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HS Code |
586520 |
| Productname | 3-(2-Methyl-1,3-Thiazol-4-Yl)Aniline |
| Casnumber | 4378-03-0 |
| Molecularformula | C10H10N2S |
| Molecularweight | 190.27 |
| Appearance | Light yellow to brown solid |
| Meltingpoint | 88-92°C |
| Purity | Typically ≥ 97% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | Cc1nc(sc1)c2cccc(N)c2 |
| Inchi | InChI=1S/C10H10N2S/c1-7-12-10(13-7)8-4-2-3-6-9(8)11/h2-4,6H,5,11H2,1H3 |
| Storageconditions | Store in a cool, dry place |
| Synonyms | 2-Methyl-4-(m-anilino)thiazole |
As an accredited 3-(2-Methyl-1,3-Thiazol-4-Yl)Aniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 25-gram amber glass bottle, featuring a white screw cap and a hazard-labeled, tamper-evident seal. |
| Shipping | 3-(2-Methyl-1,3-thiazol-4-yl)aniline is shipped in tightly sealed containers, protected from light, moisture, and extreme temperatures. Standard chemical shipping protocols apply, including labeling for laboratory use. The package complies with regulations for non-hazardous chemicals unless otherwise classified. Accompanying documentation includes safety data sheets and handling instructions to ensure secure delivery. |
| Storage | Store 3-(2-Methyl-1,3-thiazol-4-yl)aniline in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Wear appropriate personal protective equipment when handling. Clearly label the container and keep it securely stored to avoid accidental exposure or spillage. |
Applications of 3-(2-Methyl-1,3-Thiazol-4-Yl)Aniline in Industrial ManufacturingAs a direct manufacturer, we supply 3-(2-Methyl-1,3-Thiazol-4-Yl)Aniline to a select group of industries where its chemical structure provides unique functional performance. Our technical support team partners closely with these sectors to ensure each production line maximizes both quality consistency and regulatory alignment in high-end downstream production environments. Below are key industrial applications where this intermediate supports advanced formulation and product innovation. 1. Pharmaceutical Intermediate for Thiazole-based Drug SynthesisLarge-scale API producers employ this compound as a core intermediate during multi-step synthesis of patented and off-patent thiazole derivative drug substances. Its stable aniline group and thiazole ring structure facilitate key substitutions and condensation reactions in controlled reactor environments, ensuring batch-to-batch uniformity and critical impurity profile management required for regulatory submissions. Material entry typically occurs post-halogenation and before final pharmacophore assembly, when purity standards reach their highest scrutiny and chiral integrity must remain uncompromised. Industry compliance standards
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2. Agrochemical Synthesis of Thiazole-Linked HerbicidesIn agrochemical manufacturing settings, formulators use this molecule as an essential intermediate during the construction of new-generation thiazole-linked herbicides and fungicides. Its unique methyl-thiazolyl substituent allows for targeted activation in plant protection compounds, helping drive improved environmental degradation profiles and selective toxicity. The raw material enters synthesis routes after the initial methylation of base aromatic structures and just prior to final active ingredient derivatization on automated multi-ton production lines. Industry compliance standards
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3. Specialty Dye Intermediate for Reactive Textile ColorantsProducers of high-value textile dyes utilize this material in the controlled synthesis of specialty thiazole-aniline-based reactive colorants, particularly for wool and nylon substrates requiring outstanding colorfastness and molecular stability. The aniline component enhances reactivity with sulfonation agents while the thiazole ring directs chromophore orientation, resulting in deeply saturated shades with strong wash resistance. Processing teams charge the raw material during primary amination and sulfonation under rigid temperature management. Industry compliance standards
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4. Electronic Chemical: Precursor for Organic SemiconductorsElectronics industry manufacturers incorporate this chemical as a precursor in the solution-phase synthesis of organic semiconductors and photoresist materials. The compound’s aromatic-thiazole hybrid structure enables the precise engineering of electron-donating and -accepting layers in high-purity organic thin-film transistors (OTFTs) and OLED display backplanes. Producers introduce it during mid-stage oligomer assembly, utilizing inert atmosphere and ultra-dry handling to safeguard component purity for cleanroom downstream patterning. Industry compliance standards
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5. Fine Chemical Synthesis of Aroma and Flavor CompoundsProducers specializing in fine chemicals for fragrance and flavor applications employ the thiazolyl-aniline scaffold to build complex aroma compounds with characteristic roasted, nutty, or savory notes. The methylated thiazole group supports Maillard-type structures and enables precise tuning of volatility and sensory threshold required for customized flavor concentrate manufacturing. This raw material is incorporated after initial ring transformation and during strategic condensation with aldehydes under vacuum distillation protocols. Industry compliance standards
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Meeting the needs of chemists and formulation scientists demands a clear understanding of the molecules we produce. In that spirit, we’re putting the spotlight on one of our core specialty organics: 3-(2-Methyl-1,3-thiazol-4-yl)aniline. With decades behind the reactors, we’ve come to respect what this compound brings to the bench, especially for advanced intermediates and custom syntheses in pharmaceuticals, agrochemicals, and dye chemistry.
