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Methyl 4-Methyl-5-Thiazolecarboxylate

    • Product Name Methyl 4-Methyl-5-Thiazolecarboxylate
    • Alias Methyl 4-methylthiazole-5-carboxylate
    • Einecs 401-060-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    190529

    Chemical Name Methyl 4-Methyl-5-Thiazolecarboxylate
    Cas Number 5781-95-3
    Molecular Formula C6H7NO2S
    Molecular Weight 157.19 g/mol
    Appearance Light yellow to brown liquid or solid
    Boiling Point 263-265 °C
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as ethanol, DMSO
    Smiles CC1=NC(=CS1)C(=O)OC
    Inchi InChI=1S/C6H7NO2S/c1-4-7-5(3-10-4)6(8)9-2/h3H,1-2H3
    Storage Conditions Store at 2-8°C in a tightly closed container

    As an accredited Methyl 4-Methyl-5-Thiazolecarboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 100 grams, sealed with a screw cap and tamper-evident seal, labeled with chemical name, hazard, and batch details.
    Shipping Methyl 4-Methyl-5-Thiazolecarboxylate is shipped in tightly sealed containers, protected from light and moisture. It should be handled in accordance with chemical safety regulations, including use of appropriate labels and documentation. Typical shipping occurs via ground or air freight as a non-hazardous organic compound, unless otherwise specified by regional regulations.
    Storage Store Methyl 4-Methyl-5-thiazolecarboxylate in a tightly sealed container, in a cool, dry, and well-ventilated area. Keep away from heat, open flames, and sources of ignition. Protect from moisture and direct sunlight. Store separately from incompatible materials such as strong oxidizers and acids. Ensure proper labeling and restrict access to trained personnel only.
    Application of Methyl 4-Methyl-5-Thiazolecarboxylate

    Applications of Methyl 4-Methyl-5-Thiazolecarboxylate in Industrial Manufacturing

    Methyl 4-Methyl-5-Thiazolecarboxylate is a high-purity chemical intermediate, widely utilized by fine chemical, pharmaceutical, flavor, and crop-protection manufacturers. Precise control over its quality supports strict downstream specifications in synthesis, ensuring compatibility with regulatory and end-use requirements.

    1. Pharmaceutical Intermediates Synthesis

    Branded and generic pharmaceutical manufacturers rely on this compound as a key building block in thiazole-based drug synthesis, notably in anti-infective and metabolic disorder agents. Controlled specification and traceability enable cGMP batch records and downstream impurity profiling. Research and process development teams focus on achieving robust impurity control strategies during amide coupling, catalytic hydrogenation, or heterocycle transformations where this ester acts as an essential starting material.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Current Good Manufacturing Practice (cGMP) as per US FDA 21 CFR Part 210/211
    • European Pharmacopoeia monograph reference for intermediates
    • ISO 9001 certified quality management system

    Typical usage ratio

    • Ranges from 0.2 molar to 1.2 molar equivalents per downstream synthesis step, dependent on specific route and desired thiazole structure
    • Process optimization adjusts dosing to reduce excess and minimize byproducts

    Downstream process integration

    • Introduced during core coupling reactions with amines or hydrazines in synthesis blocks
    • Undergoes transformation in step-growth amidation/hydrolysis sequences in API route maps
    • Monitored by HPLC and NMR for completion and impurity analysis post-reaction

    Final product types

    • Key intermediates for cephalosporin antibiotics
    • Precursors to thiazole-based anti-diabetic and CNS drugs
    • Specialty APIs containing 5-thiazole substructures
    • Custom pharmaceutical research library compounds

    2. Agrochemical Active Ingredient Synthesis

    Leading agrochemical formulators and technical-grade manufacturers utilize this thiazolecarboxylate ester in the synthesis of selective herbicides, seed treatment agents, and insecticide intermediates. Acceptable trace heavy metal and residual solvent content must meet FAO and EU technical material standards. Processing scale and formulation route influence batch charging, ensuring final intermediates align with downstream sulfonylurea, phenylpyrrole, or neonicotinoid structures.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (FAO/WHO)
    • REACH Registration (EC 1907/2006) for hazardous intermediates
    • ISO 17025 testing for residuals and trace contaminants
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products)

