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HS Code |
719130 |
| Chemical Name | Ethyl 2-Amino-4,5-Dimethylthiophene-3-Carboxylate |
| Cas Number | 39304-71-7 |
| Molecular Formula | C9H13NO2S |
| Molecular Weight | 199.27 g/mol |
| Appearance | Yellow to brown solid |
| Melting Point | 76-78°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Storage Conditions | Store at room temperature, tightly sealed, protected from light |
| Smiles | CCOC(=O)C1=C(SC(=C1C)N)C |
| Inchi | InChI=1S/C9H13NO2S/c1-4-12-9(11)7-6(2)13-8(3)5(7)10/h4H2,1-3,10H3 |
| Synonyms | Ethyl 2-amino-4,5-dimethyl-3-thiophenecarboxylate |
As an accredited Ethyl 2-Amino-4,5-Dimethylthiophene-3-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, tightly sealed with screw cap, labeled with chemical name, formula, hazards, and manufacturer's details. |
| Shipping | **Shipping Description:** Ethyl 2-Amino-4,5-Dimethylthiophene-3-Carboxylate is shipped in tightly sealed containers, protected from light and moisture. It is handled as a laboratory chemical and may require cool, dry transport. Ensure packaging complies with relevant chemical shipping regulations. Appropriate documentation, hazard labeling, and safety precautions must accompany all shipments. |
| Storage | Store Ethyl 2-Amino-4,5-Dimethylthiophene-3-Carboxylate in a tightly sealed container, protected from moisture and light, at room temperature (15–25°C). Keep it away from strong oxidizing agents, acids, and bases. Use a well-ventilated, dry area, following standard laboratory chemical storage guidelines. Properly label the container and ensure access is restricted to trained personnel only. |
Applications of Ethyl 2-Amino-4,5-Dimethylthiophene-3-Carboxylate in Industrial ManufacturingEthyl 2-Amino-4,5-Dimethylthiophene-3-Carboxylate supports the synthesis of high-value intermediates across several mature specialty chemical sectors. As the original manufacturer, we optimize product consistency and traceability for downstream processors incorporating this advanced building block into pharmaceutical development, agrochemical production, and electronic material formulations. Below, we detail the primary industrial applications with sector-specific process requirements. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisThis compound functions as a core intermediate in the multi-step synthesis of certain heterocyclic drug candidates, especially within emerging anti-infective and metabolic disease therapy pipelines. Its insertion typically follows initial scaffold construction, introducing the amino-thiophene motif required for pharmacologically active molecules. Pharmaceutical manufacturers depend on batch purity, controlled residual solvent levels, and single-lot traceability during pilot and commercial-scale campaigns. Industry compliance standards
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2. Agrochemical Synthesis—Herbicide and Fungicide IntermediateAgrochemical manufacturers use this molecule to construct thiophene-derived heterocycles central to several selective herbicide and fungicide actives. The material enters production flows that demand strict contaminant limits and careful temperature control to preserve the sensitive heteroatom arrangement through downstream cyclization and substitution steps. Industry compliance standards
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3. Electronic Materials—Organic Semiconductor SynthesisProducers of organic semiconductors select this thiophene carboxylate as a precursor for constructing alkyl-thiophene oligomer chains, essential for high-performance organic field-effect transistors (OFETs) and OLEDs. Sensitive to air and moisture, processors require controlled microenvironment handling from intake quarantine through condensation and cross-coupling stages. Industry compliance standards
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4. Pharmaceutical Impurity Reference Standard ManufactureContract labs and pharmaceutical quality control units rely on this compound to prepare impurity reference standards and system suitability spiking materials for regulatory method validation. Accurate impurity quantification tests in finished APIs and formulations require precursor-grade input free from extraneous isomers and residual synthetic catalysts. Industry compliance standards
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5. Fine Chemical Synthesis for Fragrance and Flavor IngredientsA select group of fine chemical producers harnesses this heterocycle during the development of specialty aroma and flavor agents, capitalizing on its sulfur-based aromatic motif. Production must adhere to stringent food-grade process isolation and minimize cross-contamination risks with non-food chemicals. Industry compliance standards
Typical usage ratio
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Every specialist in our lab can recall the day we first refined a batch of Ethyl 2-Amino-4,5-Dimethylthiophene-3-Carboxylate. There’s a difference between reading about thiophene derivatives and watching golden-brown crystals separate from their solvent, clean and bright. This product, identified in industry circles by its precise nomenclature, is not a common staple pulled off a shelf or bought in bulk from untraceable sources. We synthesize it from scratch, safeguarding each step, from sourcing our dimethyl precursors to the purification processes that strip away any residual contamination. Chemical manufacturers understand the weight of these details because one missed step, one impurity, can taint an entire lot and, with it, our customer’s confidence in our expertise.
