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5-(2-Pyridyl)Thiophene-2-Sulfonyl Chloride

    • Product Name 5-(2-Pyridyl)Thiophene-2-Sulfonyl Chloride
    • Alias 2-Pyridylthiophene-2-sulfonyl chloride
    • Einecs 414-680-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    654051

    Product Name 5-(2-Pyridyl)Thiophene-2-Sulfonyl Chloride
    Cas Number 104273-86-9
    Molecular Formula C9H6ClNO2S2
    Molecular Weight 259.74 g/mol
    Appearance White to off-white powder
    Purity Typically ≥98%
    Solubility Soluble in organic solvents (e.g., dichloromethane, chloroform)
    Storage Conditions Store in a cool, dry place; protect from moisture and light
    Synonyms 2-Pyridyl-5-thienylsulfonyl chloride
    Smiles C1=CC=NC(=C1)C2=CC=C(S2)S(=O)(=O)Cl
    Hazard Statements Corrosive, may cause severe skin burns and eye damage
    Inchi InChI=1S/C9H6ClNO2S2/c10-15(12,13)9-4-3-8(16-9)7-2-1-5-11-6-7/h1-6H

    As an accredited 5-(2-Pyridyl)Thiophene-2-Sulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 5 grams of 5-(2-Pyridyl)Thiophene-2-Sulfonyl Chloride, tightly sealed with a screw cap and label.
    Shipping 5-(2-Pyridyl)Thiophene-2-Sulfonyl Chloride is shipped in tightly sealed containers under inert gas or desiccant to prevent moisture and air exposure. Transport is carried out in compliance with chemical safety regulations, using protective packaging to avoid leaks, spills, or contamination, and accompanied by relevant safety data and hazard labels.
    Storage 5-(2-Pyridyl)Thiophene-2-Sulfonyl Chloride should be stored in a tightly sealed container under a dry, inert atmosphere (such as nitrogen or argon) to prevent hydrolysis. Keep it in a cool, well-ventilated area, away from moisture, heat, and incompatible substances like strong bases or water. Use appropriate chemical storage cabinets, ideally in a cool (2–8°C) environment for optimal stability.
    Application of 5-(2-Pyridyl)Thiophene-2-Sulfonyl Chloride

    Applications of 5-(2-Pyridyl)Thiophene-2-Sulfonyl Chloride in Industrial Manufacturing

    5-(2-Pyridyl)Thiophene-2-Sulfonyl Chloride serves as a specialized intermediate for advanced functional materials, fine chemical synthesis, and pharmaceutical ingredient development. Our manufacturing facility delivers material with precise quality control standards to meet the specific requirements of downstream sectors that demand both structural selectivity and reliable performance.

    1. Pharmaceutical API Synthesis

    This compound is widely used as a sulfonylation agent in the assembly of heterocyclic building blocks for pharmaceutical actives, especially in scaffolds for kinase inhibitors and CNS-targeted drugs. Its selective reactivity toward amines allows for precise introduction of sulfonyl-pyridyl-moieties in the final synthetic steps of API production. Manufacturers depend on stable sourcing for critical batch-to-batch reproducibility within QC-monitored cGMP environments.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211
    • European Pharmacopoeia monographs for related synthetic intermediates
    • Japanese Pharmacopoeia General Notices

    Typical usage ratio

    • 0.9 – 1.1 molar equivalents relative to primary amine or phenol substrates in sulfonylation reactions. The exact ratio adjusts based on substrate reactivity and desired yield, optimized during process scaling.

    Downstream process integration

    • Added as a late-stage reagent after core scaffold assembly. Reacts under basic conditions (e.g., triethylamine in DMF or DCM) followed by aqueous workup, then purification by column chromatography or crystallization.

    Final product types

    • Kinase inhibitor drug substances
    • Neuroactive molecule APIs
    • Pyridyl-sulfonamide derivatives for further modification
    • Generic and proprietary pharmaceutical actives

    2. Agrochemical Intermediate Production

    Agrochemical formulators rely on this sulfonyl chloride to introduce pyridyl functionalities in the synthesis of selective herbicide and fungicide molecules. The functional group enhances water solubility and bioactivity. Downstream producers focus on regulated synthesis routes to maintain environmental and product safety profiles.

    Industry compliance standards

    • FAO/WHO Food and Agriculture Organization Technical Guidelines
    • REACH Regulation (EC) No 1907/2006 for chemical registration
    • US EPA Pesticide Registration Manual
    • GB 4839-2008 Safety Standards for Agricultural Chemicals (China)

    Typical usage ratio

    • 0.95 – 1.2 molar equivalents in heterocycle sulfonylation steps; precise quantity determined by target molecule structure and desired purity. Both small- and large-scale reactors adjust dosage according to reaction efficiency and downstream purity targets.

