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(2-Chloro-5-Trifluoromethyl)Phenylthiourea

    • Product Name (2-Chloro-5-Trifluoromethyl)Phenylthiourea
    • Alias 1-(2-chloro-5-(trifluoromethyl)phenyl)thiourea
    • Einecs 629-071-2
    • 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

    837329

    Iupac Name 1-[(2-chloro-5-(trifluoromethyl)phenyl)]thiourea
    Cas Number 1984-07-8
    Molecular Formula C8H6ClF3N2S
    Molecular Weight 254.66
    Appearance White to off-white solid
    Melting Point 115-117°C
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Smiles C1=C(C=C(C(=C1)Cl)NC(=S)N)C(F)(F)F
    Synonyms N-(2-Chloro-5-(trifluoromethyl)phenyl)thiourea
    Storage Temperature Store at 2-8°C
    Ec Number 217-860-9
    Hazard Statements Irritant

    As an accredited (2-Chloro-5-Trifluoromethyl)Phenylthiourea factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g (2-Chloro-5-Trifluoromethyl)Phenylthiourea comes sealed in a labeled amber glass bottle with safety and hazard warnings.
    Shipping (2-Chloro-5-Trifluoromethyl)Phenylthiourea is shipped in tightly sealed containers, protected from moisture and light. The package is labeled according to hazardous material regulations. It is transported under ambient conditions, with precautionary measures to prevent leaks or spills. Appropriate documentation and Material Safety Data Sheets (MSDS) accompany every shipment for safe handling and compliance.
    Storage Store (2-Chloro-5-Trifluoromethyl)Phenylthiourea in a tightly sealed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers. Protect from moisture, direct sunlight, and sources of ignition. Properly label the container and keep it in a designated chemical storage cabinet. Use appropriate personal protective equipment when handling the chemical to prevent exposure.
    Application of (2-Chloro-5-Trifluoromethyl)Phenylthiourea

    Applications of (2-Chloro-5-Trifluoromethyl)Phenylthiourea in Industrial Manufacturing

    (2-Chloro-5-Trifluoromethyl)Phenylthiourea is a specialty intermediate used by advanced manufacturers in several tightly regulated downstream sectors. Our material is production-proven at scale, with clearly defined use cases focused on specialty chemical synthesis, agrochemical formulation, and dye manufacturing. Each scenario detailed below relies on direct technical partnerships, practical production experience, and rigorous compliance traceability according to industry-specific demands.

    1. Pharmaceutical Intermediates Synthesis

    Process chemists in the pharmaceutical sector use this compound as a selective intermediate for synthesizing complex heterocyclic structures, particularly in targeted active pharmaceutical ingredient (API) pathways where halogen and trifluoromethyl substitutions demand strict impurity control. During multi-step API synthesis, it functions as a thiourea donor to form key sulfur-containing moieties that no direct alternatives can replace at parity for regiochemistry or stability. Manufacturers depend on fully traceable raw material supply with batch-level certification to minimize regulatory risk.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients)
    • USP–NF (United States Pharmacopeia–National Formulary) relevant impurity and residual solvent limits
    • Chinese Pharmacopoeia ChP 2025 for APIs
    • EU EudraLex GMP Vol. IV for chemical raw materials

    Typical usage ratio

    • 5–15 mole% relative to intended heterocyclic core during sulfur incorporation stage, adjusted by target API and step yield optimization data

    Downstream process integration

    • Charged during mid-sequence condensation or cyclization as a discrete batch addition under inert atmosphere; downstream purification includes aqueous workup and recrystallization to isolate clean intermediates for API finishing

    Final product types

    • Halogenated thiazole/benzothiazole API precursors
    • Anti-inflammatory and antifungal small molecules
    • Custom contract-manufactured API building blocks

    2. Agrochemical Synthesis (Herbicide & Fungicide Active Ingredients)

    Agrochemical formulators incorporate this material as a sulfur-containing intermediate when producing advanced phenylthiourea-derived pesticides, enabling controlled reactivity profiles for both contact and systemic modes of action. Unique substitution patterns boost both field stability and bioactivity, which downstream technical customers document for regulatory dossiers. Adherence to international agrochemical legislation requires full formulation transparency with respect to residuals and conversion efficiency.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 for production quality
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) for importation into the EU
    • GLP (Good Laboratory Practice) batch documentation for regulatory submission

