HEPTYL CINNAMATE
Relevant Data
Food Additives Approved in the United States
Flavouring Substances Approved by European Union:
General Information
| Synonyms: | HEPTYL beta-PHENYLACRYLATE |
| Chemical Names: | HEPTYL CINNAMATE |
| CAS number: | 10032-08-3 |
| COE number: | 2104 |
| JECFA number: | 666 |
| FEMA number: | 2551 |
| Functional Class: |
Flavouring Agent FLAVOURING_AGENT |
From apps.who.int
Evaluations
| Evaluation year: | 2000 |
| ADI: | No safety concern at current levels of intake when used as a flavouring agent |
| Report: | TRS 901-JECFA 55/22 |
| Tox Monograph: | FAS 46-JECFA 55/79 |
| Specification: | COMPENDIUM ADDENDUM 9/FNP 52 Add.9/122 (2001) |
From apps.who.int
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 6435839 |
| IUPAC Name | heptyl (E)-3-phenylprop-2-enoate |
| InChI | InChI=1S/C16H22O2/c1-2-3-4-5-9-14-18-16(17)13-12-15-10-7-6-8-11-15/h6-8,10-13H,2-5,9,14H2,1H3/b13-12+ |
| InChI Key | DCXNRXBLAGAHIL-OUKQBFOZSA-N |
| Canonical SMILES | CCCCCCCOC(=O)C=CC1=CC=CC=C1 |
| Molecular Formula | C16H22O2 |
| Wikipedia | heptyl cinnamate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 246.35 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 9 |
| Complexity | 240.0 |
| CACTVS Substructure Key Fingerprint | A A A D c e B 4 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 A A A M g I J C K A M R C C M A A k g A A I q Y e A w C 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 | 246.162 |
| Exact Mass | 246.162 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 18 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| 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+ | 0.9811 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.8253 |
| P-glycoprotein Substrate | Non-substrate | 0.5834 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8668 |
| Non-inhibitor | 0.8556 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.7871 |
| Distribution | ||
| Subcellular localization | Plasma membrane | 0.6957 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8087 |
| CYP450 2D6 Substrate | Non-substrate | 0.8816 |
| CYP450 3A4 Substrate | Non-substrate | 0.6433 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.7367 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8883 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.8733 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.6717 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.8911 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.5483 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8363 |
| Non-inhibitor | 0.8149 | |
| AMES Toxicity | Non AMES toxic | 0.9423 |
| Carcinogens | Non-carcinogens | 0.7209 |
| Fish Toxicity | High FHMT | 0.9895 |
| Tetrahymena Pyriformis Toxicity | High TPT | 1.0000 |
| Honey Bee Toxicity | High HBT | 0.6994 |
| Biodegradation | Ready biodegradable | 0.8326 |
| Acute Oral Toxicity | III | 0.8450 |
| Carcinogenicity (Three-class) | Non-required | 0.5890 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -5.1615 | LogS |
| Caco-2 Permeability | 1.4955 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.5033 | LD50, mol/kg |
| Fish Toxicity | 0.0267 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 1.8120 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Phenylpropanoids and polyketides |
| Class | Cinnamic acids and derivatives |
| Subclass | Cinnamic acid esters |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Cinnamic acid esters |
| Alternative Parents | |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Cinnamic acid ester - Styrene - Fatty acid ester - Monocyclic benzene moiety - Benzenoid - Fatty acyl - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organic oxygen compound - Carbonyl group - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as cinnamic acid esters. These are compound containing an ester derivative of cinnamic acid. |
From ClassyFire