| Weight | 284.728 g/mol |
|---|---|
| Formula | C10H9ClN4O2S |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
Sulfachloropyridazine (80-32-0)
Sulfachlorpyridazine · Monosodium Salt Sulfachlorpyridazine · Sulphachlorpyridazine
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- Electrochemical Treatment of the Antibiotic Sulfachloropyridazine: Kinetics, Reaction Pathways, and Toxicity Evolution (Environmental Science & Technology, 2012)
- The effect of pH and ionic strength on the sorption of sulfachloropyridazine, tylosin, and oxytetracycline to soil. (Environmental Toxicology and Chemistry, 2006)
- Pollution-Induced Community Tolerance of Soil Microbial Communities Caused by the Antibiotic Sulfachloropyridazine (Environmental Science & Technology, 2004)
- Monoclonal antibody-based fluorescence polarization immunoassay for sulfamethoxypyridazine and sulfachloropyridazine. (Journal of Agricultural and Food Chemistry, 2007)
- Electrochemical degradation of the antibiotic sulfachloropyridazine by hydroxyl radicals generated at a BDD anode. (Chemosphere, 2013)
- Extraction procedure for sulfachloropyridazine in porcine tissues and detection in a sulfonamide-specific enzyme-linked immunosorbent assay (ELISA) (Analytica Chimica Acta, 2003)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Sulfachlorpyridazine
- Monosodium Salt Sulfachlorpyridazine
- Sulphachlorpyridazine
-
SMILESC1=CC(=CC=C1N)S(=O)(=O)NC2=NN=C(C=C2)Cl
-
InChIKeyXOXHILFPRYWFOD-UHFFFAOYSA-N
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