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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 | 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. |
Applications of 4-Hydroxy-5-Fluorpyrimidine in Industrial ManufacturingAs 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) SynthesisPharmaceutical 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
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2. Agrochemical Intermediate ManufacturingAgrochemical 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
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3. Fluorinated Fine Chemical SynthesisChemical 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
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4. Diagnostic Imaging Reagent PreparationProducers 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
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5. Specialty Polymer Additive SynthesisManufacturers 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
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