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HS Code |
658856 |
| Product Name | 4-Methyl-2-Phenyl-1,3-Thiazole-5-Carboxylic Acid |
| Cas Number | 142137-85-1 |
| Molecular Formula | C11H9NO2S |
| Molecular Weight | 219.26 g/mol |
| Appearance | White to off-white solid |
| Solubility | Slightly soluble in water; soluble in common organic solvents |
| Purity | Typically >98% (dependent on supplier) |
| Storage Conditions | Store at room temperature, keep container tightly closed |
| Smiles | CC1=NC(=C(S1)C(=O)O)C2=CC=CC=C2 |
| Inchi | InChI=1S/C11H9NO2S/c1-7-12-9(11(13)14)15-10(7)8-5-3-2-4-6-8 |
| Synonyms | 5-Carboxy-4-methyl-2-phenylthiazole |
As an accredited 4-Methyl-2-Phenyl-1,3-Thiazole-5-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle labeled "4-Methyl-2-Phenyl-1,3-Thiazole-5-Carboxylic Acid, 25g, For laboratory use, keep tightly closed." |
| Shipping | 4-Methyl-2-Phenyl-1,3-Thiazole-5-Carboxylic Acid is shipped in tightly sealed containers to protect it from moisture and contamination. It should be packed according to standard chemical safety regulations, preferably in cool, dry conditions. Ensure clear labeling and provide appropriate documentation for safe handling and transport compliance. |
| Storage | Store **4-Methyl-2-Phenyl-1,3-Thiazole-5-Carboxylic Acid** in a tightly sealed container, protected from light, moisture, and incompatible substances. Keep in a cool, dry, and well-ventilated place, ideally at room temperature (15–25°C). Avoid exposure to strong oxidizing agents. Clearly label the container and store in accordance with all local, state, and federal chemical safety regulations. |
Applications of 4-Methyl-2-Phenyl-1,3-Thiazole-5-Carboxylic Acid in Industrial ManufacturingAs the manufacturing source of 4-Methyl-2-Phenyl-1,3-Thiazole-5-Carboxylic Acid, we supply this specialty thiazole derivative to precise downstream customers seeking reliable synthetic intermediates for regulated end uses. Our technical expertise ensures secure integration into specialized production environments across several mature sectors, where its structure and purity enable consistent product performance. 1. Pharmaceutical Intermediate for Thiazole-Based API SynthesisThis compound commonly enters controlled drug substance production routes for API manufacturers focused on heterocyclic scaffolds, particularly within anti-infective and CNS therapeutic segments. Its aromatic thiazole core acts as a foundational building block for multi-step synthetic sequences governed by rigorous quality and traceability requirements. The material is introduced after the initial condensation step, allowing for selective derivatization and subsequent coupling stages under cGMP protocols. Manufacturers rely on its high chemical purity and consistent lot analysis for uniformity throughout batch API release. Industry compliance standards
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2. Agrochemical Synthesis for Fungicidal Compound ManufacturingMajor agrochemical formulators utilize our thiazole derivative to construct advanced fungicidal frameworks. Its 1,3-thiazole ring system enables specific building block integration during the regulated synthesis of crop protection products. Controlled reaction conditions facilitate substitution or direct functionalization, typically in the presence of base catalysts, and integration occurs during intermediate coupling prior to final formulation. Downstream QC ensures absence of mutagenic or persistent by-products, in line with international pesticide safety directives. Industry compliance standards
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3. Specialty Fragrance Ingredient for Fine Aroma CompoundingOur thiazole derivative finds highly regulated application within fine fragrance and specialty aroma blending, where its distinct heterocyclic note delivers unique character to finished fragrance accords. Expert compounding operations incorporate it at the blending phase, following dilution in suitable solvents, strictly observing IFRA and safety assessment guidelines. Its use profile supports nuanced top and middle note construction in both high-end perfumes and complex flavor preparations, subject to concentration thresholds and allergen disclosure standards. Industry compliance standards
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4. Polymer Additive for Electronic Material FunctionalizationProducers of advanced polymers for electronics and specialty coatings incorporate 4-Methyl-2-Phenyl-1,3-Thiazole-5-Carboxylic Acid as a reactive modifier to impart electron-donating properties within aromatic polymer matrices. Its addition occurs during the controlled melt blending or solution polymerization stages, ensuring covalent integration across the polymer backbone. Downstream applications prioritize superior dielectric performance, thermal resistance, and regulatory-compliant leaching behavior for use in microelectronic encapsulants and antistatic coatings. Industry compliance standards
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Competitive 4-Methyl-2-Phenyl-1,3-Thiazole-5-Carboxylic Acid prices that fit your budget—flexible terms and customized quotes for every order.