Ethyl 2-Amino-4,5-Dimethylthiophene-3-Carboxylate isn’t just another line on a catalog. Our team faces every batch with an eye for control and a mind for consistency. A compound like this reflects the spirit of careful, responsible chemical production. No shortcuts, no taking quality for granted, especially in a world where more and more buyers recognize how quality at the source influences reliability downstream.
The core structure of thiophene—a sulfur-containing five-membered ring—has long proven itself in pharmaceutical research, electronic intermediates, and advanced material science. When you attach amino and carboxylate groups along with dimethyl side chains, you widen the scope of possible applications. In our experience, researchers and synthesis specialists turn to Ethyl 2-Amino-4,5-Dimethylthiophene-3-Carboxylate when designing new APIs, specialty pigments, and even as building blocks in conductive polymers.
This goes beyond speculative patent pipelines. The compound’s profile fits the demand for small-molecule starting points. For medicinal chemistry, the combination of electron-rich aromaticity and the twist added by the ethyl ester creates opportunities for modulating pharmacokinetic properties. Those investing in organic electronics appreciate its stability under process conditions and its predictable reactivity with coupling partners. When you hold a sample in your hands, the difference is not just in its crystalline clarity but also in how it behaves: solubility, response to storage, and purity all echo the experience of the team behind it.
As the people behind production, we approach each batch with the end user’s application in mind. We synthesize Ethyl 2-Amino-4,5-Dimethylthiophene-3-Carboxylate to a minimum purity of 98 percent by HPLC. We are transparent with our impurity profiles and back every shipment with batch-specific documentation generated in-house, not outsourced or blind to process details. The color and flow are consistent from order to order, and we maintain controlled moisture and ash content to avoid problems in downstream reactions. Those details can escape attention at scale, but in our experience, these are the markers customers notice after switching from low-tier alternatives.
Our batches rarely stray from a pale-yellow to amber appearance, depending on scale and lighting conditions. Solubility in common organic solvents—ethyl acetate, dichloromethane, DMF—comes standard, but we also record data for less routine solvents if our partners ask. Melting points serve as silent indicators of purity, so we catalog these with every run. Every bottle we pack carries a traceability code that can be matched straight back to our instrument logs and material records. This approach stems not from regulatory demand but from our belief in being accountable for everything we ship out.
Our in-house chemists talk often with customers who span more than one industry. Some approach us with projects in heterocyclic building blocks—synthesis of new drug scaffolds that need the unique blend of properties this thiophene offers. Others develop specialty dyes and pigment formulations, trusting in the batch-to-batch color quality and stability that more generic sources cannot guarantee.
Our relationships with university labs reinforce what we see on the shop floor: the desire for raw materials that don’t leave their research stuck troubleshooting unknown impurities or inconsistent reactivity. We’ve heard from materials researchers working on next-generation OLED materials who value the repeatability of our compound. They find that our process yields a product with negligible residual metals and solvent traces, so their prototype testing stays reliable.
Some colleagues at pharmaceutical firms have reached out after frustrating delays with poorly controlled imports from overseas intermediaries. They need a thiophene derivative that behaves as specified at every pilot run. They want answers, not sales promises. We learned to share exact chromatograms and batch histories. Full transparency conquers doubts born from previous supply headaches.
Producing Ethyl 2-Amino-4,5-Dimethylthiophene-3-Carboxylate is not a “plug-and-play” exercise. The aminomethylation step requires careful balancing; the wrong pH or mixing speed can alter yields and precipitate traces of byproducts, sometimes invisible to the naked eye. We run multiple purification cycles, track pH shift throughout, and monitor final product by high-resolution NMR and HPLC. Cross-checks matter—a single detector cannot uncover all potential flaws.
We have faced supply interruptions with precursor materials, particularly with fluctuations in high-quality dimethylthiophene stocks. Rather than lowering standards to keep volume flowing, we prefer to slow delivery and communicate delays. Customers who depend on us keep their confidence; they understand why we reject substandard starting materials. Our pride isn’t in large output, but in product our specialists are willing to stake their reputation on.
The manufacturing “sweet spot” for this compound depends on understanding the difference between lab-scale synthesis for quick analysis and the challenge of scaling up with uncompromised purity. We discovered that some filtration setups favored by larger outfits introduce minute contaminants, like fine particulate carried over from reused filter cloths, so we train our crew to test and inspect every lot visually and instrumentally. The result is rarely visible unless you’ve seen a poor batch compared side by side with a fresh, properly made product.
