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4-[3,5-Bis(Trifluoromethyl)Phenyl]-3-Thiosemicarbazide

    • Product Name 4-[3,5-Bis(Trifluoromethyl)Phenyl]-3-Thiosemicarbazide
    • Alias 4-[3,5-Bis(trifluoromethyl)phenyl]-1-(hydrazinecarbonothioylidene)hydrazine
    • Einecs 699-690-6
    • 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

    564400

    Product Name 4-[3,5-Bis(Trifluoromethyl)Phenyl]-3-Thiosemicarbazide
    Cas Number 32873-53-5
    Molecular Formula C9H7F6N3S
    Molecular Weight 303.23
    Appearance White to off-white solid
    Melting Point 152-154 °C
    Solubility Slightly soluble in DMSO and DMF
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, protect from light
    Smiles C1=C(C=C(C=C1C(F)(F)F)C(F)(F)F)NN=C(N)S
    Inchi InChI=1S/C9H7F6N3S/c10-8(11,12)5-2-4-6(7(3-5)9(13,14)15)17-18-16-1-19/h2-4H,1H2,(H3,16,17,18,19)

    As an accredited 4-[3,5-Bis(Trifluoromethyl)Phenyl]-3-Thiosemicarbazide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 25g of 4-[3,5-Bis(Trifluoromethyl)Phenyl]-3-Thiosemicarbazide supplied in an amber glass bottle with a tamper-evident screw cap.
    Shipping This chemical, 4-[3,5-Bis(Trifluoromethyl)Phenyl]-3-Thiosemicarbazide, is shipped in a tightly sealed container, protected from light, moisture, and physical damage. It is packaged according to international regulations for handling chemicals, ensuring safe transport. Proper labeling and documentation are included to comply with regulatory and safety requirements during shipping.
    Storage 4-[3,5-Bis(Trifluoromethyl)Phenyl]-3-thiosemicarbazide should be stored in a tightly sealed container, away from direct sunlight, moisture, and incompatible substances such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area, ideally in a designated chemical storage cabinet. Ensure proper labeling, and follow relevant safety protocols for handling and emergency procedures.
    Application of 4-[3,5-Bis(Trifluoromethyl)Phenyl]-3-Thiosemicarbazide

    Applications of 4-[3,5-Bis(Trifluoromethyl)Phenyl]-3-Thiosemicarbazide in Industrial Manufacturing

    As a specialized manufacturer, we provide 4-[3,5-Bis(Trifluoromethyl)Phenyl]-3-Thiosemicarbazide for sophisticated industrial segments where trifluoromethyl-functional building blocks are demanded for performance, compliance, and reliability. Our product supports downstream industries through high purity and stringent quality controls, integrating effectively in key applications where regulated performance intermediates are critical.

    1. Pharmaceutical Intermediate Synthesis

    This material functions as a privileged intermediate within the development pipeline of active pharmaceutical ingredients, specifically in heterocyclic drug syntheses targeting CNS, oncology, or antiviral APIs. It enables key nucleophilic-substitution steps and cyclization pathways, often under nitrogen atmosphere in polar solvents. Our in-house process ensures batch traceability to support DMF/CEP filings. Compliance teams rigorously test for residual solvents and heavy metals relevant to this stage.

    Industry compliance standards

    • ICH Q7: GMP for Active Pharmaceutical Ingredients
    • USP-NF General Notices and Requirements (where applicable as starting/intermediate)
    • Ph. Eur. 5.2.12: Control of Impurities of Toxicological Concern in Synthesis
    • 21 CFR Part 211: Manufacturing, Processing, Packing, or Holding of Drugs

    Typical usage ratio

    • 0.2–0.8 molar equivalent relative to the electrophilic substrate, adjusted by route constraints; final content removed by work-up and downstream purifications

    Downstream process integration

    • Grignard addition or SN2 introduction, followed by acid or base-mediated cyclization
    • Intermediate isolation and chromatographic purification prior to API finalization

    Final product types

    • Tetrazole-based CNS active pharmaceutical ingredients
    • Aromatic triazoles for antiviral drug candidates
    • Advanced pharmaceutical intermediates for oncology small molecules

    2. Agrochemical Active Ingredient Precursor

    Formulators work with this compound in the synthesis of triazole and thiadiazole derivatives for selective fungicides and insecticides. Use centers on specific heterocycle-forming reactions in medium-polarity solvents under reflux, where trifluoromethyl phenyl activation enhances metabolic stability. Careful stoichiometric balancing and work-up ensure removal of any process-related impurities, with documented support for ongoing REACH registration.

