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Muzolimine CAS NO 55294-15-0


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CAS No.:55294-15-0

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Muzolimine CAS NO 55294-15-0 is a high-purity pharmaceutical intermediate and research chemical belonging to the pyrazolone diuretic class. Its primary value lies in its role as a key building block for advanced pharmaceutical research and development, particularly in the study of renal function and diuretic agents. This compound is essential for pharmaceutical manufacturers, R&D laboratories, and academic institutions focused on cardiovascular and renal pharmacology.

Application

  • Pharmaceutical Intermediate: Critical starting material or precursor in the synthesis of specialized diuretic drug candidates.
  • Active Pharmaceutical Ingredient (API) Research: Used in preclinical and clinical research for developing novel loop diuretic agents.
  • Biochemical Research: Serves as a tool compound for studying sodium-potassium-chloride (NKCC) co-transporter inhibition in renal physiology.
  • Reference Standard: Employed as an analytical standard in quality control (QC) and quality assurance (QA) laboratories for method development and validation.
  • Academic & Institutional Research: Utilized in university and institutional labs for pharmacological studies and educational purposes.

Basic Information

Product Name Muzolimine
CAS No. 55294-15-0
Molecular Formula C₁₃H₁₃ClN₄O₃
Molecular Weight 308.72 g/mol
Synonyms Muzolimine; Bay g 2821; Edrul; 5-Amino-2-(1,3-dimethyl-5-oxo-4-pyrazolyl)-4-(2-chlorophenyl)-3-pyridazinone; 4-(2-Chlorophenyl)-2-(1,3-dimethyl-5-oxo-1H-pyrazol-4-yl)amino-2,3-dihydropyridazin-3-one
EINECS Contact for details

Quality Control

Our Muzolimine is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. We provide comprehensive analytical data supporting identity, purity, and impurity profiles. A Certificate of Analysis (COA) is supplied with each batch, detailing results from tests including assay, related substances, and residual solvents. Our quality standards are designed to meet the rigorous requirements of pharmaceutical R&D and GMP-guided production.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive); the container must be kept tightly sealed in a dry environment to prevent degradation.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time corresponds to reference standard
Assay (HPLC) ≥98.0%
Related Substances (HPLC) Total impurities ≤2.0% Any single unknown impurity ≤0.5%
Loss on Drying ≤0.5%
Residue on Ignition ≤0.1%
Heavy Metals ≤20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.

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With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.