Description

Sodium n-(3,4-Dimethylisoxazol-5-Yl)Sulphanilamidate is a specialized sulfonamide derivative with significant utility in advanced chemical synthesis and pharmaceutical research. This compound serves as a critical intermediate for developing novel active pharmaceutical ingredients (APIs), particularly in antimicrobial and anti-inflammatory drug discovery pipelines. It is essential for research and development chemists, process development scientists, and manufacturers in the fine chemical and pharmaceutical industries seeking high-purity building blocks for complex molecule construction.

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of novel sulfonamide-based therapeutics targeting bacterial infections.
• Antimicrobial Research: Used in R&D for developing new compounds with potential antibacterial or antifungal activity.
• Chemical Synthesis: Serves as a versatile precursor for creating more complex heterocyclic compounds in medicinal chemistry.
• Biochemical Research: Employed in studies investigating enzyme inhibition mechanisms, particularly those involving carbonic anhydrase.
• Process Development: Utilized in scaling up synthetic routes for pilot plant and commercial manufacturing of target molecules.
• Reference Standard: Acts as a high-purity analytical standard for quality control and method validation in pharmaceutical analysis.

Basic Information

Product Name	Sodium n-(3,4-Dimethylisoxazol-5-Yl)Sulphanilamidate
CAS No.	2200-44-4
Molecular Formula	C11H12N3NaO3S
Molecular Weight	289.29 g/mol
Synonyms	Sodium 5-(3,4-Dimethylisoxazol-5-ylsulfamoyl)anilinate; Sodium 4-Amino-N-(3,4-dimethyl-5-isoxazolyl)benzenesulfonamidate; Sulfamidate Sodium Salt; 5-Sulfanilamido-3,4-dimethylisoxazole Sodium Salt; N1-(3,4-Dimethyl-5-isoxazolyl)sulfanilamide Sodium Salt; Sulfisoxazole Impurity Sodium Salt; Sulfisoxazole Related Compound Sodium Salt
EINECS	Contact for details

Quality Control

Our Sodium n-(3,4-Dimethylisoxazol-5-Yl)Sulphanilamidate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via IR and NMR spectroscopy, to ensure it meets the stringent requirements for pharmaceutical R&D and chemical synthesis. A detailed Certificate of Analysis (COA) is provided with every shipment, documenting all relevant specifications and test results.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Water Content (KF)	≤ 2.0%
Residue on Ignition	≤ 0.5%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%

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