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4-(3,4-Dimethyl-Phenyl)-Thiazol-2-Ylamine

    • Product Name 4-(3,4-Dimethyl-Phenyl)-Thiazol-2-Ylamine
    • Alias AKOS024835502
    • Einecs 629-817-4
    • 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
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    Specifications

    HS Code

    590328

    Chemical Name 4-(3,4-Dimethyl-Phenyl)-Thiazol-2-Ylamine
    Molecular Formula C11H12N2S
    Molecular Weight 204.29 g/mol
    Appearance Solid, typically off-white to light yellow
    Melting Point Approx. 140-145 °C
    Purity Usually ≥ 97% (check lot-specific COA)
    Solubility Slightly soluble in organic solvents like DMSO, DMF, ethanol
    Cas Number 6602-47-9
    Boiling Point Decomposes before boiling
    Storage Conditions Store at room temperature, protected from light and moisture

    As an accredited 4-(3,4-Dimethyl-Phenyl)-Thiazol-2-Ylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 10g package features an amber glass bottle, sealed with a screw cap, labeled with chemical name, purity, hazard, and handling instructions.
    Shipping This chemical, 4-(3,4-Dimethyl-Phenyl)-Thiazol-2-Ylamine, is shipped in tightly sealed, chemical-resistant containers to prevent contamination and spillage. It is handled according to safety regulations, with appropriate labeling and documentation. Temperature and humidity conditions during shipping are monitored to ensure chemical integrity and compliance with all relevant transport guidelines.
    Storage Store 4-(3,4-Dimethyl-Phenyl)-Thiazol-2-Ylamine in a tightly sealed container, protected from light and moisture. Keep it at room temperature, in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers. Ensure proper labeling, and use appropriate personal protective equipment when handling. Avoid sources of ignition and store according to standard chemical storage protocols.
    Application of 4-(3,4-Dimethyl-Phenyl)-Thiazol-2-Ylamine

    Applications of 4-(3,4-Dimethyl-Phenyl)-Thiazol-2-Ylamine in Industrial Manufacturing

    4-(3,4-Dimethyl-Phenyl)-Thiazol-2-Ylamine serves as a key intermediate in select specialty chemical sectors, contributing valuable functional groups for synthesis in regulated industrial end uses. As the direct manufacturer, we supply this raw material for downstream processes requiring controlled quality, batch-to-batch reproducibility, and compliance with international standards.

    1. Advanced Pharmaceutical Intermediate Synthesis

    This compound acts as a foundational building block in custom synthesis of active pharmaceutical ingredients (APIs), particularly in thiazole-based drug discovery pipelines. Our material supports targeted synthesis of heterocyclic frameworks where strict regulatory traceability and process consistency are critical. Downstream pharmaceutical partners utilize this intermediate in multi-step protection and coupling, prior to final API crystallization and purification stages.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II for API manufacturing
    • 21 CFR 211 (USFDA current Good Manufacturing Practice)
    • Ph. Eur., USP reference standards as required by end-use API monographs

    Typical usage ratio

    • Dosages typically range from 1% to 8% by molar ratio within multi-component condensation or cyclization reactions, adjusted according to the synthetic target and impurity profile control.

    Downstream process integration

    • Introduced during initial heterocycle assembly or as a key starting material in regulated GMP synthesis suites, prior to further functionalization and final purification.

    Final product types

    • Thiazole-based oncology drugs
    • Selective kinase inhibitors
    • Anti-infective agents with thiazole cores
    • Custom intermediates for clinical and generic APIs

    2. Agrochemical Active Ingredient Development

    Agrochemical producers employ this raw material for synthesizing thiazole-containing pesticide and fungicide actives. It enables the manufacture of novel crop protection agents through precise insertion of dimethyl-phenyl-thiazole moieties, followed by targeted halogenation, esterification, or sulfonation in batch or semi-continuous processing systems.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (FAO Manual Section 4)
    • REACH Regulation (EC) No 1907/2006 for substance registration
    • ISO 9001:2015 Quality Management Systems for raw material traceability
    • OECD GLP for test item manufacturing

    Typical usage ratio

    • Formulation inclusion levels in reaction mixtures span 2%–15% depending on the specific active synthesized and yield optimization protocols.

