Highly effective potassium-based sulfonamide catalyst for selective condensation and cyclization reactions.
Enhanced thermal stability compared to sodium or ammonium analogues, supporting high-temperature process conditions.
Excellent solubility in polar aprotic solvents such as DMF, DMSO, and NMP—facilitating homogeneous reaction systems.
Low volatility and non-hygroscopic nature ensure consistent handling, storage, and dosing accuracy.
Meets stringent purity requirements for pharmaceutical intermediate synthesis and fine chemical manufacturing.
Catalyst in the synthesis of heterocyclic compounds, including benzimidazoles and triazoles.
Key promoter in Knoevenagel condensations for active methylene compound functionalization.
Enabling reagent in solid-phase peptide coupling and protected amino acid activation.
Stabilizing agent and co-catalyst in palladium-catalyzed cross-coupling reactions (e.g., Suzuki and Heck variants).
| Chemical Type | Potassium salt of di-p-toluenesulfonamide |
| Product Form | Free-flowing crystalline powder |
| Appearance | White to off-white crystalline solid |
| Assay (by HPLC) | ≥ 98.5% |
| Loss on Drying (105 °C, 2 h) | ≤ 0.5% |
| Heavy Metals (as Pb) | ≤ 10 ppm |
| Solubility | Freely soluble in DMF and DMSO; slightly soluble in ethanol; insoluble in water and aliphatic hydrocarbons |
| Storage Conditions | Store under dry, inert atmosphere at 15–25 °C in tightly sealed containers |
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