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4-Hydroxy-5-Fluorpyrimidine

    • Product Name 4-Hydroxy-5-Fluorpyrimidine
    • Alias 4-Hydroxy-5-fluoropyrimidine
    • Einecs 693-608-2
    • 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

    466134

    Product Name 4-Hydroxy-5-Fluorpyrimidine
    Cas Number 113170-01-7
    Molecular Formula C4H3FN2O
    Molecular Weight 114.08 g/mol
    Appearance White to off-white solid
    Melting Point Approx. 180°C (decomposition)
    Solubility Soluble in DMSO and methanol
    Storage Conditions Store at 2-8°C, in a dry, tightly sealed container
    Purity Typically ≥98% (HPLC)
    Smiles C1=C(C(=NC=N1)O)F
    Inchi InChI=1S/C4H3FN2O/c5-3-1-7-4(8)2-6-3/h1-2,8H

    As an accredited 4-Hydroxy-5-Fluorpyrimidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, white screw cap, chemical label displays ‘4-Hydroxy-5-Fluorpyrimidine,’ hazard symbols, and handling instructions.
    Shipping 4-Hydroxy-5-Fluorpyrimidine is shipped in tightly sealed, chemically resistant containers to prevent contamination and moisture ingress. Packaging complies with hazardous material regulations. The chemical is labeled clearly, handled with care, and transported via approved carriers to ensure safety and integrity during transit. Temperature and handling guidelines must be strictly followed.
    Storage 4-Hydroxy-5-fluoropyrimidine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers and acids. Protect from moisture and light. Label the container clearly and keep it in a designated chemical storage cabinet, following local regulations for hazardous materials.
    Application of 4-Hydroxy-5-Fluorpyrimidine

    Applications of 4-Hydroxy-5-Fluorpyrimidine in Industrial Manufacturing

    As a chemical manufacturer specialized in pyrimidine derivatives, we supply 4-Hydroxy-5-Fluorpyrimidine directly for several advanced industrial sectors. Precision synthesis and strict quality control ensure reliable performance in demanding applications. The following sections detail real downstream fields using this raw material, with industrially relevant compliance, formulation, process, and final product insights.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical companies use 4-Hydroxy-5-Fluorpyrimidine as a key heterocyclic building block in the production of antiviral and anticancer compounds. Its structure enables targeted modifications on nucleoside analogs, enhancing bioactivity and patient outcomes. Chemists introduce this intermediate during late-stage synthesis, optimizing step efficiency and purity for regulatory markets. Every batch undergoes rigorous impurity control to comply with drug master files and pharmacopoeia requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • EU Pharmacopoeia (Ph. Eur.) specifications for pharmaceutical intermediates
    • U.S. Pharmacopoeia (USP) <831> Residual Solvents
    • FDA 21 CFR Part 210-211 for drug manufacturing processes

    Typical usage ratio

    • 2%–8% relative to total API mass, adjusted per target compound’s substitution pattern and yield requirements
    • Stoichiometry varies with nucleoside coupling and protecting group chemistry

    Downstream process integration

    • Stepwise functionalization in multi-stage organic synthesis
    • Introduction before cyclization, often used with palladium or copper catalysts
    • Integration after primary amine protection for selective functional group transformation

    Final product types

    • Pyrimidine-based antiviral agents (e.g., HIV, hepatitis B drugs)
    • Oncology drug substances (cytotoxic nucleoside analogs)
    • Intermediates for cardiovascular medications
    • Reference standards for pharmaceutical analytics

    2. Agrochemical Intermediate Manufacturing

    Agrochemical formulators employ 4-Hydroxy-5-Fluorpyrimidine to synthesize modern herbicides and fungicides with enhanced selectivity and environmental profiles. The compound serves as a precursor for fluorinated pyrimidine scaffolds, a motif favored for increased mode-of-action specificity and photo-stability in crop protection agents. Industrial chemists introduce this material in condensation and cyclization steps, closely monitoring halogen substitution to manage potency and environmental persistence.

