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HS Code |
357595 |
| Cas Number | 16619-57-1 |
| Molecular Formula | C5H4Cl2S |
| Molecular Weight | 167.06 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 210-212°C |
| Density | 1.398 g/cm3 |
| Refractive Index | 1.568 |
| Purity | Typically ≥98% |
| Solubility | Insoluble in water; soluble in organic solvents |
| Flash Point | 93°C |
| Synonyms | 2,5-Dichloro-3-methylthiophene |
As an accredited 2,5-Dichloro-3-Methylthiophene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 2,5-Dichloro-3-Methylthiophene, sealed with a screw cap, labeled with hazard warnings. |
| Shipping | 2,5-Dichloro-3-Methylthiophene is shipped in tightly sealed containers made of compatible materials, protected from light and moisture. It should be handled as a hazardous chemical, transported according to relevant regulations (such as DOT or IATA), and accompanied by proper documentation and hazard labeling to ensure safe and compliant delivery. |
| Storage | 2,5-Dichloro-3-methylthiophene should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances such as strong oxidizers. Store in a cool, dry, and well-ventilated area. Ensure the storage area is equipped to contain spills. Proper chemical labeling and access for authorized personnel only are essential for safety. Avoid extreme temperatures during storage. |
Applications of 2,5-Dichloro-3-Methylthiophene in Industrial ManufacturingWe manufacture 2,5-Dichloro-3-Methylthiophene to exacting standards for demanding industrial use. Below are key application sectors and integration pathways for this intermediate chemical in actual downstream production environments. 1. Pharmaceutical Intermediates for Thienopyridine SynthesisWithin the active pharmaceutical ingredient (API) supply chain, 2,5-Dichloro-3-Methylthiophene functions as a critical intermediate during the synthesis of thienopyridine core structures, such as clopidogrel and related antiplatelet compounds. The compound’s dual chlorine substituents enable site-selective nucleophilic aromatic substitution and further cyclization steps, supporting precise structure-activity relationships in target molecules. Purity and trace impurity control remain essential for release into regulated API plants. Industry compliance standards
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2. Advanced Agrochemical Building BlocksAgrochemical manufacturers deploy this methylthiophene derivative as a building block to generate sulfur- and chlorine-bearing heterocyclic pesticides and fungicides. The material offers a reactive handle for cross-coupling and substitution steps in the protected assembly of bioactive agents. Its selectivity in substitution reactions limits side-product generation, supporting high process yields and precise regulatory documentation of starting materials. Industry compliance standards
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3. Electronic Materials and Conductive PolymersProducers of electronic components and polymeric conductors use 2,5-Dichloro-3-Methylthiophene as a functional monomer in the synthesis of thiophene-based conductive polymers. The electron-rich thiophene ring, in combination with strategic halogenation, facilitates oxidative polymerization and targeted doping with molecular dopants. Careful specification of impurities and side-chain composition impacts polymerization kinetics and performance in device integration. Industry compliance standards
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4. Fine Chemicals and Specialty Dye ProductionProducers of high-value specialty dyes and pigments utilize this dichloro-methylthiophene as a key intermediate for constructing complex aromatic and heterocyclic colorant backbones. The electron-donating methyl and electron-withdrawing chloro groups enable selective functionalization and extended conjugation, essential for tailoring light absorption and fastness properties in advanced dyes. Stringent control over lot-to-lot consistency ensures predictable color yield in batch and continuous colorant manufacture. Industry compliance standards
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5. API Impurity Reference Standards ManufacturingSpecialty reference laboratory manufacturers isolate and purify 2,5-Dichloro-3-Methylthiophene to use as a certified reference standard for impurity profiling in pharmaceutical quality control. Its known profile supports the quantitation of trace levels in related API batches, especially for structurally close thienopyridine or thiophene APIs. Rigorous certification, documentation, and trace-level purity analysis underpin this application for leading pharmaceutical QC labs worldwide. Industry compliance standards
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Years spent in the chemical manufacturing world have taught us that every intermediate brings its own strengths and challenges to the bench. 2,5-Dichloro-3-methylthiophene is one of those critical building blocks that keeps showing its value in specialties and advanced applications. Chemical plants, especially those focused on pharmaceutical actives and agrochemicals, look for starting materials with tight specifications, predictable reactivity, and reproducibility. This molecule promises just that, and as a team that synthesizes it from the ground up, we see firsthand how carefully controlled processes make all the difference for downstream users.
Our product delivers the high purity (usually above 98% by GC) chemists count on to keep side reactions at bay. The compound appears as a light-yellow liquid, a form that's easily measured, transferred, and stored in labs and manufacturing environments. The molecular structure, featuring two chlorine atoms at the 2 and 5 positions along with a methyl group at the 3 position on the thiophene ring, provides both steric and electronic characteristics sought after in synthetic chemistry. Unlike less substituted thiophenes, it offers selective sites for further functionalization — a reason it attracts interest among R&D teams developing new molecular entities.
