Isopropyl benzoate
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | Isopropyl benzoate |
| CAS number | 939-48-0 |
| COE number | 652 |
| JECFA number | 855 |
| Flavouring type | substances |
| FL No. | 09.770 |
| 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 | 13654 |
| IUPAC Name | propan-2-yl benzoate |
| InChI | InChI=1S/C10H12O2/c1-8(2)12-10(11)9-6-4-3-5-7-9/h3-8H,1-2H3 |
| InChI Key | FEXQDZTYJVXMOS-UHFFFAOYSA-N |
| Canonical SMILES | CC(C)OC(=O)C1=CC=CC=C1 |
| Molecular Formula | C10H12O2 |
| Wikipedia | isopropyl benzoate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 164.204 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Complexity | 146.0 |
| 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 B S g m A I y C I A A B A C I A i D S C A A C A A A k A A A I i A E A C M g I J j K A N R i C M Q A k w A E I q Y e I y C C 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 | 164.084 |
| Exact Mass | 164.084 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 12 |
| 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+ | 0.9727 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.8752 |
| P-glycoprotein Substrate | Non-substrate | 0.7641 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9087 |
| Non-inhibitor | 0.9617 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8912 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.8512 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8232 |
| CYP450 2D6 Substrate | Non-substrate | 0.9369 |
| CYP450 3A4 Substrate | Non-substrate | 0.6614 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.6267 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8727 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9586 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9243 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9782 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8218 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9722 |
| Non-inhibitor | 0.9624 | |
| AMES Toxicity | Non AMES toxic | 0.9723 |
| Carcinogens | Carcinogens | 0.5000 |
| Fish Toxicity | High FHMT | 0.8198 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.7260 |
| Honey Bee Toxicity | High HBT | 0.8281 |
| Biodegradation | Ready biodegradable | 0.8863 |
| Acute Oral Toxicity | III | 0.8392 |
| Carcinogenicity (Three-class) | Non-required | 0.6756 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.8272 | LogS |
| Caco-2 Permeability | 1.6738 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.6754 | LD50, mol/kg |
| Fish Toxicity | 1.8552 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.1669 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Benzoic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Benzoic acid esters |
| Alternative Parents | |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Benzoate ester - Benzoyl - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid. |
From ClassyFire