    Industry compliance standards

    • FAO/WHO Codex specifications for pesticide active ingredients
    • Regulation (EC) No 1107/2009 (EU Plant Protection Products)
    • EPA Office of Pesticide Programs (USA) product chemistry guidelines
    • ISO 9001:2015 quality system for chemical intermediates

    Typical usage ratio

    • 5%–15% in the key intermediate synthesis route (dry weight basis for heterocyclic precursors)
    • Adjustable depending on crop-specific formulation and mode of action

    Downstream process integration

    • Condensation with chlorinating agents for further substitution and derivatization
    • Integration in the heteroaromatic ring-forming reactions
    • Sequential introduction following base-catalyzed N-alkylation

    Final product types

    • Fluorinated herbicide actives (post-emergence weed control agents)
    • Pyrimidinyl fungicide actives (broad-spectrum disease prevention)
    • Crop protection intermediate stock solutions
    • Stability reference samples for formulation analysis

    3. Fluorinated Fine Chemical Synthesis

    Chemical manufacturers rely on 4-Hydroxy-5-Fluorpyrimidine to introduce selective fluorine and hydroxy substituents into specialty chemicals for electronics and material science sectors. The compound’s controlled reactivity supports building advanced intermediates with defined polarity and electronic effects. Process engineers utilize it for coupling, alkylation, and nucleophilic aromatic substitution, sustaining tight control to achieve high purity in multi-step syntheses for demanding electronics applications.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for chemical production
    • REACH registration for use in industrial fine chemicals (EC No. 1907/2006)
    • RoHS Directive (2011/65/EU) for electronics-related substances
    • IECQ QC 080000 hazardous substance process management

    Typical usage ratio

    • 1%–6% as a precursor intermediate, depending on target molecule complexity
    • Measured in mole equivalents relative to final fluorinated aromatic end group

    Downstream process integration

    • Inserted in nucleophilic aromatic substitution (SNAr) reactions
    • Employed for direct coupling with alkyl or aryl halides during intermediate synthesis
    • Incorporated before final fluorination or hydroxy protection, subject to downstream functional group compatibility

    Final product types

    • Specialty fluorinated ligands for optoelectronics
    • Fine chemical intermediates for OLED and semiconductor manufacturing
    • Precursors for electronic photoresist materials
    • Dielectric additives with controlled dipole characteristics

    4. Diagnostic Imaging Reagent Preparation

    Producers of diagnostic imaging agents integrate 4-Hydroxy-5-Fluorpyrimidine in the synthesis of fluorinated markers for PET (Positron Emission Tomography) and SPECT (Single Photon Emission Computed Tomography) radiopharmaceuticals. The compound’s defined substitution sites support radio-labeling, ensuring signal strength and biological compatibility. Reactors and solvents are validated to minimize cross-contamination and comply with strict medical device and pharmaceutical regulations.

    Industry compliance standards

    • U.S. Pharmacopoeia (USP) Chapter <823> Radiopharmaceuticals for Positron Emission Tomography
    • European Pharmacopoeia 10.0 standards for radiolabeled precursors
    • ISO 13485:2016 for medical device manufacturing
    • FDA CGMP for PET Drugs (21 CFR Part 212)

    Typical usage ratio

    • 0.5%–2.5% in radioligand precursor synthesis (calculated by substrate equivalents needed for tracer labeling)
    • Ratio adjusted based on isotope incorporation efficiency and final dose formulation

    Downstream process integration

    • Stepwise radiofluorination for preparation of labeled tracer intermediate
    • Introduction before final deprotection and purification stages
    • Integration under controlled anhydrous conditions to preserve isotope activity

    Final product types

    • PET imaging tracers (F-18 labeled pyrimidines)
    • SPECT agents containing stable or radioactive fluorine
    • Reference imaging standards for clinical calibration
    • Precursor kits for hospital radiopharmacy compounding

    5. Specialty Polymer Additive Synthesis

    Manufacturers of advanced polymers employ 4-Hydroxy-5-Fluorpyrimidine to produce functional additives and co-monomers that impart higher thermal resistance and specific chemical reactivity. The pyrimidine ring system with controlled halogenation interacts uniquely with polymer matrices. It enters copolymerization or grafting reactions, delivering enhanced performance in electronics encapsulants, membranes, and engineering plastics for demanding technical applications.

    Industry compliance standards

    • ISO 9001:2015 for specialty polymer production
    • European Commission Regulation (EU) No 10/2011 for polymer additives in food contact materials
    • FDA 21 CFR 177.1520 for polyolefin additives in food packaging
    • UL 94 plastic flammability standards for electronics

    Typical usage ratio

    • 0.1%–1.0% as an engineered additive, dependent on polymer system and target end-use properties
    • Adjusted for balance between functionality and processing performance

    Downstream process integration

    • Addition during copolymerization with olefins or vinyl monomers
    • Used as a reactive chain transfer agent in step-growth processes
    • Incorporated by melt blending for masterbatch production

    Final product types

    • Fluorinated engineering plastics for microelectronics housings
    • Polymer films and membranes with enhanced barrier function
    • Specialty copolymers for thermal and chemical resistance
    • Food contact approved packaging materials (EU/USA markets)
    Free Quote

    Competitive 4-Hydroxy-5-Fluorpyrimidine prices that fit your budget—flexible terms and customized quotes for every order.

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