Description

Sulosemide is a high-purity pharmaceutical intermediate and research chemical. This compound is of significant interest for its role in the development and synthesis of novel diuretic agents. It is primarily utilized by pharmaceutical R&D laboratories, API manufacturers, and academic research institutions engaged in cardiovascular and renal pharmacology.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of advanced diuretic and antihypertensive active pharmaceutical ingredients (APIs).
• Research & Development: Used in preclinical and pharmacological studies to investigate structure-activity relationships (SAR) for sulfonamide-derived compounds.
• Reference Standard: Serves as a certified reference material (CRM) for quality control and analytical method development in pharmaceutical analysis.
• Chemical Synthesis: Employed in organic synthesis for the preparation of more complex molecules with potential therapeutic activity.

Basic Information

Product Name	Sulosemide
CAS No.	82666-62-4
Molecular Formula	C12H11ClN2O5S2
Molecular Weight	370.81 g/mol
Synonyms	5-(Aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoic Acid; 4-Chloro-5-sulfamoyl-2-[(furan-2-ylmethyl)amino]benzoic Acid; Sulosemidum; Sulosemide (USAN); CL-85,699; CL 85699
EINECS	Contact for details

Quality Control

Our Sulosemide is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling via HPLC and other validated methods, to ensure it meets stringent specifications for research and pharmaceutical use. Certificates of Analysis (COA) documenting full compliance are provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (15-25°C). Keep the container tightly sealed to protect from moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

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