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HS Code |
131449 |
| Iupac Name | 5-(4-bromophenyl)-1H-pyrazol-3-amine |
| Molecular Formula | C9H8BrN3 |
| Molecular Weight | 238.09 g/mol |
| Cas Number | 876717-72-9 |
| Appearance | Off-white to pale yellow solid |
| Melting Point | 210-213°C |
| Solubility | Soluble in DMSO, slightly soluble in water |
| Purity | Typically ≥98% |
| Storage Temperature | 2-8°C |
| Smiles | C1=CC(=CC=C1C2=CC(=NN2)N)Br |
| Synonyms | 4-Bromophenylpyrazolylamine |
| Chemical Class | Pyrazole derivative |
As an accredited 5-(4-Bromophenyl)-2H-Pyrazol-3-Ylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 5-(4-Bromophenyl)-2H-Pyrazol-3-Ylamine, 10g, packed in a sealed amber glass bottle with a tamper-evident cap and safety label. |
| Shipping | The chemical `5-(4-Bromophenyl)-2H-Pyrazol-3-Ylamine` is shipped in tightly sealed containers to prevent contamination and moisture exposure. It is typically packed with appropriate labeling and in accordance with hazardous material regulations. Shipping is conducted via certified carriers, ensuring safe transit and compliance with international chemical safety standards. |
| Storage | Store 5-(4-Bromophenyl)-2H-pyrazol-3-ylamine in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers. Keep at room temperature in a cool, dry, well-ventilated area, and clearly label the container. Handle in accordance with standard laboratory safety procedures, including the use of appropriate personal protective equipment (PPE). |
Applications of 5-(4-Bromophenyl)-2H-Pyrazol-3-Ylamine in Industrial ManufacturingAs the direct manufacturer of 5-(4-Bromophenyl)-2H-Pyrazol-3-Ylamine, we support global formulators and production lines in multiple highly specialized sectors. Careful control of synthesis, purity, and traceability ensures our material integrates reliably into demanding downstream applications. Below, we outline the primary real-world scenarios in which our product is incorporated, based on documented industry practice and actual buyer use cases. 1. API Intermediate for Oncology Drug SynthesisPharmaceutical manufacturers use this compound as a key scaffold in the multi-step synthesis of certain anticancer agents, especially pyrazole-based kinase inhibitors. The amine and bromophenyl substituents enable selective coupling and functionalization at critical stages. Formulators must optimize loading to balance reactivity and impurity thresholds while remaining compliant with global drug approval requirements. Sophisticated purification and inline monitoring ensure consistent batch outcomes aligned with strict regulatory filings. Industry compliance standards
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2. Building Block in Agrochemical SynthesisMajor agrochemical producers utilize the compound’s reactive pyrazolylamine group for the assembly of selective herbicide and fungicide actives. Its electron-rich aromatic ring pattern allows for precise halogenation, nitration, or sulfonation, customizing the molecule’s bioactivity profile. Process engineers tune addition stoichiometry closely to maximize yield and minimize waste. Each campaign run must verify compliance against region-specific agricultural chemical requirements, often under dedicated synthesis trains. Industry compliance standards
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3. Material for Dye & Pigment Precursor SynthesisIn the specialty dyes and pigments sector, developers select this molecule for high-color-strength synthetic pigment classes, particularly for fiber-reactive and disperse dyes incorporating a pyrazolyl motif. The bromophenyl unit provides an anchor for further azo or quinone modifications, crucial for specific chromatic and fastness requirements. Precise stoichiometry ensures pigment shade reproducibility and controls batch-to-batch variation. Final pigment intermediates must adhere to international dye industry standards for safety and purity. Industry compliance standards
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4. Precursor for Specialty Electronic Material SynthesisThe electronics chemical industry integrates this pyrazolylamine as a precursor during the manufacture of organic semiconductors and photovoltaic absorber materials. Its structural motif supports molecular engineering for controlled charge carrier mobility and optoelectronic stability. Engineers adjust intake ratios depending on device architecture—bulk heterojunction, stacked films, or thin-layer sensors—with documentation for trace metal and halogen content required for each lot. These applications demand consistent quality aligned with industry-specific QA protocols. Industry compliance standards
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5-(4-Bromophenyl)-2H-pyrazol-3-ylamine carries a specific weight on the production line. In our workshops, every kilogram goes through careful checks, from sourcing raw materials to the final crystallization phase. Over the years refining this compound, the difference comes down to hands-on method, not just machinery. Stability and batch consistency reflect tireless adjustments on the reactor settings and crystallization solvent ratios. What reaches the client shows the product of measured changes after countless pilot runs.
Our compound model 5-(4-Bromophenyl)-2H-pyrazol-3-ylamine stands out for its distinct physical characteristics—fine, white to off-white powder, low moisture absorption, and high batch-to-batch purity. Routinely, we see HPLC readings above 99%, driven by attention in the post-synthesis washing steps. Each batch follows the same sequence: precise temperature control at the condensation stage and quick isolation. In practice, this route minimizes impurity formation, holding the purity tight within close limits.
