Relevant Data

Food Additives Approved by WHO:

Flavouring Substances Approved by European Union:

  • Dimethyl sulfide [show]

General Information

MaintermMETHYL SULFIDE
Doc TypeASP
CAS Reg.No.(or other ID)75-18-3
Regnum 172.515

From www.fda.gov

Computed Descriptors

Download SDF
2D Structure
CID1068
IUPAC Namemethylsulfanylmethane
InChIInChI=1S/C2H6S/c1-3-2/h1-2H3
InChI KeyQMMFVYPAHWMCMS-UHFFFAOYSA-N
Canonical SMILESCSC
Molecular FormulaC2H6S
Wikipediamethyl sulfide

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight62.13
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Complexity2.8
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 Area25.3
Monoisotopic Mass62.019
Exact Mass62.019
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


Food Additives Biosynthesis/Degradation


ADMET Predicted Profile --- Classification

Model Result Probability
Absorption
Blood-Brain BarrierBBB+0.9755
Human Intestinal AbsorptionHIA+0.9953
Caco-2 PermeabilityCaco2+0.6633
P-glycoprotein SubstrateNon-substrate0.7865
P-glycoprotein InhibitorNon-inhibitor0.9652
Non-inhibitor0.9898
Renal Organic Cation TransporterNon-inhibitor0.9140
Distribution
Subcellular localizationLysosome0.6582
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8281
CYP450 2D6 SubstrateNon-substrate0.8396
CYP450 3A4 SubstrateNon-substrate0.7094
CYP450 1A2 InhibitorNon-inhibitor0.8579
CYP450 2C9 InhibitorNon-inhibitor0.9065
CYP450 2D6 InhibitorNon-inhibitor0.9553
CYP450 2C19 InhibitorNon-inhibitor0.9168
CYP450 3A4 InhibitorNon-inhibitor0.9858
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.9150
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9625
Non-inhibitor0.9538
AMES ToxicityNon AMES toxic0.8994
CarcinogensCarcinogens 0.6312
Fish ToxicityHigh FHMT0.5816
Tetrahymena Pyriformis ToxicityLow TPT0.9054
Honey Bee ToxicityHigh HBT0.8422
BiodegradationNot ready biodegradable0.8400
Acute Oral ToxicityIII0.7954
Carcinogenicity (Three-class)Non-required0.6326

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-0.4953LogS
Caco-2 Permeability1.6061LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.2675LD50, mol/kg
Fish Toxicity3.0812pLC50, mg/L
Tetrahymena Pyriformis Toxicity-1.3175pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganosulfur compounds
ClassThioethers
SubclassDialkylthioethers
Intermediate Tree NodesNot available
Direct ParentDialkylthioethers
Alternative Parents
Molecular FrameworkAliphatic acyclic compounds
SubstituentsDialkylthioether - Sulfenyl compound - Hydrocarbon derivative - Aliphatic acyclic compound
DescriptionThis 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