≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
γ-Thiobutyrolactone undergoes copolymerization with glycidyl phenyl ether to form poly(ester-alt-sulfide).γ-Thiobutyrolactone was used to terminate the ring opening polymerization of ω-pentadecalactone to synthesize difunctional polyesters. γ-Thiobutyrolactone was used to study the mechanism of metabolism of sulphur containing heterocyclic compounds by lignin-degrading basidiomyceteCoriolus versicolor.
| Canonical Smiles | C1CC(=O)SC1 |
|---|---|
| IUPAC Name | thiolan-2-one |
| InChIKey | KMSNYNIWEORQDJ-UHFFFAOYSA-N |
| INCHI | 1S/C4H6OS/c5-4-2-1-3-6-4/h1-3H2 |
| Isomeric SMILES | C1CC(=O)SC1 |
| WGK Germany | 3 |
| RTECS | XN1930000 |
| PubChem CID | 13852 |
| Molecular Weight | 102.15 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Thiolanes |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Thiolanes |
| Alternative Parents | Carbothioic S-lactones Thiolactones Thioesters Carboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Carbothioic s-lactone - Thiolane - Thiolactone - Thiocarboxylic acid ester - Thiocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as thiolanes. These are organic compounds containing thiolane, a five-member saturated ring containing four carbon atoms and a sulfur atom. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 B2512027 | Certificate of Analysis | Nov 27, 2024 | T472178 |
| J2511104 | Certificate of Analysis | Nov 27, 2024 | T472178 |
| K2422632 | Certificate of Analysis | Nov 27, 2024 | T472178 |
| K2422633 | Certificate of Analysis | Nov 27, 2024 | T472178 |
| K2422634 | Certificate of Analysis | Nov 27, 2024 | T472178 |
| K2422635 | Certificate of Analysis | Nov 27, 2024 | T472178 |
| F2317698 | Certificate of Analysis | May 27, 2023 | T472178 |
| F2317707 | Certificate of Analysis | May 27, 2023 | T472178 |
| F2317851 | Certificate of Analysis | May 27, 2023 | T472178 |
| F2317858 | Certificate of Analysis | May 27, 2023 | T472178 |
| F2317863 | Certificate of Analysis | May 27, 2023 | T472178 |
| Solubility | THF: soluble |
|---|---|
| Refractive Index | 1.523 (lit.) |
| Flash Point(°F) | 186.8 °F |
| Flash Point(°C) | 86 °C |
| Boil Point(°C) | 39-40 °C/1 mmHg (lit.) |
| Molecular Weight | 102.160 g/mol |
| XLogP3 | 0.700 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 102.014 Da |
| Monoisotopic Mass | 102.014 Da |
| Topological Polar Surface Area | 42.400 Ų |
| Heavy Atom Count | 6 |
| Formal Charge | 0 |
| Complexity | 69.900 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
