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4-Amino-2,6-Dihydroxy-5-Nitrosopyrimidine

    • Product Name 4-Amino-2,6-Dihydroxy-5-Nitrosopyrimidine
    • Alias 5-Nitrosoisocytosine
    • Einecs 242-646-8
    • 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
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    Specifications

    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 & Storage
    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.
    Application of 4-Amino-2,6-Dihydroxy-5-Nitrosopyrimidine

    Applications of 4-Amino-2,6-Dihydroxy-5-Nitrosopyrimidine in Industrial Manufacturing

    As 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 Analogues

    Innovators 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

    • ICH Q7 Good Manufacturing Practice for API
    • US FDA 21 CFR Part 211
    • European Pharmacopoeia (Ph. Eur.) monographs applicable to nucleoside analogues
    • WHO GMP for Active Pharmaceutical Ingredients

    Typical usage ratio

    • Generally 0.12–0.38 molar equivalents per final API batch, adjusted based on substitution pattern and target nucleoside derivative

    Downstream process integration

    • Input occurs post-initial sugar derivatization during base-coupling and N-nitrosation steps under controlled temperature and pH in confined reactors

    Final product types

    • Synthetic antiviral nucleoside APIs (e.g., Lamivudine, Emtricitabine precursors)
    • Late-stage intermediate compounds for custom medicinal chemistry pipelines

    2. Specialty Dye Component in Textile Reactive Dye Manufacturing

    The 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

    • OEKO-TEX® Standard 100 – textile dye eco-certification
    • REACH Regulation (EC) No 1907/2006 – Annex XVII restrictions on azo dyes
    • ZDHC (Zero Discharge of Hazardous Chemicals) MRSL
    • ISO 9001:2015 quality system in dye synthesis

    Typical usage ratio

    • 0.5–2.8% by weight of charge in the chromophore synthesis step; varies per molecular design for target color intensity and solubility profile

    Downstream process integration

    • Introduced during early stage diazotization and subsequent condensation with sulfonated aromatic compounds

    Final product types

    • Monofunctional and bifunctional reactive dyes for polyester/cotton blends
    • High-performance textile colorants for technical and sportswear fabrics

    3. Photographic Chemicals: Light-Sensitive Emulsion Stabilizers

    Manufacturers 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

    • ISO 5-2:1985 – Density measurements for photographic films
    • DIN 19604 – Photographic chemical quality criteria
    • RoHS (Restriction of Hazardous Substances) for industrial emulsions
    • Customer-specific internal QC protocols for imaging media

    Typical usage ratio

    • 0.03–0.11% w/w relative to total emulsion solids; precisely calculated to match batch silver content and intended contrast range

    Downstream process integration

    • Added to emulsion tanks following initial gelatin and halide mixing, before proceeding to controlled ripening and crystal morphology adjustment

    Final product types

    • Photographic films (color reversal, B&W, radiographic)
    • High-sensitivity photo papers and technical imaging plates

    4. Agricultural Chemical Synthesis: Key Intermediate for Novel Herbicidal Pyrimidines

    Pyrimidine-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

    • FAO/WHO Specification for Pesticides
    • ISO 9001:2015 (applied to agrochem manufacturing)
    • European Union Regulation (EC) No 1107/2009 – Plant Protection Product Authorization
    • US EPA 40 CFR for pesticide active ingredient production

    Typical usage ratio

    • 0.09–0.24 molar equivalents per batch, tailored according to targeted substitution and desired herbicidal activity spectrum

    Downstream process integration

    • Reacted post-enamine formation as a ring-modification agent, enabling further selective methylation or chlorination steps for advanced herbicidal scaffolds

    Final product types

    • Systemic herbicidal actives for cereal and legume crop protection
    • Granular and water-dispersible concentrate formulations for direct farm application

    5. Electrochemical Sensors: Electron Mediator Precursor for Amperometric Devices

    Producers 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

    • ISO 13485:2016 (medical device manufacturing)
    • European In Vitro Diagnostic Regulation (IVDR) 2017/746
    • IEC 60601-1 – Medical electrical equipment safety
    • FDA 21 CFR Part 820 (Quality System Regulation for device manufacturers)

    Typical usage ratio

    • Between 0.14% and 1.6% by total sensor mass, depending on intended electrode functionalization density and target redox potential

    Downstream process integration

    • Functionalization step following base electrode substrate coating; incorporated in situ polymerization or direct covalent attachment to working surface

    Final product types

    • Disposable amperometric glucose and lactate test strips
    • Reusable biosensor electrodes for food contamination analysis
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