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4-Methyl-2-[4-(Trifluoromethyl)Phenyl]Thiazole-5-Carboxylic Acid

    • Product Name 4-Methyl-2-[4-(Trifluoromethyl)Phenyl]Thiazole-5-Carboxylic Acid
    • Alias GSK-3 Inhibitor XIII
    • Einecs NA
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    978200

    Chemical Name 4-Methyl-2-[4-(Trifluoromethyl)Phenyl]Thiazole-5-Carboxylic Acid
    Cas Number 1268524-69-9
    Molecular Formula C12H8F3NO2S
    Molecular Weight 287.26
    Appearance White to off-white powder
    Melting Point 144-148°C
    Solubility Slightly soluble in DMSO, methanol
    Purity Typically >98%
    Storage Conditions Store at room temperature, keep dry
    Synonyms 4-Methyl-2-(4-(trifluoromethyl)phenyl)thiazole-5-carboxylic acid
    Smiles CC1=NC(=C(S1)C(=O)O)C2=CC=C(C=C2)C(F)(F)F

    As an accredited 4-Methyl-2-[4-(Trifluoromethyl)Phenyl]Thiazole-5-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White HDPE bottle with tamper-evident cap, labeled with chemical name, hazard symbols, and batch number. Net weight: 25 grams.
    Shipping This chemical, 4-Methyl-2-[4-(Trifluoromethyl)Phenyl]Thiazole-5-Carboxylic Acid, is shipped in a sealed, chemically compatible container to ensure stability and prevent contamination. It is packaged with appropriate hazardous material labels and documentation, following federal and international shipping regulations, and typically transported via temperature-controlled priority courier services.
    Storage Store 4-Methyl-2-[4-(Trifluoromethyl)phenyl]thiazole-5-carboxylic acid in a tightly sealed container, protected from light, moisture, and incompatible substances. Keep in a cool, dry, well-ventilated area, ideally at 2–8°C. Avoid heat sources and direct sunlight. Ensure proper chemical labeling, and follow local regulations for hazardous materials storage. Use personal protective equipment when handling this compound.
    Application of 4-Methyl-2-[4-(Trifluoromethyl)Phenyl]Thiazole-5-Carboxylic Acid

    Applications of 4-Methyl-2-[4-(Trifluoromethyl)Phenyl]Thiazole-5-Carboxylic Acid in Industrial Manufacturing

    4-Methyl-2-[4-(Trifluoromethyl)Phenyl]Thiazole-5-Carboxylic Acid serves as a specialized intermediate in high-value pharmaceutical and agrochemical synthesis. As a manufacturer, we supply this raw material to customers whose production relies on stringent quality control and compliance with international standards. Below are focused applications where our product integrates into real-world, large-scale downstream processes.

    1. Active Pharmaceutical Ingredient (API) Synthesis: Thiazole-Based Antidiabetics

    This compound functions as a key building block in the synthesis of thiazole-substituted antidiabetic agents. Pharmaceutical manufacturers incorporate it in the early stage of multi-step synthesis for small-molecule APIs targeting diabetes management. The structural attributes of the thiazole moiety and trifluoromethylphenyl group support precise pharmacophore construction, directly affecting potency and selectivity.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • EU GMP Annex 13
    • United States Pharmacopeia (USP)–relevant monographs for related APIs
    • Chinese Pharmacopoeia (ChP) for regulatory filings

    Typical usage ratio

    • 0.8–3.0 molar equivalents, adjusted according to specific target molecule and synthesis yield optimization

    Downstream process integration

    • Introduced at the heterocyclic coupling stage, usually after a halogenation or Friedel–Crafts acylation step; participates as an electrophilic partner in palladium-catalyzed cross-coupling reactions

    Final product types

    • Thiazole-class small molecule antidiabetic APIs (e.g., glitazone derivatives)
    • Intermediates for advanced pharmaceutical candidates in metabolic disorder research

    2. Crop Protection Actives: Synthesis of Trifluoromethylated Fungicides

    In the agrochemical sector, manufacturers select this carboxylic acid derivative when developing high-efficiency, broad-spectrum fungicides. It integrates into the molecule at the intermediate synthesis stage, allowing precise introduction of both the thiazole ring and trifluoromethyl group, which are crucial for enhancing pathogen resistance and environmental persistence of the end product.

