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Hexoprenaline Sulphate CAS NO 32266-10-7
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CAS No.:32266-10-7
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Hexoprenaline Sulphate is a selective β2-adrenergic receptor agonist, a high-purity pharmaceutical active ingredient. It matters for its critical role in the development and formulation of specialized respiratory and tocolytic medications. This compound is primarily needed by pharmaceutical manufacturers and research institutions focused on creating treatments for conditions like asthma, chronic obstructive pulmonary disease (COPD), and premature labor.
Application
- Pharmaceutical API: Primary active ingredient in the formulation of bronchodilator and tocolytic (anti-labor) injectable solutions and tablets.
- Respiratory Therapeutics: Used in the development of medications for managing asthma, bronchitis, and other obstructive airway diseases.
- Obstetric & Gynecological Medicine: Key component in drugs designed to inhibit premature uterine contractions.
- Biochemical Research: Serves as a reference standard and tool compound for studying β2-adrenergic receptor signaling pathways and mechanisms.
- Veterinary Pharmaceuticals: Potential application in veterinary medicine for treating respiratory distress in animals.
- Analytical Standard: Used as a high-purity certified reference material (CRM) for quality control and method validation in analytical laboratories.
Basic Information
| Product Name | Hexoprenaline Sulphate |
| CAS No. | 32266-10-7 |
| Molecular Formula | C₂₂H₃₂N₂O₁₀S |
| Molecular Weight | 540.57 g/mol |
| Synonyms | Hexoprenaline Sulfate; Ipradol; 4,4'-[1,6-Hexanediylbis(iminomethylene)]bis[1,2-benzenediol] Sulfate; 1,6-Bis(3,4-dihydroxyphenyl)hexamethylenediamine Disulfate; Delaprem; GU-104; N,N'-Bis(3,4-dihydroxybenzyl)hexamethylenediamine Disulfate |
| EINECS | Contact for details |
Quality Control
Our Hexoprenaline Sulphate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, residual solvent analysis, and identification by FTIR and NMR, to ensure it meets stringent pharmaceutical-grade specifications. 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 place at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after each use to prevent degradation from atmospheric 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% - 102.0% (on anhydrous basis) |
| Water Content (KF) | ≤ 5.0% |
| Residue on Ignition | ≤ 0.1% |
| Heavy Metals | ≤ 20 ppm |
| Related Substances (HPLC) | Total impurities ≤ 2.0% Any single impurity ≤ 0.5% |
| Residual Solvents (GC) | Complies with ICH Q3C guidelines |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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