2-METHYL-1-BUTANETHIOL
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | 2-METHYL-1-BUTANETHIOL |
| Doc Type | ASP |
| CAS Reg.No.(or other ID) | 1878-18-8 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 15877 |
| IUPAC Name | 2-methylbutane-1-thiol |
| InChI | InChI=1S/C5H12S/c1-3-5(2)4-6/h5-6H,3-4H2,1-2H3 |
| InChI Key | WGQKBCSACFQGQY-UHFFFAOYSA-N |
| Canonical SMILES | CCC(C)CS |
| Molecular Formula | C5H12S |
| Wikipedia | 2-methyl-1-butanethiol |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 104.211 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 2 |
| Complexity | 27.1 |
| 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 D Q 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 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 = = |
| Topological Polar Surface Area | 1.0 |
| Monoisotopic Mass | 104.066 |
| Exact Mass | 104.066 |
| XLogP3 | None |
| XLogP3-AA | 2.2 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 6 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Isotope Atom Count | 0 |
| Covalently-Bonded Unit Count | 1 |
From Pubchem
ADMET Predicted Profile --- Classification
| Model | Result | Probability |
|---|---|---|
| Absorption | ||
| Blood-Brain Barrier | BBB+ | 0.9842 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.7524 |
| P-glycoprotein Substrate | Non-substrate | 0.7732 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9257 |
| Non-inhibitor | 0.9601 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.9059 |
| Distribution | ||
| Subcellular localization | Lysosome | 0.7433 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8450 |
| CYP450 2D6 Substrate | Non-substrate | 0.7889 |
| CYP450 3A4 Substrate | Non-substrate | 0.7609 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.7176 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8500 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.8639 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8749 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9472 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8249 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9727 |
| Non-inhibitor | 0.9235 | |
| AMES Toxicity | Non AMES toxic | 0.9793 |
| Carcinogens | Carcinogens | 0.7136 |
| Fish Toxicity | High FHMT | 0.8514 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.8307 |
| Honey Bee Toxicity | High HBT | 0.8368 |
| Biodegradation | Not ready biodegradable | 0.5595 |
| Acute Oral Toxicity | III | 0.6739 |
| Carcinogenicity (Three-class) | Non-required | 0.6466 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.2199 | LogS |
| Caco-2 Permeability | 1.7019 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.6771 | LD50, mol/kg |
| Fish Toxicity | 2.3483 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.3286 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organosulfur compounds |
| Class | Thiols |
| Subclass | Alkylthiols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Alkylthiols |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Alkylthiol - Hydrocarbon derivative - Aliphatic acyclic compound |
| Description | This 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