General Information

Chemical nameMethyl propyl sulfide
CAS number3877-15-4
COE number11541
Flavouring typesubstances
FL No.12.166
MixtureNo
Purity of the named substance at least 95% unless otherwise specified
Reference bodyEFSA

From webgate.ec.europa.eu

Computed Descriptors

Download SDF
2D Structure
CID19754
IUPAC Name1-methylsulfanylpropane
InChIInChI=1S/C4H10S/c1-3-4-5-2/h3-4H2,1-2H3
InChI KeyZOASGOXWEHUTKZ-UHFFFAOYSA-N
Canonical SMILESCCCSC
Molecular FormulaC4H10S
Wikipediamethyl propyl sulphide

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight90.184
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count2
Complexity13.1
CACTVS Substructure Key Fingerprint A A A D c c B g 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 G A Q A A A A A C A C E Q A C C A A A A A A g A A A A A A A A A A A A A A B A A A A A A A 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 = =
Topological Polar Surface Area25.3
Monoisotopic Mass90.05
Exact Mass90.05
XLogP3None
XLogP3-AA1.8
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count5
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+0.9867
Human Intestinal AbsorptionHIA+1.0000
Caco-2 PermeabilityCaco2+0.7818
P-glycoprotein SubstrateNon-substrate0.6739
P-glycoprotein InhibitorNon-inhibitor0.9350
Non-inhibitor0.9363
Renal Organic Cation TransporterNon-inhibitor0.8391
Distribution
Subcellular localizationLysosome0.6212
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8375
CYP450 2D6 SubstrateNon-substrate0.7519
CYP450 3A4 SubstrateNon-substrate0.6782
CYP450 1A2 InhibitorNon-inhibitor0.7515
CYP450 2C9 InhibitorNon-inhibitor0.9157
CYP450 2D6 InhibitorNon-inhibitor0.9241
CYP450 2C19 InhibitorNon-inhibitor0.9028
CYP450 3A4 InhibitorNon-inhibitor0.9891
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.9155
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9034
Non-inhibitor0.9141
AMES ToxicityNon AMES toxic0.9219
CarcinogensCarcinogens 0.5833
Fish ToxicityHigh FHMT0.6346
Tetrahymena Pyriformis ToxicityLow TPT0.7353
Honey Bee ToxicityHigh HBT0.7906
BiodegradationNot ready biodegradable0.5528
Acute Oral ToxicityIII0.7424
Carcinogenicity (Three-class)Non-required0.7024

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-1.7632LogS
Caco-2 Permeability1.7566LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.8648LD50, mol/kg
Fish Toxicity2.4406pLC50, mg/L
Tetrahymena Pyriformis Toxicity-0.7645pIGC50, 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