Relevant Data

Food Additives Approved by WHO:

Flavouring Substances Approved by European Union:

  • Ethane-1,1-dithiol [show]

General Information

MaintermETHANE-1,1-DITHIOL
Doc TypeEAF
CAS Reg.No.(or other ID)69382-62-3
Regnum

From www.fda.gov

Computed Descriptors

Download SDF
2D Structure
CID33645
IUPAC Nameethane-1,1-dithiol
InChIInChI=1S/C2H6S2/c1-2(3)4/h2-4H,1H3
InChI KeyDHBXNPKRAUYBTH-UHFFFAOYSA-N
Canonical SMILESCC(S)S
Molecular FormulaC2H6S2
Wikipedia1,1-ethanedithiol

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight94.19
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Complexity11.5
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 G A Q A A A A A A A C E Q A C C 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 Mass93.991
Exact Mass93.991
XLogP3None
XLogP3-AA1.3
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count4
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+0.9395
Human Intestinal AbsorptionHIA+0.9835
Caco-2 PermeabilityCaco2+0.5384
P-glycoprotein SubstrateNon-substrate0.8009
P-glycoprotein InhibitorNon-inhibitor0.9759
Non-inhibitor0.9850
Renal Organic Cation TransporterNon-inhibitor0.9254
Distribution
Subcellular localizationLysosome0.5740
Metabolism
CYP450 2C9 SubstrateNon-substrate0.7083
CYP450 2D6 SubstrateNon-substrate0.8421
CYP450 3A4 SubstrateNon-substrate0.8069
CYP450 1A2 InhibitorNon-inhibitor0.8337
CYP450 2C9 InhibitorNon-inhibitor0.7831
CYP450 2D6 InhibitorNon-inhibitor0.9529
CYP450 2C19 InhibitorNon-inhibitor0.9070
CYP450 3A4 InhibitorNon-inhibitor0.9642
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.7806
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9836
Non-inhibitor0.9607
AMES ToxicityNon AMES toxic0.9360
CarcinogensCarcinogens 0.5742
Fish ToxicityHigh FHMT0.8432
Tetrahymena Pyriformis ToxicityLow TPT0.7283
Honey Bee ToxicityHigh HBT0.8497
BiodegradationNot ready biodegradable0.7793
Acute Oral ToxicityIII0.5766
Carcinogenicity (Three-class)Non-required0.5574

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-0.6182LogS
Caco-2 Permeability1.1162LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity2.0961LD50, mol/kg
Fish Toxicity2.3646pLC50, mg/L
Tetrahymena Pyriformis Toxicity-0.7028pIGC50, 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