    Typical usage ratio

    • 0.2–2% w/w in technical concentrate synthesis as a reactive intermediate; adjusted according to target ai (active ingredient) synthesis route and pilot-scale kinetic data

    Downstream process integration

    • Introduced during sulfonation or thiourea condensation stage of pesticide synthesis, followed by neutralization and filtration; technical grade product is purified before formulation into EC, WP, or SC end-use products

    Final product types

    • Systemic fungicide actives (e.g., for rice sheath blight or wheat rust)
    • Phenylthiourea herbicide technical concentrates
    • Pre-mixed agricultural pesticide formulations

    3. Specialty Dye Intermediate

    Textile and paper dye manufacturers utilize (2-Chloro-5-Trifluoromethyl)Phenylthiourea for synthesizing high-performance sulfur dyes and vat dyes. Its halogen and trifluoromethyl groups produce unique colorfastness, shade intensity, and wash durability results, working as a coupling or color base-building agent. Our quality system tracks every batch from synthesis through blending to ensure reproducible chromatic properties, supporting downstream operations under strict industry color and migration criteria.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for restricted substances
    • EN 71-3 (Migration of certain elements for textiles and paper)
    • ISO 105 (A02–A05) fastness standards for commercial dyes
    • ZDHC MRSL Level 1/2 chemical supplier conformance

    Typical usage ratio

    • 0.5–3% based on dye bath concentration; formulation may vary depending on desired chromophore, shade, and substrate absorption dynamics

    Downstream process integration

    • Added at core stage of dye molecule synthesis via batch-wise condensation; post-reaction workup includes acidification and solvent extraction prior to solid-state blending

    Final product types

    • High-purity vat dyes for cotton and cellulosic fibers
    • Sulfur-based dyes for viscose and paper applications
    • Reactive dye intermediates used for garment and industrial textile finishing

    4. Electronic Chemicals: Organic Semiconductor Synthesis

    Specialty electronic chemical producers leverage phenylthiourea derivatives for constructing functionalized organic semiconductors, especially for optoelectronic devices and specialized sensors. Trifluoromethyl and chloro substituents tailor charge mobility and environmental robustness—essential for fabricating stable thin-film layers. Process integration focuses on purity control, with our raw material supplied under tightly closed systems and validated with comprehensive contaminant profiling as required by high-purity electronics standards.

    Industry compliance standards

    • IEC 62697 for chemicals in electronic applications
    • ISO 9001:2015 and ISO 14001:2015 for Environmental Management
    • RoHS 3 (EU Directive 2015/863) substance restrictions
    • JCSS-accredited analytical batch testing (Japanese Industrial Standards)

    Typical usage ratio

    • 1–8 mol% relative to monomer or substrate in organic semiconductor polymerization processes, defined by targeted layer thickness and device specifications

    Downstream process integration

    • Fed during functional polymer synthesis, either in solution-phase or via vapor deposition precursor preparation; purified through fractional recrystallization and chromatographic steps before device deposition

    Final product types

    • Organic thin-film transistors (OTFTs)
    • Optical sensor active coatings
    • Organic LED (OLED) material precursors

    5. Fine Chemicals: Advanced Ligand or Catalyst Precursor

    Producers of high-value fine chemicals employ this raw material for the in situ formation of custom ligands or as a building block for sulfur- and halogen-containing catalysts. Its precise stoichiometry and electron-withdrawing groups impart unique reactivity that benefits transition metal coordination and redox catalyst activity. Materials management follows validated protocols, where we provide detailed certificate of analysis (COA) and impurity trace files supporting REACH or regional chemical registration.

