Description

Nifurpirinol is a synthetic nitrofuran derivative with potent antibacterial and antiprotozoal properties. This compound is valued for its efficacy against a broad spectrum of pathogens, making it a critical active pharmaceutical ingredient (API) in specific therapeutic areas. It is primarily utilized by manufacturers in the veterinary pharmaceutical and aquaculture industries for the formulation of medicated treatments.

Application

• Veterinary Pharmaceuticals: Key ingredient in topical and systemic formulations for treating bacterial infections in livestock and companion animals.
• Aquaculture Therapeutics: Used in medicated feeds and baths to control bacterial diseases in farmed fish and shellfish.
• Antiprotozoal Agent: Employed in research and development for compounds targeting protozoan parasites.
• Antimicrobial Research: Serves as a reference standard and building block in microbiological and pharmacological research.
• API Intermediate: Acts as a crucial synthetic intermediate in the production of more complex nitrofuran-based pharmaceuticals.

Basic Information

Product Name	Nifurpirinol
CAS No.	13411-16-0
Molecular Formula	C13H12N4O4
Molecular Weight	288.26 g/mol
Synonyms	Furanace; P-7138; 1-[(5-Nitro-2-furanyl)methylene]amino]-2,4-imidazolidinedione; 1-[(5-Nitrofurfurylidene)amino]hydantoin; 1-[(5-Nitro-2-furyl)methyleneamino]imidazolidine-2,4-dione; Nifurpirinolum; 1-(5-Nitro-2-furfurylideneamino)hydantoin
EINECS	Contact for details

Quality Control

Our Nifurpirinol is manufactured under strict quality management systems. Every batch undergoes comprehensive analytical testing to ensure identity, purity, and potency meet stringent specifications. A Certificate of Analysis (COA) detailing results for assay, related substances, residual solvents, and other critical parameters is provided with each 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 controlled room temperature (15-25°C). Keep away from heat and incompatible materials.

Specification

Item	Specification
Appearance	Yellow to orange crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
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.