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HS Code |
960603 |
| Product Name | 4-(3-Bromo-Phenyl)-Thiazol-2-Ylamine |
| Cas Number | 1147726-03-9 |
| Molecular Formula | C9H7BrN2S |
| Molecular Weight | 255.14 g/mol |
| Appearance | Solid |
| Purity | Typically >98% |
| Solubility | DMSO, DMF |
| Storage Temperature | 2-8°C |
| Chemical Class | Thiazole derivative |
| Smiles | C1=CC(=CC(=C1)Br)C2=CSC(=N2)N |
As an accredited 4-(3-Bromo-Phenyl)-Thiazol-2-Ylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 1g of 4-(3-Bromo-Phenyl)-Thiazol-2-Ylamine is packaged in a sealed amber glass vial with a tamper-evident cap. |
| Shipping | The chemical **4-(3-Bromo-Phenyl)-Thiazol-2-Ylamine** is shipped in tightly sealed containers, protected from moisture and light. Packages comply with all relevant safety and hazardous material regulations. Handling is performed by trained personnel, with supporting documentation included. Shipments typically proceed via approved courier services to ensure safe and timely delivery. |
| Storage | Store 4-(3-Bromo-Phenyl)-Thiazol-2-Ylamine in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Ensure proper labeling, and use appropriate personal protective equipment when handling. Follow all local regulations for safe chemical storage and disposal. |
Applications of 4-(3-Bromo-Phenyl)-Thiazol-2-Ylamine in Industrial ManufacturingAs the direct manufacturer of 4-(3-bromo-phenyl)-thiazol-2-ylamine, we support multiple specialized downstream sectors with consistent quality and controlled specification tailoring. Our focus remains strictly on sectors where this intermediate forms a foundational building block in high-value synthesis, and we supply our partners with tailored technical support across all critical application pathways. 1. Pharmaceutical Intermediate for Thiazole-Containing Drug SynthesisPharmaceutical companies utilize this compound in the synthesis of thiazole-based drug candidates, particularly in the development of kinase inhibitors and anti-infective agents. During medicinal chemistry workflows, its unique brominated aromatic and thiazole functionalities enable targeted molecular modifications. Bulk manufacturing processes integrate this material during multi-step API synthesis, primarily at the intermediate assembly and heterocycle derivatization stages. Regulatory compliance necessitates stringent control and documentation from raw material intake through final purification. Industry compliance standards
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2. Agrochemical Intermediate for Fungicide SynthesisCompound synthesis routes in agrochemical manufacturing frequently employ this raw material for the construction of active thiazole-based fungicidal ingredients. Within multi-step crop protection chemical production, formulators introduce the compound in the creation of brominated heterocycles, serving as a precursor for targeted modifications enhancing fungal toxicity and environmental stability. Strict documentation is essential through the production chain to align with regulatory submission standards for both technical grade and formulated agrochemicals. Industry compliance standards
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3. Specialty Dye Intermediate for Electronic and Industrial ApplicationsManufacturers of specialty dyes and pigment technologies deploy this compound for its role in constructing advanced molecular backbones for liquid crystal display dyes and industrial marking inks. The thiazole ring assists in chromophore arrangement and photostability, while the 3-bromo group offers avenues for further functionalization to refine color intensity and fastness. Precise weight ratios and purification steps prove essential for downstream products to satisfy customer performance specifications in electronics and specialty coatings. Industry compliance standards
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4. Fine Chemical Intermediate for Material Science ResearchMaterial science laboratories use this compound as a modular precursor in the synthesis of advanced organic semiconductors and functional polymers, particularly those requiring custom aromatic-thiazole linkages. Such structures play a central role in organic electronics, photoconductors, and optoelectronic device prototyping. Research teams adjust input concentration and synthetic route depending on the target molecular design, ensuring the final polymer or material maintains necessary functional group integrity and purity for device-quality applications. Industry compliance standards
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Every molecule matters. At our manufacturing site, the story of 4-(3-Bromo-Phenyl)-Thiazol-2-Ylamine doesn’t begin with a catalog entry or a hasty order sheet. It starts with people—chemist to chemist—working in glass-walled labs at reactors checked daily for integrity, purity, and stability. Input materials travel tightly controlled supply chains. Our teams spend hours monitoring reaction kinetics, tuning temperatures, and purifying until the smallest trace contaminant falls below detection. No batch moves downstream until it earns the approval of our chemistry group, reviewed by team leads with decades at the bench.
This approach, built over years of customer partnerships and technical problem-solving, brings purpose to each gram we produce. We know the laboratories and manufacturing lines using this thiazole derivative demand more than an off-the-shelf standard. They seek reliability batch to batch and helpful hands ready to adapt toward downstream needs. We built our business around real-world collaboration, where conversations between you and our chemists shape our synthesis, purification, and QA/lot release workflows.