    Typical usage ratio

    • Usually 0.3–1.5 eq relative to the core amine or acid functional group in multi-step synthesis of actives
    • Ratios chosen based on yield optimization and waste minimization in pilot and full-scale plant runs

    Downstream process integration

    • Charged at the cyclization or conjugation step with sulfonyl or carbamate moieties
    • Intermediate is isolated by fractional distillation or crystallization for next-stage conversion
    • Analytical validation by GC-MS and LC-MS ensures carryover minimization

    Final product types

    • Precursors for thiazole-based herbicide actives
    • Key building blocks in neonicotinoid insecticide manufacturing
    • Seed treatment agents with modified thiazole rings
    • Intermediates for yield enhancement adjuvants

    3. Food Flavor and Aroma Ingredient Production

    Professional flavor houses and aroma chemical producers employ this compound in the creation of meaty, roasted, or umami notes. Its specific thiazole structure is valued for natural-identical flavor ingredient production under food-grade conditions. Allergen cross-contamination control, batch documentation, and compliance with global food additive lists guide process qualification, with tight control over low-level dosing essential for finished flavor profiles.

    Industry compliance standards

    • Food Chemicals Codex (FCC) requirements for thiazole derivatives
    • US FDA 21 CFR 172.515 (Synthetic flavoring substances and adjuvants)
    • EU Regulation (EC) No 1334/2008 (Flavourings and certain food ingredients)
    • ISO 22000 Food Safety Management System certification

    Typical usage ratio

    • Added at 5–500 ppm in flavor additive premix formulations
    • Adjustments based on desired flavor strength and finished product dilution factor

    Downstream process integration

    • Introduced during Maillard reaction mimetic flavor concentrate synthesis
    • Directly esterified or blended into master-batch food grade solutions
    • QC testing tracks trace residues and organoleptic profile

    Final product types

    • Flavor concentrates for snack and meat analog industries
    • Ready-to-use seasoning compounds for food service
    • Complex flavor systems for pet food applications
    • Custom natural-identical aroma ingredients for beverages

    4. Specialty Chemicals and Fine Chemical Intermediates

    Fine chemical producers and contract synthesis organizations utilize this methyl thiazolecarboxylate in the design of advanced electronic, photochemical, or catalysis agents. Customer-driven specification for purity and trace elemental content supports downstream needs in OLED or polymer additive manufacture. The compound serves as a specific heterocyclic source in process routes requiring precise substitution patterns for patented specialty applications.

    Industry compliance standards

    • ISO 9001 certified production and traceability systems
    • RoHS Directive 2011/65/EU for electronic additive raw materials
    • REACH (EC 1907/2006) for specialty intermediates
    • Custom specification agreements per final downstream client

    Typical usage ratio

    • Ranges from 0.1–2.0 eq depending on target specialty molecule and required molar incorporation
    • Shifts in usage ratio depend on yield, cost, and desired heterocycle distribution

    Downstream process integration

    • Feeds in during controlled coupling with aryl halides or polyol cores
    • Used in post-polymerization modification reactions for advanced materials
    • Requires monitoring for trace by-products using GC and ICP-MS

    Final product types

    • OLED intermediates with modified thiazole rings
    • Fine chemical ligands for catalytic systems
    • Speciality photoinitiator building blocks
    • Monomer additives in electronic-grade polymers

    5. Veterinary Active Ingredient Synthesis

    Animal health pharmaceutical producers leverage this ester intermediate in routes to thiazole-based veterinary APIs, particularly antiparasitics and antimicrobials. Veterinary batch records and identity/strength confirmation using pharmacopoeial-referenced assays are critical. Stringent process and residue controls ensure compliance with animal drug standards and traceability for feed additive approval processes.

