p-Mentha-1,8(10)-dien-9-yl acetate
Relevant Data
Food Additives Approved in the United States:
General Information
| Chemical name | p-Mentha-1,8(10)-dien-9-yl acetate |
| CAS number | 15111-97-4 |
| COE number | 10743 |
| Flavouring type | substances |
| FL No. | 09.809 |
| 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 | 61781 |
| IUPAC Name | 2-(4-methylcyclohex-3-en-1-yl)prop-2-enyl acetate |
| InChI | InChI=1S/C12H18O2/c1-9-4-6-12(7-5-9)10(2)8-14-11(3)13/h4,12H,2,5-8H2,1,3H3 |
| InChI Key | BCTDJPZNMXPMIA-UHFFFAOYSA-N |
| Canonical SMILES | CC1=CCC(CC1)C(=C)COC(=O)C |
| Molecular Formula | C12H18O2 |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 194.274 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 4 |
| Complexity | 264.0 |
| 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 g A A A A A A A A A A A A A A A A G g A A A A A A D Q C g g A I C C A A A B A C I A i D S C A A A A A A g A A A A C A A A A A g A B A I A I Q A C A A A E g A A I I A O 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 | 194.131 |
| Exact Mass | 194.131 |
| XLogP3 | None |
| XLogP3-AA | 2.7 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 14 |
| 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+ | 0.9386 |
| Human Intestinal Absorption | HIA+ | 0.9914 |
| Caco-2 Permeability | Caco2+ | 0.7448 |
| P-glycoprotein Substrate | Non-substrate | 0.6038 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.7837 |
| Non-inhibitor | 0.6620 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.7318 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.6008 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8824 |
| CYP450 2D6 Substrate | Non-substrate | 0.8623 |
| CYP450 3A4 Substrate | Non-substrate | 0.5824 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.6495 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9074 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9190 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8197 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.8499 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.6398 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8314 |
| Non-inhibitor | 0.9314 | |
| AMES Toxicity | Non AMES toxic | 0.8803 |
| Carcinogens | Non-carcinogens | 0.7227 |
| Fish Toxicity | High FHMT | 0.9927 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9991 |
| Honey Bee Toxicity | High HBT | 0.8352 |
| Biodegradation | Ready biodegradable | 0.9061 |
| Acute Oral Toxicity | III | 0.7522 |
| Carcinogenicity (Three-class) | Non-required | 0.5723 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -3.6037 | LogS |
| Caco-2 Permeability | 1.5476 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.5226 | LD50, mol/kg |
| Fish Toxicity | -0.2341 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 1.3937 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Prenol lipids |
| Subclass | Monoterpenoids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Menthane monoterpenoids |
| Alternative Parents | |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | P-menthane monoterpenoid - Monocyclic monoterpenoid - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes. |
From ClassyFire