Description

Flurandrenolone Acetate is a synthetic corticosteroid derivative with potent anti-inflammatory and immunosuppressive properties. This high-purity active pharmaceutical ingredient (API) is critical for the development and manufacturing of specialized topical and systemic pharmaceutical formulations. It is primarily utilized by pharmaceutical R&D laboratories and manufacturers requiring a reliable, high-quality raw material for advanced therapeutic applications.

Application

• Pharmaceutical API: Serves as a key active ingredient in the synthesis of corticosteroid medications.
• Topical Dermatological Preparations: Used in creams, ointments, and lotions for treating inflammatory skin conditions such as eczema, psoriasis, and dermatitis.
• Research & Development: A vital compound for pharmacological studies, mechanism of action research, and the development of new anti-inflammatory drugs.
• Veterinary Medicine: Employed in formulations for treating inflammatory disorders in animals.
• Reference Standard: Used as a certified reference material (CRM) in analytical laboratories for quality control and method validation.

Basic Information

Product Name	Flurandrenolone Acetate
CAS No.	2802-11-1
Molecular Formula	C₂₄H₃₁FO₆
Molecular Weight	434.50 g/mol
Synonyms	Fludroxycortide; Flurandrenolide Acetate; 6α-Fluoro-11β,16α,17,21-tetrahydroxypregn-4-ene-3,20-dione 16,17-acetonide 21-acetate; 6α-Fluoro-16α-hydroxyprednisolone 16,17-acetonide 21-acetate; Drenison; Haelan; Cordran; (6α,11β,16α)-6,9-Difluoro-11,16,17,21-tetrahydroxypregna-1,4-diene-3,20-dione cyclic 16,17-acetal with acetone 21-acetate
EINECS	220-548-7

Quality Control

Our Flurandrenolone Acetate is manufactured under strict quality management systems. Each batch is subjected to comprehensive analytical testing, including HPLC for purity, identification by IR and NMR spectroscopy, and tests for residual solvents and related substances, to ensure it meets stringent pharmaceutical-grade specifications. Certificates of Analysis (COA) documenting full compliance are provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). The product is light-sensitive and should be handled and stored accordingly to maintain stability and potency.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 1.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%; Any single impurity ≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Heavy Metals	≤ 20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.