2-Hexyl-4,5-dimethyl-1,3-dioxolane
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | 2-Hexyl-4,5-dimethyl-1,3-dioxolane |
| CAS number | 6454-22-4 |
| JECFA number | 1712 |
| Flavouring type | substances |
| FL No. | 06.089 |
| 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 | 94886 |
| IUPAC Name | 2-hexyl-4,5-dimethyl-1,3-dioxolane |
| InChI | InChI=1S/C11H22O2/c1-4-5-6-7-8-11-12-9(2)10(3)13-11/h9-11H,4-8H2,1-3H3 |
| InChI Key | MTNLKAOONWIMIT-UHFFFAOYSA-N |
| Canonical SMILES | CCCCCCC1OC(C(O1)C)C |
| Molecular Formula | C11H22O2 |
| Wikipedia | 2-hexyl-4,5-dimethyl-1,3-dioxolane |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 186.295 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 5 |
| Complexity | 126.0 |
| 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 S 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 B S 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 R A A I A A A A i A A A E A A A G A A G A w C 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 | 186.162 |
| Exact Mass | 186.162 |
| XLogP3 | None |
| XLogP3-AA | 3.6 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 13 |
| 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+ | 0.9854 |
| Human Intestinal Absorption | HIA+ | 0.9944 |
| Caco-2 Permeability | Caco2+ | 0.6769 |
| P-glycoprotein Substrate | Non-substrate | 0.7327 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.6256 |
| Inhibitor | 0.5000 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8822 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.3951 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8729 |
| CYP450 2D6 Substrate | Non-substrate | 0.8134 |
| CYP450 3A4 Substrate | Non-substrate | 0.5649 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.6270 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8344 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9157 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.7049 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.8522 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.7953 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8431 |
| Non-inhibitor | 0.8627 | |
| AMES Toxicity | Non AMES toxic | 0.9210 |
| Carcinogens | Non-carcinogens | 0.7360 |
| Fish Toxicity | High FHMT | 0.6111 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9792 |
| Honey Bee Toxicity | High HBT | 0.7117 |
| Biodegradation | Not ready biodegradable | 0.6791 |
| Acute Oral Toxicity | III | 0.7496 |
| Carcinogenicity (Three-class) | Non-required | 0.5744 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -3.0526 | LogS |
| Caco-2 Permeability | 1.0868 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.7094 | LD50, mol/kg |
| Fish Toxicity | 1.4628 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.7085 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Dioxolanes |
| Subclass | 1,3-dioxolanes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | 1,3-dioxolanes |
| Alternative Parents | |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Meta-dioxolane - Oxacycle - Acetal - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aliphatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as 1,3-dioxolanes. These are organic compounds containing 1,3-dioxolane, an aliphatic five-member ring with two oxygen atoms in ring positions 1 and 3. |
From ClassyFire