    Industry compliance standards

    • FAO/WHO JMPR Pesticide Specifications (Food and Agriculture Organization / Joint Meeting on Pesticide Residues)
    • ISO 9001:2015-certified quality management systems
    • Reach Regulation (EC) No 1907/2006 for chemical registration in the EU
    • China GB 2763 Maximum Residue Limits for Pesticides

    Typical usage ratio

    • Used at 1.0–2.2 molar equivalents relative to core pyrimidine or benzothiazole, depending on the target active compound's desired spectrum

    Downstream process integration

    • Forms an integral reactant during the cyclization or condensation stage, commonly in chlorination, followed by amide or ester functionalization routes

    Final product types

    • Systemic fungicide actives for rice, cereal, and fruit crop protection
    • Intermediates for strobilurin and azole-class fungicides

    3. Advanced Material Science: OLED and Electronic Intermediate Manufacturing

    Downstream producers in the electronic materials segment apply this compound in synthesizing custom thiazole derivatives for use as intermediates in OLED (organic light-emitting diode) material formulations. The unique electron-rich structure and the trifluoromethyl substituent contribute to color tuning and charge mobility, directly impacting device brightness and operational stability.

    Industry compliance standards

    • IEC 62341 standards for OLED display materials
    • ISO 14001:2015 Environmental Management in electronics manufacturing
    • RoHS (Restriction of Hazardous Substances Directive, 2011/65/EU)
    • UL 94 Flammability Testing Certification for display materials

    Typical usage ratio

    • 0.5–2.0% by weight in functional intermediate synthesis, with the proportion determined by the molecular design requirements of the final emitting layer host or dopant

    Downstream process integration

    • Used in Suzuki or Stille cross-coupling during the color emitter precursor synthesis; enters the process before vacuum deposition or inkjet printing to fabricate organic layers

    Final product types

    • Custom thiazole-derivative intermediates for red/green/blue OLEDs
    • Organic electronic materials for thin-film transistor fabrication

    4. Pharmaceutical Research: Preclinical Compound Library Expansion

    Pharmaceutical research institutes and contract research organizations (CROs) use this compound as a core scaffold for generating combinatorial analog-molecule libraries. Its thiazole-carboxylic acid structure enables rapid diversification via amide coupling or esterification, supporting the acceleration of target identification in drug discovery screening campaigns across oncology, CNS, and anti-infective fields.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • NIH Small Molecule Library Standards
    • ISO 9001:2015 for laboratory research chemicals
    • US FDA Quality System Regulation 21 CFR Part 820 (applicable for investigational new drug research materials)

    Typical usage ratio

    • 1.0–1.5 molar equivalents per reaction, depending on target compound and desired scaffold diversification density

    Downstream process integration

    • Employs direct coupling via carbodiimide-activated amidation or esterification during parallel synthesis workflows, after initial building block selection

    Final product types

    • Diverse amide/ester libraries for high-throughput biological assays
    • Early-stage preclinical candidate molecules for patent space exploration

    5. Veterinary Drug Intermediate Manufacturing

    Veterinary drug producers use this molecule to construct thiazole-modified active compounds for anti-parasitic and anti-bacterial veterinary treatments. Its chemical structure facilitates stepwise construction of complex heterocycles that are especially valued in addressing resistance development among livestock pathogens, contributing to formulations for both oral and injectable animals medicines.

    Industry compliance standards

    • VICH GL9 Good Manufacturing Practice for Active Pharmaceutical Ingredients for Veterinary Use
    • European Pharmacopoeia (Ph.Eur.) for veterinary substance monographs
    • China Veterinary Pharmacopoeia
    • ISO 9001:2015 for veterinary pharmaceutical ingredients

    Typical usage ratio

    • 1.2–2.5 molar equivalents, adjusted in multi-step synthesis based on yield and impurity profile control for the final veterinary API

    Downstream process integration

    • Involved in direct substitution and cyclization steps following initial aromatic amination, typically followed by ring closure or dehydration

    Final product types

    • Veterinary anti-parasitic active pharmaceutical ingredients
    • Bulk actives for combination animal formulations
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    Certification & Compliance
    More Introduction

    4-Methyl-2-[4-(Trifluoromethyl)Phenyl]Thiazole-5-Carboxylic Acid: Manufacturer’s Perspective

    Introducing a Key Building Block in Fine Chemical Synthesis

    As a chemical manufacturer with direct hands-on experience in high-purity heterocyclic compounds, the process of bringing 4-Methyl-2-[4-(Trifluoromethyl)Phenyl]Thiazole-5-Carboxylic Acid from initial design to shipment tells a bigger story than simple catalog listings reveal. Each batch reflects decisions made on synthetic route, purification protocol, and analysis method. Our production teams have spent years refining the processes to yield material that chemists in pharmaceuticals, agrochemicals, and advanced materials demand. Unlike traders or distributors, we witness firsthand the challenges of scale-up, the subtleties of crystallization, and the constant balance between yield and purity.

