alpha-METHYLBENZYL PROPIONATE
Relevant Data
Food Additives Approved in the United States
Flavouring Substances Approved by European Union:
General Information
| Synonyms: | METHYL PHENYL CARBINYL PROPIONATE, alpha-PHENYLETHYL PROPIONATE, STYRALLYL PROPIONATE |
| Chemical Names: | 1-PHENYLETHYL PROPIONATE |
| CAS number: | 120-45-6 |
| COE number: | 425 |
| JECFA number: | 802 |
| FEMA number: | 2689 |
| Functional Class: |
Flavouring Agent FLAVOURING_AGENT |
From apps.who.int
Evaluations
| Evaluation year: | 2001 |
| ADI: | No safety concern at current levels of intake when used as a flavouring agent |
| Report: | TRS 909-JECFA 57/61 |
| Tox Monograph: | FAS 48-JECFA 57/117 |
| Specification: | COMPENDIUM ADDENDUM 9/FNP 52 Add.9/134 |
From apps.who.int
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 8432 |
| IUPAC Name | 1-phenylethyl propanoate |
| InChI | InChI=1S/C11H14O2/c1-3-11(12)13-9(2)10-7-5-4-6-8-10/h4-9H,3H2,1-2H3 |
| InChI Key | WCIQNYOXLZQQMU-UHFFFAOYSA-N |
| Canonical SMILES | CCC(=O)OC(C)C1=CC=CC=C1 |
| Molecular Formula | C11H14O2 |
| Wikipedia | α-methylbenzyl propionate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 178.231 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 4 |
| Complexity | 160.0 |
| CACTVS Substructure Key Fingerprint | A A A D c c 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 B S 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 C I g I J i K A M R i C M A A k w A E I q 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 | 178.099 |
| Exact Mass | 178.099 |
| XLogP3 | None |
| XLogP3-AA | 2.5 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 13 |
| 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+ | 0.9829 |
| Human Intestinal Absorption | HIA+ | 0.9970 |
| Caco-2 Permeability | Caco2+ | 0.8672 |
| P-glycoprotein Substrate | Non-substrate | 0.7542 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8081 |
| Non-inhibitor | 0.9525 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8928 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.7433 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8543 |
| CYP450 2D6 Substrate | Non-substrate | 0.9286 |
| CYP450 3A4 Substrate | Non-substrate | 0.6694 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.5112 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8824 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9307 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8662 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9514 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.6099 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9396 |
| Non-inhibitor | 0.9019 | |
| AMES Toxicity | Non AMES toxic | 0.9706 |
| Carcinogens | Carcinogens | 0.5875 |
| Fish Toxicity | High FHMT | 0.5264 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9732 |
| Honey Bee Toxicity | High HBT | 0.7794 |
| Biodegradation | Ready biodegradable | 0.8833 |
| Acute Oral Toxicity | III | 0.5151 |
| Carcinogenicity (Three-class) | Non-required | 0.5970 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.7580 | LogS |
| Caco-2 Permeability | 1.4532 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.5037 | LD50, mol/kg |
| Fish Toxicity | 2.0588 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.4163 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Benzyloxycarbonyls |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Benzyloxycarbonyls |
| Alternative Parents | |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Benzyloxycarbonyl - 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 benzyloxycarbonyls. These are organic compounds containing a carbonyl group substituted with a benzyloxyl group. |
From ClassyFire