Description

Diclofenacbeta-Dimethylaminoethanol is a key pharmaceutical intermediate and salt form of the widely used non-steroidal anti-inflammatory drug (NSAID) diclofenac. This compound is valued for its role in enhancing the solubility, stability, and bioavailability of the active pharmaceutical ingredient in various formulations. It is primarily required by manufacturers in the pharmaceutical and fine chemical industries for the development and production of topical analgesics, anti-inflammatory creams, and other advanced drug delivery systems.

Application

• Pharmaceutical Intermediate: Critical synthesis component for producing diclofenac diethylamine and other diclofenac salts used in topical formulations.
• Topical Analgesic Creams & Gels: Used in the manufacture of medicated creams, gels, and patches for localized pain and inflammation relief.
• Transdermal Drug Delivery Systems: Serves as a key ingredient in advanced formulations designed for controlled release through the skin.
• Veterinary Pharmaceuticals: Employed in the production of anti-inflammatory treatments for animals.
• Research & Development: Utilized in pharmaceutical R&D for exploring new drug delivery mechanisms and formulation stability.
• Generic Drug Manufacturing: A vital raw material for companies producing generic versions of diclofenac-based medications.

Basic Information

Product Name	Diclofenacbeta-Dimethylaminoethanol
CAS No.	81811-14-5
Molecular Formula	C20H25Cl2N2O2
Molecular Weight	396.33 g/mol
Synonyms	Diclofenac Diethylamine; Diclofenac N,N-Diethylethanolamine; 2-[(2,6-Dichlorophenyl)amino]benzeneacetic acid compd. with 2-(Diethylamino)ethanol (1:1); Diclofenac DEA; Diclofenac Diethylammonium; Voltaren Emulgel Active Ingredient; Diclofenac Epolamine (related salt); UNII-8GQZ6W219M
EINECS	Contact for details

Quality Control

Our Diclofenacbeta-Dimethylaminoethanol is produced under strict quality management systems. Each batch undergoes rigorous analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. A comprehensive Certificate of Analysis (COA) documenting identity, purity, and impurity profiles is provided with every shipment to ensure full traceability and compliance.

Storage

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

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	98.0% - 102.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Individual Unknown Impurity	≤ 0.5%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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