Relevant Data

Food Additives Approved in the United States:

Food Additives Approved by WHO:


General Information

Chemical nameMethyl hexanoate
CAS number106-70-7
COE number319
JECFA number1871
Flavouring typesubstances
FL No.09.069
MixtureNo
Purity of the named substance at least 95% unless otherwise specified

From webgate.ec.europa.eu

Computed Descriptors

Download SDF
2D Structure
CID7824
IUPAC Namemethyl hexanoate
InChIInChI=1S/C7H14O2/c1-3-4-5-6-7(8)9-2/h3-6H2,1-2H3
InChI KeyNUKZAGXMHTUAFE-UHFFFAOYSA-N
Canonical SMILESCCCCCC(=O)OC
Molecular FormulaC7H14O2

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight130.187
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count5
Complexity79.0
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 A A A A C A C A g A I C C A A A B A 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 A B I A A A A A A A A E A 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 Area26.3
Monoisotopic Mass130.099
Exact Mass130.099
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count9
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
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+0.9880
Human Intestinal AbsorptionHIA+0.9859
Caco-2 PermeabilityCaco2+0.8050
P-glycoprotein SubstrateNon-substrate0.6885
P-glycoprotein InhibitorNon-inhibitor0.9029
Non-inhibitor0.9101
Renal Organic Cation TransporterNon-inhibitor0.9049
Distribution
Subcellular localizationMitochondria0.4752
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8538
CYP450 2D6 SubstrateNon-substrate0.8884
CYP450 3A4 SubstrateNon-substrate0.6393
CYP450 1A2 InhibitorNon-inhibitor0.5637
CYP450 2C9 InhibitorNon-inhibitor0.9369
CYP450 2D6 InhibitorNon-inhibitor0.9475
CYP450 2C19 InhibitorNon-inhibitor0.9449
CYP450 3A4 InhibitorNon-inhibitor0.9820
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.9109
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9378
Non-inhibitor0.8925
AMES ToxicityNon AMES toxic0.9679
CarcinogensCarcinogens 0.5528
Fish ToxicityHigh FHMT0.7234
Tetrahymena Pyriformis ToxicityLow TPT0.6846
Honey Bee ToxicityHigh HBT0.7641
BiodegradationReady biodegradable0.8920
Acute Oral ToxicityIII0.9021
Carcinogenicity (Three-class)Non-required0.6829

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-2.0627LogS
Caco-2 Permeability1.3418LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.4471LD50, mol/kg
Fish Toxicity1.4969pLC50, mg/L
Tetrahymena Pyriformis Toxicity-0.2506pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
ClassFatty Acyls
SubclassFatty acid esters
Intermediate Tree NodesNot available
Direct ParentFatty acid methyl esters
Alternative Parents
Molecular FrameworkAliphatic acyclic compounds
SubstituentsFatty acid methyl ester - Methyl ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as fatty acid methyl esters. These are compounds containing a fatty acid that is esterified with a methyl group. They have the general structure RC(=O)OR', where R=fatty aliphatic tail or organyl group and R'=methyl group.

From ClassyFire