Ethyl propyl sulfide
General Information
| Chemical name | Ethyl propyl sulfide |
| CAS number | 4110-50-3 |
| COE number | 11479 |
| Flavouring type | substances |
| FL No. | 12.127 |
| 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 | 20063 |
| IUPAC Name | 1-ethylsulfanylpropane |
| InChI | InChI=1S/C5H12S/c1-3-5-6-4-2/h3-5H2,1-2H3 |
| InChI Key | ZDDDFDQTSXYYSE-UHFFFAOYSA-N |
| Canonical SMILES | CCCSCC |
| Molecular Formula | C5H12S |
| Wikipedia | ethyl propyl sulfide |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 104.211 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 3 |
| Complexity | 19.9 |
| CACTVS Substructure Key Fingerprint | A A A D c c B g 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 A A A A A A A A A A A A A A A G A Q A A A A A C A C E Q A C C A A A A A A g A A A A A A A A A A A A A A B A A A A A A A A A A A A A g A A A A A A 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 A A A A A A A A A A A A = = |
| Topological Polar Surface Area | 25.3 |
| Monoisotopic Mass | 104.066 |
| Exact Mass | 104.066 |
| XLogP3 | None |
| XLogP3-AA | 2.1 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 6 |
| 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+ | 0.9848 |
| Human Intestinal Absorption | HIA+ | 0.9972 |
| Caco-2 Permeability | Caco2+ | 0.7599 |
| P-glycoprotein Substrate | Non-substrate | 0.5662 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9052 |
| Non-inhibitor | 0.9428 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8365 |
| Distribution | ||
| Subcellular localization | Lysosome | 0.7475 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8481 |
| CYP450 2D6 Substrate | Non-substrate | 0.7620 |
| CYP450 3A4 Substrate | Non-substrate | 0.7109 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.7047 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8899 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9051 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8808 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9721 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8574 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8372 |
| Non-inhibitor | 0.7923 | |
| AMES Toxicity | Non AMES toxic | 0.9708 |
| Carcinogens | Carcinogens | 0.6416 |
| Fish Toxicity | High FHMT | 0.8453 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.7523 |
| Honey Bee Toxicity | High HBT | 0.7566 |
| Biodegradation | Not ready biodegradable | 0.7813 |
| Acute Oral Toxicity | III | 0.6296 |
| Carcinogenicity (Three-class) | Non-required | 0.5303 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.4424 | LogS |
| Caco-2 Permeability | 1.5629 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.8150 | LD50, mol/kg |
| Fish Toxicity | 1.1579 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.1317 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organosulfur compounds |
| Class | Thioethers |
| Subclass | Dialkylthioethers |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Dialkylthioethers |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Dialkylthioether - Sulfenyl compound - Hydrocarbon derivative - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as dialkylthioethers. These are organosulfur compounds containing a thioether group that is substituted by two alkyl groups. |
From ClassyFire