Price range: $150.00 through $750.00

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

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.