Description

Levomecol is a high-purity pharmaceutical compound, recognized for its critical role in advanced therapeutic formulations. This active pharmaceutical ingredient (API) is essential for ensuring product efficacy and batch-to-batch consistency in regulated manufacturing. It is primarily utilized by pharmaceutical companies and research institutions engaged in the development and production of specialized medications.

Application

• Pharmaceutical API: Serves as the active ingredient in the formulation of prescription medications.
• Topical Preparations: Used in the development of creams, ointments, and gels for dermatological applications.
• Wound Care Products: A key component in advanced formulations designed for infection control and tissue repair.
• Veterinary Pharmaceuticals: Incorporated into medicinal products for animal health.
• Clinical Research: Employed as a reference standard or raw material in pharmacological and toxicological studies.
• Generic Drug Manufacturing: Used in the production of bioequivalent generic pharmaceutical products.

Basic Information

Product Name	Levomecol
CAS No.	118573-58-3
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Levomecol; Levomecolum; (8S,9R,10S,11S,13S,14S,16R,17R)-9-Fluoro-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-3-one; 9α-Fluoro-11β,17α,21-trihydroxy-16β-methylpregna-1,4-diene-3,20-dione 21-acetate; A related corticosteroid acetate.
EINECS	Contact for details

Quality Control

Our Levomecol is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets stringent specifications for identity, purity, and potency. A Certificate of Analysis (COA) documenting results against relevant pharmacopeial standards (such as USP/EP) is provided with every shipment to guarantee regulatory compliance and supply chain integrity.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (typically 15-25°C). Keep the container tightly sealed to protect from moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to standard
Assay (HPLC)	98.0% - 102.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Single Unknown Impurity	≤ 0.5%
Residual Solvents (GC)	Complies with ICH guidelines
Loss on Drying	≤ 1.0%
Heavy Metals	≤ 20 ppm

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