    Why Molecular Design Matters

    Molecule design impacts every step of synthesis, purification, and application. The particular substitution pattern in 4-Methyl-2-[4-(Trifluoromethyl)Phenyl]Thiazole-5-Carboxylic Acid—combining a thiazole ring, a methyl group, and a trifluoromethylphenyl moiety—requires robust chemistry to install each portion cleanly. This is not a trim-and-snap operation. Precision in temperature control, reagent quality, and reaction sequence all play into the outcome. Over the years, early routes suffered from batch irreproducibility and side products that fouled solid-liquid separations. Now, with both lab-scale and plant-scale runs harmonized, we see consistent NMR profiles, high-resolution mass spectra, and rare out-of-spec events. Our experience shows that control over each synthetic step doesn’t just boost numbers on a certificate. It changes the way customers use the product downstream.

    Model and Specifications: More Than Just a Number

    The industry often references products by catalog numbers or models, but in our facility, the product becomes a physical result of real-world effort. For this compound, purity measures above 98% by HPLC, and we guarantee moisture below 0.5%. Our in-house GC-MS and NMR screening guard against trace organics. Customers often notice how fine batch-to-batch consistency translates to easier method development—whether preparing for clinical trials or industrial intermediates. Some buyers scrutinize the presence of residual impurities left from starting thiazoles or the impact of trace trifluoromethyl contaminants. Rather than just quoting numbers, our chemists invite discussion of quantifiable results and encourage analytical transparency. Years of feedback from repeat users reinforce that tangible, consistent outcomes matter more than flashy marketing language.

    Applications: Direct Insights from the Field

    Many research clients approach us with requests not only for material but for practical guidance. In medicinal chemistry, the trifluoromethyl and carboxylic acid combination offers unique options for tuning compound properties. Molecular engineers have integrated this compound into kinase inhibitor scaffolds, protease modulators, and selective G-protein coupled receptor binders. From conversations with leading users, its electron-withdrawing profile stands out for balancing hydrophobicity with metabolic stability, helping optimize oral bioavailability in emerging drug candidates.
    In crop protection, the same compound serves as a foundation for fine-tuning biological activity and selectivity. Process chemists at major agrochemical companies comment that the mix of methyl and trifluoromethyl substitution gives them a valuable launching point for optimizing resistance profiles while minimizing environmental off-target effects. Our own development scientists regularly explore how batch purity influences the reproducibility of downstream coupling reactions, helping users avoid false negatives in screening campaigns.

    From Lab Bench to Pilot Plant: Quality Control in Action

    Scaling up from a few grams in the research lab to multi-kilogram quantities in production presents real challenges. No amount of catalog copy can prepare one for the difference between glassware bubbling on a hotplate and reactor vessels holding hundreds of liters. Our operators manage material flow, solvent recovery, and filtration on a daily basis. With every order, we keep logs detailing reaction parameters and quality attributes from raw materials through finished packaging. Unexpected events like power dips, atmospheric moisture swings, or minor equipment wear teach us the real discipline of manufacturing. We have learned to communicate openly about any lot anomalies, however rare, because honest partnership with clients builds long-term trust.

    Why This Compound Stands Apart

    In an industry with thousands of substituted thiazoles, the blend of a para-trifluoromethylphenyl group and methyl substitution on the ring distinguishes this molecule. Competitor products with ortho- or meta- substitution show unpredictable reactivity in Suzuki and Buchwald-type coupling reactions. Some suppliers cut corners on process control or push material out with higher solvent residue. We see how an extra chromatographic polish, an extra lyophilization, or a switch in drying technique can mean the difference between a flaky, difficult-to-handle powder and a reproducible, easy-to-weigh solid. These are not small distinctions—researchers need to trust what’s inside the bottle without constantly retesting every new batch.

