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HS Code |
444795 |
| Iupac Name | ethyl 3-amino-thieno[2,3-b]pyridine-2-carboxylate |
| Molecular Formula | C10H10N2O2S |
| Molecular Weight | 222.27 g/mol |
| Cas Number | 51941-58-9 |
| Appearance | Solid (usually off-white to pale yellow powder) |
| Melting Point | 178-182°C |
| Solubility In Water | Slightly soluble |
| Smiles | CCOC(=O)C1=NC2=CC=CC=C2SC1N |
| Inchi | InChI=1S/C10H10N2O2S/c1-2-14-10(13)8-6-12-9-5-3-4-7(11)15-9(8)9/h3-6H,2,11H2,1H3 |
As an accredited thieno[2,3-b]pyridine-2-carboxylic acid, 3-amino-, ethyl ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Supplied in a 25g amber glass bottle with tamper-evident cap, labeled with chemical name, formula, and safety information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 8MT (200kg/drum, 40 drums) of thieno[2,3-b]pyridine-2-carboxylic acid, 3-amino-, ethyl ester. |
| Shipping | **Shipping Description:** Thieno[2,3-b]pyridine-2-carboxylic acid, 3-amino-, ethyl ester should be shipped in a tightly sealed container, protected from moisture and light. Transport should comply with all applicable regulations for chemicals. Ensure appropriate labeling, and include safety data. Avoid extreme temperatures and handle as a potentially hazardous laboratory chemical. |
| Storage | **Storage Description:** Store thieno[2,3-b]pyridine-2-carboxylic acid, 3-amino-, ethyl ester in a tightly sealed container, away from moisture, light, and incompatible substances. Keep it at room temperature (15–25°C) in a well-ventilated, dry area designated for chemicals. Avoid excessive heat and direct sunlight. Clearly label the container and follow all safety protocols for handling and storing organic esters and acids. |
| Shelf Life | Shelf life: Store thieno[2,3-b]pyridine-2-carboxylic acid, 3-amino-, ethyl ester in a cool, dry place; stable for two years. |
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Purity 98%: thieno[2,3-b]pyridine-2-carboxylic acid, 3-amino-, ethyl ester with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal impurity formation. Melting Point 154°C: thieno[2,3-b]pyridine-2-carboxylic acid, 3-amino-, ethyl ester with a melting point of 154°C is used in solid-state formulation development, where it provides thermal stability during processing. Molecular Weight 234.26 g/mol: thieno[2,3-b]pyridine-2-carboxylic acid, 3-amino-, ethyl ester with molecular weight 234.26 g/mol is used in medicinal chemistry research, where it enables accurate dosing and reproducible biological assays. Particle Size ≤10 μm: thieno[2,3-b]pyridine-2-carboxylic acid, 3-amino-, ethyl ester with particle size ≤10 μm is used in nanoformulation development, where it allows for enhanced solubility and bioavailability. Stability Temperature up to 120°C: thieno[2,3-b]pyridine-2-carboxylic acid, 3-amino-, ethyl ester with stability temperature up to 120°C is used in high-throughput screening, where it maintains compound integrity under assay conditions. Viscosity Grade Low: thieno[2,3-b]pyridine-2-carboxylic acid, 3-amino-, ethyl ester with low viscosity grade is used in liquid formulation design, where it allows for ease of mixing and homogeneous dispersion. |
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Working at the crossroads of research and industry, we stand behind the chemistry we produce. Thieno[2,3-b]pyridine-2-carboxylic acid, 3-amino-, ethyl ester has gained a real following in laboratories and upscaled production facilities. We’ve been involved with this heterocyclic scaffold since early-stage medicinal chemistry researchers highlighted its versatility. The exacting need for reliable building blocks with specific molecular frameworks has driven much of our development work, particularly for the pharmaceutical, agrochemical, and advanced materials markets. Direct feedback from our partners—those in hands-on synthetic roles—shows a strong demand for high-purity, consistent thieno[2,3-b]pyridine derivatives.
Synthesizing this compound involves detailed process control, from choosing raw materials to final purifications. We avoid short-cuts. Every batch gets full characterization using HPLC and NMR. Chemical purities above 98% don’t come from chance; they result from focusing on solvent selection, reaction optimization, and filtration that removes trace byproducts which could compromise downstream chemistry. Observing trends in pilot-scale and full-scale synthesis, we noted that the presence of just a small amount of unresolved precursor or isomer can derail further functionalization. That’s why every run ties back to practical application—what works in a kilogram batch must also work reliably in a 50-kilogram drum.
