Potassium thioethanoate
Potassium thioacetate
CAS: 10387-40-3
Molecular Formula: C2H3KOS
Potassium thioethanoate - Names and Identifiers
| Name | Potassium thioacetate |
| Synonyms | Kaliumthioacetat Potassium thioacetat Potassium Thioacetic Potasium thioacetate Potassium thioacetate Potassium thioaccetate Potassium thiolacetate Thioacetamide Potassium potassium ethanethioate Potassium thioethanoate Thioacetic acid potassium Thioacetic acid potassium salt Thioacetic acid S-potassium salt Ethanethioic acid, potassium salt Acetic acid, thio-, potassium salt |
| CAS | 10387-40-3 |
| EINECS | 233-848-7 |
| InChI | InChI=1/C2H4OS.K/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1/rC2H3KOS/c1-2(4)5-3/h1H3 |
Potassium thioethanoate - Physico-chemical Properties
| Molecular Formula | C2H3KOS |
| Molar Mass | 114.21 |
| Density | 1.58 g/cm3 |
| Melting Point | 173-176 °C (lit.) |
| Boling Point | 130.6℃ at 760 mmHg |
| Water Solubility | soluble |
| Solubility | soluble |
| Appearance | White crystal |
| Color | White to light brown |
| BRN | 3595448 |
| Storage Condition | Inert atmosphere,Room Temperature |
| Sensitive | 4: no reaction with water under neutral conditions |
| MDL | MFCD00137704 |
| Physical and Chemical Properties | Melting Point: 173 - 176 |
| Use | For the synthesis of anti-AIDS drugs |
Potassium thioethanoate - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. S37/39 - Wear suitable gloves and eye/face protection |
| UN IDs | UN 3335 |
| WGK Germany | 3 |
| FLUKA BRAND F CODES | 3-9-13-23 |
| TSCA | Yes |
| HS Code | 29309070 |
| Hazard Class | 9 |
Potassium thioethanoate - Reference Information
| EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
| introduction | potassium thioacetate is white crystalline powder with a melting point of 173°C-176°C. it is mainly used for the introduction of sulfur atoms in molecular structure and the synthesis of anti-AIDS drugs. |
| Biological activity | In the synthesis of sulfur-containing organic compounds, Potassium thioacetate are widely used as a source of sulfur. It is applied to the synthesis of heterocyclic compounds, polymers, transition metal ligands, nanoparticles, bioactive molecules and complexes containing macromolecules. |
| Use | Used for the introduction of sulfur atoms in the molecular structure. used to synthesize anti-AIDS drugs, etc. |
Last Update：2024-04-09 20:49:11
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Potassium thioethanoate
Cystine Disodium Salt
2-Formyltetrahydrofuran
Bis(p-chlorophenyl) sulfide
Vat Brilliant Green Ffb
Cystine Disodium Salt
2-Formyltetrahydrofuran
Bis(p-chlorophenyl) sulfide
Vat Brilliant Green Ffb