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HS Code |
735027 |
| Chemical Name | 2-Iodo-5-Methylthiophene |
| Molecular Formula | C5H5IS |
| Molecular Weight | 223.06 g/mol |
| Cas Number | 73074-96-9 |
| Appearance | Yellow to brown liquid |
| Boiling Point | 85-87°C at 20 mmHg |
| Density | 1.99 g/cm³ |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents |
| Synonyms | 5-Methyl-2-iodothiophene |
| Storage Temperature | Store at 2-8°C |
| Smiles | CC1=CC=CS1I |
As an accredited 2-Iodo-5-Methylthiophene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2-Iodo-5-Methylthiophene (5 grams) is packaged in an amber glass bottle with a secure screw cap, labeled for safety. |
| Shipping | 2-Iodo-5-Methylthiophene is shipped in secure, chemical-resistant containers, compliant with relevant hazardous materials regulations. Packaging ensures protection from moisture, light, and physical damage. Appropriate labeling, documentation, and safety data sheets (SDS) are included. Shipments follow IATA, IMDG, and DOT guidelines, with temperature control as needed to maintain product integrity during transit. |
| Storage | 2-Iodo-5-Methylthiophene should be stored in a tightly sealed container, protected from light and moisture, and kept in a cool, dry, and well-ventilated area. Store away from incompatible substances such as strong oxidizers. Ensure appropriate labeling and keep in a chemical storage cabinet, preferably dedicated to halogenated organics, to prevent contamination and accidental reactions. |
Applications of 2-Iodo-5-Methylthiophene in Industrial ManufacturingAs a direct manufacturer, we supply 2-Iodo-5-Methylthiophene for various specialty chemical production chains. Our expertise supports integrated downstream operations in advanced materials, life sciences intermediates, and electronic industries. Below, we outline key application fields with detailed industrial integration and process data. 1. Pharmaceutical Intermediate Synthesis2-Iodo-5-Methylthiophene serves as an essential building block in the preparation of certain active pharmaceutical ingredient (API) intermediates, particularly within the thiophene-based heterocyclic compounds. Major API manufacturers use this material predominantly in Suzuki-Miyaura and Stille coupling steps to introduce methylthiophene motifs into antihypertensive and antiepileptic drug intermediates. This approach facilitates substitution precision and maintains consistency with global regulatory dossier requirements for impurity profiles. The compound commonly enters multi-step organic syntheses, often in gram-to-multikilogram batch campaigns, followed by several purification stages to meet stringent pharma-grade impurity limits. Industry compliance standards
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2. Agrochemical R&D and Fine Chemical SynthesisProducers of advanced agrochemical ingredients employ 2-Iodo-5-Methylthiophene as a key halogenated aromatic precursor for lead diversification in fungicide and herbicide discovery programs. Researchers use this compound in targeted synthesis of sulfur-containing analogs to improve selectivity and activity against economically important crop pathogens. The iodinated motif supports rapid halogen exchange and cross-coupling chemistry, adaptable across gram to pilot plant scaleouts. Downstream fine chemical workshops leverage its reactivity for route scouting and impurity characterization, subject to extensive quality control in accordance with global supply agreements. Industry compliance standards
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3. OLED and Organic Electronics Material ManufacturingIn the development of organic light emitting diode (OLED) materials, 2-Iodo-5-Methylthiophene provides a functional precursor for constructing custom thiophene-based π-conjugated structures. Downstream processors employ palladium-catalyzed couplings to insert 5-methylthiophene units into electron-rich polymer and small-molecule semiconductors, targeting improved carrier mobility and emission efficiency. Material scientists in display technology operations apply rigorous quality controls on all incoming raw material batches, as these affect thin-film purity and device yield within cleanroom fabrication environments. Industry compliance standards
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4. Custom Dyestuff and Specialty Pigments ProductionDyestuff and pigment manufacturers utilize 2-Iodo-5-Methylthiophene as a core intermediate for synthesizing high-value sulfur-heterocyclic colorants. Synthesis teams use this building block to introduce electron-rich aromatic units, which modify colorfastness and solubility in advanced pigment systems targeting plastics, inks, and coatings. The compound enters specialized reaction sequences such as electrophilic aromatic substitution and subsequent condensation, with stringent monitoring for purity and color index conformity. Downstream production integrates these custom thiophene units into dye molecules to meet performance benchmarks under light exposure and temperature stress tests. Industry compliance standards
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5. Building Block in Heterocyclic Research ChemicalsAcademic and industrial research laboratories order 2-Iodo-5-Methylthiophene as a reliable halogenated starting block for novel heterocycle creation and advanced synthetic route development. Researchers typically employ this material in cross-coupling, cyclization, and alkylation reactions to obtain libraries of functionalized thiophenes, which serve as lead structures in material science and medicinal chemistry. These applications demand analytical purity and complete spectroscopic characterization, with variable synthetic scales from milligrams to several hundred grams, following best practice in laboratory chemical safety and inventory management. Industry compliance standards
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At our manufacturing site, we’ve watched the development and use of 2-Iodo-5-Methylthiophene (CAS 6937-38-0) shift over the years, as customers and industrial researchers have driven the demand for specialized building blocks in pharmaceuticals, advanced materials, and fine chemical synthesis. We produce this compound consistently in batches ranging from multi-kilogram to small pilot lots, supporting both innovative research programs and routine commercial projects.