The thieno[2,3-b]pyridine motif offers a compact, fused bicyclic structure featuring an electron-rich thiophene ring meshed to a pyridine. We modify the core by introducing an ethyl ester at the 2-carboxylic acid position, and an amino group at the 3-position. This combination appeals to synthetic chemists who need a versatile intermediate. The ethyl ester allows for smooth hydrolysis or transesterification in common transformations, while the amino substituent gives extra leverage for further derivatization—amines can punch through a host of reactions, from acylations to cross-couplings. We see this compound emerge most often in custom synthesis orders for pharmaceutical lead compounds, where the thieno[2,3-b]pyridine backbone shows up as a privileged motif for kinase inhibitors and CNS-active agents.
Through our direct work with academic groups and contract synthesis labs, we've learned how crucial ease of handling becomes. Some compounds with similar backbones powderize or clump, but the crystalline nature of our product—and the way batches pour and dissolve in solvents—matters to those running multi-step syntheses. No one wants gummed-up glassware or unreliable weighing. Some teams report that our material offers straightforward solubility in DCM, methanol, and ethyl acetate—an operational edge over other derivatives with larger esters or bulkier substituents. Our process minimizes colored impurities that signal decomposition or early-stage oxidation.
Many chemists ask how the ethyl ester, amino-substituted variant compares with methyl or bulkier ester analogues, or with non-amino thieno[2,3-b]pyridine-2-carboxylic acids. In our experience, those with larger ester groups delay or hamper hydrolysis steps. Omitting the 3-amino group limits post-derivatization flexibility, especially when the aim is to build a focused library. We’ve tested these scenarios at different scales—results consistently show that the ethyl ester produces faster, cleaner conversions, and the free amino group supplies a key site for diversification. Higher molecular weight esters often show sluggish reaction rates, while the parent acid variant introduces solubility challenges in organic solvents and can throw off analytical baselines. Our clients appreciate a consistent melting point, pure white appearance, and reaction performance batch after batch.
We take practical safety considerations seriously. No batch leaves our plant without records of controlled moisture, proper containment, and documented chain of custody. This compound doesn't exhibit the malodor or rapid oxidation of some sulfur-containing moieties; it stores without advanced precautions. Still, we advise all users to work with appropriate gloves and eye protection, and to store sealed containers in cool, dry rooms. Several process chemists report trouble-free weighing and dissolution, even over long-term storage, since our storage recommendations are based on our own on-site stability studies.
The transition from gram-scale to multi-kilogram supply often reveals where laboratory talk doesn't match industry reality. Manufacturing thieno[2,3-b]pyridine-2-carboxylic acid, 3-amino-, ethyl ester at scale presents challenges in terms of solvent management, heat transfer, and process reproducibility. We solved bottlenecks around byproduct removal and phase separation early in our scale-up work. Our years spent in both development and production show that even minor in-process deviations can ripple into downstream product performance. Consistency matters most to our repeat customers, especially those feeding our product into their ISO-audited development channels.
Based on published research and direct feedback, this compound fits straight into targeted screening programs. Researchers choose it for its dual reactivity—both ester and amino functionalities can act as springboards for quickly accessing analog series. One project, aimed at kinase inhibitor development, selected our compound precisely because the core skeleton supported critical SAR modifications without extra purification headaches. Some groups focus on insecticide discovery and value the residue profile and manageable toxicity of our preparations.
As the direct manufacturer, we build long-standing relationships in research and industry. Users tell us that working straight with a chemist-owned facility eliminates confusion around origin, batch authentication, and technical support. We understand process challenges at bench and plant levels, bringing an eye for detail and problem-solving that extends beyond rote specification sheets. We supply all supporting analytical data, including extended NMR, MS, and HPLC reports with each consignment. We don’t just ship molecules — we answer questions about crystallization, filtration, or formulation from hands-on experience.
At every scale, unwanted color, odor, or trace metal contamination throws plenty of synthetic campaigns off track. We worked extensively on optimizing reagents and workup steps to take our product beyond lab-use quality. Labs working with standard methyl esters or non-amino analogues reported sticky residues and inconsistent MS response. We invested in additional purification steps to eliminate reaction stoppers that can slip through lesser-controlled routes, based on customer requests and internal R&D.
Projects running combinatorial synthesis or rapid parallel SAR place a premium on versatile intermediates. This ester-amino derivative lets teams move straight to amide couplings, Suzuki-Miyaura couplings, or selective reductions. One pharmaceutical team told us their library expanded more quickly—and their results improved—using this intermediate as a platform, compared to more rigid building blocks lacking free amino groups. The ethyl ester cleaves cleanly under mild basic conditions, simplifying downstream purification by crystallization or extraction.
We base every manufacturing lot on measured results. Each batch comes with full analytical data, from melting point (usually tight within 2-3°C) to residual solvent content and trace element levels. Where projects need to meet REACH or FDA technical standards, we support documentation down to the lot level, with impurity profiling and controlled process conditions. Customers entering regulated supply chains rely on consistent data, not guesswork.
