1.0 2010-04-08 22:10:54 UTC 2025-11-19 00:35:13 UTC FDB013779 2-Methyl-gamma-butyrolactone Present in Mangifera indica (mango). 2-Methyl-gamma-butyrolactone is found in fruits. 2-Methyl-&laquo;gamma&raquo;-butyrolactone 2-Methyl-4-butanolide 2-Methyl-gamma-butyrolactone 2-Methyl-laquo gammaraquo -butyrolactone 2-Methylbutanolide 2(3H)-Furanone, dihydro-3-methyl- 3-Methyldihydro-2(3H)-furanone 3-Methyldihydrofuran-2(3H)-one 4-Hydroxy-2-methylbutanoic acid lactone 4-Hydroxy-2-methylbutyric acid lactone 4,5-Dihydro-3-methyl-2(3H)-furanone a-Methyl-g-butyrolactone alpha -Methyl-alpha -methylbutyrolactone alpha -Methyl-laquo gammaraquo -butyrolactone alpha -Methylbutyrolactone alpha-Methyl-gamma-butyrolactone Dihydro-3-methyl-2(3H)-furanone C5H8O2 100.1158 100.0524295 3-methyloxolan-2-one 3-methylbutyrolactone 1679-47-6 CC1CCOC1=O InChI=1S/C5H8O2/c1-4-2-3-7-5(4)6/h4H,2-3H2,1H3 QGLBZNZGBLRJGS-UHFFFAOYSA-N belongs to the class of organic compounds known as gamma butyrolactones. Gamma butyrolactones are compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-member ring with four carbon atoms, one oxygen atom, and bears a ketone group on the carbon adjacent to the oxygen atom. Gamma butyrolactones Organic compounds Organoheterocyclic compounds Lactones Gamma butyrolactones Aliphatic heteromonocyclic compounds Carbonyl compounds Carboxylic acid esters Hydrocarbon derivatives Monocarboxylic acids and derivatives Organic oxides Oxacyclic compounds Tetrahydrofurans Aliphatic heteromonocyclic compound Carbonyl group Carboxylic acid derivative Carboxylic acid ester Gamma butyrolactone Hydrocarbon derivative Monocarboxylic acid or derivatives Organic oxide Organic oxygen compound Organooxygen compound Oxacycle Tetrahydrofuran logp 0.36 ALOGPS logs -0.03 ALOGPS solubility 9.31e+01 g/l ALOGPS logp 0.69 ChemAxon pka_strongest_basic -7.1 ChemAxon iupac 3-methyloxolan-2-one ChemAxon average_mass 100.1158 ChemAxon mono_mass 100.0524295 ChemAxon smiles CC1CCOC1=O ChemAxon formula C5H8O2 ChemAxon inchi InChI=1S/C5H8O2/c1-4-2-3-7-5(4)6/h4H,2-3H2,1H3 ChemAxon inchikey QGLBZNZGBLRJGS-UHFFFAOYSA-N ChemAxon polar_surface_area 26.3 ChemAxon refractivity 24.88 ChemAxon polarizability 10.09 ChemAxon rotatable_bond_count 0 ChemAxon acceptor_count 1 ChemAxon donor_count 0 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 19418 Specdb::CMs 136183 Specdb::CMs 143917 Specdb::MsIr 6817 Specdb::MsIr 6818 Specdb::MsMs 100275 Specdb::MsMs 100276 Specdb::MsMs 100277 Specdb::MsMs 165552 Specdb::MsMs 165553 Specdb::MsMs 165554 Specdb::MsMs 2382350 Specdb::MsMs 2382351 Specdb::MsMs 2382352 Specdb::MsMs 2579946 Specdb::MsMs 2579947 Specdb::MsMs 2579948 Specdb::NmrOneD 130138 Specdb::NmrOneD 130139 Specdb::NmrOneD 130140 Specdb::NmrOneD 130141 Specdb::NmrOneD 130142 Specdb::NmrOneD 130143 Specdb::NmrOneD 130144 Specdb::NmrOneD 130145 Specdb::NmrOneD 130146 Specdb::NmrOneD 130147 Specdb::NmrOneD 130148 Specdb::NmrOneD 130149 Specdb::NmrOneD 130150 Specdb::NmrOneD 130151 Specdb::NmrOneD 130152 Specdb::NmrOneD 130153 Specdb::NmrOneD 130154 Specdb::NmrOneD 130155 Specdb::NmrOneD 130156 Specdb::NmrOneD 130157 HMDB35143 #<Reference:0x000055ce307d66e0> Fruits Unknown generic