≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal 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.
It undergoes desulfurization reaction with hydrosilane under photo irradiation in the presence of a methyl iron complex. It forms a deep-orange complex with anhydrous bismuth(III) trifluoromethanesulfonate.
It was used as sulfur donor solvent to investigate the coordination chemistry of lead(II).
| Pubchem Sid | 488184405 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488184405 |
| Sonrisas canónicas | CN(C)C=S |
| IUPAC Name | N,N-dimethylmethanethioamide |
| InChIKey | SKECXRFZFFAANN-UHFFFAOYSA-N |
| INCHI | 1S/C3H7NS/c1-4(2)3-5/h3H,1-2H3 |
| Isómeros SMILES | CN(C)C=S |
| WGK Alemania | 3 |
| Peso molecular | 89.16 |
| Beilstein | 1737191 |
| Reaxy-Rn | 1737191 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1737191&ln= |
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 | Organic acids and derivatives |
| Clase | Thiocarboxylic acids and derivatives |
| Subclass | Thiocarboxylic acid amides |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Thiocarboxylic acid amides |
| Alternative Parents | Organosulfur compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Thiocarboxylic acid amide - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organosulfur compound - Organonitrogen compound - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as thiocarboxylic acid amides. These are organic compounds containing an amide of thiocarboxylic acid, with the general structure R1C(=S)N(R2)R3 (R1-R3=H, alkyl, aryl). |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 D2609040 | Certificate of Analysis | Apr 16, 2026 | N139246 |
| K2110691 | Certificate of Analysis | Aug 04, 2023 | N139246 |
| K2110692 | Certificate of Analysis | Aug 04, 2023 | N139246 |
| K2110697 | Certificate of Analysis | Aug 04, 2023 | N139246 |
| K2110698 | Certificate of Analysis | Aug 04, 2023 | N139246 |
| E1917028 | Certificate of Analysis | Jan 20, 2023 | N139246 |
| Solubilidad | Fully miscible in water. |
|---|---|
| Punto de inflamación (°F) | 210.2 °F |
| Punto de inflamación (°C) | 99 °C |
| Punto de ebullición (°C) | 98°C/10mmHg(lit.) |
| Punto de fusión (°C) | -9°C |
| Peso molecular | 89.160 g/mol |
| XLogP3 | 0.300 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 89.0299 Da |
| Monoisotopic Mass | 89.0299 Da |
| Topological Polar Surface Area | 35.300 Ų |
| Heavy Atom Count | 5 |
| Formal Charge | 0 |
| Complexity | 33.900 |
| 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 |
