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Galantamine Hydrobromide CAS NO 1953-04-4
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CAS No.:1953-04-4
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Galantamine Hydrobromide is a high-purity alkaloid salt derived from natural sources and synthesized for pharmaceutical applications. It serves as a potent and selective acetylcholinesterase inhibitor, making it a critical active pharmaceutical ingredient (API) for cognitive support. This compound is essential for manufacturers in the pharmaceutical industry developing treatments for neurological conditions. We supply it with a focus on stringent quality control and reliable global supply chains.
Application
- Pharmaceutical API: Primary use as the active ingredient in prescription medications for the treatment of mild to moderate Alzheimer's disease and other memory-related cognitive disorders.
- Neurological Research: A key reference standard and biochemical tool in neuroscience research for studying cholinergic systems, enzyme inhibition, and cognitive function.
- Finished Dosage Formulation: Used in the development and production of various oral solid dosage forms, including tablets and capsules.
- Veterinary Medicine: Investigated for potential applications in cognitive dysfunction syndrome (CDS) in aging pets.
- Reference Standard: Serves as a high-purity certified reference material (CRM) for quality control laboratories in pharmacopeial testing (USP, EP).
Basic Information
| Product Name | Galantamine Hydrobromide |
| CAS No. | 1953-04-4 |
| Molecular Formula | C17H21NO3 • HBr |
| Molecular Weight | 368.27 g/mol |
| Synonyms | Galantamine HBr; Galanthamine Hydrobromide; Lycoramine; Jilkon; Nivalin; Reminyl (as API); (4aS,6R,8aS)-4a,5,9,10,11,12-Hexahydro-3-methoxy-11-methyl-6H-benzofuro[3a,3,2-ef][2]benzazepin-6-ol hydrobromide |
| EINECS | 217-796-2 |
Quality Control
Our Galantamine Hydrobromide is manufactured and tested to meet high-grade pharmaceutical standards. Quality assurance protocols are designed to ensure identity, purity, strength, and composition, referencing pharmacopeial monographs such as USP and EP. A comprehensive Certificate of Analysis (COA) is provided with each batch, detailing results for assay, related substances, residual solvents, and other critical parameters.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation. For long-term storage, consider desiccants or inert atmosphere conditions.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to reference standard |
| Identification (HPLC) | Retention time corresponds to reference |
| Assay (HPLC) | 98.0% - 102.0% (on anhydrous basis) |
| Related Substances (HPLC) | Total impurities ≤ 1.0% Any single impurity ≤ 0.5% |
| Water Content (KF) | ≤ 1.0% |
| Residue on Ignition | ≤ 0.1% |
| Heavy Metals | ≤ 20 ppm |
| Residual Solvents (GC) | Complies with ICH Q3C guidelines |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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