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Every manufacturer faces the test of consistency and transparency, especially in the world of specialty chemicals. In our production facility, the synthesis and supply of 4-Methyl-2-Phenyl-1,3-Thiazole-5-Carboxylic Acid has shaped our operations for years. This compound, often referenced by its CAS number, marks a critical building block for both pharmaceutical intermediates and agrochemical development. Our team handles the entire production, from raw material selection through to purification and packaging. We are not resellers—we create the molecule from scratch, using controlled reaction pathways we have refined over countless batches. Our customers—chemists who design advanced molecules, process engineers configuring new syntheses—depend on us to reduce noise in their results by giving them a product with tight, reliable specifications.
From an industrial chemist’s point of view, every compound tells a different story. 4-Methyl-2-Phenyl-1,3-Thiazole-5-Carboxylic Acid contains both thiazole and phenyl groups, making it compatible with a range of target molecules for pharmaceutical and agricultural synthesis. The carboxylic acid group gives clear points for downstream reactivity, a feature process chemists look for when devising novel analogues. Our own batch records demonstrate that only rigorous control of reaction temperature and stoichiometry yields the distinct crystal form favored by our largest clients. Many manufacturers struggle to minimize side reactions that insert impurities at the aromatic sites. Our investment in high-performance liquid chromatography (HPLC) lets us measure and confirm the purity of every lot before it leaves the reactor. These steps make a difference because off-specification material leads to wasted downstream steps in R&D or plant-scale synthesis.
Some producers cut corners on solvent quality or drying techniques, hoping for quicker production cycles. Experience teaches a different lesson—shortcuts translate to unpredictable byproducts that surface later, sometimes after months of downstream research investment. With thiazole-based acids, trace-level impurities can trigger unexpected results during amide coupling or cyclization. Our team once received feedback from a pharmaceutical R&D group that a trace impurity—less than 0.05%—introduced complications in an enzyme inhibition test. This prompted us to revise not only our workup procedure but also to double-check incoming solvents and reagents. It means more hours in the lab, more stringent lot testing, and tighter release criteria, but the return comes through long-term customer trust and fewer problem reports. Quality starts at batch one, and poor results can ripple through dozens of invested projects. That’s why our technicians scrutinize each run the way an analytical chemist would.
We manufacture 4-Methyl-2-Phenyl-1,3-Thiazole-5-Carboxylic Acid in multiple scales to respond to both kilo-lab and larger process needs. Our larger reactors have carefully controlled stirring rates, and jacketed cooling prevents local overheating—a frequent cause of colored byproducts in aromatic thiazoles. Technicians trained in gravimetric measurement and pH control run every process. One recurring challenge lies in the control of reaction pH during the carboxylation step, which, if not managed, shifts product purity from above 99% to the low nineties. We document these lessons in our batch records and use them to refine each repeat production. Because certification as a trusted manufacturer comes not from a single good batch, but from consistently high purity across every shipment.
Most customers sourcing this compound from us request the crystalline solid, typically in the 100 g to multi-kilo scale. The melting point remains a key indicator; our in-process team records a range with tight limits in every certificate of analysis we generate. The typical melting point hovers around 180-185°C, uncorrected, but we observe variations if carrier solvents aren’t fully removed. Moisture content, checked by Karl Fischer titration, features in our finished product checks. Low moisture not only avoids product clumping during transit, but it also reduces the risk of hydrolysis when customers use the acid in sensitive steps. Packaged in HDPE bottles and sealed under inert gas, each shipment passes a checklist where IR, NMR, and purity by HPLC form the backbone of our documentation. If a buyer requests it, we can cross-check by GC-MS to confirm the absence of overlooked low-mass volatiles. Through these controls, our clients in Europe, North America, and Asia receive material that genuinely matches our stated purity, color, and form.
The acid’s value lies in its application versatility. Medicinal chemists often use it as an intermediate for further coupling, with downstream steps involving amidation or esterification. Our clients highlight the clear color, fine particle size, and the way the compound dissolves in polar aprotic solvents—a testament both to synthesis quality and consistent particle engineering. Agrochemical researchers opt for this thiazole-based acid because it integrates into novel pesticide candidates where sulfur and nitrogen heterocycles are essential. In both sectors, failed reactions waste material and time; our own experience has taught us that every truncated chain reaction, every crystallization that doesn’t proceed as planned, runs up the costs for formulation teams working under strict deadlines. We field frequent questions about compatibility with new green chemistry coupling agents; our technical service team draws on hands-on process knowledge, not just a data sheet.
In the crowded world of thiazole derivatives, molecular structure makes a significant difference. A methyl group in the 4-position and a phenyl at the 2-position give our acid properties distinct from simple 1,3-thiazole carboxylates. This combination brings improved stability and a more predictable reactivity during condensation steps. We have synthesized dozens of related molecules—clients often compare our material to 2-Phenyl-1,3-thiazole-5-carboxylic acid (lacking the methyl group), or to 4-Methylthiazole-5-carboxylic acid (missing the phenyl). Our compound dissolves in organic solvents like DMF and DMSO at higher concentrations, which supports chemists handling batch reactions at scale. Many analogs crystallize as sticky oils or unstable powders. Our product’s solid state, with defined crystals, avoids dispersion challenges, especially during automated dispensing.
