3-MERCAPTOHEXYL HEXANOATE
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | 3-MERCAPTOHEXYL HEXANOATE |
| Doc Type | EAF |
| CAS Reg.No.(or other ID) | 136954-22-8 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 536987 |
| IUPAC Name | 3-sulfanylhexyl hexanoate |
| InChI | InChI=1S/C12H24O2S/c1-3-5-6-8-12(13)14-10-9-11(15)7-4-2/h11,15H,3-10H2,1-2H3 |
| InChI Key | KVXKOWZLYWBURN-UHFFFAOYSA-N |
| Canonical SMILES | CCCCCC(=O)OCCC(CCC)S |
| Molecular Formula | C12H24O2S |
| Wikipedia | 3-mercaptohexyl hexanoate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 232.382 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 10 |
| Complexity | 160.0 |
| CACTVS Substructure Key Fingerprint | A A A D c e B w M 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 g Q A A A A A C A C k w A K C C A A A B A Q I A A C Q C A A A A A A A A A A A A A E A A A A A A B I A A A A C A A A E A A A A A A G I S A A A A A A A A A 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 | 27.3 |
| Monoisotopic Mass | 232.15 |
| Exact Mass | 232.15 |
| XLogP3 | None |
| XLogP3-AA | 4.0 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 15 |
| 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+ | 0.9807 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.7222 |
| P-glycoprotein Substrate | Non-substrate | 0.6864 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8750 |
| Non-inhibitor | 0.9194 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.9093 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.6282 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8452 |
| CYP450 2D6 Substrate | Non-substrate | 0.8623 |
| CYP450 3A4 Substrate | Non-substrate | 0.6559 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.5430 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8592 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9237 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8901 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9033 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8354 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9725 |
| Non-inhibitor | 0.7968 | |
| AMES Toxicity | Non AMES toxic | 0.9390 |
| Carcinogens | Non-carcinogens | 0.6053 |
| Fish Toxicity | High FHMT | 0.9688 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9923 |
| Honey Bee Toxicity | High HBT | 0.8040 |
| Biodegradation | Ready biodegradable | 0.8938 |
| Acute Oral Toxicity | III | 0.6495 |
| Carcinogenicity (Three-class) | Non-required | 0.6935 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -3.4094 | LogS |
| Caco-2 Permeability | 1.4553 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.9186 | LD50, mol/kg |
| Fish Toxicity | 1.1751 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.5587 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Fatty Acyls |
| Subclass | Fatty acid esters |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Fatty acid esters |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Fatty acid ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Alkylthiol - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid. |
From ClassyFire