|
HS Code |
623068 |
| Productname | 2-Phenyl-1,3-Thiazole-4-Carboxylic Acid |
| Casnumber | 18844-45-6 |
| Molecularformula | C10H7NO2S |
| Molecularweight | 205.24 g/mol |
| Appearance | Off-white to pale yellow solid |
| Meltingpoint | Approx. 225-230°C |
| Solubility | Slightly soluble in water; soluble in DMSO and methanol |
| Purity | Typically ≥98% |
| Smiles | C1=CC=C(C=C1)C2=NC(=CS2)C(=O)O |
| Inchi | InChI=1S/C10H7NO2S/c12-10(13)8-6-14-9(11-8)7-4-2-1-3-5-7/h1-6H,(H,12,13) |
| Storagetemperature | Store at room temperature, keep container tightly closed |
As an accredited 2-Phenyl-1,3-Thiazole-4-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 5 grams of 2-Phenyl-1,3-Thiazole-4-Carboxylic Acid, sealed, with hazard labeling and product information. |
| Shipping | 2-Phenyl-1,3-Thiazole-4-Carboxylic Acid is shipped in tightly sealed containers, protected from moisture and light. It is packed according to safety regulations for chemical transport, typically at ambient temperature. Proper labeling and documentation are included to ensure safe and compliant delivery. Suitable for standard or expedited shipping, depending on customer requirements. |
| Storage | Store 2-Phenyl-1,3-thiazole-4-carboxylic acid in a tightly sealed container at room temperature, away from direct sunlight and moisture. Keep in a dry, cool, and well-ventilated area, isolated from strong oxidizing agents and bases. Employ standard laboratory precautions and ensure proper labeling. Avoid exposure to heat and incompatible materials during storage for maximum stability and safety. |
Applications of 2-Phenyl-1,3-Thiazole-4-Carboxylic Acid in Industrial Manufacturing2-Phenyl-1,3-Thiazole-4-Carboxylic Acid plays a vital role as a fine chemical intermediate within several demanding industrial verticals. Our manufacturing experience supports end users in regulated markets who require strict process control, accurate formulation, and reliable supply for high-value downstream synthesis. The following sections detail precise applications across the pharmaceutical, agrochemical, specialty dye, and electronic material sectors. 1. Pharmaceutical Intermediate for Thiazole-Containing APIsMultiple active pharmaceutical ingredients rely on this compound as a key building block. Manufacturers incorporate it during heterocyclic scaffolding, particularly within synthetic routes for antimicrobial, anti-inflammatory, and antineoplastic APIs. Its carboxylic acid group offers site-selective functionalization for achieving specific bioactive profiles. The precise quality and impurity profile are crucial for successful integration into cGMP production schemes. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Synthesis for Fungicidal and Herbicidal ActivesThis material serves as an essential intermediate in the synthesis of thiazole-based fungicides and selective herbicides. Its molecular structure enables downstream modification towards the development of protective agents demonstrating high selectivity and efficacy in crop protection. Agrochemical formulators exploit the thiazole ring to engineer molecules with improved environmental stability and target specificity. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Advanced Dye and Pigment ManufacturingThe compound introduces reactive sites and chromophoric properties in the formulation of specialty dyes and pigments. Industrial colorant producers employ it in the manufacture of thiazole-derived azo and heterocyclic dyes, which deliver enhanced lightfastness and chemical resistance. The substituent pattern permits fine-tuning of hue and solubility profiles, supporting value-added applications in textile and polymer coloration. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Organic Semiconductor and Conductive Polymer PrecursorIn the electronics industry, the thiazole structure forms an integral part of organic semiconductors and conjugated polymers for advanced functional materials. Device developers integrate this acid during the synthesis of heteroaromatic building blocks to achieve specific electron-withdrawing effects and improved charge transport. Gain in performance for organic field-effect transistors and light-emitting diodes often depends on molecular design enabled by thiazole-carboxylic acid intermediates. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2-Phenyl-1,3-Thiazole-4-Carboxylic Acid prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
As a manufacturer rooted in daily chemical plant work, I’ve watched 2-Phenyl-1,3-thiazole-4-carboxylic acid grow from a niche intermediate to a core piece in the modern chemical toolkit. Years on the shop floor make priorities clear: consistency, clarity, and reliability in each drum or flask that leaves the finishing line. Many customers who visit our site want to understand not just what this compound is but why its synthesis matters and how it’s different from near neighbors in the thiazole family. After handling this compound up close for over a decade, I’m happy to unpack what stands out.
We supply 2-Phenyl-1,3-thiazole-4-carboxylic acid with model designation PTC-403. Our process delivers a pale, off-white crystalline material that tends to hold up well against humidity and typical storage temperatures. In practice, the carboxylic acid group makes it easier to control solubility compared to more hydrophobic thiazole derivatives, easing purification and formulation for downstream users. Each batch goes through strict checks—not just for purity, but particle distribution and ease of dissolution in standard laboratory solvents like DMF or DMSO. After packaging tons of this stuff, our focus has shifted to managing trace impurities at consistently low levels, which our longtime clients notice in fewer downstream troubles.