Another key technical difference rests with the electronic effects of the methyl and phenyl combination. As any medicinal chemist will explain, electron-donating and -withdrawing groups shift the molecule’s behavior under reaction conditions. The modified electron density pattern makes our carboxylic acid more predictable in stepwise additions or metal-catalyzed couplings. Feedback from industrial clients often centers around how our compound reliably gives cleaner conversion in urea or amide construction. Engineers in pilot plants appreciate a product that translates from lab to plant scale without shifting impurity profiles—a challenge common with less rigorously manufactured analogs from other suppliers. We share our customers’ data (with consent) with our QA team, closing the loop between maker and user, turning every production run into a lesson for the next.
Manufacturing is only the beginning. Our 4-Methyl-2-Phenyl-1,3-Thiazole-5-Carboxylic Acid finds its way into candidate drugs and new crop protection compounds. In every field trial, every bench chemistry experiment, stability and purity become the measure of our effort. Clinical researchers and agrochemical developers report that off-color, poorly characterized batches slow down their screens and sometimes stop development cold. Over the years, we have worked in partnership with several pilot plants and contract research organizations. Problems traced to inconsistent input material often circle back to inferior handling during manufacture, drying, or storage. Our logistics chain includes tight monitoring of humidity and temperature from production through delivery. Shelf life, as reported from our own stability tests, consistently reaches two years when stored in original sealed packaging, away from direct sunlight and high temperatures.
Customers have commented that switching to our product reduced purification steps in downstream modifications. One synthetic route, for example, went from a three-step to a single-step workup due to the absence of byproducts we previously saw from lower-grade acids. Every hour saved and kilo reclaimed makes a difference, not just in the chemical cost, but in project timelines and regulatory filings. In a field where processes scale from grams to hundreds of kilos, predictability at the input stage helps projects clear regulatory and internal review quicker. That benefits everybody involved—from the lab technician running the first synthesis to managers balancing project budgets.
We’ve always put a premium on safety, both for people and the environment. Production of 4-Methyl-2-Phenyl-1,3-Thiazole-5-Carboxylic Acid deals with precursors that demand care—care in handling, in ventilation design, and in responsible waste treatment. Over the last decade, we’ve retooled our process to manage residues, recycling as much solvent as possible and sending only residue-rich fractions to licensed waste facilities. Staff in our plant undergo recurring safety training and maintain up-to-date records of exposure and incident drills. Our QA audits regularly cross-check every operator protocol, and every lot shipped includes traceable batch records in compliance with global chemical regulations. The customers we work with expect transparent documentation, and our experience tells us that well-documented, reproducible production not only ensures repeatable results, but also helps our partners meet their own quality management standards.
Shifts in global chemical stewardship have encouraged us to rethink waste streams and solvent use, transitioning to more benign carrier systems and adopting closed-loop recycling wherever technically feasible. Energy use has dropped over the years due to continuous process upgrades, but maintaining product quality always comes first. We have declined at times to adopt more “efficient” processes simply because our batch tests showed even slight increases in impurity levels. These hard choices reflect the balance between sustainable manufacture and uncompromising quality our team maintains as core values. Regulatory oversight continues to tighten, but long experience has prepared us to meet and exceed those demands, batch after batch, year after year.
Every lot we produce represents a living link with our customers’ research and business goals. Over time, we have extended our synthesis to customized analogs—a direct response to bioassay data received from client labs. Dialogue with research departments shapes process tweaks, new purification approaches, and parallel synthesis routes. Internal R&D spends part of each year exploring higher purity targets and faster synthesis pathways, but never at the expense of reliability. Direct feedback—both positive and negative—guides these investments. We conduct regular workshops with synthetic chemists and scale-up engineers to align our molecular offerings with the shifting demands of biopharma, crop science, and materials companies. More than just a catalog item, our 4-Methyl-2-Phenyl-1,3-Thiazole-5-Carboxylic Acid stands as proof that precise, traceable, reproducible manufacturing has a real, daily impact on outcomes in the industrial laboratory.
Every kilogram we supply helps launch new molecules, complete clinical design studies, and fill analytical labs with material that meets their highest hopes, rather than just minimum requirements. We see the trust our customers place in us as the most valuable asset, earned through transparent practice, relentless learning, and shared experience. In the evolving landscape of fine chemical manufacture, producing 4-Methyl-2-Phenyl-1,3-Thiazole-5-Carboxylic Acid is a calling that continues to sharpen our skills, deepen our knowledge, and connect us with those shaping the science of tomorrow.