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HS Code |
874739 |
| Cas Number | 52973-18-7 |
| Molecular Formula | C6H7NO2S |
| Molecular Weight | 157.19 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Purity | Typically ≥98% |
| Boiling Point | 246-247 °C |
| Density | 1.232 g/cm³ |
| Solubility | Soluble in organic solvents |
| Refractive Index | 1.549 |
| Flash Point | 110 °C |
| Smiles | CCOC(=O)c1csnc1 |
| Inchi | InChI=1S/C6H7NO2S/c1-2-9-6(8)5-3-10-4-7-5/h3-4H,2H2,1H3 |
As an accredited Ethyl Thiazole-4-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Ethyl Thiazole-4-Carboxylate is packaged in a 25g amber glass bottle, labeled with chemical details, hazard symbols, and batch information. |
| Shipping | **Shipping Description for Ethyl Thiazole-4-Carboxylate:** Ethyl Thiazole-4-Carboxylate is shipped in tightly sealed, chemical-resistant containers, protected from light and moisture. Packaging complies with relevant chemical transport regulations. The material is transported under ambient conditions, with careful labeling and documentation to ensure safe and compliant handling throughout transit. |
| Storage | Store **Ethyl Thiazole-4-Carboxylate** in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep it away from incompatible substances such as strong oxidizing agents. For safety, use with appropriate personal protective equipment (PPE) and follow all relevant chemical handling guidelines. Store at room temperature unless otherwise specified by the manufacturer. |
Applications of Ethyl Thiazole-4-Carboxylate in Industrial ManufacturingEthyl Thiazole-4-Carboxylate serves as an essential intermediate in several high-value industrial manufacturing sectors, supporting both stringent compliance regimes and advanced production chains. We leverage years of experience in synthesis and process integration to supply this raw material for precise use within specialized downstream domains. Explore real-world applications, compliance requirements, integration points, and main formulations in established industrial scenarios. 1. Pharmaceutical Intermediate for Thiazole-Based APIsProducers of thiazole-containing active pharmaceutical ingredients (APIs) utilize Ethyl Thiazole-4-Carboxylate as a key heterocyclic building block, particularly for drugs targeting metabolic, anti-infective, and anti-inflammatory pathways. Downstream API manufacturers integrate the compound at the initial condensation and acylation stage, enabling specific ring transformations crucial for patented structures. Compliance with global pharmacopoeias and regulatory standards governs each batch, while formulation ratios depend on both molecular route and impurity profiles. The resulting APIs enter finished dosage form manufacturing for regulated markets. Industry compliance standards
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2. Aroma Chemicals for Food Flavor SynthesisMajor flavor manufacturers include Ethyl Thiazole-4-Carboxylate as a precursor to develop thiazole-based aroma molecules, critical for imparting roasted, nutty, or meaty notes in processed foods and ready-to-eat meals. The material enters flavor compound synthesis under strictly controlled food additive regulations, with formulation levels determined by target aroma threshold and end-use regulatory approval. Production integrates batch synthesis followed by distillation and purity analysis for food-grade deployment. Industry compliance standards
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3. Agrochemical Synthesis: Pesticide and Fungicide IntermediatesEthyl Thiazole-4-Carboxylate functions as a critical intermediate for agrochemical suppliers manufacturing specific thiazole-derived pesticides and fungicides. The compound integrates into multi-step synthesis chains, specifically during precursor functionalization for sulfur-heterocycle-based crop protection agents. Strict adherence to agrochemical purity and residue limits guides its use, combined with robust quality testing prior to final formulation. Industry compliance standards
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4. Custom Chemical Intermediate for Dye and Pigment ManufactureSpecialty dye and pigment producers employ Ethyl Thiazole-4-Carboxylate as a unique intermediate to deliver color-fast thiazole-based structures, particularly for textile or paper applications requiring resistance to high temperatures and UV exposure. The intermediate enters diazotization or coupling stages, undergoing targeted molecular modifications tracked by batch QC and standard textile chemical regulations. Industry compliance standards
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The world of heterocyclic chemistry pushed us forward rapidly, and Ethyl Thiazole-4-Carboxylate stands as a product that keeps up with the pace of modern laboratories and innovative industrial projects. At its core, this molecule serves as a stable foundation for constructing more intricate chemical structures. Each time our synthesis team completes a batch, the familiar blend of robustness and reactivity reminds us why this compound has won a place on the bench of countless chemists.
We manufacture Ethyl Thiazole-4-Carboxylate to meet a tight set of quality markers formed by years of close work with R&D departments and production engineers. Our standard model delivers a consistently high purity, regularly hitting greater than 98% on an HPLC assay. Shelf-life stability has proven solid when stored under dry, cool conditions, which matters for those working with tight timelines or bulk quantities. Color and odor provide quick first-glance indicators—a faint yellow, free-flowing powder with a mild, characteristic thiazole aroma.