    Industry compliance standards

    • VICH GL10 Good Manufacturing Practice for Veterinary Pharmaceutical Products
    • US FDA CVM Guidance for Industry #61 API Procedures
    • European Pharmacopoeia (Ph. Eur.) directives for veterinary raw materials
    • ISO 9001 documented process control

    Typical usage ratio

    • Generally 0.2–1.0 eq in stepwise synthesis, set per target API yield requirement
    • Adjustment based on minimization of unreacted starting material and animal safety data

    Downstream process integration

    • Added in early or mid-stage condensation reactions, forming thiazole-containing veterinary actives
    • Followed by purification and crystallization to meet regulatory-defined purity
    • Batch QC includes HPLC identity and titration for content uniformity

    Final product types

    • Active veterinary ingredients in oral or injectable form
    • Premixes for medicated animal feeds
    • Intermediate APIs for further veterinary R&D
    • Finished antiparasitic pharmaceuticals
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    Certification & Compliance
    More Introduction

    Methyl 4-Methyl-5-Thiazolecarboxylate: From the Production Line to Practical Use

    What Sets This Compound Apart

    Every batch of Methyl 4-methyl-5-thiazolecarboxylate that leaves our manufacturing site reflects years of dedicated experience. This compound—built on the thiazole ring—delivers much more than a list of chemical properties. The unique methyl group and ester function, properly positioned, shape both its reactivity and the applications customers rely on daily. Chemical structure always guides function. Here, methylation at the fourth position and the carboxylate ester at the fifth provide the stability and selectivity demanded in modern chemical development.

    As a manufacturer, we don't just see a catalog item. Each kilogram represents careful control: purity reaches 98% or higher, moisture remains tightly managed, and organoleptic testing confirms batch-to-batch consistency. The distinctive aroma alone can serve as a quick authenticity check for those who know their raw materials; even trace impurities stand out. Our internal protocol monitors color, melting point, and solubility every time. Handling hundreds of tons over the years means problems become apparent long before they reach downstream users. Feedback from formulators and process engineers shapes our practices—packaging keeps the material dry and stable, and particle sizing helps avoid surprises in automated feeding systems.

    Why the Origin of Your Chemical Matters

    Not all manufacturers take responsibility for every step. As producers, we pay close attention to every reaction phase. Our chemists track precursor quality, maintain optimal reaction temperature, and use high-performance distillation to separate the final product. Rigorous filtration removes color bodies and polymeric side-products that can build up if shortcuts are taken. Customers often bring us issues with other sources: inconsistent color, unexpected odors, or solvent residues that interfere with catalysts. We avoid these pitfalls through robust process validation. Production means much more than filling an order; it means protecting downstream processes from hidden risks.

    Building Methyl 4-methyl-5-thiazolecarboxylate on a commercial scale presents challenges unseen in the lab. Reactions that work in small glassware behave unpredictably in multi-ton vessels. Exotherms, agitation rates, and raw material purity all affect reproducibility. Our shopfloor workers and chemical engineers resolve issues with a direct understanding of how each condition affects the target molecule. The solution often comes not from textbooks but from the memory of what happened last quarter or last year. Improvement means tracing minor color changes back to minute traces of oxidized sulfur or out-of-spec methanol. Results travel immediately into the next cycle—this is the continuous loop of learning that real chemical production relies upon.

    Applications: Focusing on Real-World Results

    Methyl 4-methyl-5-thiazolecarboxylate finds its place at the beginning of many synthetic routes, especially in pharmaceutical research and specialty chemicals. Medicinal chemists use it to build complex thiazole-based drugs—here, the ester group welcomes further transformation, while the thiazole ring delivers biological relevance. Downstream reactions include amide formation and substitution with tailored side chains for drug discovery. Performance matters: impurities at the percent or even parts per million level can compromise synthesis, lower yield, and trigger regulatory rework.

