2-Hexyl-5-hydroxy-1,3-dioxane
Relevant Data
Food Additives Approved by WHO:
General Information
| Chemical name | 2-Hexyl-5-hydroxy-1,3-dioxane |
| CAS number | 1708-36-7 |
| COE number | 2016 |
| Flavouring type | substances |
| FL No. | 06.102 |
| 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 | 74361 |
| IUPAC Name | 2-hexyl-1,3-dioxan-5-ol |
| InChI | InChI=1S/C10H20O3/c1-2-3-4-5-6-10-12-7-9(11)8-13-10/h9-11H,2-8H2,1H3 |
| InChI Key | ZIWLHBBLQRQFSA-UHFFFAOYSA-N |
| Canonical SMILES | CCCCCCC1OCC(CO1)O |
| Molecular Formula | C10H20O3 |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 188.267 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 5 |
| Complexity | 119.0 |
| 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 k A A A A A A A A A A A A A A A A G g A A C A A A C B S w g A M C C A A A B g 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 E A I A A A A i A A A F A A A H 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 | 38.7 |
| Monoisotopic Mass | 188.141 |
| Exact Mass | 188.141 |
| XLogP3 | None |
| XLogP3-AA | 2.1 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 13 |
| 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+ | 0.8780 |
| Human Intestinal Absorption | HIA+ | 0.9565 |
| Caco-2 Permeability | Caco2+ | 0.5858 |
| P-glycoprotein Substrate | Substrate | 0.5409 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.7894 |
| Non-inhibitor | 0.9595 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8296 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.6234 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8581 |
| CYP450 2D6 Substrate | Non-substrate | 0.8218 |
| CYP450 3A4 Substrate | Non-substrate | 0.6788 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.8726 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9409 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9413 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.7794 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9357 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9765 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8895 |
| Non-inhibitor | 0.8596 | |
| AMES Toxicity | Non AMES toxic | 0.8079 |
| Carcinogens | Non-carcinogens | 0.9157 |
| Fish Toxicity | Low FHMT | 0.8157 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9634 |
| Honey Bee Toxicity | High HBT | 0.6190 |
| Biodegradation | Not ready biodegradable | 0.7383 |
| Acute Oral Toxicity | III | 0.8086 |
| Carcinogenicity (Three-class) | Non-required | 0.6139 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.2110 | LogS |
| Caco-2 Permeability | 0.9094 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.4335 | LD50, mol/kg |
| Fish Toxicity | 2.7105 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.5381 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Dioxanes |
| Subclass | 1,3-dioxanes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | 1,3-dioxanes |
| Alternative Parents | |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Meta-dioxane - Secondary alcohol - Oxacycle - Acetal - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as 1,3-dioxanes. These are organic compounds containing 1,3-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 3. |
From ClassyFire