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HS Code |
926924 |
| Productname | 2,4-Diamino-6-Hydroxy-5-Nitrosopyrimidine |
| Iupacname | 2,4-diamino-6-oxo-5-nitrosopyrimidine |
| Molecularformula | C4H5N5O2 |
| Molecularweight | 155.12 g/mol |
| Casnumber | 51917-12-9 |
| Appearance | Yellow to orange crystalline powder |
| Solubility | Slightly soluble in water |
| Meltingpoint | 263-265 °C (decomposition) |
| Synonyms | 2,4-diamino-5-nitroso-6-hydroxypyrimidine |
| Pubchemcid | 11756466 |
| Smiles | C1=NC(=O)C(=C(N1N=O)N)N |
| Inchikey | IXOOVGJXSBKHJY-UHFFFAOYSA-N |
As an accredited 2,4-Diamino-6-Hydroxy-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 2,4-Diamino-6-Hydroxy-5-Nitrosopyrimidine, labeled with safety data and batch information. |
| Shipping | 2,4-Diamino-6-hydroxy-5-nitrosopyrimidine should be shipped in tightly sealed containers, protected from moisture and light. Transport according to local, national, and international regulations for chemical safety. Ensure labeling complies with hazard communication standards. Use secondary containment to prevent leaks, and handle with appropriate personal protective equipment (PPE). Store in a cool, dry place. |
| Storage | **2,4-Diamino-6-hydroxy-5-nitrosopyrimidine** should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers and acids. Store at a cool, dry, and well-ventilated location. Ensure the storage area is secure, labeled, and complies with local chemical safety regulations. Avoid exposure to heat or sources of ignition. |
Applications of 2,4-Diamino-6-Hydroxy-5-Nitrosopyrimidine in Industrial Manufacturing2,4-Diamino-6-Hydroxy-5-Nitrosopyrimidine is an intermediate widely employed by specialty manufacturers in select regulated downstream sectors. Its molecular structure brings targeted reactivity for high-value syntheses. Below are application scenarios reflecting actual current industrial usage, addressed from a producer’s perspective to support formulation, technical detailing, and compliance in each field. 1. Synthesis of Reactive Dyes for Wool and Polyamide FibersDyestuff manufacturers incorporate this pyrimidine derivative to supply amino and nitroso functionalities in defining the chromophore segment of azo and anthraquinone structures. The reagent enters the diazotization or coupling stage to produce customized reactive dye molecules with strong fixation capacity and robust wash-fastness on protein-based and polyamide substrates. Controlled addition ratios and rigorous process parameters maintain color specification and chemical purity as demanded by downstream textile finishing experts. Industry compliance standards
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2. Pharmaceutical Synthesis: Production of Antiviral Pyrimidine DerivativesActive pharmaceutical ingredient (API) processors deploy 2,4-diamino-6-hydroxy-5-nitrosopyrimidine as a precursor for developing antiviral compounds targeting nucleic acid analogues. This intermediate participates in nucleophilic substitution and selective amination protocols, supporting GMP-compliant synthesis of regulatory dossier-backed APIs. QC protocols monitor impurity profiles at each reaction stage, and all systems operate under strict pharmaceutical documentation and traceability controls. Industry compliance standards
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3. High-Performance Polymer Additive ManufacturingCompounders for engineering plastics may utilize this substituted pyrimidine as a high-efficiency polymerization modifier, conferring improved thermal stability and chain branching in specialized polyamides or polyimides. In melt-phase or solvent-aided synthesis, QC teams strictly control addition points and temperatures to prevent side reactions while supporting required resin molecular weights and performance certifications for end-users in automotive and electronics. Industry compliance standards
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4. Intermediate for Agrochemical Synthesis: Herbicide and Fungicide Active CompoundsAgrochemical formulators turn to this pyrimidine molecule as a customizable scaffold for active ingredient development in selective herbicides and systemic fungicides. Its electron-rich and nucleophilic sites lend themselves to substitution and alkylation reactions generating target-specific actives for modern crop management. All handling and residue control follow international food safety and chemical traceability protocols. Industry compliance standards
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