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Nebivolol Hcl CAS NO 169293-50-9
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CAS No.:169293-50-9
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Nebivolol Hcl CAS NO 169293-50-9 is a high-purity active pharmaceutical ingredient (API) and a highly selective β-1 adrenergic receptor antagonist. It is a critical component in the formulation of cardiovascular medications, primarily used to manage hypertension and heart failure. This compound is essential for pharmaceutical manufacturers and research institutions engaged in the development and production of advanced cardiology drugs, requiring a reliable supply of material that meets stringent pharmacopeial standards.
Application
- Pharmaceutical API: Primary active ingredient in antihypertensive and anti-anginal medication formulations.
- Cardiovascular Drug Synthesis: Key intermediate in the synthesis of finished dosage forms such as tablets and capsules.
- Clinical Research: Reference standard and material for pharmacological studies and clinical trials.
- Analytical Development: Used as a certified reference material (CRM) for method development and validation in quality control laboratories.
- Generic Drug Manufacturing: Sourcing for the production of bioequivalent generic versions of branded nebivolol medications.
- Preclinical Studies: Utilized in animal models to study hemodynamic effects and receptor selectivity.
Basic Information
| Product Name | Nebivolol Hcl |
| CAS No. | 169293-50-9 |
| Molecular Formula | C22H25F2NO4 • HCl |
| Molecular Weight | 441.90 g/mol (as hydrochloride) |
| Synonyms | Nebivolol Hydrochloride; (αR,α'R,2R,2'S)-α,α'-[Iminobis(methylene)]bis[6-fluoro-3,4-dihydro-2H-1-benzopyran-2-methanol] Hydrochloride; Bystolic (brand name); R 65-824; R-65824; UNII-5V5IOJ8338; Nebilet; Lobivon |
| EINECS | Contact for details |
Quality Control
Our Nebivolol Hcl is manufactured under strict quality management systems, targeting compliance with major pharmacopeial standards such as USP and EP. Each batch undergoes comprehensive analytical testing including identification, assay, impurity profiling, and residual solvent analysis. A Certificate of Analysis (COA) documenting all test results is provided with every shipment to ensure full traceability and regulatory support for our clients.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a low-humidity environment to prevent moisture absorption and degradation.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white powder |
| Identification (IR) | Conforms to reference standard |
| Identification (HPLC) | Retention time corresponds to reference |
| Assay (HPLC) | 98.0% - 102.0% (on anhydrous basis) |
| Water Content (KF) | ≤ 1.0% |
| Residue on Ignition | ≤ 0.1% |
| Related Substances (HPLC) | Individual impurity: ≤ 0.5% Total impurities: ≤ 1.5% |
| 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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