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4-Thiazolecarboxylic Acid

    • Product Name 4-Thiazolecarboxylic Acid
    • Alias 4-Thiazolecarboxylic acid
    • Einecs 221-977-0
    • 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

    288333

    Chemical Name 4-Thiazolecarboxylic acid
    Molecular Formula C4H3NO2S
    Molecular Weight 129.14 g/mol
    Cas Number 3973-08-8
    Appearance Off-white solid
    Melting Point 172-176 °C
    Solubility In Water Moderately soluble
    Smiles C1=CSC(=N1)C(=O)O
    Inchi InChI=1S/C4H3NO2S/c6-4(7)3-1-2-8-5-3/h1-2H,(H,6,7)
    Pka 2.87 (carboxylic acid group)
    Storage Temperature Room temperature
    Synonyms Thiazole-4-carboxylic acid

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

    Packing & Storage
    Packing 4-Thiazolecarboxylic Acid, 25g, is supplied in a sealed amber glass bottle with a screw cap and tamper-evident seal.
    Shipping 4-Thiazolecarboxylic Acid is shipped in tightly sealed containers to prevent moisture uptake and contamination. Packages are clearly labeled with hazard information and handled according to chemical safety regulations. During transit, temperature and handling controls are maintained to ensure product integrity. Appropriate documentation accompanies each shipment for regulatory compliance.
    Storage 4-Thiazolecarboxylic Acid should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, and well-ventilated area away from incompatible substances, such as strong bases and oxidizing agents. Ensure proper labeling of the container and avoid exposure to heat. Follow all standard laboratory safety and chemical hygiene protocols when handling and storing.
    Application of 4-Thiazolecarboxylic Acid

    Applications of 4-Thiazolecarboxylic Acid in Industrial Manufacturing

    Our 4-Thiazolecarboxylic Acid, manufactured under strict quality protocols, delivers consistent performance across specialty downstream sectors. Below, we detail core industrial application areas where direct value is realized by process manufacturers and formulators through verified use cases of this specialty intermediate.

    1. Pharmaceutical Intermediate for Thiazole-Based APIs

    Pharmaceutical synthesis utilizes our material as a key intermediate for constructing thiazole-containing active compounds, widely used in infection control and metabolic therapies. Its reactivity and purity profile ensure precise cyclization and acylation stages in multi-step synthesis for patented drugs and regulated generics, where traceability and quality assurance directly impact batch outcomes.

    Industry compliance standards

    • Complies with ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Used per standards in USP, EP, and JP for related substances and impurity controls
    • Subject to FDA 21 CFR Part 210/211 for finished pharmaceuticals
    • Traceability supported for regulatory submission batches

    Typical usage ratio

    • Typically 0.5–2.5 molar equivalents depending on the target molecule structure and yield requirements
    • Adjusted based on stoichiometry of coupling and ring-formation stages

    Downstream process integration

    • Introduced early as building block in the initial heterocycle assembly
    • Undergoes specific amide, ester, or halogenation reactions according to API core synthesis
    • Subject to in-process control for intermediate purity (HPLC, NMR monitored)

    Final product types

    • Cephalosporin antibiotics
    • Thiazole-derived antidiabetic drugs
    • New chemical entities (NCEs) with thiazole motifs
    • Generic pharmaceuticals requiring thiazole intermediates

    2. Agrochemical Active Ingredient Precursor

    Plant protection manufacturers leverage this thiazolecarboxylic acid for producing crop-protection actives, especially in the synthesis of fungicides and seed treatment agents. It participates in acylation and ring-functionalization steps, delivering selectivity and reliability for scalable agricultural chemical production where field performance and residue standards are critical.