    Industry compliance standards

    • EU REACH Regulation (EC 1907/2006)
    • ISO 9001:2015 Quality Management for Production Site Validation
    • FAO/WHO Manual on Development and Use of Specifications for Plant Protection Products
    • EPA 40 CFR Part 180 (tolerance for residues in or on food)

    Typical usage ratio

    • 0.15–0.55 mole equivalents, modulated by specific crop protection synthesis needs and desired end-point purity

    Downstream process integration

    • Condensation reaction with diketone or carboxamide functional blocks
    • Heterocycle ring closure performed before formulation into technical-grade concentrate

    Final product types

    • Selective triazole fungicides
    • Insecticidal active intermediates for seed treatment or foliar sprays
    • Precursor to fluorinated herbicides for rice and corn protection

    3. Advanced Dye and Pigment Manufacturing

    Specialty dye producers utilize this compound for high-performance pigment synthesis, particularly in the formulation of metal complex dyes and functionalized azo colorants. Its electron-withdrawing trifluoromethyl groups enable enhanced chroma and chemical resistivity in textiles and plastics. Manufacturing uses controlled high-temperature coupling in aprotic environments, with stringent in-process QA to meet export regulatory thresholds.

    Industry compliance standards

    • OEKO-TEX Standard 100 for chemical substances
    • European Directive 2004/42/EC on VOC content in coatings
    • EN 71-3: Toy Safety (heavy metals migration for pigment use in toys)
    • ISO 9001:2015 for batch release and QC traceability

    Typical usage ratio

    • 0.05–0.12 mass fraction in dye synthesis, determined by dye class and substrate load

    Downstream process integration

    • Chemoselective coupling with activated diazonium salts
    • Introduction into pigment condensation reactors for subsequent complexation

    Final product types

    • Trifluoromethylated azo dyes for polyester textiles
    • High-durability pigments for automotive coatings
    • Colorants resistant to aggressive washing and UV exposure

    4. Specialty Polymer Additive Synthesis

    This thiosemicarbazide derivative is incorporated into polymer modifier synthesis, especially for introducing fluorinated side chains in engineering plastics and specialty elastomers. Industrial implementation includes addition to pre-polymer blends under controlled temperatures, allowing the targeted grafting of functional groups. The material supports downstream performance validation for anti-fouling, dielectric, and chemical resistance use-cases, with robust documentation for RoHS and food contact compliance where relevant.

    Industry compliance standards

    • EU Regulation (EU) No 10/2011 (food contact plastics)
    • Directive 2011/65/EU (RoHS) for restricted substances in electronics polymer components
    • ASTM D638: Standard Test Method for Tensile Properties of Plastics
    • ISO 14001: Environmental Management for additive production processes

    Typical usage ratio

    • 0.8–2.5% by weight in pre-polymer or additive blends, optimized for end-use mechanical/chemical targets

    Downstream process integration

    • Reactive blending during masterbatch production for engineering resins
    • Grafting or curing phase at elevated temperature (typically 180–220°C for engineering plastics)

    Final product types

    • Fluorinated engineering polymer pellets
    • Anti-fouling additive concentrates for coatings and marine paints
    • Dielectric-enhanced specialty elastomers
    Free Quote

    Competitive 4-[3,5-Bis(Trifluoromethyl)Phenyl]-3-Thiosemicarbazide prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 4-[3,5-Bis(Trifluoromethyl)Phenyl]-3-Thiosemicarbazide: Our Manufacturing Experience and Perspective

    Our Commitment to Real Chemistry

    In today’s specialty chemical landscape, standing out comes from experience in manufacturing, not just repackaging or trading. As a producer with decades of hands-on practice in the field, we face the everyday pressures – from selecting the right raw materials, to fine-tuning purification steps, to controlling each batch for consistency. This is especially true with compounds as complex as 4-[3,5-Bis(Trifluoromethyl)Phenyl]-3-Thiosemicarbazide. We believe in sharing not just a product, but the understanding and insights gained from countless runs, optimizations, and problem-solving sessions on the plant floor.

    What 4-[3,5-Bis(Trifluoromethyl)Phenyl]-3-Thiosemicarbazide Brings to the Table

    This compound shows up often in research circles. Its backbone–a phenyl ring decorated at the 3 and 5 positions with trifluoromethyl groups, coupled to a thiosemicarbazide moiety–offers a unique blend of electronic and structural features. We first began producing it in response to demand from pharmaceutical and agrochemical developers who sought a scaffold with pronounced lipophilicity, strong electron-withdrawing groups, and sulfur-nitrogen functionalities.

