Description

Deprodone is a synthetic corticosteroid with potent anti-inflammatory and immunosuppressive properties. This high-purity active pharmaceutical ingredient (API) is critical for developing targeted dermatological and ophthalmic treatments. It is primarily utilized by pharmaceutical manufacturers and research institutions in the development of topical creams, ointments, and eye drops for managing inflammatory skin conditions and ocular inflammation.

Application

• Pharmaceutical API: Core active ingredient in topical corticosteroid formulations for eczema, psoriasis, and dermatitis.
• Dermatological Preparations: Manufacture of anti-inflammatory creams, ointments, and lotions.
• Ophthalmic Solutions: Used in eye drops and suspensions to treat uveitis, conjunctivitis, and post-operative ocular inflammation.
• Veterinary Medicine: Component in topical treatments for inflammatory skin conditions in animals.
• Research & Development: Reference standard and building block in steroid chemistry and pharmacological research.
• Combination Therapies: Used in fixed-dose combination products with antimicrobial agents.

Basic Information

Item	Detail
Product Name	Deprodone
CAS No.	6795-60-4
Molecular Formula	C₂₄H₃₃FO₅
Molecular Weight	420.52 g/mol
Synonyms	Deprodone; 9α-Fluoro-11β,17α,21-trihydroxy-16β-methylpregna-1,4-diene-3,20-dione; 9α-Fluoro-16β-methylprednisolone; Desoximetasone Impurity C; Desoximetasone Related Compound C; (11β,16β)-9-Fluoro-11,17,21-trihydroxy-16-methylpregna-1,4-diene-3,20-dione; Fluocortin Butyl Impurity D
EINECS	Contact for details

Quality Control

Our Deprodone is manufactured under cGMP conditions and undergoes rigorous analytical testing to ensure it meets stringent pharmaceutical-grade specifications. Each batch is supported by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. We adhere to relevant ICH guidelines for stability and validation.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation.

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%
Residue on Ignition	≤ 0.1%
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 1.5%
Heavy Metals	≤ 20 ppm

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