METHYLTHIO 2-(PROPIONYLOXY) PROPIONATE
Relevant Data
Food Additives Approved in the United States
Flavouring Substances Approved by European Union:
General Information
| Synonyms: | PROPIONYLLACTIC ACID THIOMETHYL ESTER |
| Chemical Names: | S-METHYL 2-(PROPIONYLOXY)PROPANETHIOATE |
| CAS number: | 93940-60-4 |
| JECFA number: | 493 |
| FEMA number: | 3790 |
| Functional Class: |
Flavouring Agent FLAVOURING_AGENT |
From apps.who.int
Evaluations
| Evaluation year: | 1999 |
| ADI: | No safety concern at current levels of intake when used as a flavouring agent |
| Report: | TRS 896-JECFA 53/32 |
| Tox Monograph: | FAS 44-JECFA 53/125 |
| Specification: | COMPENDIUM ADDENDUM 10/FNP 52 Add.10/40 (2002) |
From apps.who.int
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 16205885 |
| IUPAC Name | S-methyl 2-propoxypropanethioate |
| InChI | InChI=1S/C7H14O2S/c1-4-5-9-6(2)7(8)10-3/h6H,4-5H2,1-3H3 |
| InChI Key | LCIGYKJDIBCNQK-UHFFFAOYSA-N |
| Canonical SMILES | CCCOC(C)C(=O)SC |
| Molecular Formula | C7H14O2S |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 162.247 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 5 |
| Complexity | 104.0 |
| CACTVS Substructure Key Fingerprint | A A A D c c B g 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 B S g w A K C A A A A B A g I A A A Q A A I A A A A A A B A A A A F A A A A A A A A g A A Q C 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 Area | 51.6 |
| Monoisotopic Mass | 162.071 |
| Exact Mass | 162.071 |
| XLogP3 | None |
| XLogP3-AA | 1.8 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 10 |
| 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+ | 0.9834 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.7050 |
| P-glycoprotein Substrate | Non-substrate | 0.7366 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.7003 |
| Non-inhibitor | 0.6195 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8660 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.6532 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8327 |
| CYP450 2D6 Substrate | Non-substrate | 0.8233 |
| CYP450 3A4 Substrate | Non-substrate | 0.5169 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.6130 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8683 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9324 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8261 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9500 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8033 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9808 |
| Non-inhibitor | 0.7913 | |
| AMES Toxicity | Non AMES toxic | 0.7242 |
| Carcinogens | Carcinogens | 0.5537 |
| Fish Toxicity | Low FHMT | 0.6488 |
| Tetrahymena Pyriformis Toxicity | Low TPT | 0.7618 |
| Honey Bee Toxicity | High HBT | 0.8432 |
| Biodegradation | Ready biodegradable | 0.8938 |
| Acute Oral Toxicity | III | 0.7909 |
| Carcinogenicity (Three-class) | Non-required | 0.6656 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -1.0964 | LogS |
| Caco-2 Permeability | 1.5614 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 2.0198 | LD50, mol/kg |
| Fish Toxicity | 2.3950 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.1563 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Class | Thiocarboxylic acids and derivatives |
| Subclass | Thioesters |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Thioesters |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Carbothioic s-ester - Thiocarboxylic acid ester - Sulfenyl compound - Ether - Dialkyl ether - Carboxylic acid derivative - 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 thioesters. These are organic compounds containing an ester of thiocarboxylic acid, with the general structure RC(=S)XR' (R=H, alkyl, aryl; R'=alkyl, aryl; X=O,S). |
From ClassyFire