Allyl undec-10-enoate
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | Allyl undec-10-enoate |
| CAS number | 7493-76-7 |
| COE number | 441 |
| JECFA number | 9 |
| Flavouring type | substances |
| FL No. | 09.146 |
| Mixture | No |
| Purity of the named substance at least 95% unless otherwise specified | |
| Reference body | JECFA |
From webgate.ec.europa.eu
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 61412 |
| IUPAC Name | prop-2-enyl undec-10-enoate |
| InChI | InChI=1S/C14H24O2/c1-3-5-6-7-8-9-10-11-12-14(15)16-13-4-2/h3-4H,1-2,5-13H2 |
| InChI Key | VJOZUTGJXVDWDJ-UHFFFAOYSA-N |
| Canonical SMILES | C=CCCCCCCCCC(=O)OCC=C |
| Molecular Formula | C14H24O2 |
| Wikipedia | allyl 10-undecenoate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 224.344 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 12 |
| Complexity | 197.0 |
| 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 A C A A A B A C I A C D S C A A A A A A g A A A I A A E A A A g A B B I A I Q A C A A A E g A A A I A G I y K C 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 | 224.178 |
| Exact Mass | 224.178 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 16 |
| 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+ | 0.9723 |
| Human Intestinal Absorption | HIA+ | 0.9693 |
| Caco-2 Permeability | Caco2+ | 0.6528 |
| P-glycoprotein Substrate | Non-substrate | 0.8293 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8723 |
| Non-inhibitor | 0.8033 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8235 |
| Distribution | ||
| Subcellular localization | Plasma membrane | 0.5004 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8747 |
| CYP450 2D6 Substrate | Non-substrate | 0.9039 |
| CYP450 3A4 Substrate | Non-substrate | 0.7238 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.6624 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8655 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9570 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8675 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9273 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8042 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8303 |
| Non-inhibitor | 0.9599 | |
| AMES Toxicity | Non AMES toxic | 0.8000 |
| Carcinogens | Non-carcinogens | 0.5548 |
| Fish Toxicity | High FHMT | 0.9521 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9691 |
| Honey Bee Toxicity | High HBT | 0.8163 |
| Biodegradation | Ready biodegradable | 0.8178 |
| Acute Oral Toxicity | III | 0.6101 |
| Carcinogenicity (Three-class) | Non-required | 0.6011 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.1749 | LogS |
| Caco-2 Permeability | 1.2747 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 2.2390 | LD50, mol/kg |
| Fish Toxicity | -0.3660 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.1034 | 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 - 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