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(-)-Bevantolol CAS NO 135531-41-8
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CAS No.:135531-41-8
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
(-)-Bevantolol CAS NO 135531-41-8 is a high-purity, single-enantiomer pharmaceutical intermediate and research chemical belonging to the class of β-adrenergic blocking agents. This compound is critical for the development and production of enantiomerically pure cardiovascular drugs, where the specific stereochemistry is essential for targeted biological activity and reduced side-effect profiles. It is primarily utilized by pharmaceutical R&D laboratories, API (Active Pharmaceutical Ingredient) manufacturers, and academic institutions engaged in cardiovascular and receptor pharmacology studies.
Application
- Pharmaceutical Intermediate: Key chiral building block in the synthesis of enantiomerically pure β-blocker APIs.
- Research & Development: Used as a reference standard and pharmacological tool in cardiovascular and adrenergic receptor research.
- Active Pharmaceutical Ingredient (API) Synthesis: Integral component in multi-step synthetic routes for producing final drug substances.
- Metabolite Studies: Employed in the investigation of drug metabolism and pharmacokinetics (DMPK) for related therapeutic agents.
- Analytical Standard: Serves as a high-purity certified reference material (CRM) for quality control and method validation in analytical laboratories.
Basic Information
| Product Name | (-)-Bevantolol |
| CAS No. | 135531-41-8 |
| Molecular Formula | C20H25NO4 |
| Molecular Weight | 343.42 g/mol |
| Synonyms | (-)-Bevantolol; (2R)-1-{[3,4-Dimethoxyphenethyl]amino}-3-(3-methylphenoxy)propan-2-ol; Levobevantolol; (R)-Bevantolol; Bevantolol (S-enantiomer); CL 77555; L-Bevantolol; NCI 60_003529 |
| EINECS | Contact for details |
Quality Control
Our (-)-Bevantolol is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including chiral purity verification by HPLC, to ensure it meets the stringent requirements for pharmaceutical research and development. A detailed Certificate of Analysis (COA) is provided with every shipment, documenting identity, purity, and impurity profiles.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). The product is hygroscopic (moisture-sensitive); ensure the container is sealed tightly after each use to prevent degradation.
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) | ≥ 98.5% |
| Chiral Purity (Enantiomeric Excess) | ≥ 99.0% |
| Related Substances (HPLC) | Total impurities ≤ 1.0% Any single impurity ≤ 0.5% |
| Residual Solvents (GC) | Complies with ICH Q3C guidelines |
| 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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