    Beyond pharma, flavors and fragrance formulators rely on the building blocks we produce. The distinctive notes of this compound often serve as the backbone for roasted, meaty, or bread-like aromas. Reliability makes all the difference: inconsistent starting material impacts finished products across multiple batches. We’ve worked with development teams who struggled with seasonal aroma shifts—often traced back to unstable supply or poorly monitored synthesis steps from less careful sources.

    Electronic and advanced material firms benefit from the thiazole scaffold in their polymeric systems. Here, stability and control over trace metal content become crucial; unknown byproducts or catalyst residues can poison sensitive electronic processes. Our experience in managing trace contaminants allows specialty clients to push their formulations harder, avoiding bake-off failures and downstream defects.

    Real Differences from Other Candidates

    Comparisons with similar materials reveal differences that impact both performance and handling in real plants. Many engineers consider simply replacing Methyl 4-methyl-5-thiazolecarboxylate with an analog, only to discover significant changes in product properties or reactivity. For example, swapping in a thiazolecarboxamide or an unsubstituted ethyl ester can drive yield drops, waste formation, or even regulatory headaches due to impurity formation. Position and type of substituent matter—removal of the methyl triggers changes in solubility and volatility that disrupt downstream mixing and separation steps.

    From a manufacturer's perspective, these are not theoretical issues. We track data on outcomes across hundreds of production lots, working with purchasing teams to evaluate alternatives only after extensive trials. Each change in molecular structure comes with process risks: increased corrosion under distillation, new profiles in thermal decomposition, or altered crystallization behaviors. Over the years, our technical staff has supported countless scale-ups gone wrong when users switched to nonstandard substitutes without considering these knock-on effects.

    On a logistical front, product stability under varied shipping climates often exposes the difference between substances that sound similar on paper. Moisture uptake, light-sensitivity, and packaging compatibility aren't evident in the chemical formula—but they shape real-world costs and success. Our in-house test program exposes all grades to temperature and humidity extremes ahead of shipping, ensuring that received material matches the certificate of analysis.

    Supplier Experience Shapes Reliability

    As a direct manufacturer, we witness firsthand the spectrum of supplier reliability. Many companies focus on price and overlook the impact of minor quality drifts, but our clients tell a different story. Batch failures, unexpected scrap, and requalification costs all trace back to poorly controlled manufacturing elsewhere. This is why we adhere to independent audits, maintain certification to ISO standards, and employ experienced staff at every stage—from raw material assay to final drum checkoff. Our in-plant training covers not only the technical operation of equipment but also the contextual understanding of customer processes downstream.

    We never underestimate the cumulative impact of lived experience. The knowledge gained on yesterday’s shift shapes tomorrow’s process improvement. Over the course of running year after year, even minute optimizations—in solvent recovery, lot scheduling, or waste reduction—feed into the consistency that global customers notice.

    Working With Formulators and Research Teams

    Many of our long-term partners began with simple questions—troubleshooting off-odors, seeking a finer or coarser product, or battling process residue. Process transparency leads to solutions. We track reaction yields at every stage, immediately sharing relevant deviations with customers so that reformulation or process tweaks occur before costly failures appear. Some clients require modified particle size for dosing systems; others demand enhanced purity for clinical research. In both cases, feedback loops keep the line of communication open, and we adapt as their requirements evolve.

    Our R&D chemists have collaborated with pharmaceutical scientists to push the boundaries of where this compound fits within drug discovery. This has driven changes in drying procedures, new methods for impurity detection, and tailored drying agents. Not all improvements originate in-house; often, the best ideas come from a customer’s tough question or unique requirement.

    For smaller laboratories, production consistency supports traceability in their own reporting and helps maintain their accreditations. For large-scale plants, bulk deliveries match scale-up timelines without unexpected shipment delays. Whether the need involves a few kilograms or several metric tons, production scheduling remains flexible—a commitment backed by central control over supply chain and inventory.

