CAS 23282-55-5
:Sulfachloropyridazine sodium
Description:
Sulfachloropyridazine sodium is a sulfonamide antibiotic characterized by its broad-spectrum antibacterial activity, primarily against Gram-positive and some Gram-negative bacteria. It is a sodium salt of sulfachloropyridazine, which features a pyridazine ring substituted with a sulfonamide group and a chlorine atom. This compound is typically used in veterinary medicine for the treatment of bacterial infections in livestock and poultry. Its mechanism of action involves the inhibition of bacterial folic acid synthesis, which is essential for nucleic acid production and overall bacterial growth. Sulfachloropyridazine sodium is generally administered orally or through injection, depending on the specific application. It is important to note that, like other sulfonamides, it may cause allergic reactions or adverse effects in some animals, and its use is regulated in food-producing animals to prevent antibiotic residues in meat and milk. Proper dosage and adherence to withdrawal times are crucial to ensure food safety and efficacy in treatment.
Formula:C10H9ClN4O2S·Na
InChI:InChI=1S/C10H9ClN4O2S.Na/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);
InChI key:InChIKey=GHQJXOBLWKFNAD-UHFFFAOYSA-N
SMILES:S(NC1=CC=C(Cl)N=N1)(=O)(=O)C2=CC=C(N)C=C2.[Na]
Synonyms:- 201-269-9
- 3-Chloro-6-sulfanilamidopyridazine
- 3-Sulfanilamido-6-chloropyridazine
- 4-Amino-N-(6-chlor-3-pyridazinyl)benzolsulfonamid
- 4-Amino-N-(6-chloro-3-pyridazinyl)benzenesulfonamide
- 4-amino-N-(6-chloropyridazin-3-yl)benzenesulfonamide
- Benzenesulfonamide, 4-amino-N-(6-chloro-3-pyridazinyl)-, monosodium salt
- Benzenesulfonamide, 4-amino-N-(6-chloro-3-pyridazinyl)-, sodium salt (1:1)
- Prinzone
- Sodium [(4-Aminophenyl)Sulfonyl](6-Chloropyridazin-3-Yl)Azanide
- Sodium sulfachloropyridazine
- Sodium sulfachlorpyridazine
- Spdz
- Sulfachloropyridazine Sodium
- Sulfachlororyridazine sodium
- Sulfachlorpyridazine Sodium
- Sulfachlorpyridazine sodium salt
- Sulfanilamide, N<sup>1</sup>-(6-chloro-3-pyridazinyl)-, monosodium salt
- Vetisulid
- benzenesulfonamide, 4-amino-N-(6-chloro-3-pyridazinyl)-
- See more synonyms
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Found 9 products.
Benzenesulfonamide, 4-amino-N-(6-chloro-3-pyridazinyl)-, sodium salt (1:1)
CAS:Formula:C10H9ClN4NaO2SPurity:98%Color and Shape:SolidMolecular weight:307.7118Sulfachloropyridazine sodium
CAS:Formula:C10H8ClN4NaO2SPurity:≥ 98.0%Color and Shape:White to light yellow powderMolecular weight:306.7Sodium ((4-Aminophenyl)Sulfonyl)(6-Chloropyridazin-3-Yl)Amide
CAS:<p>Sodium ((4-Aminophenyl)Sulfonyl)(6-Chloropyridazin-3-Yl)Amide</p>Purity:98%Molecular weight:306.70g/molMinistry of Agriculture Veterinary Drug Mixture 348 10 µg/mL in Acetonitrile:Water
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Color and Shape:MixtureSulfachlorpyridazine Sodium
CAS:<p>Applications Sulfachlorpyridazine is an antibacterial compound.<br>References Wammer, K.: Environ. Toxicol. Chem. 25, 1480 (2006).<br></p>Formula:C10H8ClN4NaO2SColor and Shape:BeigeMolecular weight:306.7Sodium N-(6-chloropyridazin-3-yl)sulphanilamidate
CAS:<p>Sodium N-(6-chloropyridazin-3-yl)sulphanilamidate (NPS) is a sulfa drug that has been shown to have an effect on the enzyme activities of some endoparasites, such as Giardia lamblia and Entamoeba histolytica. The active form of NPS is metabolized through a number of metabolic transformations, including hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid. It also specifically binds to markers expressed at high levels in Mycobacterium tuberculosis strains (e.g., ESX-1 secretion system protein) and inhibits cell growth in culture.</p>Formula:C10H8ClN4O2SNaPurity:Min. 95%Molecular weight:306.7 g/molSulfachloropyridazine sodium
CAS:<p>Sulfachloropyridazine (sodium) is a sulfonamide antibiotic that impedes bacterial proliferation [1].</p>Formula:C10H8ClN4NaO2SPurity:98%Color and Shape:SolidMolecular weight:306.7









