5-Methylhexan-2,3-dione
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | 5-Methylhexan-2,3-dione |
| CAS number | 13706-86-0 |
| COE number | 11148 |
| JECFA number | 414 |
| Flavouring type | substances |
| FL No. | 07.093 |
| 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 | 26204 |
| IUPAC Name | 5-methylhexane-2,3-dione |
| InChI | InChI=1S/C7H12O2/c1-5(2)4-7(9)6(3)8/h5H,4H2,1-3H3 |
| InChI Key | PQCLJXVUAWLNSV-UHFFFAOYSA-N |
| Canonical SMILES | CC(C)CC(=O)C(=O)C |
| Molecular Formula | C7H12O2 |
| Wikipedia | 5-methyl-2,3-hexanedione |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 128.171 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Complexity | 125.0 |
| 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 A C A A A A A A A I A I A Q A 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 A A A A A A A E 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 | 34.1 |
| Monoisotopic Mass | 128.084 |
| Exact Mass | 128.084 |
| XLogP3 | None |
| XLogP3-AA | 0.9 |
| 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+ | 0.9848 |
| Human Intestinal Absorption | HIA+ | 0.9928 |
| Caco-2 Permeability | Caco2+ | 0.6557 |
| P-glycoprotein Substrate | Non-substrate | 0.7384 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.5984 |
| Non-inhibitor | 0.7766 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.9285 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.7052 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8344 |
| CYP450 2D6 Substrate | Non-substrate | 0.8521 |
| CYP450 3A4 Substrate | Non-substrate | 0.6148 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.7759 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9081 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9263 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9080 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9633 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9464 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9711 |
| Non-inhibitor | 0.9416 | |
| AMES Toxicity | Non AMES toxic | 0.8436 |
| Carcinogens | Carcinogens | 0.7025 |
| Fish Toxicity | High FHMT | 0.6120 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.5829 |
| Honey Bee Toxicity | High HBT | 0.7415 |
| Biodegradation | Ready biodegradable | 0.7904 |
| Acute Oral Toxicity | III | 0.8013 |
| Carcinogenicity (Three-class) | Non-required | 0.7401 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -1.4155 | LogS |
| Caco-2 Permeability | 1.2209 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.4401 | LD50, mol/kg |
| Fish Toxicity | 2.2093 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.2019 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Class | Organooxygen compounds |
| Subclass | Carbonyl compounds |
| Intermediate Tree Nodes | Ketones |
| Direct Parent | Alpha-diketones |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Alpha-diketone - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as alpha-diketones. These are organic compounds containing two ketone groups on two adjacent carbon atoms. |
From ClassyFire