DIMETHYLBENZYL CARBINYL HEXANOATE
Relevant Data
Food Additives Approved by WHO:
General Information
| Mainterm | DIMETHYLBENZYL CARBINYL HEXANOATE |
| Doc Type | EAF |
| CAS Reg.No.(or other ID) | 891781-90-1 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 71587848 |
| IUPAC Name | (2-methyl-1-phenylpropan-2-yl) hexanoate |
| InChI | InChI=1S/C16H24O2/c1-4-5-7-12-15(17)18-16(2,3)13-14-10-8-6-9-11-14/h6,8-11H,4-5,7,12-13H2,1-3H3 |
| InChI Key | IRKDZQZMTAKZKQ-UHFFFAOYSA-N |
| Canonical SMILES | CCCCCC(=O)OC(C)(C)CC1=CC=CC=C1 |
| Molecular Formula | C16H24O2 |
| Wikipedia | dimethylbenzyl carbinyl hexanoate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 248.366 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 8 |
| Complexity | 240.0 |
| CACTVS Substructure Key Fingerprint | A A A D c e B 4 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 E S A m A A y C I A A B A C I A i D S C A A C A A A g A A A I i A E A A I g I I D K A E R C C I A A k w A E I i A e I y O 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 | 248.178 |
| Exact Mass | 248.178 |
| XLogP3 | None |
| XLogP3-AA | 4.6 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 18 |
| 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+ | 0.9842 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.7957 |
| P-glycoprotein Substrate | Non-substrate | 0.5138 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.7186 |
| Non-inhibitor | 0.5337 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8594 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.5595 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8484 |
| CYP450 2D6 Substrate | Non-substrate | 0.9102 |
| CYP450 3A4 Substrate | Substrate | 0.5559 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.6114 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.6950 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.8283 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.6799 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.8256 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.7647 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9363 |
| Non-inhibitor | 0.6955 | |
| AMES Toxicity | Non AMES toxic | 0.9551 |
| Carcinogens | Non-carcinogens | 0.5098 |
| Fish Toxicity | High FHMT | 0.9661 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9998 |
| Honey Bee Toxicity | High HBT | 0.7711 |
| Biodegradation | Not ready biodegradable | 0.6730 |
| Acute Oral Toxicity | III | 0.7671 |
| Carcinogenicity (Three-class) | Non-required | 0.5264 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -4.8520 | LogS |
| Caco-2 Permeability | 1.4615 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.7833 | LD50, mol/kg |
| Fish Toxicity | 0.3644 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 2.2420 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Phenylpropanes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Phenylpropanes |
| Alternative Parents | |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Phenylpropane - Fatty acid ester - Fatty acyl - 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 phenylpropanes. These are organic compounds containing a phenylpropane moiety. |
From ClassyFire