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HS Code |
494932 |
| Cas Number | 1073-72-9 |
| Molecular Formula | C4H3ClO2S2 |
| Molecular Weight | 182.65 |
| Appearance | Colorless to pale yellow liquid |
| Melting Point | -3 °C |
| Boiling Point | 96-98 °C (14 mmHg) |
| Density | 1.503 g/cm3 at 20 °C |
| Solubility | Decomposes in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Refractive Index | 1.596 |
| Synonyms | Thiophene-2-sulfonyl chloride |
| Flash Point | 97 °C |
| Storage Condition | Keep tightly closed and store in a cool, dry, well-ventilated place |
As an accredited 2-Thiophenesulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Thiophenesulfonyl Chloride, 25g, is supplied in a tightly sealed amber glass bottle with a tamper-evident cap for protection. |
| Shipping | 2-Thiophenesulfonyl Chloride is shipped in tightly sealed containers, protected from moisture and light. It is classified as a hazardous material and transported under strict regulatory guidelines. Packages are clearly labeled, and handled by trained personnel to ensure safety during transit and storage. Appropriate documentation accompanies every shipment for compliance and tracking. |
| Storage | 2-Thiophenesulfonyl chloride should be stored in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong bases and oxidizers. Keep the container tightly closed and protected from direct sunlight. Store in a corrosion-resistant container with a resistant inner liner. Handle under inert atmosphere if possible, and avoid exposure to air to prevent hydrolysis and decomposition. |
Applications of 2-Thiophenesulfonyl Chloride in Industrial Manufacturing2-Thiophenesulfonyl chloride acts as a key intermediate in advanced chemical synthesis, featuring high reactivity and selectivity for various specialty manufacturing fields. Our facility supports pharmaceutical, agrochemical, material science, and dye sectors with direct integration into critical process steps, ensuring strict adherence to international standards. 1. Pharmaceutical Sulfonamide SynthesisPharmaceutical manufacturers rely on this material for targeted sulfonamide group installation during intermediate or API synthesis, especially in anti-infective agents and enzyme inhibitors. The reagent reacts with amines under controlled, anhydrous conditions, allowing for fine-tuning substitution patterns. Precise process control ensures minimization of potential impurities, with in-process monitoring for residual chloride content and reaction completion before downstream processing. Advanced purification follows, preparing intermediates for stringent pharma quality requirements. Industry compliance standards
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2. Agricultural Fungicide Intermediate ProductionCrop protection manufacturers use this compound as a pivotal sulfonylating agent in the development of heterocyclic fungicidal actives. Its role focuses on attaching sulfonyl groups to thiophene backbones, generating potent precursors for triazole or azole-class fungicides. The process requires rigid moisture control and validated quenching steps to eliminate unreacted material, and finished intermediates undergo residue and purity checks aligned with global agrochemical directives. Industry compliance standards
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3. Advanced Organic Electronic Material SynthesisSpecialty electronic material firms integrate this intermediate into thiophene-based polymer and oligomer fabrication, especially for high-performance organic field-effect transistors (OFETs) and conductive coatings. In this application, the material drives sulfonylation reactions expanding conjugation or tailoring electronic affinity. Clean-room handling, confirmed by low halide contamination, is essential, and each batch must meet electronic grade criteria before polymerization steps. Industry compliance standards
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4. Specialty Dye ManufacturingIndustrial dye producers employ this building block for introducing sulfonyl groups into aromatic or heterocyclic dye frameworks. Selectively increasing dye solubility or imparting unique color fastness, this material reacts at targeted points to form dispersal or reactive dye families. Strict controls for purity and trace sulfonic acid by-products are enforced, with analytical verification before formulation into pigments or concentrates. Industry compliance standards
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Every day on the production line, we run careful checks on purity, handling, and yield. Our 2-Thiophenesulfonyl Chloride sits at the intersection of theory and practical application, especially among pharmaceutical and fine chemical producers. Over the years, requests for 2-Thiophenesulfonyl Chloride (commonly known by its CAS number 1120-36-1) have increased in step with the market’s shift toward heterocyclic building blocks. We see this demand from shops aiming to design next-generation agrochemicals or new classes of anti-infectives—a sign that molecular design is evolving. From direct customer feedback, chemists look for reagents able to introduce a sulfonyl group onto heteroaromatic rings without extraneous by-products or technical headaches.
Our seasoned operators blend long practice with strong traceability. The powder leaves our reactors at a purity we keep above 98%, and we always verify this through triple-point HPLC and precise titration. This means that when chemists open up a drum from our process, they see material free of oiling or abnormal particulate. The appearance: white to pale yellow crystalline solid, mild, pungent, often with just a trace of sulfurous sharpness that hints at its potent reactivity. We never compromise on minimizing moisture content—in our experience, trace water degrades sulfonyl chlorides quickly—so we use double-sealed bags under inert nitrogen atmospheres. Transport conditions matter, because even modest heat or humidity can prompt unwanted hydrolysis. From vat to drum, we enforce tight controls pinpointed by careful data logging, because real work in the lab starts with clean, predictable material.
