Altrenogest – Pharmaceutical Grade Intermediate
Veterinary Reproductive Health Formulation Material
Altrenogest is supplied as a pharmaceutical-grade intermediate intended for the formulation of veterinary reproductive health products. Delivered in a controlled solid form with verified purity, this material is designed to support formulation scientists, quality control teams, and regulatory departments with reliable analytical documentation and consistent performance.
Please note: This product is not a finished veterinary medicine. It is a raw material intended for further processing, formulation, and regulatory approval by qualified manufacturers.
Technical Specifications
- CAS Number: 850-52-2
- Physical Form: Fine, off-white crystalline powder
- Purity / Assay: ≥ 98% (HPLC)
- Solubility: Soluble in common organic solvents
Storage Conditions
▸ Short-term: 2–8 °C, sealed and dry
▸ Long-term: −20 °C recommended
▸ Protection: Store away from light and moisture
Documentation
- Certificate of Analysis (COA)
- MSDS / TDS
- Impurity profile and stability summary
Packaging
- Small vials for sample evaluation
- Larger packaging for bulk supply
- OEM and customized packaging available
Practical Considerations for Formulation & QC
Material Behavior
As a steroidal compound, Altrenogest requires controlled handling. Exposure to heat, moisture, or light may accelerate degradation pathways if not properly managed.
Formulation Implications
Early evaluation of solubility limits and pH compatibility is recommended before scale-up.
Batch Integration & Traceability
Each batch is assigned a unique ID and accompanied by full documentation for QC and ERP traceability.
Handling & Storage Notes
- Transfer promptly to controlled storage
- Avoid prolonged humidity exposure
- Use appropriate PPE
- Prevent inhalation and skin contact
- Align solvents with stability strategy
Packaging & Logistics
- Moisture-resistant sealed vials
- Temperature-controlled transport options
- Complete documentation packets included
Procurement Pathway
Sample Verification
Order samples to evaluate compatibility.
Documentation Review
QC teams assess COA and impurity profiles.
Scale to Production
Transition to bulk supply after validation.
Frequently Asked Questions (FAQs)
Q: What quality documentation is provided?
A: COA, impurity summary, and stability data.
Q: Can I order samples?
A: Yes, sample orders are standard.
Q: How should it be stored?
A: 2–8 °C short term, −20 °C long term, protect from light.
Q: Is custom packaging available?
A: Yes, OEM options are supported.
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