| Identification | Back Directory | [Name]
2-dimethylamino-1,3-bis(sulfosulfanyl)propane | [CAS]
98968-92-4 | [Synonyms]
thiosultap
2-dimethylamino-1,3-bis(sulfosulfanyl)propane
S,S'-(2-(dimethylamino)-1,3-propanediyl)thiosulfuric acid ester
Thiosulfuric acid (H2S2O3), SS,SS'-[2-(dimethylamino)-1,3-propanediyl] ester | [Molecular Formula]
C5H13NO6S4 | [MDL Number]
MFCD09955120 | [MOL File]
98968-92-4.mol | [Molecular Weight]
311.42 |
| Chemical Properties | Back Directory | [density ]
1.695±0.06 g/cm3(Predicted) | [solubility ]
Methanol (Slightly, Heated), Water (Slightly) | [form ]
Solid | [pka]
-4.79±0.30(Predicted) | [color ]
White to Off-White | [Stability:]
Hygroscopic |
| Hazard Information | Back Directory | [Uses]
Thiosultap Sodium Salt is used as an insecticide. | [Definition]
ChEBI: A nereistoxin analogue insecticide that is 2-(dimethylamino)propane-1,3-dithiol with both sulfhydryls bearing sulfate groups. | [Production Methods]
Thiosultap is commercially produced through a multi-step synthesis involving the reaction of dimethylamino-propane derivatives with thiosulphuric acid to form a disodium or monosodium thiosulphuric acid ester. This process begins with the preparation of 2-dimethylamino-1,3-propanedithiol, which is then reacted with thiosulphuric acid or its salts under controlled conditions to yield thiosultap. The reaction typically occurs in aqueous or methanolic media, followed by purification steps such as crystallisation or filtration to isolate the active compound. | [Mechanism of action]
Stomach poison with some contact and systemic action. It is a nereistoxin analogue, meaning it disrupts nerve function in insects, leading to paralysis and death | [Pesticide Type]
Insecticide |
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