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HS Code |
893727 |
| Cas Number | 96-43-5 |
| Molecular Formula | C4H3ClS |
| Molecular Weight | 118.59 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 148-150°C |
| Melting Point | -41°C |
| Density | 1.286 g/cm3 at 25°C |
| Refractive Index | 1.560 |
| Flash Point | 39°C |
| Solubility In Water | Insoluble |
| Pubchem Cid | 7290 |
| Iupac Name | 3-chlorothiophene |
As an accredited 3-Chlorothiophene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3-Chlorothiophene is supplied in a 100 mL amber glass bottle, tightly sealed, with a clear chemical label and hazard warnings. |
| Shipping | 3-Chlorothiophene is shipped in tightly sealed, chemical-resistant containers to prevent leaks or contamination. It is classified as a hazardous material and must be transported according to relevant international regulations, such as DOT and IATA. Appropriate labeling, documentation, and safety measures—including temperature and ventilation controls—are required during shipping. |
| Storage | 3-Chlorothiophene should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Store away from direct sunlight and heat. Ensure proper labeling and keep the container away from moisture. Use appropriate safety measures to prevent inhalation, ingestion, or contact with skin and eyes. |
Applications of 3-Chlorothiophene in Industrial Manufacturing3-Chlorothiophene serves as a specialty intermediate for chemical synthesis across agrochemicals, pharmaceutical APIs, electronic material manufacturing, and dye sectors. The following sections detail industrial-specific utilization, compliance, blending ratios, integration steps, and resulting manufactured goods. 1. Synthesis of Agrochemical Active Ingredients3-Chlorothiophene plays a critical role as a heterocyclic intermediate in the synthesis of select herbicide and insecticide actives. Agrochemical manufacturing groups employ this compound for constructing bioactive thiophene linkages, integrating it in multi-step Grignard reactions or Suzuki coupling, strictly controlling purity for downstream crop protection formulations. Batch consistency and traceability remain paramount to meet regulatory registrations and pre-marketing trials. Common usage scenarios include the advancement of herbicidal pyrazole and thiophene-based scaffolds that demonstrate soil selectivity or improved photostability in the field. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Intermediate for API (Active Pharmaceutical Ingredient) ManufacturePharmaceutical firms use 3-Chlorothiophene as a building block for synthesizing select heterocyclic APIs, notably in anti-inflammatory and CNS therapeutic classes. The compound supports the formation of chlorinated thiophene rings essential for drug actives that display metabolic stability. In cGMP manufacturing, control points include residual solvent monitoring and compliance with European and US monographs on residual impurities. This intermediate enters amidation, cyclization, and alkylation reactions under validated protocols before isolation and QP release for drug substance integration. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Precursor in Conductive Polymer Manufacturing for Electronics3-Chlorothiophene finds application in advanced electronic material production, especially as a starting material for synthesizing thiophene-based oligomers and monomers. Electronic materials companies rely on this compound for developing organic semiconductors, OLED layers, and antistatic agents. Production settings emphasize ultra-high purity, low halide content, and tight specification on residual metallic impurities. Integration typically occurs in controlled solvent polymerization lines, targeting high charge mobility and consistent electronic properties in the final device applications. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Intermediate for Dye and Pigment SynthesisSpecialty dye producers incorporate 3-Chlorothiophene in the manufacture of high-performance organic pigments. The molecule facilitates the construction of thiophene core structures that impart strong visible and near-IR absorption in textile and polymer colorants. Process chemists use controlled acylation, sulfonation, or ring substitution procedures, monitoring by-product halides and ensuring compliance with global textile and food contact pigment regulations. Formulated pigments undergo standardized QC for color fastness and toxicity prior to releasing for downstream blending in masterbatch operations or finishing lines. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Working with 3-Chlorothiophene every day, we see its practical value in chemical synthesis. With the formula C4H3ClS and CAS Number 872-31-1, this compound has built a reputation as an effective building block for pharmaceuticals, agrochemicals, and advanced materials. Over several years of manufacturing, we've watched industries lean on chlorothiophenes for their unique reactivity and versatility. Our experience tells us that the practical advantages of 3-Chlorothiophene reach far beyond basic literature descriptions. Reliable sourcing, consistency, and stringent purity standards are the daily challenges we tackle in our plant, knowing that any deviation can ripple into our customers’ research and production lines.
Every step in synthesizing 3-Chlorothiophene shapes the quality and suitability of the final product. As manufacturers, we observe firsthand the nuances in chlorination processes. Small shifts in temperature or feed ratios lead to noticeable differences in by-product formation. We keep our reactions under close control and use in-line analytical systems to ensure purity meets or exceeds 99%, knowing a single impurity can complicate downstream chemistry. The result is a transparent, pale-yellow liquid with a sharp, distinctive odor. Our operators consistently report that even minor adulteration alters the color or viscosity, so every batch receives careful visual scrutiny on top of automated QA.
