Description

Nifuratel is a synthetic nitrofuran derivative with potent antimicrobial and antiprotozoal properties. This compound is valued for its broad-spectrum efficacy against a range of pathogens, including fungi, bacteria, and protozoa. It is a critical active pharmaceutical ingredient (API) primarily required by pharmaceutical manufacturers for the formulation of gynecological and urological treatments.

Application

• Primary API in the manufacture of antifungal and antibacterial medications.
• Key ingredient in topical creams, ointments, and vaginal suppositories for treating gynecological infections such as vulvovaginal candidiasis and bacterial vaginosis.
• Used in formulations for treating urogenital trichomoniasis and other protozoal infections.
• Component in combination therapies for complex genitourinary tract infections.
• Subject of research for potential applications in other antimicrobial indications.
• Used by fine chemical suppliers for further synthesis and distribution to the pharmaceutical industry.

Basic Information

Item	Detail
Product Name	Nifuratel
CAS No.	4936-47-4
Molecular Formula	C10H11N3O5S
Molecular Weight	285.28 g/mol
Synonyms	5-(Methylthio)-3-[(5-nitrofurfurylidene)amino]-2-oxazolidinone; 3-[(5-Nitrofurfurylidene)amino]-5-(methylthio)-2-oxazolidinone; Macmiror; Methylmercadone; Nifuratelum; Polmiror; Magnilor
EINECS	225-580-9

Quality Control

Our Nifuratel is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical use. A detailed Certificate of Analysis (COA) confirming identity, purity, and impurity profiles is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its light-sensitive and easily oxidized nature, it is recommended to store the product under an inert atmosphere for long-term stability. Keep away from strong oxidizing agents.

Specification

Item	Specification
Appearance	Yellow to orange-yellow 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)
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%
Related Substances (HPLC)	Total impurities ≤ 1.0% Any individual impurity ≤ 0.5%
Heavy Metals	≤ 20 ppm

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