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HS Code |
751225 |
| Chemical Name | 6-Phenyl-2-Thiouracil |
| Cas Number | 103-85-5 |
| Molecular Formula | C10H8N2OS |
| Molecular Weight | 204.25 g/mol |
| Appearance | White to pale yellow crystalline powder |
| Melting Point | 284-288°C |
| Solubility | Slightly soluble in water, soluble in ethanol |
| Purity | Typically ≥98% |
| Iupac Name | 6-phenyl-2-sulfanylidene-2,3-dihydropyrimidin-4(1H)-one |
As an accredited 6-Phenyl-2-Thiouracil factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with screw cap, labeled "6-Phenyl-2-Thiouracil, 25g, For laboratory use only." Store in a cool, dry place. |
| Shipping | 6-Phenyl-2-Thiouracil is shipped in secure, chemically compatible containers, clearly labeled per regulatory standards. Packages are cushioned and sealed to prevent leaks or contamination. Shipping follows all relevant safety and environmental guidelines, typically via ground or air, with appropriate documentation, handling instructions, and hazard communication as required for laboratory chemicals. |
| Storage | 6-Phenyl-2-Thiouracil should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizers. Store at room temperature, avoiding excessive heat and humidity. Ensure proper labeling and restrict access to authorized personnel trained in handling hazardous chemicals. |
Applications of 6-Phenyl-2-Thiouracil in Industrial ManufacturingAs an established manufacturer of 6-Phenyl-2-Thiouracil, we supply this intermediate for specialized downstream sectors where its chemical properties enable precise functional outcomes. Below, we detail its primary industrial applications, with each scenario reflecting actual field deployment standards and manufacturing practices. 1. Pharmaceutical Intermediate for Antithyroid Drug Synthesis6-Phenyl-2-Thiouracil functions as a critical building block in the synthesis of antithyroid drugs. Its chemical structure enables efficient construction of molecular frameworks essential for controlling thyroid hormone production in finished pharmaceuticals. Manufacturers introduce it during multi-step synthesis of active pharmaceutical ingredients (APIs) for the treatment of hyperthyroidism, leveraging its reactivity and high purity for consistent end-product performance aligned with stringent regulatory compliance in international markets. Industry compliance standards
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2. Agrochemical Active Ingredient PrecursorDownstream agrochemical manufacturers apply 6-Phenyl-2-Thiouracil as an intermediate for formulating specific classes of herbicides and plant growth regulators. Its sulfur- and nitrogen-containing heterocycle supports targeted synthesis of actives with selectivity for broadleaf weed management. Detailed process control is critical, as this raw material undergoes condensation and further derivatization to yield products with regulated environmental persistence. Industry compliance standards
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3. Dye and Pigment Intermediate for Specialty ColorantsManufacturers of specialty dyes leverage 6-Phenyl-2-Thiouracil for its ability to introduce stable chromophore motifs into high-performance colorants. The aromatic and thioamide functionalities serve as key motifs in azo dye synthesis, ensuring robust colorfastness demanded by industrial textile and leather processing. Stakeholders in this sector specify purity and trace side-reaction controls to meet end-product regulatory demands. Industry compliance standards
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4. Analytical Reagent Component in Laboratory DiagnosticsProducers of laboratory diagnostics integrate 6-Phenyl-2-Thiouracil in specialized colorimetric reagents for biochemical assays, especially those evaluating thyroid function or enzymatic activity. Its specificity in reacting with oxidizing species enables precise quantitative measurements under controlled clinical laboratory protocols. Strict batch consistency and trace impurity controls are maintained by customers to satisfy validated test kit performance. Industry compliance standards
Typical usage ratio
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In our laboratories and on the plant floor, we pay close attention to the workhorse molecules that drive research, pharmaceuticals, and specialty synthesis. 6-Phenyl-2-Thiouracil stands out for its dependable profile and unique chemical character. Over years of hands-on manufacturing, this compound has taught us about its subtleties—both in its immediate behavior during synthesis and later in how clients from varied industries choose to apply it.
This compound balances a phenyl group and a thiouracil backbone, resulting in distinct reactivity and stability. It doesn’t just slot into the usual array of organosulfur or heterocyclic molecules—there’s a reason researchers keep coming back to it when seeking specificity in their work.
At our facility, the 6-Phenyl-2-Thiouracil we produce meets stringent purity standards. That matters because impurities, even at trace levels, skew outcomes in pharmaceutical and fine-chemical settings. We invest in analytical controls and reliable batch processing equipment to meet target purity every cycle—our QC team lives by their NMR spectra and HPLC traces, not just datasheet promises.
