Description

Moxonidine is a highly selective imidazoline I1-receptor agonist with antihypertensive properties. This compound is a critical active pharmaceutical ingredient (API) valued for its efficacy in managing essential hypertension. It is primarily required by pharmaceutical manufacturers and research institutions engaged in cardiovascular drug development and production.

Application

• Pharmaceutical API: Primary use as the active ingredient in finished dosage forms for the treatment of hypertension.
• Cardiovascular Research: A key reference standard and investigational compound in pharmacological studies targeting imidazoline receptors.
• Formulation Development: Used in R&D for developing new tablet, capsule, or controlled-release formulations.
• Generic Drug Manufacturing: Sourcing of the API for the production of generic antihypertensive medications.
• Biochemical Standard: Serves as a high-purity analytical standard for quality control laboratories.

Basic Information

Product Name	Moxonidine
CAS No.	75438-57-2
Molecular Formula	C9H12ClN5O
Molecular Weight	241.68 g/mol
Synonyms	4-Chloro-N-(4,5-dihydro-1H-imidazol-2-yl)-6-methoxy-2-methylpyrimidin-5-amine; BDF 5895; CYNT; Physiotens; Moxon; Lomox; Moxogamma
EINECS	Contact for details

Quality Control

Our Moxonidine is manufactured and tested under a quality management system. We provide material that meets stringent internal specifications aligned with ICH guidelines. A comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles is supplied with each batch to ensure traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Related Substances (HPLC)	Individual impurity: NMT 0.5% Total impurities: NMT 1.5%
Water (KF)	NMT 1.0%
Residue on Ignition	NMT 0.1%
Heavy Metals	NMT 20 ppm

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