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1-(3-Bromophenyl)-1H-Pyrrole

    • Product Name 1-(3-Bromophenyl)-1H-Pyrrole
    • Alias 3-Bromophenylpyrrole
    • Einecs 697-664-5
    • 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
    VTB
    Specifications

    HS Code

    660471

    Cas Number 83857-96-9
    Molecular Formula C10H8BrN
    Molecular Weight 222.08
    Iupac Name 1-(3-bromophenyl)-1H-pyrrole
    Smiles c1cc(ccc1Br)N2C=CC=C2
    Appearance Solid
    Solubility Soluble in organic solvents such as DMSO and chloroform
    Purity Typically >98%
    Synonyms 3-Bromophenylpyrrole
    Storage Conditions Store at room temperature, dry and away from light

    As an accredited 1-(3-Bromophenyl)-1H-Pyrrole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 1-(3-Bromophenyl)-1H-Pyrrole, tightly sealed, labeled with hazard symbols and product information.
    Shipping 1-(3-Bromophenyl)-1H-Pyrrole is shipped in tightly sealed containers, under ambient or controlled temperature conditions, depending on stability data. Standard chemical shipping protocols are followed, including secondary containment and appropriate hazard labeling. All shipments comply with relevant local and international regulations for hazardous chemicals to ensure safe transport and handling.
    Storage 1-(3-Bromophenyl)-1H-pyrrole should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from sources of heat, ignition, and incompatible substances such as strong oxidizers. Ensure proper labeling and handle under a fume hood to minimize exposure to vapors. Use appropriate safety precautions and protective equipment.
    Application of 1-(3-Bromophenyl)-1H-Pyrrole

    Applications of 1-(3-Bromophenyl)-1H-Pyrrole in Industrial Manufacturing

    As a direct manufacturer of 1-(3-Bromophenyl)-1H-pyrrole, we work closely with process engineers and formulation chemists across established specialty chemical sectors. Below are the industrial application scenarios where this building block is currently integrated at a commercial scale, with a focus on operational parameters, regulatory frameworks, and functional outcomes.

    1. Pharmaceutical Intermediates for Heterocyclic Drug Synthesis

    This intermediate is widely applied in the synthesis of targeted heterocycle-containing APIs, where the 3-bromophenyl moiety directs regioselective C-C coupling and the pyrrole ring facilitates key cyclization routes. Downstream manufacturers deploy it in route design for anti-infective, oncology, and neuroactive agent pipelines, strictly adhering to validated GMP protocols. Purity profiles and traceability remain systematic priorities throughout the API lifecycle due to regulatory expectations and stringent customer audits.

    Industry compliance standards

    • IFPMA GMP for Active Pharmaceutical Ingredients
    • ICH Q7 (Good Manufacturing Practice for APIs)
    • European Pharmacopoeia (Ph. Eur.), USP standards
    • FDA 21 CFR Part 210/211

    Typical usage ratio

    • Mol ratios range from 0.8:1 to 1.2:1 relative to core starting units; actual ratio determined by target API yield optimization and impurity control studies

    Downstream process integration

    • Charged as an early-stage build block during Suzuki or Buchwald-Hartwig cross-coupling reactions
    • Undergoes catalytic transformations and functionalization prior to final cyclization and purification steps

    Final product types

    • Anti-cancer compounds (e.g., pyrrole-based kinase inhibitors)
    • Neuropsychiatric drugs featuring pyrrole scaffolds
    • Anti-bacterial and anti-fungal small molecules
    • Intermediates supplied to pharmaceutical CMOs

    2. Advanced Materials for Organic Electronic Devices

    In the organic electronics industry, the brominated pyrrole unit serves as a crucial donor monomer for constructing π-conjugated polymers used in optoelectronic components. Material science teams exploit its electron affinity to finely tune polymer backbone properties, impacting charge mobility and stability in the final device. Purity, batch reproducibility, and residual metal content are critical control points, especially for OLED and OFET fabrication lines.

