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R-Benproperine CAS NO 124678-30-4
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CAS No.:124678-30-4
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
R-Benproperine is a high-purity pharmaceutical intermediate and active ingredient, identified by CAS NO 124678-30-4. This compound is a key chiral building block in the synthesis of advanced active pharmaceutical ingredients (APIs), valued for its specific stereochemistry and consistent quality. It is primarily required by pharmaceutical manufacturers and R&D organizations engaged in the development and production of respiratory therapeutics and other specialized medications.
Application
- Pharmaceutical Synthesis: A critical chiral intermediate in the production of benproperine and related antitussive (cough suppressant) APIs.
- Active Pharmaceutical Ingredient (API) Manufacturing: Serves as a direct precursor or building block in GMP-compliant API production lines.
- Research & Development: Used in medicinal chemistry research for developing new therapeutic agents targeting the central nervous and respiratory systems.
- Process Development & Scale-Up: Employed in optimizing synthetic routes and scaling up from laboratory to commercial production.
- Reference Standard: Utilized as an analytical standard for quality control and method validation in pharmaceutical testing laboratories.
Basic Information
| Product Name | R-Benproperine |
| CAS No. | 124678-30-4 |
| Molecular Formula | C21H27NO |
| Molecular Weight | 309.45 g/mol |
| Synonyms | (R)-Benproperine; (R)-1-[2-(2-Benzylphenoxy)-1-methylethyl]piperidine; (R)-1-[1-Methyl-2-(2-benzylphenoxy)ethyl]piperidine; R-Benproperine phosphate intermediate; Dextro-Benproperine; R-Form Benproperine; Benproperine R-Isomer; UNII-8V8W7Q7K8P (component) |
| EINECS | Contact for details |
Quality Control
Our R-Benproperine is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles. We support compliance with ICH Q7 guidelines and relevant pharmacopeial standards 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 (15-25°C). Keep away from incompatible materials.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to structure |
| Assay (HPLC) | ≥98.5% |
| Optical Rotation [α] | Specific range provided on COA |
| Related Substances (HPLC) | Total impurities ≤1.5% |
| Residual Solvents (GC) | Meets ICH Q3C guidelines |
| Heavy Metals | <20 ppm |
| Loss on Drying | ≤0.5% |
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.






