Description

Linogliride is a synthetic chemical compound belonging to the sulfonylurea class, recognized for its specific biological activity. This high-purity intermediate is critical for research and development in metabolic and endocrine pharmacology. It is primarily utilized by pharmaceutical R&D laboratories, academic research institutions, and fine chemical manufacturers focused on developing novel therapeutic agents.

Application

• Pharmaceutical Research & Development: Serves as a key reference standard and active pharmaceutical ingredient (API) intermediate in metabolic disorder studies.
• Biochemical Assay Development: Used as a tool compound for in vitro screening and validation of biological targets related to insulin secretion and glucose metabolism.
• Academic & Clinical Research: Employed in preclinical investigations to study the mechanisms of sulfonylurea drugs and their effects.
• Fine Chemical Synthesis: Acts as a specialized building block for the synthesis of more complex molecules and analogs in medicinal chemistry programs.

Basic Information

Product Name	Linogliride
CAS No.	75358-37-1
Molecular Formula	C15H21N3O3S
Molecular Weight	323.41 g/mol
Synonyms	1-Cyclohexyl-3-[[p-[2-(5-methylpyrazinecarboxamido)ethyl]phenyl]sulfonyl]urea; McN-3495; McN 3495; LY217266; McN3495; U-24973A; Linoglirida; Linogliridum
EINECS	Contact for details

Quality Control

Our Linogliride 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 exacting research-grade standards. A Certificate of Analysis (COA) detailing all specifications 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). The product is hygroscopic (moisture-sensitive) and should be handled under anhydrous conditions to maintain stability.

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.