In global markets, sourcing molecules like thieno[2,3-b]pyridine-2-carboxylic acid, 3-amino-, ethyl ester often means drifting between resellers or unverified manufacturers. We’ve seen products arrive with incomplete documentation, inconsistent color, or batch-to-batch variability that disrupts scale-up. By controlling production from raw material through isolation and quality testing, we eliminate these pain points for developers. We take transparency seriously and work with customers to meet their internal analytical requirements, not just our own.
Open communication with end users shapes our manufacturing practices. Synthetic teams working under tight project deadlines need products that perform, not surprises. Reported field results show that our batches retain consistent chemical and physical properties; this reliability reduces the risk of rework, delays, or unexpected dilution. Several groups also commented on the lower frequency of filtration problems and faster cleanups, compared to some commonly cited competitors.
Keeping pace with research demands for new chemical scaffolds, our role is to supply ready-to-use, high-quality materials. Teams focused on rapid hit-to-lead programs require compounds that integrate seamlessly into their automated systems or traditional protocol benches. Working with thieno[2,3-b]pyridine-2-carboxylic acid, 3-amino-, ethyl ester lets chemists bypass several low-yielding steps or lengthy purifications, jumpstarting multi-step syntheses that might stall with less refined materials.
Our customers serve sectors from pharmaceutical R&D to veterinary health, crop protection, and more specialized applications like chemical biology probes. The tailored reactivity of this compound enables creative solutions for difficult synthetic targets. In agrochemical fields, researchers rely on manageable physical properties and known low-toxicity profiles, which our team supports through further analytical work. In academic settings, students and postdocs tackle total synthesis or probe modification with confidence, thanks to our consistent and well-documented manufacturing.
From early development, we noticed recurring batch quality spikes traced to feedstock purity, reactor design, or temperature control. Investing in closed-loop feedback systems, improved reaction monitoring, and incremental workup optimization paid off in rising customer satisfaction and fewer out-of-spec lots. We pull from both literature precedents and process troubleshooting in the trenches of full-scale chemical manufacturing. Every process improvement springs from practical need—not theoretical guesswork, but decades of combined experience between our synthetic and production teams.
We do more than manufacture to order. We consult with customers on suitable solvents, agitation approaches, or even how to adapt our product into continuous processing. Technical support doesn’t mean reading a manual. It means sharing what we’ve learned about optimal storage, blending ratios, and the kinds of byproducts that appear with specific downstream chemistries. Our team communicates directly with operators and formulators, not just purchasing departments, so we solve issues before they become bottlenecks.
We strive for responsible chemistry. Thieno[2,3-b]pyridine-2-carboxylic acid, 3-amino-, ethyl ester presents manageable risk profiles and waste streams compared with many advanced intermediates. We recover and recycle solvent wherever practical, and write process safety into every step. Customers with sustainability mandates depend on documentation of emissions, handling, and disposal, and we respond with transparency on these fronts.
No supply route remains static. We examine every returned container and every customer memo for possible improvements in packaging, labeling, or shipping. Insights gained from direct handling—not arm’s-length analysis—drive changes in bottle sizes, seal types, or desiccant selections. Whether it’s fast delivery for a strict deadline or an emergency resupply after an accident at the customer’s lab, our logistics gear up to real-world requirements.
Our approach ensures you know what's inside every drum or bottle. All analytical records—chromatograms, spectra, and batch histories—back up the physical product delivered. Chemists value a straightforward relationship between product documentation and observed performance. If additional testing is needed, we can perform expanded impurity screening, thermal analysis, or compatibility testing and add the data to each customer file.
Our continued involvement in direct manufacturing transforms customer collaborations. Teams that rely on our experience receive more than a shipment—they receive backup, troubleshooting, and guidance tailored to their challenges. Building blocks like thieno[2,3-b]pyridine-2-carboxylic acid, 3-amino-, ethyl ester matter most in hands-on research environments, where a missed batch or impurity hiccup causes months of delay, not just minutes. We work with our customers to anticipate new directions, support pilot runs, or troubleshoot purification setbacks in the real world.
With years in the lab and on the plant floor, we developed a deep appreciation for what consistent, application-ready intermediates contribute to advanced synthesis. Thieno[2,3-b]pyridine-2-carboxylic acid, 3-amino-, ethyl ester stands out for its practical reactivity, straightforward handling, and clean analytical profile. By investing in robust process control and fostering direct communication, we continue to earn the trust of chemists, project managers, and bench scientists worldwide. This is more than producing commodity chemicals—it’s about supporting research and industry with every lot.