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4-Fluorothiobenzamide

    • Product Name 4-Fluorothiobenzamide
    • Alias 4-Fluorobenzenecarbothioamide
    • Einecs 240-928-2
    • 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
    VTB
    Specifications

    HS Code

    195630

    Chemical Name 4-Fluorothiobenzamide
    Cas Number 456-59-7
    Molecular Formula C7H6FNS
    Molecular Weight 155.19 g/mol
    Appearance White to off-white solid
    Melting Point 106-108°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Pubchem Cid 22583
    Smiles C1=CC(=CC=C1C(=S)N)F
    Inchi InChI=1S/C7H6FNS/c8-6-3-1-2-5(4-6)7(9)10/h1-4H,(H2,9,10)
    Storage Conditions Store in a cool, dry place; keep container tightly closed
    Synonyms 4-Fluorobenzenecarbothioamide

    As an accredited 4-Fluorothiobenzamide 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 screw cap, labeled "4-Fluorothiobenzamide," includes hazard warnings and lot information.
    Shipping 4-Fluorothiobenzamide is shipped in tightly sealed containers, compliant with relevant chemical transport regulations. Packaging protects against moisture, physical damage, and contamination. Proper labeling, including hazard identification and handling instructions, ensures safe transit. Shipments may require temperature control and documentation in accordance with local, national, and international shipping standards for hazardous substances.
    Storage 4-Fluorothiobenzamide should be stored in a tightly sealed container, away from moisture and incompatible substances (such as oxidizing agents). Store it in a cool, dry, well-ventilated area, protected from light and sources of ignition. Properly label the container, and ensure only trained personnel have access. Follow local regulations and safety guidelines when handling and storing this chemical.
    Application of 4-Fluorothiobenzamide

    Applications of 4-Fluorothiobenzamide in Industrial Manufacturing

    Our 4-Fluorothiobenzamide supports specialized synthesis processes across several regulated industries. Below, we detail critical downstream application scenarios, compliance requirements, dosage ranges, process stages, and the resulting end products as used by large-scale manufacturers worldwide.

    1. Pharmaceutical Intermediate for Thiazole Synthesis

    Major active pharmaceutical ingredient (API) producers use this material to synthesize substituted thiazoles, which are key structural elements in advanced antibiotics and selective antifungal agents. The compound delivers a consistent nucleophilic sulfur source for building thioamide functionalities during multi-step organic synthesis. Controlled batch-reactor addition and monitored reaction environments underpin in-process quality control, in alignment with global GMP and pharmacopoeial norms.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • European Pharmacopoeia section 04/2015:2570 (Thiazole derivatives)
    • US FDA 21 CFR Part 211 for finished pharmaceuticals
    • Chinese Pharmacopoeia Part II (API synthesis)

    Typical usage ratio

    • 5–14 mol% relative to aromatic thioamide precursors; precise adjustment based on target thiazole yield and downstream purity demands

    Downstream process integration

    • Introduced post-nitrile hydrolysis, immediately before heterocyclization stage; subsequent purification aligns with solvent extraction and column chromatography process flows

    Final product types

    • Bactericidal thiazole drugs
    • Anti-fungal excipients
    • API intermediates for clinical pipeline compounds
    • Registered pharmaceutical intermediates for export formulations

    2. Agrochemical Intermediate for Fluorinated Pesticides

    Leading agrochemical synthesis plants utilize this raw material as a building block for next-generation sulfur-fluorinated pesticide actives, especially in the construction of thioamide-bridge intermediates. These serve as core scaffolds for selective herbicides and pest-resistance enhancers, with precise input volumes guided by reaction kinetics and downstream formulation physicochemical profiles. Continuous-feed reactors and on-line impurity monitoring form part of the compliance and quality assurance workflow for all export-compliant production lots.

    Industry compliance standards

    • FAO/WHO Specification for Agricultural Pesticide Ingredients
    • ISO 9001:2015 Quality Management Systems
    • REACH Registration (EC 1907/2006) for novel intermediates
    • China National Standard GB 20800 (Pesticide Technical)

    Typical usage ratio

    • 0.8–2.5% by mass per batch, fine-tuned according to yield optimization models and active ingredient concentration targets

    Downstream process integration

    • Dosed during the early condensation phase, upstream of heterocyclic ring closure; in-line FTIR analysis validates batch progress prior to extraction and drying

    Final product types

    • Precursor intermediates for triazole fungicides
    • Active herbicidal agents for industrial crop protection
    • Process intermediates in patented insecticide pathways
    • Custom asymmetric pesticide actives with sulfur-fluorine motifs

    3. Fine Chemical Synthesis for Specialty Organic Intermediates

    Producers of specialty organic chemicals leverage this compound during synthesis of aromatic fluorinated thioamides, which serve as functional intermediates in dye, photoinitiator, and polymer additive industries. Process chemists employ precise stoichiometry to control substitution reactions, with attention to impurity profiles and recycling procedures for spent solvents to meet both product specification and sustainability goals.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management Systems for chemical synthesis plants
    • US EPA TSCA Inventory for synthetic organics
    • OECD Good Laboratory Practice for industrial chemicals
    • Japan Chemical Substances Control Law (CSCL) standards

    Typical usage ratio

    • 0.5–6.0 mol% in condensation or substitution steps depending on targeted product substitution pattern and downstream compatibility requirements

    Downstream process integration

    • Dosed during electrophilic aromatic substitution or coupling phase, frequently under inert atmosphere; work-up involves phase separation and vacuum distillation for quality assurance

    Final product types

    • Fluorescent dye intermediates
    • Photoinitiator bases for UV-cured coatings
    • Additive intermediates for engineering polymers
    • Specialty reagents for custom synthesis houses

    4. Advanced Material Precursor for Electronic Chemicals

    Manufacturers producing semiconductor process chemicals employ this material as a precursor for synthesizing sulfur- and fluorine-containing modifiers used in dielectric films and high-performance polymeric photoresists. Purity controls, trace-metal analysis, and micro-contaminant filtering are enforced from raw material reception through final intermediate isolation. Application-specific grades are validated through batch certification and spectroscopic fingerprinting.

    Industry compliance standards

    • SEMI C47 Specification for Electronic Grade Chemicals
    • ISO 9001:2015 and ISO 14644 (Cleanroom standards)
    • RoHS Directive (2011/65/EU) for restricted substances in electronics
    • IPC-5704 Clean Handling of Electronic Chemicals

    Typical usage ratio

    • 1.2–5 wt% for precursor formation, with ratio controlled by required degree of fluorination and electronic application purity standards

    Downstream process integration

    • Enters at the modifier synthesis stage, followed by high-vacuum distillation and multi-stage micro-filtration; chemical is tracked to prevent ion migration in sensitive device applications

    Final product types

    • Sulfur-fluorine modified dielectric polymers
    • Photoresist intermediates for advanced lithography
    • Semiconductor-grade anti-etch coatings
    • Functionalized surface treatment chemicals
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