Every year, customers from research outfits and production lines use this compound in a range of breakthrough pathways. Medicinal chemistry outfits prize its scaffold when building kinase inhibitors and antifungal drug candidates; the unique blend of aromatic and heterocyclic chemistry brings options for hydrogen bonding, π-stacking, and derivatization. From an industrial point of view, it’s far more than a library filler. Our pharma clients often call out how the acid group allows straightforward coupling reactions. One group running pilot-scale synthesis described clean conversion under peptide coupling conditions, shaving hours off their regular timelines. Bioactive compound synthesis in the agrochemical world also leans on its rigidity and ease of functional group access, making late-stage diversification less painful.
Not every thiazole product brings this much flexibility to the table. For example, basic phenylthiazole without the carboxylic acid clocks in as less reactive under mild conditions, nudging teams to use harsher chemistry. We’ve watched industrial chemists return to our version for that reason. Downstream, that difference reshapes scale-up: better reactivity leads to higher selectivity, smaller waste streams, and less time at the purification step. This is not lost on teams racing to meet clinical trial deadlines or push crop protection products through regulatory approval.
Several features of 2-Phenyl-1,3-thiazole-4-carboxylic acid have kept it in demand. The balance of electron density in its core ring system and the electron-withdrawing acid group enables reactivity without overreacting during functionalization. In my time troubleshooting production, the compound’s stability during storage and shipping helped keep customer complaints almost non-existent—compared to, say, thiazole-aldehydes, which degrade or discolor before arriving.
In laboratory usage, chemists prefer our product for Suzuki coupling and amidation steps. The acid functionality enables mild-base activation, so researchers can avoid running high-pressure reactors or added catalysts that complicate waste handling. Some get creative: combinatorial libraries for testing enzyme interactions, fluorescein dye modifications, advanced material coatings—all draw on the carboxylate for linker attachment. No matter the industry, the material’s clean spectral characteristics help save time in analytical workups, which can make a difference in quick-turnaround environments.
From a manufacturer’s perspective, perhaps what stands out most is the middle ground this molecule occupies. There are more complex thiazole scaffolds, but those often bring increased handling costs or regulatory headaches. There are simpler ones, but they don’t offer as much tunability or application breadth. Engineers and chemists want flexibility, consistent performance, and sensible costs—this compound delivers on all three. Direct feedback from R&D partners continues to shape our process tuning, ensuring each lot goes out with batch documentation that means something in the real world, not just on paper.
Working with 2-Phenyl-1,3-thiazole-4-carboxylic acid at production scale revealed early on where the bottlenecks lurk. High temperatures during synthesis can skew substitution patterns, so we run a tightly controlled process using temperature ramping and in-line monitoring to avoid overreaction. Good yields also depend on water content management—our reactors run with multi-stage drying cycles and nitrogen blankets throughout. Process waste is a major reality in industrial synthesis. Over the years, we improved solvent recovery in our steps, keeping emissions and disposal costs down. Several years ago, we switched to a new filtration media that handled fine crystal agglomerates better, cutting filter blockages that used to shut lines down for hours.
Another key challenge involves maintaining bleach-resistant product in final fill. We adjusted our hydrogen peroxide work-up protocol after field reports highlighted trace oxidation in overseas shipments, which raised red flags for regulatory acceptance in the EU. Fielding call-backs and examining product returned from customers holds manufacturers to a different accountability standard than distant brokers or traders. We respond by running real shipment stress tests—high humidity, extended storage, agitation—and feeding test outcomes back into our QC protocols.
Chemical buyers watch material prices with intensity, especially when commodity thiazole intermediates come into play. Yet we’ve seen from customer-side studies that the savings from switching to cut-rate or unverified sources get offset by downstream failure points—variable reactivity, failed couplings, inconsistent purity, or extra purification runs. Several pharmaceutical clients mentioned failed reactions or inconsistent data linked to off-brand thiazoles, which set their pipeline back weeks. The lesson here is direct: consistent, well-documented material saves money and hours in the long run, especially when scaling from bench to pilot plant.
As a manufacturer, we’ve kept tight price control by automating several handling and quality sampling steps, reducing labor without cutting corners in oversight. We bulk source starting materials only from vetted, audited producers, minimizing batch-to-batch fluctuations. After years of hearing how untraceable materials muddied synthetic work, we designed an end-to-end tracking system for every lot of 2-Phenyl-1,3-thiazole-4-carboxylic acid that leaves our gate—a barcoded chain running from raw material entry through finished product shipment. Clients regularly ask for this level of traceability as a due diligence requirement, and we build it directly into our process, not as an afterthought.
It’s tempting to believe that one grade fits all, but actual lab and plant performance shows otherwise. Over the years, academic and pharma customers have pointed out the value of extra high-purity grades. Even a 0.1% impurity, undetectable in broad-stroke analytical sweeps, can cook a high-yield reaction or interfere with NMR readings. Responding to these trends, we offer a 99.5% minimum purity guaranteed on most production runs, with option for custom purification on larger lots.