    Industry compliance standards

    • RoHS Directive (2011/65/EU)
    • IEC 62321 for hazardous substance analysis
    • ISO 9001:2015 for quality management
    • Customer-driven material safety disclosure and conflict mineral declarations

    Typical usage ratio

    • 0.5-5% molar as a co-monomer in polymer feed formulation; loading level tuned based on target emission wavelengths and desired electrical properties

    Downstream process integration

    • Introduced as monomer to Stille or Suzuki polymerization for backbone engineering
    • Post-polymerization purification performed to below 250 ppm inorganic residues as specified by device manufacturers

    Final product types

    • OLED emissive layers
    • P-type semiconducting polymers for OFETs
    • Organic photovoltaic absorber or donor materials
    • Functional coatings for flexible electronics

    3. Agrochemical Active Intermediate Synthesis

    Manufacturers of advanced crop protection agents select this pyrrole derivative to introduce heteroaryl diversity into novel fungicides and insecticides. The bromine substituent allows site-selective transformations while maintaining ring stability during large-scale batch processing. Ensuring regulatory clearance for pesticidal intermediates, including strict monitoring of potential carry-over impurities, forms part of the compliance protocol in this downstream sector.

    Industry compliance standards

    • OECD Guidelines for Testing of Chemicals
    • EU Regulation 1107/2009 (Plant Protection Products)
    • FAO/WHO Specification for Pesticide Technical Grade Materials
    • ISO 17025 for laboratory testing accuracy

    Typical usage ratio

    • Typically 1.0-1.5 mole equivalent per target heterocycle core; ratio customized for each synthetic pathway to achieve desired yield without excess unreacted starting material

    Downstream process integration

    • Used in metal-catalyzed arylation or halogen exchange steps during intermediate construction
    • Feeds directly into condensation and ring-extension stages prior to formulation of the technical concentrate

    Final product types

    • Selective fungicides with pyrrolyl pharmacophores
    • Insecticide active ingredient intermediates
    • Ready-to-formulate crop protection technical concentrates
    • Co-formulant intermediates for seed treatment blends

    4. Dye and Pigment Synthesis for Specialty Colorants

    The compound’s electron-rich core and halogen functionality make it a preferred starting unit for synthesizing specialty azo and heteroaromatic dyes, allowing color chemists to generate novel shades with high lightfastness and solvent resistance. Manufacturing processes emphasize the removal of unreacted intermediates and control of heavy metal content to meet textile and ink end-use regulations. Custom batch records track all critical material transfer and blending steps for compliance audits.

    Industry compliance standards

    • REACH Regulation (EC 1907/2006) for registration and safety
    • OEKO-TEX Standard 100 for textile safety
    • EN 71-3 (Toy Safety, for pigment use in toy applications)
    • ISO 14001 for environmental management

    Typical usage ratio

    • 2-6% by weight in dye batch, with actual amount optimized for color intensity and performance; higher dose used in high-chroma and deep-tone pigment production

    Downstream process integration

    • Reacted via palladium-catalyzed coupling for pre-azo or aryl-pyrrolic dye precursors
    • Enter pigment blending and dispersion units post-reaction and high-vacuum drying

    Final product types

    • High-performance liquid inks for industrial printing
    • Disperse dyes for synthetic fiber coloration
    • Specialty pigments for automobile coatings
    • Non-migratory textile colorants

    5. Specialty Polymer Additives in Flame Retardant Applications

    This heteroaryl compound supports synthesis of advanced brominated additives, where the 3-bromophenyl-pyrrole structure forms the precursor for flame retardant building blocks compatible with engineering plastics. Quality control teams focus on minimizing oligomeric byproducts and halogen volatility during compounding. The downstream industry rigorously verifies additive performance metrics for fire resistance and material compatibility through accredited test protocols.

