P-TOLYL ISOBUTYRATE
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | P-TOLYL ISOBUTYRATE |
| Doc Type | ASP |
| CAS Reg.No.(or other ID) | 103-93-5 |
| Regnum |
172.515 |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 7685 |
| IUPAC Name | (4-methylphenyl) 2-methylpropanoate |
| InChI | InChI=1S/C11H14O2/c1-8(2)11(12)13-10-6-4-9(3)5-7-10/h4-8H,1-3H3 |
| InChI Key | UPPSFGGDKACIKP-UHFFFAOYSA-N |
| Canonical SMILES | CC1=CC=C(C=C1)OC(=O)C(C)C |
| Molecular Formula | C11H14O2 |
| Wikipedia | p-cresyl isobutyrate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 178.231 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Complexity | 167.0 |
| CACTVS Substructure Key Fingerprint | A A A D c c 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 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 Q S A m A A y D o A A B A C I A i D S C A A C C A A g I A A I i A E G C I g M J i K E M R q C O i C k w B E I q A e A w A A O I A A A A A A A A A B 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 | 178.099 |
| Exact Mass | 178.099 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 13 |
| 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+ | 0.9223 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.8689 |
| P-glycoprotein Substrate | Non-substrate | 0.7430 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8749 |
| Non-inhibitor | 0.9663 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8993 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.8926 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.7906 |
| CYP450 2D6 Substrate | Non-substrate | 0.7730 |
| CYP450 3A4 Substrate | Non-substrate | 0.5386 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.6240 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9399 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9634 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8930 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9725 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8469 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9482 |
| Non-inhibitor | 0.9604 | |
| AMES Toxicity | Non AMES toxic | 0.8871 |
| Carcinogens | Non-carcinogens | 0.6538 |
| Fish Toxicity | High FHMT | 0.9205 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.8489 |
| Honey Bee Toxicity | High HBT | 0.9081 |
| Biodegradation | Ready biodegradable | 0.7136 |
| Acute Oral Toxicity | III | 0.9034 |
| Carcinogenicity (Three-class) | Non-required | 0.6075 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -3.3704 | LogS |
| Caco-2 Permeability | 1.5766 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.8159 | LD50, mol/kg |
| Fish Toxicity | 0.7380 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.6721 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Phenol esters |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Phenol esters |
| Alternative Parents | |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Phenol ester - Phenoxy compound - Toluene - Monocyclic benzene moiety - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as phenol esters. These are aromatic compounds containing a benzene ring substituted by a hydroxyl group and an ester group. |
From ClassyFire