    Purity and precise specification play a huge role for our clients. For this compound, trace byproducts left over from the trifluoromethylation step or incomplete hydrazine conversions throw off analytical results or impact downstream application in bioassays and further synthetic work. Unlike simple reselling, manufacturing this compound has drawn us deep into the nuances. For example, slight variations in solvent polarity or temperature ramp rates during the coupling step can shift impurity profiles, something that would rarely show up in basic third-party screening.

    Why This Molecule Emerges in Modern Research

    4-[3,5-Bis(Trifluoromethyl)Phenyl]-3-Thiosemicarbazide isn’t just another thiosemicarbazide derivative. The double -CF3 substitution pattern on the aromatic ring drives its unique behavior. It changes everything from solubility in organic solvents to the electron density across the azo and amide bonds. Researchers in medicinal chemistry have gravitated toward this structure in the hunt for kinase inhibitors and other enzyme modulators. The high electronegativity of the trifluoromethyl groups influences hydrogen bonding interactions, making the compound an agent of choice for those screening for new ligands or exploring receptor selectivity.

    Synthetic chemists employ this compound as a precursor for tailoring libraries of bioactive molecules. The sulfur on the thiosemicarbazide allows for further elaboration—cyclization, for example, to imidazo or triazole rings, where the trifluoromethylated phenyl ring can modulate pharmacokinetic performance. From our vantage point on the plant floor, it’s clear that slight changes in the backbone–whether in position or substitution–induce large swings in downstream product profiles. Our experience meeting project demands has led us to tweak everything from hydrogen source to crystallization solvent, each time learning more about how this molecule likes to behave.

    Physical Characteristics: Nuances Beyond Appearance

    We’ve encountered batches that look identical yet perform differently in clients’ screens. Our rigorous control goes beyond typical melting point or visual checks. Besides the characteristic white to pale yellow powder form, we pay close attention to subtle phase changes during drying. For quality assurance, not just analytical spectrum—but granular observations, such as the precise way the compound compacts under storage conditions or responds to temperature cycling—are tracked in our batch histories.

    Moisture uptake sometimes creeps in if ambient controls slip, which alters handling characteristics and dilutes potency in downstream reactions. Comparison samples stored for months under varied light exposure reveal photostability limits that informed our packaging hike—shifting from plain drums to lined, light-blocking containers. These changes didn’t come from a manual, but from troubleshooting with users who needed reliable results over extended project timelines.

    Reliable Delivery Rooted in Experience

    Supplying a specialty intermediate, especially one often needed in sub-kilo to multi-kilo lots, means mastering logistics and scale. Requests often come up with tight timelines. By owning the production process—right down to in-house purification and custom particle-size control—we share responsibility directly for the quality that goes out the door. This is a far cry from traders, who must defer to others up the supply chain.

    Our regular shipment lots often trigger customer questions about potential batch-to-batch variation. The solution lies not just in final QC, but in documenting and understanding the full process. For example, earlier iterations had variable formation of colored impurities traceable to subtle exotherms during the hydrazinolysis phase. We now employ multiple temperature probes along the reactor jacket, catching “hot spots” that could previously go undetected. This hands-on refinement over many cycles means consistency, not just on the analytical certificate but in any real-world application, whether that’s further functionalization or direct biological assessment.

    Handling Differences: Why Our Approach Matters

    Years of technical support taught us the pitfalls users meet. Compared to simpler thiosemicarbazides, the double trifluoromethyl functionality makes this product oddly sticky at certain humidities, clumping with some solvents even below saturation. Researchers using cheap imitations or older stocks often report poor solubility or failed reactions. Each formulation batch here undergoes humidity cycle testing, not just standard vacuum oven drying, specifically to flag batches at risk for clumping or agglomeration.

    While some products can tolerate basic post-processing, this molecule does not forgive poorly handled steps. For instance, harsh rotary evaporation at too high a vacuum will alter its character—the product forms a tacky mass that resists redissolution. Manual intervention, fine-tuning process controls, and keeping careful process notes helps us deliver a material that meets analytical claims and actually works in synthesis or screening applications. That track record stems from living with both minor annoyances and rare mishaps, not from reading standard chemical supply specifications.

    Use in Synthesis: Real-Life Applications, Not Just Theories

    Much of the published literature on this compound hails from academic and industrial labs using it as a starting scaffold. Peering behind the paper-trail, our experience supplying to those groups shows a few surprises. Direct cyclization reactions proceed smoothly when batch quality is high, but the minute levels of oxidized byproducts—often undetectable by basic tests—can shut down yields in trickier one-pot procedures.