    Industry compliance standards

    • REACH Annex VII-VIII registration for fine and specialty chemicals
    • ISO 17034:2016 for reference material producers
    • Responsible Care® chemical supplier code
    • Local customs registration for advanced intermediates

    Typical usage ratio

    • 0.1–1.5 molar equivalents per metal center or target catalyst compound, defined by reaction type and scale-up reports

    Downstream process integration

    • Metered during batch or continuous flow synthesis of ligand frameworks or pre-catalyst assemblies; followed by downstream metalation, scavenging, and performance validation against application targets

    Final product types

    • Palladium or platinum complex catalysts for fine chemical synthesis
    • Heterogeneous supported catalyst beads
    • Advanced chelate ligands for process chemistry
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    Certification & Compliance
    More Introduction

    Introducing (2-Chloro-5-Trifluoromethyl)Phenylthiourea: Built for Precision Applications

    Real Experience with Chemical Manufacturing

    Years in the chemical synthesis field have shown which molecules offer both consistency and versatility. Among the compounds in our catalogue, (2-Chloro-5-Trifluoromethyl)Phenylthiourea stands out for its stability, distinct functional groups, and compatibility with demanding synthesis routes. We have spent years refining its synthesis, keeping batch-to-batch purity above industry benchmarks. Every step, from raw input selections to precise reactor controls, contributes to a product intended for laboratories and pilot-scale manufacturing lines that demand material uniformity and reliable performance.

    Model and Specifications: Standards Informed by Real Chemistry

    Through direct feedback from partner labs and clients, our current model reflects a careful balancing of practical purity and manageable handling. (2-Chloro-5-Trifluoromethyl)Phenylthiourea presents itself as a pale, crystalline solid, typically melted and recrystallized in a nitrogen blanket to protect against degradation. Typical testing, including HPLC and NMR, places our minimum assay at 98%. Chloride and trifluoromethyl substitutions reinforce oxidative stability. Trace moisture and solvent residues remain consistently low, a result of attention to post-processing protocols.

    Practicing chemists will recognize the benefit of narrow melting point ranges; the typical melting point (routinely confirmed with each new batch) ensures predictable behavior during subsequent use. We use analytical tools like titration and mass-spec to confirm the absence of unreacted starting materials and process byproducts, not just to meet regulatory norms, but to save chemists from unwelcome surprises during synthesis or formulation.

    Core Advantages Over Related Products

    Most phenylthiourea derivatives offer a selection of substitution patterns, each modifying reactivity and environmental resistance. Through in-house side-by-side trials, we have observed that introducing both a chloro and a trifluoromethyl group, positioned at 2 and 5 respectively, uniquely balances electron density and steric profiles. This translates to selective reactivity in cross-coupling or heterocycle-building steps. The presence of these groups also extends shelf-life and reduces batch-aging during storage, particularly when compared to analogues lacking fluorinated moieties.

    Some labs opt for simpler thiourea cores or phenyl rings substituted solely with electron-donating groups. Over time, many discover unanticipated side reactions or decomposition when ramping conditions or scaling up. By contrast, our version allows predictable transition metal coordination and double-bond formation, as documented through both our internal application studies and external customer feedback.

    Usage: Value for Synthesis, Materials, and Research

    Our specialty teams regularly engage with academic and industrial users to help match the molecule to its most promising reactions. (2-Chloro-5-Trifluoromethyl)Phenylthiourea commonly finds itself as a precursor or intermediate in the assembly of complex organosulfur frameworks. Its precise reactivity profile makes it popular for the production of crop protection agents, fine chemicals, and pharmaceutical research where subtle electronic effects determine product success.

    With each new application, fresh insight emerges. In pesticide R&D, this compound has found value as an intermediate supporting the introduction of unique sulfur-nitrogen motifs, widely pursued for resistance-breaking formulations. In pharmaceuticals, the trifluoromethyl group’s electron-withdrawing properties offer metabolic stability and improved bioavailability profiles, sought after when building new scaffolds. The chloro group supports downstream coupling reactions without excessive activation, letting medicinal chemists conserve valuable feedstocks.

    Several of our process partners utilize this molecule as a starting point for ligand design. Here, fine control over reactivity and geometry proves critical. Repeated trials have demonstrated that Friedel-Crafts acylation chemistries, sulfenylation, and oxidation protocols yield higher conversion rates and less impurity formation when initiated with our optimized material. Customers point out reduced byproduct formation, which translates directly into easier work-ups and streamlined purification. Efficiency and reproducibility matter when process times are measured in days, not hours.

