Description

n-Methyl-3-(5-Nitrofuran-2-Yl)-n-Nitroso-1H-1,2,4-Triazol-5-Amine is a specialized heterocyclic compound featuring a unique molecular architecture combining nitrofuran and nitroso-triazole moieties. This structure makes it a valuable advanced pharmaceutical intermediate and a key building block in organic synthesis for research and development. It is primarily sought by pharmaceutical R&D laboratories and fine chemical manufacturers engaged in developing novel therapeutic agents and high-value chemical entities.

Application

• Pharmaceutical Intermediate: Serves as a critical precursor in the synthesis of novel drug candidates, particularly those targeting infectious diseases.
• Antimicrobial Agent Research: The nitrofuran moiety is historically associated with antimicrobial activity, making this compound a scaffold for developing new antibacterial and antiprotozoal agents.
• Chemical Biology Probe: Used in research to study biological pathways and enzyme interactions due to its reactive functional groups.
• Organic Synthesis Building Block: Employed in constructing complex heterocyclic systems for material science and agrochemical research.
• Reference Standard: Utilized in analytical laboratories as a high-purity standard for method development and quality control testing.

Basic Information

Item	Detail
Product Name	n-Methyl-3-(5-Nitrofuran-2-Yl)-n-Nitroso-1H-1,2,4-Triazol-5-Amine
CAS No.	41735-28-8
Molecular Formula	C8H7N7O4
Molecular Weight	265.18 g/mol
Synonyms	5-Amino-1-methyl-3-(5-nitro-2-furyl)-1H-1,2,4-triazole; 1-Methyl-3-(5-nitro-2-furyl)-1H-1,2,4-triazol-5-amine N-nitroso derivative; 1-Methyl-3-(5-nitro-2-furanyl)-N-nitroso-1H-1,2,4-triazol-5-amine; 5-Amino-1-methyl-3-(5-nitro-2-furyl)-1,2,4-triazole; N-Methyl-3-(5-nitrofuran-2-yl)-N-nitroso-1H-1,2,4-triazol-5-amine; 41735-28-8; 1H-1,2,4-Triazol-5-amine, N-methyl-3-(5-nitro-2-furanyl)-N-nitroso-
EINECS	Contact for details

Quality Control

Our n-Methyl-3-(5-Nitrofuran-2-Yl)-n-Nitroso-1H-1,2,4-Triazol-5-Amine is produced under strict quality management systems. Every batch undergoes comprehensive analytical testing including HPLC for purity, IR and NMR for structural confirmation, and residual solvent analysis to ensure it meets the stringent requirements for research and synthesis. A detailed Certificate of Analysis (COA) is provided with each shipment to guarantee traceability and compliance with your specifications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its light-sensitive nature and propensity for oxidation, it is recommended to handle under an inert atmosphere for long-term storage and to minimize exposure to air and moisture.

Specification

Item	Specification
Appearance	Yellow to orange crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 97.0%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.5%
Single Unknown Impurity (HPLC)	≤ 1.0%
Total Impurities (HPLC)	≤ 3.0%

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