Dimethyl trisulfide
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | Dimethyl trisulfide |
| CAS number | 3658-80-8 |
| COE number | 539 |
| JECFA number | 582 |
| Flavouring type | substances |
| FL No. | 12.013 |
| 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 | 19310 |
| IUPAC Name | (methyltrisulfanyl)methane |
| InChI | InChI=1S/C2H6S3/c1-3-5-4-2/h1-2H3 |
| InChI Key | YWHLKYXPLRWGSE-UHFFFAOYSA-N |
| Canonical SMILES | CSSSC |
| Molecular Formula | C2H6S3 |
| Wikipedia | dimethyl trisulfide |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 126.25 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 2 |
| Complexity | 12.4 |
| CACTVS Substructure Key Fingerprint | A A A D c Y B 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 A A A A A A A A A A A A A A A E A Q A A A A A A A A A A A C 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 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 A A A A A A A A A A A = = |
| Topological Polar Surface Area | 75.9 |
| Monoisotopic Mass | 125.963 |
| Exact Mass | 125.963 |
| XLogP3 | None |
| XLogP3-AA | 1.3 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 5 |
| 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
Food Additives Biosynthesis/Degradation
ADMET Predicted Profile --- Classification
| Model | Result | Probability |
|---|---|---|
| Absorption | ||
| Blood-Brain Barrier | BBB+ | 0.9778 |
| Human Intestinal Absorption | HIA+ | 0.9866 |
| Caco-2 Permeability | Caco2+ | 0.5937 |
| P-glycoprotein Substrate | Non-substrate | 0.8441 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9623 |
| Non-inhibitor | 0.9954 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.9237 |
| Distribution | ||
| Subcellular localization | Lysosome | 0.4968 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8139 |
| CYP450 2D6 Substrate | Non-substrate | 0.8406 |
| CYP450 3A4 Substrate | Non-substrate | 0.7343 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.7773 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8126 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9040 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8261 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9650 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8321 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9393 |
| Non-inhibitor | 0.9593 | |
| AMES Toxicity | Non AMES toxic | 0.8675 |
| Carcinogens | Carcinogens | 0.6799 |
| Fish Toxicity | Low FHMT | 0.5422 |
| Tetrahymena Pyriformis Toxicity | Low TPT | 0.6093 |
| Honey Bee Toxicity | High HBT | 0.8557 |
| Biodegradation | Not ready biodegradable | 0.7094 |
| Acute Oral Toxicity | II | 0.6252 |
| Carcinogenicity (Three-class) | Non-required | 0.6515 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -1.5400 | LogS |
| Caco-2 Permeability | 1.5049 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 2.4653 | LD50, mol/kg |
| Fish Toxicity | 1.9903 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -1.0717 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organosulfur compounds |
| Class | Organic trisulfides |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Organic trisulfides |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Organic trisulfide - Sulfenyl compound - Hydrocarbon derivative - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as organic trisulfides. These are organosulfur compounds with the general formula RSSSR' (R,R'=alkyl, aryl). |
From ClassyFire