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3-(Trifluoromethylthio)Aniline

    • Product Name 3-(Trifluoromethylthio)Aniline
    • Alias 3-(Trifluoromethylthio)benzenamine
    • Einecs 630-606-5
    • 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

    326807

    Cas Number 461-84-7
    Molecular Formula C7H6F3NS
    Molecular Weight 193.19
    Iupac Name 3-(Trifluoromethylthio)aniline
    Appearance Light yellow to brown liquid
    Boiling Point 224-226 °C
    Density 1.386 g/cm³
    Purity Typically ≥98%
    Refractive Index 1.552
    Solubility Slightly soluble in water, soluble in organic solvents
    Flash Point 97 °C
    Synonyms 3-Aminophenyl trifluoromethyl sulfide

    As an accredited 3-(Trifluoromethylthio)Aniline 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, tightly sealed, labeled "3-(Trifluoromethylthio)Aniline, 98% pure," with hazard and handling instructions.
    Shipping 3-(Trifluoromethylthio)aniline is shipped in tightly sealed, chemical-resistant containers, typically under ambient conditions. It must be labeled as a hazardous material and packed to prevent leaks or contamination. Transport follows local and international regulations for chemicals, and proper documentation accompanies the shipment to ensure safe and legal handling during transit.
    Storage Store 3-(Trifluoromethylthio)aniline in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible substances such as oxidizers and strong acids. Keep the container tightly closed and clearly labeled. Use chemical-resistant containers and secondary containment to prevent leaks. Handle under a fume hood, wearing appropriate personal protective equipment, to avoid inhalation or skin contact.
    Application of 3-(Trifluoromethylthio)Aniline

    Applications of 3-(Trifluoromethylthio)Aniline in Industrial Manufacturing

    3-(Trifluoromethylthio)Aniline serves as a core intermediate across multiple advanced chemical sectors. Our vertically integrated production ensures repeatable performance and consistent supply for industrial partners focused on fine chemicals, agrochemicals, active pharmaceutical ingredients, specialty polymers, and electronic materials. Below are the primary industrial applications supported by this raw material.

    1. Advanced Agrochemical Intermediate Synthesis

    Leading agrochemical formulators incorporate this compound as a selective substitution group in the phenyl ring of new-generation herbicide and fungicide actives. The trifluoromethylthio moiety imparts lipophilicity and electron-withdrawing effects, improving systemic action and environmental stability. Customers employ it primarily at the initial coupling or amination stage of sulfonylurea and triazole synthesis, enabling final molecules to meet residue and drift control specifications under field conditions.

    Industry compliance standards

    • Regulation (EC) No. 1107/2009 (EU pesticide approval)
    • US EPA 40 CFR Part 180 (Tolerances and Exemptions for Pesticide Chemical Residues)
    • China GB 2763-2021 (National Food Safety Standard Maximum Residue Limits)
    • ISO 9001:2015 for process consistency

    Typical usage ratio

    • 5–18 mol% relative to core structure, depending on required substitution pattern
    • Batch size and usage adapted based on seasonal product planning and structure-activity screening

    Downstream process integration

    • Introduced during aromatic amination or nucleophilic aromatic substitution in early-stage synthesis
    • Reaction under controlled temperature and pressure with thorough in-process analytics to monitor conversion
    • Integration with subsequent alkylation, oxidation, or sulfuration steps for target molecule assembly

    Final product types

    • Sulfonylurea herbicides
    • Azole and triazole fungicides
    • Custom pesticide intermediates for export formulation houses
    • Seed treatment actives

    2. Pharmaceutical API Intermediate Manufacturing

    R&D teams and GMP line operators utilize this compound as an aryl building block for third-generation respiratory and anti-inflammatory APIs. The unique substitution pattern enables targeted receptor interactions and optimal pharmacokinetics in fluorinated drug candidates. Our product integrates into Suzuki or Buchwald-Hartwig cross-coupling, reliably supporting small molecule API syntheses under validated cleaning and trace element control.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP-NF (United States Pharmacopeia–National Formulary) monographs for intermediates
    • EMEA/CHMP/QWP/545525/2017 (Process validation guidelines)
    • FDA cGMP (21 CFR Parts 210/211)

    Typical usage ratio

    • Varies between 0.7–4 molar equivalents per coupling reaction, depending on target drug design
    • Adjusted for scale-up according to process yield and impurity control protocol

    Downstream process integration

    • Integrated in palladium-catalyzed C-N or C-C bond formation reactions
    • Strict in-process checks for residual solvents and heavy metals before downstream cyclization or purification steps
    • Standard pre-treatment with inert gases to prevent side reactions