We fill every drum after confirming specifications using modern chromatographic analysis. Typically, customers want minimal presence of non-chlorinated thiophene or other halogenated isomers. Over time, working directly with processors, we found that some formulations allow wider impurity ranges, but most pharmaceutical partners demand an even tighter purity specification. We do not cut corners, knowing how these standards affect clinical trials, regulatory filings, and product reputation downstream. Our own teams prefer using our own 3-Chlorothiophene as a benchmark because we trust our batch consistency and raw material traceability.
We supply 3-Chlorothiophene primarily for intermediate synthesis. In pharmaceutical plants, chemists favor it for building heterocyclic scaffolds, especially when preparing drug candidates that require selective aromatic substitution. The chlorine atom at the third position on the thiophene ring directs further chemical functionalization, helping researchers create complex structures with reliable regioselectivity. As we talk to R&D partners, process optimization often takes center stage—they rely on our technical expertise to reduce side-reactions, streamline scaling, and minimize waste.
In crop protection synthesis, 3-Chlorothiophene is indispensable. Over the years, most of our agricultural clients sought it for manufacturing herbicides and fungicides sensitive to the purity and moisture content of raw materials. These products frequently undergo halogen exchange, Grignard reactions, or cross-coupling, all demanding starting materials with handled oxidation and monitored trace metal levels. Our plant is equipped to address these technical details, adapting production to deliver application-ready material. Through countless audits and feedback loops, we learned that reducing batch-to-batch variability saves our clients hours of requalification, even when the end-use is as far-flung as a pilot plant in another hemisphere.
Direct comparison with other thiophene derivatives—such as 2-Chlorothiophene or 2,5-Dichlorothiophene—shows sharp differences in both physical properties and chemical behavior. From a manufacturer’s perspective, 3-Chlorothiophene’s chlorine atom sits on the ring in a position that encourages nucleophilic attack at selective sites. This makes it a preferred intermediate for Suzuki, Stille, and Heck reactions, as well as other metal-catalyzed couplings.
Our technical team often receives requests for advice on substituting other chlorothiophene isomers. We’ve found no perfect one-to-one drop-in, since 2-chloro and 3-chloro thiophenes behave differently in both substitution and oxidation. 2-Chlorothiophene, for instance, reacts more predictably in certain ring-opening reactions, but its increased reactivity can generate side products that don’t appear with the 3-chloro isomer. In industrial practice, 3-Chlorothiophene’s reactivity profile delivers more selective transformations, reducing purification steps in complex synthetic schemes.
Another frequent point of comparison arises with brominated or iodinated thiophenes. While heavier halogens often yield higher reactivity in cross-coupling reactions, they come with cost and environmental burdens that our buyers wish to avoid. Chlorinated thiophenes like ours strike a practical balance between performance and sustainability. Brominated intermediates, we’ve observed, require more elaborate waste treatment and carry higher regulatory scrutiny. We’re seeing a clear industry shift towards chlorine-based intermediates, echoing our early design decisions. Throughout years of feedback, our customers have praised the cost-effectiveness and manageable handling requirements of 3-Chlorothiophene, particularly compared to higher halogen analogues.
On the production line, the essential physical parameters carry real implications. 3-Chlorothiophene has a boiling point near 117°C under atmospheric pressure. This makes it amenable to standard distillation and easy purification, which we employ to remove unwanted by-products and moisture. Our technical teams developed customized glassware and inert gas systems to maintain low water and oxygen content, as even trace levels speed up discoloration or resin formation in storage. We package and ship under nitrogen for long-distance export, relying on time-tested procedures rather than fancy claims in catalogs.
Batch homogeneity relies on strict process controls, not luck. With a density around 1.2 g/mL, loading and unloading drums require careful pumping and regular drum scale checks, a lesson we learned after early losses due to overfilling. In the colder months, we heat storage tanks to prevent crystallization or viscosity spikes. For large-scale users, we also offer railcar and tanker truck options, adapting our filling procedures as demands evolve.
We don’t shy away from the day-to-day complexities behind every delivered kilogram. Raw material sourcing sets the tone for all downstream quality. Over the years, we’ve vetted and re-vetted suppliers of elemental sulfur, chlorinating agents, and solvents. Early issues with inconsistent byproduct formation, stemming from impurity-laden sulfur batches, taught us to develop direct supply agreements with miners and refineries. We supervise the delivery of every lot, because relaxed acceptance rules in warehousing create manufacturing headaches that ripple down to our customers.