    Clients in pharma or crop-protection sectors often drive formulation work with high-throughput screening. Here, impurity thresholds must drop to near-invisible levels, since reactive contaminants can mislead activity results or even damage valued screening hardware. With those researchers, we work directly to adjust specifications and validate process tweaks, keeping contaminants low: no simple feat but critical for reproducible science.

    In materials science, this molecule acts as a building block for fluoroaromatic polymers and functionalized resins. Some batches have landed in hands-on engineering projects, where slight color or powder-flow differences have led to retooling feed hoppers and blending tanks. Our engineers behind the scenes have visited client sites to analyze process bottlenecks, feeding back lessons into future production runs.

    What Sets It Apart in Our Eyes

    Producers bump into real constraints that traders never see. Bulk synthesis of 4-[3,5-Bis(Trifluoromethyl)Phenyl]-3-Thiosemicarbazide looks simple on paper but turns complex in scale-out. The multiple trifluoromethylations demand fluorinated intermediates that, in our experience, behave quite differently than the more common alkyl halides. The handling of potassium fluoride, for example, taught us hard lessons about reactor seals and PPE—lessons learned by fire rather than formula.

    Older production routes relied heavily on extended refluxes or inefficient solvent swaps. We overhauled this by introducing staged additions and better agitation profiles, greatly reducing cycle times and lowering the formation of persistent minor byproducts. The energy savings and cleaner chromatography outcomes present a unique edge over products sourced from suppliers still using legacy methods. This continuous improvement is not a matter of regulatory compliance, but of pride in our craft.

    Compared to classic unsubstituted thiosemicarbazides, the increased hydrophobicity here calls for different solvent and handling approaches. This rarely shows up in technical data sheets, but we field daily troubleshooting questions that only hands-on production experience can equip us to answer.

    Our Long-Term Perspective on Safety, Quality, and Environmental Impact

    The growing regulatory push for sustainable chemistry has forced every reputable manufacturer to re-examine processes. In our operations, this started with tracking all waste streams—organic, fluoride-bearing, and otherwise—through both manual logs and automated monitoring. We don’t just ship product and forget it. Instead, regular reviews of incoming raw material standards and secondary containment systems keep us ahead of environmental audits.

    A significant portion of headache in large-scale production comes from managing HF byproducts. Early years in batch work led to corrosion setbacks and downtime. Plant investment into specialized alloy reactors improved both safety and yield. These upgrades don’t show up in product brochures, but they fundamentally change the safety profile for every gram produced.

    Ongoing dialogue with end users also influences packaging changes. Strong demand for smaller, manageable unit sizes led us to pilot lab busters, offering flexible handling without breaking bulk unnecessarily. Experimenting with new types of fluoropolymer liners, we found that these not only preserve purity but also reduce microleaching, which can be critical in long-term stability testing.

    Why Trust the Manufacturer?

    What most customers never see is the troubleshooting that happens behind the scenes. We have reworked entire process trains when a single raw supplier changed their spec, and documented the ripple effects down to the user’s bench. Our analysts cross-check HPLC, GC-MS, and even FTIR spectra on every lot, flagging anomalous patterns that reflect changes in upstream chemistry, not just anomalies in final output.

    This level of oversight is impossible without vertical integration. Site lockdowns during public health emergencies, port disruptions, and raw-market volatility stress-test weak supply chains. By keeping production in-house and maintaining a team with decades navigating fine chemical processes, we commit ourselves to reliability over mere price competition.

    We also devote resources to customer-facing support, guiding users through not just order fulfillment but also application troubleshooting and even downstream product design. Our technical services piece is built off the real-world lessons that only a manufacturer can collect—half from scheduled process validations, half from fielding frantic calls as project deadlines loom.

    Forward-Looking: Where This Product’s Journey Leads

    With the rise in demand for fluorinated scaffolds, especially for drug and advanced material programs, 4-[3,5-Bis(Trifluoromethyl)Phenyl]-3-Thiosemicarbazide holds steady as a core ingredient. Sourcing directly from a seasoned manufacturer delivers not just a drum of powder, but assurance that each step—reaction, purification, packaging—reflects a deeper understanding of what is truly required for success in modern chemical applications.

    Looking forward, we invest not just in scaling capacity, but also in making production cleaner and safer. Each run, each delivery, and each customer conversation feeds new data back into our manufacturing process. The road from lab bench through pilot reactor and into full-scale tanks shows us that chemical production is not just science on paper, but a daily exercise in continuous learning and improvement.

    In a world crowded with intermediaries, real chemical manufacturing brings hard-won expertise to the table. For those who demand reliability, performance, and genuine technical partnership, our role goes beyond selling a product—it is about backing each order with decades of lived experience on the ground, supporting progress wherever our compounds make a difference.