    Downstream process integration

    • Acts as a core substrate in the lead step of active ingredient synthesis, typically under inert nitrogen and solvent-controlled conditions for further derivatization before isolation and formulation into commercial-grade actives.

    Final product types

    • Broad-spectrum fungicides
    • Herbicide intermediates
    • Seed treatment actives
    • Crop-specific pesticide formulations

    3. Specialty Dye and Pigment Manufacturing

    Dye producers use this compound as a precursor for thiazole-based chromophores incorporated in high-performance pigments. These applications require strict control over color consistency and lightfastness, often for demanding textile and plastics coloration markets. Its substituent profile enables unique hue modification in advanced dye structures.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile safety
    • ISO 9001 for pigment batch consistency
    • REACH (EC) No 1907/2006 for pigment intermediates
    • GB/T 31888-2015 Safety Technical Specifications for Children’s Textile Products (for downstream applications)

    Typical usage ratio

    • Employed at 1%–5% by weight in condensative or oxidative coupling recipes; batch ratios depend on targeted chromatic intensity and required stability.

    Downstream process integration

    • Integrated into the initial coupling or cyclization stage of pigment synthesis, followed by sulfonation or metallation steps, then granulation and milling for downstream blending or dispersion.

    Final product types

    • Sulfur-based azo dyes
    • High-fastness textile pigments
    • Plastics masterbatch colorants
    • Inkjet printing pigments

    4. Electronic and Functional Material Synthesis

    Manufacturers of specialty materials leverage this molecule as a thiazole-source in high-purity organic functional compounds, particularly for materials science research and advanced application in OLEDs, organic semiconductors, and specialty polymers. Its methylated phenyl configuration imparts favorable electronic properties and processability for tailored polymer backbones and donor–acceptor systems.

    Industry compliance standards

    • RoHS 2 Directive 2011/65/EU (for downstream electronics)
    • ISO 14001 Environmental Management System in specialty chemical operations
    • IEC 61249-2-21 Halogen-free requirements (for further downstream use in circuit boards)
    • Internal QC protocols for trace metal impurities & purity profile (≥99%)

    Typical usage ratio

    • Loaded at 0.5%–3% of total organic content in synthesis runs, precisely adjusted for target bandgap, charge mobility, and solubility relevant to each downstream function.

    Downstream process integration

    • Charged into monomer synthesis reactors under dry, oxygen-free conditions for polymerization or oligomer assembly, often followed by vacuum distillation and high-performance purification for device-grade use.

    Final product types

    • Electroluminescent polymer layers for OLED displays
    • Organic transistor (OFET) materials
    • Advanced photoactive coatings
    • Custom research-grade functional monomers

    5. Chemical Reference Standard and Analytical Synthesis

    Laboratory and analytical reagent suppliers use this compound as a characterized reference standard or as a starting material for synthesis of labeled analogs in LC-MS and GC-MS method validation, process monitoring, or pharmaceutical impurity profiling. This application requires documented batch traceability and comprehensive spectral libraries.

    Industry compliance standards

    • ISO/IEC 17034 General Requirements for Reference Material Producers
    • ISO/IEC 17025 General requirements for the competence of testing and calibration laboratories
    • USP/NF standards for analytical reference materials where applicable
    • CFR Title 21 Part 58, Good Laboratory Practice for Nonclinical Laboratory Studies

    Typical usage ratio

    • Directly used at 0.1 mg to 10 mg per analytical run, and at 0.2%–2% for further downstream derivatization or isotopic labeling workflows based on equipment sensitivity and method development goals.

    Downstream process integration

    • Weigh-out for standard solution preparation, comparison spiking, or as first-step reactant in small-scale syntheses of isotope-labeled analogs, followed by stringent purity verification.

