","pka_strongest_basic":"-7.033186743608634","pka_strongest_acidic":null,"bioavailability":"1","number_of_rings":"0","rule_of_five":"1","ghose_filter":"0","veber_rule":"1","mddr_like_rule":"0","synonyms":[],"pathways":[],"growth_conditions":[],"references":[{"pubmed_id":19845354,"citation":"Robinson AL, Ebeler SE, Heymann H, Boss PK, Solomon PS, Trengove RD. (2009). \"Interactions between wine volatile compounds and grape and wine matrix components influence aroma compound headspace partitioning.\" J Agric Food Chem. 2009 Nov 11;57(21):10313-22."}],"proteins":[]}