METHYL SULFIDE
Relevant Data
Food Additives Approved in the United States
Flavouring Substances Approved by European Union:
General Information
| Synonyms: | 2-THIAPROPANE, THIOBISMETHANE |
| Chemical Names: | DIMETHYL SULFIDE |
| CAS number: | 75-18-3 |
| COE number: | 483 |
| JECFA number: | 452 |
| FEMA number: | 2746 |
| Functional Class: |
Flavouring Agent FLAVOURING_AGENT |
From apps.who.int
Evaluations
| Evaluation year: | 1999 |
| ADI: | No safety concern at current levels of intake when used as a flavouring agent |
| Report: | TRS 896-JECFA 53/32 |
| Tox Monograph: | FAS 44-JECFA 53/125 |
| Specification: | COMPENDIUM ADDENDUM 7/FNP 52 Add.7/110 |
From apps.who.int
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 1068 |
| IUPAC Name | methylsulfanylmethane |
| InChI | InChI=1S/C2H6S/c1-3-2/h1-2H3 |
| InChI Key | QMMFVYPAHWMCMS-UHFFFAOYSA-N |
| Canonical SMILES | CSC |
| Molecular Formula | C2H6S |
| Wikipedia | methyl sulfide |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 62.13 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Complexity | 2.8 |
| CACTVS Substructure Key Fingerprint | A A A D c Y B A 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 E A Q A A A A A A A A A A A C C 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 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 | 25.3 |
| Monoisotopic Mass | 62.019 |
| Exact Mass | 62.019 |
| XLogP3 | None |
| XLogP3-AA | 0.9 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 3 |
| 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+ | 0.9755 |
| Human Intestinal Absorption | HIA+ | 0.9953 |
| Caco-2 Permeability | Caco2+ | 0.6633 |
| P-glycoprotein Substrate | Non-substrate | 0.7865 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9652 |
| Non-inhibitor | 0.9898 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.9140 |
| Distribution | ||
| Subcellular localization | Lysosome | 0.6582 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8281 |
| CYP450 2D6 Substrate | Non-substrate | 0.8396 |
| CYP450 3A4 Substrate | Non-substrate | 0.7094 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.8579 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9065 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9553 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9168 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9858 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9150 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9625 |
| Non-inhibitor | 0.9538 | |
| AMES Toxicity | Non AMES toxic | 0.8994 |
| Carcinogens | Carcinogens | 0.6312 |
| Fish Toxicity | High FHMT | 0.5816 |
| Tetrahymena Pyriformis Toxicity | Low TPT | 0.9054 |
| Honey Bee Toxicity | High HBT | 0.8422 |
| Biodegradation | Not ready biodegradable | 0.8400 |
| Acute Oral Toxicity | III | 0.7954 |
| Carcinogenicity (Three-class) | Non-required | 0.6326 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -0.4953 | LogS |
| Caco-2 Permeability | 1.6061 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.2675 | LD50, mol/kg |
| Fish Toxicity | 3.0812 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -1.3175 | 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