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Fluticasone Furoate CAS NO 397864-44-7
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CAS No.:397864-44-7
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Fluticasone Furoate is a synthetic corticosteroid of the glucocorticoid class, widely recognized for its potent anti-inflammatory and immunosuppressive properties. This high-purity active pharmaceutical ingredient (API) is critical for the development of advanced therapeutic formulations targeting chronic inflammatory conditions. It is essential for pharmaceutical manufacturers and R&D facilities focused on respiratory and dermatological treatments, where consistent quality and reliable supply are paramount for product efficacy and regulatory compliance.
Application
- Pharmaceutical API: Primary active ingredient in prescription medications for asthma and chronic obstructive pulmonary disease (COPD).
- Nasal Spray Formulations: Key component in treatments for allergic and non-allergic rhinitis.
- Topical Dermatological Preparations: Used in creams and ointments for managing inflammatory skin conditions such as eczema and psoriasis.
- Drug Delivery System Research: Investigated in advanced delivery mechanisms, including dry powder inhalers (DPIs) and nano-formulations.
- Reference Standard: Serves as a high-purity analytical standard for quality control and regulatory testing in laboratories.
- Veterinary Pharmaceuticals: Applied in anti-inflammatory treatments for companion animals.
Basic Information
| Product Name | Fluticasone Furoate |
| CAS No. | 397864-44-7 |
| Molecular Formula | C27H29F3O6S |
| Molecular Weight | 538.58 g/mol |
| Synonyms | Fluticasone 17-Furoate; GW685698; (6α,11β,16α,17α)-6,9-Difluoro-17-{[(fluoromethyl)sulfonyl]carbonyl}-11-hydroxy-16-methyl-3-oxoandrosta-1,4-dien-17-yl 2-furoate; Flutiform (component); Avamys/Veramyst (component); Fluticasone Furoate USP; Fluticasone Furoate EP |
| EINECS | Contact for details |
Quality Control
Our Fluticasone Furoate is manufactured under strict quality management systems, targeting compliance with USP, EP, and ICH Q7 guidelines for active pharmaceutical ingredients. Each batch undergoes comprehensive analytical testing, including identification, assay, and impurity profiling via HPLC, to ensure it meets stringent purity specifications. A Certificate of Analysis (COA) documenting all test results is provided with every shipment to guarantee traceability and support your regulatory submissions.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation. For long-term storage, consider using desiccants.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white powder |
| Identification (IR) | Conforms to reference standard |
| Identification (HPLC) | Conforms to reference standard |
| Assay (HPLC) | 98.0% - 102.0% |
| Related Substances (HPLC) | Total impurities ≤ 1.0% Any single impurity ≤ 0.5% |
| Residual Solvents (GC) | Complies with ICH Q3C |
| Loss on Drying | ≤ 1.0% |
| 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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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
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