Carvyl acetate
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | Carvyl acetate |
| CAS number | 97-42-7 |
| COE number | 2063 |
| JECFA number | 382 |
| Flavouring type | substances |
| FL No. | 09.215 |
| 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 | 7335 |
| IUPAC Name | (2-methyl-5-prop-1-en-2-ylcyclohex-2-en-1-yl) acetate |
| InChI | InChI=1S/C12H18O2/c1-8(2)11-6-5-9(3)12(7-11)14-10(4)13/h5,11-12H,1,6-7H2,2-4H3 |
| InChI Key | YTHRBOFHFYZBRJ-UHFFFAOYSA-N |
| Canonical SMILES | CC1=CCC(CC1OC(=O)C)C(=C)C |
| Molecular Formula | C12H18O2 |
| Wikipedia | (1S,5R)-carvyl acetate |
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 | 3 |
| Complexity | 276.0 |
| 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 R S 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 E A A E g A A I I A O A g A 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 | 2.6 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 14 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 2 |
| 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+ | 0.8340 |
| Human Intestinal Absorption | HIA+ | 0.9927 |
| Caco-2 Permeability | Caco2+ | 0.7637 |
| P-glycoprotein Substrate | Non-substrate | 0.7076 |
| P-glycoprotein Inhibitor | Inhibitor | 0.6819 |
| Non-inhibitor | 0.9356 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8173 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.7629 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8740 |
| CYP450 2D6 Substrate | Non-substrate | 0.8536 |
| CYP450 3A4 Substrate | Substrate | 0.5554 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.8789 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9650 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9401 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.7156 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.8310 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8208 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8678 |
| Non-inhibitor | 0.9342 | |
| AMES Toxicity | Non AMES toxic | 0.9132 |
| Carcinogens | Non-carcinogens | 0.7505 |
| Fish Toxicity | High FHMT | 0.9414 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.8737 |
| Honey Bee Toxicity | High HBT | 0.9116 |
| Biodegradation | Ready biodegradable | 0.6691 |
| Acute Oral Toxicity | III | 0.8429 |
| Carcinogenicity (Three-class) | Non-required | 0.6412 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -3.0568 | LogS |
| Caco-2 Permeability | 1.4090 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.6646 | LD50, mol/kg |
| Fish Toxicity | 0.7556 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.2705 | 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