    Downstream process integration

    • Charged into the reaction after primary aromatic coupling for direct sulfonylation. Used under controlled temperature conditions with inorganic or organic bases to prevent degradation of active intermediates.

    Final product types

    • Selective pyridine-based herbicides
    • Triazole fungicide intermediates
    • Sulfonamide crop protection agents
    • Regulated pre-formulated technical materials

    3. Material Science Functionalization

    Advanced material manufacturers utilize this intermediate for surface modification in electronic and sensor applications. Incorporation of the pyridyl-thiophene sulfonyl group enhances electronic properties and enables subsequent functional attachment in polymer backbones or nano-structured surfaces.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • IEC 62474 Material Declaration Standard
    • RoHS Directive 2011/65/EU for hazardous substances
    • ASTM D6288 Standard Guide for Material Selection

    Typical usage ratio

    • 1.0 – 5.0 wt% relative to base polymer or substrate, depending on the degree of functionalization required for specific conductivity or surface reactivity.

    Downstream process integration

    • Integrated in the polymerization process or through post-polymerization surface reaction, typically via solution phase immobilization or covalent attachment protocols. Reacted with activated surfaces in controlled atmospheres.

    Final product types

    • Functionalized polymer films for OLEDs
    • Sensors and biosensor chips with modified surfaces
    • Electroactive coatings for printed electronics
    • Microelectronic device substrates

    4. Specialty Dye and Pigment Manufacturing

    Dye producers select this sulfonyl chloride for the targeted synthesis of pyridyl-modified thiophene dyes. Its role enables covalent linkage to chromophore cores via sulfonyl bridges, improving solubility and lightfastness in pigment applications. Quality-focused synthesis ensures tight control of byproducts and heavy metal residues, which is critical for textile and ink applications.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (textile chemicals)
    • REACH Regulation Annex XVII (pigment restrictions)
    • EN 71-3 Safety of Toys – Migration of Certain Elements (for children’s ink)
    • ISO 787-2 General methods of test for pigments and extenders

    Typical usage ratio

    • Separate batch processes employ 1.2 – 1.5 molar equivalents depending on the dye core structure. Ratio optimized for maximum chromophore yield and minimal side reaction formation.

    Downstream process integration

    • Applied after main dye chromophore synthesis under microwave or conventional heating. Reaction monitored by HPLC, followed by aqueous extraction and filtration to increase color purity and washing properties.

    Final product types

    • Pyridyl-sulfonyl dyes for digital textile printing
    • Colorants for water-based industrial inks
    • UV-stable pigments for plastic and coating sectors
    • Chromatic markers for specialty security printing
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    Certification & Compliance
    More Introduction

    5-(2-Pyridyl)Thiophene-2-Sulfonyl Chloride: An Insight from a Manufacturer’s Bench

    Getting Close with 5-(2-Pyridyl)Thiophene-2-Sulfonyl Chloride

    In our labs, 5-(2-Pyridyl)thiophene-2-sulfonyl chloride goes by more than its catalog entry. Crafting this molecule requires a careful choreography of reaction control, solvent selection, and an eye for stability. The demand for this compound roots itself in its usefulness as a sulfonyl chloride building block, often landing in the hands of chemists working on pharmaceuticals, agrochemicals, and advanced materials. Model T5283 at our site stands out for two things: consistently sharp purity and tightly controlled particle size, both of which matter tremendously once synthesis begins.

    What Sets This Compound Apart?

    If you’ve ever scaled up thiophene derivatives, you know that substitution patterns can introduce process headaches. The 5-(2-pyridyl) orientation gives a precise spatial arrangement that influences both reactivity and compatibility with a suite of nucleophiles. Tweaking the position even slightly—say, placing the pyridyl ring on the third or fourth carbon—changes reactivity in the next step. It’s not a matter of theoretical speculation. In practice, we have seen yields drop or purification become difficult when customers try alternatives that lack this exact configuration.

    Practical differences emerge during handling and storage as well. While some sulfonyl chlorides are notorious for hydrolyzing on exposure to air, this variant, when properly stabilized during packing, offers longer shelf stability. That’s come from both rigorous QC and careful investment in packaging infrastructure. Packing crew and chemists trade feedback, refining the way we bottle and seal the product to keep moisture where it belongs—outside, not in the drum. Our experience shows that properly protected, the product maintains reactivity and color for extended periods without significant decomposition.

