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Prenalterol Sulfate Ester CAS NO 81924-67-6
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CAS No.:81924-67-6
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Prenalterol Sulfate Ester CAS NO 81924-67-6 is a key pharmaceutical intermediate and reference standard of significant interest in medicinal chemistry. Its primary value lies in its role as a precursor or derivative in the synthesis and analytical profiling of β-adrenergic receptor agonists. This compound is essential for research and development laboratories, pharmaceutical manufacturers, and quality control units focused on cardiovascular and respiratory therapeutics.
Application
- Pharmaceutical Intermediate: Critical precursor in the synthesis of β-adrenergic agonists and related active pharmaceutical ingredients (APIs).
- Analytical Reference Standard: Used for method development, validation, and quality control (QC) testing in HPLC, LC-MS, and other chromatographic systems.
- Metabolite Studies: Employed in pharmacokinetic and drug metabolism research to study the biotransformation pathways of prenalterol and similar compounds.
- Process Chemistry & Impurity Profiling: Serves as a known impurity or degradation product standard to ensure the purity and stability of final drug substances.
- Biochemical Research: Utilized in vitro studies to investigate the structure-activity relationships (SAR) of β-agonist drugs.
Basic Information
| Product Name | Prenalterol Sulfate Ester |
| CAS No. | 81924-67-6 |
| Molecular Formula | C₁₂H₁₈N₂O₅S |
| Molecular Weight | 302.35 g/mol |
| Synonyms | Prenalterol Sulfate; (±)-Prenalterol Sulfate Ester; 1-(4-Hydroxyphenoxy)-3-[(1-methylethyl)amino]-2-propanol Sulfate Ester; 3-[(2RS)-2-Hydroxy-3-[(1-methylethyl)amino]propoxy]phenyl Sulfate; Hydroxyprenalterol Sulfate Ester; Prenalterol Ester Sulfate; Isopropanolamine Sulfate Ester Derivative |
| EINECS | Contact for details |
Quality Control
Our Prenalterol Sulfate Ester is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling, to ensure it meets stringent specifications for pharmaceutical research and development. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and compliance with your quality requirements.
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). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white 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 ≤ 1.0% |
| Water Content (KF) | ≤ 1.0% |
| Residue on Ignition | ≤ 0.1% |
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.