In our experience, the true test of 6-Phenyl-2-Thiouracil’s quality reveals itself downstream: does it behave the same way every time, regardless of which lot is opened? Some differences in crystallinity, particle size, or residual moisture may escape the attention of those removed from synthesis, but anyone who has scaled up from benchtop to pilot plant quickly learns that “close enough” isn’t good enough.
We keep our synthesis process simple and robust. Each batch is monitored through the final recrystallization, not only to deliver an analytically pure product but to ensure the physical handling, dissolution profile, and storage stability support real-world workflows. Solubility in standard laboratory solvents, consistent melting point, and a low tendency to agglomerate—these details, often overlooked in generic descriptions, become make-or-break when scientists need reproducible results.
This compound's most frequent destination is the pharmaceutical laboratory. Researchers explore how 6-Phenyl-2-Thiouracil modulates biological targets related to the thyroid and beyond. Our technical team collaborates closely with researchers to support them in drug discovery and development, offering insights from the manufacturing side that translate directly into better results at the bench or in the reactor.
6-Phenyl-2-Thiouracil carries structural features appreciated by medicinal chemists. Its substitution pattern allows for fine-tuning derivative synthesis—this flexibility benefits those screening for new pharmacological activities. Over time, we have seen how increased demand for selectivity and lower toxicity has pushed users to scrutinize every intermediate that enters their synthesis. Our customers want confidence in both the structural integrity and the trace impurity profile of what they’re using—not just because regulators ask for documentation, but because robust science demands it from the first step.
Beyond drug research, 6-Phenyl-2-Thiouracil also appears in advanced materials development and as a lead scaffold for agrochemical compounds. Synthetic chemists regularly modify the uracil core for new electronic and biological outcomes, so our product must align with both the exploratory and production-focused approaches seen across industries.
Not all thiouracil derivatives behave the same. In our manufacturing practice, we see distinct personality shifts between simple thiouracil, methylated variants, and the phenyl-substituted version. Adding a phenyl ring changes more than just the molecular weight. It pushes solubility profiles away from the parent compound, adjusts reactivity toward common electrophiles, and alters ring aromaticity. These aren’t just textbook curiosities—they show up as real differences in synthesis, storage, and eventual biological activity.
For instance, researchers appreciate that 6-Phenyl-2-Thiouracil’s increased hydrophobicity compared to unsubstituted thiouracil expands its application in certain drug delivery formats. The phenyl group changes both how the molecule partitions and how it fits in binding pockets—a subtle but significant distinction. Certain synthetic routes that work for simple uracils stall or give lower yields here, which has pushed us over the years to optimize solvent systems, choose catalysts with better selectivity, and rethink our purification methods.
What our customers notice immediately is that 6-Phenyl-2-Thiouracil offers a balance: enough stability for handling and storage, but enough reactivity at the sulfur and ring positions for subsequent transformations. Where other derivatives either degrade too quickly under routine laboratory conditions or resist functionalization, this molecule often delivers the desired performance, provided it’s correctly made.
Handling matters, too—the compound in our experience forms stable crystals, resists cake formation in storage, and doesn’t develop odors or color changes that signal degradation. Our warehouse staff appreciates these subtle advantages as much as our analytical chemists.
Over time, we’ve learned to guide clients beyond generic grades like “lab,” “industrial,” or “pharma” quality—those buckets don’t always reflect what truly matters in the lab or plant. For 6-Phenyl-2-Thiouracil, we focus on clear, relevant parameters: chemical purity, NMR spectral consistency, melting range, water content, and particle distribution. We list what actually matters for performance in synthesis and storage, not just the regulatory minimum.
Our technical sheets back up the rigorous batch release standards. Each unit has an unambiguous lot number connected to its test results. We also archive retention samples, so if a question arises months down the line, we can re-analyze and confirm details. It's this feedback loop between manufacturing, analytical, and customer use that produces a stronger, more transparent product.
Procurement specialists and research heads commonly express concern about supply interruptions or inconsistent performance between lots. We take control of the manufacturing process—not just the last stage, but right from raw material qualification. Volatility in raw chemical pricing or availability does impact the industry, so we’ve forged stable relationships with our raw materials suppliers and maintain safety stocks in our inventory. This strategy lets us deliver not just a one-off shipment, but reliable year-round supply.
