Pentadecan-1-ol
General Information
| Chemical name | Pentadecan-1-ol |
| CAS number | 629-76-5 |
| Flavouring type | substances |
| FL No. | 02.202 |
| Mixture | No |
| Purity of the named substance at least 95% unless otherwise specified |
From webgate.ec.europa.eu
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 12397 |
| IUPAC Name | pentadecan-1-ol |
| InChI | InChI=1S/C15H32O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h16H,2-15H2,1H3 |
| InChI Key | REIUXOLGHVXAEO-UHFFFAOYSA-N |
| Canonical SMILES | CCCCCCCCCCCCCCCO |
| Molecular Formula | C15H32O |
| Wikipedia | pentadecyl alcohol |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 228.42 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 13 |
| Complexity | 112.0 |
| CACTVS Substructure Key Fingerprint | A A A D c f B w 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 A C 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 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 | 20.2 |
| Monoisotopic Mass | 228.245 |
| Exact Mass | 228.245 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 16 |
| 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+ | 0.9579 |
| Human Intestinal Absorption | HIA+ | 0.9947 |
| Caco-2 Permeability | Caco2+ | 0.7688 |
| P-glycoprotein Substrate | Non-substrate | 0.6180 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9201 |
| Non-inhibitor | 0.9092 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8735 |
| Distribution | ||
| Subcellular localization | Lysosome | 0.7017 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.7931 |
| CYP450 2D6 Substrate | Non-substrate | 0.8437 |
| CYP450 3A4 Substrate | Non-substrate | 0.7094 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.5000 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8798 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9262 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9330 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9142 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8928 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8578 |
| Non-inhibitor | 0.7525 | |
| AMES Toxicity | Non AMES toxic | 0.9872 |
| Carcinogens | Non-carcinogens | 0.5579 |
| Fish Toxicity | High FHMT | 0.7423 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.8899 |
| Honey Bee Toxicity | High HBT | 0.6964 |
| Biodegradation | Ready biodegradable | 0.8849 |
| Acute Oral Toxicity | III | 0.8548 |
| Carcinogenicity (Three-class) | Non-required | 0.7292 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.9473 | LogS |
| Caco-2 Permeability | 1.3872 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.5561 | LD50, mol/kg |
| Fish Toxicity | 1.2558 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.7150 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Fatty Acyls |
| Subclass | Fatty alcohols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Long-chain fatty alcohols |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Long chain fatty alcohol - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as long-chain fatty alcohols. These are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms. |
From ClassyFire