2-METHYLPENTANAL
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | 2-METHYLPENTANAL |
| Doc Type | ASP |
| CAS Reg.No.(or other ID) | 123-15-9 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 31245 |
| IUPAC Name | 2-methylpentanal |
| InChI | InChI=1S/C6H12O/c1-3-4-6(2)5-7/h5-6H,3-4H2,1-2H3 |
| InChI Key | FTZILAQGHINQQR-UHFFFAOYSA-N |
| Canonical SMILES | CCCC(C)C=O |
| Molecular Formula | C6H12O |
| Wikipedia | 2-methylvaleraldehyde |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 100.161 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 3 |
| Complexity | 50.1 |
| CACTVS Substructure Key Fingerprint | A A A D c c B g 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 C g g A I C A A A A A A A I A A g Q g 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 A 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 | 17.1 |
| Monoisotopic Mass | 100.089 |
| Exact Mass | 100.089 |
| XLogP3 | None |
| XLogP3-AA | 1.7 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 7 |
| 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
Food Additives Biosynthesis/Degradation
ADMET Predicted Profile --- Classification
| Model | Result | Probability |
|---|---|---|
| Absorption | ||
| Blood-Brain Barrier | BBB+ | 0.9885 |
| Human Intestinal Absorption | HIA+ | 0.9956 |
| Caco-2 Permeability | Caco2+ | 0.8767 |
| P-glycoprotein Substrate | Non-substrate | 0.7093 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9323 |
| Non-inhibitor | 0.8940 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.9084 |
| Distribution | ||
| Subcellular localization | Lysosome | 0.3903 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8170 |
| CYP450 2D6 Substrate | Non-substrate | 0.8551 |
| CYP450 3A4 Substrate | Non-substrate | 0.7354 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.5790 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9545 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9612 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9568 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9919 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9045 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9269 |
| Non-inhibitor | 0.9509 | |
| AMES Toxicity | Non AMES toxic | 0.9152 |
| Carcinogens | Carcinogens | 0.6726 |
| Fish Toxicity | High FHMT | 0.7673 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9388 |
| Honey Bee Toxicity | High HBT | 0.7544 |
| Biodegradation | Ready biodegradable | 0.8310 |
| Acute Oral Toxicity | III | 0.8220 |
| Carcinogenicity (Three-class) | Non-required | 0.7155 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -1.1630 | LogS |
| Caco-2 Permeability | 1.7318 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.5271 | LD50, mol/kg |
| Fish Toxicity | 1.1920 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.3974 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Class | Organic oxides |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Organic oxides |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aldehyde - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as organic oxides. These are organic compounds containing an oxide group. |
From ClassyFire