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HS Code |
698917 |
| Chemical Name | 3-(4-Chloro-1,2,5-thiadiazol-3-yl)pyridine |
| Cas Number | 748815-01-2 |
| Molecular Formula | C7H4ClN3S |
| Molecular Weight | 197.65 |
| Appearance | Off-white to yellow solid |
| Melting Point | 122-126°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in organic solvents such as DMSO and DMF |
| Storage Conditions | Store in a cool, dry place and keep tightly closed |
| Inchi | InChI=1S/C7H4ClN3S/c8-6-7(12-10-6)5-2-1-3-9-4-5/h1-4H |
| Smiles | C1=CC(=CN=C1)C2=NSN=C2Cl |
| Synonyms | 3-(4-Chlorothiadiazol-3-yl)pyridine |
As an accredited 3-(4-CHLORO-1,2,5-THIADIAZOL-3-YL)PYRIDINE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 10g of 3-(4-chloro-1,2,5-thiadiazol-3-yl)pyridine is packaged in a sealed amber glass bottle with tamper-evident cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 3-(4-CHLORO-1,2,5-THIADIAZOL-3-YL)PYRIDINE: Securely packed drums or bags, maximizing space, ensuring safe chemical transport. |
| Shipping | The chemical **3-(4-chloro-1,2,5-thiadiazol-3-yl)pyridine** should be shipped in tightly sealed containers, protected from light and moisture. Transport should comply with relevant chemical regulations, ensuring clear labeling and documentation. Ship at ambient temperature, unless otherwise specified by the manufacturer. Handle with care, avoiding extreme temperatures or physical damage during transit. |
| Storage | Store 3-(4-chloro-1,2,5-thiadiazol-3-yl)pyridine in a tightly closed container, in a cool, dry, and well-ventilated area. Keep away from incompatible materials such as strong oxidizers and acids. Protect from moisture, heat, and direct sunlight. Use in a chemical fume hood with appropriate personal protective equipment. Clearly label the storage container and restrict access to authorized personnel. |
| Shelf Life | Shelf life: Store 3-(4-chloro-1,2,5-thiadiazol-3-yl)pyridine in a cool, dry place; stable for at least 2 years. |
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Purity 98%: 3-(4-CHLORO-1,2,5-THIADIAZOL-3-YL)PYRIDINE with purity 98% is used in pharmaceutical intermediate synthesis, where high-purity ensures efficient yield and minimal by-product formation. Melting Point 123°C: 3-(4-CHLORO-1,2,5-THIADIAZOL-3-YL)PYRIDINE with melting point 123°C is used in agrochemical formulation, where consistent melting behavior supports uniform blending. Particle Size <10 µm: 3-(4-CHLORO-1,2,5-THIADIAZOL-3-YL)PYRIDINE with particle size less than 10 µm is used in catalyst development, where fine particle size enhances surface area and reaction rates. Stability Temperature up to 150°C: 3-(4-CHLORO-1,2,5-THIADIAZOL-3-YL)PYRIDINE with stability up to 150°C is utilized in high-temperature polymerization processes, where thermal stability maintains structural integrity. Moisture Content <0.5%: 3-(4-CHLORO-1,2,5-THIADIAZOL-3-YL)PYRIDINE with moisture content below 0.5% is applied in electronic material preparation, where low moisture reduces risk of unwanted hydrolysis. Assay ≥99%: 3-(4-CHLORO-1,2,5-THIADIAZOL-3-YL)PYRIDINE with assay not less than 99% is employed in chemical reference standards, where high assay enables accurate analytical calibration. Residue on Ignition <0.1%: 3-(4-CHLORO-1,2,5-THIADIAZOL-3-YL)PYRIDINE with residue on ignition less than 0.1% is used in specialty coating formulations, where low residue contributes to product purity and film clarity. Solubility in DMSO >50 mg/mL: 3-(4-CHLORO-1,2,5-THIADIAZOL-3-YL)PYRIDINE with solubility in DMSO greater than 50 mg/mL is utilized in medicinal chemistry screening, where excellent solubility facilitates compound delivery. |
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Over the past decade, demand has grown fast for aromatic heterocyclic intermediates that serve the agrochemical and pharmaceutical sectors. Our own experience as a manufacturer revealed a shifting landscape, marked by higher expectations on purity, batch reproducibility, and regulatory compliance. 3-(4-Chloro-1,2,5-thiadiazol-3-yl)pyridine fills a unique space in this market, and production at scale brings its own set of challenges and valuable lessons.