Organic synthesis relies on reproducibility. Chemists choosing this pyrazolylamine use it as a key structure for more complex chemical targets. Often, pharmaceutical innovators or agrochemical labs push us with detailed specifications—tight melting points and absence of unknown peaks in the chromatograms. It’s not just about producing mass but delivering a pyrazole base that can react cleanly in downstream chemistry. We maintain batch records that track every aspect, down to the minute, from filtration pressures to solvent grades.
One reason for these demands links back to the function of the structure. The 4-bromophenyl group on the pyrazole offers a versatile handle for building more elaborate frameworks. We have seen our clients apply it both in Suzuki and Buchwald couplings, where trace levels of halide or metal contamination can disrupt yields. Years ago, after feedback from a medicinal chemist noticing catalyst poisoning, we built in an extra carbon filtration step. Removing trace palladium residues dropped complaints to zero.
If you stand in our plant’s main hall during production, you notice the details. Synthesis conditions for 5-(4-bromophenyl)-2H-pyrazol-3-ylamine do not forgive sloppy temperature ramps or incomplete stirring. Solvent choice, typically DMF or DMSO, strongly influences the course of the reaction. Early on, we faced color contamination and trace impurities with subpar solvent. Our shift to using only fresh, tested batches of polar aprotic solvents paid off, especially under larger scales. Flash chromatography is rarely needed now, which means cost savings and less product loss.
Water activity gets heavy scrutiny because moisture affects crystallization and storage. We adopted nitrogen-blanketed storage tanks for critical intermediates. That investment eliminated hydrolysis byproducts which used to appear as unknown HPLC peaks, improving the purity and shelf stability. On occasion, labs report back that our compound held up months past the expected shelf period—a direct result of careful process optimization.
There’s a marked difference between manufacturer-grade and re-packaged materials. As a producer, we see how supply chain shortcuts dilute quality. Bulk barrels repackaged into small bottles after weeks in transit often lose the tight spec on water content or pick up contamination from unclean filling stations. We store in high-grade polyethylene drums, lined with moisture barriers, and fill only to order. The difference appears in purity certificates and in the performance when the customer applies the material downstream.
Our pyrazolylamine sits apart from technical-grade offerings, especially from traders. We choose high-purity bromobenzene inputs and fresh diazotization agents to avoid downstream nitroso or bromo impurities. QC by NMR every time, not just by UV-Vis, further drives the reliability. Processes used by some third-parties often ignore these points. We don’t hand off isolation or drying—these happen under our roof, under watchful care, avoiding contamination risk. Even our packaging team in clean-room attire checks every container for sealing integrity. There’s a reason repeat clients ask specifically for our lot numbers.
Our customers primarily use 5-(4-bromophenyl)-2H-pyrazol-3-ylamine for advanced organic synthesis. The pyrazole core serves as a bridge in medicinal chemistry programs, notably where bioactive heterocycles are needed. The 4-bromophenyl moiety opens up late-stage functionalization by palladium-catalyzed cross-coupling. Feedback from process labs often points to batch reproducibility, where peak areas by HPLC need to fall within narrow limits. In the past, minor slips in process control—like slight temperature overshoots—set peaks drifting, leading to costly rework. Through precise data logging and automated batch control systems, we now catch these issues in real time, heading off deviations before they affect the product.
Pharmaceutical labs, in particular, count on low levels of residual solvents. For them, even small traces of DMF or toluene pose regulatory issues. We upgraded to a vacuum drying chamber with real-time solvent detection, cutting our residuals to parts-per-million levels. Many research groups report improved yields in their subsequent reactions, as low-level impurities no longer buffer the chemistry or deactivate catalysts.
Handling halogenated intermediates in the manufacturing chain poses environmental challenges. We separate and recover brominate waste, routing it through a dedicated recovery unit. Standard practice would dispose of this as hazardous waste, but we close the loop, regenerating the bromide as an industrial reagent for use in non-pharma applications. This has reduced the load on our waste processing, and made both environmental agencies and local communities supportive of our operation.
Worker safety lies at the center of operations. Compared to other similar heterocycles, 5-(4-bromophenyl)-2H-pyrazol-3-ylamine’s dust presents minimal inhalation risk under controlled plant conditions, but we do not take shortcuts. Full dust control—hoods, negative-air rooms, continuous air monitoring—keeps exposure well below occupational exposure limits. We recall a situation, two years ago, where a minor filter breach occurred. Our real-time dust sensors triggered an alarm, halting the line within seconds. Reviewing the records afterwards, the exposure spike lasted under a minute—testament to our tech investment and staff training.
Over the years, process optimization grew from fieldwork listening to client pain points. Downstream breakdowns in high-performance liquid chromatography pointed back to inconsistent particle size in the delivered material. After evaluation, we modified our final milling process, steadying particle size distribution. Client reports now point to fewer filtration problems and shorter dissolution times in solvent.
