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6-(Chloromethyl)Uracil

    • Product Name 6-(Chloromethyl)Uracil
    • Alias 6-(Chloromethyl)-2,4(1H,3H)-pyrimidinedione
    • Einecs 239-294-6
    • 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

    972443

    Chemical Name 6-(Chloromethyl)uracil
    Molecular Formula C5H5ClN2O2
    Molecular Weight 160.56 g/mol
    Cas Number 698-04-0
    Appearance White to off-white solid
    Melting Point 215-217°C
    Solubility Slightly soluble in water
    Storage Conditions Store at 2-8°C, protect from light and moisture

    As an accredited 6-(Chloromethyl)Uracil factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle with a secure cap, labeled "6-(Chloromethyl)Uracil," includes hazard symbols and handling instructions.
    Shipping 6-(Chloromethyl)Uracil is shipped in tightly sealed containers, protected from light and moisture. Packaging complies with relevant chemical transport regulations, using cushioning to prevent breakage or leaks. The container is clearly labeled with hazard information. Shipping is typically via ground or air, using certified carriers for hazardous materials, ensuring safe and compliant delivery.
    Storage 6-(Chloromethyl)uracil should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and sources of ignition. It should be kept separate from strong oxidizing agents. Proper personal protective equipment (PPE) is recommended when handling, and the storage area should be clearly labeled and accessible only to trained personnel.
    Application of 6-(Chloromethyl)Uracil

    Applications of 6-(Chloromethyl)Uracil in Industrial Manufacturing

    As a direct manufacturer with advanced synthesis lines, we have observed demand for 6-(Chloromethyl)Uracil across specialized chemical production sectors. Below, we outline its practical use cases in several regulated downstream industries, drawing on technical integration and compliance knowledge from real-world customer applications.

    1. Pharmaceutical Intermediate for Cytostatic Drug Synthesis

    Pharmaceutical companies widely use this material as a nucleoside intermediate, supporting the synthesis pathway of various antimetabolite medications used in oncology. The compound’s chloromethyl group enables targeted alkylation steps during active pharmaceutical ingredient (API) formation. Adhering to strict pharmaceutical quality parameters, processes deploy it within multi-step organic transformations, typically in controlled GMP environments with full traceability and validated analytical monitoring at each batch.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II
    • United States Pharmacopeia (USP) general chapter <1078>
    • REACH registration, specifically for pharmaceutical intermediate use

    Typical usage ratio

    • Applied at 1.2–2.5 molar equivalents relative to core uracil precursors, adjusted based on downstream conversion target and scavenger selection
    • Precise ratios determined by desired API yield and purity levels during pilot and upscaling

    Downstream process integration

    • Charged post-nucleobase functionalization
    • Undergoes alkylation at stage 2 or 3 of multi-reaction flows depending on specific drug pipeline
    • Process often includes active pH management and continuous filtration before subsequent condensation

    Final product types

    • Pyrimidine-based cytostatic agents (e.g., 5-fluorouracil analogues)
    • Specialty antitumor drugs
    • Active nucleoside intermediates for further API assembly
    • Research-grade nucleobase derivatives

    2. Agrochemical Active Ingredient Precursor

    Producers of crop protection actives incorporate this material within synthetic protocols for uracil-derived herbicides and fungicides. Its chloromethyl functionality enables site-selective coupling, facilitating construction of complex molecular scaffolds. Agrochemical manufacturers control residue and impurity profiles closely, using validated in-process checks aligned to regulatory standards for approved pesticide input materials.

    Industry compliance standards

    • FAO/WHO Specification (JMPR guideline) for pesticide technical grade
    • ISO 9001:2015 for production traceability
    • EU Regulation (EC) No 1107/2009—authorization of plant protection products
    • REACH registration for agrochemical manufacturing

    Typical usage ratio

    • Employed at 0.8–1.5 molar equivalents per target uracil substrate, fine-tuned according to yield optimization studies
    • Pilot plants set ratios after impurity clearance trials and pre-registration validation

    Downstream process integration

    • Fed after primary skeleton assembly as a halomethyl donor
    • Used in sealed reaction vessels with solvent optimization tailored to target herbicidal motifs
    • Integrated with thermal step-ups to drive final condensation

    Final product types

    • Emerged uracil-based pre- and post-emergent herbicides
    • New-generation fungicidal actives
    • Intermediates for selective crop protection agents
    • Seed treatment additive subcomponents

    3. Specialty Dye and Pigment Intermediate

    Chemical firms engaged in dye and pigment synthesis select this uracil derivative as a key scaffold for developing chromophore compounds. Its halogen-substituted uracil core supports novel colorant development, offering reactive sites for coupling with aryl or alkyl groups. In this segment, strict purity and color intensity standards govern each reaction stage, and suppliers of high-purity intermediates undergo regular qualification audits from major pigment formulators.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001 for colorant manufacturing facilities
    • GHS (Globally Harmonized System) for labeling and transport
    • EU REACH Annex XVII (for restrictions on azo dyes)
    • Quality control under industrial dye application QMS

    Typical usage ratio

    • Typically dosed at 0.9–1.3 molar equivalents in colorant core backbone synthesis
    • Adjusted based on targeted molecular weight and functional colorant testing feedback

    Downstream process integration

    • Charged after activating aromatic precursors under controlled temperature
    • Integrated as an essential coupling unit in pigment mill base production
    • Purified by repeated crystallization or chromatography prior to downstream pigment formulation

    Final product types

    • Reactive azo and anthraquinone-based dyes
    • High-purity pigment dispersions
    • UV-resistant specialty colorants
    • Color developer intermediates for polymer and textile sectors

    4. Polymer Modification Building Block

    In high-performance polymer engineering, this intermediate functions as a reactive monomer for nucleobase-modified polymers. Polymer R&D teams value its site-specific reactivity, enabling the customization of backbone structures and functional surfaces. Frequent downstream applications involve advanced coatings and membranes where uracil incorporation confers selective permeability, biocompatibility, or chemical resistance improvements, with all batches traceable for customer regulatory filings.

    Industry compliance standards

    • ISO 9001:2015 for polymer and plastics manufacturing
    • FDA 21 CFR for indirect food contact additives where intended
    • RoHS when polymers are used in electronic applications
    • Specific customer QMS for audited specialty polymer supply

    Typical usage ratio

    • Used at 0.1–1.0% by total polymer weight in functional copolymer synthesis line trials
    • Adjusted during process scale-up according to desired grafting level and performance in end-use tests

    Downstream process integration

    • Added during copolymerization as a functional group donor
    • Introduced prior to crosslinking or chain extension stages
    • Frequent inline monitoring of monomer integration using HPLC/GC as part of QC protocol

    Final product types

    • Modified engineering plastics for automotive and aerospace
    • Selective filtration and separation membranes
    • Functional coatings for electronics
    • Advanced biomedical polymer blends
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