Description

1-Glyceryl n-[7-Chloro-4-Quinolyl]Anthranilate Hydrochloride is a specialized quinoline derivative with significant potential in pharmaceutical research and development. This compound is valued for its structural complexity, which serves as a key intermediate or active moiety in the synthesis of novel therapeutic agents. It is primarily sought by research institutions and pharmaceutical companies engaged in the development of new chemical entities, particularly for applications in medicinal chemistry and as a precursor for advanced active pharmaceutical ingredients (APIs).

Application

• Pharmaceutical Intermediate: A critical building block in the synthesis of novel quinoline-based drug candidates, particularly for anti-malarial or other therapeutic research.
• Medicinal Chemistry Research: Used in structure-activity relationship (SAR) studies to develop and optimize new pharmacologically active molecules.
• Active Pharmaceutical Ingredient (API) Synthesis: Serves as a key precursor or intermediate in the multi-step synthesis of complex APIs.
• Biochemical Research: Employed in laboratory studies to investigate biological pathways and mechanisms of action.
• Reference Standard: Can be utilized as an analytical standard for quality control and method development in pharmaceutical analysis.

Basic Information

Product Name	1-Glyceryl n-[7-Chloro-4-Quinolyl]Anthranilate Hydrochloride
CAS No.	65513-72-6
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	7-Chloro-4-quinolyl anthranilate glyceryl ester hydrochloride; 1-Glyceryl N-(7-chloro-4-quinolyl)anthranilate hydrochloride; Glyceryl 1-(7-chloro-4-quinolinyl)anthranilate hydrochloride; 1-O-Glyceryl N-(7-chloro-4-quinolyl)anthranilate HCl; (7-Chloro-4-quinolylamino)benzoic acid 2,3-dihydroxypropyl ester hydrochloride
EINECS	Contact for details

Quality Control

Our 1-Glyceryl n-[7-Chloro-4-Quinolyl]Anthranilate Hydrochloride is manufactured under a strict quality management system. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide a detailed Certificate of Analysis (COA) with key parameters including assay, impurity profile, and identification. Our quality commitment aligns with cGMP principles where applicable for pharmaceutical intermediates, ensuring reliability for critical research and development applications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area. Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture. Recommended storage temperature is 2-8°C for long-term stability.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Loss on Drying	≤ 2.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Single Maximum Impurity	≤ 1.0%

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