|
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 | 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. |
Applications of 4-[3,5-Bis(Trifluoromethyl)Phenyl]-3-Thiosemicarbazide in Industrial ManufacturingAs 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 SynthesisThis 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
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Active Ingredient PrecursorFormulators 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
Typical usage ratio
Downstream process integration
Final product types
3. Advanced Dye and Pigment ManufacturingSpecialty 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
Typical usage ratio
Downstream process integration
Final product types
4. Specialty Polymer Additive SynthesisThis 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
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 4-[3,5-Bis(Trifluoromethyl)Phenyl]-3-Thiosemicarbazide prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.