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Galantamine Hydrobromide Racemic (15 Mg) CAS NO 193146-85-9
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CAS No.:193146-85-9
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Galantamine Hydrobromide Racemic (15 Mg) is a high-purity pharmaceutical intermediate and reference standard. This compound is critical for research and development in neuropharmacology, serving as a key building block for the synthesis of active pharmaceutical ingredients (APIs). It is primarily utilized by pharmaceutical manufacturers, analytical laboratories, and research institutions focused on developing treatments for cognitive disorders.
Application
- Pharmaceutical Intermediate: A key starting material for the synthesis of Galantamine-based active pharmaceutical ingredients (APIs).
- Analytical Reference Standard: Used in quality control laboratories for method development, validation, and assay calibration in HPLC and other chromatographic systems.
- Biochemical Research: Employed in *in vitro* and *in vivo* studies to investigate acetylcholinesterase inhibition and mechanisms related to cognitive function.
- Process Development & Scale-up: Serves as a critical material for optimizing synthetic routes and manufacturing processes in pilot plants.
- Impurity Profiling: Used as a marker or precursor in the identification and quantification of related substances in finished drug products.
Basic Information
| Product Name | Galantamine Hydrobromide Racemic (15 Mg) |
| CAS No. | 193146-85-9 |
| Molecular Formula | C17H21NO3 • HBr |
| Molecular Weight | 368.27 g/mol |
| Synonyms | (±)-Galantamine Hydrobromide; Rac-Galantamine HBr; Galanthamine Hydrobromide Racemate; 4a,5,9,10,11,12-Hexahydro-3-methoxy-11-methyl-6H-benzofuro[3a,3,2-ef][2]benzazepin-6-ol hydrobromide; Lycoramine hydrobromide (racemic); Jilkon; Nivalin (racemic form); Reminyl precursor |
| EINECS | Contact for details |
Quality Control
Our Galantamine Hydrobromide Racemic is manufactured under strict quality management systems. Each batch is tested to ensure it meets stringent specifications for identity, purity, and composition, suitable for research and pharmaceutical development. A comprehensive Certificate of Analysis (COA) detailing all test results, including assay by HPLC, related substances, residual solvents, and heavy metals, is provided with every shipment.
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 maintain stability and purity.
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% |
| Related Substances (HPLC) | Total impurities ≤ 2.0% |
| 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.
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