Our operators stand by the reactors as reagents slowly feed in, monitoring temperature profiles and chloride concentrations with digital and manual checks. Process deviations never go unnoticed, because even small variations in addition speed can throw off yield and product quality. Our factory culture prizes vigilance; everyone who handles 3-Chlorothiophene production owns a part of the final outcome. We build traceability directly into our batch records, since more than once a customer traced an unexpected impurity to a single missed step in the initial chlorination run.
Transportation remains a reality check for any specialty chemical. 3-Chlorothiophene’s class as a hazardous flammable liquid means we work closely with shipping and logistics partners. We pack in steel drums or IBCs, using UN-approved packaging. Through the years, timely delivery has come to depend on not just paperwork but actual hands-on familiarity with each carrier’s risk tolerances, inspection schedules, and customs handling. Several times, we have stepped in to resolve last-minute snagged shipments, hands-on, because suppliers can’t afford production delays waiting for an intermediate stuck in transit.
Real-world feedback from research labs and production plants steers our manufacturing priorities. Chemists repeatedly request assurance on impurity content, especially for scalable pharmaceutical syntheses. End users in pilot-scale and full production settings need reassurance that property shifts between lots won’t derail established methods. We actively collect data from post-delivery product testing and visit facilities using our compound, a hands-on approach that improves our own processes and supports quality arguments during regulatory submissions.
For agricultural applications, speed and reliability take priority. Customers tell us that ordering delays or nonconforming batches translate directly into missed planting windows and frustrated growers. By hearing the direct impact, we ramped up inventory finishes in high-volume months and created surge capacity during spring. We’ve developed close working relationships with formulators, sometimes troubleshooting process issues onsite, especially when the final product involves emulsification or granulation stages that amplify minor upstream differences.
No discussion about a chlorinated building block escapes debate on safety and environmental impact. Our compliance team faces regular audits for air and wastewater discharge. We have invested in closed-loop reactor systems and real-time monitoring to minimize fugitive emissions. Sometimes, we receive requests for life-cycle assessments or environmental footprints, especially from multinational pharmaceutical partners operating in tightly regulated markets. Our long-term records and transparency have opened up collaborative conversations, where we share practical insights on solvent recycling, energy management, and waste minimization in chlorination chemistry.
Handling 3-Chlorothiophene safely matters for everyone along the chain. We train every operator in spill avoidance, drum handling, and personal protective equipment use. Over the years, we worked with industrial hygiene consultants to beef up engineering controls—local ventilation, leak sensors, and scrubbers keep both employees and the environment safe. Customer audits offer new perspectives; we take their feedback seriously to maintain industry-leading safeguards. Fine-tuning safety data sheets and updating response plans has become second nature, not just regulatory compliance.
Once a drum leaves our warehouse, support continues. Our technical service team fields questions about compatibility, blending, and troubleshooting in reaction setups. We track batch numbers and feedback on every problem solved, whether the issue is an unexpected inhibitor requirement or a change in product coloration at scale. Some partners have leveraged our analytical data packages to troubleshoot slowdowns on pilot lines, saving them weeks of post-mortem investigation.
Education is part of our relationship with buyers. We organize regular webinars, send out application notes, and visit key accounts for process walk-throughs. These outreach efforts surfaced new applications for 3-Chlorothiophene—from specialty coatings to materials research—stretching beyond the products we originally expected to serve.
Decades of making 3-Chlorothiophene have given us a deep understanding of what truly matters to end users. Reliable quality starts with experienced teams controlling every ingredient, every reaction, and every shipment. Our consistency gives chemists the confidence to use our product in advanced areas—including medicinal chemistry, active ingredient creation, and polymer development—where substitution simply will not produce the same results. Batch records, hands-on checks, and clear technical communication keep surprises to a minimum, saving headaches and cost for everyone involved.
What truly differentiates our 3-Chlorothiophene runs deeper than the molecule itself. Experience in manufacturing, hard-won lessons about material variability, and a culture of ongoing improvement guide our product philosophy. Customers value this more than any marketing claim. Technical innovations, continuous feedback, and careful environmental practices are not optional. They shape the product delivered each day.
As global chemistry grows more demanding, 3-Chlorothiophene offers a unique combination of accessibility, reactivity, and performance that we are proud to deliver—backed by a track record built over years, not weeks. Through every challenge, from formulation tweaks to regulatory shifts, our manufacturing know-how stands behind each shipment, helping customers push boundaries in synthesis, create new solutions, and advance their fields with confidence in the quality of the building blocks they use.