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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.
O,O,S-Triethyl thiophosphate (TETP) stands as an organosulfur compound renowned for its diverse applications in the realm of science and technology. It presents itself as a colorless solid, readily soluble in organic solvents, and exhibits a pungent odor. TETP finds widespread use in the synthesis of various organic compounds, contributing to advancements in materials and catalyst development. Moreover, it plays a significant role in the manufacturing of pesticides, dyes, and other industrial products. Within the domain of scientific research, O,O,S-Triethyl thiophosphate (TETP) holds a broad spectrum of applications. It serves as a key ingredient in organic compound synthesis, aiding in the creation of novel materials and catalysts. TETP has proven instrumental in exploring biochemical processes. The exact mechanism by which O,O,S-Triethyl thiophosphate operates is yet to be fully elucidated. It is hypothesized that TETP acts as a catalyst in organic compound synthesis, promoting the formation of covalent bonds between different molecules. Additionally, it is believed to partake in the formation of polymeric structures, assuming the role of a cross-linking agent.
| Canonical Smiles | CCOP(=O)(OCC)SCC |
|---|---|
| IUPAC Name | 1-[ethoxy(ethylsulfanyl)phosphoryl]oxyethane |
| InChIKey | YEXTYUIZRKSYHA-UHFFFAOYSA-N |
| INCHI | 1S/C6H15O3PS/c1-4-8-10(7,9-5-2)11-6-3/h4-6H2,1-3H3 |
| Isomeric SMILES | CCOP(=O)(OCC)SCC |
| Molecular Weight | 198.22 |
| Reaxy-Rn | 1705782 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1705782&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organophosphorus compounds |
| Class | Organothiophosphorus compounds |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Organothiophosphorus compounds |
| Alternative Parents | Sulfenyl compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Sulfenyl compound - Organothiophosphorus compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as organothiophosphorus compounds. These are organic derivatives of thiophosphonic acid, thiophosphoric acid, dithiophosphoric acid, or phosphorotrithioic acid, or derivatives thereof. Thiophosphonic acid, dithiophosphoric acid, thiophosphoric acid, and phosphorotrithioic acid are thiophosphorus compounds with the formula OP(O)(=S), OP(S)(=S)O, OP(O)(=S)O, and OP(=S)(S)S, respectively. |
| 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 |
|---|---|---|---|
| Certificate of Analysis | Jun 29, 2024 | O356870 | |
| Certificate of Analysis | Jun 29, 2024 | O356870 | |
| Certificate of Analysis | Jun 29, 2024 | O356870 | |
| Certificate of Analysis | Jun 29, 2024 | O356870 |
| Molecular Weight | 198.220 g/mol |
|---|---|
| XLogP3 | 1.300 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 6 |
| Exact Mass | 198.048 Da |
| Monoisotopic Mass | 198.048 Da |
| Topological Polar Surface Area | 60.800 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 130.000 |
| 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 |