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2-(Trifluoromethyl)Phenylthiourea

    • Product Name 2-(Trifluoromethyl)Phenylthiourea
    • Alias TFMTU
    • Einecs 246-211-2
    • 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
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    Specifications

    HS Code

    119411

    Chemical Name 2-(Trifluoromethyl)Phenylthiourea
    Molecular Formula C8H7F3N2S
    Molecular Weight 220.22 g/mol
    Cas Number 1114-97-8
    Appearance White to off-white solid
    Melting Point 140-143°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=CC=C(C(=C1)C(F)(F)F)NC(=S)N
    Inchi InChI=1S/C8H7F3N2S/c9-8(10,11)6-3-1-2-5(4-6)13-7(12)14/h1-4H,(H3,12,13,14)

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

    Packing & Storage
    Packing A 25-gram amber glass bottle sealed with a screw cap, labeled "2-(Trifluoromethyl)Phenylthiourea," including hazard symbols and lot information.
    Shipping 2-(Trifluoromethyl)Phenylthiourea is shipped in tightly sealed containers to prevent moisture and contamination, complying with chemical safety regulations. It is transported as a non-hazardous material under normal conditions, but should be stored in a cool, dry place and handled with appropriate personal protective equipment during transit.
    Storage 2-(Trifluoromethyl)Phenylthiourea should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Store at room temperature and avoid excessive heat. Ensure the storage area is clearly labeled, and handle with appropriate personal protective equipment to prevent skin and eye contact.
    Application of 2-(Trifluoromethyl)Phenylthiourea

    Applications of 2-(Trifluoromethyl)Phenylthiourea in Industrial Manufacturing

    2-(Trifluoromethyl)Phenylthiourea is a specialized intermediate favored in high-value industries requiring tightly controlled functionalization. Our large-scale, high-purity production supports integrated supply for diverse chemical markets. Below we detail major industrial application routes, each with associated quality, process, and formulation guidance.

    1. Pharmaceutical Intermediate for Thiohydantoin Synthesis

    Pharmaceutical manufacturers apply 2-(Trifluoromethyl)Phenylthiourea as a key reactant in the synthesis of advanced thiohydantoin-based drug scaffolds. Its electron-withdrawing group supports selectivity and efficiency during heterocycle formation, crucial for structure-activity optimization in API development. The raw material enters multi-step syntheses after initial condensation, and precise control over input ratio and purity safeguards compliance with regulatory standards for traceability and impurity limits in human therapeutics.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • Ph. Eur. and USP monograph guidelines on raw material purity
    • 21 CFR Part 211: US cGMP for finished pharmaceuticals
    • EDQM trace impurity requirements

    Typical usage ratio

    • 0.90–1.10 molar equivalents in heterocycle-forming reactions relative to partner amine or carbonyl functional groups
    • Adjustments depend on target molecule substitution pattern and reaction scale from pilot to commercial batches

    Downstream process integration

    • Added directly to condensation or cyclization reaction vessels following raw material assay and preblending
    • Often dissolved in polar aprotic solvents for enhanced reactivity and controlled temperature ramping
    • Integrated into multi-step synthesis with rigorous intermediate sampling for quality control

    Final product types

    • Thiohydantoin-based oncology agent precursors
    • CNS-active pharmaceutical intermediates
    • Sulfur-containing modulators for cardiovascular drug leads
    • Custom research molecules with CF3-substituted heterocyclic cores

    2. Agrochemical Synthesis – Herbicide and Pesticide Intermediates

    Agrochemical firms employ 2-(Trifluoromethyl)Phenylthiourea during the early-stage synthesis of thiourea-linked active substances. Its fluorinated aromatic moiety boosts bioactivity and field stability. Integration occurs in the construction of heterocycle or urea bridges, and downstream plants enforce strict monitoring to comply with global environmental and residue legislation for crop protection agents. Ratio tuning ensures target molecule yield and minimizes waste.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH (EC 1907/2006) substance registration for European markets
    • EPA Pesticide Registration Guidelines
    • ISO 9001 Quality Management System Certification