Each batch we produce of 3-(4-Chloro-1,2,5-thiadiazol-3-yl)pyridine brings focus to precision, especially in ensuring consistent chlorination and heterocyclic ring integrity, which define the product's reactivity. Unlike less complex fused heterocycles, this molecule combines a pyridine ring with a chlorinated thiadiazole. The resulting structure produces a more stable product under storage, and that matters for manufacturers further along the supply chain. During development, synthesis parameters needed adjustment to keep impurity profiles especially low, so downstream users can predict performance. That consistency took rounds of pilot runs in full-sized reactors, not laboratory glassware. We realized that minor fluctuations in oxidation control or temperature shifts would tilt the ratio of positional isomers, which directly affects subsequent catalytic or coupling reactions.
Real-world performance depends on more than just nominal assay. Over years of production and collaboration with formulation teams, it became clear that trace isomer content or off-spec residues could trigger unexpected color reactions or even hinder crystallization in active ingredient synthesis. It’s one thing to hit 98% HPLC on a results sheet, it’s another to keep batch-to-batch UV and NMR profiles aligned, so formulation chemists avoid sudden troubleshooting periods in their own operations. Our on-site quality team, working with process engineers, takes multiple samples per batch at different points of the run to catch these early, before packaging begins. We authenticate our material against both internal standards and industry-wide benchmarks, an approach that simplifies audits and makes it easier to respond to traceability requests from end users.
Chemists approach us with a slate of uses for this compound, but demand primarily centers on its value as an intermediate in two areas: selective herbicides and advanced pharmaceutical building blocks. Structurally, the molecule allows targeted functionalization at both the pyridine and thiadiazole rings. This two-site versatility means it supports routes requiring nucleophilic substitution, cross-coupling, or ring-opening reactions — all within a single skeleton. In our customer network, some synthesis teams explore this intermediate as a scaffold to rapidly access active pharmaceutical ingredients targeting CNS disorders or emerging infectious diseases. On the crop science side, researchers turn to it as an anchor molecule when they want to introduce sulfur and nitrogen into ring systems, which often boosts the selectivity profile of modern herbicides.
In our own testing, the stability window for 3-(4-Chloro-1,2,5-thiadiazol-3-yl)pyridine lets it handle controlled heating steps or mild acidic conditions, which opens possibilities that less robust analogues simply don’t handle well. Scale-up partners especially appreciate the low exotherm risk during storage and blending, which cuts down on hazard assessments or insurance concerns in their own plants.
From a hands-on perspective, production teams note a few specific attributes that differentiate this molecule during actual handling. The chlorinated thiadiazole ring brings a characteristic odor, quickly detected in the air, so our plant upgraded localized fume extraction in reaction and packing areas. Operators note that standard nitrile gloves and splash goggles provide adequate protection, but powder handling benefits from a dust-free environment, as the crystalline product can cake under high humidity. We realized during shipping trials that usual steel drums sufficed at standard loads, but poly-liner bags or HDPE containers help with longer-term storage and prevent minor contamination if weather perturbations arise.
Waste management always draws regulatory scrutiny, especially in Europe and North America, so process water streams undergo on-site peroxide treatment to break down residual ring structures before final disposal. We tracked local air and water for trace chlorinated discharge and made infrastructure upgrades, rather than rely only on out-of-facility treatment, so we can submit cleaner compliance records during audits. Our staff attends annual training on evolving regulations, especially where heterocyclic chlorinated byproducts attract more attention from environmental agencies.
Across the catalog, our customers often weigh this product against similar pyridine or thiadiazole derivatives. Side-by-side in a process line, 3-(4-Chloro-1,2,5-thiadiazol-3-yl)pyridine stands out for tighter melting range and a lower residual solvent uptake. Our analytics group established that the thiadiazole motif delivers higher electron density versus standard pyridines, streamlining electrophilic substitution during synthesis. In feedback sessions with R&D chemists, they noticed fewer unwanted side-products in comparison trials against 4-chloropyridine or 1,2,5-thiadiazole-3-yl analogues, especially when processed in continuous flow reactors.
Compared to raw materials sourced from trade houses or batch resellers, our controlled full-route synthesis also ensures that each batch offers verifiable chain-of-custody details. This enables scale-up projects to satisfy not only quality but traceability requirements that are fast becoming standard, especially for global registrants in the plant protection and pharmaceutical industries.
Rosters of regulatory authorities and major buyers ask more probing questions about material sourcing than ever before. Years spent responding to audits and regulatory documentation confirmed the value of tracking every movement, from raw material intake to final sealed drum. Detailed batch logs, digital access to analytical results, and a focus on transparency mean that correction cycles are measured in hours, not weeks, if a customer or regulator flags an issue. Supply disruptions in recent years—spurred by logistics swings and regional unrest—highlighted how essential local and regional warehousing becomes, rather than banking only on bulk ocean freight.
We put effort into backward integration with reliable base chemical suppliers, ensuring that every ton of precursor thiadiazole comes with the same level of documentation and purity. This forward-thinking approach helps not only in day-to-day logistics, but also during inevitable external reviews and customer site visits. Globally, as new frameworks for chemical traceability arrive, the foundation laid by persistent documentation pays for itself—not just in smoother sales, but in lower risk of safety holds or fines.