    Final product types

    • Certified chemical reference standards
    • Isotopically-labeled thiazoles
    • Pharmaceutical impurity markers
    • Analytical grade working solutions for method validation
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    Certification & Compliance
    More Introduction

    Introducing 4-(3,4-Dimethyl-Phenyl)-Thiazol-2-Ylamine: Advancing Chemical Synthesis with Authenticity and Integrity

    In the chemical manufacturing field, experience reveals that some molecules consistently offer more value for research, formulation, and industrial use than others. Over the years, we have worked with countless aromatic amines and thiazoles, and many share similar features on paper. Yet only a handful deliver the consistency, purity, and reliability that synthesis work demands. 4-(3,4-Dimethyl-Phenyl)-Thiazol-2-Ylamine stands apart for its focused structure and broad utility, and our direct experience proves this daily.

    Direct Synthesis and Careful Manufacturing

    The story of every compound begins with where and how it is made. From sourcing raw precursors to refining the final product, each step affects what chemists and formulators see in their flask. Our own process for 4-(3,4-Dimethyl-Phenyl)-Thiazol-2-Ylamine emphasizes transparent supply chain control and modern synthetic routes. Instead of relying on intermediaries, we manage sourcing for each aromatic and thiazole building block ourselves. Batch after batch, we stick to high-performance purification, keeping side-products and contaminants in their place—out of the final crystalline powder.

    Technical staff test every lot for melting point, residue on ignition, and elemental composition using trusted methods like HPLC and NMR validation. We run each batch in stainless steel or glass-lined reactors when appropriate, using closed-system handling to preserve chemical integrity. Over years of production, we learned that shortcuts—skipping a wash, relaxing a temp control step—lead to differences in color, purity, and behavior during use. Skipped steps mean more cleaning downstream for processors and chemists. Care at our level keeps the work moving smoothly for customers. That’s responsibility.

    Specifications Based on Real-World Lab Demands

    Each research and production setting brings its own needs. Nobody benefits from a product that looks good only on paper yet acts unpredictably in actual lab protocols. We focus on making 4-(3,4-Dimethyl-Phenyl)-Thiazol-2-Ylamine that responds to real research. Melting point falls within a tight range—our QC results usually read 154–157 °C, supporting reliable solid handling and crystallization behaviour. HPLC area purity for production batches runs >99%, minimizing surprises in downstream applications.

    Moisture sensitivity often causes trouble for aromatic amines, and thiazoles with electron-donating substituents aren’t immune. We pack in sealed, heavy-gauge lined containers and store in controlled environments, ensuring minimal drift in assay and appearance during transport or storage. This matters for users who depend on batch integrity at every stage.

    The Structure and Its Benefits

    The chemical makeup of 4-(3,4-Dimethyl-Phenyl)-Thiazol-2-Ylamine brings together features valued by both bench chemists and process engineers. Two methyl substituents at the 3 and 4 positions of the phenyl ring create steric and electronic effects uncommon in unsubstituted thiazolamino analogs. These methyl groups shift electronic density, dampen ring reactivity in specific environments, and affect solubility profiles. With the thiazol-2-ylamine core, this molecule bridges classic heterocyclic chemistry with modern functional needs.

    Users working in medicinal chemistry, photochemistry, or materials design can leverage these features. The substitution pattern influences how the molecule couples, condenses, or inserts into new scaffolds. Methyl groups, for example, can boost lipophilicity or block metabolic attack at common oxidation sites. In dye precursor synthesis, the pattern controls chromophore alignment, affecting light absorption. Decades of hands-on chemical work confirm that these subtle features make or break synthesis projects.

    Practical Uses as Seen in Industry

    Given our years of supplying 4-(3,4-Dimethyl-Phenyl)-Thiazol-2-Ylamine, we see customers using it in many applications, each drawing out strengths tied to its structure. In labs aiming to build modified thiazole rings for pharmaceutical lead development, the starting amine group delivers efficient coupling points. Synthetic chemists exploiting Suzuki or Buchwald-Hartwig methods often comment on the clean conversion and manageable by-product profile they get compared with unsubstituted analogs.

