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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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