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Dinoprost CAS NO 146388-90-1
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CAS No.:146388-90-1
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Dinoprost is a synthetic prostaglandin analog, chemically identical to naturally occurring PGF2α, and is a critical active pharmaceutical ingredient (API) in veterinary medicine. Its primary value lies in its potent luteolytic and uterotonic properties, which are essential for precise reproductive management in livestock. This compound is therefore indispensable for manufacturers of veterinary pharmaceuticals targeting the global animal health industry, particularly for applications in cattle and swine breeding programs.
Application
- Veterinary Pharmaceutical Synthesis: As the core API for injectable solutions used to induce luteolysis and control the estrous cycle in cattle and other farm animals.
- Estrus Synchronization: A key component in protocols for timed artificial insemination (TAI) to improve breeding efficiency and herd management.
- Treatment of Pyometra and Endometritis: Used in therapeutic formulations to treat uterine infections in cattle by promoting uterine clearance.
- Induction of Parturition: Employed to initiate controlled farrowing in sows and calving in cows, facilitating supervised births.
- Abortion Induction: Used in cases of unwanted pregnancy or for the termination of mummified fetus in livestock.
- Research and Development: Serves as a reference standard and key intermediate in pharmacological research focused on prostaglandin pathways and reproductive biology.
Basic Information
| Product Name | Dinoprost |
| CAS No. | 146388-90-1 |
| Molecular Formula | C₂₀H₃₄O₅ |
| Molecular Weight | 354.48 g/mol |
| Synonyms | Prostaglandin F2α (PGF2α); 9α,11α,15S-Trihydroxy-5Z,13E-prostadienoic acid; (5Z,9α,11α,13E,15S)-9,11,15-Trihydroxyprosta-5,13-dien-1-oic acid; U-14583; Enzaprost; Lutalyse (brand name equivalent); Dinolytic (brand name equivalent); Prostarmon F |
| EINECS | Contact for details |
Quality Control
Our Dinoprost is manufactured under strict quality management systems to ensure it meets the high-purity standards required for pharmaceutical use. Each batch is subjected to comprehensive analytical testing, including identity confirmation, potency assay, and impurity profiling via advanced techniques like HPLC. A Certificate of Analysis (COA) documenting full compliance with agreed specifications is provided with every shipment.
Storage
Preserve in a tightly closed container, protected from light. Store in a freezer at or below -20°C for long-term stability. This product is hygroscopic (moisture-sensitive); ensure the container is sealed under an inert atmosphere or with desiccant to prevent degradation. Allow the sealed container to reach room temperature before opening to avoid condensation.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to reference spectrum |
| Identification (HPLC) | Retention time matches reference standard |
| Assay (HPLC) | ≥ 98.0% |
| Related Substances (HPLC) | Total impurities ≤ 2.0% Any single impurity ≤ 1.0% |
| Water Content (KF) | ≤ 1.0% |
| Residue on Ignition | ≤ 0.1% |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
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