Galantamine Hydrobromide API Powder

Galantamine Hydrobromide Powder - High Purity API Grade CAS No.: 1953-04-4 Molecular Formula: C₁₇H₂₂BrNO₃ Molecular Weight: 368.27 g/mol Form: White to off-white crystalline powder Product Overview Galantamine Hydrobromide is a premium-grade Active Pharmaceutical Ingredient (API) widely used in neurological and cognitive research. Known for its dual action as an acetylcholinesterase inhibitor and nicotinic receptor modulator, this compound is essential for studies related to memory, cognition, and neurodegenerative diseases. Our high-purity powder ensures excellent performance, consistency, and reliability for laboratory, formulation, and R&D applications. Key Features High Purity (≥98% HPLC): Ensures superior quality and accuracy in research and formulation. Pharmaceutical Grade: Suitable for advanced R&D, formulation development, and analytical studies. Stable & Consistent: Manufactured under strict quality control for batch-to-batch reliability. Highly Soluble: Soluble in water, methanol, and DMSO for versatile laboratory use. Reliable Mode of Action: Acts as a reversible acetylcholinesterase inhibitor and allosteric potentiator of nicotinic acetylcholine receptors. Technical Specifications PropertyDetails CAS Number 1953-04-4 Molecular Weight 368.27 g/mol Purity ≥ 98% (HPLC) Appearance White to off-white crystalline powder Melting Point ~256 °C Solubility Water, methanol, DMSO Storage Conditions Store at 2-8 °C, protect from light & moisture Applications / Uses 1. Neurodegenerative Disease Research Widely used in studies on Alzheimer's disease and other forms of dementia due to its ability to enhance acetylcholine levels and support cognitive function. 2. Cognitive & Memory Research Ideal for exploring memory formation, cognitive enhancement, synaptic plasticity, and cholinergic neurotransmission. 3. Pharmaceutical Development Used as an API in the development of formulations targeting cognitive impairment. Supports pharmacokinetic, bioavailability, and stability studies. 4. Mechanistic & Analytical Research Helps investigate biochemical pathways, neuroprotective mechanisms, and neural receptor interactions. Also suitable for method development (HPLC/UV/Spectroscopy). Quality & Compliance Manufactured under GMP-oriented quality systems COA, MSDS, and batch documentation provided Excellent stability under recommended storage conditions Available in multiple custom pack sizes for bulk or research needs Handling & Safety Use appropriate PPE while handling Avoid exposure to moisture and direct sunlight Store in a cool, dry place at 2-8 °C About the Company Legal Status of Firm: Partnership Number of Employees: 11 To 25 People Annual Turnover: 0 - 40 L company-description: Zesla Chemicals and Pharmaceuticals leverages its cost-effective operations in India, coupled with extensive expertise and advanced production capabilities, to deliver competitive and exceptional custom manufacturing services to a global clientele. Our Contract Manufacturing Services stand out with top-notch units adhering to WHO-GMP standards. Our manufacturing process is fully automated, ensuring precision and efficiency. We excel in creating dosage forms in both sterile and general categories, encompassing every pharmaceutical aspect, from small to large volume parenterals. With dedicated production facilities for Beta-Lactam and Cephalosporin products, we boast a qualified and experienced specialized team overseeing all aspects of Pharma Contract Manufacturing, including QC, QA, and Product Development. Choose Zesla for a superior and reliable partner in the pharmaceutical manufacturing industry.