DIMERCAPTOMETHANE
Relevant Data
Food Additives Approved in the United States
Flavouring Substances Approved by European Union:
General Information
| CAS number: | 6725-64-0 |
| JECFA number: | 1661 |
| FEMA number: | 4097 |
| Functional Class: |
Flavouring Agent FLAVOURING_AGENT |
From apps.who.int
Evaluations
| Evaluation year: | 2007 |
| ADI: | No safety concern at current levels of intake when used as a flavouring agent |
| Report: | TRS 947-JECFA68/ |
| Tox Monograph: | FAS 59-JECFA68/ |
| Specification: | FAO JECFA Monographs 4-JECFA 68/ . N |
From apps.who.int
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 138818 |
| IUPAC Name | methanedithiol |
| InChI | InChI=1S/CH4S2/c2-1-3/h2-3H,1H2 |
| InChI Key | INBDPOJZYZJUDA-UHFFFAOYSA-N |
| Canonical SMILES | C(S)S |
| Molecular Formula | CH4S2 |
| Wikipedia | methanedithiol |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 80.163 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Complexity | 2.8 |
| CACTVS Substructure Key Fingerprint | A A A D c Y A 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 A A A A A A A Q 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 | 2.0 |
| Monoisotopic Mass | 79.975 |
| Exact Mass | 79.975 |
| 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
ADMET Predicted Profile --- Classification
| Model | Result | Probability |
|---|---|---|
| Absorption | ||
| Blood-Brain Barrier | BBB+ | 0.9355 |
| Human Intestinal Absorption | HIA+ | 0.9753 |
| Caco-2 Permeability | Caco2+ | 0.5827 |
| P-glycoprotein Substrate | Non-substrate | 0.8549 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9618 |
| Non-inhibitor | 0.9261 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8735 |
| Distribution | ||
| Subcellular localization | Lysosome | 0.5389 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8463 |
| CYP450 2D6 Substrate | Non-substrate | 0.8191 |
| CYP450 3A4 Substrate | Non-substrate | 0.8096 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.7251 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.7375 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9389 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8184 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9118 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.6685 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9586 |
| Non-inhibitor | 0.9598 | |
| AMES Toxicity | Non AMES toxic | 0.7455 |
| Carcinogens | Carcinogens | 0.6249 |
| Fish Toxicity | High FHMT | 0.5737 |
| Tetrahymena Pyriformis Toxicity | Low TPT | 0.8703 |
| Honey Bee Toxicity | High HBT | 0.8136 |
| Biodegradation | Not ready biodegradable | 0.8078 |
| Acute Oral Toxicity | II | 0.6800 |
| Carcinogenicity (Three-class) | Non-required | 0.4838 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -0.3847 | LogS |
| Caco-2 Permeability | 1.1854 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 2.5694 | LD50, mol/kg |
| Fish Toxicity | 2.6047 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.4802 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organosulfur compounds |
| Class | Thiols |
| Subclass | Alkylthiols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Alkylthiols |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Alkylthiol - Hydrocarbon derivative - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as alkylthiols. These are organic compounds containing the thiol functional group linked to an alkyl chain. |
From ClassyFire