Consistency forms the backbone of our reputation as direct manufacturers. We use carefully sourced raw materials, under tightly monitored temperature and pressure controls, to maintain batch-to-batch uniformity. The synthetic protocol, including chlorination and methylation, follows a closed-loop monitoring system to catch impurities below the threshold levels (typically less than 1% for any single impurity, by our analysis). Our finished 2,5-dichloro-3-methylthiophene meets a water content specification below 0.5%, so users avoid hydrolytic degradation in moisture-sensitive syntheses.
Each batch passes through a dedicated distillation train, separating the desired product from close-boiling byproducts. Sampling crews take vials from each drum and run GC-MS and NMR validation, cross-checking against previous lots as well as published literature. We never skip these steps, as downstream complaints about reactivity or solubility almost always tie back to lapses in the early stages of production. Decades of feedback — both positive and corrective — from long-term clients have shaped our inspection routines.
Research routes for new pharmaceuticals and agrochemicals keep returning to substituted thiophenes as privileged scaffolds. Our experience with regulatory filings exposed us to the recurring need for this compound in advanced intermediates and fine chemical libraries. Chemists gravitate to it for its clean reactivity, especially on the unsubstituted positions of the ring. The presence of two chlorine atoms offers anchor points for various cross-coupling and substitution reactions, expanding the playbook for medicinal chemistry and development teams.
Formulations involving 2,5-dichloro-3-methylthiophene often depend on its unique balance of electron withdrawal and ring activation. The methyl group at the 3 position blocks regioselectivity, steering further functionalization toward the open 4-position or facilitating reductive coupling. This makes our product a reliable starting point for new library members or patentable active molecules. Some of our customers design thiophene-based ligands from scratch, while others focus on scale-up and pilot production tied to this versatile intermediate.
We see a steady pipeline of requests from innovators working in performance materials as well, where designing structure-property relationships needs precision at the atomic level. Our formulation team keeps track of customer feedback to refine downstream compatibility, especially for those running automated synthesis or parallel chemistry protocols. The product’s physical properties — manageable viscosity, moderate polarity, and reasonable volatility — blend well into existing workflows, limiting downtime or equipment recalibration.
Over the years, we’ve handled a wide range of chlorinated thiophenes, each with its own challenge. Simple thiophene offers little selectivity, often demanding lengthy protection-deprotection sequences. Mono-chlorinated thiophenes suit some applications but lack the tunable reactivity that the 2,5-dichloro motif brings. Introducing a methyl group at the 3 position as we do in our product changes the chemistry, making it possible to access chemical space otherwise blocked with unsubstituted rings.
Customers sometimes ask whether it’s worth choosing this compound over related analogs. In our view, 2,5-dichloro-3-methylthiophene’s pattern of substitution prevents unwanted side reactions and leads to higher yields for targeted couplings, especially in Suzuki or Buchwald-Hartwig cross-coupling chemistry. We’ve tracked scale-up data and batch records from partner pilot plants; these show better yields and purer end-products when starting from this specific compound, compared to congeners like 2,3-dichloro- or 2,5-dibromothiophenes.
In practice, what keeps clients confident returning to us isn’t just the technical properties of the molecule; it’s the traceable path from raw material to finished drum. We design control points throughout synthesis to record time, temperature, pressure, and addition rates along the way. These records stay archived for every batch, accessible at audit and on demand by clients with documentation requirements. We support filings for regulatory bodies and quality management systems along the supply chain, so every kilogram delivered tallies with a clear data trail.
We also keep direct feedback channels open for upgrading or troubleshooting customer experience. If a batch shows performance anomalies in a reaction, our technical support team engages immediately, running side-by-side comparatives with retained samples and adjusting future runs if needed. This dynamic response wasn’t possible back in the early days of manual batch records and paper logs; today’s digital tracking gives us a flexible edge and a culture of constant learning.
From a manufacturer’s perspective, maximizing both yield and worker safety sets the agenda. Our production teams work in training cycles to identify bottlenecks in purification or reaction setup. Reactor cleaning protocols, drum labeling, and in-process controls all come out of lessons learned from actual downtime and operational interruptions. By reducing off-specification runs, we keep unnecessary rework and waste to a minimum. Losses from side reactions can be costly both in raw material use and in hours lost for reprocessing, so process improvement meetings focus on efficient transfer and accurate distillation cuts.
In earlier years, occasional troubleshooting pinpointed corrosion issues in process lines carrying chlorinated organics. Shifting to corrosion-resistant alloys for key transfer lines and seals reduced downtime and contamination risk. Similarly, we responded to feedback about odor management and safe handling, investing in vapor containment hoods and sealed pump systems for transfer. These steps were driven not by regulatory pressure but by on-the-ground feedback and an understanding of the hazards specific to chlorinated thiophenes.