    Typical usage ratio

    • 0.95–1.05 molar ratios vs. chlorinated or carbonyl partner compounds
    • Application rates tailored by synthesis route and target agrochemical activity profile

    Downstream process integration

    • Dosed via automated feed at the cyclization, urea coupling, or thiolation stage
    • Tested for residual contaminants and conversion efficiency before intermediate isolation
    • Processed under inert gas to protect sensitive functional groups

    Final product types

    • Thiocarbamate herbicide intermediates
    • CF3-aryl substituted fungicide scaffolds
    • Systemic pesticide key building blocks
    • Nematicide precursors for soil treatments

    3. Dye and Pigment Manufacture—Functional Dye Intermediates

    Specialty dye manufacturers use 2-(Trifluoromethyl)Phenylthiourea as a modifying agent in synthesizing sulfur-rich, electron-withdrawing dye intermediates. Its specific reactivity helps create unique chromophores with altered photophysical properties required for high-performance textile, inkjet, and optical dyes. Puity profile and byproduct minimization align with current industry standards for colorant safety and performance testing.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textiles
    • GHS (Globally Harmonized System) label requirements
    • EU REACH Annex XVII restrictions on amine contaminants
    • ISO 1833 and EN 71-3 for pigment analysis

    Typical usage ratio

    • 0.85–1.20 equivalents based on desired chromophore functionalization degree
    • Adjusted to control shade depth and fastness properties

    Downstream process integration

    • Charged at diazotization or coupling reaction stage in closed vessels
    • Dissolved in alkaline or buffered media to enhance coupling efficiency
    • Process includes real-time monitoring of conversion and color strength

    Final product types

    • Sulfur-bridged anthraquinone dyes
    • CF3-phenyl azo dye intermediates
    • High-performance inkjet pigment precursors
    • Fluorescent textile dye molecules

    4. Electronic Chemicals—Organic Semiconductor Synthesis

    Producers of organic semiconductors utilize 2-(Trifluoromethyl)Phenylthiourea in constructing sulfur linkages for small-molecule and polymeric compounds in electronic device fabrication. The introduction of trifluoromethyl and thio functionalities modulates electron transport and stability, especially for organic field-effect transistors (OFETs) and organic photovoltaics. Manufacturing mandates enhanced material purity and trace-metal controls in line with advanced electronics protocols.

    Industry compliance standards

    • IEC 60749 testing protocols for semiconductor materials
    • JEDEC JESD22 standards for organic electronic substrates
    • RoHS Directive (Restriction of Hazardous Substances)
    • Customer-specific purity specs for high-mobility semiconductor grades

    Typical usage ratio

    • Targeted usage of 1.00 molar equivalent in thiourea-forming stages
    • Fine tuning based on molecular weight and charge carrier mobility targets of the polymer or oligomer

    Downstream process integration

    • Blended with aryl halides or diimines in controlled-atmosphere reactors
    • Reaction steps synchronized with continuous-flow synthesis for batch uniformity
    • Analytical validation at each stage for trace contamination and homogeneity

    Final product types

    • Charge-transport polymer intermediates
    • OFET active layer precursors
    • Solution-processable organic photovoltaic components
    • CF3-substituted electron transport materials

    5. Analytical Chemistry—Selective Reagents for Metal Detection Kits

    Analytical kit manufacturers incorporate 2-(Trifluoromethyl)Phenylthiourea as a selective chelating reagent for trace metal ion detection. Its high affinity for soft metal cations forms colorimetric complexes used in rapid testing solutions. Precise formulation with controlled substance ratios ensures robust detection sensitivity and shelf-life for commercial lab kits under regulatory chemical safety regimes.