Our manufacture of 3-(2-Methyl-1,3-thiazol-4-yl)aniline reflects close attention to consistency. Every batch aligns to the structure: a phenyl ring bound to a thiazole moiety, with a methyl at the 2-position of the thiazole and an amino at the 4-position of the aniline. The product’s purity often exceeds 98% by HPLC, and moisture control is maintained at strict levels to preserve its chemical behavior. We avoid excessive residual solvents, and run routine checks for possible isomeric or oxidative impurities, since even trace levels can interrupt downstream processing or color stability in end use.
In our experience, customers reach for this aniline derivative during not just routine routes, but processes where the thiazole plays a specific electronic or steric role. For example, in pharmaceutical research, the thiazole ring enables medicinal chemists to introduce heterocyclic character into lead molecules, lending both metabolic stability and electronic modulation to the scaffold. We have supported projects seeking new kinase inhibitors, CNS actives, and anti-infective agents, where the fine-tuning of hydrogen bond donors and acceptors—afforded by this molecule—makes a notable difference in binding behavior.
For dye and pigment ventures, this aniline structure allows integrators to design precursors for azo or heterocyclic dyes with improved bathochromic shift or lightfastness. The methyl substitution brings fresh variation compared to unsubstituted thiazole analogs, often shifting solubility, color tone, or ease of formulation for specialty dyes in textiles or plastics. We continue to follow up on feedback from color chemists who ask for assistance optimizing process scale-up, ink formulation, or stability in environmental testing, using our material’s performance as a guide.
Sourcing matters. Over time, we have learned the hard way that inconsistent 2-methylthiazole sources can introduce problematic byproducts, so we developed in-house controls over the intermediate steps. Each synthesis run is validated with pre-production checks on raw materials, reacting vessels, and cleaning procedures. This isn’t just bureaucracy—trace metal ions or cross-contamination can tarnish the end product’s utility in sensitive, high-purity syntheses.
By maintaining tight pH and temperature controls during the coupling reaction, and carefully working up the product prior to crystallization, we retain the intended isomer and minimize degradation. Our downstream team steps in early, confirming melting point, spectral identity, and ensuring residues or side products have been sufficiently stripped. This attention not only protects our reputation, but saves customers rework or downtime. Few things frustrate a chemist more than having to halt a reaction due to unforeseen contaminants or out-of-specification batches.
Feedback from both internal and external project teams shows a clear distinction between our 3-(2-methyl-1,3-thiazol-4-yl)aniline and commodity grade phenyl- or thiazole-based intermediates. The presence of the methyl group at the 2-position influences both steric and electronic interactions—details that emerge only in lab notebooks and process notes, yet make a world of difference in real chemistry. The compound’s nucleophilicity and solubility in common organic solvents are altered enough to change reaction tempos, purification stages, and even the type of analytical methods required.
Comparing to unsubstituted analogs, chemists often comment that our version enables selectivity in coupling reactions or Pd-catalyzed processes. In one collaborative medicinal chemistry program, optimization studies using generic aniline led to uncontrolled regioisomeric products, but the methylated thiazole ring, as supplied by our process, provided the anticipated selectivity and minimized side formation. In pigment chemistry, darker tones and altered fastness emerge thanks to altered electronic delocalization brought by this group.
Supply chain disruptions have prompted us to scale up in-house all critical raw materials. While some manufacturers opt for toll synthesis or third-party blending to save costs, we keep major steps internal. This way, we avoid the batch-to-batch variation that downstream users have flagged as an issue from alternative sellers. Analytical tracking and batch records allow our clients to request specific lot histories, building the trust that research and production managers look for.
We ship the product in crystalline or powder form, usually pale yellow to off-white, avoiding excess clumping through careful drying and inert packaging. Standard packaging sizes range from grams for early R&D through to multi-kilogram batches for pilot and commercial runs, with each lot supported by a full CoA and spectral data.
Logistics teams in our company run compatibility and stability checks prior to shipment, particularly in months of high temperature or humidity. This helps our partners prevent caking, hydrolysis, or polymerization during transport—common issues with this class of amine-thiazole compounds if handled with less vigilance. While minor variations in hue or particle size occur (as every lot has its own fingerprint), we work to ensure core reactivity and solubility stay in the tight ranges requested by synthetic chemists.
End users benefit not just from a molecule, but from direct line access to our technical experts. Many synthetic challenges can be traced back to subtle differences in starting materials. We readily discuss optimal solvent choices, temperature profiles, or work-up protocols based on past troubleshooting efforts. In fast-paced research environments, chemists do not have weeks to source alternative lots or repeat failed runs. Our process team actively compiles feedback from users who synthesize custom heterocycles, or attempt late-stage functionalization—often providing tips that aren’t found in published literature, informed by decades running our own bench and pilot reactors.
