Description

Hydroxygliclazide is a high-purity pharmaceutical intermediate and research chemical. This compound is of significant interest for its role in the development and synthesis of advanced therapeutic agents. It is primarily required by pharmaceutical R&D laboratories, API manufacturers, and academic institutions engaged in metabolic disorder research.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of novel gliclazide analogs and related sulfonylurea compounds.
• Active Pharmaceutical Ingredient (API) Research: Used in preclinical and clinical research for developing new diabetes medications.
• Metabolic Disorder Studies: Serves as a reference standard or experimental compound in biochemical studies targeting insulin secretion and glucose metabolism.
• Process Chemistry: Employed in scale-up and optimization of synthetic routes for pharmaceutical production.
• Analytical Standard: Used as a high-purity standard in HPLC, LC-MS, and other analytical methods for quality control and method validation.

Basic Information

Product Name	Hydroxygliclazide
CAS No.	87368-00-1
Molecular Formula	C15H21N3O4S
Molecular Weight	339.41 g/mol
Synonyms	1-(3-Azabicyclo[3.3.0]oct-3-yl)-3-(4-methylphenylsulfonyl)urea; Hydroxy Gliclazide; Gliclazide Impurity; Gliclazide Related Compound; 3-(4-Methylphenylsulfonyl)-1-(octahydro-2H-pyrrolo[3,4-c]pyrrol-2-yl)urea
EINECS	Contact for details

Quality Control

Our Hydroxygliclazide is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation (IR, NMR), to ensure it meets the stringent requirements for pharmaceutical research and development. A Certificate of Analysis (COA) detailing all test results is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Keep the container tightly sealed in a dry environment to maintain stability.

Specification

Item	Specification
Appearance	White to off-white 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% Any single impurity ≤ 1.0%
Residual Solvents (GC)	Complies with ICH guidelines
Loss on Drying	≤ 0.5%

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