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Neriproct CAS NO 117803-69-7
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CAS No.:117803-69-7
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Neriproct CAS NO 117803-69-7 is a high-purity pharmaceutical intermediate and active ingredient of significant commercial importance. Its primary value lies in its role as a key building block for the synthesis of advanced therapeutic agents, particularly in specialized pharmaceutical formulations. This compound is essential for manufacturers and R&D facilities in the pharmaceutical and fine chemical industries seeking reliable, high-quality raw materials for production and development.
Application
- Pharmaceutical Synthesis: A critical intermediate in the production of active pharmaceutical ingredients (APIs) for various therapeutic classes.
- Research & Development: Used in laboratory settings for the discovery and development of new drug candidates and novel chemical entities.
- Fine Chemical Manufacturing: Serves as a key precursor in multi-step synthesis processes for complex organic molecules.
- Contract Manufacturing (CMO): Supplied to contract manufacturing organizations for the production of client-specific pharmaceutical compounds.
- Reference Standard: Utilized as an analytical reference standard for quality control and method validation in pharmaceutical analysis.
Basic Information
| Item | Detail |
|---|---|
| Product Name | Neriproct |
| CAS No. | 117803-69-7 |
| Molecular Formula | Contact for details |
| Molecular Weight | Contact for details |
| Synonyms | Neriproct; 117803-69-7; Neriproctum; Neripract; (Chemical name based on structure to be confirmed); (IUPAC name to be confirmed) |
| EINECS | Contact for details |
Quality Control
Our Neriproct is produced under a strict quality management system. Each batch undergoes rigorous analytical testing to ensure it meets the high-purity standards required for pharmaceutical applications. A comprehensive Certificate of Analysis (COA) is provided, detailing purity, identity, and impurity profiles. We adhere to relevant GMP guidelines for the manufacture of 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 (typically 15-25°C). Keep the container tightly sealed to protect from moisture.
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% |
| 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.
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.






