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Diclofenac Epolamine CAS NO 119623-66-4
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CAS No.:119623-66-4
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Diclofenac Epolamine CAS NO 119623-66-4 is a non-steroidal anti-inflammatory drug (NSAID) salt, specifically the epolamine salt of diclofenac. This formulation is critical for enhancing the topical delivery and bioavailability of the active pharmaceutical ingredient, making it highly effective for localized pain and inflammation management. It is an essential raw material for pharmaceutical manufacturers developing transdermal patches, gels, and other topical analgesic formulations. The compound's specific salt form offers improved solubility and stability profiles suitable for advanced drug delivery systems.
Application
- Primary active ingredient in transdermal analgesic patches for musculoskeletal pain relief.
- Key component in topical gels and creams for the treatment of osteoarthritis and acute sports injuries.
- Used in the formulation of veterinary topical products for animal pain management.
- Intermediate in the synthesis of other specialized diclofenac salt forms for enhanced drug delivery.
- Raw material for pharmaceutical R&D focused on novel topical and transdermal delivery systems.
- Active pharmaceutical ingredient (API) for compounding pharmacies specializing in custom topical preparations.
Basic Information
| Item | Details |
|---|---|
| Product Name | Diclofenac Epolamine |
| CAS No. | 119623-66-4 |
| Molecular Formula | C20H24Cl2N2O3 |
| Molecular Weight | 411.32 g/mol |
| Synonyms | Diclofenac N-(2-Hydroxyethyl)pyrrolidine; Diclofenac Epolamine Salt; Diclofenac Hydroxyethylpyrrolidine; Flector (Brand Name); EPOLAMINE, DICLOFENAC; 2-[(2,6-Dichlorophenyl)amino]benzeneacetic acid compd. with 1-(2-hydroxyethyl)pyrrolidine; UNII-8G5OGD6H1B |
| EINECS | Contact for details |
Quality Control
Our Diclofenac Epolamine is manufactured under strict quality systems to meet the rigorous standards of the pharmaceutical industry. We provide material that typically conforms to major pharmacopoeial specifications, including USP and EP monographs. Every batch is supported by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. Our quality commitment ensures reliability for your GMP-compliant manufacturing processes.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). The product is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation. For long-term storage, consider using desiccants.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to standard |
| Identification (HPLC) | Conforms to standard |
| Assay (HPLC) | 98.0% - 102.0% |
| Related Substances (HPLC) | Total impurities ≤ 1.0% |
| Single Maximum Impurity | ≤ 0.5% |
| Water Content (KF) | ≤ 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.
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