Name | sulfachloropyridazine |
Synonyms | Prinz Soxilyn AKOS B014357 Nefrosul (TN) VetisullideNefrosul sulfachlorpyridazine sulfachloropyridazine Sulphachlorpyridazine Sulfachlorpyridazine (USP) N1-3-chloropyridazin-6-ylsulphanilamide N'-(6-Chloro-3-pyridazinyl)sulfanilamide |
CAS | 80-32-0 |
EINECS | 201-269-9 |
InChI | InChI=1/C10H9ClN4O2S/c11-9-5-6-10(14-13-9)15-18(16,17)8-3-1-7(12)2-4-8/h1-6H,12H2,(H,14,15) |
Molecular Formula | C10H9ClN4O2S |
Molar Mass | 284.72 |
Density | 1.588 |
Melting Point | 186-187℃ |
Boling Point | 559.7±60.0 °C(Predicted) |
Solubility | 0.5 M NaOH: soluble 50 mg/mL |
Appearance | off-white to light yellow |
Color | off-white to light yellow |
BRN | 261558 |
pKa | pKa 6.10 (Uncertain) |
Storage Condition | Keep in dark place,Inert atmosphere,2-8°C |
Refractive Index | 1.6300 (estimate) |
MDL | MFCD00057371 |
Use | Used as anti-inflammatory antibacterial |
Hazard Symbols | Xi - Irritant |
Risk Codes | 43 - May cause sensitization by skin contact |
Safety Description | 36/37 - Wear suitable protective clothing and gloves. |
WGK Germany | 3 |
HS Code | 2935909550 |
Hazard Class | IRRITANT |
Reference Show more | 1. Kollinger, Kefei, niudejun, et al. Screening of sulfonamide sensitive strains by UV mutagenesis and its application in the detection of milk sulfonamide antibiotics [J]. Modern food science and technology, 2019, 35(5):296-303. 2. [IF = 4.821] Lang et al Jin-Ye. "Preparation of boronate-modified." Microchem J. 2022 Apr;175:107193 |