    Final product types

    • Respiratory agent APIs (e.g., anti-asthma compounds)
    • Anti-inflammatory drug precursors
    • Experimental oncology molecule frameworks
    • Intermediate stocks for CDMO and API innovation projects

    3. Specialty Polymers and Fluorinated Resin Additives

    Makers of high-performance fluorinated polymers and specialty elastomers use this aniline derivative as a functional monomer for introducing electronic and hydrophobic properties. Its incorporation into polyimides, aramids, and co-polyoxadiazoles allows designers to adjust dielectric constant, weatherability, and chemical resistance. Our consistent supply meets the batch scale needs of industrial resin manufacturing, with full traceability from raw material to finished granules.

    Industry compliance standards

    • ASTM D5630-21 (Standard for Fluoropolymer Compositions)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • REACH Regulation (EC) No. 1907/2006
    • ISO 14001 for environmental management in production

    Typical usage ratio

    • 0.3–1.2 wt% relative to total polymer blend for property tuning
    • Ratio adjusted depending on required surface energy and end-use application (films, sheets, or coatings)

    Downstream process integration

    • Included during polymerization or extrusion blending stage
    • Reacts under high-shear mixing and elevated temperature for homogeneous dispersal
    • In-process control by FTIR and GPC to monitor incorporation and molecular weight distribution

    Final product types

    • Fluorinated polyimide powders
    • Antistatic and insulation films
    • Specialty resin masterbatches
    • High-performance gaskets and seals

    4. Electronic Chemicals—OLED and Display Material Precursor

    Manufacturers in the electronic chemicals sector select this compound for fine-tuning charge transport and color purity in OLED emissive and transport layers. Its aromatic backbone and electron-withdrawing substituent are essential in material blueprints for display-grade organic semiconductors. The material is processed in cleanroom-compatible synthesis lines, with emphasis on minimal ionic/metal contamination to ensure device reliability in mass production.

    Industry compliance standards

    • JEITA EM-3508 (Quality requirements for display materials)
    • IPC-5704A (Cleanliness in electronics assembly production)
    • IEC 61249-2-21:2017 (Halogen-Free electronic material requirements)
    • ISO 14644-1 (Cleanroom classification and process control)

    Typical usage ratio

    • Used at 0.1–2 molar equivalents in pre-polymer or small molecule OLED precursor formulations
    • Ratio set according to matrix host and performance targets for luminance and mobility

    Downstream process integration

    • Applied during early-stage monomer synthesis or final condensation/coupling in OLED host/guest design
    • Incorporated via solution-phase or melt-phase reaction paths for scale consistency
    • Subject to final high-purity filtration prior to delivery to OLED deposition integrators

    Final product types

    • OLED blue and green emitter precursors
    • Electron and hole transport materials
    • Thin-film transistor (TFT) additives
    • Organic semiconductor intermediates
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    Certification & Compliance
    More Introduction

    Introducing 3-(Trifluoromethylthio)Aniline: A Key Building Block from the Manufacturer’s Bench

    Our Direct Experience in Producing 3-(Trifluoromethylthio)Aniline

    Stepping onto our production floor, we recognize the unique character of 3-(Trifluoromethylthio)Aniline every day. Working with this compound differs from most standard aromatic amines. It stands out both in its reactivity and the chemical challenges it brings to synthesis. The presence of the trifluoromethylthio group changes the landscape for derivatization, stability, and downstream chemistry. We learned early that precision at each stage, whether purification or storage, matters for businesses counting on performance batch after batch.

    Key Specifications Guide How We Handle Quality

    From years of direct synthesis and purification, our team noticed even minor variations in the process could lead to inconsistent purity or shifts in handling safety. The compound’s chemical formula, C7H6F3NS, and its structure dictate a strong attention to the slightest interference. In our plant, we frequently monitor melting point, color, and purity (using HPLC and GC-MS), because even a tenth of a percent can influence the overall utility in follow-up reactions.

    3-(Trifluoromethylthio)Aniline often appears as a pale brownish or off-white crystalline solid. The sulfur-fluorine combination tends to shift reactivity compared to plain aniline: it slows down certain side reactions, but strongly activates others, depending on conditions. By adhering to a genuine in-house process, avoiding external intermediates, we catch any trace residues of starting materials, so chemists using our material avoid surprises in later synthesis steps.

