Description

Sulconazle Nitrate is a synthetic organic compound belonging to the azole class, widely recognized for its potent antifungal properties. This high-purity active pharmaceutical ingredient (API) is critical for ensuring the efficacy and safety of antifungal formulations. It is primarily utilized by pharmaceutical manufacturers and research institutions in the development and production of topical and systemic antifungal medications.

Application

• Pharmaceutical API: Core active ingredient in the manufacture of antifungal creams, ointments, and oral formulations.
• Veterinary Medicine: Used in antifungal treatments for livestock, poultry, and companion animals.
• Agricultural Fungicide: Intermediate or active component in crop protection agents to combat fungal plant diseases.
• Research & Development: Standard reference material for biochemical studies, antifungal mechanism research, and new drug discovery.
• Personal Care Products: Incorporated into specialized antifungal soaps, shampoos, and medicated powders.

Basic Information

Product Name	Sulconazle Nitrate
CAS No.	82382-23-8
Molecular Formula	C18H15Cl3N2O3S
Molecular Weight	461.75 g/mol
Synonyms	Sulconazole Nitrate; 1-[2,4-Dichloro-β-[(4-chlorobenzyl)thio]phenethyl]imidazole Nitrate; Sulconazole Mononitrate; RS-44872; RS-44872-00-10-3; Exelderm (brand/trade name); Myk (brand/trade name)
EINECS	Contact for details

Quality Control

Our Sulconazle 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. A detailed Certificate of Analysis (COA), including results for assay, related substances, and residual solvents, is provided with every shipment to guarantee traceability and compliance.

Storage

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

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% - 102.0% (on anhydrous basis)
Related Substances (HPLC)	Total impurities ≤ 2.0%
Loss on Drying	≤ 0.5%
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.