3-HEXANOL
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | 3-HEXANOL |
| Doc Type | ASP |
| CAS Reg.No.(or other ID) | 623-37-0 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 12178 |
| IUPAC Name | hexan-3-ol |
| InChI | InChI=1S/C6H14O/c1-3-5-6(7)4-2/h6-7H,3-5H2,1-2H3 |
| InChI Key | ZOCHHNOQQHDWHG-UHFFFAOYSA-N |
| Canonical SMILES | CCCC(CC)O |
| Molecular Formula | C6H14O |
| Wikipedia | 3-hexanol |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 102.177 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 3 |
| Complexity | 35.2 |
| CACTVS Substructure Key Fingerprint | A A A D c c B g 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 C A A A C B S g g A I C A A A A A 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 A E A I A A A A A Q A A E 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 = = |
| Topological Polar Surface Area | 20.2 |
| Monoisotopic Mass | 102.104 |
| Exact Mass | 102.104 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 7 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| 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+ | 0.9784 |
| Human Intestinal Absorption | HIA+ | 0.9942 |
| Caco-2 Permeability | Caco2+ | 0.8376 |
| P-glycoprotein Substrate | Non-substrate | 0.6078 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8902 |
| Non-inhibitor | 0.9248 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.9263 |
| Distribution | ||
| Subcellular localization | Lysosome | 0.4228 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8435 |
| CYP450 2D6 Substrate | Non-substrate | 0.8405 |
| CYP450 3A4 Substrate | Non-substrate | 0.6548 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.6009 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9191 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9205 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9231 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9560 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8884 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8775 |
| Non-inhibitor | 0.7435 | |
| AMES Toxicity | Non AMES toxic | 0.9735 |
| Carcinogens | Carcinogens | 0.5326 |
| Fish Toxicity | High FHMT | 0.5000 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.5377 |
| Honey Bee Toxicity | High HBT | 0.7361 |
| Biodegradation | Ready biodegradable | 0.8580 |
| Acute Oral Toxicity | III | 0.8788 |
| Carcinogenicity (Three-class) | Non-required | 0.7288 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -0.9190 | LogS |
| Caco-2 Permeability | 1.4023 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.8334 | LD50, mol/kg |
| Fish Toxicity | 1.6952 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.6056 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Class | Organooxygen compounds |
| Subclass | Alcohols and polyols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Secondary alcohols |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Secondary alcohol - Hydrocarbon derivative - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as secondary alcohols. These are compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R') (R,R'=alkyl, aryl). |
From ClassyFire