    The Craft of Synthesis: Lessons Learned on the Floor

    Producing this compound takes more than off-the-shelf glassware and stock reagents. We’ve honed stepwise addition techniques in controlled environments because uncontrolled addition spikes temperature and can generate unwanted side products, especially during the sulfonylation step. Lab experiments have taught us that a few degrees in exotherm can demand extra purification. Operators require real skill mastering this—that experience comes only after repeated process runs. Over the years, we invested in automated controls and real-time monitoring, which help clamp down on variability. There is no shortcut; raw practical know-how breeds tight, repeatable specs.

    We pay close attention to the incoming thiophene starting material. Trace levels of contaminant pyridine, halides, or oxidants shift the final product profile, so we source and test with intent. LC-MS and NMR have taught us that even reputable compounds from familiar names can sometimes ride in with unexpected ghosts. Old-timers in the lab can spot subtle differences in product appearance and flag things before analytical work even begins. One lesson holds true: as a manufacturer, trust, but always verify your starting points.

    Why Purity and Consistency Matter for End Users

    People at the bench, carrying out sulfonamide couplings, know that byproduct control is not academic. In peptide and pharmaceutical R&D, sensitive substrates respond poorly to even minute levels of hydrolysis products or symmetrical sulfonates. Colleagues have reported poor conversion or messy chromatography when the upstream intermediate contains these flaws. Most literature procedures, fine-tuned for small batches, don’t translate unless the incoming reagents are top-notch.

    Feedback cycles with our customers push us to customize drying protocols and filtration based on real-world performance. One team in a medicinal chemistry group compared our product with a generic version and flagged that our batch consistently accelerated reaction kinetics and minimized tarry residues. We adjusted our processes after hearing how a slight boost in chemical stability led to higher isolated yields further down the pipeline.

    Role in Modern Research and Industrial Application

    Over the last decade, requests for 5-(2-pyridyl)thiophene-2-sulfonyl chloride have shifted. It’s no longer just about supporting academic groups or lone drug discovery projects. Catalysis researchers, polymer chemists, and agrochemical teams reach out. Some customers push the boundaries, using the sulfonyl chloride in click chemistry, others as a platform intermediate for heterocyclic scaffolds. We stay close to this evolution, noticing nuances in how different sectors deploy the molecule.

    Pharmaceutical demand for thiophene-containing moieties traces back to structure-activity relationships uncovered in anticancer and antiviral research. Synthetically versatile sulfonyl chlorides provide handle points for downstream amines, opening routes to novel sulfonamides with diverse pharmacological profiles. The pyridyl group brings additional benefits—nitrogen coordination can fine-tune interactions in biological systems or with transition metals in complex catalysis.

    Beyond life sciences, our partners in materials chemistry use the product to impart unique electronic characteristics into polythiophene backbones. These tweaks sometimes make or break device performance in organic electronics. Directly connected pyridyl rings, naturally, influence solubility and oxidative stability, two features critical for producing stable thin films and device layers.

    Specifications That Reflect Experience

    Beyond a number on a data sheet, specs echo our accumulated lessons. For our T5283 model, we commit to >98.5% purity by HPLC, with close monitoring for moisture and color. The color metric matters: off-color batches usually point to thermal stress, indicating decomposition or byproduct formation. When asked about differences in melting point or solubility, we keep updated records from production runs, sharing data with downstream users for process design. Purity, moisture content, physical consistency—each ties directly to batch reliability.

    Batches undergo inline Fourier-transform infrared (FTIR) checks to catch residual chlorination byproducts. Since some application stages show hypersensitivity to these, we keep limits stricter than what typical commodity houses would tolerate. Our teams have revisited the drying and sealing step after seeing how trace water affects shelf life—an effort driven not by theory but by repeated real-world slip-ups that cost more in customer troubleshooting than in preventive process upgrades.

    Operational Safety and Sustainability

    People tend to overlook safety beyond rote protocol. In regular runs, personnel use specialized PPE and local exhaust not just for regulatory compliance, but because sulfonyl chlorides bite—skin and airway. Our plant’s approach combines sensors for hydrochloric acid emission, improved containment design, and continuous staff training. Past incidents inform incremental improvement. For example, after an unexpected hydrolysis event during humid weather, we implemented traffic pattern changes and upgraded humidity controls.

    Customers increasingly ask about sustainability. Sourcing thiophene and pyridine rings from greener, lower-impact routes has become more viable thanks to improvements in feedstock refining outside our plant. On-site, efforts to reclaim solvents and minimize chlorinated waste ramped up after we started quantifying environmental impact more rigorously. Steps like solvent distillation, improved scrubbing, and packed column neutralization went from optional to standard. Our chemists and engineers go beyond compliance—each change tightens both quality and environmental care.

