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Granisetron Nitrogen Oxide CAS NO 160177-68-4
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CAS No.:160177-68-4
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Granisetron Nitrogen Oxide is a key pharmaceutical intermediate and research chemical. This compound is of significant interest for its role in the development and synthesis of advanced antiemetic agents. It is primarily utilized by pharmaceutical manufacturers and research institutions engaged in the development of new drug formulations and chemical synthesis pathways. The material is handled under controlled conditions to ensure its integrity for high-value applications.
Application
- Pharmaceutical Intermediate: Critical precursor in the synthesis of Granisetron and its related analogs.
- Research & Development: Used in medicinal chemistry for structure-activity relationship (SAR) studies and new drug discovery projects.
- Process Chemistry: Serves as a building block in the scale-up and optimization of active pharmaceutical ingredient (API) manufacturing processes.
- Analytical Reference Standard: Employed as a high-purity standard for quality control and analytical method development (e.g., HPLC, LC-MS).
- Chemical Synthesis: Utilized in organic synthesis for introducing specific functional groups or creating novel molecular architectures.
Basic Information
| Product Name | Granisetron Nitrogen Oxide |
| CAS No. | 160177-68-4 |
| Molecular Formula | Contact for details |
| Molecular Weight | Contact for details |
| Synonyms | 1-Methyl-N-((1R,3r,5S)-9-methyl-9-azabicyclo[3.3.1]nonan-3-yl)-1H-indazole-3-carboxamide N-oxide; Granisetron N-Oxide; Granisetron Oxide; 1-Methyl-1H-indazole-3-carboxylic acid (1R,3r,5S)-9-methyl-9-azabicyclo[3.3.1]non-3-yl ester N-oxide |
| EINECS | Contact for details |
Quality Control
Our Granisetron Nitrogen Oxide is produced and tested under a strict quality management system. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. A detailed Certificate of Analysis (COA) is provided with every shipment, documenting key parameters such as assay and impurity profiles. We support compliance with cGMP and ICH guidelines for pharmaceutical intermediates.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature. Keep away from incompatible materials.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white powder |
| Identification (IR) | Conforms to reference spectrum |
| Assay (HPLC) | ≥ 98.0% |
| Related Substances (HPLC) | Total impurities ≤ 2.0% |
| Residual Solvents (GC) | Complies with ICH limits |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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Why choose US
Trusted Manufacturer
With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.
Rigorous Quality Assurance
Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
Advanced R&D Expertise
Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.






