2,6-Dimethyloctanal
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | 2,6-Dimethyloctanal |
| CAS number | 7779-07-9 |
| COE number | 112 |
| JECFA number | 273 |
| Flavouring type | substances |
| FL No. | 05.023 |
| Mixture | No |
| Purity of the named substance at least 95% unless otherwise specified |
From webgate.ec.europa.eu
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 5463910 |
| IUPAC Name | 2,6-dimethyloctanal |
| InChI | InChI=1S/C10H20O/c1-4-9(2)6-5-7-10(3)8-11/h8-10H,4-7H2,1-3H3 |
| InChI Key | CBOBADCVMLMQRW-UHFFFAOYSA-N |
| Canonical SMILES | CCC(C)CCCC(C)C=O |
| Molecular Formula | C10H20O |
| Wikipedia | 2,6-dimethyloctanal |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 156.269 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 6 |
| Complexity | 99.0 |
| 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 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 E I i M C 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 | 156.151 |
| Exact Mass | 156.151 |
| XLogP3 | None |
| XLogP3-AA | 3.5 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 11 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 2 |
| 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+ | 0.9861 |
| Human Intestinal Absorption | HIA+ | 0.9947 |
| Caco-2 Permeability | Caco2+ | 0.8370 |
| P-glycoprotein Substrate | Non-substrate | 0.6737 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8774 |
| Non-inhibitor | 0.5388 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.9043 |
| Distribution | ||
| Subcellular localization | Lysosome | 0.3691 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8329 |
| CYP450 2D6 Substrate | Non-substrate | 0.8386 |
| CYP450 3A4 Substrate | Non-substrate | 0.6885 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.5347 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9218 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9557 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9624 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9890 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8670 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8595 |
| Non-inhibitor | 0.8258 | |
| AMES Toxicity | Non AMES toxic | 0.9856 |
| Carcinogens | Carcinogens | 0.6616 |
| Fish Toxicity | High FHMT | 0.9350 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9993 |
| Honey Bee Toxicity | High HBT | 0.7538 |
| Biodegradation | Ready biodegradable | 0.6108 |
| Acute Oral Toxicity | III | 0.7034 |
| Carcinogenicity (Three-class) | Non-required | 0.6922 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -3.3374 | LogS |
| Caco-2 Permeability | 1.4192 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.3798 | LD50, mol/kg |
| Fish Toxicity | -0.3540 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.6343 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Class | Organooxygen compounds |
| Subclass | Carbonyl compounds |
| Intermediate Tree Nodes | Aldehydes |
| Direct Parent | Medium-chain aldehydes |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Medium-chain aldehyde - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as medium-chain aldehydes. These are an aldehyde with a chain length containing between 6 and 12 carbon atoms. |
From ClassyFire