Nolvadex Powder Overview
Nolvadex Powder (Tamoxifen Citrate Powder) is a nonsteroidal selective estrogen receptor modulator engineered for advanced pharmaceutical and biochemical research applications. Known for its stable molecular structure, excellent formulation adaptability, and high analytical reliability, Tamoxifen Citrate is extensively utilized in hormone-related studies and pharmaceutical development environments.
Manufactured using GMP-oriented production systems and advanced purification technologies, Nolvadex Powder undergoes comprehensive analytical verification including HPLC assay analysis, impurity profiling, residual solvent testing, and heavy metal screening to ensure pharmaceutical-grade quality and superior batch consistency.
The powder generally appears as a white to slightly off-white crystalline material with strong stability under controlled storage conditions.
Technical Product Specification
| Parameter | Specification |
|---|---|
| Product Name | Nolvadex Powder |
| Chemical Name | Tamoxifen Citrate |
| CAS Number | 54965-24-1 |
| Molecular Formula | C32H37NO8 |
| Molecular Weight | 563.64 g/mol |
| Appearance | White to off-white crystalline powder |
| Assay (HPLC) | ≥99.0% |
| Identification | HPLC / IR / UV Compliant |
| Melting Point | 140–144°C |
| Solubility | Soluble in methanol, ethanol, DMSO |
| 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
Nolvadex Powder is refined using advanced purification technologies to achieve ultra-high purity levels with minimal impurity content and superior production consistency.
Optimized Formulation Compatibility
Tamoxifen Citrate demonstrates excellent compatibility with common pharmaceutical solvents and laboratory formulation systems, supporting advanced research and analytical applications.
Enhanced Molecular Stability
Its stable crystalline structure provides excellent resistance to degradation under recommended storage conditions, helping preserve long-term product integrity and analytical reliability.
Comprehensive Analytical Validation
Every production batch undergoes rigorous quality testing using advanced instrumentation, including:
- High Performance Liquid Chromatography (HPLC)
- Infrared Spectroscopy (IR)
- Ultraviolet Spectral Identification (UV)
- Residual Solvent Analysis
- Heavy Metal Screening
- Moisture Content Verification
- Impurity Profile Evaluation
- Particle Size Distribution Testing
Pharmaceutical Manufacturing Standards
- GMP-oriented production environment
- Controlled cleanroom manufacturing 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 Nolvadex Powder in tightly sealed, moisture-resistant containers within a cool, dry, and well-ventilated environment.
Recommended Conditions
- Temperature: 2–8°C
- Humidity: Below 50%
- Protection: Avoid direct sunlight, oxidation, and excessive heat exposure
Proper storage conditions help preserve product purity, stability, and analytical performance.
