Description

Triamcinolone Furetonide is a synthetic corticosteroid derivative with potent anti-inflammatory and immunosuppressive properties. This compound is a critical intermediate in the synthesis of advanced topical and injectable pharmaceutical formulations. It is primarily utilized by pharmaceutical R&D laboratories and manufacturers specializing in dermatological and anti-inflammatory medications. The high-purity grade ensures consistency and reliability for sensitive production processes.

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of potent corticosteroid APIs (Active Pharmaceutical Ingredients).
• Dermatological Research: Used in the development of novel creams, ointments, and lotions for treating eczema, psoriasis, and dermatitis.
• Anti-inflammatory Drug Development: Serves as a precursor for investigational drugs targeting chronic inflammatory conditions.
• Veterinary Medicine: Employed in the formulation of anti-inflammatory treatments for animals.
• Reference Standard: Used as an analytical standard in quality control laboratories for HPLC and LC-MS methods.
• Academic & Contract Research: Utilized in university and CRO settings for pharmacological and metabolic studies.

Basic Information

Product Name	Triamcinolone Furetonide
CAS No.	4989-94-0
Molecular Formula	C₂₄H₃₁FO₆
Molecular Weight	434.50 g/mol
Synonyms	9α-Fluoro-11β,16α,17α,21-tetrahydroxypregna-1,4-diene-3,20-dione cyclic 16,17-acetal with acetone; Fluoro Triamcinolone Acetonide; Triamcinolone-16,17-acetonide; SQ-15101; NSC-92339; Kenalog (related derivative); Aristocort (related derivative)
EINECS	225-658-5

Quality Control

Our Triamcinolone Furetonide is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical R&D and intermediate use. We provide detailed Certificates of Analysis (COA) with each shipment, which include data for identity, purity, and related substances. Our quality commitment aligns with cGMP principles for active pharmaceutical ingredients (APIs) and intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed in a dry environment to prevent degradation. For long-term storage, consider using desiccants.

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 ≤ 0.5%
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.