    Impact on Downstream Chemistry

    The thiazole-5-carboxylic acid motif with a trifluoromethyl aromatic unit unlocks a variety of synthetic transformations. Our most experienced clients cite compatibility with common coupling reagents, reduced side-product load, and easier purification in both batch and automated flow setups. As a manufacturer, we provide technical bulletins summarizing observed reactivity trends rather than theoretical speculation. Over time, user feedback and our own R&D pilots confirm that sharper melting profiles and uniform solubility data make the compound a reliable tool for scale-up runs in both discovery and pre-commercial settings.

    Analytical Rigor: Not Just a Checkbox

    Our QA teams monitor every critical control point: reaction conversions, residual solvents, and trace metals from equipment lines. Each lot ships with a full panel—HPLC, NMR, FTIR, and, for particularly reactive intermediates, elemental analysis and residual moisture checks using Karl Fischer. We run actual comparison tests on key parameters to ensure consistency. Unusual findings, such as a trace signal in mass spec or a deviation in water content, prompt immediate communication with end-users. Our laboratory’s accuracy comes from both state-of-the-art equipment and rigorous training. Many of our analytical chemists have backgrounds in real-world problem solving, not just running standards, and this perspective strengthens our entire workflow. We welcome requests for additional data, not just as a formality but to strengthen the partnership with our clients.

    Stability Matters: Practical Handling on the Lab Floor

    Many users focus first on the headline purity number, but practical stability and ease of handling make or break a batch’s usefulness. Thanks to the electron-withdrawing trifluoromethyl group and rigid aromatic structure, the molecule resists degradation under ambient light and temperature, unlike some thiazole derivatives that darken or degrade during storage. Our packaging crew selects moisture-barrier pouches to discourage any hydrolysis during shipment. Over years of observation, no significant decomposition has shown up in QC retesting, even after months on storage shelves—provided the containers stay tightly capped. Scientists working on tight timelines appreciate material that doesn’t require special atmospheric precautions or last-minute purification.

    Feedback from the Field: Practical Advantages

    Returning clients often report sharper chromatographic performance and easier phase separation when using our batches compared to those from bulk traders. Some academic teams have told us that time saved by not having to rerun purification offsets a slightly higher unit cost. For industrial partners, repeatability in downstream transformations, especially C–C bond formations and amide couplings, drives both solvent reduction and process optimization targets. We keep a log of troubleshooting calls—missed peaks, unexpected byproducts, or difficulties in scale-up. Each becomes a lesson not just for our next batch but for clients, through collaborative problem-solving and iterative process refinement.

    Environmental and Regulatory Considerations

    With increasing global scrutiny on both process and product, strict attention to environmental compliance forms a daily part of our routines. Each kilogram produced involves recovery and reuse of solvents, minimizing organic waste, and tracking effluent purity. We continually update waste handling based on the latest best practices and maintain records of full traceability from raw materials through finished product shipment. We keep a close eye on evolving chemical control lists and work with industry associations to stay ahead of new registration or reporting requirements. Our staff are trained to recognize both the environmental and human health implications of each step in manufacturing, and we encourage responsible use down the product’s life cycle.

    Challenges in Sourcing and Scalability

    The raw materials needed for this compound, especially the halogenated aromatics and specialty thiazoles, often present unpredictable lead times and quality issues. Over the past few years, global disruptions have forced many of our peers to delay deliveries or compromise on input quality. We contract directly with trusted suppliers, often running our own qualification tests before integration. Direct purchasing reduces risk of off-odor or colored contaminants making their way into the final product. Our purchasing and QC teams collaborate to screen incoming lots, ensuring we never build scale at the expense of reliability. Stable sources for high-purity precursors reduce our internal troubleshooting and give users peace of mind.

    Customization and Technical Support

    Bespoke chemistry happens only when all parties communicate. Often, customers require more than a standard bottle—they may need specific particle sizes, alternate salt forms, or certificate details attuned to regulatory filings. We work together to clarify intended use and any critical process parameters. It’s common for a project to start with small quantities and scale up to multi-kilogram requests on tight timelines. Our technical teams bridge R&D and plant operations, offering process insights to fine-tune purification steps or suggest alternative handling methods. Honest dialogue saves time and money on both sides, and years of experience in rapid-turnaround customization allows us to respond without delays.