    Industry compliance standards

    • UL 94 (Flammability of Plastic Materials)
    • EN 45545-2 (Railway Applications, fire protection requirements)
    • VDE 0472 for electrical insulation materials
    • ISO 178 for flexural properties (when testing compounded plastics)

    Typical usage ratio

    • 8-15% by weight as flame retardant precursor, depending on targeted V-0 or V-1 flammability rating in the host polymer

    Downstream process integration

    • Introduced during additive batch synthesis as a key aryl halide unit
    • Melt compounded with base resin pellets in twin-screw extrusion systems

    Final product types

    • Flame-retarded polyamides and polyesters
    • High-performance electronic enclosure housings
    • Wire and cable compounds meeting IEC flammability specs
    • Engineering resins for public transport interiors
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    Certification & Compliance
    More Introduction

    Introducing 1-(3-Bromophenyl)-1H-Pyrrole: Insights from the Manufacturer’s Bench

    Developing 1-(3-Bromophenyl)-1H-Pyrrole on the Production Floor

    Manufacturing specialty pyrroles takes more than technical know-how. From the first kilogram produced, 1-(3-bromophenyl)-1H-pyrrole has stood out for its direct impact in building advanced organic molecules. Each batch that comes off our line reflects a combination of process precision, smart sourcing of brominated aromatics, and careful fine-tuning of reaction conditions. For years, chemical creators and developers in pharmaceutical and material science laboratories have relied on this compound’s unique electronic character. From coupling partners to building blocks for heterocyclic scaffolds, 1-(3-bromophenyl)-1H-pyrrole bridges a critical gap between simple aromatics and complex targets.

    Every day, pounding solvents, heating glassware, and patenting small improvements in yields, our team understands what it takes to deliver reliable, pure material. The significance of the 3-bromo substitution on the phenyl ring has not been lost on those developing next-generation drug candidates or novel polymers. The electron-withdrawing nature of the bromine atom at the meta position directly influences reactivity, offering a different path from the more commonly used ortho or para isomers. Certain research focuses demand steric control and fine-tuned reactivity, and that’s where 1-(3-bromophenyl)-1H-pyrrole earns its place.

    Quality and Reliability Beyond the Barrel

    True consistency only comes through deliberate attention at every step—from vetting raw phenyl bromides for purity to exacting washing, dry-down, and vacuum handling during workup. Our analytical equipment works overtime running NMR, HPLC, and GC-MS checks because customers’ syntheses rely on predictable results, batch after batch. Color, particle properties, and moisture content tell stories about process hygiene that spreadsheets cannot. Regardless of how ambitious the end use, nobody wants to troubleshoot their synthesis around vendor impurities.

    Years of customer feedback have taught us that specification sheets are just a starting point. The real trust comes from trouble-free reactions and clean research data. Our technical team goes beyond posted specs, routinely pushing purity benchmarks, minimizing trace contaminants, and sharing practical feedback straight from the QC bench. Not all brominated pyrrole compounds behave the same during storage or dissolution, and experience has led us to optimize packaging and shipment for safer handling and more straightforward transfer into sensitive reaction settings.

    Specifications with End-Use in Mind

    The unique structure of 1-(3-bromophenyl)-1H-pyrrole, C10H8BrN, puts electronic and steric influences right where advanced synthesis needs them. The melting point, color, and volatility all track closely with final purity. Most research-grade customers expect a product that is white to pale yellow and free of oily residues. Integrating spectroscopic tests routinely prevents cross-contamination, especially for customers pursuing drug intermediates or specialty conductive polymers. With years of production behind us, we have honed our process to meet the exacting thresholds demanded by custom and commercial-scale users alike.

    Compound stability, air sensitivity, and ease of redissolution aren’t afterthoughts. Pyrrole derivatives like this sometimes challenge even experienced chemists with their susceptibility to oxidation or polymerization. Early in our manufacturing journey, small issues with color drift and shelf life forced us to revisit our purification approach and rethink storage. Now, all outgoing material gets attention to oxygen exclusion, minimizing light exposure, and seamless packaging that suits not just large-scale, but also gram-quantity pilot runs.