Documented stability testing, impurity profiling, and analytical reports find their way directly to project leads and QC teams for both large firms and niche startups. This transparency emerges from hard lessons learned: intermediate grades with suspect color or unexpected solubility can derail project timelines and increase costs, so we over-communicate before materials even ship.
Real-world workflows rarely follow textbook routes, and small modifications in scale, order of addition, or solvent ratio can make the difference between success and an intractable emulsion. Our most successful project collaborations have come when R&D chemists contact us before finalizing their scale-up. During one discovery campaign, a project engineer experienced fouling and precipitation issues after switching to a competitor’s lot. After discussion, we traced it to elevated moisture and a subtle shift in melting point due to trace thiazole oxidation. The chemist reverted to our supply—with full batch analysis on hand—and regained the reproducibility required to secure pilot batch approval.
We encourage feedback loops from every project. Synthetic failures, purification slow-downs, or unexpected reactivity trends tend to have root causes in raw material variability. Instead of burying such issues, we prioritize open reporting and documentation. Even incremental improvements in particle size control or solvent washing have led to markedly easier process filtrations or better yields, as reported by customers and confirmed in our process notes.
For specialty users working at gram to multi-kilogram scales, it pays to plan with input from those producing the actual molecule. Many of our product improvements—such as enhanced drying steps, optimized filtration techniques, or stronger batch analytical packages—trace directly back to direct user feedback, testing, and field experience.
Each dispatch includes not just standard analytical data but expanded reports upon request, covering everything from NMR and mass spectra to trace metals and residual solvents. Over time, customers have come to value the completeness of our CoAs, recognizing how upstream transparency can reduce the uncertainties of multi-step synthesis. In exploratory and regulated environments alike, certainty beats guesswork. Our operations chemists and analytical team openly answer questions as technical issues arise—whether it’s reproducibility of coupling, concern over latent contaminants, or the need for advice on storage stability for delayed campaigns.
Problems do arise, and by owning our manufacturing chain, we respond with direct corrective actions. During an early lot shipment for an agrochemical partner, we discovered slight excess in unmethylated thiazole impurity—well below safety limits, but flagged by the recipient’s analysts. After retracing our upstream raw material sulfonation and adjusting pH control, we eliminated the deviation in future runs and updated our standard operating notes. Repeat clients often cite this technical engagement and willingness to own results as decisive in sticking with us versus the sometimes-anonymous supply from traders or re-packagers.
Years of handling this aniline derivative have shaped our business philosophy. Pricing pressure may tempt some organizations to push wider specification windows, outsource critical steps, or keep customers at arm’s length to avoid difficult conversations. We have concluded that deeper engagement, control over supply, and fielding the tough technical inquiries boosts long-term value for both sides. Research chemists, production managers, and purchasing professionals have all echoed this in feedback: reliability, traceability, and technical transparency must underpin any claim of quality.
The challenges of handling amine-thiazole heterocycles go beyond the initial assay, and only those manufacturing at scale learn the importance of shipping, batch homogeneity, handling air and moisture, and dealing with variable end-user process conditions. We continually reinvest in both our analytical and process equipment, recognize the nuances of scale-dependent impurity formation, and carry forward the discipline of pre-testing lots in target application conditions before scaling output shipments. Every week, a technical question or process hiccup somewhere in the world links back to a small choice at the manufacturing bench—this cycle of learning, reporting, and adjusting now anchors our manufacturing ethos.
From the outside, an aromatic amine with a thiazole and methyl substitution might seem just another line item on a chemical catalog. For those of us producing, testing, and partnering in its countless applications, it’s a lesson in the value of precision, transparency, and honest feedback. Small design elements—choice of methyl location, trace moisture content, rigor of raw material treatment—add up to big advantages or headaches for chemists in the real world. Each jar shipped reflects improvements and adjustments made possible by the demands and insights of those at the research and production front lines.
Our experience says that supplying a specialty building block amounts to far more than rotating a valve or running a reactor. Multiple teams—process chemists, analytical experts, packaging handlers, logistics coordinators—coordinate to deliver not just a chemical substance, but the confidence that each gram or kilogram meets the highest standards of reliability and traceability. Decades of serving diverse chemistries, through tight timelines and demanding specs, have reinforced that lesson.
As new discoveries, therapeutic agents, colorants, and specialty materials emerge from today’s labs, reliable access to pure, well-characterized chemicals remains essential. We remain committed to that mission—not as a slogan or a sales pitch, but as a hard-earned reality rooted in the daily details of manufacturing and technical partnership. Each lot of 3-(2-Methyl-1,3-thiazol-4-yl)aniline serves as another step in that ongoing journey.