1,1-Di-isobutoxyethane
Relevant Data
Food Additives Approved in the United States:
General Information
| Chemical name | 1,1-Di-isobutoxyethane |
| CAS number | 5669-09-0 |
| COE number | 10023 |
| Flavouring type | substances |
| FL No. | 06.053 |
| 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 | 79753 |
| IUPAC Name | 2-methyl-1-[1-(2-methylpropoxy)ethoxy]propane |
| InChI | InChI=1S/C10H22O2/c1-8(2)6-11-10(5)12-7-9(3)4/h8-10H,6-7H2,1-5H3 |
| InChI Key | KIELJSVPUISYCI-UHFFFAOYSA-N |
| Canonical SMILES | CC(C)COC(C)OCC(C)C |
| Molecular Formula | C10H22O2 |
| Wikipedia | acetaldehyde di-isobutylacetal |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 174.284 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 6 |
| Complexity | 88.0 |
| 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 D Q 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 A A A A A i A A A A A A A E 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 = = |
| Topological Polar Surface Area | 18.5 |
| Monoisotopic Mass | 174.162 |
| Exact Mass | 174.162 |
| XLogP3 | None |
| XLogP3-AA | 3.1 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 12 |
| 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+ | 0.9616 |
| Human Intestinal Absorption | HIA+ | 0.9879 |
| Caco-2 Permeability | Caco2+ | 0.6568 |
| P-glycoprotein Substrate | Non-substrate | 0.7701 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9126 |
| Non-inhibitor | 0.8398 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8760 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.5968 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8442 |
| CYP450 2D6 Substrate | Non-substrate | 0.8641 |
| CYP450 3A4 Substrate | Non-substrate | 0.6773 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.8833 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9375 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9503 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9382 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9873 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9311 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9491 |
| Non-inhibitor | 0.9568 | |
| AMES Toxicity | Non AMES toxic | 0.8683 |
| Carcinogens | Carcinogens | 0.7632 |
| Fish Toxicity | High FHMT | 0.9149 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.5352 |
| Honey Bee Toxicity | High HBT | 0.8491 |
| Biodegradation | Not ready biodegradable | 0.5243 |
| Acute Oral Toxicity | III | 0.6751 |
| Carcinogenicity (Three-class) | Non-required | 0.6358 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.1608 | LogS |
| Caco-2 Permeability | 1.2401 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.2820 | LD50, mol/kg |
| Fish Toxicity | 1.5199 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.3360 | 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