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2,4-Diamino-6-Hydroxy-5-Nitrosopyrimidine

    • Product Name 2,4-Diamino-6-Hydroxy-5-Nitrosopyrimidine
    • Alias 6-Hydroxy-2,4-diamino-5-nitrosopyrimidine
    • Einecs 207-433-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of 2,4-Diamino-6-Hydroxy-5-Nitrosopyrimidine

    Applications of 2,4-Diamino-6-Hydroxy-5-Nitrosopyrimidine in Industrial Manufacturing

    2,4-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 Fibers

    Dyestuff 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

    • Oeko-Tex Standard 100 (Class I-IV as applicable)
    • REACH Annex XVII restricted substances
    • ZDHC MRSL compliance (Zero Discharge of Hazardous Chemicals)
    • ISO 9001:2015 for dye production quality control

    Typical usage ratio

    • 2.5%–6% by weight in chromophore-forming stages, fine-tuned per shade intensity and substrate absorption profile. Optimized via pilot batch testing.

    Downstream process integration

    • Feeds into azo-coupling or anthraquinone synthesis vessels after diazotization, preceding filtration and spray-drying to produce powder pigment standards for textile customers.

    Final product types

    • Powdered reactive dyes (various CI Reactive classifications)
    • Liquid dye concentrates for yarn and piece dyeing
    • Textile auxiliaries for protein fiber treatment
    • Colorant masterbatches for synthetic fiber spinning

    2. Pharmaceutical Synthesis: Production of Antiviral Pyrimidine Derivatives

    Active 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

    • ICH Q7 Good Manufacturing Practices for APIs
    • European Pharmacopoeia (Ph. Eur.) monographs
    • United States Pharmacopoeia (USP) for pyrimidine derivatives
    • FDA 21 CFR Part 211

    Typical usage ratio

    • 0.8–2.0 molar equivalents relative to key ring closure reagents; amount adjusted for yield maximization and impurity control based on route selectivity.

    Downstream process integration

    • Introduced as a major building block during heterocycle formation in multi-step synthesis, directly upstream of final purification, crystallization, and API isolation under cGMP control.

    Final product types

    • Antiviral bulk APIs (e.g., nucleoside analogues)
    • Research-grade reference standards for regulated laboratories
    • Preclinical intermediate compounds for pharma R&D
    • Finished dosage form precursors (pending further formulation)

    3. High-Performance Polymer Additive Manufacturing

    Compounders 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

    • UL 94 Vertical Burning Test for polymers
    • ISO 9001:2015 Quality Management System (polymer manufacturing)
    • EU RoHS Directive 2011/65/EU
    • GADSL (Global Automotive Declarable Substance List)

    Typical usage ratio

    • 0.1–1.2 wt% as a chain branching or stabilization co-monomer, optimized via end-use property specification and extrusion trial runs.

    Downstream process integration

    • Added directly to the polymerization reactor during pre-polymer or melt-stage reactions, followed by extrusion and pelletizing before compounding with fillers and modifiers.

    Final product types

    • Engineering polymer resin pellets for injection molding
    • Thermally stable polyimide sheets and films
    • Masterbatches for automotive components
    • High-performance wire insulation compounds

    4. Intermediate for Agrochemical Synthesis: Herbicide and Fungicide Active Compounds

    Agrochemical 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

    • FAO/WHO JMPR Pesticide Specifications and Evaluations
    • ISO 17025:2017 for analytical controls
    • EU Regulation 1107/2009 on plant protection products
    • China GB 2763 Maximum Residue Limits

    Typical usage ratio

    • 1.2–4.0 molar equivalents, depending on the structural complexity of final active; ratios optimized to balance conversion and downstream purification overheads during scale-up.

    Downstream process integration

    • Employed as a core intermediate in multi-stage synthesis, before halogenation or alkyl group introduction; product then proceeds to technical concentrate formulation for field application testing.

    Final product types

    • Herbicide technical powders (e.g., pyrimidinylcarboxylic acids derivatives)
    • Fungicide actives (e.g., substituted pyrimidine molecules)
    • Water-dispersible granules for field blending
    • Emulsifiable concentrates for foliar spraying
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