Diallyl sulfide
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | Diallyl sulfide |
| CAS number | 592-88-1 |
| COE number | 11846 |
| JECFA number | 458 |
| Flavouring type | substances |
| FL No. | 12.088 |
| Mixture | No |
| Purity of the named substance at least 95% unless otherwise specified | |
| Reference body | JECFA |
From webgate.ec.europa.eu
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 11617 |
| IUPAC Name | 3-prop-2-enylsulfanylprop-1-ene |
| InChI | InChI=1S/C6H10S/c1-3-5-7-6-4-2/h3-4H,1-2,5-6H2 |
| InChI Key | UBJVUCKUDDKUJF-UHFFFAOYSA-N |
| Canonical SMILES | C=CCSCC=C |
| Molecular Formula | C6H10S |
| Wikipedia | allyl sulfide |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 114.206 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 4 |
| Complexity | 49.2 |
| 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 A A A A A A A i A A C B C A A A A A A A A A B A I A A A A A A A A A A A A A Q 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 | 114.05 |
| Exact Mass | 114.05 |
| XLogP3 | None |
| XLogP3-AA | 2.2 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 7 |
| 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+ | 0.9730 |
| Human Intestinal Absorption | HIA+ | 0.9901 |
| Caco-2 Permeability | Caco2+ | 0.7134 |
| P-glycoprotein Substrate | Non-substrate | 0.7909 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9187 |
| Non-inhibitor | 0.9579 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8325 |
| Distribution | ||
| Subcellular localization | Lysosome | 0.5392 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8584 |
| CYP450 2D6 Substrate | Non-substrate | 0.8557 |
| CYP450 3A4 Substrate | Non-substrate | 0.7960 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.6525 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8034 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9623 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.7404 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9586 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.6960 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8476 |
| Non-inhibitor | 0.9691 | |
| AMES Toxicity | Non AMES toxic | 0.6775 |
| Carcinogens | Carcinogens | 0.6993 |
| Fish Toxicity | High FHMT | 0.9328 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.7303 |
| Honey Bee Toxicity | High HBT | 0.8655 |
| Biodegradation | Not ready biodegradable | 0.9744 |
| Acute Oral Toxicity | III | 0.8261 |
| Carcinogenicity (Three-class) | Non-required | 0.3817 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -1.0789 | LogS |
| Caco-2 Permeability | 1.6915 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 2.0903 | LD50, mol/kg |
| Fish Toxicity | 0.7187 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.4921 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organosulfur compounds |
| Class | Allyl sulfur compounds |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Allyl sulfur compounds |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Allyl sulfur compound - Dialkylthioether - Sulfenyl compound - Thioether - Hydrocarbon derivative - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as allyl sulfur compounds. These are compounds containing an allylsulfur group, with the general structure H2C(=CH2)CS. |
From ClassyFire