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3-Chloro-5-(Trifluoromethyl)Pyridine-2-Thiol

    • Product Name 3-Chloro-5-(Trifluoromethyl)Pyridine-2-Thiol
    • Alias 3-Chloro-5-(trifluoromethyl)-2-pyridinethiol
    • Einecs 697-404-3
    • 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
    VTB
    Specifications

    HS Code

    409178

    Cas Number 89856-27-7
    Molecular Formula C6H2ClF3NS
    Molecular Weight 215.61
    Appearance Solid
    Purity Typically ≥98%
    Solubility Slightly soluble in organic solvents
    Synonyms 2-Mercapto-3-chloro-5-(trifluoromethyl)pyridine
    Smiles C1=CC(=C(N=C1Cl)S)C(F)(F)F
    Inchi InChI=1S/C6H2ClF3NS/c7-4-2-3(6(8,9)10)1-5(11)12-4/h1-2,11H

    As an accredited 3-Chloro-5-(Trifluoromethyl)Pyridine-2-Thiol 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, tightly sealed with a screw cap; labeled with hazard warnings, chemical name, and supplier details.
    Shipping **Shipping Description:** 3-Chloro-5-(trifluoromethyl)pyridine-2-thiol is shipped in tightly sealed containers under ambient conditions. It should be protected from moisture, extreme temperatures, and direct sunlight. Ensure compliance with local regulations for handling hazardous chemicals. Label containers appropriately and include safety documentation. Handle with care to avoid spillage and environmental contamination during transit.
    Storage Store **3-Chloro-5-(Trifluoromethyl)Pyridine-2-Thiol** tightly sealed in a cool, dry, well-ventilated area, away from sources of ignition, incompatible chemicals (oxidizers, strong acids, bases), and moisture. Use containers made of materials compatible with thiols. Avoid excessive heat or sunlight. Store under inert gas if sensitive to air. Clearly label storage containers, and restrict access to trained personnel using appropriate personal protective equipment (PPE).
    Application of 3-Chloro-5-(Trifluoromethyl)Pyridine-2-Thiol

    Applications of 3-Chloro-5-(Trifluoromethyl)Pyridine-2-Thiol in Industrial Manufacturing

    As the original manufacturer of 3-Chloro-5-(Trifluoromethyl)Pyridine-2-Thiol, we enable global industry partners with reliable supply for core synthesis processes. Our expertise ensures consistent quality and technical parameters for diverse manufacturing value chains across agrochemicals, pharmaceuticals, specialty chemicals, and advanced materials.

    1. Synthesis of Agrochemical Active Ingredients

    This compound serves as a targeted intermediate in the manufacturing chains of modern agrochemicals, where its electron-withdrawing trifluoromethyl group and chloro-substitution facilitate further introduction of functional moieties. In herbicide and fungicide synthesis, downstream processors incorporate it in multi-step condensation and coupling reactions to achieve final molecules with high selectivity and field stability. The application requires compliance with detailed ecological and worker safety standards, and integration into highly-controlled synthesis suites.

    Industry compliance standards

    • European Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market
    • US EPA 40 CFR Part 158 (Data Requirements for Pesticides)
    • China GB/T 38562-2020 (General rules for pesticide production)
    • ISO 9001:2015 for production site QMS

    Typical usage ratio

    • Acts as a key intermediate at 0.5%–8% by weight of total batch depending on process yield, targeted molecular structure, and downstream reaction step

    Downstream process integration

    • Input during nucleophilic aromatic substitution or cross-coupling stage of actives’ core-ring assembly; handled in enclosed, automated reactors for batch synthesis

    Final product types

    • Aryl-pyridine herbicides (e.g., systemic pre-emergence weed control agents)
    • Trifluoromethylated fungicide actives for cereal and fruit protection

    2. Pharmaceutical API Intermediate Manufacturing

    Pharmaceutical synthesis routes utilize this raw material in the preparation of advanced intermediates for certain small-molecule APIs, especially within the anti-infective and CNS agent classes. Its chemical framework allows for regioselective transformations, facilitating substitution, cross-coupling, and reduction steps at critical reaction stages. Each batch manufactured for this purpose must adhere to stringent GMP and traceability requirements, supporting downstream consistency for regulatory filings and validation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211 (cGMP in Manufacturing, Processing, Holding of Drugs)
    • European Pharmacopoeia (Ph.Eur.) standards for impurities and residual solvents
    • ISO 17025 (analytical test method validation)

