Description

Triamcinolone is a potent synthetic glucocorticoid corticosteroid, widely recognized for its significant anti-inflammatory and immunosuppressive properties. This high-purity active pharmaceutical ingredient (API) is essential for formulating effective therapeutic solutions that require precise biological activity and consistent quality. It is primarily utilized by pharmaceutical manufacturers and research institutions in the development of topical creams, ointments, injectable suspensions, and other advanced medicinal products targeting dermatological, ophthalmic, and rheumatic conditions.

Application

• Pharmaceutical API: Core ingredient in the manufacture of topical corticosteroids for treating eczema, psoriasis, dermatitis, and other inflammatory skin disorders.
• Ophthalmic Preparations: Used in eye drops and ointments to manage inflammatory conditions of the eye, such as uveitis and allergic conjunctivitis.
• Injectable Formulations: Key component in intra-articular and intramuscular injections for the treatment of joint inflammation, bursitis, and severe allergic reactions.
• Veterinary Medicine: Employed in anti-inflammatory and anti-pruritic treatments for companion animals and livestock.
• Research & Development: Serves as a critical reference standard and biochemical tool in pharmacological studies and steroid receptor research.
• Compound Formulations: Used in combination with other APIs, such as antifungals or antibiotics, in compounded medications for enhanced therapeutic effect.

Basic Information

Product Name	Triamcinolone
CAS No.	124-94-7
Molecular Formula	C21H27FO6
Molecular Weight	394.44 g/mol
Synonyms	Triamcinolone; 9α-Fluoro-11β,16α,17,21-tetrahydroxypregna-1,4-diene-3,20-dione; 9α-Fluoro-16α-hydroxyprednisolone; Aristocort; Kenalog; Triamcinolone acetonide (related compound); Volon; Adcortyl; Fluoxyprednisolone; Triamcinolone base
EINECS	204-716-4

Quality Control

Our Triamcinolone is manufactured under strict quality management systems to ensure it meets the stringent requirements for pharmaceutical actives. Each batch is subjected to comprehensive analytical testing, including identification, purity assay, and impurity profiling, to confirm compliance with relevant pharmacopeial standards such as USP and EP. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and batch-to-batch consistency for our global B2B clients.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation. Ensure the storage area is well-ventilated and away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to standard
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water (KF Titration)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Specific Rotation	+65° to +72° (c=1 in dioxane)

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