Description

Naflocort is a synthetic corticosteroid compound with significant anti-inflammatory and immunosuppressive activity. This high-purity active pharmaceutical ingredient (API) is essential for the development and manufacturing of advanced topical and systemic pharmaceutical formulations. It is primarily utilized by pharmaceutical companies and research institutions focused on dermatology, allergy, and autoimmune therapies.

Application

• Pharmaceutical API: Core active ingredient in topical creams, ointments, and lotions for treating inflammatory skin conditions such as eczema, psoriasis, and dermatitis.
• Veterinary Medicine: Used in formulations for managing inflammation and allergic reactions in animals.
• Research & Development: Critical reference standard and building block in medicinal chemistry for developing new corticosteroid derivatives with optimized efficacy and safety profiles.
• Dermatological Preparations: Key component in compounded medications for specialized dermatological treatments.

Basic Information

Product Name	Naflocort
CAS No.	59497-39-1
Molecular Formula	C24H31FO6
Molecular Weight	434.50 g/mol
Synonyms	9α-Fluoro-11β,17α,21-trihydroxy-16α-methylpregna-1,4-diene-3,20-dione; 9α-Fluoro-16α-methylprednisolone; Flunisolide related compound; 16α-Methyl-9α-fluoroprednisolone; SQ-16360; Naflocort
EINECS	Contact for details

Quality Control

Our Naflocort is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. Certificates of Analysis (COA) detailing purity, identity, and impurity profiles are provided with every shipment.

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). Due to its hygroscopic nature, the container must be kept tightly sealed to prevent moisture absorption.

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%
Loss on Drying	≤ 1.0%
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.