    Typical usage ratio

    • Utilized as a synthetic intermediate at 1.5%–6% by weight in total process mass, adjusted according to structure-activity requirements of the API

    Downstream process integration

    • Introduced at the selective thiolation or halogen-exchange step in the synthesis of central nervous system and anti-microbial drug intermediates

    Final product types

    • Active pharmaceutical ingredients for anti-epileptic formulations
    • API derivatives used in anti-infective drug products

    3. Manufacture of Specialized Dye Intermediates

    Producers of specialty dyes select this compound for its ability to impart heterocyclic stability and enhanced lightfastness in final dye molecules. Integrations often include its use in forming pyridine-based chromophores and auxiliary ligands for pigments. It is added in dye precursor synthesis when precise control of substituent orientation and side chain reactivity is required for targeted dye shades and fastness characteristics. Handling and documentation fall under colorant manufacturing regulations and specific purity controls.

    Industry compliance standards

    • REACH (EC No 1907/2006) chemical registration and evaluation
    • ISO 9001:2015 (quality control for dyes manufacture)
    • OEKO-TEX® Standard 100 (certification for restricted substances in textiles)
    • EU 2004/648/EC (detergents and surfactants regulation, for dye applications in detergents)

    Typical usage ratio

    • Typically used at 3%–7% by weight of active dye mass, customized to target molecular structure for depth of color and stability

    Downstream process integration

    • Employed during the initial condensation or coupling reaction for dye base assembly; subsequent modification carries the functional group into the finished pigment or dye

    Final product types

    • Reactive dyes for fiber textiles
    • UV-stable pigments for plastics and polymer coatings

    4. Industrial Corrosion Inhibitor Synthesis

    Within the specialty chemicals sector, manufacturers employ this compound as a key raw material in synthesizing sulfur- and nitrogen-containing corrosion inhibitors for water treatment and oilfield applications. Its integration supports molecular frameworks that offer adsorption affinity on metal surfaces, forming durable, hydrophobic barriers during harsh operational conditions. End-use products must adhere to international water safety, oil extraction, and anti-corrosion quality benchmarks.

    Industry compliance standards

    • ASTM D2688 (Standard Test Method for Corrosiveness of Water)
    • API RP 932-B (Materials Selection for Amine Units)
    • EU Biocidal Products Regulation (BPR, Regulation (EU) No 528/2012)
    • AWWA B306-15 (corrosion inhibitor standards for potable water)

    Typical usage ratio

    • Introduced at 0.2%–2% weight of total inhibitor formulation, with dosage adjusted based on application system pH and required film persistence

    Downstream process integration

    • Added at the inhibitor precursor condensation phase or as a thiol source during ligand formation for anti-corrosion actives

    Final product types

    • Corrosion protection additives for oil field water injection systems
    • Closed-loop industrial cooling system inhibitors

    5. Advanced Electronic Material Precursor

    Producers of high-performance electronic and optoelectronic materials use this compound to create specialized organic compounds for semiconductor processing. Its molecular structure enables downstream synthesis of pyridine-based ligands and electron-transport materials with high chemical and thermal stability. During integration, precise traceability, contamination control, and adherence to semiconductor grade requirements are necessary to ensure quality in circuit fabrication.

    Industry compliance standards

    • IPC-6012DA (Qualification and Performance Specification for High Reliability Printed Boards)
    • JEDEC JESD22 (Material stress testing for electronics)
    • ISO 14644-1 (cleanroom and contamination control)
    • RoHS 3 (Directive 2015/863/EU – restriction of hazardous substances)

    Typical usage ratio

    • Used at 1%–4.5% by formulation weight, determined by targeted molecular design for electronic layer deposition or organic semiconducting films

    Downstream process integration

    • Introduced during ligand precursor synthesis for thin film deposition or as a functional group donor in polymeric insulator material production

    Final product types

    • Organic electron-transport layers for OLED and TFT-LCD manufacturing
    • Specialty insulating materials for PCB microelectronics
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