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HS Code |
313971 |
| Name | Dithiouracil |
| Synonyms | 2-Thiouracil-4-thiol |
| Chemical Formula | C4H4N2O2S2 |
| Molecular Weight | 176.22 g/mol |
| Cas Number | 141-90-2 |
| Appearance | Pale yellow crystalline powder |
| Melting Point | 327-329 °C (decomposes) |
| Solubility In Water | Slightly soluble |
| Pka | 7.6 |
| Storage Conditions | Store in a cool, dry place, protected from light |
| Iupac Name | 2,4-dithiouracil |
| Pubchem Cid | 70293 |
As an accredited Dithiouracil factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White plastic bottle labeled "Dithiouracil, 25g" with hazard symbols, batch number, and manufacturer details; tightly sealed with a screw cap. |
| Shipping | Dithiouracil should be shipped in tightly sealed containers, protected from light and moisture. Transport under ambient temperature is typically acceptable, but consult relevant regulations. Ensure proper labeling as a chemical substance, and ship with appropriate documentation. Handle with care to avoid breakage or contamination during transit. Follow local, national, and international shipping regulations. |
| Storage | Dithiouracil should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature and avoid exposure to heat or open flames. Ensure appropriate labeling and keep away from sources of ignition to prevent decomposition or hazardous reactions. |
Applications of Dithiouracil in Industrial ManufacturingAs a specialized manufacturer of Dithiouracil, we supply global industries relying on its chemical properties for advanced process control, stability modification, and targeted synthesis. Below, we present verified industrial uses with details on integration, formulation, standards, and delivered end-product types. 1. Photographic Chemical IntermediatesDithiouracil serves as an essential intermediate for the synthesis of certain silver halide stabilizers and photographic developer agents. Its sulfur-containing structure enables it to modulate reduction-oxidation reactions during the preparation of developer solutions and image stabilizers, particularly for high-resolution imaging materials. Customers choose our material for consistent performance in large-scale film and printed plate manufacturing lines. Industry compliance standards
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2. Pharmaceutical Intermediate for Thyroid ModulatorsPharmaceutical manufacturers use Dithiouracil as a structural precursor in the synthesis of specific thyroid medication and antithyroid compounds. Its controlled reactivity allows precise functionalization in active pharmaceutical ingredient (API) production under cGMP protocols, supporting global supply chains for anti-hyperthyroid treatments. Industry compliance standards
Typical usage ratio
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3. Corrosion Inhibition for Industrial Cooling SystemsDithiouracil provides specialty corrosion inhibition in open and closed-loop industrial water circulation systems, including power plant cooling towers and petrochemical heat exchangers. By adsorbing on metal surfaces and interrupting cathodic oxygen reduction pathways, it preserves asset longevity in aggressive scaling and oxidizing chemistries, where high sulfur donor affinity is essential. Industry compliance standards
Typical usage ratio
Downstream process integration
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4. Polymerization Chain Transfer Agent in Specialty ResinsIn advanced polymer synthesis, Dithiouracil operates as a chain transfer and molecular weight control agent, essential for preparing high-end resins with predefined branching and functional group density. Processing engineers in resin and plastics manufacturing value its sulfur donor profile for enabling precision design of backbone architecture, especially in polythioamide and related specialty elastomeric polymers. Industry compliance standards
Typical usage ratio
Downstream process integration
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At our production facility, we’ve had hands-on involvement with Dithiouracil for over a decade, refining both process and purity to meet a wide spectrum of practical demands. Dithiouracil, a sulfur-containing heterocyclic compound, sits among unique organosulfur agents recognized for their ability to engage directly with both biological and industrial targets. In manufacturing, you learn quickly that not all analogs with similar ring structures offer the same level of reliability; Dithiouracil bridges gaps that few other sulfur compounds address. Every batch delivers an unmistakable yellowish powder, crystalline and consistent in physical profile. Near-millimeter granules flow readily from our production lines, reflecting controlled temperature and humidity throughout our synthesis cycles.
Our experience shows that subtle impurities in this class can derail downstream performance, especially in applications where redox reactions rule outcomes. We maintain batch records of the structure—predominantly 2,4-dithiouracil—backed by multiple layers of quantitative analysis. It’s not just a matter of running TLC or HPLC to check purity. During the final stage, we rely on sulfur analysis and melting point checks, since slight deviations will surface as sluggish reactivity or poor solubility. Lab teams here know that sulfidic notes—the odor profile—signal freshness and unadulterated content, while unusual browning warns of oxidation. Our finished product consistently lands in the melting range around 330°C, distinctly higher than many structurally related sulfur analogs, showing the robust bonding inside the ring.
