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Flutamide CAS NO 13311-84-7
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CAS No.:13311-84-7
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Flutamide CAS NO 13311-84-7 is a potent, non-steroidal antiandrogen pharmaceutical compound. It is a critical active pharmaceutical ingredient (API) used in the treatment of androgen-dependent conditions, most notably prostate cancer. This high-purity compound is essential for pharmaceutical manufacturers and research institutions developing and producing advanced hormone therapies. Its specific mechanism of action makes it a key component in therapeutic regimens worldwide.
Application
- Pharmaceutical API: Primary use as the active ingredient in the manufacture of antiandrogen medications for the treatment of metastatic prostate cancer.
- Hormone Therapy Formulations: Used in combination therapy protocols, such as with luteinizing hormone-releasing hormone (LHRH) agonists, for advanced prostate cancer management.
- Biomedical Research: Serves as a critical tool compound in preclinical and clinical research studying androgen receptor pathways, hormone-dependent cancers, and endocrine disorders.
- Reference Standard: Utilized as a high-purity analytical reference standard in quality control laboratories for drug testing and method validation.
- Dermatological Applications: Investigated for use in treating androgen-dependent skin conditions such as hirsutism and acne.
Basic Information
| Product Name | Flutamide |
| CAS No. | 13311-84-7 |
| Molecular Formula | C11H11F3N2O3 |
| Molecular Weight | 276.21 g/mol |
| Synonyms | 2-Methyl-N-[4-nitro-3-(trifluoromethyl)phenyl]propanamide; 4'-Nitro-3'-trifluoromethylisobutyranilide; SCH 13521; Eulexin®; Flutamida; Flutamidum; Fugerel®; Niftolide |
| EINECS | 236-318-8 |
Quality Control
Our Flutamide is manufactured under strict quality management systems to ensure it meets the stringent requirements for pharmaceutical active ingredients. Each batch is subjected to comprehensive analytical testing, including identification, purity assay, and impurity profiling via HPLC, to confirm compliance with in-house specifications and relevant pharmacopeial guidelines. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and quality assurance for our global B2B clients.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Keep the container tightly sealed to protect from moisture.
Specification
| Item | Specification |
|---|---|
| Appearance | Yellowish crystalline powder |
| Identification (IR) | Conforms to structure |
| Identification (HPLC) | Retention time matches reference standard |
| Assay (HPLC) | ≥ 99.0% |
| Related Substances (HPLC) | Total impurities ≤ 1.0% Any single impurity ≤ 0.5% |
| Loss on Drying | ≤ 0.5% |
| Residue on Ignition | ≤ 0.1% |
| Heavy Metals | ≤ 20 ppm |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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