Description

Clofedanol is a synthetic chemical compound primarily recognized for its antitussive (cough-suppressing) properties. It is a high-purity active pharmaceutical ingredient (API) essential for the formulation of effective cough medications. This compound is critical for pharmaceutical manufacturers and R&D laboratories focused on respiratory therapeutics. We supply Clofedanol CAS NO 791-35-5 to meet the stringent quality demands of the global pharmaceutical industry.

Application

• Pharmaceutical API: Primary use as the active ingredient in prescription and over-the-counter (OTC) antitussive syrups, lozenges, and tablets.
• Respiratory Drug Formulation: Key component in the development and production of medications targeting dry, non-productive coughs.
• Veterinary Pharmaceuticals: Used in formulations for cough suppression in animals.
• Clinical Research: Serves as a reference standard and raw material in pharmacological studies and drug discovery programs related to cough reflex pathways.
• Generic Drug Manufacturing: Essential for companies producing generic versions of established cough suppressant medications.

Basic Information

Product Name	Clofedanol
CAS No.	791-35-5
Molecular Formula	C17H20ClNO
Molecular Weight	289.80 g/mol
Synonyms	Clofedanol; Chlophedianol; 1-(2-Chlorophenyl)-3-dimethylamino-1-phenyl-1-propanol; Detigon; Ulone; Tussiplegyl; SKF-478; NSC-526063
EINECS	212-339-0

Quality Control

Our Clofedanol is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity pharmacopeial standards, including identity, potency, and impurity profile. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming compliance with specifications for pharmaceutical use.

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). The product is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	98.0% - 102.0% (on dried basis)
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Related Substances (HPLC)	Total impurities ≤ 1.0% 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.