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HS Code |
273770 |
| Name | 4-Amino-2,6-Dihydroxy-5-Nitrosopyrimidine |
| Chemical Formula | C4H4N4O3 |
| Molecular Weight | 156.10 g/mol |
| Cas Number | 36377-93-4 |
| Appearance | Pale yellow to light brown solid |
| Solubility | Soluble in water |
| Melting Point | Decomposes above 260°C |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Synonyms | 4-Amino-5-nitroso-2,6-pyrimidinediol |
| Structure Type | Pyrimidine derivative |
| Hazard Class | May cause skin and eye irritation |
| Stability | Stable under recommended storage conditions |
| Inchi | InChI=1S/C4H4N4O3/c5-1-2(9)7-4(11)8-3(1)6-10/h9,11H,5H2 |
As an accredited 4-Amino-2,6-Dihydroxy-5-Nitrosopyrimidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle containing 25 grams of 4-Amino-2,6-Dihydroxy-5-Nitrosopyrimidine, labeled with safety information and chemical identifiers. |
| Shipping | 4-Amino-2,6-Dihydroxy-5-Nitrosopyrimidine is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Packaging complies with relevant chemical transport regulations. Labeling includes hazard identification according to GHS. Ensure prompt delivery via reliable couriers, maintaining ambient temperatures. Material Safety Data Sheet (MSDS) accompanies each shipment for safe handling and storage information. |
| Storage | 4-Amino-2,6-Dihydroxy-5-Nitrosopyrimidine should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers. Store at room temperature and clearly label the container. Use appropriate personal protective equipment when handling and consult the compound’s safety data sheet (SDS) for detailed guidance. |
Applications of 4-Amino-2,6-Dihydroxy-5-Nitrosopyrimidine in Industrial ManufacturingAs a direct manufacturer of 4-Amino-2,6-Dihydroxy-5-Nitrosopyrimidine, we supply this pyrimidine-based intermediate to specialized sectors that demand precise molecular functions for efficient downstream synthesis. Below outlines several distinctive and fully proven industrial application scenarios enabled by this raw material, with each use-case reflecting real manufacturing standards, input ratios, process steps, and corresponding output products. 1. Pharmaceutical API Synthesis: Antiviral Nucleoside AnaloguesInnovators in antiviral research utilize this pyrimidine derivative for constructing nucleoside analogue APIs, where its unique functional groups streamline the formation of structurally specific bases. Molecular specificity in this compound reduces by-product formation during N-alkylation and ring substitution, supporting stringent compliance in regulated synthesis of active pharmaceutical ingredients for viral hepatitis and HIV treatments. Industry compliance standards
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2. Specialty Dye Component in Textile Reactive Dye ManufacturingThe nitroso and amino functionalities of this compound play a critical role as a core intermediate for reactive dye molecule assembly. Superior chromophore stability and reproducibility can be traced to the presence of the pyrimidine ring, which underpins consistent quality in color-fast textile dyes formulated for synthetic fiber applications in regulated export markets. Industry compliance standards
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3. Photographic Chemicals: Light-Sensitive Emulsion StabilizersManufacturers of high-purity light-sensitive emulsions incorporate this pyrimidine compound as a stabilizer for silver halide crystals in color reversal and high-contrast black-and-white films. Its strong chelating behavior assists with controlled reduction kinetics, supporting batch-to-batch reproducibility and minimizing fog under defined light exposure cycles demanded by photographic industry QC. Industry compliance standards
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4. Agricultural Chemical Synthesis: Key Intermediate for Novel Herbicidal PyrimidinesPyrimidine-based herbicide manufacturers utilize this intermediate for its ability to introduce tailored nitrogen-oxygen moieties, critical for structure-activity relationships targeting difficult weed species. The material’s reactivity profile directly affects downstream yield and selectivity in the synthesis of selective, low-application-rate agrochemicals, where regulatory compliance and traceability are mandatory. Industry compliance standards
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5. Electrochemical Sensors: Electron Mediator Precursor for Amperometric DevicesProducers of high-sensitivity electrochemical sensors leverage this compound as a building block for pyrimidine-derived redox mediators. The specific structure ensures reproducible electron transfer kinetics when functionalized onto working electrode surfaces or immobilized within membrane matrices, vital for analytical devices requiring narrow detection thresholds under food safety and biomedical QC testing. Industry compliance standards
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