    Industry compliance standards

    • Manufactured following ISO 9001:2015 and ISO 14001:2015 for environmental and quality management
    • Integrated in manufacturing per FAO/WHO specifications for pesticide technical material
    • Downstream use consistent with EPA and REACH agrochemical ingredient registration
    • Adheres to global MRL (maximum residue limit) requirements in finished use

    Typical usage ratio

    • Applied at 1–6% weight basis in active ingredient synthesis routes
    • Varies with yield optimization and target fungicide molecular type

    Downstream process integration

    • Added during early-stage condensation and cyclization at the active ingredient plant
    • Subject to reaction monitoring for functional group transformation efficiency
    • Post-reacted intermediates further processed to technical material and formulated products

    Final product types

    • Systemic fungicides for cereals and fruits
    • Synthetic crop protection mixtures containing thiazole moieties
    • Seed coating agents containing derived actives

    3. Dye and Pigment Intermediate for Specialty Colorants

    Industrial colorant producers utilize our thiazolecarboxylic acid for manufacturing sulfur-containing dyes and functional pigments. The material’s scaffold supports synthesis of heterocyclic color bases used in plastics, textiles, and functional inks, providing distinct colorfastness and UV-resistance properties demanded by contemporary processing lines.

    Industry compliance standards

    • Compliant with EN 71-3 and Oeko-Tex Standard 100 for consumer-safe dyes
    • Upholds REACH Annex XVII restrictions on hazardous substances in pigments
    • Formulation per ISO 9001:2015 quality management in colorant compounding

    Typical usage ratio

    • Utilized at 0.8–4.0% by weight, subject to targeted chromophore intensity and substrate compatibility

    Downstream process integration

    • Incorporated early during heterocycle core assembly in dye synthesis lines
    • Reacted via sulfonation, halogenation, or azo-coupling with other dye intermediates
    • Post-reaction blending to produce finished pigment concentrates

    Final product types

    • Sulfur dyes for cellulosic fibers
    • Colorfast pigments for engineering plastics
    • Specialty inks for industrial and security printing

    4. Fine Chemical Intermediate for Electronic Chemical Synthesis

    Producers in the semiconductor and electronic chemical sectors integrate this compound into functional molecule development, including assembly of corrosion inhibitors and electron-transporting materials in device fabrication. High-purity, analytically confirmed shipments support sensitive process thresholds required in advanced electronics manufacturing, where elemental impurities and trace organics must consistently meet narrow process windows.

    Industry compliance standards

    • Production monitored per SEMI E49 and IEC 62474 for chemical purity in electronics
    • Meets ISO 9001:2015 and QC tested under ICP and ion chromatography methodologies
    • Supported by material traceability documentation for audit trail compliance

    Typical usage ratio

    • Formulated at 0.3–2.0% in precursor batches for functional film or specialty microelectronic chemical synthesis
    • Variations depend on required thickness, conductive/insulating properties, and final device application

    Downstream process integration

    • Added to synthesis reactors during functional group introduction on segment molecule
    • Processed by solution-phase or vapor-phase growth depending on downstream substrate
    • Batch-level controlled for trace impurities

    Final product types

    • Corrosion inhibitor additives for microelectronic interconnects
    • Charge transport layers in organic electronic displays
    • Functionalized intermediates for specialty electronic polymers

    5. Synthesis of Veterinary Pharmaceutical Compounds

    Veterinary active pharmaceutical ingredient manufacturers use this specialty heterocycle in the synthesis of anthelmintic and antimicrobial actives for animal health formulations. Controlled supply ensures regulatory audit ability and process documentation for GMP veterinary finished dose manufacturing.

