Description

Glidazamide is a high-purity sulfonylurea compound, widely recognized for its role as a key pharmaceutical intermediate. Its primary commercial value lies in the synthesis of advanced active pharmaceutical ingredients (APIs), particularly in the development of therapeutic agents. This product is essential for manufacturers and research institutions in the pharmaceutical and fine chemical sectors seeking reliable, high-quality building blocks for complex synthesis.

Application

• Pharmaceutical Intermediate: A critical precursor in the synthesis of sulfonylurea-based active pharmaceutical ingredients (APIs).
• Research & Development: Used in medicinal chemistry for the discovery and development of new therapeutic compounds.
• Fine Chemical Synthesis: Serves as a specialized building block for constructing complex organic molecules in custom synthesis projects.
• Reference Standard: Employed as an analytical standard in quality control laboratories for method development and validation.

Basic Information

Product Name	Glidazamide
CAS No.	3074-35-9
Molecular Formula	C15H21N3O3S
Molecular Weight	323.41 g/mol
Synonyms	1-(Hexahydro-1H-azepin-1-yl)-3-[(4-methylphenyl)sulfonyl]urea; Gliclazamide Impurity A; Gliclazamide Related Compound A; N-(Hexahydro-1H-azepin-1-yl)-N'-[(4-methylphenyl)sulfonyl]urea; 1-(4-Methylphenylsulfonyl)-3-(hexahydroazepin-1-yl)urea; Gliclazamide EP Impurity A
EINECS	Contact for details

Quality Control

Our Glidazamide is manufactured under a strict quality management system. Each batch undergoes comprehensive analytical testing to ensure it meets the high-purity standards required for pharmaceutical applications. A Certificate of Analysis (COA) detailing purity, identity, and impurity profiles is provided with every shipment to guarantee traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area 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.

Specification

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

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