    Sustainability and Safety at the Plant Level

    Manufacturing experience brings clarity on sustainable practices. Waste minimization comes not from abstract goals but from detailed mass balances. Shifting to more efficient solvent systems, recovering excess reagents, and reusing process utilities drive both cost and environmental benefits. As emission regulations tighten, our plant invests in scrubber upgrades, continuous monitoring, and low-residual waste generations. Years of firsthand interaction with inspectors keep our safety documentation robust, and our team undergoes regular hazard simulation to minimize operator risk.

    We enforce direct traceability for every lot, linking raw material origin to final product shipping. Deviations trigger real-time corrective actions—not after regulatory audit, but at the source. External partners and end users gain peace of mind knowing that each certificate reflects true batch history, with transparent reporting if deviation occurs.

    On safety, detailed process hazard analysis underpins each shift. The presence of sulfur compounds and methylating reagents demands both experience and vigilance. Secondary containment, rigorous PPE protocols, and real-world emergency drills supplement written SOPs. These are living processes—constantly reviewed as near-misses and performance metrics reveal new areas for improvement.

    What We’ve Learned Over Years of Production

    Some compounds follow predictable paths in both lab and plant. Methyl 4-methyl-5-thiazolecarboxylate does not always fit this mold. Reaction intermediates can drift based on the source of thiazole starting material, or minor fluctuations in reagent grade. The lessons of hundreds of reaction scale-ups have shaped experienced troubleshooting: slow precipitation of byproducts, color drift, and odor changes all leave clues for root cause analysis. Our senior operators refer directly to batch records—not just to tick boxes, but to guide in-the-moment adjustments.

    Failures present the best teachers. One memorable incident involved an unexpected darkening of final product color, traced back to a slight over-temperature incident in a single reactor loop. Documentation, root-cause analysis, and a commitment to incremental process change prevented recurrence. From that event, we built redundancy into our monitoring systems—and now rely on dual sensors and extra oversight each production run.

    Long-term supply contracts provide us insight into global market swings: spikes in demand for thiazole derivatives can arise from pharmaceutical patent cliffs, flavor trend shifts, or supply crunches for raw precursors. Advanced warning systems, careful stockpiling, and robust supplier relationships—all built through the practical, day-to-day management of a chemical operation—give us the resilience to honor delivery even as external shocks ripple through the supply chain.

    Supporting Innovation Without Compromising Core Values

    Many R&D-driven industries push for new materials, and raw material reliability anchors successful innovation. We've contributed feedback to regulatory bodies as manufacturers, addressing proposed changes in impurity thresholds and trace contaminant reporting. Participation in working groups for sustainable production gives our team insight on global best practices while keeping us grounded in the realities of continuous plant operation.

    Our labs run round-the-clock quality control, and our scientists write and revise process documentation based on what works, not just on compliance language. This loop—exposure to real use cases, regulatory evolution, and hands-on operational improvement—continues to distinguish direct producers from brokers or generic suppliers. Customers value this not for its own sake, but for the visible reduction in troubleshooting time, fewer field failures, and better overall results.

    As manufacturers, we have a stake in every downstream project that uses our material. Whether building the next generation of pharmaceuticals or enhancing consumer goods for global markets, we see each order not as a transaction but as an extension of our commitment to careful chemistry. Our role includes sharing deep experience, tracking new application trends, and delivering a level of stewardship only practical manufacturing can offer.

    Conclusion: Direct Manufacturing Benefits Everyone Downstream

    Years spent producing Methyl 4-methyl-5-thiazolecarboxylate shape how we see both the molecule and its users. Quality depends on more than certification—it calls for observation, adaptation, and improvement at every stage. Consistency reflects more than equipment or raw materials; it’s the product of skilled people, well-maintained processes, and transparent communication from order to shipment.

    We invite questions, technical challenges, and new partnerships as the field continues to evolve. Direct connection between manufacturer and user benefits the entire supply chain—ensuring the reliability, performance, and innovation our partners have come to expect.