Demand for 2,5-dichloro-3-methylthiophene closely follows the cycles of innovation in pharmaceuticals and crop protection. As drug molecule complexity climbs, reliance on tailored building blocks like chlorinated thiophenes grows. Our main clients share the need for kilogram-to-multiton supply, each with specific requirements for documentation, purity, and on-time delivery. We’ve learned that early-stage projects often start with gram-scale orders, scaling up quickly as projects move to phase II trials or field studies for agrochemicals.
Our production planning team watches market signals to align capacity expansions with customer trial phases and commercial launches. In years marked by regulatory changes or sudden shifts in compound portfolios, we adapt supply schedules to avoid bottlenecks. Recently, increased scrutiny on impurity profiles and trace contaminants means that we run extended chromatography and advanced analytics to ensure compatibility with pharmaceutical-grade applications. For some end uses, we provide further cleaning steps, giving chemists a head start on downstream purification.
Not every batch walks the same path — we’ve seen 2,5-dichloro-3-methylthiophene used in work targeting cancer therapies, as well as crop science breakthroughs. Relationships with customer teams let us track success stories and gather detailed performance data, especially in multi-step syntheses. Chemical engineers appreciate the predictable boiling point and defined reactivity; analytical chemists turn to our batch data during impurity investigations.
Learning from each application, we’ve improved not only the chemical itself, but also the container materials and label durability for extended storage. There’s no substitute for field data, particularly when intermediates travel long distances in varied conditions. Issues with temperature swings, moisture ingress, or labeling confusion are all brought back to our operations team for fast resolution and continuous improvement in packing and logistics.
As direct manufacturers, we feel a responsibility to environmental performance, not just for compliance but as a matter of principle. Chlorinated organics require robust emissions controls, and decades of investment in scrubber systems and closed vapor loops cut emissions to well below regulatory limits. We recover heat from exothermic reactions, channeling it to pre-warm raw material feeds, which cuts energy waste plant-wide. For waste product streams, we operate neutralization and incineration systems before safe disposal, audited regularly by independent agencies.
Input materials sourcing has shifted toward partners with transparent supply chains and certified practices. We scrutinize every link — from mine to feedstock processor — for environmental and labor credentials. This approach reduces risks in our supply chain and aligns us with partners who share long-term goals for responsible chemistry. Responding to increasing requests for “green” process documentation, we continue gathering and sharing data on solvent recovery, closed-loop operations, and process intensification.
No two customers request exactly the same thing, and that’s where our cumulative on-floor expertise sets us apart. Projects seeking custom specifications on assay or packaging bring out the best in our team, who handle fine-tuning every order in line with customer feedback. Modifications to the distillation route, solvent choices, or drying cycles for specific project needs receive detailed attention in plant meetings. As manufacturers, we actively invite this level of collaboration, knowing it leads to better-designed products and solutions.
On request, we can trace specific synthesis variables and offer extra product analyses — such as residual solvent reports or impurity fingerprints — supporting client filings or special formulation needs. For multinational programs needing locked process parameters, we document every change and run periodic full validations to support reproducibility. The open-door policy between our lab, production, and quality assurance teams means every special order, whether for a few kilograms or larger scale, gets treated with the rigor and respect it deserves.
Our own R&D team keeps a steady eye on new catalytic methods or alternative feedstocks that could improve future batches. Current test runs focus on lowering solvent use and expediting cleaning cycles, further reducing emissions and downtime. Materials science collaborations aim to reduce odor and vapor risks during shipping. Practical lessons from warehouse to reactor continue to inform both incremental and step-change improvements in our plant.
We draw innovation from real-world operator feedback, supplier partner updates, and — ultimately — the inventive ways our clients deploy 2,5-dichloro-3-methylthiophene. No two projects mirror one another, so ongoing dialogue remains the backbone of our ongoing improvement. As regulations change and the demand for specialty building blocks grows, we rely on accumulated manufacturing practice and a commitment to transparent communication across all stakeholders.
After years on the shop floor and in client meetings, it’s clear that quality, operational transparency, and flexible support secure more loyalty than buzzwords or claims. Our responsibility, as manufacturers of 2,5-dichloro-3-methylthiophene, is to deliver consistency — not just in chemical purity, but in every aspect of the customer experience. Whether developing a new therapy or advancing specialty materials, teams count on reliable partners who fundamentally understand the chemistry and the demands of production, shipping, and long-term storage.
Being present through each stage of synthesis, quality assurance, and customer support allows us to continually refine the product. Our best ideas don’t come from marketing; they come from seeing what works in practice, listening to customer pain points, and solving the unique puzzles that every batch presents. In every ton produced or test vial shipped, our knowledge and investments reflect not only today’s needs, but also a vision for the future of responsible chemical manufacturing.