    Handling Variability in Customer Requirements

    Few orders fit the same mold. Some partners prize highest purity for immediate R&D needs; others request bulk lots for pilot or production campaigns where cost and throughput matter as much as performance. Our flexibility stems from real manufacturing experience—batch sizes scale to need, but not at the expense of core quality markers. This isn’t always easy; larger scale introduces mixing, heat transfer, and impurity management challenges that do not show up on a six-gram flask run, but become all too real in a 100-kilo reactor. Maintaining spec means routine attention even when the volume changes.

    Once, we adjusted the drying and milling parameters for a polymer customer whose application failed when using larger, unmodified particles. By listening directly to their feedback and replicating conditions on our small-scale lines, we defined new screening and grinding steps. Later, the customer noted increased uniformity in the application-layer films, reporting less batch-to-batch opacity. Modifications like this only come from direct process control.

    Looking Ahead: Challenges and Opportunities

    As demand grows from fields like combinatorial chemistry and specialty materials, we keep refining production. Upscaling remains a continuous process. New reactor coatings and process intensification have increased both output and operator safety. It’s not enough to chase quantity alone—process drift eventually seeps into the most robust set-ups and catches seasoned operators off guard.

    Supply chain security and quality are joined at the hip. Geopolitical factors, raw material availability, and transportation unpredictability add pressure. By maintaining deep and diversified supplier relationships, with backup systems and regular qualification rounds, risks are contained before they threaten reliability. Investing in both supplier evaluation and in-house processing gives control most traders cannot match.

    Weaving user feedback back into production doesn’t come from a suggestion box. It takes sitting down with customers, reviewing failed runs together, and tracing problems to root causes—be they upstream processes or downstream formulations. Through pilot collaborations, we co-develop process tweaks, sometimes shaving hours off the end-user’s workflow or improving compatibility with automated dosing systems.

    How 5-(2-Pyridyl)Thiophene-2-Sulfonyl Chloride Stands Out from Similar Products

    Within the sulfonyl chloride family, subtle molecular shifts make all the difference. Compounds based on plain thiophene, without the 2-pyridyl group, show different reactivity when paired with complex nucleophiles. The nitrogen atom within the pyridyl ring directs regioselectivity, promotes clean product formation, and sometimes eliminates extra steps downstream. Reduction in purification complexity pays dividends, particularly at larger scales, saving time and materials on the back end of a project.

    We have fielded requests for custom analogs—switching thiophene substitution or introducing alternate heterocycles—and find that most customers return to this classic configuration due to the blend of ease of handling, performance, and versatility. Some competitors attempt to push less pure, lower-spec alternatives under the guise of commodity pricing, but user reports circle back with issues of haze, bad yields, or need for rework. Our own comparative runs have shown that off-purity or wrong isomer content hits conversion percentages and escalates downstream impurity profiles, resulting in greater hassle.

    Maintaining Trust and Delivering Value

    Our factory walls remind every staff member of the accountability inherent in every batch. Delivering on promises is not just a business value—it is the only way to nurture long-term partnerships. In-depth knowledge of how 5-(2-pyridyl)thiophene-2-sulfonyl chloride behaves throughout its full lifecycle, from synthesis to packaging, makes the difference in troubleshooting bottlenecks or resolving customer concerns. No certificate of analysis replaces the comfort of direct dialogue and the readiness to respond immediately if a batch or shipment comes up short.

    Customers depend on simplicity and clarity. We offer direct technical support, not scripted phone lines. Teams who make, test, and dispatch the product stay on call should questions or challenges arise mid-project. Lessons from years of handling sulfonyl chlorides, both good and challenging, shape every improvement, extension, and adjustment undertaken on the line.

    Conclusion: The Manufacturer’s Commitment in Every Drum

    Reflecting on years of shipping 5-(2-pyridyl)thiophene-2-sulfonyl chloride across continents and industries, the core philosophy remains the same: every drum carries the sum of accumulated knowledge and care, shaped as much by past errors as by successes. The molecule represents not just a product code or line on an invoice, but a bridge between intention and innovation. Staying close to real-world challenges, listening to those who trust us with their research and production, and pursuing continuous technical and process improvement are part of the ethos woven through each batch.

    As new projects and unexpected demands emerge, experience shows one truth—commitment to quality, transparency, and practical support will always define what sets a manufacturer apart from those who just trade. Through this approach, we keep building both better products and stronger partnerships, one batch at a time.