2-Thiophenesulfonyl Chloride offers a reliable entry point for sulfonamide synthesis. We know that for bench chemists, a strong sulfonylating agent with high selectivity for nucleophilic aromatic substitution reactions means one less purification headache downstream. Every production cycle, we ensure our product supports high yields in the synthesis of thiophene sulfonamides and in turn, the intermediates for pharmaceuticals and advanced materials. Customer requests often point to the need for batch-to-batch reproducibility and robust performance in Buchwald-Hartwig amination or Suzuki coupling protocols. That’s why we build up every vessel charge by tracking raw material sources, monitoring our columns, and verifying end-point active chlorine content.
In industrial-scale use, sulfonyl chlorides can be finicky. During synthesis, the shallow distinction between a clean, rapid sulfonation and an over-chlorinated by-product matters. Our formulation minimizes by-product generation thanks to tuned reaction times and optimized acid chlorination. End users often tell us that alternative sulfonyl chlorides cause darkening, excessive residue, or impurity issues in column purification. By contrast, our 2-Thiophenesulfonyl Chloride consistently delivers a single, clean spot under TLC, reflecting the practical decisions we make upstream—tight temperature profiles, efficient separations, strict exclusion of DMSO impurities (which are notorious quenchers), and continuous in-house analytics for contaminants.
A lot of questions from the field center around thionyl chloride residuals. Low-level SO2 or HCl impurities can sabotage scale-up. We respond by purging all batch vessels post-reaction and running post-synthesis scavenging before final drying. We set our residual SO2 content below 0.1% and keep chloride traces to a minimum. In practice, this means one less uncertainty for R&D teams chasing tricky nucleophilic aromatic substitutions and no interruptions from equipment corrosion or ghost peaks during chromatography.
Our plant workers suit up in full PPE and move deliberately through each stage, not out of rote habit but because sulfonyl chlorides, especially 2-Thiophenesulfonyl Chloride, demand a focus on containment. A single open drum in humid air could start its exothermic decomposition, so we move product only within shielded, nitrogen-purged workspaces. We have learned that air-sensitive handling and proper sealing are more than certifications—they preserve product lifetime and functional reactivity.
Operations teams on-site ensure every package leaves with consistent particle size distribution. We granulate to a median of 400-600 microns, since too fine particles increase dust and inhalation risk, while overly coarse lumps slow dissolution during charge-in. Our colleagues at pharmaceutical plants report smoother dosing into process reactors using this calibrated spec. Drums remain sealed until use and we train partners on correct scoop-and-pour techniques to minimize operator exposure and avoid static discharge near the workbench.
There has never been a shortcut when it comes to waste management on the factory floor. By working closely with local authorities and keeping up with current guidelines, we neutralize waste streams on site. The safest route involves alkaline hydrolysis and careful ventilation, which our experience shows pins down both odor and corrosivity before offsite disposal.
Over years of customer visits and R&D partnerships, we have found that not all sulfonyl chlorides react the same in the real world. Bench chemists often reach for benzenesulfonyl chloride out of habit, only to run into low regioselectivity or more frequent side-chain rearrangements. By contrast, 2-Thiophenesulfonyl Chloride consistently outperforms in heterocyclic frameworks, especially when the synthetic targets involve nitrogen or oxygen nucleophiles attached to challenging aryl groups.
We have seen that in comparison to its close cousin 3-thiophenesulfonyl chloride, the 2-position product leads to intermediates ideally positioned for downstream cross-coupling. Pharmaceutical research teams have demonstrated higher functional group compatibility for 2-isomers, which translates to safer scale-up and reduced by-product load.
From a cost-of-goods viewpoint, we know large buyers often compare the total performance package. While aromatic sulfonyl chlorides (such as p-toluenesulfonyl chloride) remain less expensive in bulk, their lack of selectivity in heterocycle applications generates more by-products and costly rework steps. 2-Thiophenesulfonyl Chloride punches above its price tag for complex sulfonamide and sulfonylurea preparations—areas where a misstep can spike expenses.
We have made enough batches to understand how even minor process tweaks impact the end user. Small shifts in raw material source, temperature drift, or solvent ratios ripple through to customer labs, sometimes with unexpected results. To avoid this, every campaign, we qualify incoming sulfur, thiophene, and chlorinating agents against pre-set specs. Our staff runs tighter QC than any external standard requires, and we adjust plant parameters to hit repeatable yields—month in, month out. There is no room for “close enough”.