    Industry compliance standards

    • ISO/IEC 17025 for laboratory reagent traceability
    • EU CLP Regulation (EC No 1272/2008) for chemical labeling
    • Good Laboratory Practice (GLP) for analytical kit assembly
    • ASTM D3223 test procedures for water analysis

    Typical usage ratio

    • 5–20 mg per reaction vial for trace detection (sub-ppm sensitivity)
    • Formulation optimized for specific kit design and detection threshold

    Downstream process integration

    • Premeasured and sealed into single-use test kits under dry nitrogen
    • Homogenized in aqueous or mixed-solvent buffers during final assembly
    • Subjected to QC checks for batch-to-batch reagent performance

    Final product types

    • Copper ion test strips
    • Nickel and mercury rapid screening kits
    • Trace heavy metal detection panels for environmental labs
    • Analytical test packs for industrial water systems
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    More Introduction

    2-(Trifluoromethyl)Phenylthiourea—A Manufacturer’s Perspective

    Understanding 2-(Trifluoromethyl)Phenylthiourea From the Ground Up

    From our production floor, 2-(Trifluoromethyl)Phenylthiourea—sometimes recognized by its structural shorthand, TFPTU—arrives in a crystalline form with a purity surpassing 98%. After years of refining both process and quality control, the outcome rarely leaves any doubts in its clarity or stability. For clients who demand a reliable base chemical for synthesis or advanced research, clear batch consistency spells confidence. Over our decades working in fine chemistry, consistency isn’t an empty promise, it’s a track record built through strict controls, disciplined raw material sourcing, and regular in-house quality testing.

    TFPTU’s uniqueness comes from its core structure: a phenylthiourea ring decorated with a trifluoromethyl group at the ortho position. This particular arrangement helps steer reactivity and offers properties seldom matched by thiourea analogues. Down the years, we have seen demand grow along with the increasingly sophisticated needs of those working at the interface of medicinal chemistry, agrochemical development, and specialty material synthesis. Customers often approach us after less specific thiourea derivatives fail to deliver selectivity, solubility, or thermal stability in their target reactions.

    What Sets TFPTU Apart in the Real World?

    Some ask why a trifluoromethyl group in the 2-position changes the game. We have watched the evolution ourselves. Standard phenylthiourea serves as a building block for many applications, but lacks the electron-shifting capabilities the fluoroalkyl group brings to the table. The result: TFPTU offers stronger electron-withdrawing effects, which opens new doors in synthesis. Take pharmaceuticals, for example—adding trifluoromethyl groups tends to boost metabolic stability and bioavailability. That simple upgrade in molecular structure translates into real-world improvements in shelf life and performance of the resulting drug candidates. In agrochemicals, similar substituents often mean greater resistance to environmental breakdown and greater selectivity toward target species.

    Compared to straight thiourea or its alkyl-substituted cousins, our TFPTU provides better lipophilicity and chemical versatility. Reactions, particularly those involving nucleophilic aromatic substitution or targeted thiourea condensation, see cleaner conversions and fewer by-products—the kind of efficiency that matters when you run larger batches. During scale-up, minor differences can cost hours and kilograms. These are the details that stand out on the plant floor, not just in the textbook.

    From Synthesis to Storage—Production Insights and Specifications

    TFPTU does not just roll off the line. Our process involves a careful reaction between 2-trifluoromethylaniline and thiocyanate reagents under controlled temperature and pH. Over the years, tweaks in reagent ratios and solvent selection have reduced impurity carryover and ensured that specifications don’t sag as volumes swing up and down. Most of our batches offer a melting point in the 112–115°C range, clear identity spectrum, and low moisture content. Hazard controls keep dust and vapors in check, not only for product quality but for the well-being of crews who handle open reactors and dryers.

    What matters most on the user side is stability and ease of handling. TFPTU holds up well in ambient storage. It resists caking and degradation, even over extended periods, as long as it’s shielded from direct moisture and oxidizing agents. This resilience simplifies inventory strategies for formulators and researchers alike—no chorus of complaints about tricky storage, lost potency, or unexpected contamination. Standard polyethylene drums or double-lined fiber containers work for bulk; smaller jobs go out in sealed glass or fluoropolymer bottles.