    Learning from Batch Anomalies

    In a perfect world, every batch runs to completion, and every spec passes. Real manufacturing means real risk: a faulty batch of solvent, a sticky filter pad, or a temperature probe reading off by a few degrees can impact yield and purity. We share these stories, keeping detailed deviation logs—because root-cause analysis makes the difference between a temporary setback and a repeated error. We act fast to quarantine affected lots, engage in transparent discussions with users, and remake product if required. Each hiccup spurs a procedural update. Over time, this “rough edge awareness” builds resilience into the whole operation.

    How Certification and Documentation Support Your Science

    Buyers, especially in regulated industries, rely on thorough documentation. Every shipment carries certificates showing actual test data, not generic forms. We keep archivable records for each lot—chromatograms, spectra, calibration logs—so if a question arises, our teams respond promptly with signed, time-stamped files. This attention has paid off not just for our business, but for clients facing inspections, audit requests, or filing deadlines. Our front-line staff undergo annual compliance training to stay current with evolving documentation standards, so data supplied stays relevant and reliable.

    Supply Chain Sustainability and Future Readiness

    The last few years have forced every chemical manufacturer to plan for resilience, not just efficiency. We maintain buffer stocks of critical raw materials, diversify packaging options, and audit logistics partners to prevent shipping delays. Rapid response to global disruption—whether caused by natural disasters, trade policy shifts, or unforeseen demand surges—separates lasting partnerships from temporary suppliers. We continue to invest in energy-efficient plant upgrades, solvent recycling, and process digitization, keeping a close watch on both regulatory requirements and future market shifts.

    Supporting New Applications and Scientific Progress

    Scientists continue to discover novel uses for 4-Methyl-2-[4-(Trifluoromethyl)Phenyl]Thiazole-5-Carboxylic Acid. Recent medicinal chemistry programs cite its role in fragment-based screening libraries. Research on enzyme inhibitors and modulators finds the thiazole-carboxylic acid moiety helpful in probing binding sites where traditional motifs fail. Some material scientists, working in surface functionalization or specialty dyes, report benefits from its distinctive electronic effects. We share literature reviews with clients, highlight promising data trends, and remain open to collaboration as new possibilities arise. The more we learn from diverse fields, the better our support for those pushing scientific boundaries.

    Differences from Other Heterocyclic Carboxylic Acids

    Buyers often compare this compound to other carboxylic acids—pyridines, imidazoles, benzimidazoles—seeking the right fit for a particular biological target or reactivity profile. Our long-term storage studies and cross-batch reactivity trials show this compound’s unique behavior. Typical analogues without the trifluoromethyl group tend to show higher solubility but lower metabolic robustness. Analogues with a different aromatic substitution pattern often give less predictable downstream reactivity, leading to purification bottlenecks or poor scale-up reproducibility. Firm control at each process stage, along with a knowledge-driven approach, lets us deliver material that opens more options and fewer stumbling blocks for chemists under deadline pressure.

    The Human Side of Fine Chemical Manufacturing

    The process of transforming raw blocks of starting material into high-purity specialty chemicals involves more than equipment and protocols—it reflects daily efforts of skilled workers, iterative learning, and open communication between production, QC, and sales. We value expertise, from veteran operators who sense when a distillation “smells right” to the analytical chemists who recognize trace signals before they become problems. Our clients know that a short phone call or a quick email exchange can resolve most questions without red tape. A commitment to learning and adapting is the real foundation for reliable fine chemical manufacture.

    Transparency, Traceability, and Trust

    Business partners look for honest answers—whether on typical lead times, unusual impurity profiles, or suggestions for alternate routes. We document each production run from raw material intake to batch release, storing data securely and making it available as needed. Mistakes or anomalies happen in any real manufacturing environment; what matters is direct communication, quick correction, and willingness to share knowledge. Our relationships with repeated buyers, from local startups to multinational firms, rest on this trust. If a project needs a tailored solution or urgent support, our doors stay open and our response time reflects our belief in real partnership.

    Final Words: A Commitment to Consistency and Scientific Progress

    The journey from chemical idea to useful product brings daily challenges and regular moments of satisfaction. 4-Methyl-2-[4-(Trifluoromethyl)Phenyl]Thiazole-5-Carboxylic Acid holds promise for researchers and developers across many fields. As a manufacturer, we stay committed to practical, hands-on expertise, detailed analytical support, and a partnership approach that goes beyond ordinary product supply. Years of solving real-world problems together with our clients give us confidence in both the molecule and the people who use it. The feedback we earn helps us refine practice and keep pace with new discoveries, making each batch a new chapter in the shared progress of science.