It took years of iterative process development and real-world troubleshooting to land at the routine procedure we use today. Early technical hurdles included managing color formation during ring closure and dealing with unpredictable yields from standard chlorination agents. After repeated pilot runs, our chemists modified the solvent system and swapped oxidizing agents—eventually boosting yield by over 15% and trimming total reaction time by several hours. Investments in automation, including inline analytics, now allow finer tuning of reaction endpoints and feed addition rates.
Strong engagement between our R&D and production groups means innovations in laboratory scale ups get stress-tested on plant-sized equipment under actual batch volumes. Sometimes it means pausing to learn from a surprise—such as a runaway exotherm in summer months with higher ambient humidity—and adjusting protocols over the next few cycles to avoid similar occurrences. This spirit of continuous improvement still drives our teams, leading to the consistency and reliability that end users expect from a direct manufacturer.
Engagements with downstream application labs exposed the importance of reliable intermediates. In both agricultural and pharmaceutical lines, development chemists reported that inconsistent upstream material turned into yield hits or delays that cascaded through entire quarterly plans. We started seeing these feedback loops not as complaints, but as opportunities to engineer better control of our own processes.
By maintaining direct dialogue with development partners, we learned to prioritize not only chemical purity but also packaging formats that matched process needs—less bulk for pilot plants, larger drums for continuous processes. Each year, customer requests for tailored impurity profiles or matching color indices reveal evolving regulatory and research constraints, especially as the push for greener synthesis ramps up. The insights gathered fuel ongoing refinements, keeping our offerings closely aligned with the shifting requirements of those bringing new active ingredients to market.
Recent years placed a spotlight on the environmental footprint of specialty chemicals. We echo those concerns in day-to-day actions. Waste minimization starts with reaction optimization: lower solvent use, solvent recycling, and minimizing off-gas byproducts. Internal audits, sometimes running in parallel to third-party reviews, help spot parts of the process that generate excess waste or risk. Rather than treat environmental compliance as an afterthought, our teams collaborate with local experts to ensure that all effluent and emissions sit at or under regional targets.
We work closely with local authorities and community advisory boards—not just because regulations demand it, but because operational transparency is the best way to maintain a license to operate long-term. Site tours, regular reporting, and open question sessions create understanding that, while chemical manufacturing remains complex, responsible management benefits both business and the public.
Ongoing partnerships with university labs and independent researchers feed novel uses for 3-(4-Chloro-1,2,5-thiadiazol-3-yl)pyridine. Grants and co-authored studies often focus on developing active pharmaceutical ingredients or exploring new crop protection chemistries. In several collaborations, we’ve supplied technical samples, real-time process data, and sometimes full access to analytical results. Researchers benefit from direct insight, while we gain a preview of future commercial opportunities or regulatory demands. With broader moves toward sustainable synthesis, invested researchers look to this intermediate for cross-coupling experiments using green reagents or flow chemistry platforms, which has guided our own investments in continuous processing infrastructure.
Making this molecule consistently and safely is never “set and forget.” Raw material volatility, energy costs, and evolving occupational safety rules keep us vigilant. Longer-term, we expect more scrutiny over trace environmental residues, so finding ways to further cut waste or move to fully green oxidants and solvents will form the backbone of ongoing improvement. We continue to participate in industry working groups focused on safer heterocyclic chemistry, and actively invest in new analytical tools that promise better in-process control. The know-how built over thousands of batches allows nimble response to new application requirements from the pharmaceutical, crop protection, and specialty chemical sectors.
Supply reliability remains a core concern for buyers. As a direct manufacturer, we know the pitfalls of depending solely on spot markets or trading houses for key inputs. By holding a portion of production for on-demand dispatch and maintaining long-term supply agreements with key accounts, we balance efficiency and resilience. Feedback from global customers highlights how sudden logistics bottlenecks or customs delays risk entire projects. Our local and regional stockpiles, as well as multi-modal shipping capabilities, address these interruptions faster than remote resellers ever could.
We also work to educate customers about safe handling, regulatory filings, and the realities of downstream operational integration—not simply providing material, but sharing decades of practical manufacturing experience to aid their own teams. In an era where information is as valuable as product, this mutual knowledge transfer often distinguishes direct manufacturers from intermediaries.
Decades making 3-(4-Chloro-1,2,5-thiadiazol-3-yl)pyridine, paired with open lines of communication to application chemists and industrial partners, built our technical base. Our investments in process control, quality assurance, and compliance are directly informed by real production lessons—not abstract textbook formulations. We focus on enabling our partners to innovate and commercialize new products with lower risk and greater confidence, offering not just material on a datasheet, but a track record backed by transparency and responsiveness.
This is how a chemical manufacturer views an intermediate — as both a technical achievement and a trust-based product, woven into the shared progress of clients and communities alike.