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4-Hydroxy-6-(Trifluoromethyl)Pyrimidine-2-Thiol

    • Product Name 4-Hydroxy-6-(Trifluoromethyl)Pyrimidine-2-Thiol
    • Alias 4-Hydroxy-6-(trifluoromethyl)-2(1H)-pyrimidinethione
    • Einecs 425-900-4
    • 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

    646385

    Product Name 4-Hydroxy-6-(Trifluoromethyl)Pyrimidine-2-Thiol
    Cas Number 117311-90-1
    Molecular Formula C5H3F3N2OS
    Molecular Weight 196.16
    Appearance White to off-white solid
    Melting Point 122-126°C
    Purity ≥98%
    Solubility Slightly soluble in water, soluble in DMSO
    Storage Condition Store at 2-8°C, protect from light and moisture

    As an accredited 4-Hydroxy-6-(Trifluoromethyl)Pyrimidine-2-Thiol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, screw-capped amber glass bottle labeled "4-Hydroxy-6-(Trifluoromethyl)Pyrimidine-2-Thiol, 10 grams," with safety and batch information.
    Shipping 4-Hydroxy-6-(Trifluoromethyl)Pyrimidine-2-Thiol is shipped in tightly sealed containers, protected from light and moisture. It is packed according to hazardous chemical regulations, usually with cold packs if required, and includes clear labeling. Shipping is typically by ground or air, following all local and international safety and documentation protocols.
    Storage Store **4-Hydroxy-6-(Trifluoromethyl)Pyrimidine-2-Thiol** 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 oxidizing agents and acids. Ensure proper labeling and access only to trained personnel. Follow standard chemical storage protocols and consult the Safety Data Sheet (SDS) for specific requirements.
    Application of 4-Hydroxy-6-(Trifluoromethyl)Pyrimidine-2-Thiol

    Applications of 4-Hydroxy-6-(Trifluoromethyl)Pyrimidine-2-Thiol in Industrial Manufacturing

    As the direct producer of 4-Hydroxy-6-(Trifluoromethyl)Pyrimidine-2-Thiol, we focus on core industrial segments where this advanced pyrimidine derivative delivers measurable impact on molecule design, process yield, and regulatory compliance. The applications below reflect our technical support and regular supply for large-scale operations in pharmaceuticals, agrochemicals, specialty materials, and diagnostic reagent production. Each scenario details practical integration based on actual downstream manufacturing use, regulatory compliance concerns, and formulation experience.

    1. Pharmaceutical Intermediate for Antiviral and Oncology APIs

    Major API manufacturers incorporate this pyrimidine thiol as a critical fragment in the synthesis of fluorinated heterocycles found in third-generation antivirals and targeted anticancer agents. The reactive thiol and fluoromethyl functionalities allow introduction of metabolic stability and receptor selectivity in late-stage pharmaceutical intermediates. We support formulation chemists to optimize purity, impurity profiles, and crystallization yields with this building block.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF Monographs on related synthesis intermediates
    • EMA Guidelines on Genotoxic Impurities
    • ISO 9001 Quality Management Systems, validated traceability

    Typical usage ratio

    • 5–25% (molar equivalent) as a terminal or penultimate intermediate depending on target structure; process chemists adjust based on stoichiometric requirements and impurity control objectives

    Downstream process integration

    • Direct coupling during Suzuki, Buchwald-Hartwig, or S-alkylation steps of API syntheses; typically introduced after main ring assembly but before side-chain or salt formation; temperature- and pH-controlled reactors used for quality assurance

    Final product types

    • Cutting-edge antiviral drugs (e.g., nucleoside analogs)
    • Pyrimidine-based oncology APIs
    • Late-stage pharmaceutical intermediates supplied to innovators and CDMOs

    2. Agrochemical Synthesis — Selective Herbicide Building Block

    Agricultural chemical producers use the unique trifluoromethyl-pyrimidine motif to construct new generations of selective herbicides with enhanced crop tolerance and environmental breakdown profiles. The compound’s thiol moiety serves as a reactive site for further derivatization, enabling the creation of molecules effective against resistant weed biotypes. Our production team supplies material to maximize batch-to-batch reproducibility in large-scale synthesis.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Plant Protection Products
    • OECD Guidelines for the Testing of Chemicals
    • ISO 17025 for Analytical Testing of Agrochemical Ingredients
    • Chinese National Standard GB 2763 for Pesticide Residue Limits

    Typical usage ratio

    • 10–18% by weight in pre-herbicide molecular fragment assembly, fine-tuned during scale-up to balance conversion efficiency and cost

    Downstream process integration

    • Initial building block during nucleophilic substitution with halo-organic precursors; processed in jacketed glass-lined reactors for heat-sensitive steps; followed by post-purification to remove residual starting materials

    Final product types

    • Selective herbicide actives (e.g., for cereals or rice paddies)
    • Patent-pending herbicide intermediate stocks
    • Combination active ingredients for broad-spectrum weed control

    3. Electronic Chemical Synthesis — Fluorinated Heterocycle for Photoresists

    Producers of advanced photoresist formulations incorporate this pyrimidine derivative to enhance fluorine content and UV transparency in microelectronics industry resins. Its chemical profile supports the design of photoacid generators and blocking groups, critical for fine-line lithography applications. We deliver high-purity, low-ionic grade to ensure strict process compatibility and device yield.

    Industry compliance standards

    • SEMI C3 Standard — Specification for Photoresist Materials
    • ISO 14644 Cleanroom and Controlled Environments Protocols
    • RoHS Directive 2011/65/EU (for electronic components)
    • UL 94 (Flammability of plastic materials)

    Typical usage ratio

    • 3–10% as weight percentage in resin masterbatch formulation; adjusted according to target exposure wavelength and required resolution

    Downstream process integration

    • Blend addition during prepolymerization of photoresist resin; introduced in high-shear mixing under inert atmosphere to minimize moisture uptake and ion contamination; followed by filtration and spin-coating

    Final product types

    • Deep-UV and EUV photoresist systems for semiconductor lithography
    • Custom fluorinated coatings for printed circuit boards
    • Fine-line mask materials used in microelectronic packaging

    4. Diagnostic Reagent Synthesis — Heterocyclic Labeling Agent

    In molecular diagnostics, reagent manufacturers rely on derivatives of this pyrimidine compound as heterocyclic scaffolds for modifying oligonucleotide probes and enzyme substrates. The trifluoromethyl group confers distinct NMR and mass spectrometry signals, supporting multiplex detection assays. Our QC protocol guarantees high assay purity and spectral reproducibility suitable for bioanalytical workflows.

    Industry compliance standards

    • ISO 13485 Quality Management Systems for Medical Devices
    • CLSI EP10-A3 Standard for Preliminary Evaluation of Quantitative Clinical Laboratory Methods
    • 21 CFR Part 820 (Quality System Regulation for IVD products)
    • REACH Registration for laboratory chemicals

    Typical usage ratio

    • 0.5–5% by molar proportion in probe modification reactions; optimized according to probe length and required detection sensitivity

    Downstream process integration

    • Introduced during phosphoramidite or solid-phase synthesis of nucleic acid probes; typically handled in small-batch reaction vessels under controlled temperature/humidity for high-purity output; followed by HPLC purification

    Final product types

    • Fluorescent or mass-tagged DNA/RNA probes for PCR and isothermal amplification
    • Enzyme-modified reporter molecules for ELISA kits
    • Reference standards for clinical diagnostic reagent development
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