    Polymer and advanced material applications also benefit. The dimethylated phenyl ring imparts tailored rigidity and hydrophobicity when built into thermosetting or flexible polymer systems. R&D teams working with conductive polymers or OLED precursors value the fine-tuned electronic properties resulting from this core. In the dye industry, the dual methyl groups enhance both solubility and thermal resistance—essential for melt-processing and high-temperature formulation.

    In specialty chemical research, our contacts routinely highlight that this amine behaves more predictably than mixed phenyl-thiazoles with halogen or alkoxy substitutions. Other groups introduce unwanted reactivity, self-condensation, or challenging purification steps. The dimethyl arrangement seems simple but solves a number of common bench-scale headaches.

    Consistency and Performance in Your Synthesis

    Success on the bench or production line counts on more than just a name or CAS number. Real gains come from consistent, verifiable performance. Working directly as the manufacturer, we experience these needs firsthand whenever an order rolls off the line. Consistency shows in the physical appearance and bulk powder handling. Crystals pour cleanly from the bottle, leaving minimal residue behind. No persistent odors or dust cling to scoops and tools, making cleanup more straightforward.

    Analytical teams downstream validate what we see by eye. NMR spectra display sharp, well-isolated peaks, and each lot’s chromatographic profile matches historical standards set from years of production data. Feedback from buyers, especially those scaling to pilot or kilo-lot projects, consistently points out the lack of batch-to-batch drift—lab results at gram scale map directly onto kilo runs, reducing troubleshooting.

    Comparing 4-(3,4-Dimethyl-Phenyl)-Thiazol-2-Ylamine Against Alternatives

    Over time we have manufactured and compared a broad set of thiazolylamines, including mono-methylated, non-methylated, and ring-substituted versions. Many alternatives offer some advantages: faster coupling reactions, higher solubility, or different melting points. Yet, the trade-offs show up where reliability matters. Halogen-substituted phenyl thiazolylamines, for instance, sometimes show better activity in nucleophilic aromatic substitution, but they complicate the purification stage. Methoxy or tert-butyl analogs open up new synthesis routes yet introduce greater air sensitivity and instability on storage.

    Our production process for 4-(3,4-Dimethyl-Phenyl)-Thiazol-2-Ylamine yields clean, stable material with a shelf life that matches customer schedules instead of forcing rushed use. In mixed synthesis campaigns, users report greater control over both site-selectivity and by-product profile. This compound behaves robustly without special storage or handling tricks. For customers looking to avoid repeated small-batch verifications, it means less time patching protocols and more time making genuine progress.

    Addressing Supply Chain and Authenticity Challenges

    Experienced practitioners know that many problems in chemistry begin with unreliable source material. Subtle batch variations mean scale-up processes break, bioassay results shift, and purification costs spiral. We address these issues every day at the manufacturer level. Rigorous documentation supports each batch, including origin of raw materials and chain of custody through production. Our transparency stands as a direct answer to the flood of off-spec, repacked, or relabelled material too often seen in the marketplace.

    Several partners have told stories about long delays, ambiguous documentation, or unexpected analytical results from resellers. Sourcing direct from a qualified, experienced primary producer mitigates those risks. Our facility maintains internal batch reserves, traceable records, and qualified technical staff available for troubleshooting. Customers dealing with patent filings, regulatory review, or stringent sourcing requirements find these factors not just helpful, but essential.

    Supporting Advanced Research and Development

    Today’s chemical landscape demands more than basic compliance or reproducible melting points. Researchers working at the frontiers of pharmaceutical discovery, fine chemical synthesis, or advanced materials require compounds that perform in real-world conditions—not just under idealized laboratory scenarios. Our direct factory experience means that requests for custom adaptations, alternate salt forms, or unique purities actually receive knowledgeable support, not vague promises.

