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HS Code |
100526 |
| Chemical Name | 2,4-Dimethylthiazole-5-Carboxylic Acid |
| Cas Number | 13073-25-1 |
| Molecular Formula | C6H7NO2S |
| Molecular Weight | 157.19 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 137-140°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥ 98% |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Iupac Name | 2,4-dimethyl-1,3-thiazole-5-carboxylic acid |
| Smiles | CC1=NC(=C(S1)C(=O)O)C |
| Synonyms | 2,4-Dimethyl-5-thiazolecarboxylic acid |
As an accredited 2,4-Dimethylthiazole-5-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250 mg of 2,4-Dimethylthiazole-5-Carboxylic Acid is supplied in a sealed, amber glass vial with a secure screw cap. |
| Shipping | **2,4-Dimethylthiazole-5-Carboxylic Acid** is shipped in secure, leak-proof containers, protected from light and moisture. It is packaged following regulatory guidelines for chemical transport, with clear hazard labeling and documentation. Standard shipping is via ground or air freight, adhering to all relevant safety and handling protocols for laboratory chemicals. |
| Storage | **2,4-Dimethylthiazole-5-Carboxylic Acid** should be stored in a tightly sealed container, protected from light and moisture. Keep it at room temperature, ideally between 2-8°C, in a well-ventilated, dry area away from incompatible substances such as strong oxidizers and bases. Proper labeling and handling procedures should be followed to avoid contamination and ensure safety. |
Applications of 2,4-Dimethylthiazole-5-Carboxylic Acid in Industrial Manufacturing2,4-Dimethylthiazole-5-carboxylic acid is an essential intermediate used in advanced industrial synthesis. Our direct manufacturing enables precision control of quality for downstream sectors requiring high-purity thiazole derivatives. Below, we detail core application areas with specific compliance, usage, process, and end-product requirements. 1. Pharmaceutical Active Ingredient SynthesisPharmaceutical companies utilize our material primarily in the synthesis of thiazole-based APIs used for anti-infective and metabolic disorder treatment drugs. Controlled integration of this acid enables targeted heterocyclic assembly directly into advanced intermediates. Regulatory systems demand validated traceability and documented impurity profiles throughout synthesis. We provide precise batch consistency supporting strict validation protocols in tableted and injectable end products. Industry compliance standards
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2. Flavor and Fragrance Ingredient ProductionManufacturers in the flavor and fragrance sector employ 2,4-dimethylthiazole-5-carboxylic acid as a high-purity precursor for thiazole-derived aroma compounds. The thiazole core imparts roasted, nutty, or meaty flavor notes in processed foods, beverages, and fragrances. Accurate dosing and compliance with global food additive norms are crucial, particularly for products exported to regulated markets. Industry compliance standards
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3. Agrochemical Intermediate ManufacturingAgrochemical producers deploy this raw material in syntheses of thiazole-structured fungicides and plant growth regulators. High selectivity and purity are essential for agrochemical actives that must meet strict environmental residue standards. Our product supports reproducible outcomes for pesticide manufacturers, including dedicated agrochemical GMP integration and field application QA approvals. Industry compliance standards
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4. Specialty Chemical Synthesis for Electronic MaterialsProducers of specialty chemicals for the electronics sector exploit this acid for the molecular construction of photoinitiators and optoelectronic intermediates. High-purity compound delivery ensures reproducibility in advanced photoresist formulation, OLED material manufacturing, and sensor chemical design. Stringent electronic-grade quality control governs incoming raw materials for downstream process yield and device reliability. Industry compliance standards
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5. Fine Chemical Intermediate for Diagnostic ReagentsDiagnostic and research reagent manufacturers require consistent thiazole intermediates for use in assay buffer formulations, labeling compounds, and biochemical marker synthesis. Biomedical quality parameters and analytical performance rely on raw material reproducibility, including confirmation through spectroscopic and chromatographic QC. Direct traceability from manufacturer to finished diagnostic lot remains essential for end-user and regulatory acceptance. Industry compliance standards
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In our plant, 2,4-Dimethylthiazole-5-Carboxylic Acid comes off the line with a purity that meets the needs of researchers and process engineers. Developing this compound means more than ticking off quality boxes. It shows the steady hand and real-world judgment that comes from scaling reactions beyond glassware. While the molecular structure of this compound may look simple—thiazole ring, two methyl groups and a carboxylic acid moiety—the nuances in achieving a tight, controlled synthesis pave the way for reliability in application.
Our standard batch yields a high-purity crystalline powder that stands up to rigorous analysis. We submit every lot to practices we trust—HPLC, NMR—because ambiguous results tie up downstream processes. Direct feedback from users in both pharmaceutical and specialty chemical sectors keeps us grounded in the real utility of such testing. While some labs settle for loose interpretation of melting point or NMR data, we hold each batch to predictable chromatographic retention and clear spectral signatures. You won’t get the uneven color or erratic color change that sometimes signals the presence of byproducts. Moisture content lands within tight limits, as even small shifts can alter reactivity for end use.
