Description

Paramethasone Acetate (200 Mg) is a synthetic glucocorticoid corticosteroid, widely recognized for its potent anti-inflammatory and immunosuppressive properties. This high-purity active pharmaceutical ingredient (API) is critical for ensuring the efficacy and safety of advanced pharmaceutical formulations. It is primarily utilized by pharmaceutical manufacturers and research institutions in the development and production of specialized injectable and topical medications for treating severe inflammatory and autoimmune conditions.

Application

• Pharmaceutical API: Core active ingredient in the manufacture of injectable corticosteroid formulations.
• Anti-inflammatory Medications: Used in drugs targeting severe inflammatory disorders such as rheumatoid arthritis and lupus.
• Immunosuppressive Therapy: Key component in therapies designed to manage autoimmune diseases and prevent organ transplant rejection.
• Dermatological Preparations: Incorporated into high-potency creams and ointments for treating severe skin conditions like psoriasis and eczema.
• Ophthalmic Solutions: Used in specialized eye drops to treat inflammatory eye conditions.
• Veterinary Pharmaceuticals: Applied in anti-inflammatory treatments for companion and livestock animals.
• Biomedical Research: Serves as a reference standard and key reagent in pharmacological and endocrinological research studies.

Basic Information

Product Name	Paramethasone Acetate (200 Mg)
CAS No.	1597-82-6
Molecular Formula	C₂₄H₃₁FO₆
Molecular Weight	434.50 g/mol
Synonyms	Paramethasone 21-Acetate; 6α-Fluoro-11β,17α,21-trihydroxy-16α-methylpregna-1,4-diene-3,20-dione 21-acetate; 1-Dehydro-6α-fluoro-16α-methylhydrocortisone 21-acetate; Haldrate; Monocortin; Dilar; (11β,16α)-21-(Acetyloxy)-6-fluoro-11,17-dihydroxy-16-methylpregna-1,4-diene-3,20-dione
EINECS	Contact for details

Quality Control

Our Paramethasone Acetate is manufactured under strict quality management systems, targeting purity levels suitable for pharmaceutical applications. Each batch undergoes comprehensive analytical testing, including identification, assay, and impurity profiling via HPLC and other pharmacopeial methods. Certificates of Analysis (COA) detailing all test results are provided to ensure full traceability and compliance with cGMP and relevant ICH guidelines.

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. For long-term storage, consider desiccated conditions.

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% 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.