    Industry compliance standards

    • Supplied under VICH GL3 GMP for active ingredient manufacturing
    • Registers to main veterinary pharmacopoeias, including Ph. Eur. and USP Vet
    • Production validated under ISO 9001:2015 and traceability to batch records

    Typical usage ratio

    • Applied at 0.9–3.5% in main-stage intermediate assembly, based on animal species and active substance concentration requirements
    • Adjusted to optimize reaction yields for veterinary active structures

    Downstream process integration

    • Reacted in early-stage synthesis for construction of veterinary active ingredient molecules
    • Processed and purified prior to formulation step for oral or injectable medications
    • Release testing conducted according to veterinary pharmacopoeia monographs

    Final product types

    • Anthelmintic veterinary tablets and boluses
    • Antibacterial veterinary oral suspensions
    • Veterinary injectable solutions
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    Certification & Compliance
    More Introduction

    4-Thiazolecarboxylic Acid: The Practical Benefits of a Reliable Building Block

    Experience Behind Every Batch

    Decades on the floor and in the lab have shaped how we approach every product, and 4-Thiazolecarboxylic Acid serves as a good reminder of why attention to detail doesn’t go out of style. Each time we run production, we focus on purity, color, and consistency, since downstream reactions won’t forgive careless work. Our team relies on continuous monitoring, traceable raw materials, and equipment that we maintain according to the schedules we’ve refined over the years. The product usually comes in free-flowing crystalline powder, with a pale yellow shade that tells the experienced eye something about cleanliness. Any deviation in the process—too much moisture, hasty heating, or sloppiness in pH control—tricks the eye at once, creating lumps or discoloration. Taking time to address these small things keeps both reprocessing and customer issues at bay.

    Understanding 4-Thiazolecarboxylic Acid

    4-Thiazolecarboxylic acid, known in-house by its CAS number, brings together a thiazole ring with a carboxylic acid function. Several years back, this molecule started gaining traction as a starting point for a range of reactions, especially in pharmaceutical synthesis. Chemists find it appealing because of its chemical backbone—it resists unwanted side reactions and holds up well when you’re working under more aggressive conditions. For anyone scaling a route for an API intermediate, these are real advantages. You don’t have to keep contending with hidden impurities or unexpected process headaches.

    The carboxylic acid group lets researchers couple this molecule with amines and alcohols, opening up a stream of downstream chemistry. Oxidative steps, protective group strategies, and ring manipulations all begin here. We keep our product set up so that batch-to-batch variability stays low; this comes from practical tweaks like sieving, careful rinsing before drying, and documenting every in-process measurement. Over the years, inquiries from clients pushed us to raise our bar for trace heavy metals, moisture content, and residual solvents—all critical for anyone planning GMP work downstream.

    Bridging Research and Production

    Our main experience with 4-thiazolecarboxylic acid involves supporting both bench chemists and full-scale API manufacturers. Lab-scale customers request gram quantities, but large pharma houses work with multiple kilograms at a time. There are differences in usage at these two scales, and the needs vary as well. For instance, research labs often focus on purity and ease of handling, asking for detailed spectral data, while manufacturing partners might grill us on documentation, impurity profiles, or our filtration and drying methods that affect bulk flow and shelf-life.

    Anecdotes stick with us. One customer, struggling with another source’s frequent out-of-spec batches, turned to us for material their med-chem department could rely on. Our team visited their site, exchanged notes with their QC folks, swapped insights about trace pH shifts impacting coupling efficiency, and changed our own crystallization protocol to minimize these subtle drifts. It showed how process tweaks on our end deliver direct benefits to someone else’s workflow.

    Pharmaceutical work rarely leaves room for excuse-making. We’ve seen how contamination—even barely detectable—can derail multi-step syntheses. Unreacted raw materials, trace metals, or color bodies block crystallization or require costly column purification steps downstream. The thiazole ring, if not handled right, sometimes co-crystallizes tiny amounts of starting material. Careful monitoring of the synthesis up front—via HPLC, TLC, and NMR—shaves hours off downstream troubleshooting.

    Model, Specifications, and Practical Choices

    Our facility manufactures several grades of 4-thiazolecarboxylic acid, shaped directly by the demands of our customers. The pharma-intermediate grade meets a minimum purity of 99% by HPLC, while a technical variant, more suitable for industrial processes or academic R&D, runs slightly lower in specification. Both come with validated analytical data—usually covering melting point, NMR, IR, and trace element profiles.