This molecule acts as a fundamental building block in fields ranging from medicinal chemistry to agriculture. Chemists have turned to it as a scaffold for heterocyclic development, especially where nuanced reactivity or bioactivity is called for. Within our walls, we learned the true meaning of batch consistency after early feedback showed that minor impurities lead to challenging isolation or unexpected side reactions. Now, synthetic teams rely on repeatable yields, avoiding headaches over purification bottlenecks or unplanned experiments trying to “tweak out” interfering peaks.
The carboxylic acid functionality stays responsive for coupling reactions. We see it put to work in amide formation and esterification, serving both research bench needs and larger scale process chemistry. It takes real experience to stay below limits of trace-metal contamination, which matters for follow-up cyclization or amidation. In cases where purity has drifted at the milligram scale, we’ve watched the knock-on effects: stalled assays, wasted time, frustrated downstream partners. That led us to standardize every part of material handling, ensuring containers, balances, and mills don’t introduce extra variables.
Outside our doors, we’ve seen this thiazole derivative become established in intermediate steps for active pharmaceuticals, flavor development, and as a monomer in targeted polymer synthesis. Despite the variety, the foundational role remains: feedstock that introduces molecular rigidity and defined reactivity.
We don’t chase trends by frivolously adjusting specifications just to stand out. Our edge rests on proven feedback: reproducibility, clean batch records, and clear communication with chemists who rely on dependable supply. Several years ago, demand shifted toward higher throughput. Early on, large-scale drying steps introduced subtle yellow-brown tint that signaled thermal breakdown—a costly lesson in overzealous heating. By retooling crystallization parameters and switching to lower-impact drying, material now retains the color and chemical reactivity that downstream users expect, even in multi-kilogram lots.
Some suppliers focus only on the molecule’s name on a datasheet. From our vantage point, being the actual producer means tracking raw input quality, scaling reaction vessels, maintaining solvent purge cycles, and controlling temperature ramp rates in every run. Small changes here show up as real issues later: incomplete reactions, odor, or atypical dissolution in organic or aqueous setups. Working closely with development chemists helped reinforce which attributes matter—flowability for automated feeders, solubility in diverse solvents, or predictable performance in condensation reactions. Unlike generic offerings that sidestep these details, we listened closely and adjusted.
Another difference shows up in safety and batch handling. In our experience, losses and cross-contamination risk multiply if personnel become complacent about labeling or dedicated equipment. Every operator goes beyond routine SOPs, verifying identities at multiple steps. Chemistry will always throw curveballs, so direct oversight—a person who knows the quirks of this acid—prevents accidental blending with other thiazole derivatives or ring-substituted analogs.
Scaling up from grams in a flask to tens of kilograms created its own breed of problems. The reaction between starting methylthiazole and carboxyl precursor evolves sharp odors, and strict air handling is not optional. We tackled this by investing in upgraded ventilation and real-time atmospheric monitoring, which protected both staff and product. On the bench, pH swings during purification once led to lumpy crystallization and unpredictable particle size. After collaboration between technical, safety, and production teams, a multi-stage crystallization protocol removed these hurdles—so now, each lot dissolves as expected in downstream coupling without leaving stubborn residues.
Purity troubles and mismatched expectations sometimes sprouted across global sites. At one point, shipments raised eyebrows with varying NMR baseline, even though GC data looked spotless. Investigation led us back to trace residuals from a supplier who quietly altered a raw material’s purification method. Instead of resting on internal paperwork, we flew out to audit the partner’s site, tracing the subtle difference in quitpoint. That experience shaped our current documentation process and showed us that total supply-chain visibility isn’t optional for reproducible results.
Solvent selection for final washes once seemed a minor point. Over time, we saw how residual traces impacted next-stage reactions and even caused flavor taints. By tightening release specification and investing in better in-house analytical calibration, the product now comfortably passes muster with those who care about spectroscopic purity and flavor/aroma carryover. This opened doors in food chemistry and fragrance development, allowing downstream partners to trust not only the main thiazole component but also its inertness in their matrices.
End users include both research labs and bulk pharmaceutical intermediates teams who don’t walk in lockstep. Some need small glass bottles with detailed spectra, others want multi-kilo fiber drums with robust seals. Keeping pace means more than just clean paperwork. Direct calls from users have alerted us to practical issues—blockages in automated feeder lines if static charges build up, sticking during powder transfer on humid days, or spills during charging that ruin a batch. Our operators have learned how to control for these issues in-house—antistatic agents, careful grounding, and staged container filling.