Customers rely on our transparency. We provide batch analysis and full traceability with every shipment. In customer audits, our partners have the right to observe not only the final product but also the cleaning logs of each reactor, the titration records of every delivery, and environmental monitoring reports. If a batch shows even a slight deviation in color or melting point, we trace root cause all the way back to the catalyst charge and auxiliary agent lots. Years of running production lines have shown us that openness keeps our processes sharp and earns long-term trust down the value chain.
Delivering to customers in Asia, Europe, and America, we navigate a range of regulatory and safety requirements. We never take shortcuts on documentation. Each drum carries an unbroken certificate of analysis, MSDS, and batch record. Safety for the end user begins on our side: we train every operator not just in handling, but also incident response. Even a small leak draws an immediate plant-wide lock-down, full air monitoring, and root-cause investigation. This engrained culture of safety ensures that 2-Thiophenesulfonyl Chloride doesn’t introduce risk into downstream labs.
In major export markets, we know customs and port inspection are not just “boxes to tick.” Material held up for missing or incomplete paperwork can paralyze customer timelines. That’s why each consignment includes full nomenclature, hazard identification, packing group data, and traceable lot information. In regions where REACH registration comes into play, we maintain a shelf of in-house dossiers ready for inspection, with completed risk assessments. Our direct compliance saves time and money for everyone in the supply chain.
Feedback forms the backbone of our process improvement. Every year, our technical sales team and process chemists visit hundreds of labs. Reports from research partners give us a steady flow of ideas—from shifting moisture spec limits down by 0.01%, to exploring smaller pack sizes for university trial orders. One large producer of API intermediates credited a 15% increase in isolated yield simply to improved material consistency from our site. Other partners in electronics chemistry remarked on improved device yields, thanks to the narrow impurity window we hold.
We know that direct contact with users pays dividends. By supporting even small pilot-lab scaleups with samples, technical notes, and troubleshooting on reaction scaling, we deepen our own process experience. This practical collaboration—reaction troubleshooting by phone or on-site—has, in many cases, resulted in route modifications and cost savings. For example, a client in Germany found that replacing an aromatic sulfonyl chloride with our product cut two recrystallization steps out of their purification sequence. We, in turn, identify potential tweaks to our formulation or packaging, bringing cross-industry learning back to our production teams.
Like any specialty chemical, 2-Thiophenesulfonyl Chloride presents challenges around both supply reliability and downstream safety. Raw material sourcing comes with swings in thiophene pricing and international logistics volatility—storms or customs delays in major ports can disrupt the schedule. Thanks to dual-sourcing and local inventory buffers, we keep delivery times predictable. Years with supply chain surprises shaped our approach: we run continuous forecasting and partner with multiple freight lines to sidestep overdue shipments.
Another real hurdle: long-term stability during storage. Even in double bags and nitrogen-flushed drums, prolonged heat or accidental seal compromise during transport accelerates decomposition and lowers active ingredient levels. As a solution, we advise refrigerated storage and rapid inbound inspection upon arrival. This has meant investing in insulated shipping and taggable TTI (time-temperature indicator) labels, plus online shipment tracking for time-sensitive orders. Educating logistics partners made a clear difference; fielding a phone call the moment a delay crops up can save thousands in lost material.
On the technical front, some reactions crave ever tighter purity thresholds. Customers in electronics formulation or pharmaceutical intermediate work push for even lower metal and solvent residue levels. We constantly trial new purification stages—charcoal scrubbing, multi-stage crystallization, and advanced filtration systems. Every innovation here later translates to enriched research results and lower background interference for the end users.
From the earliest pilot batches years ago, we saw the downstream impact of chemical handling. Like many synthetic intermediates in this class, 2-Thiophenesulfonyl Chloride breaks down to acidic by-products. We re-engineered our production plant to recover heat wherever practical, and capture emissions through triple-scrubber stacks. Waste minimization focuses on solvent recapture, and we set up on-site treatment before off-site disposal in certified facilities. Partners know we will never pass along unneutralized effluent or off-spec by-products.
Good manufacturing practice runs parallel with environmental protection. We tune batch sizes, minimize solvent waste, and train field partners on accidental spill management. Regular third-party audits confirm our compliance, and we share environmental performance data upon request, building trust with our community and downstream users.
In the end, a successful reagent means reliability—not just on paper, but in the hands of the chemists and engineers who use it day in and day out. Our 2-Thiophenesulfonyl Chloride stands not as an isolated product, but as a core enabler for those pushing boundaries in molecule making. Past years have taught us that continuous refinement, attentive listening, and honest feedback from real users drive better chemistry. Each drum carries not only a high-purity sulfonylating agent, but the experience of a team dedicated to meeting evolving challenges across labs and factories worldwide.
For those looking to cut through the noise and source a reagent that stands up to the demands of pharmaceutical synthesis, electronic materials, and specialty chemistry, we remain committed to a partnership founded on consistency and transparency. As processes scale up and innovation pushes forward, we back every order with the hard-won insights of our crew and a track record of results and reliability.