    Moisture content has been a recurring focus. With carboxylic acids, water binding is a constant risk, especially during extended storage or shipment in humid climates. We package using moisture-barrier liners, continuously monitoring shelf samples for changes. If a customer requests tighter limits tailored to their process—especially those operating in high-precision peptide coupling or azide chemistry—we can accommodate through additional drying and real-time Karl Fischer titration. Some companies let materials sit idly in storage; we rotate stock and use date stamps and full-trace audit trails, so sourcing departments never worry about surprises down the line.

    Our packaging options grew from real-world experience. Smaller glass bottles for research, steel drums and HDPE liners for bulk buyers. Too many times we’ve seen inferior packaging leave residue, leach plasticizers, or admit moisture, harming process yields. We source liners and containers only after confirming their compatibility with both the product’s chemistry and the reality of international shipping warehouses.

    Application and Real-World Usage

    The core utility of 4-thiazolecarboxylic acid shows in the range of coupling reactions, transformations, and derivatizations it supports. Medicinal chemists see it as a core intermediate for thiazole-linked pharmaceuticals, especially cephalosporin-type antibiotics, antifungal agents, and novel kinase inhibitors. In our experience, even clients outside pharmaceuticals—such as specialty polymer and agricultural developers—have explored its reactivity for new compound classes. Here, inconsistent product quality puts scale-up at risk.

    We’ve worked closely with several researchers who operate under pressure to meet tight synthetic deadlines. During one collaboration with a biotech startup, their team called late one afternoon about batch failure. Quick troubleshooting over video chat revealed that slight off-white coloration in their prior raw material blocked the key coupling with an expensive amine. We sent rapid replacement, and this saved them both time and substantial cost on their entire synthetic pathway. This sort of practical, responsive interaction often means more than the documentation; it comes from being an actual manufacturer and having the ability to trace problems to their source, fix them, and share troubleshooting insights openly.

    Quality Assurance from Start to Finish

    We control every step—starting with secure sourcing of precursor chemicals, maintaining real-time logs during production, to final batch-release protocols. Batch records include precise reactant weights, pH logs at critical stages, temperature profiles, filtration notes, and full analytical reports. Some customers want more: longitudinal impurity mapping, or specific trace element data for metals like iron, copper or sodium, due to their impact on catalytic processes downstream. Responding to these needs comes naturally to us. If quality falls short, we halt release, revise, document, and share exact findings with the customer. Manufacturing, not trading, backs up this kind of transparency and accountability.

    Environmental controls matter, and we learned the hard way after an HVAC mishap let humidity spike, which increased the lot’s water content outside acceptable limits. Tracking every deviation with clear corrective actions ensures reliability across future runs. Our people walk the plant floor, check packaging for integrity, monitor airlocks for dust intrusion, and test new batches on-site well before shipping. Repeat business, we find, comes not from grand claims, but from tight, flaw-free batches that perform as promised.

    Setting 4-Thiazolecarboxylic Acid Apart from Similar Products

    Some clients ask how 4-thiazolecarboxylic acid lines up against related carboxylic acids, such as 2-thiazolecarboxylic acid or simple thiazole derivatives. The 4-position carboxylic group introduces distinct steric and electronic effects—making it more suited for certain coupling or ring-extension reactions. We see this first-hand in customer feedback: chemists needing better selectivity or reactivity routinely report success in switching to the 4- variant after problems with other isomers.

    Raw material purity directly impacts the success of researchers working under regulatory inspection. Many facilities hope that “close enough” meets spec, but that rarely holds up during a challenging synthetic transformation. We run validation checks specifically for isomeric contamination, process by-products, and carry out forced degradation studies, so everyone—from development labs to commercial manufacturers—works with the same reliability. Years ago, a batch of structurally similar 2-thiazolecarboxylic acid stalled downstream amid persistent trace impurities and sluggish reactivity; switching to the 4-isomer from our line solved these bottlenecks, with direct improvement in yield and throughput.

