Cyproterone Acetate Powder Overview
Cyproterone Acetate Powder is a synthetic steroidal antiandrogen and progestogenic compound engineered for advanced pharmaceutical and biochemical research applications. Known for its stable molecular structure and excellent formulation compatibility, Cyproterone Acetate is widely utilized in hormone-related laboratory studies and analytical development environments.
Produced under GMP-oriented manufacturing systems, the raw powder undergoes comprehensive analytical testing including HPLC purity verification, residual solvent analysis, impurity profiling, and heavy metal screening to ensure pharmaceutical-grade quality and performance consistency.
The powder generally appears as a white to slightly yellow crystalline material with excellent stability under controlled storage conditions.
Technical Product Specification
| Parameter | Specification |
|---|---|
| Product Name | Cyproterone Acetate Powder |
| Chemical Name | Cyproterone Acetate |
| CAS Number | 427-51-0 |
| Molecular Formula | C24H29ClO4 |
| Molecular Weight | 416.94 g/mol |
| Appearance | White to slightly yellow crystalline powder |
| Assay (HPLC) | ≥99.0% |
| Identification | HPLC / IR / UV Compliant |
| Melting Point | 200–204°C |
| Solubility | Soluble in chloroform, ethanol, methanol |
| Specific Rotation | Meets internal specification |
| Loss on Drying | ≤0.5% |
| Sulfated Ash | ≤0.1% |
| Heavy Metals | ≤10 ppm |
| Residual Solvents | USP / EP Standard |
| Particle Size | Micronized / Customizable |
| Microbial Limits | Pharmaceutical compliant |
| Storage Conditions | Cool, dry, light-resistant environment |
| Shelf Life | 24 months |
Advanced Product Features
Pharmaceutical-Grade Purity
Cyproterone Acetate Powder is refined using advanced purification and filtration technologies to achieve ultra-high purity with low impurity content and superior production consistency.
Optimized Formulation Compatibility
The compound demonstrates excellent compatibility with pharmaceutical solvents and laboratory formulation systems, supporting advanced research and analytical applications.
Enhanced Stability Profile
Its chemically stable crystalline structure provides strong resistance to degradation under properly controlled environmental conditions, supporting long-term storage reliability.
Comprehensive Analytical Testing
Every production batch is verified using advanced analytical methodologies, including:
- High Performance Liquid Chromatography (HPLC)
- Infrared Spectroscopy (IR)
- Ultraviolet Spectral Identification (UV)
- Residual Solvent Testing
- Heavy Metal Screening
- Moisture Content Verification
- Impurity Profile Analysis
- Particle Size Distribution Testing
Pharmaceutical Manufacturing Standards
- GMP-oriented manufacturing procedures
- Controlled cleanroom production systems
- Batch-to-batch consistency verification
- Strict raw material traceability
- International export packaging compliance
- Advanced quality assurance protocols
Packaging Options
| Packaging Type | Available Sizes |
|---|---|
| Aluminum Foil Vacuum Bag | 10g / 50g / 100g |
| Pharmaceutical Vacuum Packaging | 500g |
| Fiber Drum with Double PE Lining | 1kg / 5kg / 25kg |
OEM packaging and private labeling services available for wholesale and bulk supply.
Storage Recommendations
Store Cyproterone Acetate Powder in tightly sealed, moisture-resistant containers within a cool, dry, and well-ventilated environment.
Recommended Storage Conditions
- Temperature: 2–8°C
- Humidity: Below 50%
- Protection: Avoid direct sunlight, oxidation, and excessive heat exposure
Proper storage conditions help maintain purity, stability, and analytical performance.