Many fine chemicals come across our workbenches every day, but a good iodo-thiophene intermediate still turns heads in the lab. This particular chemistry owes much of its importance to the balance of reactivity and selectivity that the iodo group introduces on the thiophene ring, alongside the activating effects of the methyl function at the 5-position. We’ve seen firsthand how this arrangement opens new paths in heterocyclic transformations that non-iodinated or differently substituted thiophenes just can’t match.
The molecular structure—an iodine atom at position two and a methyl group at position five—gives this compound a coupling potential that matches the demands of modern Suzuki, Sonogashira, and Stille reactions. Processes that need reliable arylation or heteroarylation frequently zero in on precisely this motif, because the iodine increases reactivity without triggering unwanted side-reactions, and the methyl lock offers site differentiation otherwise hard to achieve. Our chemists appreciate being able to offer this distinct profile to customers facing synthesis bottlenecks.
Every chemist knows that trace impurities drag down reaction reliability and increase troubleshooting headaches. In our facility, we target 98% minimum purity by GC and NMR confirmation for all lots, and we keep water content tightly controlled using Karl Fischer titration. Each delivery comes in amber glass, not just for tradition’s sake, but because the material’s stability stands up best in low-light, dry conditions. Regular requests from customers to compare our compound’s shelf-life versus open-market material show a difference born directly from carefully managed production and storage.
We produce 2-Iodo-5-Methylthiophene using iodine halogen-exchange routes that minimize metal contamination, and every run is checked for residual base metals by ICP-OES. Our experience has shown that even trace palladium or copper left over from prior reaction steps can sideline a well-planned coupling strategy downstream. That’s why we clean up and test to tight standards, so the synthetic scalability our customers need matches what they receive—not just on paper, but at bench scale and beyond.
Most buyers approach us because they’ve hit a wall with commercially available thiophene derivatives that either lack the right leaving group or introduce unwanted side chains. 2-Iodo-5-Methylthiophene’s structure makes it a highly effective intermediate in pharmaceutical and agrochemical R&D, especially where the build-out of complex thiophene cores proves tricky. Medicinal chemists rely on it for late-stage diversification, since the iodo group offers coupling flexibility and the methyl substitution fine-tunes electronic properties—altering compound solubility, potency, and metabolic fate. Our pharma partners note fewer byproducts during scale-up, giving this intermediate an edge in both cost and time savings.
Organic materials researchers make it clear how difficult it can be to introduce functionalized thiophenes into conducting polymers or OLED precursors. Here again, the 2-iodo-5-methyl substitution solves two problems at once: the selective reactivity of the ring and a methyl group’s resistance to oxidative degradation. Some of our most recurring orders have come from groups investigating next-generation organic semiconductors and light-modulating materials. They cite batch-to-batch consistency and cleanliness as being as important as theoretical reactivity.
We’ve worked with a broad range of thiophene halides, from 2-bromo and 2-chloro through to unsubstituted thiophenes. Differences often come down to reactivity, stability, and regulatory issues. The iodo leaving group moves cross-coupling reactions forward under milder conditions, which cuts down on side reactions and the need for elaborate purification protocols. This means customers waste less precious starting material and avoid costly post-reaction cleanups.