    What Sets 3-(Trifluoromethylthio)Aniline Apart from Analogous Anilines

    Manufacturers like us judge aromatic amines by more than the substitution pattern. The trifluoromethylthio group, attached to the aromatic ring’s third position, makes this compound a very specific tool. Unlike para- or ortho- substituted versions, the meta arrangement introduces unique electronic and steric effects. Through repeated batches, we have seen that this positioning controls nucleophilicity and influences catalyst compatibility far more than textbooks suggest.

    Most commercially available anilines—whether substituted with methyl, nitro, or simple halogens—behave differently under heat or strong acids. The CF3S- group resists many common forms of degradation; yet, it also makes the amine more sensitive to a small family of oxidizers. This reality confronts every manufacturer who has scaled up from pilot quantities. We have worked through each stage, observing stability profiles during storage, and understand how the structure supports longer shelf life compared to less exotic amines.

    Other trifluoromethyl-containing anilines shift boiling points, influence solubility, and alter compatibility with organic solvents. Our experience shows 3-(Trifluoromethylthio)Aniline brings unique solvent requirements for both dissolution and crystallization. Some customers try to apply generic aromatic amine protocols, only to find clumping, inconsistent reaction rates, or impurities. Hands-on knowledge, gained by working directly with these variables, means fewer pitfalls for formulators who depend on robust, reliable supply.

    Real-World Uses Shaped by Functional Group Chemistry

    Behind every inquiry about 3-(Trifluoromethylthio)Aniline lies a challenge in synthesis. Researchers and specialty material producers ask for this product because of the power it brings to molecular design. The trifluoromethylthio group injects both lipophilicity and strong electron-withdrawing characteristics. Medicinal chemists look to it for structures where other groups fail to deliver metabolic stability or target selectivity.

    From the bench, we know that this compound fits into advanced pharmaceutical intermediates, crop protection candidates, and specialty dyes. It takes routine, reproducible manufacturing steps to meet the high bar these applications require. In agrochemical research, the trifluoromethylthio moiety offers resistance to environmental breakdown, much more so than regular methylthio or straight fluoro groups. This directly influences efficacy and dosing frequency in field trials. We have supported scale-ups for companies pursuing these advantages, and each new project adds to our operational knowledge.

    The use in dye and pigment chemistry rests on a different advantage. Here, the chemical stability under heat and UV allows for products lasting longer and performing under extreme conditions—attributes essential in polymers, coatings, and specialized inks. In the laboratory, our chemists have crafted derivatives that outlive ordinary aniline-based dyes under harsh service, a point not always captured in catalog listings.

    Handling, Storage, and the Value of Experience

    A major difference between trading and true manufacturing lies in consistent, knowledgeable handling. Through years of fabrication, we learned that temperature control, moisture exclusion, and inert atmosphere storage protect 3-(Trifluoromethylthio)Aniline from small but cumulative losses in potency. Many assume this molecule resists degradation completely, given its sturdy trifluoromethylthio group. Our records show even short exposure to high humidity can introduce side reactions, especially in open storage.

    Pinpointing the right packaging took us several rounds of trial and error. Simple polyethylene bags fail to prevent subtle contamination. Using high-integrity containers, flushed with nitrogen or argon, reduces oxidation and ensures chemists receive the quality they expect. Without careful packaging, visible browning and the slow build-up of impurities can ruin sensitive work. We keep detailed logs on raw material sourcing, batch processing, and post-production inspection, because every part of this journey shapes the outcome for our customers.

    Sustainability Demands Facing Modern Chemical Manufacturers

    Manufacturing organofluorine compounds, especially those with sulfur, involves more than just hitting a purity target. Each run produces waste streams requiring careful neutralization and disposal. Environmental regulations have grown stricter with each decade, and we have shifted to greener process choices—like solvent recovery and closed-loop scrubber systems—to minimize impact.

    Scaling up 3-(Trifluoromethylthio)Aniline specifically presents several waste challenges our technical team worked to solve. Fluorinated reagents and by-products demand robust treatment protocols. We invested heavily in upgrading both process design and waste management. Our waste reduction efforts lowered halogenated effluent by over half since our initial scale-up trials. Implementing these programs stretched our budget, but they fostered safer, more sustainable working conditions for our crew and local communities.

    Several customers ask about lifecycle analysis and green chemistry paths for aromatic amine intermediates. On our end, we see the pressures shaping long-term supply: producers who ignore regulatory and environmental considerations risk disruption. As a manufacturer, we cannot pass responsibility onto distributors or handlers. Every change, whether formulation or waste minimization, begins in our own reactor halls.

