1,1-Diethoxynonane
General Information
| Chemical name | 1,1-Diethoxynonane |
| CAS number | 54815-13-3 |
| COE number | 10016 |
| Flavouring type | substances |
| FL No. | 06.065 |
| 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 | 108625 |
| IUPAC Name | 1,1-diethoxynonane |
| InChI | InChI=1S/C13H28O2/c1-4-7-8-9-10-11-12-13(14-5-2)15-6-3/h13H,4-12H2,1-3H3 |
| InChI Key | RJMSGTVQHHFVLK-UHFFFAOYSA-N |
| Canonical SMILES | CCCCCCCCC(OCC)OCC |
| Molecular Formula | C13H28O2 |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 216.365 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 11 |
| Complexity | 109.0 |
| CACTVS Substructure Key Fingerprint | A A A D c e B w 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 C A C w g A M C C A A A B 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 Q A A I A A A A i A A A E A A A E A A G A w K 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 = = |
| Topological Polar Surface Area | 18.5 |
| Monoisotopic Mass | 216.209 |
| Exact Mass | 216.209 |
| XLogP3 | None |
| XLogP3-AA | 4.8 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 15 |
| 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+ | 0.9752 |
| Human Intestinal Absorption | HIA+ | 0.9839 |
| Caco-2 Permeability | Caco2+ | 0.7412 |
| P-glycoprotein Substrate | Non-substrate | 0.6966 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8721 |
| Non-inhibitor | 0.8585 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8629 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.4584 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8741 |
| CYP450 2D6 Substrate | Non-substrate | 0.8694 |
| CYP450 3A4 Substrate | Non-substrate | 0.6389 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.7688 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9307 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9192 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9037 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9451 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8311 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8289 |
| Non-inhibitor | 0.8165 | |
| AMES Toxicity | Non AMES toxic | 0.9032 |
| Carcinogens | Carcinogens | 0.6783 |
| Fish Toxicity | High FHMT | 0.7263 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9436 |
| Honey Bee Toxicity | High HBT | 0.7788 |
| Biodegradation | Ready biodegradable | 0.5938 |
| Acute Oral Toxicity | III | 0.8905 |
| Carcinogenicity (Three-class) | Non-required | 0.6398 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -3.0743 | LogS |
| Caco-2 Permeability | 1.1701 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.6022 | LD50, mol/kg |
| Fish Toxicity | 1.0180 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.6184 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Class | Organooxygen compounds |
| Subclass | Ethers |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Acetals |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Acetal - Hydrocarbon derivative - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as acetals. These are compounds having the structure R2C(OR')2 ( R' not Hydrogen) and thus diethers of geminal diols. Originally, the term was confined to derivatives of aldehydes (one R = H), but it now applies equally to derivatives of ketones (neither R = H ). Mixed acetals have different R' groups. |
From ClassyFire