Other products like 2-Bromo-5-methylthiophene frequently require tougher coupling conditions and can lead to increased metal scavenging or more byproducts. In contrast, the iodo derivative supports a broader catalytic toolkit—especially handy for labs trying to streamline their catalyst inventory or for projects sensitive to traces of base metals. Products based on 2-chloro-5-methylthiophene often price more attractively, but the chemistry can drift or stall, driving up costs in development work and making scale-up less predictable. Our long-term customers often report switching to the iodo version as soon as challenging couplings or complex molecular architectures are needed.
Some customers used to prefer non-methylated iodo-thiophenes under pressure from procurement departments, but consistent feedback shows that the methyl group at the 5-position shifts both reactivity and product profiles in key target molecules, especially in pharmaceutical leads. The methyl group is not a benign passenger—it actually limits unwanted ring formation and shifts the electron density in downstream applications.
Our in-house manufacturing team faces tough reality checks every time they scale up a batch. The handling of iodine-based reagents always demands strict attention to air and moisture control, as small slips in atmosphere lead to batch degradation or off-odors. We use both automatic and manual monitoring throughout each reaction run, taking corrective action when readings stray even a little out of spec. This vigilance brings down waste and ensures every drum we ship works exactly the same way as the last.
We’ve also responded to customer needs by adjusting lot sizes and packaging. Academic researchers typically want small bottles to avoid product hang-up and minimize exposure, so we fill these by weight and double-seal them for peace of mind. Larger R&D teams and scale-up labs appreciate full- or half-kilo containers with both nitrogen and desiccant backfill, preserving product activity for extended projects. Fielding these requests directly means we get feedback straight from use—not filtered through sales reps.
Several years ago, customers flagged the presence of volatile trace states on startup batches that caused inconsistent GC profiles. Our quality team followed those findings back to minor process contaminants in one raw input line. Adjusting reagent sequence and introducing extra drying steps corrected this issue across all future production runs. These incremental, feedback-driven improvements define long-term partnerships far more than pricelists or certificates ever could.
Nobody wants regulatory setbacks to stand between them and project success. Many customers in pharma and electronics ask about analytical file support for regulatory filings with the FDA, EMA, or patent offices. We keep well-archived batch records and maintain the full suite of analytical data—GC, NMR, MS, and IR—on file for each lot. Thanks to robust documentation and traceable, in-process controls, customers can close out their validation programs without having to chase missing or incomplete data.
Whenever customers contact us for clarification, our technical team responds directly rather than deferring to third-party QA teams. Over the years, this approach has built real trust, especially on questions about trace metals, elemental impurities, or process origins. Most buyers tell us that upstream transparency and direct access to manufacturing support gives them the confidence to bring our material into regulated or mission-critical workflows.
Over the years, we’ve paid close attention to safe shipment and storage. 2-Iodo-5-Methylthiophene travels as a light-sensitive, moisture-sensitive organic liquid, so we use shock-resistant, amber glass containers and as little headspace as possible. All outgoing shipments include up-to-date Safety Data Sheet documentation. Common questions relate to controlled temperature protocols. Outside of high-temperature or long-term storage, regular warehouse temperatures suffice for stability, but we recommend refrigeration for open containers or storage beyond six months.
On arrival, most users appreciate the clear labeling and tamper-evident packaging. Occasionally, new users reach out regarding odor or residue which stems from trace sulfur volatiles—a normal artifact that quickly dissipates in fume hoods. These details matter far more than data sheet lines or generic shipping advice, and our logistic teams treat every order as a critical mission to the end user’s bench.
Ten years of continuous shipment and customer surveys proved that chemistry is only half the story—ongoing, real-world feedback provides the other half. Our relationship with both academic and commercial users keeps us alert to process changes their side and shifts in practical demand. Most product adjustments over the years sprang from direct requests—a more selective drying step, direct-to-lab labeling for easy shelf ID, extra testing for elemental contaminants, and even tailored advice for end-use transformations in specific reaction classes.
Some of the most insightful input came from customers who hit unanticipated snags in scale-up, like unexpected batch heterogeneity or color change during purification. Rapid, transparent discussion followed by changes in in-process controls solved these issues, often before formal complaints could arise. We adjust not just based on “the book” but on outcomes in the diverse, pressure-filled work environments our customers face.
