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SULFACHLOROPYRIDAZINE

CAS No.
80-32-0
Chemical Name:
SULFACHLOROPYRIDAZINE
Synonyms
SULFACHLORPYRIDAZINE;SULPHACHLOROPYRIDAZINE;Sulfochlorpyridazine;Sulphachlorpyridazine;Prinz;Soxilyn;Sonilyn;Cosulid;NEFROSUL;Cluricol
CBNumber:
CB6724544
Molecular Formula:
C10H9ClN4O2S
Molecular Weight:
284.72
MDL Number:
MFCD00057371
MOL File:
80-32-0.mol
MSDS File:
SDS
Last updated:2024-11-25 20:05:57

SULFACHLOROPYRIDAZINE Properties

Melting point 186-187℃
Boiling point 559.7±60.0 °C(Predicted)
Density 1.588
refractive index 1.6300 (estimate)
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility 0.5 M NaOH: soluble50mg/mL
pka pKa 6.10 (Uncertain)
form powder
color off-white to light yellow
BRN 261558
FDA 21 CFR 556.630
FDA UNII P78D9P90C0
EPA Substance Registry System Benzenesulfonamide, 4-amino-N-(6-chloro-3-pyridazinyl)- (80-32-0)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H317
Precautionary statements  P280
Hazard Codes  Xi
Risk Statements  43
Safety Statements  36/37
WGK Germany  3
HazardClass  IRRITANT
HS Code  2935909550

SULFACHLOROPYRIDAZINE price More Price(25)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 46778 Sulfachloropyridazine VETRANAL 80-32-0 250mg $80.4 2024-03-01 Buy
Sigma-Aldrich 1624505 Sulfachlorpyridazine United States Pharmacopeia (USP) Reference Standard 80-32-0 200mg $436 2024-03-01 Buy
Sigma-Aldrich S9882 Sulfachloropyridazine 80-32-0 100g $87.1 2022-05-15 Buy
TRC S689061 Sulfachloropyridazine 80-32-0 250mg $65 2021-12-16 Buy
Usbiological S8016-60A Sulfachlorpyridazine 80-32-0 500ul $523 2021-12-16 Buy
Product number Packaging Price Buy
46778 250mg $80.4 Buy
1624505 200mg $436 Buy
S9882 100g $87.1 Buy
S689061 250mg $65 Buy
S8016-60A 500ul $523 Buy

SULFACHLOROPYRIDAZINE Chemical Properties,Uses,Production

Description

It is a sulfonamide antibiotic that is usually used as antibacterial anti-inflammatory drug, which has been applied in the treatment of acute urinary tract infections in childhood. Specifically, due to its antibiotic activity, this chemical has been selected as an ingredient to prepare antibacterial composition.1 Moreover, this substance can be introduced in the drinking water to fabricate aqueous liquid formulations for combating bacterial and protozoal in animals.2 In addition, this compound can act as an eco-friendly inhibitor for corrosion of mild steel in H2SO4 solution.3 Besides, sulfachloropyridazine associated to tripelennamine hydrocholoride has been demonstrated to function as an anti-stress agent in poultry after vaccinations.4

Brand Name(s) in US

Vetisulid

Reference

  1. Stolar, M. E., Synergistic antibacterial composition US Patent 4470978 1984.
  2. Gerhard Lukas; Atasoy, K., Aqueous liquid formulations for control of bacterial and protozoal diseases US Patent 4423043 1983.
  3. Omar A. Hazazi; Ahmed Fawzy; Awad, M. I., Sulfachloropyridazine as an Eco-Friendly Inhibitor for Corrosion of Mild Steel in H2SO4 Solution Chemical Science Review and Letters 2015, 4, 67-79.
  4. M. Nakano; M.N. Narimatsu; Portugal, M. A. S. C., Use of sulfachloropyridazine associated to tripelennamine hydrochloride as anti-stress agent in poultry after vaccinations. Biologico 1977.

Originator

Sonilyn,Mallinckrodt Inc.,US,1962

Uses

Sulfachloropyridazine is an antibacterial compound.This compound is a contaminant of emerging concern (CECs).

Definition

ChEBI: A sulfonamide antimicrobial used for urinary tract infections and in veterinary medicine.

Manufacturing Process

1.9 parts of 3,6-dichloropyridazine, 3.4 parts of sulfanilamide, 2.7 parts of potassium carbonate and 1 part of sodium chloride were ground together. The solid mixture was heated with stirring and as the dichloropyridazine and sulfanilamide melted, the mixture became a slurry. When the bath temperature had reached 140°C a sudden evolution of carbon dioxide occurred which lasted about 5 minutes, after which the mixture set in fine granules. When no more carbon dioxide was evolved, heating was stopped and the reaction mixture was heated with sufficient water to dissolve it and the solution allowed to cool. Unreacted sulfanilamide was collected by filtration. Excess dichloropyridazine was removed from the filtrate by extraction with a water immiscible organic solvent such as ether.
The basic solution was chilled and poured into one-half volume of 1:3 acetic acid. Sufficient hydrochloric acid was added to bring the mixture to pH 4. The crude 3-sulfanilamido-6-chloropyridazine which precipitated was purified by solution in 6 parts of 1:100 ammonium hydroxide, charcoal treatment and precipitation by pouring of the filtrate into dilute acetic acid.

brand name

Nefrosul (3M Pharmaceuticals); Sonilyn,(Carter-Wallace); Vetisulid [Veterinary] (Fort Dodge Animal Health).