    Practical Considerations in Handling and Storage

    In the real world, a promising molecule often faces trouble if handling proves impractical. Years of own experience, plus constant client conversations, have driven our batch workflow towards reliability. Each drum, each bag, is delivered under conditions that mitigate moisture uptake and breakdown. Our QA teams spend as much time checking particulate load, packing density, and seal integrity as they do on analytical purity.

    Feedback from bulk chemical handlers has spurred improvements in packaging. Moisture-barrier liners and oxygen-absorbing sachets are standard, a direct response to observations of caking or oxidation with lesser materials. Our preferred packing formats are based on real-world handling characteristics rather than abstract standards—chemical and physical integrity remain priorities from factory door to end-user storage.

    Beyond logistics, attention must also stay on workplace safety and process efficiency. Our in-house chemists routinely run process simulations to confirm that dust generation, off-gassing, and thermal decomposition are absent at user-friendly temperatures. Practical field studies confirm that managed environments—well-sealed, with simple nitrogen overlay—bring years of stable storability. The end result: real-world productivity paired with robust supply chain predictability.

    Bench and Pilot-Scale Experiences: Lessons Learned

    No amount of literature review replaces hands-on experience. Over years of in-house process optimization, our teams have dealt with every common problem: recrystallization bottlenecks, batch inhomogeneity, inconsistent color, trace metal contamination. Direct engagement with the molecule informs every production run.

    For instance, pilot-scale stakeholders often press for rapid cycle times; shortcutting recrystallization can tempt risk. On multiple occasions, we discovered that even small compromises in solvent removal or temperature ramping ended up aggravating downstream color stability and, in one memorable campaign, almost doubled impurity carryover in a scale-up. This feedback loop, and the discipline to carry process improvements across all batches, helps ensure end-users receive consistent, trouble-free product.

    Analogs—those with minor ring modifications or alternate substituents—sometimes behave unpredictably. In multiple pilot campaigns outside our main facility, partners reported poor yields, color changes, or fouling equipment with alternative commercial sources. Follow-up, with side-by-side comparative analyses, almost always favored our own process: fewer purification steps, lower waste output, and simpler equipment cleaning.

    Lab staff point to small touches that reduce real-life headaches: packaging formats that match bench-top workflows, clear labeling, and reliable batch record traceability. Not all value lies directly in the molecule; years working with chemists inform even these supporting details.

    Piece by Piece: Downstream Considerations

    Those who work in scale-up, process engineering, or regulatory submission understand the true difference between catalog compounds and field-ready intermediates. New reaction technologies—flow reactors, continuous manufacturing, or automation—require reagents resistant to heat shock, variable stir rates, or fluctuating concentrations. We've seen, firsthand, that deviation from strict process protocols with less refined thiourea materials quickly spores lost product, wasted time, and unpredictable waste hazards.

    It becomes clear, application by application, that the right substitution pattern unlocks a batch’s full yield potential. In phenylthiourea chemistry, electron-withdrawing groups tightly control reactivity and improve functional group compatibility. Both internal and collaborative studies demonstrate that, for diverse coupling, cyclization, or substitution steps, the (2-Chloro-5-Trifluoromethyl) core rarely triggers side reactions—something not often true of less stable analogs. Process waste shrinks, and documentation headaches evaporate when extractions, crystallizations, or distillations move forward without the rogue peaks and ghost spots that plague standard alternatives.

    Quality, Data Transparency, and Traceability

    Practicing chemists care about what’s actually in the drum, not just the label. For us, absolute process transparency governs everything from raw material selection through to individual sample release. Each (2-Chloro-5-Trifluoromethyl)Phenylthiourea lot runs through a defined analytics chain—HPLC, NMR, GC-MS if needed, and Karl Fischer for residual water levels. Certificates record precise impurity profiles, not just blanket statements about technical grade or general purity.

    Every batch gets kept aside for internal benchmarking. If questions ever turn up in the field—whether about melting point drift, yield fluctuations, or trace contaminant carryover—samples are immediately available for retesting. This habit of holding reference is not regulatory box-ticking. From the start, it’s a lesson learned through real production setbacks—there are no shortcuts around accountability or data transparency.

    Our quality team constantly audits manufacturing records and cross-verifies with field reports. If customer feedback highlights a new impurity or stability issue not caught in standard analysis, methods are revised. Results get discussed in cross-departmental meetings, and process improvements are implemented on the next production run. This cycle of continuous improvement carries respect for the chemists who rely on clean, well-characterized intermediates. It’s the only way to guarantee both trust and progress.

