PHENETHYL BUTYRATE
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | PHENETHYL BUTYRATE |
| Doc Type | ASP |
| CAS Reg.No.(or other ID) | 103-52-6 |
| Regnum |
172.515 |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 7658 |
| IUPAC Name | 2-phenylethyl butanoate |
| InChI | InChI=1S/C12H16O2/c1-2-6-12(13)14-10-9-11-7-4-3-5-8-11/h3-5,7-8H,2,6,9-10H2,1H3 |
| InChI Key | WFNDDSQUKATKNX-UHFFFAOYSA-N |
| Canonical SMILES | CCCC(=O)OCCC1=CC=CC=C1 |
| Molecular Formula | C12H16O2 |
| Wikipedia | phenethyl butyrate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 192.258 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 6 |
| Complexity | 160.0 |
| 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 A 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 w A E I i A e A w K A 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 | 192.115 |
| Exact Mass | 192.115 |
| 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 | 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+ | 0.9692 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.8191 |
| P-glycoprotein Substrate | Non-substrate | 0.6849 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8973 |
| Non-inhibitor | 0.9069 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8175 |
| Distribution | ||
| Subcellular localization | Plasma membrane | 0.5069 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8335 |
| CYP450 2D6 Substrate | Non-substrate | 0.9023 |
| CYP450 3A4 Substrate | Non-substrate | 0.7089 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.6569 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8108 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9017 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.6230 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9429 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.6881 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8356 |
| Non-inhibitor | 0.8954 | |
| AMES Toxicity | Non AMES toxic | 0.9616 |
| Carcinogens | Non-carcinogens | 0.6859 |
| Fish Toxicity | High FHMT | 0.9394 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9993 |
| Honey Bee Toxicity | High HBT | 0.6766 |
| Biodegradation | Ready biodegradable | 0.8927 |
| Acute Oral Toxicity | III | 0.8062 |
| Carcinogenicity (Three-class) | Non-required | 0.5075 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -3.8816 | LogS |
| Caco-2 Permeability | 1.6414 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.7025 | LD50, mol/kg |
| Fish Toxicity | 0.8997 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.8511 | 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