Description

Levofuraltadone is a synthetic nitrofuran derivative with potent antibacterial and antiprotozoal activity. This compound is valued for its efficacy against a broad spectrum of Gram-positive and Gram-negative bacteria, making it a critical intermediate in specific therapeutic applications. It is primarily utilized by the pharmaceutical industry for research and development, as well as in the synthesis of veterinary medicinal products.

Application

• Pharmaceutical Intermediate: Serves as a key building block in the synthesis of advanced antibacterial and antiprotozoal APIs (Active Pharmaceutical Ingredients).
• Veterinary Medicine: Used in the development of treatments for bacterial infections in livestock and poultry.
• Antimicrobial Research: A valuable reference standard and tool compound in microbiological and pharmacological research to study nitrofuran mechanisms.
• Chemical Synthesis: Employed in organic synthesis for the preparation of more complex nitrofuran-based molecules with targeted biological activity.

Basic Information

Product Name	Levofuraltadone
CAS No.	3795-88-8
Molecular Formula	C13H16N4O6
Molecular Weight	324.29 g/mol
Synonyms	(S)-Furaltadone; L-Furaltadone; Levofuraltadon; (5S)-3-[[(5-Nitro-2-furanyl)methylene]amino]-5-morpholinomethyl-2-oxazolidinone; (S)-5-Morpholinomethyl-3-[(5-nitrofurfurylidene)amino]-2-oxazolidinone; 5-Morpholinomethyl-3-[(5-nitrofurfurylidene)amino]-2-oxazolidinone (S)-; (S)-5-Morpholinomethyl-3-[(5-nitrofurfurylidene)amino]-2-oxazolidinone
EINECS	223-272-5

Quality Control

Our Levofuraltadone is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation (IR, NMR), to ensure it meets exacting standards for research and synthesis. A detailed Certificate of Analysis (COA) is provided with every shipment to guarantee traceability and batch-to-batch consistency.

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 incompatible materials.

Specification

Item	Specification
Appearance	Yellow to orange-yellow crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

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