Description

Eberconazole Nitrate is a synthetic antifungal agent belonging to the azole class, valued for its potent activity against a broad spectrum of pathogenic fungi. Its primary commercial significance lies in its use as the active pharmaceutical ingredient (API) in topical formulations for treating dermatological infections. This compound is essential for manufacturers in the pharmaceutical and personal care industries developing antifungal creams, ointments, and solutions. Eberconazole Nitrate CAS NO 130104-32-4 offers a reliable therapeutic option for conditions like athlete's foot, ringworm, and cutaneous candidiasis.

Application

• Pharmaceutical API: Primary use as the active ingredient in topical antifungal medications for human use.
• Dermatological Creams & Ointments: Formulated into over-the-counter (OTC) and prescription treatments for superficial fungal skin infections.
• Antifungal Powders & Sprays: Used in medicated powders and sprays designed for foot care and hygiene.
• Veterinary Pharmaceuticals: Incorporated into topical treatments for fungal infections in animals.
• Cosmecutical Products: Potential use in dandruff-control shampoos and other personal care items targeting fungal-related issues.
• Research & Development: Serves as a reference standard and key intermediate in antifungal drug discovery and development programs.

Basic Information

Product Name	Eberconazole Nitrate
CAS No.	130104-32-4
Molecular Formula	C18H15Cl3N2O3
Molecular Weight	413.68 g/mol
Synonyms	Eberconazole Nitrate; Eberconazol Nitrate; 1-(2,4-Dichloro-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)-1H-imidazole Nitrate; Eberconazole Mononitrate; Piconazole Nitrate (obsolete); Eberconazol [Spanish]; Eberconazolum [Latin]; ZP 1694; CAS 130104-32-4
EINECS	Contact for details

Quality Control

Our Eberconazole Nitrate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. Specifications typically align with pharmacopeial guidelines, and a detailed Certificate of Analysis (COA) documenting identity, purity, and impurity profiles is provided with every shipment to ensure full traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed to prevent absorption of atmospheric moisture, which can affect stability and handling properties.

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% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Microbial Limits	Meets Ph. Eur./USP criteria

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