Relevant Data

Food Additives Approved by WHO:

Flavouring Substances Approved by European Union:

  • Pentane-2-thiol [show]

General Information

Mainterm2-PENTANETHIOL
Doc TypeEAF
CAS Reg.No.(or other ID)2084-19-7
Regnum

From www.fda.gov

Computed Descriptors

Download SDF
2D Structure
CID62424
IUPAC Namepentane-2-thiol
InChIInChI=1S/C5H12S/c1-3-4-5(2)6/h5-6H,3-4H2,1-2H3
InChI KeyQUSTYFNPKBDELJ-UHFFFAOYSA-N
Canonical SMILESCCCC(C)S
Molecular FormulaC5H12S
Wikipedia2-pentanethiol

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight104.211
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count2
Complexity27.1
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 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 I A A A A A A A A A A A A A A A A A A A A A A A A A A A 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 Area1.0
Monoisotopic Mass104.066
Exact Mass104.066
XLogP3None
XLogP3-AA2.2
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count6
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
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+0.9810
Human Intestinal AbsorptionHIA+1.0000
Caco-2 PermeabilityCaco2+0.7609
P-glycoprotein SubstrateNon-substrate0.7102
P-glycoprotein InhibitorNon-inhibitor0.9109
Non-inhibitor0.9313
Renal Organic Cation TransporterNon-inhibitor0.9282
Distribution
Subcellular localizationLysosome0.6593
Metabolism
CYP450 2C9 SubstrateNon-substrate0.7940
CYP450 2D6 SubstrateNon-substrate0.7549
CYP450 3A4 SubstrateNon-substrate0.7418
CYP450 1A2 InhibitorNon-inhibitor0.6120
CYP450 2C9 InhibitorNon-inhibitor0.8391
CYP450 2D6 InhibitorNon-inhibitor0.8642
CYP450 2C19 InhibitorNon-inhibitor0.8155
CYP450 3A4 InhibitorNon-inhibitor0.9673
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.7228
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9699
Non-inhibitor0.9071
AMES ToxicityNon AMES toxic0.9549
CarcinogensCarcinogens 0.5137
Fish ToxicityHigh FHMT0.9495
Tetrahymena Pyriformis ToxicityHigh TPT0.8861
Honey Bee ToxicityHigh HBT0.8420
BiodegradationReady biodegradable0.6864
Acute Oral ToxicityIII0.4739
Carcinogenicity (Three-class)Non-required0.6583

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-3.0600LogS
Caco-2 Permeability1.7946LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.9409LD50, mol/kg
Fish Toxicity1.4053pLC50, mg/L
Tetrahymena Pyriformis Toxicity-0.2612pIGC50, 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