Description

Moguisteine CAS NO 119637-67-1 is a non-narcotic antitussive agent, a peripherally acting cough suppressant. It is valued for its selective action on the cough reflex without causing central nervous system depression or significant side effects. This compound is primarily required by the pharmaceutical industry for the formulation of effective and safe cough relief medications.

Application

• Active Pharmaceutical Ingredient (API) in antitussive (cough suppressant) formulations.
• Key component in the development of prescription and over-the-counter (OTC) cough syrups and lozenges.
• Research and development of novel respiratory therapeutics targeting peripheral cough receptors.
• Manufacturing of combination drug products for treating symptoms of bronchitis, colds, and flu.
• Reference standard in analytical laboratories for quality control and pharmacokinetic studies.

Basic Information

Item	Detail
Product Name	Moguisteine
CAS No.	119637-67-1
Molecular Formula	C19H24N2O4S
Molecular Weight	376.47 g/mol
Synonyms	Moguisteine; (±)-Moguisteine; 2-(2-Methoxyphenoxy)-N-[2-(4-morpholinyl)ethyl]acetamide; 4-[2-[[(2-Methoxyphenoxy)acetyl]amino]ethyl]morpholine; AF-389; FK-888; Moguisteinum
EINECS	Contact for details

Quality Control

Our Moguisteine is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical use. A Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment to guarantee traceability and compliance with relevant guidelines.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after each use to prevent degradation from atmospheric moisture.

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)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Heavy Metals	≤ 20 ppm

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