Traceability isn’t a formality—it keeps confidence high. We subscribe to batch-level identification for all outgoing shipments, accompanied by analytical documentation directly from our in-house team. A chemist receiving our product knows not only the date of manufacture but also how the batch performed against our internal benchmarks. These measures keep surprises out of the equation, whether the project is at R&D scale or trending toward commercial volumes.
Collaboration between manufacturer and end user changes the product for the better. Our technical team fields questions daily about solubility limits, reactivity modifications, and impurity control strategies. Real-world labs need advice that draws from manufacturing history, not just textbook procedure. For instance, some researchers have found that re-drying the compound prior to certain couplings enhances yields, while others have discovered that minor modifications to their dissolution protocols reduce induction times. We don’t just hand over a product—we engage with users to interpret intricate results and suggest suitable adjustments.
Such feedback has led us to experiment with different drying techniques and container types until we found what minimizes caking and preserves free-flowing powder, even if humidity fluctuates in warehouse or shipping containers. As a result, our process supports both short-term benchwork and long-term storage, which is rarely addressed by bulk traders or generic resellers.
We don’t operate in a vacuum. Repeat users share stories of trial and error with competitive products—crystals too small to filter, unexpected discoloration, poor shelf-life, or reactivity that falls short under real laboratory conditions. Our in-house R&D examines every deviation, compares it against historical records, and refines manufacturing steps accordingly. Sometimes it means tweaking solvent systems, sometimes investing in better filtration equipment, sometimes updating how we pack and label for transit. Each variation is a chance to learn, and that learning cycles back into the next run.
For everything from benchtop reaction monitoring to scale-up in jacketed reactors, consistency pays dividends. Even seemingly minor deviations—a shift in particle size, a slightly wider melting range—can complicate a reaction pathway or introduce an unnecessary variable. We keep a practical focus: does the product perform in a real synthetic workflow, not just on the datasheet?
Responsibility doesn’t end when the shipment leaves our facility. Our environmental health and safety group keeps watch over solvent use, waste streams, and emissions during the manufacturing of 6-Phenyl-2-Thiouracil. We employ closed-loop systems and solvent recycling where feasible, reducing unnecessary discharge and maintaining a clean workplace.
We’ve adopted more efficient purification and drying steps to cut down on energy use and to avoid heavy-metal residues in the product. Some of our modifications may increase production costs in the short term, but they support a safer pipeline for both users and the environment. Our safety data and material handling guidelines stem from firsthand experience, stressing clear protocols for dust management, ventilation, and spill response. These practices don’t just meet rules—they make long-term business sense, because skilled staff and careful operators trust us when we show the “why” behind each procedure.
The story of 6-Phenyl-2-Thiouracil isn’t static; demand for specialty heterocycles is rising as novel drugs, advanced materials, and biotechnology solutions progress. Customers are asking for new forms: finer powders, micronized versions for rapid dissolution, or pre-screened materials tailored to automated synthesis platforms. We have begun investigating these developments through pilot projects and ramped up small-scale test batches for select partners. Real-life feedback cycles help us validate changes faster than broad-market guesswork.
With pharmaceutical pipelines growing more complex, compound purity and analytical transparency matter more than ever. We’re enhancing our in-line monitoring and data sharing platforms so that clients in regulated industries see what we see, immediately and without friction. Not every request turns into a standard product overnight, but our process grows stronger with every exchange.
There is no substitute for experience—those who have run reactors overnight, scrubbed glassware after failed reactions, or navigated the tangle of regulatory documentation know this better than anyone. Every batch of 6-Phenyl-2-Thiouracil comes through our doors not only as a bag of crystals but as a record of careful choices and lessons learned. Production staff handle the real risks and rewards, and analytical chemists scrutinize every detail so that surprises show up only in the data, not in the customer’s results.
This culture of care sets us apart from the reseller or distributor model. In our world, a single variable—a shift in raw input, a tweak to drying time, a modification to the filtering apparatus—has consequences. We celebrate every challenge because each one builds a tighter, more trusted pathway from reactor to end user.
Stepping back, 6-Phenyl-2-Thiouracil reminds us daily why manufacturing matters—the crucial link between the vision of the scientist and the reality inside the flask or reactor. Each inquiry about the compound’s behavior, every request for a novel form or tailored impurity profile, and all troubleshooting sessions coalesce into a product that reflects both technical insight and practical wisdom.
What we make is more than a set of numbers or bullet points on a brochure; it is the sum of collective hands-on experience and ongoing investment in process, people, and partnership. As new challenges arise—whether due to shifting project goals, regulatory tightening, or the pursuit of the next big breakthrough—we stand ready to serve, drawing from the lessons learned directly from our own factory floor.