Ethyl 2-ethyl-3-phenylpropionate
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | Ethyl 2-ethyl-3-phenylpropionate |
| CAS number | 2983-36-0 |
| COE number | 10587 |
| JECFA number | 1475 |
| Flavouring type | substances |
| FL No. | 09.802 |
| Mixture | No |
| Purity of the named substance at least 95% unless otherwise specified | |
| Reference body | EFSA |
From webgate.ec.europa.eu
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 62469 |
| IUPAC Name | ethyl 2-benzylbutanoate |
| InChI | InChI=1S/C13H18O2/c1-3-12(13(14)15-4-2)10-11-8-6-5-7-9-11/h5-9,12H,3-4,10H2,1-2H3 |
| InChI Key | QDCUBAFTOOPBFR-UHFFFAOYSA-N |
| Canonical SMILES | CCC(CC1=CC=CC=C1)C(=O)OCC |
| Molecular Formula | C13H18O2 |
| Wikipedia | ethyl 2-ethyl-3-phenylpropanoate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 206.285 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 6 |
| Complexity | 183.0 |
| 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 w A A A A A A A A A A A B A A A A G g A A A A A A D Q C g m A I y C I A A B A C I A i D S C A A C A A A g A A A I i A E A A I g I I D K A E R C C I A A k g A A I i A e I y O C O 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 | 206.131 |
| Exact Mass | 206.131 |
| XLogP3 | None |
| XLogP3-AA | 3.3 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 15 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| 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+ | 0.9689 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.8586 |
| P-glycoprotein Substrate | Non-substrate | 0.7152 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9386 |
| Non-inhibitor | 0.9193 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8346 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.7756 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8427 |
| CYP450 2D6 Substrate | Non-substrate | 0.9027 |
| CYP450 3A4 Substrate | Non-substrate | 0.7350 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.7051 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8682 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9198 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8735 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9563 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.7285 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9627 |
| Non-inhibitor | 0.9596 | |
| AMES Toxicity | Non AMES toxic | 0.9434 |
| Carcinogens | Carcinogens | 0.5000 |
| Fish Toxicity | High FHMT | 0.9650 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9988 |
| Honey Bee Toxicity | High HBT | 0.7758 |
| Biodegradation | Ready biodegradable | 0.8425 |
| Acute Oral Toxicity | III | 0.7919 |
| Carcinogenicity (Three-class) | Non-required | 0.7626 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -3.1441 | LogS |
| Caco-2 Permeability | 1.6045 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.6399 | LD50, mol/kg |
| Fish Toxicity | 1.3725 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.4674 | 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 | Aromatic homomonocyclic compounds |
| Substituents | Fatty acid ester - Benzenoid - Monocyclic benzene moiety - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic homomonocyclic 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