METHYL 4-METHYLVALERATE
Relevant Data
Flavouring Substances Approved by European Union:
General Information
| Mainterm | METHYL 4-METHYLVALERATE |
| Doc Type | ASP |
| CAS Reg.No.(or other ID) | 2412-80-8 |
| Regnum |
172.515 |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 17008 |
| IUPAC Name | methyl 4-methylpentanoate |
| InChI | InChI=1S/C7H14O2/c1-6(2)4-5-7(8)9-3/h6H,4-5H2,1-3H3 |
| InChI Key | KBCOVKHULBZKNY-UHFFFAOYSA-N |
| Canonical SMILES | CC(C)CCC(=O)OC |
| Molecular Formula | C7H14O2 |
| Wikipedia | methyl 4-methylvalerate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 130.187 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 4 |
| Complexity | 86.9 |
| 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 C A g A I C C A A A B A A I A A C Q C A A A A A A A A A A A A A E A A A A A A B I A A A A A A A A E A A A A A A C I A A A 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 = = |
| Topological Polar Surface Area | 26.3 |
| Monoisotopic Mass | 130.099 |
| Exact Mass | 130.099 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 9 |
| 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+ | 0.9867 |
| Human Intestinal Absorption | HIA+ | 0.9702 |
| Caco-2 Permeability | Caco2+ | 0.7505 |
| P-glycoprotein Substrate | Non-substrate | 0.7531 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8986 |
| Non-inhibitor | 0.8480 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8966 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.6383 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8196 |
| CYP450 2D6 Substrate | Non-substrate | 0.8759 |
| CYP450 3A4 Substrate | Non-substrate | 0.5380 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.8455 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9346 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9679 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9465 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9885 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9627 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9560 |
| Non-inhibitor | 0.9452 | |
| AMES Toxicity | Non AMES toxic | 0.9477 |
| Carcinogens | Carcinogens | 0.5798 |
| Fish Toxicity | High FHMT | 0.6959 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.5350 |
| Honey Bee Toxicity | High HBT | 0.8086 |
| Biodegradation | Ready biodegradable | 0.8328 |
| Acute Oral Toxicity | III | 0.8368 |
| Carcinogenicity (Three-class) | Non-required | 0.6596 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.2143 | LogS |
| Caco-2 Permeability | 1.4028 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.3853 | LD50, mol/kg |
| Fish Toxicity | 1.4786 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.3245 | 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 methyl esters |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Fatty acid methyl ester - Methyl ester - 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 methyl esters. These are compounds containing a fatty acid that is esterified with a methyl group. They have the general structure RC(=O)OR', where R=fatty aliphatic tail or organyl group and R'=methyl group. |
From ClassyFire