TERPINYL FORMATE
Relevant Data
Food Additives Approved in the United States
Flavouring Substances Approved by European Union:
General Information
| Chemical Names: | p-MENTH-1-EN-8-YL FORMATE |
| CAS number: | 2153-26-6 |
| COE number: | 348 |
| JECFA number: | 367 |
| FEMA number: | 3052 |
| Functional Class: |
Flavouring Agent FLAVOURING_AGENT |
From apps.who.int
Evaluations
| Evaluation year: | 1998 |
| ADI: | No safety concern at current levels of intake when used as a flavouring agent |
| Report: | TRS 891-JECFA 51/79 |
| Tox Monograph: | FAS 42-JECFA 51/293 |
| Specification: | COMPENDIUM ADDENDUM 9/FNP 52 Add.9/118 (2001) |
From apps.who.int
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 16537 |
| IUPAC Name | 2-(4-methylcyclohex-3-en-1-yl)propan-2-yl formate |
| InChI | InChI=1S/C11H18O2/c1-9-4-6-10(7-5-9)11(2,3)13-8-12/h4,8,10H,5-7H2,1-3H3 |
| InChI Key | IPYLQIQMGUZFCK-UHFFFAOYSA-N |
| Canonical SMILES | CC1=CCC(CC1)C(C)(C)OC=O |
| Molecular Formula | C11H18O2 |
| Wikipedia | terpinyl formate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 182.263 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Complexity | 216.0 |
| 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 U S A g A M C C A A A B A C I A i B C i A A A A A A g A A A A C A A A A A g A A A I A A Q A A A A A E g A A I A A O A w E A O g 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 | 182.131 |
| Exact Mass | 182.131 |
| XLogP3 | None |
| XLogP3-AA | 2.4 |
| 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+ | 0.9429 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.7264 |
| P-glycoprotein Substrate | Non-substrate | 0.5155 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.6760 |
| Inhibitor | 0.5970 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8197 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.6558 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8647 |
| CYP450 2D6 Substrate | Non-substrate | 0.9042 |
| CYP450 3A4 Substrate | Substrate | 0.6255 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.8316 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.7372 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9325 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.5656 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9003 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.7554 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9332 |
| Non-inhibitor | 0.8681 | |
| AMES Toxicity | Non AMES toxic | 0.9426 |
| Carcinogens | Non-carcinogens | 0.6462 |
| Fish Toxicity | High FHMT | 0.9352 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9467 |
| Honey Bee Toxicity | High HBT | 0.8786 |
| Biodegradation | Ready biodegradable | 0.7716 |
| Acute Oral Toxicity | III | 0.7462 |
| Carcinogenicity (Three-class) | Non-required | 0.4913 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -3.7837 | LogS |
| Caco-2 Permeability | 1.5843 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.6185 | LD50, mol/kg |
| Fish Toxicity | 0.6080 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 1.1089 | 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