Description

Zidapamide is a high-purity pharmaceutical intermediate and research chemical with the CAS registry number 75820-08-5. This compound is valued for its specific chemical structure, making it a critical building block in the synthesis of advanced active pharmaceutical ingredients (APIs). It is primarily sought by research institutions and manufacturers in the pharmaceutical and life sciences sectors for development and production purposes.

Application

• Pharmaceutical Intermediate: A key precursor in the synthesis of novel therapeutic agents and active pharmaceutical ingredients (APIs).
• Research & Development: Used in academic and industrial laboratories for pharmacological studies and the development of new drug candidates.
• Chemical Synthesis: Serves as a specialized building block in organic synthesis for creating complex molecular structures.
• Analytical Reference Standard: Employed as a high-purity standard in analytical testing (e.g., HPLC, LC-MS) for method development and quality control.

Basic Information

Product Name	Zidapamide
CAS No.	75820-08-5
Molecular Formula	C13H11ClN2O3S
Molecular Weight	310.76 g/mol
Synonyms	3-(Aminosulfonyl)-4-chloro-N-(2,3-dihydro-2-methyl-1H-indol-1-yl)benzamide; 4-Chloro-3-sulfamoyl-N-(2-methylindolin-1-yl)benzamide; Zidapamide; Zidapamidum; Zidapamida
EINECS	Contact for details

Quality Control

Our Zidapamide is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide Certificates of Analysis (COA) with detailed results from advanced techniques like HPLC, GC, and NMR. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates, ensuring reliable supply for critical research and production needs.

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). Keep away from incompatible materials and sources of ignition.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
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.