Our version of 4-(3-Bromo-Phenyl)-Thiazol-2-Ylamine, identified by its CAS number and regulatory notifications, traces its design to the very core reactions that power pharmaceutical discovery and next-generation materials science. This compound stands out with its fused heterocycle, combining the bromo-substituted phenyl group with a thiazole ring. Both structural pieces offer distinct reactivity:
We produce this material in multi-kilo reactors, then purify using columns paired to the exact solubility and retention profile of each batch. Standard lots come tightly milled, clean, and ready for weighing by automatic balances on your site. Our chemists keep residual solvents in check—whether you need the lot for library generation, hit-to-lead expansion, or as a protected intermediate for agrochemical scaffolds.
We’ve watched what happens when corners are cut. Earlier in our journey, residual bromide and inconsistent moisture hurt downstream yields for researchers at an oncology startup. After seeing their purification time triple, we changed tack. Now, every batch clears residual halide and water using optimized drying and in-line analytic verification. Customers pressing forward in fragment-based drug discovery, or building elaborate target molecules, can waste time if each building block need extra post-purchase cleaning. This small attention to detail around individual lots delivers tangible gains for users scaling reactions above gram levels.
Typical product leaves our hands as an off-white to light tan powder, free-flowing and easily divided. Each drum and pack lists precise batch and retest dates, and supporting chromatograms come with shipment or are accessible on request. No generic notification, no silence if you have questions. If your route needs a solvent-specific adjustment, we check stability, then adapt our drying and packing to ensure no clumping or caking from atmospheric moisture. You won’t see variable performance in NMR or LC-MS trace work—from extraction through to final bioassay—because we personally stand behind each lot.
Medicinal chemists often start with simple, structurally tractable building blocks before modifying leads for solubility, potency, or selectivity. Our 4-(3-Bromo-Phenyl)-Thiazol-2-Ylamine first found users among those running iterative parallel synthesis, where batch-to-batch differences in such intermediates become an operational headache. Our attention to trace contaminants paid off for teams running amination and coupling steps side by side in plate arrays; reactions containing our material produced cleaner, more predictable spectra and higher yields, moving more candidates forward to screening.
Large pharma synthesis chemists engage with this molecule's thiazole core for ongoing kinase inhibitor projects and antibacterial series. Many enzyme inhibitors or receptor antagonists rely on diversified thiazole fragments to probe for SAR. Substituted aryl-thiazoles also feature in pest control agents and fungicides needing rapid, single-flask modifications. We’ve worked with suppliers of these industries—sometimes fielding midnight emails troubleshooting a reaction sequence—so we understand our customers operate under unrelenting time constraints.
We observed the most successful users validated intermediates with both LC-MS and NMR at each step. They documented that our thiazolylamine often delivered higher incorporation rates in arylation and urea coupling with minimal side products. Post-reaction workups turned up fewer traces of hydrolysis or dehalogenation. These victories seem modest at the bench, but they accumulate—meaning your team spends less time purifying, more time discovering.
Direct comparison between our 4-(3-Bromo-Phenyl)-Thiazol-2-Ylamine and other products on the market taught us a hard lesson: not all thiazole building blocks perform equally. Years ago, one of our R&D colleagues tested competitor samples. Minor, yet unreported, levels of des-bromo impurity or low-level di-substitution on the ring altered final yields. Product with poorly controlled particle size led to powder packing, requiring endless stirring or regrinding before dissolution. We set a higher bar.
Our process starts with pharmaceutical-grade bromoaniline and high-purity thiazole-forming reagents, qualifying each raw material supplier against a rigid blacklist of known contamination and stability risks. We check every batch not only for main peak purity—but also for ultraviolet impurities, solvent traces, and off-pathway byproducts—across at least two orthogonal analytics. Customers dealing with time-sensitive custom synthesis projects turn to us for one critical reason: our lots do what we say, when we say, without variance that delays a program or derails optimization.
We know chemical manufacturing doesn't happen in a vacuum. Even so, we’ve documented increased reproducibility when using our 4-(3-Bromo-Phenyl)-Thiazol-2-Ylamine in outside partners’ Suzuki-Miyaura couplings, as well as cleaner coupling intermediates in regioselective oxidations and alkylations. Compared to resold material from generic inventory lots, our product stands out by avoiding secondary peaks and demonstrating longer shelf stability under inert storage. Customers described lower rates of batch failure related to variable solubility or inconsistent melting profiles, important for multi-step campaigns where one off-spec jar can compromise months of work.
Troubles sometimes emerge not from the molecule, but through what surrounds it—humidity leeching in during transport, glassware residues, or even bottle cap failures. We saw real-world examples where late-stage intermediates struggled to dissolve. Rather than shifting responsibility, our team returned to process chemistry and adjusted drying protocols with staged vacuum steps. One customer facing solvent compatibility issues during an organometallic transformation reached out; our technical support responded with data from accelerated aging trials and provided fresh samples with validated moisture content. Such hands-on involvement—driven by lived experience, not templates—anchors our work.