    Teams developing combinatorial libraries request consistency and freedom from cross-contamination. Analytical users who need single-digit ppm limits on related substances rely on direct technical assurance from our side, supported by detailed batch documentation. Production facilities appreciate being able to request tailored packing, shipping, and documentation formats for their own checked protocols. By working directly from the manufacturer, the conversation becomes technical and practical, not just commercial.

    Safety and Compliance in Manufacturing and Handling

    Any discussion about aromatic amines and thiazoles must account for safety in both manufacturing and usage. Over the years, our operations teams have implemented material-specific controls. Closed reaction systems, real-time gas monitoring, and temperature modulation come standard, reducing both worker exposure risks and product variability. Trained staff monitor every transfer and filling operation, so packaging arrives clean and sealed. Upon request, material supplied with specialized handling training or usage protocols, supporting responsible use in sensitive research or production environments.

    Sustainability plays a growing role in all manufacturing decisions. We devote resources to improved solvent recovery, reduced waste, and energy-efficient process optimization. This means that both start-to-finish chain of custody and environmental records ship with each batch. End users not only achieve compliance with regulatory frameworks but also contribute to broader sustainability targets without compromising on raw material performance.

    Challenges with Scale-Up and Solutions from the Production Floor

    Moving from gram-scale laboratory work to full production brings familiar pain points. Some molecules change color, lose activity, or pick up trace impurities during kilogram-scale synthesis. We encounter and resolve such issues not only through process chemistry skill, but also through attention to equipment configuration and material movement strategies. Stainless steel batch vessels, optimized temperature and stirring profiles, and validated filtration protocols all help lock down quality.

    Sometimes, supply chain interruptions challenge both delivery and price stability. As a manufacturer, we respond by holding extra stock of hard-to-source precursors, qualifying multiple raw material suppliers, and regularly reviewing long-term logistics contracts. This ‘boots on the ground’ approach means that not only can we deliver urgent or unusual orders, but also maintain the same rigorous quality that bench research expects.

    Feedback Loops and Real-World Continuous Improvement

    Year after year, the strongest insight comes not from a marketing trend but from feedback in the lab and the plant. Chemists tell us when impurity profiles disrupt HPLC detection. Production foremen note when a lot handles differently on a screw-feeder or gains static in dry rooms. Each piece of feedback has shaped our batchwork, order fulfilment, and customer service models. When a recurring challenge appears—a stickier than expected powder, a temperature cross-sensitivity in storage, or an unexpected signal in an NMR run—we act directly and openly. Troubleshooting happens with the data in hand and the next batch improves.

    This ethos keeps the compound relevant across an ever-changing spectrum of applications. The partnership between real data, factory equipment, and clear, fact-driven conversations with users produces a product that not only meets technical data sheets but also delivers when weighed, measured, dissolved, or built into vital research and production projects.

    Trust and Direct Support from the Manufacturer

    In a market crowded by intermediaries, authenticity becomes rare. From years of firsthand production experience, we have seen the benefits of direct lines between factory and bench, chemist and process engineer, needs and solutions. Our focus on genuine information, consistent QC reporting, and candid support creates a foundation of trust. Many repeat customers return simply because they know that every challenge, question, or specific requirement is met with direct, authentic answers—not generic responses copied from a brochure.

    Whether you need scalable quantities for pilot campaigns or continuous analytical feedback for assay validation, our team operates with the direct experience of actually making each batch, monitoring its performance, and supporting its application. This practical, transparent approach makes 4-(3,4-Dimethyl-Phenyl)-Thiazol-2-Ylamine more than just another compound: it represents collaboration, accountability, and craftsmanship in the world of advanced intermediates.

    Conclusion: Value Gained Through Direct Manufacture

    Every day on the production floor, choices about raw materials, process steps, and quality controls directly impact the value researchers and manufacturers receive. Years of hands-on manufacturing have shown that these decisions make the difference between a product that simply fills a need and one that advances discovery and enables new solutions. The story of 4-(3,4-Dimethyl-Phenyl)-Thiazol-2-Ylamine continues with each batch produced, each order dispatched, and each research result built on a foundation of real quality and direct support.