Determine the necessary mass, volume, or concentration for preparing a solution.
≥98% 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.
2-(Ethylthio)ethylamine forms complexes with Pd(II) and Pt(II)
2-(Ethylthio)ethylamine hydrochloride was used in the preparation of (syn, syn)-2,7-Bis(N-2-ethylthioethylmethylimino)-1,8-naphthyridine. It was used in the synthesis of N-functionalized bis(phosphino)amine ligands with ether, thioether and pyridyl ethers.
| Pubchem Sid | 504762312 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504762312 |
| Sorrisi canonici | CCSCCN.Cl |
| IUPAC Name | 2-ethylsulfanylethanamine;hydrochloride |
| InChIKey | AZQOTRRSHMSXFJ-UHFFFAOYSA-N |
| INCHI | 1S/C4H11NS.ClH/c1-2-6-4-3-5;/h2-5H2,1H3;1H |
| Isomeri SMILES | CCSCCN.Cl |
| WGK Germania | 3 |
| Peso molecolare | 141.66 |
| Reaxy-Rn | 3906671 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3906671&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 | Organosulfur compounds |
| Classe | Thioethers |
| Subclass | Dialkylthioethers |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Dialkylthioethers |
| Alternative Parents | Sulfenyl compounds Monoalkylamines Hydrochlorides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Dialkylthioether - Sulfenyl compound - Organic nitrogen compound - Hydrocarbon derivative - Hydrochloride - Primary amine - Organonitrogen compound - Primary aliphatic amine - Amine - Aliphatic acyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as dialkylthioethers. These are organosulfur compounds containing a thioether group that is substituted by two alkyl groups. |
| External Descriptors | Not available |
| Punto di fusione (°C) | 144-146°C |
|---|---|
| Peso molecolare | 141.660 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Exact Mass | 141.038 Da |
| Monoisotopic Mass | 141.038 Da |
| Topological Polar Surface Area | 51.300 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 23.500 |
| 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 | 2 |