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Galdansetron CAS NO 116684-43-6
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CAS No.:116684-43-6
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Galdansetron is a high-purity pharmaceutical intermediate and active ingredient. This compound is critical for ensuring the quality and efficacy of advanced therapeutic formulations. It is primarily required by pharmaceutical manufacturers and research institutions engaged in the development and production of specialized medications.
Application
- Key intermediate in the synthesis of novel pharmaceutical actives.
- Research and development of new chemical entities (NCEs) in medicinal chemistry.
- Production of high-value reference standards for analytical and quality control laboratories.
- Precursor for advanced drug discovery programs targeting specific therapeutic areas.
- Used in process development and scale-up activities within GMP manufacturing facilities.
Basic Information
| Product Name | Galdansetron |
| CAS No. | 116684-43-6 |
| Molecular Formula | C₁₈H₂₀N₄O₂ |
| Molecular Weight | 324.38 g/mol |
| Synonyms | Galdansetron; 1H-Indazole-3-carboxamide, 1,2-dihydro-2-oxo-N-(8-methyl-8-azabicyclo[3.2.1]oct-3-yl)-; (3-endo)-N-(8-Methyl-8-azabicyclo[3.2.1]oct-3-yl)-1,2-dihydro-2-oxo-1H-indazole-3-carboxamide; Bemesetron; BRL 43694; Granisetron Impurity F |
| EINECS | Contact for details |
Quality Control
Our Galdansetron is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation, to ensure it meets the stringent requirements for pharmaceutical use. Certificates of Analysis (COA) detailing all specifications are available upon request.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white powder |
| Identification (IR) | Conforms to reference spectrum |
| Identification (HPLC) | Retention time matches reference standard |
| Assay (HPLC) | ≥ 98.5% |
| Related Substances (HPLC) | Total impurities ≤ 1.5% Any single impurity ≤ 0.5% |
| Loss on Drying | ≤ 0.5% |
| Residue on Ignition | ≤ 0.1% |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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Trusted Manufacturer
With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.
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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
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Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.