    Direct Applications—Where TFPTU Works Best

    Across our customer base, TFPTU’s sweet spot shows up in three main arenas: intermediate synthesis for specialty organics, pharmaceutical research, and crop science. In research labs, TFPTU serves as a flexible ligand or as a scaffold for complex heterocyclic compounds. Medicinal chemists value the fluoro group’s contribution to metabolic stability—sometimes it’s the only way new candidates pass key bioassays. TFPTU derivatives have appeared in patent filings for fungicides, anti-inflammatory agents, and enzyme inhibitors.

    For manufacturing routes, TFPTU often ends up as a step in multi-stage syntheses, where its sulfur and nitrogen atoms provide handles for further functionalization. Sulfur chemistry brings a lot of challenge, and the predictable reactivity of TFPTU beats less stable thioureas for condensation or cyclization steps. We often field requests for custom scale batches where TFPTU forms the fulcrum between commodity building blocks and unique end products. This position in the synthesis chain means reliability and reproducibility matter more than in lab-only use cases; we have to keep impurity levels low and batch variations even lower.

    Agrochemical formulators line up for TFPTU when seeking alternatives to basic thiourea because environmental agencies keep tightening the noose on persistence and non-specific toxicity. The added trifluoromethyl group can deliver both better selectivity and improved breakdown profiles, which makes for easier compliance—regulatory approval moves faster and finished formulations perform more predictably under field conditions.

    Typical Customer Challenges—And Manufacturer Solutions

    Producing 2-(Trifluoromethyl)Phenylthiourea at scale, cost, purity, and batch-to-batch reliability throws out some hurdles. Over the years, we have adapted our oxidation and filtration steps to reduce secondary product formation. Early on, even minor fluctuations in pH or mixing speed at the thiourea formation stage could tilt impurity profiles unfavorably. By investing in automated in-line pH monitoring, tighter temperature controls, and higher-purity input streams, we have lowered reject rates and held purity levels firm.

    Once, moisture uptake during packaging led to some caking and analytical drift in summer shipments. Now, we run our final drying in controlled-atmosphere chambers, then seal under nitrogen. These tweaks don’t show up in the brochure, but they show up in fewer support calls and repeated orders.

    Some users, especially in pilot plants, want more than purity. Particle size, bulk density, and flow characteristics matter, especially when dosing by weight or integrating into continuous reactor feeds. On the production floor, a dusting issue can turn an otherwise tidy process into a headache for both operator safety and metering accuracy. To address this, we calibrate our milling and screening operations to hit a 150–300 microns size spread—tight enough for predictable handling, loose enough to keep it from packing like flour. Shipment includes a certificate listing these granular details, so customers see exactly what they’re working with.

    Regulatory and Environmental Considerations

    Sourcing and offering TFPTU brings us face-to-face with the escalating patchwork of regulatory frameworks. Whether it’s REACH registration in Europe, TSCA listings in North America, or new chemical inventory requirements in Asia, the scrutiny grows each year. As manufacturers, we commit to providing full analytical dossiers, updated toxicological data, and product stewardship documentation. End-users demand traceability—where did the raw materials come from, what are the byproducts, what are the hazard codes? Our investment in third-party verification and internal hazard mapping means when a customer calls for proof or additional data, we are ready.

    Waste reduction and emission control are not just environmental buzzwords—they are now critical cost and compliance factors. By closing solvent loops and installing on-site abatement units, our process effluent contains a fraction of the organosulfur load typical of older generation plants. We return spent catalysts to reclaim facilities and offer take-back programs for empty bulk packaging at customer sites. These steps grew from the need to comply, but now form part of our standard operating procedures; over the long haul, both the environment and our bottom line benefit.

    Customers in Europe and Japan have asked for evidence on both bioaccumulation potential and environmental breakdown of TFPTU. By commissioning independent studies, we can provide solid data that the fluoromethyl substitution does not increase persistent bioaccumulative properties compared to basic phenylthiourea. Regulatory comfort with this reality keeps downstream users free from late-stage surprises during their product registrations.

