Relevant Data

Food Additives Approved in the United States

Flavouring Substances Approved by European Union:

  • Methyl oct-4(cis)-enoate [show]

General Information

Chemical Names: (Z)-METHYL OCT-4-ENOATE
CAS number: 21063-71-8
COE number: 10834
JECFA number: 337
FEMA number: 3367
Functional Class: Flavouring Agent
FLAVOURING_AGENT

From apps.who.int


Evaluations

Evaluation year: 1998
ADI: No safety concern at current levels of intake when used as a flavouring agent
Report: TRS 891-JECFA 51/68
Tox Monograph: FAS 42-JECFA 51/267
Specification: COMPENDIUM ADDENDUM 11/FNP 52 Add.11/96 (2003)

From apps.who.int


Computed Descriptors

Download SDF
2D Structure
CID5352774
IUPAC Namemethyl (Z)-oct-4-enoate
InChIInChI=1S/C9H16O2/c1-3-4-5-6-7-8-9(10)11-2/h5-6H,3-4,7-8H2,1-2H3/b6-5-
InChI KeySSPBQLGVUAXSMH-WAYWQWQTSA-N
Canonical SMILESCCCC=CCCC(=O)OC
Molecular FormulaC9H16O2
Wikipedia(Z)-methyl 4-octenoate

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight156.225
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count6
Complexity128.0
CACTVS Substructure Key Fingerprint A A A D c e B w 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 C I A C D S C A A A A A A g A A A I C A E A A A g A A B A A A Q A A A A A E g A A I A A I 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 = =
Topological Polar Surface Area26.3
Monoisotopic Mass156.115
Exact Mass156.115
XLogP3None
XLogP3-AA2.4
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count11
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count1

From Pubchem


ADMET Predicted Profile --- Classification

Model Result Probability
Absorption
Blood-Brain BarrierBBB+0.9838
Human Intestinal AbsorptionHIA+0.9941
Caco-2 PermeabilityCaco2+0.8177
P-glycoprotein SubstrateNon-substrate0.6747
P-glycoprotein InhibitorNon-inhibitor0.8472
Non-inhibitor0.6780
Renal Organic Cation TransporterNon-inhibitor0.8934
Distribution
Subcellular localizationPlasma membrane0.6788
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8474
CYP450 2D6 SubstrateNon-substrate0.8876
CYP450 3A4 SubstrateNon-substrate0.6171
CYP450 1A2 InhibitorInhibitor0.5466
CYP450 2C9 InhibitorNon-inhibitor0.9433
CYP450 2D6 InhibitorNon-inhibitor0.9530
CYP450 2C19 InhibitorNon-inhibitor0.9415
CYP450 3A4 InhibitorNon-inhibitor0.9705
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.8518
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.8861
Non-inhibitor0.9003
AMES ToxicityNon AMES toxic0.9321
CarcinogensCarcinogens 0.5217
Fish ToxicityHigh FHMT0.9580
Tetrahymena Pyriformis ToxicityHigh TPT0.9958
Honey Bee ToxicityHigh HBT0.7976
BiodegradationReady biodegradable0.8105
Acute Oral ToxicityIII0.6390
Carcinogenicity (Three-class)Non-required0.7273

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-3.8977LogS
Caco-2 Permeability1.2275LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.7357LD50, mol/kg
Fish Toxicity0.3195pLC50, mg/L
Tetrahymena Pyriformis Toxicity1.1527pIGC50, 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