The thiazole core in this ester form presents a handle for diversification, all while maintaining ease of solubility in many common organic solvents. This chemical form travels safely and can be stored for months, offering flexibility during prolonged projects or scale-ups. Every batch undergoes spectral validation; we confirm structure using NMR and IR, with the CO2Et group giving a crisp IR stretch that our QC chemists can spot without a second guess.
Our own team started making Ethyl Thiazole-4-Carboxylate to serve the needs in pharmaceutical intermediate synthesis, since the 4-position on the thiazole ring provides a strategic spot for further transformations. Medicinal chemists come back for this compound because they rely on the predictable reactivity of the ester function. Working directly with their teams over the years has taught us that clean coupling reactions—especially those using Suzuki, Sonogashira, or Buchwald-Hartwig protocols—benefit from a pure, dry starting material. We cut down on the off-odors and side reactions that plagued earlier processes by revising our purification method a few years ago after feedback on kettle fouling and yield loss.
In our plant, scale-up to kilogram quantities never sacrifices reproducibility. The same batch consistency required by a start-up research lab extends to the large-scale pharmaceutical producer. Material moves through our reactor trains with checks at each step, and with every completed lot, we catch the nuances only those making the product notice—a sharper odor with slightly higher purity, a more cohesive granule bed when mixing larger volumes. We don’t outsource our production or depend on third-party processing, and that shows in the unique fingerprints of every batch.
This compound didn’t earn its foothold by accident. Those working in API synthesis often require fragments that carry both sulfur and nitrogen, features that the thiazole structure supplies in one five-membered ring. The ester group streamlines downstream modification, so when material reaches our customers, they cut steps and save time getting to more complex thiazole derivatives. We’ve worked through dozens of custom orders to make related esters and acids, but Ethyl Thiazole-4-Carboxylate keeps its place as a go-to building block because it doesn’t produce the byproducts universal acids or free thiazoles tend to.
Over the last decade, we’ve watched as agricultural research programs expanded their calls for thiazole-based compounds. Our own tests pairing Ethyl Thiazole-4-Carboxylate with electrophilic partners uncovered routes toward new fungicide and plant-protectant classes. This versatility became clear as we gathered customer reports showing novel biocidal activities tied to custom derivatives. In fragrances, the subtle, baked-bread aroma of the thiazole core finds its way into high-end product formulations. These specialty markets seek unique molecules with traceable manufacturing and clear batch histories—not generic catalogs filled with uncertain sources.
Our Ethyl Thiazole-4-Carboxylate stands distinct from simple thiazole or its acid and methyl ester cousins for several reasons. The ethyl ester brings an optimal blend of stability and reactivity. We encountered pain points with methyl thiazole-4-carboxylate in our own labs—more volatility, more rapid hydrolysis, and inconsistency in certain downstream condensations. The ethyl chain, at once short and hydrophobic, smooths those edges and handles process solvents with less fuss.
Our customers tell us that acid forms suffer from excessive sticking and variable shelf life; the solid ethyl ester avoids these pitfalls. You can open a container at room temperature without a strong acid vapor, and when it comes to filtration, we’ve dialed our crystal size so users cut labor in their own labs. From batch to batch, material pours easily, sets well in process trays, and permits handling at scales from gram jars to multi-kilo drums.
Creative chemists selecting building blocks for combinatorial libraries appreciate the selective reactivity of the ethyl ester. Nucleophilic or electrophilic partners proceed with minimal protection steps. In the realm of advanced materials development, this reactivity opens routes to modified surfaces and new polymer blends that don’t suffer the instability seen with other ester variations. We’ve tackled several custom modifications for electronics firms that needed a robust, sulfur-nitrogen motif tethered to a hydrocarbon chain.
The thiazole motif in Ethyl Thiazole-4-Carboxylate draws on a century of heterocycle chemistry. Modern research confirms the utility of this core—study after study describes its prevalence in FDA-approved drugs, pesticides, and advanced materials. In our own plant, we run a full suite of quality checks, not only performing routine spectroscopic confirmation but also testing reactivity with established coupling partners. Over years of adjusting and fine-tuning our process, we strengthened our crystallization and washing steps, cutting down on residual acids and heavy metals that can derail sensitive downstream transformations.
The benefit of keeping manufacturing in-house extends to traceability—each incremental change in process conditions and cleaning protocols reflects in our lot records and batch-level analytics. We maintain full documentation for all shipments, supporting audits by major pharmaceutical buyers and offering extensive technical support to troubleshooting teams worldwide. Few outside our facility see how repeatable and robust the process becomes only from years of immersion in the practical details: solvent choices adjusted for season, filtration speed tweaks for alternate particle sizes, constant debate over drying endpoints for high humidity periods.
