Relevant Data

Food Additives Approved by WHO:

Flavouring Substances Approved by European Union:

  • Dimercaptomethane [show]

General Information

MaintermDIMERCAPTOMETHANE
Doc TypeEAF
CAS Reg.No.(or other ID)6725-64-0
Regnum

From www.fda.gov

Computed Descriptors

Download SDF
2D Structure
CID138818
IUPAC Namemethanedithiol
InChIInChI=1S/CH4S2/c2-1-3/h2-3H,1H2
InChI KeyINBDPOJZYZJUDA-UHFFFAOYSA-N
Canonical SMILESC(S)S
Molecular FormulaCH4S2
Wikipediamethanedithiol

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight80.163
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Complexity2.8
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 Area2.0
Monoisotopic Mass79.975
Exact Mass79.975
XLogP3None
XLogP3-AA0.9
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count3
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count1

From Pubchem


ADMET Predicted Profile --- Classification

Model Result Probability
Absorption
Blood-Brain BarrierBBB+0.9355
Human Intestinal AbsorptionHIA+0.9753
Caco-2 PermeabilityCaco2+0.5827
P-glycoprotein SubstrateNon-substrate0.8549
P-glycoprotein InhibitorNon-inhibitor0.9618
Non-inhibitor0.9261
Renal Organic Cation TransporterNon-inhibitor0.8735
Distribution
Subcellular localizationLysosome0.5389
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8463
CYP450 2D6 SubstrateNon-substrate0.8191
CYP450 3A4 SubstrateNon-substrate0.8096
CYP450 1A2 InhibitorNon-inhibitor0.7251
CYP450 2C9 InhibitorNon-inhibitor0.7375
CYP450 2D6 InhibitorNon-inhibitor0.9389
CYP450 2C19 InhibitorNon-inhibitor0.8184
CYP450 3A4 InhibitorNon-inhibitor0.9118
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.6685
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9586
Non-inhibitor0.9598
AMES ToxicityNon AMES toxic0.7455
CarcinogensCarcinogens 0.6249
Fish ToxicityHigh FHMT0.5737
Tetrahymena Pyriformis ToxicityLow TPT0.8703
Honey Bee ToxicityHigh HBT0.8136
BiodegradationNot ready biodegradable0.8078
Acute Oral ToxicityII0.6800
Carcinogenicity (Three-class)Non-required0.4838

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-0.3847LogS
Caco-2 Permeability1.1854LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity2.5694LD50, mol/kg
Fish Toxicity2.6047pLC50, mg/L
Tetrahymena Pyriformis Toxicity-0.4802pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganosulfur compounds
ClassThiols
SubclassAlkylthiols
Intermediate Tree NodesNot available
Direct ParentAlkylthiols
Alternative Parents
Molecular FrameworkAliphatic acyclic compounds
SubstituentsAlkylthiol - Hydrocarbon derivative - Aliphatic acyclic compound
DescriptionThis 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