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Fluocortin CAS NO 33124-50-4


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CAS No.:33124-50-4

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Fluocortin is a synthetic corticosteroid derivative with potent anti-inflammatory and immunosuppressive properties. This compound is a critical intermediate in the synthesis of advanced topical pharmaceutical formulations designed to treat dermatological conditions. It is primarily utilized by pharmaceutical manufacturers and research institutions engaged in the development of new therapeutic agents. Our supply of Fluocortin CAS NO 33124-50-4 ensures high purity and consistent quality for demanding production and research applications.

Application

  • Pharmaceutical Intermediate: Key starting material or intermediate in the synthesis of potent topical corticosteroids.
  • Anti-inflammatory Drug Research: Used in preclinical and clinical research to develop new treatments for skin inflammation, eczema, and psoriasis.
  • Active Pharmaceutical Ingredient (API) Manufacturing: Serves as a core building block in the production of finished dosage forms like creams and ointments.
  • Biochemical Research: A tool compound for studying glucocorticoid receptor activity and signal transduction pathways.
  • Veterinary Medicine: Potential application in developing anti-inflammatory treatments for animals.
  • Reference Standard: Used as a high-purity standard in analytical laboratories for quality control and method validation.

Basic Information

Product Name Fluocortin
CAS No. 33124-50-4
Molecular Formula C₂₄H₃₁FO₆
Molecular Weight 434.50 g/mol
Synonyms Fluocortin; Fluocortin Butyl; 6α-Fluoro-11β,21-dihydroxy-16α-methylpregna-1,4-diene-3,20-dione 21-acetate; 6α-Fluoro-11β,21-dihydroxy-16α-methylpregna-1,4-diene-3,20-dione 21-acetate; Fluocortin Butylester; SH K 203; SHK-203; Fluocortine
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Quality Control

Our Fluocortin is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, residual solvent analysis, and identification by IR and NMR spectroscopy, to ensure it meets stringent specifications for pharmaceutical intermediates. Certificates of Analysis (COA) documenting full compliance are available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Keep the container tightly sealed in a dry environment to maintain stability.

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%
Related Substances (HPLC) Total impurities ≤2.0%
Single Unknown Impurity ≤0.5%
Residual Solvents (GC) Complies with ICH guidelines
Loss on Drying ≤0.5%

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

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Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.