Therapeutic Function

Antibacterial

SULFACHLOROPYRIDAZINE Preparation Products And Raw materials

Global( 239)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Weibang Biotechnology Co., Ltd
+8615531157085 abby@weibangbio.com China 8811 58
Hebei Mojin Biotechnology Co., Ltd
+86 13288715578 +8613288715578 sales@hbmojin.com China 12839 58
Shaanxi TNJONE Pharmaceutical Co., Ltd
+8618092446649 sarah@tnjone.com China 1143 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418679 +8618949832763 info@tnjchem.com China 2986 55
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29882 58
Xiamen AmoyChem Co., Ltd
+86-86-5926051114 +8618959220845 sales@amoychem.com China 6383 58
Chongqing Chemdad Co., Ltd
+86-023-6139-8061 +86-86-13650506873 sales@chemdad.com China 39894 58
Masteam Bio-tech Co., Ltd.
+86-15200345168 +86-15200345168 bruce.lei@masteam.com CHINA 151 58
SIMAGCHEM CORP
+86-13806087780 sale@simagchem.com China 17365 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 32165 58

View Lastest Price from SULFACHLOROPYRIDAZINE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
SULFACHLOROPYRIDAZINE pictures 2024-11-25 SULFACHLOROPYRIDAZINE
80-32-0
US $10.00 / KG 1KG 99% 10 mt Hebei Weibang Biotechnology Co., Ltd
Sulfachloropyridazine pictures 2024-11-19 Sulfachloropyridazine
80-32-0
US $50.00 / mg 99.87% 10g TargetMol Chemicals Inc.
Sulfachloropyridazine pictures 2024-04-05 Sulfachloropyridazine
80-32-0
US $0.00 / kg 1kg 99% 1000kg Shaanxi TNJONE Pharmaceutical Co., Ltd
N’-(6-Chloro-3-pyridazinyl)sulfanilamide Soxilyn VetisullideNefrosul AKOS B014357 Nefrosul (TN) Prinz Sulfachlorpyridazine (USP) Vetisulid (Veterinary) SULFACHLOROPYRIDAZINE NEFROSUL TIMTEC-BB SBB001158 4-AMINO-N-(6-CHLORO-3-PYRIDAZINYL)BENZENESULFONAMIDE sulfachloropyridazine Solution, 100ppm Sulfachlorpyridazine solution,100ppm Cluricol N(sup 1)-(6-Chloro-3-pyridazinyl)sulfanilamide N1-(6-Chlor-3-pyridazinyl)sulfanilamid LABOTEST-BB LT00772309 ART-CHEM-BB B014357 N1-3-chloropyridazin-6-ylsulphanilamide 6-Chloro-3-sulfanilamidopyridazine sulfachlorpyridazine sulfachloropyridazine Sulfachlorpyridazine (base and/or unspecified salts) Ba-10370 Consulid Durasulf Renalsulfa Sonilyn Sulpirazina 4-amino-N-(6-chloropyridazin-3-yl)benzenesulfonamide benzenesulfonamide, 4-amino-N-(6-chloro-3-pyridazinyl)- 4-azanyl-N-(6-chloropyridazin-3-yl)benzenesulfonamide SULFACHLOROPYRIDAZINE VETRANAL, 250 SulfachloropyridazineSodiumSalt 3-Chloro-6-sulfanilamidopyridazine Sulfachloropyridazine,4-Amino-N-(6-chloro-3-pyridazinyl)benzenesulfonamide Sulfachlorpyridazine (200 mg) Sulfaclorazina Sulfarene. 6-Sulfanilamido-3-chloropyridazine Bactolin Ciba 10370 Cosulid N1-(6-Chloro-3-pyridazinyl)sulfanilamide Sulfachloropy 4-Amino-N-(6-chloropyridazin-3-yl)benzenesulphonamide Sulfachloropyridazine Solution in Methanol, 100μg/mL SULFACHLOROPYRIDAZINE USP/EP/BP Sulfachlorpyridazine USP/EP/BP Sulphachlorpyridazine SULFACHLORPYRIDAZINE SULPHACHLOROPYRIDAZINE Sulfochlorpyridazine Sulfachloropyridazine 100 μg/mL in Acetonitrile Sulfachlordazine SUIFACHIOROPYRIDAZINE C16990100 Sulfachloropyridazine Sulfachloropyridazine 100 μg/ml Acetonitrile