One challenge that crops up every year stems from changes in global supply dynamics. Sourcing the starting materials, especially sulfur and specialized reagents, sometimes gets complicated. Over time, we learned to secure long-term contracts with trusted raw-material producers and keep a larger inventory buffer on site. This move kept us shipping even during disruptions, ensuring chemists relying on our compounds did not get delayed by global volatility.
Another hurdle comes from handling waste byproducts—thiazole chemistry sometimes produces sulfur-rich residues that require careful disposal. We invested in scrubber systems and re-engineered some unit operations to cut our environmental load. Local regulations evolve, and we keep adapting, talking directly with regulators to prove we manage hazardous components responsibly. The days of venting odorous solvents unchecked to the air are over, and we hold ourselves to the standards our customers expect from a long-term supplier.
Labs that count on reliable starting materials save time and reduce research setbacks. Over years of collaboration with academic groups and industrial formulation teams, it’s been clear that the smallest inconsistencies—from minor impurity spikes to color variations—can delay patent filings or stall scale-up. Our technical liaison team receives frequent requests for extra batch data, early samples, and reaction troubleshooting. We’ve built protocols to support these needs, offering tailored documentation and log files for every prepared batch.
Smaller labs working at bench scale won’t always see the full supply chain behind a bottle of Ethyl Thiazole-4-Carboxylate. We open our lines for technical support, from confirming solubility profiles in unusual solvents to discussing synthetic routes that avoid hazardous reagents. We spotted recurring questions about batch stability under different conditions, so we studied storage effects systematically, giving more tailored recommendations to customers—results that help avoid unnecessary losses from temperature excursions or humidity slip-ups.
The impact goes beyond mere supply. Advanced formulation teams at global consumer goods giants draw on thiazole derivatives to create new fragrances and flavors, some recognized for years as natural or nature-identical. Our products, which meet rigorous trace impurity specifications, help customers avoid market recalls and regulatory challenges. We share real data, not marketing fluff, every time a new customer puts a purchase order in, because that’s how you build lasting partnerships.
Ethyl Thiazole-4-Carboxylate isn’t the only option in heterocyclic fragment chemistry, but it speaks to a middle ground between stability and synthetic leverage. Moving to methyl esters, you may gain volatility at the cost of product loss and inconvenience during storage. Using the free acid, you can tune your route for rapid amidations or other transformations, but risk lower yields and more challenging purification. The ethyl ester gives a measured path, taking the best from both alternatives while limiting their drawbacks.
We’ve produced a range of analogues—propyl, butyl, even isopropyl esters—each offering some adjustment in reactivity and solubility. Our data show, though, that the ethyl variant remains the workhorse across most applications, neither too slow in saponification nor too fast to hydrolyze during purification. Thiazole-2-carboxylates and 5-carboxylates cross the bench every so often, but the 4-position targets downstream modifications more reliably; synthetic chemists recognize the distinct geometry and electronics catered to their goals.
Making comparisons invites consideration of source as much as structure. Sourcing from the manufacturer offers benefits beyond cost: full process knowledge, direct documentation, and support for scale-up or troubleshooting. Traders and resellers can’t provide the same transparency or explain subtle variations in an impurity from one batch to the next. Working with us puts real manufacturing expertise at your disposal, and the conversation runs both ways—feedback from real usage has driven process improvements and more robust supply chains.
The story of Ethyl Thiazole-4-Carboxylate at our facility doesn’t just lie in the chemistry textbooks. Collaboration, adaptability, and hands-on problem solving brought us to where we are. We run regular reviews of our processes, spurred as much by field reports as by in-house analytics. Each time a customer flags an issue or shares a new downstream use, we reevaluate quality and workflow. Those moments drive innovation, guiding equipment upgrades, procedural changes, and new stability studies.
Demand evolves as new discoveries unfold—drug pipelines shift, flavor profiles trend, eco-friendly chemicals find bigger markets. Our commitment remains to keep pace, not by jumping on trends, but by strengthening our base. Volumes grow, and so does our investment in staff training and analytical instrumentation. Only by keeping our production grounded in the details can we consistently provide a product that supports both routine work and ambitious projects alike.
Ethyl Thiazole-4-Carboxylate shows what focused expertise produces—a chemical whose reliability, traceability, and responsiveness to customer needs keeps it at the forefront of synthetic work. Our ongoing improvements ensure that each order brings the same careful attention we relied on to develop this product in the first place. For those seeking more than just a bottle off a shelf, the experience borne of daily hands-on practice makes a meaningful difference, project after project.