    We never cut corners by substituting raw materials, altering drying params to pad out yields, or mixing regrind. Following reliable, transparent protocols sets apart our processes compared to some third-party channels, who sometimes scramble to resell materials sourced without origin or process control. We value the relationship that grows when customers know they’re talking to the team actually making the product, who pick up the phone for questions, adjustments, and prompt fixes.

    Product Improvements and Unseen Challenges

    Routine doesn’t mean static. Over years, our QC chemists have dialed in new analytical methods for this molecule, including advanced HPLC and GC-MS impurity profiling, and NMR shutdowns to confirm structure—especially after customer requests for even lower impurity levels ahead of clinical candidate submissions. Documentation grows, and with it our own awareness of how even trace changes in input solvent lots or grade can leave a fingerprint on the final product. Oftentimes, this kind of process insight stays out of third-party “certificate of analysis” documents seen elsewhere, but our operations team keeps these datasets ready for audit or just to solve mysteries for R&D staff who notice subtle shifts in their own yields.

    We confront sourcing challenges, too. Sometimes a precursor’s availability or regulatory status creates headaches. Long-term relationships with suppliers matter as much as reaction conditions. Our purchasing team meets regularly with our R&D and production managers, sharing feedback about how batch-to-batch variability up the supply chain can echo through to our customers’ syntheses. We have learned that immediate, honest disclosure about potential sourcing pinch-points lets partners plan alternatives and avoid surprise disruptions to critical production.

    Environmental Responsibility and Waste Reduction

    Thiazole chemistry, like most sulfur-containing processes, brings its own environmental burdens. Our waste capture, filtration systems, and off-gas treatment minimize the environmental load, meeting strict local and international guidelines. Each year brings additional pressure—by regulators or end customers—to improve. We have responded by investing in solvent recovery systems and reducing hazardous discharge. Our plant safety and environmental team invests hours reviewing near-misses and exploring process intensification strategies that use less solvent, energy, or consumables without sacrificing quality. Our records, available for inspection, show a steady improvement trend—less downtime, fewer rejected lots, more efficient production turns.

    We include our customers in these conversations. Several times, specialty buyers have asked for guidance on waste treatment for spent acid or thiazole intermediates. Our technical service staff offers methods developed in-house for safe neutralization and disposal, rather than pushing the problem downstream. Improving our own sustainability practices lets us offer real advice instead of vague assurances, which builds trust across the supply chain.

    Facing Market Shifts and Future Needs

    In our experience, staying close to the market is the only way to manage unpredictable changes. Regulatory shifts, swings in demand, or shifts in preference for green chemistry alternatives—these become our daily concerns. To keep up, we track regulatory developments and voluntarily adapt our documentation, traceability, and analytical offerings. Customers need more than a static product; they need answers to technical questions, compliant documentation, and a partner prepared to share both good news and challenges.

    It has become clear that ease of access to reliable 4-thiazolecarboxylic acid—whether for developing a new antihypertensive drug, a specialty coating, or a peptide linker—directly supports global innovation. This only works if the manufacturer cares enough to maintain fresh supply, robust technical support, and full transparency across every step. From our perspective, walking the line between cost control and ongoing improvement isn’t a one-off project, but a daily commitment driven by feedback and real-world challenges.

    Conclusion: Value through Practical Expertise

    Whether developed into a high-value pharmaceutical intermediate or a critical step in agrochemical synthesis, 4-thiazolecarboxylic acid stands apart based on reliability, transparency, and practical understanding of both the molecule and its users’ actual needs. Our long-term success keeps coming from a simple idea—stay hands-on in both production and customer support, keep improving based on feedback, and value every chance to see things through the eyes of the people using the product every day. By staying close to both chemistry and customers, we keep raising our standards and delivering solutions that hold up in practice.