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

    • Product Name 2-Amino-4,6-Dihydroxy-5-Nitropyrimidine
    • Alias 5-Nitroisocytosine
    • Einecs 237-015-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    986989

    Cas Number 940-54-9
    Molecular Formula C4H4N4O4
    Molecular Weight 172.10 g/mol
    Appearance Yellow to orange crystalline powder
    Melting Point Above 300°C (decomposes)
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Chemical Class Nitropyrimidine derivative
    Synonyms 2-Amino-5-nitro-4,6-pyrimidinediol
    Smiles Nc1nc([N+](=O)[O-])c(O)nc1O
    Storage Conditions Store at room temperature in a tightly closed container
    Stability Stable under normal conditions

    As an accredited 2-Amino-4,6-Dihydroxy-5-Nitropyrimidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 2-Amino-4,6-Dihydroxy-5-Nitropyrimidine is sealed in an amber glass bottle with a tamper-evident screw cap.
    Shipping 2-Amino-4,6-Dihydroxy-5-Nitropyrimidine is shipped in tightly sealed containers to protect from moisture and contamination. It is packaged according to chemical safety regulations, with appropriate labeling and documentation. Transport is typically via ground or air in compliance with local, national, and international hazardous materials guidelines, ensuring safe delivery to the destination.
    Storage 2-Amino-4,6-Dihydroxy-5-Nitropyrimidine should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep it in a cool, dry, well-ventilated area, separated from incompatible substances such as strong oxidizers and acids. Personal protective equipment should be used when handling. Ensure appropriate labeling and secure storage to prevent unauthorized access or accidental release.
    Application of 2-Amino-4,6-Dihydroxy-5-Nitropyrimidine

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

    As a direct manufacturer of 2-Amino-4,6-Dihydroxy-5-Nitropyrimidine, we support technical teams and procurement specialists across regulated markets. Our product integrates into multiple downstream chemical sectors where strict quality control and precise performance are required. Below we detail the authentic industrial applications that utilize this specialty intermediate with reference to applicable industry compliance, practical formulation ratios, process steps, and the finished goods created.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    This pyrimidine derivative is frequently adopted as a nucleophilic building block in the synthesis of APIs, especially within pyrimidine-based oncology and antiviral drugs. Its structure allows for targeted functionalization during heterocyclic ring construction, streamlining the creation of potent drug candidates and reducing the number of synthetic steps in GMP-compliant plants.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP, EP, JP monograph requirements for starting materials
    • FDA 21 CFR Part 211 (USA) and EudraLex Volume 4 (EU) for pharmaceutical production
    • ISO 9001:2015 for quality management systems

    Typical usage ratio

    • Ranges from 0.5% to 3% molar ratio relative to total batch reactants, adjusted based on desired yield and targeted API structure

    Downstream process integration

    • Added during nucleophilic aromatic substitution or amidation steps, often as an initial heterocycle formation stage before further derivatization and purification

    Final product types

    • Pyrimidinyl pharmaceutical intermediates
    • Oncology drug precursor compounds
    • Antiviral active ingredients

    2. Specialty Dye and Pigment Synthesis

    This compound provides essential amino and nitro functionalities for the construction of high-performance azo and pyrimidine dyes, primarily used in textile printing and inkjet ink manufacturing. Its role as a diazo component enables precise control over color fastness, molecule reactivity, and suitability for demanding printing applications.

    Industry compliance standards

    • OEKO-TEX Standard 100 (textile safety)
    • REACH Annex XVII for restricted dye intermediates (EU)
    • ZDHC MRSL Level 1 (zero discharge program)
    • ISO 105 (series) for textile colorfastness tests

    Typical usage ratio

    • Usually 0.2–2% by weight of total dye formulation, optimized according to targeted hue intensity and desired application substrate

    Downstream process integration

    • Incorporated during azo coupling reaction steps; acts as a controlled source for diazotization and dye side chain modification before dilution and finishing

    Final product types

    • Reactive dyes for cotton and synthetics
    • Digital inkjet textile inks
    • High-stability azo pigments

    3. Agrochemical Active Ingredient Manufacturing

    Leading agrochemical formulators use this raw material for constructing pyrimidine-based herbicide and fungicide cores, benefiting from its dual hydroxy and nitro substituents that drive selective reactivity. It helps streamline ring closure steps and facilitates the production of active ingredients with targeted biological activity for crop protection.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EPA OPPTS Guidelines (USA)
    • ISO 17025 for laboratory testing of actives
    • GMP+ Feed Safety Assurance for agrochemical supply (where applicable)

    Typical usage ratio

    • Ranges from 1% to 4% based on the specific compound synthesis pathway and the active load required per batch

    Downstream process integration

    • Utilized during cyclization or condensation stages in the synthesis of key herbicide/fungicide chemicals, preceding chlorination or amide introduction steps

    Final product types

    • Selective herbicide actives
    • Pyrimidine-derived fungicides
    • Pre-emergent weed control formulations

    4. Veterinary Drug Intermediate Production

    Veterinary pharmaceutical manufacturers incorporate this heterocycle as an intermediate in formulating antimicrobial and antiparasitic actives for livestock and companion animals. The specific substitution pattern permits effective synthesis of biologically relevant pyrimidinone derivatives critical to animal health solutions.

    Industry compliance standards

    • Veterinary Drug GMP Guidelines (China, EU, USA)
    • VICH GL quality requirements
    • Ph. Eur. and USP standards for veterinary substances
    • ISO 22716:2007 (cosmetic GMP, where topical veterinary drugs are relevant)

    Typical usage ratio

    • Typically between 0.3% and 2% as calculated by molar proportion to the main substrate in multi-step syntheses

    Downstream process integration

    • Engaged at ring assembly or reductive amination phases to introduce essential pharmacophores before final compound isolation and formulation

    Final product types

    • Veterinary antibiotic actives
    • Antiparasitic intermediates
    • Livestock feed additives with pesticidal action

    5. Analytical Reagent and Diagnostic Kit Component

    Leading IVD and diagnostics producers employ this compound for the synthesis of pyrimidine-based chromogenic substrates and selective staining reagents. Its functionality enables the production of reagents with improved analytical specificity and signal generation for clinical laboratory applications.

    Industry compliance standards

    • ISO 13485:2016 for IVD medical device quality management
    • CLSI EP standard for reagent validation
    • 21 CFR 820 (USA) for medical device current good manufacturing practice
    • IVDR (EU Regulation 2017/746) for IVD ingredients

    Typical usage ratio

    • Ranges from 0.05% to 1% of total reagent weight, depending on detection threshold and platform compatibility

    Downstream process integration

    • Integrated during substrate coupling chemistry or indicator reagent synthesis prior to formulation in standardized diagnostic kits

    Final product types

    • Enzyme substrate reagents for ELISA
    • Chromogenic test strips
    • Diagnostic indicator reagents for clinical kits
    Free Quote

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    Email: sales7@sinochem-nanjing.com

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