Relevant Data

Food Additives Approved by WHO:

Flavouring Substances Approved by European Union:

  • Methyl 3-hydroxyhexanoate [show]

General Information

MaintermMETHYL 3-HYDROXYHEXANOATE
Doc TypeASP
CAS Reg.No.(or other ID)21188-58-9
Regnum

From www.fda.gov

Computed Descriptors

Download SDF
2D Structure
CID519845
IUPAC Namemethyl 3-hydroxyhexanoate
InChIInChI=1S/C7H14O3/c1-3-4-6(8)5-7(9)10-2/h6,8H,3-5H2,1-2H3
InChI KeyACCRBMDJCPPJDX-UHFFFAOYSA-N
Canonical SMILESCCCC(CC(=O)OC)O
Molecular FormulaC7H14O3
Wikipediamethyl 3-hydroxyhexanoate

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight146.186
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count5
Complexity101.0
CACTVS Substructure Key Fingerprint A A A D c c B g M A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A G g A A C A A A C B S g g A I C C A A A B g A I A A C Q C A A A A A A A A A A A A A E A A A A A E B Y A A A A A Q A A F I A A A A A G I S A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A = =
Topological Polar Surface Area46.5
Monoisotopic Mass146.094
Exact Mass146.094
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count10
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count1

From Pubchem


ADMET Predicted Profile --- Classification

Model Result Probability
Absorption
Blood-Brain BarrierBBB+0.9574
Human Intestinal AbsorptionHIA+0.9859
Caco-2 PermeabilityCaco2+0.7078
P-glycoprotein SubstrateNon-substrate0.5546
P-glycoprotein InhibitorNon-inhibitor0.8379
Non-inhibitor0.7735
Renal Organic Cation TransporterNon-inhibitor0.9255
Distribution
Subcellular localizationMitochondria0.7292
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8691
CYP450 2D6 SubstrateNon-substrate0.8830
CYP450 3A4 SubstrateNon-substrate0.6410
CYP450 1A2 InhibitorNon-inhibitor0.7300
CYP450 2C9 InhibitorNon-inhibitor0.9161
CYP450 2D6 InhibitorNon-inhibitor0.9450
CYP450 2C19 InhibitorNon-inhibitor0.9175
CYP450 3A4 InhibitorNon-inhibitor0.9681
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.9440
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9651
Non-inhibitor0.8633
AMES ToxicityNon AMES toxic0.9546
CarcinogensNon-carcinogens0.6559
Fish ToxicityHigh FHMT0.5834
Tetrahymena Pyriformis ToxicityHigh TPT0.9340
Honey Bee ToxicityHigh HBT0.7536
BiodegradationReady biodegradable0.9314
Acute Oral ToxicityIII0.4973
Carcinogenicity (Three-class)Non-required0.6875

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-1.5722LogS
Caco-2 Permeability1.0852LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.9355LD50, mol/kg
Fish Toxicity2.2570pLC50, mg/L
Tetrahymena Pyriformis Toxicity0.4163pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClassHydroxy acids and derivatives
SubclassBeta hydroxy acids and derivatives
Intermediate Tree NodesNot available
Direct ParentBeta hydroxy acids and derivatives
Alternative Parents
Molecular FrameworkAliphatic acyclic compounds
SubstituentsBeta-hydroxy acid - Fatty acid ester - Fatty acid methyl ester - Fatty acyl - Methyl ester - Carboxylic acid ester - Secondary alcohol - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Organic oxide - Alcohol - Carbonyl group - Organic oxygen compound - Organooxygen compound - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as beta hydroxy acids and derivatives. These are compounds containing a carboxylic acid substituted with a hydroxyl group on the C3 carbon atom.

From ClassyFire