    Why Choose TFPTU Over Similar Thioureas?

    We regularly field questions about how 2-(Trifluoromethyl)Phenylthiourea performs against the broader field of thioureas—methyl, ethyl, or cycloalkyl variants, and even pyridyl or naphthyl analogues. In real applications, the distinction comes down to both physical-chemical properties and regulatory footing. Methyl- and ethylphenylthioureas offer some increase in selectivity and reactivity profile, but they falter in physical stability under heat or aggressive reaction conditions. TFPTU shrugs off most such stresses without discoloration or rapid breakdown.

    Some customers point to price differences—why not just cut cost with a non-fluorinated substitute? The answer lies in yields and performance. Substituting TFPTU with a bulkier or less electron-deficient thiourea often means more unreacted starting material, lower selectivity, and more time cleaning up by-products. For customers producing high-value pharmaceuticals or advanced intermediates, these material inefficiencies quickly swamp any savings from cheaper feedstocks. As a rule, the value proposition for TFPTU is strongest in high-complexity, high-reliability applications. Lower-value processes can stick to the basics.

    Users who have switched often tell us that analytical profiles for their downstream products tighten considerably. Melting point ranges distill down, HPLC traces show fewer tailing peaks, and required purification steps shrink. These feedback loops have allowed us, as manufacturers, to refine TFPTU grades further for mission-critical pharmaceutical and specialty chemical applications.

    Supporting Customers—Beyond the Drum

    In manufacturing, the conversation does not end once we ship. We stay on call for cross-lab method transfer, pilot scale troubleshooting, and on-site technical support. New reaction projects sometimes hit snags that trace back to unforeseen reactivity quirks or physical blending issues. Because we control our entire process, we can pull batch records, run targeted analyses, and supply tailored application notes to help partners keep their timelines intact.

    Flexibility in packaging, custom purifications, or co-processing requests happens routinely. Our ability to produce TFPTU in lots from grams to hundreds of kilograms, and to deliver under hazardous material protocols, owes itself to an integrated plant-floor organization. Customers in regulated industries prefer a direct pipeline to the actual producer, not just a logistics middleman. We maintain transparency about production changes, batch releases, and analytical testing so users know the real status of their supply chains.

    Inventory reliability stands as another competitive edge. Every year brings spikes in commodity costs, changes in regulatory status for amine and fluorine-derived inputs, or disruptions from weather or geopolitics. Longstanding partnerships with raw material suppliers, plus contingency stocks for mission-critical reagents, keep us from running short or offering excuses about delays. In the world of specialty chemicals, dependability often matters more than any individual test parameter.

    Looking Forward—TFPTU’s Future in Fine Chemistry and Beyond

    As markets for specialty organosulfur compounds expand, we see TFPTU taking on more roles outside the classic pharmaceutical and agrochemical domains. Polymer and coating industries, in particular, are starting to explore fluoro-substituted thioureas as chain extenders or adhesion promoters where resistance to harsh conditions is prized. Our continued R&D includes partnering with academic and industrial teams on new application areas, sharing our data, and visiting customer sites to understand pain points that lab-scale literature often overlooks.

    Industry focus on sustainability and tighter regulation puts pressure on both price and performance. By investing early in greener chemistry routes, waste minimization, and real-time process analytics, we not only future-proof our offerings but help our customers navigate their own compliance and innovation challenges. By building trust through data, delivering consistently reliable batches, and leaning into customer-specific needs, we see both the science and business of TFPTU production delivering for everyone involved.

    2-(Trifluoromethyl)Phenylthiourea is more than just a chemical SKU for us: it is a reflection of how hands-on production, accountability, and customer-driven improvements build better results. Our years in the trenches—dealing with process upsets, customer emergencies, and regulatory curveballs—have shown us that chemistry rarely takes the easy path. But with clear communication from the factory floor to the bench, problems get solved, and innovation moves forward.