Technical Specifications of Testosterone Enanthate | CAS 315-37-7
Product Introduction of Testosterone Enanthate
Analytical Specifications & In-House Quality Control (Self-Inspection)
Certified laboratories evaluate the structural integrity and impurity profile via validated chromatographic methods, ensuring the complete absence of unauthorized synthetic cross-contaminants:
Analytical Parameters | Technical Baseline Criteria | Primary Verification Methodology |
Assay (Purity Profile) | Must align precisely with compendial limits | HPLC-UV (High-Performance Liquid Chromatography) |
Identification Criteria | Must match designated reference spectrum | FT-IR Spectroscopy / Mass Spectrometry |
Melting Range | 34.0°C – 39.0°C | Capillary Melting Point Apparatus |
Specific Rotation | +77° to +82° (in chloroform) | Automatic Digital Polarimeter |
Organic Impurities | Individual unknown impurities ≤ 0.1% | High-Resolution Liquid Chromatography |
Loss on Drying | ≤ 0.5% | Vacuum Desiccation over Phosphorus Pentoxide |
Product Packaging
Application of Testosterone Enanthate
Within specialized chemical engineering and pharmacodynamics mapping, the utilization of this compound is restricted strictly to authorized downstream loops:
- Reference Standard Material: Employed as a chemical reference standard in high-performance liquid chromatography (HPLC) calibration and gas chromatography-mass spectrometry (GC-MS) matrix validation within accredited forensic and testing laboratories.
- Synthetic Tracer Substrates: Utilized in advanced metabolic research and endocrine pathway elucidation models to trace steroid receptor binding affinities under laboratory-controlled conditions.
Related Questions:
Q1: What structural factors govern the low melting point and thermal stability of this esterified compound?
Q2: How must laboratories manage environmental exposure to prevent hydrolysis of the ester linkage?
A: Although the ester link at the 17-beta position is hydrophobic, prolonged exposure to atmospheric moisture in the presence of trace acidic or alkaline catalytic residues can trigger slow hydrolytic cleavage, releasing free enanthic acid and degrading the compound’s purity profile. Storage protocols require hermetically sealed container systems blanketed under high-purity dry nitrogen gas, protected from light, and maintained consistently within specialized refrigeration zones (2°C–8°C).
International Regulatory Frameworks & Compliance Auditing
Given the complex global legal statuses associated with esterified steroid intermediates, operations must align thoroughly with localized country-specific regulatory bodies:
- Import/Export Verification Tracking: In accordance with international drug enforcement and pharmaceutical management mandates, distribution requires specific licensing, end-user declarations (EUD), and strict compliance with the destination country’s competent authorities.
- Facility Auditing Verification: Manufacturing loops must strictly separate any hormonal production areas from standard fine chemical processing blocks to prevent cross-contamination, adhering to rigorous atmospheric filtration and occupational hygiene exposure limits.
Manufacturer of Testosterone Enanthate
API, usually referring to chemical raw materials, is the active ingredient in chemical drug formulations.
Testosterone Enanthate Safety Information
| Hazard Codes | T |
| Risk Statements | 45-63 |
| Safety Statements | 53-22-36/37/39-45 |
| WGK Germany | 3 |
| RTECS | XA3080000 |
| HS Code | 2937290000 |
| Storage Class | 6.1C – Combustible acute toxic Cat.3 toxic compounds or compounds which causing chronic effects |
OrganicIntermediate is a professional foreign trade enterprise specializing in chemical raw materials. Upholding people-oriented values and cooperating with reliable manufacturers, we aim to become the world’s most trusted chemical supplier. Our production plant is located 50 meters south of the intersection of North Ring Road and 13th Road, Chenwang Street, Juancheng County, Heze City, Shandong Province. Our R&D laboratory is situated at R&D Base : F5, Yinfeng Biomedical City, Free Trade Zone, Jinan, Shandong. Integrating R&D and production, we strictly control product quality. With stable supply and sincere service, we welcome global customers for consultation and procurement.
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This article was written by William, the chief chemist of Shandong Zhishang New Materials Co., Ltd.
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