Methyl 2-oxo-3-methylvalerate
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | Methyl 2-oxo-3-methylvalerate |
| CAS number | 3682-42-6 |
| JECFA number | 591 |
| Flavouring type | substances |
| FL No. | 09.550 |
| 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 | 545106 |
| IUPAC Name | methyl 3-methyl-2-oxopentanoate |
| InChI | InChI=1S/C7H12O3/c1-4-5(2)6(8)7(9)10-3/h5H,4H2,1-3H3 |
| InChI Key | ZPSBJVARKCHQDF-UHFFFAOYSA-N |
| Canonical SMILES | CCC(C)C(=O)C(=O)OC |
| Molecular Formula | C7H12O3 |
| Wikipedia | methyl 2-oxo-3-methylpentanoate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 144.17 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 4 |
| Complexity | 140.0 |
| CACTVS Substructure Key Fingerprint | A A A D c c B g 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 A 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 Q S A g A I C C A A A B A A I A I C Q C A I A A A A A A A A A A A F A A A A A A B I A A A Q A A A A E A A A A A A C I A A A K 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 | 43.4 |
| Monoisotopic Mass | 144.079 |
| Exact Mass | 144.079 |
| XLogP3 | None |
| XLogP3-AA | 1.4 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 10 |
| 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+ | 0.9618 |
| Human Intestinal Absorption | HIA+ | 0.9892 |
| Caco-2 Permeability | Caco2+ | 0.5994 |
| P-glycoprotein Substrate | Non-substrate | 0.7600 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.6380 |
| Inhibitor | 0.6136 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.9491 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.8130 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8715 |
| CYP450 2D6 Substrate | Non-substrate | 0.9014 |
| CYP450 3A4 Substrate | Non-substrate | 0.6668 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.8741 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8983 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9571 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9389 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9780 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9167 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9861 |
| Non-inhibitor | 0.9576 | |
| AMES Toxicity | Non AMES toxic | 0.7730 |
| Carcinogens | Carcinogens | 0.6704 |
| Fish Toxicity | High FHMT | 0.6096 |
| Tetrahymena Pyriformis Toxicity | Low TPT | 0.8990 |
| Honey Bee Toxicity | High HBT | 0.8222 |
| Biodegradation | Ready biodegradable | 0.8329 |
| Acute Oral Toxicity | III | 0.7331 |
| Carcinogenicity (Three-class) | Non-required | 0.5830 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -0.2512 | LogS |
| Caco-2 Permeability | 0.9273 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.4441 | LD50, mol/kg |
| Fish Toxicity | 2.2747 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.6526 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Fatty Acyls |
| Subclass | Fatty acid esters |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Fatty acid esters |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Fatty acid ester - Keto acid - Alpha-keto acid - Methyl ester - Ketone - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid. |
From ClassyFire