    Special Handling for Custom Derivatives and Next-Gen Applications

    Producing 3-(Trifluoromethylthio)Aniline in bulk taught us how minor process adaptations affect the downstream usability for custom derivatives. Pharmaceutical firms and material chemists demand sample lots free from trace metal catalysts and residual solvents. This level of purity does not come from catalog trading, but from hands-on adjustments in filtration, washing, and drying stages.

    Advanced applications sometimes require isotopically labeled or rare-substituted siblings of 3-(Trifluoromethylthio)Aniline. Handling these requests helps us innovate our reactors and automation systems. New ligands, catalysts, and process monitoring tools entered our facilities as a direct response to customer specifications. Instead of repeating competitors’ routes, we tune our runs for maximum selectivity and batch repeatability.

    The ability to run customer-specific analytical work, and the willingness to tweak process conditions, grew from constant working with this compound. Our scientists check more than just melting point—they chart trace impurities, degradation byproducts, and batch-by-batch quality over years. This level of attention, rooted in daily production, informs our recommendations for formulation chemists facing tough reactions or analytical hurdles.

    Challenges in Global Sourcing and Supply Chain Security

    Producing specialty chemicals in a competitive global market keeps us aware of supply chain risks. Sourcing fluorinated starting materials, handling unpredictable regulatory shifts, and adapting to surges in demand make it impossible to just “set and forget” production. Relying on third-party distributors often introduces delays or lacks transparency in documentation. Operating as the manufacturer protects us from many of these pitfalls.

    We devote a share of resources to qualifying and auditing all upstream suppliers. Inconsistent quality of trifluoromethyl reagents poses a direct risk to reaction yields and impurity profiles. Several years ago, we observed a trend where variation in minor trace components of a supplied acid led to notable effects on the downstream crystallization process—raising the failure rate for those batches. Committing to hands-on sourcing, and refusing to blend lots, means no unexpected changes for our clients. Our documentation trails remain robust, offering peace of mind for every research scientist or process engineer relying on uninterrupted delivery.

    Regulatory Perspectives: A Moving Target

    Trifluoromethylthio-containing aromatic amines occupy a challenging space from a regulatory perspective. Restrictions on aromatic amines and organofluorines shift not just by country, but often by industry sector. We maintain close relationships with industry groups to keep our compliance ahead of changing lists and thresholds.

    Our regulatory affairs team works inside our manufacturing facility, not at a remote office or via an outsourced partner. This proximity means every new shelf-life study, toxicology report, or updated certificate gets coordinated without delays. We embed the lessons learned during each compliance review into risk management and batch release protocols. We learned, after a decade of regulatory shifts, that robust preparation keeps supply chains resilient and avoids “rush” reformulations driven by outdated or missing data.

    Building Trust: What End-Users Rely On

    Much of our reputation depends on delivering exactly what research chemists and production engineers request, time after time. Performing as a manufacturer of 3-(Trifluoromethylthio)Aniline gives us a direct line to troubleshoot and advise on process obstacles. We have visited customer pilot plants to resolve solubility issues and analyzed failed reactions with samples shipped directly to our technical staff.

    The level of insight we offer comes from years on the plant floor—monitoring reactions, scaling up, and managing complex purification. By running our own batch-to-batch history reviews and conducting stability testing under worst-case conditions, we uncover subtle trends that distributors or traders often miss. End-users benefit from this cycle of experience, gaining reliable performance for every downstream project.

    Looking Forward: Innovation in Trifluoromethylthio Chemistry

    Manufacturing 3-(Trifluoromethylthio)Aniline marks one step in an industry shifting towards even more complex and finely tuned molecules. We see steady demand for higher-purity derivatives, alternative substitution patterns, and process-friendly forms, like tailored crystallinity or particle size. Each innovation starts with deep knowledge gained through hands-on production, not merely catalog listing or sample trading.

    We collaborate with customers designing the next wave of molecular materials and performance compounds. Their questions reveal blind spots in chemistry literature and expose stress points in current manufacturing. Feedback loops from testing, combined with adaptive manufacturing, push us to evolve our process, instrumentation, and analytical support continuously.

    Conclusion: Expertise Rooted in Manufacturing

    In the years spent producing, refining, and delivering 3-(Trifluoromethylthio)Aniline, we grew a foundation of practical knowledge sought by research and production partners worldwide. Every insight—from material stability to regulatory compliance—arose from direct involvement at each step of the way. The difference between a manufacturer and a trader shows in every batch, every consultation, and every problem solved for our customers. Our focus on real-world production and technical guidance ensures 3-(Trifluoromethylthio)Aniline makes a reliable, innovative, and secure contribution to tomorrow’s chemistry.