Competitors may produce similar molecules, but in practice, differences quickly show. Substituting other thiophene carboxylates might appear trivial on a specification sheet, yet side reactions behave differently due to electron density shifts across the ring. Our material’s dimethyl substitution pattern, combined with the ethyl ester group, impacts both reactivity and solubility profile. These are not academic points—they shape reaction times in the customer’s own lab, and even the waste profiles post-use.
When a client used a mono-methyl thiophene alternative for a medicinal study, they found lower yields in their final coupling reactions and impurities that took hours to resolve by preparative HPLC. After a switch back to our Ethyl 2-Amino-4,5-Dimethylthiophene-3-Carboxylate, purification steps shortened, overall yield increased, and their process teams spent less time diagnosing side reactions. Deep experience in the lab breeds sharper instincts about which details to pay attention to, and those lessons guide our process control here.
We maintain open channels for feedback. Customers sometimes report differences in solubility between comparable thiophene esters from other producers. Most of these arise from subtle impurities—sometimes polymeric byproducts, other times traces of starting alcohols or sulfur compounds. We’ve tailored our syntheses to address these, not through guessing, but by systematic process reviews and validation. That kind of problem-solving is possible only at the source. Distributors and repackers seldom have the insight to track back to precise cause.
Years of answering technical calls have shown us what matters most to researchers: supply reliability, product purity, and honest dialogue about shelf-life or stability risks. Sometimes a customer’s application falls outside our field of production, but they need a custom batch or unusual quantity. We welcome challenges that force us to re-examine our own controls, or to run additional quality checks. Even when we’ve met specifications, we recognize unexpected results may come from differences in scale, equipment, or reaction setup outside our facility.
We make every HPLC trace from our production accessible to customers on request, not just the typical certificate summary. Direct conversations between our process chemists and the customer’s own project teams clear up many small issues before they grow into bigger problems. Whether dealing with high-throughput screening in pharma or pilot-scale syntheses for emerging organic semiconductors, we emphasize the experience behind every gram we supply.
Feedback from university labs proved that many younger researchers assume all sources of rare thiophene derivatives are identical. After a failure to reproduce published work, they often trace the problem to inconsistent starting materials. Those customers appreciate seeing our approach firsthand during site audits or video calls—no attempt to obscure the raw data, just openness about the good runs and the rare failed batch.
We’ve watched the market for thiophene derivatives change. Demand for high-purity intermediates climbs across Asia, North America, and Europe. At the same time, the pressure from trading houses and resellers grows. They press for price over pedigree, quantity over conversation. Holding the line on standards means we decline some opportunities, but the value of trust from advanced users more than compensates for lost volume. No distributor can replicate the perspective earned from having to fix your own processing mistakes, or from seeing firsthand how cross-contamination ruins a customer’s six-month trial run.
Responsible production for us goes beyond the latest compliance badge. We’ve been forced to discard entire runs when trace contaminants crept in from reused glassware or poorly stored solvents. Our team treats this as a learning tool, not a failure. We document every step, update our internal SOPs, and invite our clients to learn with us if they wish. This culture is hard to copy—no marketing message replaces real transparency.
The biggest issue for buyers of rare intermediates continues to be clarity on quality and traceability. Unlabeled or poorly documented chemical shipments persist because corners get cut downstream. We tackle this by over-communicating, documenting origin, purification history, and even unexpected troubleshooting steps for each made-to-order batch. Critical buyers realize that cheap, untraceable product means expensive troubleshooting later. A laboratory’s performance often hangs on a reagent’s purity, not just the sticker price.
Across our industry, new analytical methods—like real-time NMR and advanced mass spectrometry—help narrow the gap between process reality and claimed specifications. We invested early in these technologies. This doesn’t mean flashy tools make all the difference; rather, our team’s willingness to scrutinize each anomaly and to reject batches that miss the mark makes the long-term difference. Our end users appreciate being engaged in the results, not forced to accept faceless supply chains.
Manufacturers bear the deepest responsibility for every bottle shipped out. By owning our process from raw material to packaged product, we learn from delayed reactions, filtration errors, and customer feedback alike. These lessons become part of every subsequent run. Ethyl 2-Amino-4,5-Dimethylthiophene-3-Carboxylate doesn’t just represent another niche chemical—it stands for the sum of every failed re-crystallization, every sudden impurity spike, and every late-night troubleshooting call.
Chemical manufacturing at this level rarely looks glamorous. The care shows in clear audit trails, in hours spent revalidating old batch data, and in our willingness to say “no” to a shipment when it doesn’t meet our own standard. For the users who put their trust in our product, that commitment means lower risk, fewer surprises, and more reliable progress in their own projects. That’s the difference you feel when you work with a manufacturer who owns the details, the process, and the reputation that comes with it.