5-Methylheptan-3-one
General Information
| Chemical name | 5-Methylheptan-3-one |
| CAS number | 541-85-5 |
| Flavouring type | substances |
| FL No. | 07.182 |
| 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 | 7822 |
| IUPAC Name | 5-methylheptan-3-one |
| InChI | InChI=1S/C8H16O/c1-4-7(3)6-8(9)5-2/h7H,4-6H2,1-3H3 |
| InChI Key | PSBKJPTZCVYXSD-UHFFFAOYSA-N |
| Canonical SMILES | CCC(C)CC(=O)CC |
| Molecular Formula | C8H16O |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 128.215 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 4 |
| Complexity | 86.6 |
| CACTVS Substructure Key Fingerprint | A A A D c e B w I 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 g A 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 | 17.1 |
| Monoisotopic Mass | 128.12 |
| Exact Mass | 128.12 |
| XLogP3 | None |
| XLogP3-AA | 2.2 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 9 |
| 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+ | 0.9881 |
| Human Intestinal Absorption | HIA+ | 0.9967 |
| Caco-2 Permeability | Caco2+ | 0.7957 |
| P-glycoprotein Substrate | Non-substrate | 0.7488 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.7586 |
| Non-inhibitor | 0.7868 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.9141 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.4656 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8549 |
| CYP450 2D6 Substrate | Non-substrate | 0.8506 |
| CYP450 3A4 Substrate | Non-substrate | 0.6564 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.6027 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9374 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9411 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9443 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9769 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8902 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9166 |
| Non-inhibitor | 0.8511 | |
| AMES Toxicity | Non AMES toxic | 0.9789 |
| Carcinogens | Carcinogens | 0.7863 |
| Fish Toxicity | High FHMT | 0.6607 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.8140 |
| Honey Bee Toxicity | High HBT | 0.7962 |
| Biodegradation | Ready biodegradable | 0.7739 |
| Acute Oral Toxicity | III | 0.7945 |
| Carcinogenicity (Three-class) | Non-required | 0.7219 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -1.8968 | LogS |
| Caco-2 Permeability | 1.3457 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.5951 | LD50, mol/kg |
| Fish Toxicity | 1.8367 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.0662 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Class | Organooxygen compounds |
| Subclass | Carbonyl compounds |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Ketones |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Ketone - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as ketones. These are organic compounds in which a carbonyl group is bonded to two carbon atoms R2C=O (neither R may be a hydrogen atom). Ketones that have one or more alpha-hydrogen atoms undergo keto-enol tautomerization, the tautomer being an enol. |
From ClassyFire