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(R)-Ambrisentan CAS NO 1007358-76-0
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CAS No.:1007358-76-0
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
(R)-Ambrisentan CAS NO 1007358-76-0 is the single enantiomer form of the potent and selective endothelin A (ETA) receptor antagonist, ambrisentan. This high-purity chiral intermediate is critical for the research and development of targeted pulmonary arterial hypertension (PAH) therapies. It is primarily utilized by pharmaceutical R&D laboratories, contract research organizations (CROs), and advanced chemical synthesis facilities focused on producing enantiomerically pure active pharmaceutical ingredients (APIs).
Application
- Pharmaceutical Intermediate: Key chiral building block in the synthesis of the API Letairis® (ambrisentan) for treating pulmonary arterial hypertension (PAH).
- Research & Development: Used in preclinical and clinical studies to investigate the specific pharmacological profile of the (R)-enantiomer.
- Process Chemistry: Serves as a reference standard and starting material for developing and optimizing asymmetric synthesis routes.
- Analytical Standard: Employed as a high-purity standard for method development and validation in HPLC and chiral analysis.
- Academic Research: Utilized in biochemical studies exploring endothelin receptor signaling pathways and structure-activity relationships (SAR).
Basic Information
| Product Name | (R)-Ambrisentan |
| CAS No. | 1007358-76-0 |
| Molecular Formula | C22H22N2O4 |
| Molecular Weight | 378.42 g/mol |
| Synonyms | (R)-Ambrisentan; (2R)-2-[(4,6-Dimethylpyrimidin-2-yl)oxy]-3-methoxy-3,3-diphenylpropanoic Acid; (R)-(-)-Ambrisentan; BSF 208075 (R)-enantiomer; LU 208075 (R)-enantiomer; (R)-Form of Ambrisentan; (R)-BSF 208075; (R)-LU 208075 |
| EINECS | Contact for details |
Quality Control
Our (R)-Ambrisentan is manufactured under strict quality management systems. Every batch undergoes comprehensive analytical testing, including chiral purity determination by HPLC, to ensure it meets the stringent requirements for pharmaceutical R&D. A detailed Certificate of Analysis (COA) is provided with each shipment, documenting identity, purity, and enantiomeric excess.
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 light-sensitive and should be handled under appropriate conditions to maintain stability.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white powder |
| Identification (IR) | Conforms to structure |
| Identification (HPLC) | Retention time matches reference standard |
| Assay (HPLC) | ≥98.0% |
| Enantiomeric Purity (Chiral HPLC) | ≥99.0% |
| Related Substances (HPLC) | Total impurities ≤2.0% |
| Residual Solvents (GC) | Complies with ICH 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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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
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