Bulk grades for early-phase screening and non-pharma applications come in a slightly broader specification. We'll always note impurity profiles for each batch, ensuring end users know what’s present before the codes go to their sysadmin. In the rare cases where feedback brought up out-of-specification issues, we investigated root causes and either refined our purification or advised on compatible solvents or pre-treatment steps. Sometimes a basic pre-wash or switch in dissolution solvent resolves otherwise time-eating application roadblocks.
Beside 2-Phenyl-1,3-thiazole-4-carboxylic acid, the thiazole landscape includes several near cousins, each with quirks and strengths. Standard 2-phenylthiazole, lacking the acid group, sees less uptake in greener chemistry pursuits due to lower solubility and functionalization options. Others, like 2-(4-hydroxyphenyl) thiazole, play a bigger role in dye chemistry but introduce more oxidative instability, triggering product complaints during hot months. Organophosphorus-substituted thiazoles offer high reactivity, but at a cost—more challenging handling, higher hazard classification, and greater regulatory oversight, which can derail synthesis in regulated facilities.
End-users looking for easy coupling find few better alternatives than the carboxylic acid version. The acid serves as a reliable anchor point for further chemical modifications. Whether constructing peptidomimetics, linking dye molecules, or building out new material properties, chemists keep coming back to this product for its workhorse character and manageable risk profile. This feedback loop between our customers and plant ensures we refine our offering for practical reality rather than theoretical optimums that never see a real fume hood.
No chemical producer can ignore tightening regulations around waste management and product stewardship. Our site runs a closed-loop cleaning system on thiazole intermediates, capturing and reusing wash solvents and reducing total organic emissions. As REACH regulations tightened in the EU, we shifted intermediates to registered, compliant suppliers and overhauled our MSDS documentation for end-clients. Customers now demand not only proof of compliance but full transparency around life cycle impacts. These concerns shape everything from process design to waste hauling to secondary packaging choices.
Several years back, we faced a challenge in meeting new South Korean chemical inventory requirements for phenylthiazole derivatives. Our regulatory affairs team caught it early and worked with consultant partners to file correct documents and answer government queries before shipments faced dock delays. This ongoing diligence means when regulatory questions land in our inbox, we can produce chain-of-custody documents, certifications, and testing data promptly. This isn’t just a box-ticking exercise; it’s what keeps product moving and investigations off the critical path for our clients.
Every so often, our technical team works directly with client R&D to address new synthetic goals or stuck projects. One memorable case came from an academic lab facing tough solubility limits with standard thiazole derivatives. By tuning our recrystallization protocol, we offered a batch with improved dissolution in polar aprotic solvents, which allowed their team to run high-throughput screening at twice their former rate. This type of on-the-ground collaboration turns an off-the-shelf intermediate into a tailored piece of a research pipeline.
Pharmaceutical formulators sometimes approach us with the request to reduce trace metal contamination to single-digit ppm. While such tight control adds cost and process steps, our partnership mindset means we set up targeted purification runs and additional ICP-MS monitoring. Over time, these efforts return in client loyalty and long-term supply agreements, reinforcing that deep technical capability, not just price, keeps manufacturers and end-users working together year after year.
Safe, stable transport is another area worth close attention. Shelf life for our 2-Phenyl-1,3-thiazole-4-carboxylic acid typically stretches past two years in sealed containers at ambient temperature, provided the stock stays dry. Bulk orders leave our plant in double-lined drums or sealed high-density polyethylene pails, always labeled with lot trace codes and tested for seal integrity. If exposure or seal compromise occurs, the compound is more forgiving than many acylated thiazoles, which can hydrolyze or discolor rapidly.
Several remote clients have integrated RFID scanning on their receiving docks using our label tracking features; this keeps their digital inventory in sync with what arrives on-site. Customer experience has taught us that clear, minimal-excess packaging helps reduce warehouse waste—so we designed shipping units that cut out unnecessary cardboard or fill materials, addressing both environmental considerations and end-user convenience. Should returns or disposal be necessary, our technical team responds with solvent management recommendations based on real process observations, not boilerplate procedures.
Years in this field taught us that manufacturing is less about one-time perfection and more about sustained attention to detail. Improvements rarely rest on price or paperwork alone. It’s feedback from bench chemists, production managers, and QC labs that shows us which tweaks in granularity, drying schedules, or impurity thresholds will pay dividends in actual use.
The labs using our 2-Phenyl-1,3-thiazole-4-carboxylic acid remind us often of what works. Many feed back that they see higher coupling yields, less off-target reactivity, or tidier chromatography profiles when using our recently optimized product. One customer in the peptide synthesis space remarked that lot-to-lot reproducibility cut out redundant validation steps for his QA team. This is where real-world value emerges—removing friction from the daily practice of science.
All claims aside, trust grows from every delivery that matches or exceeds expectations. It resides in every lab notebook entry where reactions run as planned, chromatography columns separate easily, and analysts confirm identity and purity without surprises. Down-to-earth, open communication between manufacturer and customer groups means ongoing improvement is possible, problems get solved rapidly, and new applications become tangible faster. For us, keeping 2-Phenyl-1,3-thiazole-4-carboxylic acid at the core of these workflows remains less about headlines and more about time-tested collaboration—resulting in better science, better business, and more reliable outcomes all round.