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Penirolol CAS NO 58503-83-6
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CAS No.:58503-83-6
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Penirolol CAS NO 58503-83-6 is a high-purity pharmaceutical intermediate and research chemical belonging to the class of β-adrenergic blocking agents. This compound is critical for the development and synthesis of active pharmaceutical ingredients (APIs) targeting cardiovascular conditions. It is primarily utilized by pharmaceutical manufacturers and advanced research institutions engaged in drug discovery and process chemistry.
Application
- Pharmaceutical Intermediate: Key building block in the synthesis of β-blocker APIs for hypertension and angina treatment.
- Research & Development: Used in preclinical and clinical studies to investigate cardiovascular pharmacology and drug mechanisms.
- Reference Standard: Serves as an analytical standard for quality control and method validation in pharmaceutical laboratories.
- Process Chemistry: Employed in scale-up and optimization of synthetic routes for commercial drug manufacturing.
- Academic Research: Utilized in university and institutional labs for studying adrenergic receptor interactions and structure-activity relationships.
Basic Information
| Item | Details |
|---|---|
| Product Name | Penirolol |
| CAS No. | 58503-83-6 |
| Molecular Formula | C16H25NO3 |
| Molecular Weight | 279.38 g/mol |
| Synonyms | Penirolol; (±)-Penirolol; 1-(tert-Butylamino)-3-[2-(cyclopentyloxy)phenoxy]-2-propanol; 2-Propanol, 1-[(1,1-dimethylethyl)amino]-3-[2-(cyclopentyloxy)phenoxy]-; Penirolol [INN]; BRN 2933977; UNII-7V8A4U7985; (RS)-Penirolol |
| EINECS | Contact for details |
Quality Control
Our Penirolol is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, IR and NMR for structural confirmation, and residual solvent analysis. We provide full traceability and Certificates of Analysis (COA) are available for all shipments, ensuring 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 (15-25°C). Keep the container tightly sealed to protect from moisture.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to reference spectrum |
| Identification (HPLC) | Retention time matches reference standard |
| Assay (HPLC) | ≥ 98.0% |
| Related Substances (HPLC) | Total impurities ≤ 2.0% Any single impurity ≤ 0.5% |
| Residual Solvents (GC) | Meets ICH Q3C guidelines |
| Loss on Drying | ≤ 0.5% |
| Heavy Metals | ≤ 20 ppm |
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.