    Comparisons Through Experience: Why the Details Matter

    On paper, some see only small differences between phenylthiourea derivatives—perhaps a different halogen or a varied fluorinated moiety. In execution, those differences spell reliability or lost opportunity in the lab or plant. Over countless trial runs, an extra chlorine or a misplaced methyl group alters melting point, shifts reactivity profiles, and sometimes introduces stubborn impurities. Extended experience with (2-Chloro-5-Trifluoromethyl)Phenylthiourea, particularly using our established process, consistently shows fewer issues.

    Many clients have reported a smoother transition from bench scale to pilot batches, fewer failed runs, and less solubility mystery when working with our carefully prepared material. The combination of strong electron withdrawers and careful process hygiene limits byproducts. During pressure vessel reactions or more aggressive hydrogenations, feedback shows measurable advantages over competitors’ materials: no unwanted residue, less color formation, and lower time spent troubleshooting extraction or filtration.

    Quite a few alternative sources overlap in basic specification numbers but miss the hidden variables: polymorph formation, process dust, or color irregularities that skew downstream testing. Through ongoing user feedback and our own process data, these issues are directly traced to crude post-processing, minimal purification, or inadequate analytical verification elsewhere.

    Supporting Innovation: Open Lines and Real-World Feedback

    From the earliest days of product development, it became clear that insight flows from open dialogue with chemists actually pushing the frontiers of research. We learn as much from customer process data and novel application reports as from classical literature. Direct collaborations have allowed us to tweak impurity profiles, suggest changes to packaging, and occasionally overhaul production methodology to better serve application-specific needs.

    Whenever end-users face a new synthesis puzzle, our technical support teams share process diagrams, risk evaluations, and—when requested—co-develop scaled-up demonstration batches. In a recent example, a leading agrochemical group hoping to lengthen the service life of new actives found unexpected improvements when switching over to our material, specifically reporting fewer batch failures at high temperature and improved yield on final coupling.

    Direct access to the manufacturing know-how—and openness to critiques and suggestions—also helps remove long-term reliability worries for both routine and exotic chemistry projects. Real-world feedback and lived experience count as much as raw purity, perhaps more.

    Continuous Process and Product Optimization

    Process efficiency remains a moving target. New regulations, updated customer requirements, and changes in raw material sourcing all force regular time on the production line. Our operations team works with synthesis chemists and QA engineers to examine sources of yield loss, product instability, or byproduct drift. This includes actively reviewing literature and in-house data regarding alternative solvents, reactor technologies, and green chemistry initiatives.

    Recently, a push to shorten cycle times while keeping thermal profile tight led to an overhaul in solvent exchange and fine filtration systems. As we run design-of-experiment trials, regular feedback guides even minor formulation changes. Each increment in efficiency or purity doesn’t just serve the bottom line—it actively supports our partners’ capacity to innovate.

    For customers working to minimize regulatory hurdles, our attention to trace impurity and analytical transparency smooths their own approval processes. It’s a two-way path: as our quality climbs, their own compliance and laboratory throughput see less friction.

    Conclusion: Chemical Manufacturing That Delivers What Real Chemists Need

    Every batch of (2-Chloro-5-Trifluoromethyl)Phenylthiourea is the product of not just chemical process, but ongoing conversation, field feedback, and hard lessons from demanding project partners. Our history with this compound goes deeper than a catalogue listing or an invoice; it reflects repeated cycles of adaptation, problem-solving, and meticulous quality management.

    As both a manufacturer and a partner-in-innovation, we recognize what matters in real laboratories and scalable processes—the subtle differences that separate routine from exceptional, and theory from valuable, reproducible chemistry. Building a robust supply and feedback chain for this compound has meant staying grounded in the needs of the people actually using it.

    The story of (2-Chloro-5-Trifluoromethyl)Phenylthiourea is still unfolding. Future applications, improved process methodologies, and new customer challenges will continue to shape the product’s evolution. We remain ready for that next challenge, armed with decades of practical experience and a clear-eyed approach to chemical manufacturing excellence.