Reliability stretches into shipping logistics too. More than once, improper boxing caused caking near container walls. Packing modifications on our end now keep the powder free-flowing, preventing lumps or compressed cakes at the bottom. Our warehouse processes occasionally had to pivot—investing in better environmental control rather than just clockwork timetables or routine methods.
Some synthetic chemists raised concerns about the interaction of this acid with water-sensitive intermediates. Open communication led us to invest in tailored desiccant protocols, and now storage and transit ensure the product arrives without absorbing excess moisture. Practical safeguards built around real feedback pulled quality metrics higher than laboratory benchmarks would have suggested.
We have also worked with flavor and fragrance houses who value sharp NMR peaks and the absence of sulfurous tints or odd notes. They flagged issues in pilot-scale runs that textbook procedures never foresaw. Day-to-day cooperation with these teams built our appreciation for how subtle impurities can derail both analytical readings and sensory panels.
Academic teams and industrial R&D groups often pursue exploratory syntheses, feeding new analogs into bioassays and advanced screens. Several of our long-term partners detailed cases where even slight drift in melting point or color hampered performance, either by creating solubility issues or triggering unwanted reactivity. In the past, relying only on “standard” parameters wasn’t enough. By adapting both our chromatography protocols and work-up steps, we push for consistency from lot to lot—resolving microimpurities or oddball contaminants that escape crude analytical checklists.
Pharma researchers have drilled down on batch-to-batch reproducibility for explorations in enzyme inhibition and receptor modeling. Some have flagged failures in scale-up due to invisible background contaminants—something we uncovered by running our own reference syntheses in parallel with customer recipes. We then adjusted our in-process controls and expanded our chromatographic checks, closing the loop on sources of deviation.
Polymer chemists and materials scientists reach for this carboxylic acid because the thiazole ring introduces both rigidity and a handle for functionalization. In one instance, the necessity for accurate particle sizing emerged when users described filter clogging on custom reactors. This triggered an internal project that reviewed and stabilized our grind and sieving steps, helping us meet precise demand for free-flowing powder across different markets.
Our manufacturing team looks beyond internal metrics to track wider environmental impact. The production of 2,4-Dimethylthiazole-5-Carboxylic Acid can raise questions about solvent disposal and energy load during purification. Several years in, we replaced higher-toxicity solvents with greener choices, aligning our practice with both regulatory and practical demands from partners who prize sustainable chemistry. The transition forced a reexamination of reaction pathways and post-treatment, rewarding us with leaner, less hazardous waste streams and more satisfied users.
Energy savings often come in increments. Small changes to temperature ramping and agitation, for instance, improved both output and staff safety. Sharing these learnings with customers what’s possible in process improvement—even if it means only minor cost savings per kilo, the benefits add up.
Every team member sees the value in closing feedback loops, whether rooted in environmental response, process safety, or real-world application. What started as a routine chemical has grown into a benchmark for how upstream diligence brings downstream results.
In the competitive space of specialty building blocks, buyers can’t afford unreliable sourcing or unproven supply chains. We learned early from customer setbacks—delays when purity dips, retooling labs due to unexpected color changes, or scrambling to salvage a project on the brink due to off spec shipments. Real partnerships grew out of resolving these pain points, not just affirming delivery numbers but reworking internal procedures so that each order, large or small, travels with a trusted track record.
Chemists return not for branding or packaging, but because our bulk lots and kilogram-scale shipments deliver consistent performance, supported by the kind of direct engagement and iterative improvement that only the producer achieves. Internal traceability charts the history of every kilogram back to its starting material, and technical support lines connect end users directly with those who run day-to-day production. Not every hiccup can be prevented, but real-world transparency solves the inevitable ones faster.
Unlike some secondary traders or online resellers, the direct producer knows the idiosyncrasies of a product at every stage, from raw procurement through final washing and shipment. Our plant managers step onto the processing floor to see for themselves if a blend’s humidity rises or if packaging absorbs static. Operators swap stories and troubleshooting tips not out of obligation, but because each lesson translates to fewer field problems and helps uphold the reputation of the product and everyone involved.
The journey from laboratory curiosity to industrial staple reveals the forces shaping not just the chemical itself but the whole approach to manufacturing. From our vantage point, there’s no shortcut for hands-on attention and a culture that welcomes feedback instead of avoiding it. The future will bring new challenges—novel bioapplications, stricter purity standards, or even automated handling systems that expose gaps in handling or stability. These coming turns don’t unsettle us; they drive our operating principles.
In the end, 2,4-Dimethylthiazole-5-Carboxylic Acid is more than a compound in our catalog. It stands as a testament to what care, persistence, and mutual respect between producer and real-world chemists achieve. By keeping every stage accountable, by learning alongside our partners, and by acting on each lesson from the shop floor to the bench, we continue building the kind of credibility and product quality that outlasts trends and bypasses the pitfalls of generic supply.