Regulatory and documentation requirements also push more chemists to confront problems around transparency. We make batch-specific analytical data standard, not optional, and respond to custom documentation requests from regulatory groups in the US, Europe, and Asia. We focus on speed with accuracy; documents go out with shipments, not as afterthoughts. If a customer’s regulatory or import officials need clarification, we're at the ready with plain-language chemistry explanations relevant for both small chemical users and major multi-site plants.
Environmental waste and safe storage represent another reality seldom mentioned in standard product descriptions. Over years of direct conversations with environmental safety teams, we developed custom packing solutions capable of withstanding variable site conditions, reducing risk of punctures or cross-contamination. For larger users disposing waste, our product doesn’t carry unreported secondary or quaternary amines that would complicate classification or create surprises during incineration or EHS reporting.
Reliable manufacturing doesn’t translate only to cleaner powders. Failures upstream can mean failed screens, lost production time, or regulatory delays. We learned—sometimes the hard way—that a missed analytical step or a skipped drying protocol can cascade through your supply chain. Customer feedback shapes our process improvement: scientists doing gram-scale route scouting need small lots without excess lead times or intermediary packaging, while major production lines demand tons, always available, never interrupted by upstream shortages. We handle both needs without sacrificing quality or hands-on communication.
In late-phase development, when materials need to cross from discovery to pilot or full-scale synthesis, differences in impurity profile, stability, and moisture sensitivity become amplified. Our technical support and on-site chemists regularly provide additional chromatograms, impurity breakdowns, and update packaging to match individual workflow preferences. You rarely find us silent; ongoing improvement means continual benefit for all customers, big or small.
We don’t just sell molecules; we help solve problems. During a pandemic-induced logistics crisis, shipping delays forced several research groups to reach out for real-time status tracking and rush replacements. Our logistics team quickly updated every affected customer, re-routing stock, and in some cases, hand-delivering replacement product through local partners. Such responsiveness isn’t dictated from a manual—it grows from prioritizing long-term, person-to-person relationships.
We track global changes in regulatory, purity, and supply chain standards, keeping technical teams updated whenever guidance impacts analytical methodologies or labeling standards. When customers in fast-evolving fields—CRISPR, high-throughput screening, synthetic biology—request custom cuts or niche documentation, we gather requirements, set realistic delivery windows, and deliver consistently. This feedback loop, grounded in daily communication, ensures product and support evolve with users’ demands.
Our R&D team never stands still. Recent requests for alternative packaging, solvent swaps, and rare isotope labeling led to tailored pilot runs. Several users now run direct, in-plate derivatizations; our team responded with stability profiles and delivery options fit for microplate workflows. If you require a format or grade outside standard, we actively explore viability rather than simply refusing the request.
Every lot comes with a full traceability pedigree: batch number, synthesis log, purification method, and post-production analytics including NMR, HPLC, and melting point data. For larger partners, our technical files provide full chain-of-custody, change control tracking, and data archiving to comply with cGMP standards wherever demanded. Each deviation, if any ever occurs, is flagged and explained with remedial action—never hidden from view.
We often engage in technical reviews both before and after product shipment. Customers send feedback reporting success in medicinal chemistry screens, and—on occasion—report discrepancies. Every such note prompts immediate re-testing, batch retention, and problem-solving sessions with the users. Our open-door approach doesn’t always mean every obstacle vanishes, but it guarantees clear answers, accessible support, and collaborative progress.
Our facility leaders invest in technology and training to maintain robust analytical infrastructure—multi-field NMR, advanced mass spec, inert-atmosphere gloveboxes—alongside seasoned chemists who trust each other to speak up when off-nominal findings arise. Team members take pride reaching out to customers before problems can escalate. We want 4-(3-Bromo-Phenyl)-Thiazol-2-Ylamine to set a standard: reliable structure, strong documentation, and a support team who knows what it means to run reactions against a tight deadline.
By keeping synthesis in-house, we avoid uncertainty from unreliable subcontractors or fluctuating quality grades. Increasing demand and changing regulatory standards across continents create pressure to cut corners, but experience shows such shortcuts rarely pay. Instead, we build trusted partnerships by staying transparent, reducing surprises, and maintaining product reliability across the changing research and production landscape.
4-(3-Bromo-Phenyl)-Thiazol-2-Ylamine stands as more than a chemical name or a string of digits on a label. It represents a set of commitments: to purity, process consistency, ongoing support, and transparent improvement. Our experience proves the value of direct connection between manufacturer and user, shortening the path between need and solution. Every request for this compound reflects trust—trust that we’ve earned through tireless focus and honest business. We continue refining our approach every day—adapting, listening, delivering value through experience and care.