In the world of lab chemistry, end-users often compare Dithiouracil to 2-thiouracil and standard uracil derivatives. From our side, the dual sulfur insertion delivers a more reactive nucleophile profile. Researchers and process engineers trust it when seeking stronger metal-chelation properties without sacrificing stability. Dithiouracil outperforms typical mono-thio compounds in forming complexes with soft transition metals. This compound lends itself to heavy metal detection and recovery, particularly in gold and mercury systems, because its two sulfur atoms present an enhanced binding motif. For this category, speed of complexation and lack of unwanted side products always matter—two parameters tied directly to the way we crystallize and dry each lot.
In scale-up, Dithiouracil holds its own when big reactors start running. Unlike many related agents, it doesn’t off-gas ammonia or produce toxic fragments easily under heating in a closed system. People in our technical service department often advise formulators dealing with downstream discoloration or off-odors to consider swapping in Dithiouracil over other sulfur donors or reducing agents. It controls itself better under moderate pH shifts and doesn’t foster runaway polymerization which other sulfur heterocycles sometimes do.
From a physical handling perspective, our Dithiouracil avoids the caking and lumping issues seen with granular elemental sulfur. It pours cleanly. Production workers, loading hoppers or pressing tablets, regularly comment on its minimal dust generation — a comfort when measuring for kilograms instead of grams. In actual processing, its dense form cuts down on losses during equipment transfer, with fewer fines discharged through air filters.
End users usually first encounter Dithiouracil in very targeted reactions. Medicinal chemists looking for unique analog substitution or bioconjugation possibilities call on it because of this reactivity. Our relationships with R&D teams emphasize purity, since even minor halide residues, left over from other synthetic routes, can complicate pharmaceutical assays. Our batches restrict these side residues, so folks in downstream synthesis don’t waste time troubleshooting aberrant solubility profiles.
Industrially, Dithiouracil fits well for electrochemical metal stripping or as a selective corrosion inhibitor. Several plating shops in Asia switched to our grade due to tighter control over anodic passivation. They reported longer bath longevity and less unpredictable deposition. Textile dyeing partners approach us for the compound’s ability to break down stubborn azo bonds — helping with color removal in effluent treatment. Biologists and enzymologists, who once depended on milder sulfur donors, now replace them with Dithiouracil due to its sharper, more predictable response in thiolating nucleic acids or proteins.
In our own pilot work, we’ve trialed Dithiouracil for synthesis of photoswitches and as part of advanced polymer projects—areas where sulfur’s electron-donating effect imparts noteworthy new characteristics. More chemical engineers are pushing for greener, less toxic routes to organosulfur compounds, steering away from older, hazardous byproducts. Through hands-on batch trials at scale, our Dithiouracil offerings have allowed those teams to pursue cleaner, higher-yield pathways for these novel materials.
Producing Dithiouracil at scale presents its own set of lessons. Our synthesis relies on tightly regulated thermal conditions and accurate sulfur gauging. If temperature drifts or reagents stray out of spec, off-color intermediates signal a probable drop in activity. Workers at our plant are trained to spot these changes long before they reach quality control — it marks the difference between consistent reactivity and product returned due to customer complaints.
Our operators weigh out solid sodium derivatives for reaction. Steam-jacketing of kettles ensures reliable phase separation, and the transfer process steers clear of cross-contamination that could encourage unexpected side reactions. In our experience, the difference between good Dithiouracil and merely passable material lies more in these process controls than in the initial starting materials. Over time, we’ve found that skipping a deep vacuum drying step leaves in trace moisture, resulting in product that clumps or ages prematurely. So, we always maintain full vacuum cycles that drive off loosely bound water — avoiding surprises on the customer’s bench.
Quality assurance pulls random samples for FT-IR and NMR spectroscopy, making certain that batch variability doesn’t creep in. Over the last year, we’ve responded to customer feedback about trace iron content in competitor’s materials, and doubled down on filtering every intermediate through micron-level mesh. By sharing these QC routines directly with returning clients, confidence builds organically, not through generic certificates but through proven experience.
We also address environmental responsibility in every production run. Our energy systems recover waste heat from exothermic stages, channeling it back into reactor feedstock warming. Our waste sulfur streams are reverted into subsequent batches where purity specs permit, keeping operational footprints tight and minimizing emissions from sulfur combustion. Across several campaigns, this has reduced our overall sulfur procurement bill, cut waste, and let us pass along pricing consistency.
Comparing Dithiouracil to 2-thiouracil, thiosemicarbazide, or thioacetamide paints a clear picture for formulators seeking performance without compromise. The extra sulfur atom in Dithiouracil offers increased affinity in metal chelation settings, producing complexes that resist breakdown even in acidic streams. Personnel handling gold cyanidation always highlight how this difference cuts reagent costs by improving each pass in the extraction cycle.