We maintain direct control over all stages of manufacturing and purification. This isn’t just a matter of pride—it’s necessary to achieve the product consistency required for high-precision work in pharmaceutical and electronics synthesis. If a process step drifts even slightly, problems show up immediately in downstream coupling reactions or material quality analysis. Our technical team watches for even minor deviations, taking preventive steps before these ever reach customer hands.
Requests for documentation, technical support, or application advice never bounce around third-party desks. Customers have access to the chemists and engineers directly overseeing their batch, which keeps conversations grounded in the realities of process chemistry and not just sales bullet points. This direct interaction has made our company a preferred supplier for groups who value the assurance that each delivered batch matches both internal expectations and external regulatory needs.
R&D never stands still. Over the last five years, market interest in specialized iodo-thiophene building blocks has grown, driven by demands in green chemistry, low-temperature catalysis, selective metabolite mimicry, and advanced functional materials. We take signals for future capacity plus evolving purity requirements straight from conversations with end users. Whether for rapid analog synthesis in drug discovery, or precision-tuned polymers in electronics, next-gen applications continually reshape our approach to what and how we deliver.
We’ve increasingly collaborated with university and contract labs to fine-tune process details or share best-practices. For example, one collaboration with a European research group led to a tweak in our distillation regime, trimming trace artifact formation and securing a cleaner, more reproducible starting material for new OLED emitters. Open exchange of real manufacturing experience and end-use results pushes both our technology and customer science forward.
Many traders and resellers offer similar-sounding products, but distance between producer and user complicates troubleshooting and slows process improvements. As direct manufacturers, we see and manage every batch, and stay close to the chemistry, handling, and feedback cycles driving each delivery. If a challenge comes up, we can trace the source to the production line, adjust workflows quickly, and inform customers honestly about what has changed and what supports their next synthesis mission.
Over decades in the fine chemicals sector, direct customer dialogue and in-house control have repeatedly turned minor setbacks into improved protocols. This ongoing relationship makes each lot of 2-Iodo-5-Methylthiophene not just a commodity but a tool shaped for the complex, evolving needs of chemistry professionals.
No lot leaves our facility without full validation. On-site teams perform in-process monitoring throughout synthesis, including control of reagent charge, atmospheric exclusion, and post-reaction purification. Our investment in real-time batch analytics isn’t just for compliance—it cuts waste, boosts reliability, and supports repeatable performance in sensitive coupling reactions. The real test happens when a chemist opens a new bottle, sets up a reaction, and sees expected results with little troubleshooting. That level of predictability is the standard we work toward in every production run.
This approach pays off most when end users find themselves in time-critical stages of development or scale-up. Rather than chase substitutes or patch process gaps, they reach for our material knowing it will hit published specifications with transparency behind every lot history. In the rare event of an out-of-spec or problematic batch, our direct support team responds immediately, sharing not only findings but practical corrective options to keep research and production on track. The trust built over years of direct interaction, rather than through layers of intermediaries, brings real peace of mind.
Demand for highly tailored building blocks only intensifies. Environmental concerns, tighter regulations on halogens and process contaminants, and the push for sustainable catalysis all impact how we approach both material sourcing and synthetic methodology. We track regulatory developments in Europe, North America, and East Asia, adapting process or documentation formats as rules tighten. For several big users, we’ve implemented extended impurity profiles and customizable batch records to suit quality audits, responding with the technical documentation expected from a true manufacturing partner.
We continue scaling up green chemistry protocols in the iodo-thiophene line, piloting lower-waste iodination routes and solvent reclamation at intermediate steps. What started as an internal project to save on waste disposal ultimately provided clean product, with fewer residual reagents and lower environmental impact, which proved attractive to many customers committed to their own sustainability goals.
In a competitive world of chemical manufacturing, 2-Iodo-5-Methylthiophene stands out not just because of unique chemistry or technical specifications, but due to the accumulated trust between end users and our direct manufacturing team. Production, packaging, and delivery have evolved based on real-world challenges, user feedback, and a science-driven commitment to performance and reliability. With every lot that leaves our facility, we uphold standards of quality, documentation, and support that go well beyond commodity supply, aiming always to be the responsive partner professional chemists count on for their next breakthrough.