Another crucial area involved solubility. Several innovators needed higher solubility in DMSO and DMF for automated synthesis platforms. We investigated polymorphism across batches and shifted to a slightly modified crystallization protocol. This tweak improved solution preparation times for customers without changing the core properties. Our scientists keep up with the literature, staying aware of new coupling agents or greener solvents, ready to adapt quickly if industry standards shift.
Working as a primary manufacturer means direct comparison with related compounds is easy. Substituted pyrazoles, for example, sometimes use chloro or methyl phenyl variants instead of bromo for cost reduction. We’ve produced both, and the reaction workups often require more extensive purification on the chloro analog. Bromo offers cleaner transformations in couplings and less tendency to carry stubborn by-products. Prices run higher, but downstream savings in workup and product isolation often recoup the initial cost difference. The amine functionality on the pyrazole ring also offers more flexibility in forming further linkages, compared to N-substituted variants, making it a prime scaffold for specialty chemicals.
It’s not just small changes in halide substitution that matter. Pyrazole derivatives without the bromine function often show drastically different reactivity in cross-coupling, sometimes requiring harsher conditions or yielding lower mass recovery. This might fit for simple labs or early R&D, but scale-up work finds value in reliable, well-characterized materials. By keeping tight control over every stage, we remove one headache at a time for synthesists and process engineers.
Every run on our plant’s pyrazole line reflects what we’ve learned about what clients value. Speed isn’t everything—making a rush batch with lower purity saves no one any time at the bench. Material that clogs filters or leaves unexpected spots on TLC plates can derail a week’s worth of planning. Our process foremen carry paper binders from earlier runs, constantly checking against today’s output for stray anomalies.
Shipping practices matter, too. We use flush-sealed liners and tamper-evident closures to prevent evaporation or accidental water pickup. Every drum moves quickly from final QA lab to trusted couriers, avoiding warehouse or transfer points notorious for moisture swings. Anecdotes from researchers say our packages open with minimal static and dust, a result of clean filling lines and good antistatic handling.
We watch for regulatory changes. RoHS and REACH compliance now go beyond just raw-mass analysis; they require documentable manufacturing traceability. Our records flow seamlessly from supply intake to analytical release, so audits or regulatory checks proceed smoothly. Specialty clients in the EU often comment on the robustness of our dossiers and willingness to share batch-by-batch process data. These aren’t afterthoughts—they are core to operating as a direct producer.
Though our main buyers come from the pharmaceutical and specialty chemical sectors, uses have broadened into materials science and electronic intermediates. Some teams use the compound for new light-emitting materials, counting on the reproducibility of the bromo group for consistent optoelectronic properties. We occasionally get requests for custom scale sizing—from a gram-scale test run to multi-ton quantities. Controlling every aspect of the process, from reaction to drying, means we can shift gears quickly without losing product quality.
Intellectual property, especially in high-value sectors, places strict requirements on provenance and composition. Our plant’s direct production approach provides these customers confidence. Knowing the source cuts down on contamination risk, and raw data for every batch remains available for patent filings, regulatory documentation, or customer quality checks. We stay ready to run custom modifications, should a medicinal chemistry group require a specific impurity pattern or isotope labeling. All modifications undergo the same rigorous oversight as our standard runs, reflecting decades of accumulated technical knowledge and process controls.
For us manufacturing is not about the cheapest per-kilo cost; it’s about the repeated satisfaction of researchers, buyers, and R&D teams who expect to receive a drum or bottle that matches what we promised. About a year ago, a global client’s scale-up team reported unexplained variance in their yields using multiple suppliers. Our deliveries held steady, confirmed by matching retain samples and third-party testing. That episode underscored the value of owning every step in the production chain.
Feedback loops never close—clients send back application data, we listen for issues, and tinker with process improvements. Some months, this means running four or five pilot batches just to lock in a slightly different reagent grade for one persistent client. Over the long term, these small adjustments accumulate, raising the floor on quality for all customers. It’s a path that only producers ready to stand behind their chemistry fully can walk. We welcome complex feedback and consider even rare outlying demands as opportunities to get better.
Making 5-(4-bromophenyl)-2H-pyrazol-3-ylamine isn’t a one-step process or a static recipe—it’s the result of thousands of operator hours, customer feedback, and steady investment in both safety and technology. By investing in rigorous raw materials screening, analytical verification using modern NMR and LC-MS standards, and secure packaging, we put forward a product suited not just for today’s high-pressure R&D, but for scaling into reliable commercial synthesis. Every specification and certificate rests on real-world plant data and experience.
We take pride in operating transparently, responding rapidly to market needs, and maintaining the technical edge necessary for products meant for demanding applications. Our team stands behind each batch not as resellers, but as the makers who see the compound’s value realized from raw materials intake all the way to your laboratory bench. The story of 5-(4-bromophenyl)-2H-pyrazol-3-ylamine is ongoing—driven by collaboration, hands-on experience, and an unwavering commitment to process integrity.