We’ve sent analytical samples to direct users for side-by-side heat stability and reaction yield evaluations. Reactions which demand prolonged heating, such as wrapping up heterocycle synthesis or slowly reducing metal ions, see none of the premature volatility issues that crop up with competing compounds. Dithiouracil retains integrity where 2-thiouracil or monothio variants fizz or discolor, especially as batch sizes move up from grams to multiple kilograms.
Our downstream users in research and industry have noted that the sulfur content in Dithiouracil avoids over-reducing target substrates, so side products stay low. Standard thioamides, by contrast, demand extra cleanup stages — not a welcome sight for continuous production lines or pharmaceutical QA teams pressed for time.
Comparing solubility, Dithiouracil dissolves best in alkaline water or polar organic solvents, making formulation planning smoother for water-based or mixed solvent systems. In spot checks with partners in the electroplating sector, better reaction profiles resulted from this combination of solubility and redox stability against standard thio reagents.
At the plant, handling Dithiouracil takes straightforward precautions. Unlike volatile organothio compounds, it does not create explosive dust clouds, nor does it break down into hazardous fumes under routine temperature excursions. Workers suit up with minimum PPE—mainly gloves and safety goggles—with more intense protocols reserved for open mixing. Morning toolbox talks on the plant floor focus less on exothermic risk and more on house-keeping: an approach that reflects both the material’s stable handling profile and our real-world experience bundling tons into shipment drums.
While Dithiouracil holds together robustly under most warehouse conditions, we keep all inventory sealed tightly in lined drums, away from direct sunlight or acids. This avoids avoidable aging of the sulfur bonds and inhibits formation of breakdown products. Our plant logs traceability on every outgoing lot—all the way from raw feedstock intake to final testing—providing transparency for all risk audits and compliance reviews. Our familiarity with handling similar sulfur chemicals pays off here, allowing us to anticipate possible challenges, especially in transit through humid or variable climates.
Demand for Dithiouracil runs steadily year by year, mainly due to the combination of better metal recovery rates, reliable biological incorporation, and unique reactivity. Production efficiency on our end lets us adjust to volume swings — from custom pilot-scale batches for specialty researchers to ongoing multi-ton commitments for industrial partners. Teams here keep a close eye on regulatory shifts involving organosulfur production. As tighter purity controls and environmental restrictions emerge, our in-house systems adapt rather than resist these tides.
Sharing technical documentation with all stakeholders, from procurement managers to end-application chemists, keeps expectations realistic. We learned long ago that sending out heavy stacks of templated certificates often raises more questions than answers. Instead, our support engineers engage directly, offering batch-specific analytic details and supporting on-site troubleshooting.
Over time, clients in the electronics and renewable sectors have pointed toward additional avenues for Dithiouracil’s strengths. For example, in battery formulation, its sulfur donor capacity finds usage as chemical intermediates for electrolyte additives. Teams developing novel photovoltaics test its ring system as a basis for light-absorbing assemblies. Every time a new sector picks up our product, our in-house team learns alongside, tweaking our synthetic methods in small increments to keep apace with their discoveries.
Direct feedback from end users shapes nearly every technical tweak we introduce. We recall a case from a year back when a pharmaceutical client reported inconsistent binding in a critical downstream reaction. Joint review of their application and our batch process uncovered that a minor shift in reagent ratio — corrected in future syntheses — solved problems both for them and for users down the line. Such improvements flow directly into updated batch protocols, avoiding recurrence and giving future users access to stronger, more reliable lots.
Support goes well beyond the sale. Our technical team provides preparation support, checks reactor compatibility, and troubleshoots unexpected outcomes on both pilot and full-scale production runs. A recurring challenge in international logistics—humidity-induced caking—resulted in us swapping out container liners and adjusting drying end-points. Problems encountered inside our factory rarely remain siloed; we broadcast solutions to all clients, embedding reliability into all outgoing shipments.
From the perspective of the actual manufacturer, Dithiouracil stands out for its balance of reactivity, stability, and manageable handling. Production, testing, and packaging echoes decades of trial, adaptation, and technical partnership. Each drum shipped reflects not just process optimization but hundreds of micro-decisions across the entire workforce, responding to both market signals and hands-on customer insight. Whether in a tightly controlled pharmaceutical synthesis or a challenging industrial metal recovery application, the reliability of this compound pays back in saved time, fewer interruptions, and more consistent results batch after batch.
As a specialty chemical manufacturer, we treat feedback and evolving practice as drivers for better materials and safer, more efficient production. Dithiouracil may appear to outsiders as just another yellow powder, but for those who depend on it — and those who make it — every step matters.