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5-(4-Bromophenyl)-2H-Pyrazol-3-Ylamine

    • Product Name 5-(4-Bromophenyl)-2H-Pyrazol-3-Ylamine
    • Alias MFCD09972095
    • Einecs 821-615-0
    • 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

    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 & Storage
    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).
    Application of 5-(4-Bromophenyl)-2H-Pyrazol-3-Ylamine

    Applications of 5-(4-Bromophenyl)-2H-Pyrazol-3-Ylamine in Industrial Manufacturing

    As 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 Synthesis

    Pharmaceutical 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

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211 (Finished Pharmaceuticals and Intermediates)
    • European Pharmacopoeia (Ph. Eur.) Monographs for process residues
    • Japan Pharmacopoeia purity and impurity limits

    Typical usage ratio

    • 0.8–2.3 molar equivalents per downstream target molecule, adjusted per batch scale and observed conversion yields; loading is defined by ligand exchange efficiency and desired substitution pattern in the final API intermediate.

    Downstream process integration

    • Charged after protection/deprotection or Suzuki coupling, often entering at Stage 2 or 3 of the synthetic route. Incorporated during batch addition or continuous flow setup, monitored by in-line HPLC until completion of amination or cyclization steps.

    Final product types

    • Active pharmaceutical ingredient intermediates for kinase inhibitors (e.g., pyrazolyl-based oral chemotherapeutics)
    • Final oncology drug substances following further derivatization
    • Analytical reference compounds for clinical research batches

    2. Building Block in Agrochemical Synthesis

    Major 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

    • FAO/WHO Specifications for Plant Protection Products
    • EPA 40 CFR Part 180 (Pesticide Residue Tolerances)
    • REACH (EC) No 1907/2006 registration for agrochemical intermediates
    • China GB/T 37963 General Rules for Safe Use of Pesticides

    Typical usage ratio

    • 1.0–1.1 molar equivalents for coupling reactions, slightly in excess for reactions with less than 93% yield; process chemists may adjust based on impurity formation and cost of raw materials.

    Downstream process integration

    • Fed into the main reaction kettle as one of the primary building blocks post-activation of the substrate, frequently under inert atmosphere with automated mass flow measurement and reaction temperature control.

    Final product types

    • Pyrazole-based herbicide technical concentrates
    • Fungicidal active ingredient masterbatches
    • Finished crop protection products (granular/powdered or liquid)

    3. Material for Dye & Pigment Precursor Synthesis

    In 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

    • ETAD/ECO (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) Recommendations
    • OEKO-TEX® Standard 100 for textile colorants
    • ISO 9001 certified process controls for pigment intermediates
    • REACH Annex XVII restrictions on aromatic amines

    Typical usage ratio

    • 0.5–1.4 molar equivalents per azo or dye backbone, selected to tailor hue, tinctorial strength, and cost per kilogram of final pigment; incremental scale-up performed for new shades.

    Downstream process integration

    • Added as a key monomer after diazotization or during coupling with naphthol derivatives, with staged temperature ramping and controlled pH to direct selectivity and minimize byproduct formation.

    Final product types

    • Synthetic dye intermediates for polyester and nylon fibers
    • High-performance organic pigments for inks, coatings, and plastics
    • Specialty shade dispersions used in textile printing

    4. Precursor for Specialty Electronic Material Synthesis

    The 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

    • IEC 61249-2-21 (Halogen free materials for electronic applications)
    • RoHS Directive 2011/65/EU for hazardous substance limitation
    • JEDEC JESD625 Handling of Electrostatic Discharge Sensitive Devices
    • ISO/TS 16949 for automotive electronics (when used for specialty sensors)

    Typical usage ratio

    • 0.2–0.6 molar equivalents per target molecule or polymer unit; process optimization considers purity, volatility, and metal content, with pilot scale trials establishing the baseline for mass production campaigns.

    Downstream process integration

    • Introduced during monomer preparation—prior to oligomerization or copolymerization—with dissolution in electronic grade solvents and filtration to 0.2 micron to remove particulates; subsequent steps performed under controlled moisture and oxygen conditions.

    Final product types

    • Organic light emitting diode (OLED) intermediate materials
    • Photoactive molecules for thin-film solar cells
    • High-purity organic semiconductors for flexible electronics and chemical sensors
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    Certification & Compliance
    More Introduction

    5-(4-Bromophenyl)-2H-Pyrazol-3-Ylamine: An Insight from the Manufacturing Floor

    Overview and Experience

    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.

    Why Quality Matters in Pyrazole Synthesis

    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.

    Process Control and Its Impact

    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.

    Comparisons: Setting Ourselves Apart

    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.

    Meeting Application Needs: What We’ve Learned

    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.

    Environmental and Safety Responsibility

    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.

    Continuous Improvement and Response to Client Feedback

    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.

    Looking at Other Compounds in Our Portfolio

    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.

    From Manufacturing Floor to Research Lab

    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.

    Supporting Breakthroughs across Industries

    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.

    Real-world Value: Consistency and Integrity

    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.

    Our Commitment Moving Forward

    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.