3-HEXENYL 2-HEXENOATE
Relevant Data
Food Additives Approved in the United States
Flavouring Substances Approved by European Union:
General Information
| Chemical Names: | (Z)-3-HEXENYL (E)-2-HEXENOATE |
| CAS number: | 53398-87-1 |
| JECFA number: | 1279 |
| FEMA number: | 3928 |
| Functional Class: |
Flavouring Agent FLAVOURING_AGENT |
From apps.who.int
Evaluations
| Evaluation year: | 2003 |
| ADI: | No safety concern at current levels of intake when used as a flavouring agent |
| Report: | TRS 922-JECFA 61/101 |
| Tox Monograph: | FAS 42-JECFA 51/267 (1998) |
| Specification: | COMPENDIUM ADDENDUM 11/FNP 52 Add. 11/119 |
From apps.who.int
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 5367679 |
| IUPAC Name | [(Z)-hex-3-enyl] (E)-hex-2-enoate |
| InChI | InChI=1S/C12H20O2/c1-3-5-7-9-11-14-12(13)10-8-6-4-2/h5,7-8,10H,3-4,6,9,11H2,1-2H3/b7-5-,10-8+ |
| InChI Key | WAZKUHYKUCORDK-SUTBWYPISA-N |
| Canonical SMILES | CCCC=CC(=O)OCCC=CCC |
| Molecular Formula | C12H20O2 |
| Wikipedia | (3Z,2E)-3-hexenyl 2-hexenoate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 196.29 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 8 |
| Complexity | 193.0 |
| 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 g 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 A A A E g A B A A A I Q A C E A A A w A A I I Y 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 Area | 26.3 |
| Monoisotopic Mass | 196.146 |
| Exact Mass | 196.146 |
| XLogP3 | None |
| XLogP3-AA | 3.7 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 14 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 2 |
| Undefined Bond Stereocenter Count | 0 |
| Isotope Atom Count | 0 |
| Covalently-Bonded Unit Count | 1 |
From Pubchem
ADMET Predicted Profile --- Classification
| Model | Result | Probability |
|---|---|---|
| Absorption | ||
| Blood-Brain Barrier | BBB+ | 0.9842 |
| Human Intestinal Absorption | HIA+ | 0.9968 |
| Caco-2 Permeability | Caco2+ | 0.7984 |
| P-glycoprotein Substrate | Non-substrate | 0.7344 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8578 |
| Non-inhibitor | 0.7596 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8886 |
| Distribution | ||
| Subcellular localization | Plasma membrane | 0.5104 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8639 |
| CYP450 2D6 Substrate | Non-substrate | 0.9008 |
| CYP450 3A4 Substrate | Non-substrate | 0.6194 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.5000 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9408 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9266 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9403 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9431 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.7162 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8888 |
| Non-inhibitor | 0.8852 | |
| AMES Toxicity | Non AMES toxic | 0.8177 |
| Carcinogens | Carcinogens | 0.5838 |
| Fish Toxicity | High FHMT | 0.8717 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9804 |
| Honey Bee Toxicity | High HBT | 0.7835 |
| Biodegradation | Ready biodegradable | 0.9052 |
| Acute Oral Toxicity | III | 0.7494 |
| Carcinogenicity (Three-class) | Non-required | 0.5692 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.3945 | LogS |
| Caco-2 Permeability | 1.2636 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.5264 | LD50, mol/kg |
| Fish Toxicity | 0.5557 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.3035 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Fatty Acyls |
| Subclass | Fatty acid esters |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Fatty acid esters |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Fatty acid ester - Alpha,beta-unsaturated carboxylic ester - Enoate 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 |
| Description | This compound belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid. |
From ClassyFire