    Why the 3-Bromo Variant?

    In our own hands, the choice between the 2-, 3-, and 4-bromophenyl pyrroles comes down to more than a CAS number. Electrophilic aromatic substitution patterns, cross-coupling compatibility, and ring electronics all shift with each isomer, impacting both ease of installation and downstream transformations. Medicinal chemistry teams exploring new kinase inhibitors, or material scientists chasing unique electronic properties, often specify the 3-bromo isomer over the others for its unique blend of reactivity and selectivity.

    Feedback from pilot plant collaborators and academic partners has repeatedly confirmed that this isomer unlocks synthetic shortcuts not accessible with ortho or para substituents. We’ve seen success stories where challenging Suzuki-Miyaura couplings transition from marginal to robust simply by using the 3-position substitution. That kind of direct evidence keeps our process engineers motivated to keep yields and purity high, precisely because the downstream savings are real.

    Where 1-(3-Bromophenyl)-1H-Pyrrole Finds Its Home

    The most seasoned researchers bring this molecule into projects ranging from medicinal lead discovery to organic electronics. In custom synthesis work, 3-bromophenyl pyrrole opens routes to complex heterocyclic compounds, often acting as a responsive handle for further functionalization. Quality in this context means more than numbers. It means project deadlines kept and downstream chemistry that proceeds as expected—outcomes we hear about directly during customer visits or calls for technical support.

    With our compounds supporting professional teams across research and development, we often supply not just kilograms but also guidance, answering questions on reaction compatibility and practical storage tips based on years of experience. Whether going into a multistep pharmaceutical intermediate or forming monomers for specialty polymers, this compound’s performance helps research teams accelerate—not slow down—progression from ideas to published results.

    Experience on the Production Line

    Every new lot represents a learning opportunity. Improving our bromination stage or adjusting the pyrrole cyclization protocol keeps efficiency high and production waste low. Staff on the plant floor monitor color, texture, and scent at every phase—not just relying on machine readings—to flag subtle shifts that can mean the difference between a straightforward purification and a time-consuming rework. Over the past decade, we’ve refined our process to hold batch-to-batch variability to a minimum, because repeat customers from both the start-up and academic sectors depend on repeat outcomes.

    GMP guidelines shape our plant setup and upgrade paths, but it’s lived experience in solving real-world synthesis snags that drives practical quality improvements. Early on, our tech team documented issues caused by air and light in packaging, leading to improved containment protocols that now serve as industry benchmarks. Direct communication flows between chemists at the bench and engineers in production, speeding up troubleshooting and minimizing lost time.

    Safety and Handling: Lessons Earned on the Shop Floor

    There’s a temptation to treat solid aromatics as easy to manage. Yet, pyrrole compounds can interact with moisture and air in ways that don’t show up until warmth or light application in the reaction pot. Some customers learned the hard way about early-stage degradation or byproduct formation due to overlooked storage quirks. Our plant staff faced these same challenges early, and over time, worked out safest handling methods for shipping and storage.

    Most safe practices aren’t printed, they’re taught: avoiding static-prone environments, separating sensitive stock from strongly oxidizing chemicals, and using moisture-resistant liners in all packaging. The longevity and performance of the compound in a customer’s hands often depends as much on these details as on purity statistics. Direct feedback loops with users have driven our choices for containers and quality checks. Each input gets tracked not just on paper, but via team memory and lived experience from hundreds of successful shipments.

    Customer Success Stories Drive Us Forward

    Some of the most rewarding moments come from learning how a well-behaved batch made an unlikely coupling reaction work or a convoluted medicinal chemistry synthesis run more smoothly. One research group scaled their project simply by switching from a generic vendor’s product to our tightly controlled pyrrole, eliminating stepwise purification headaches. Another lab completed urgent proof-of-concept testing after we fast-tracked a customized lot, keeping their milestone on track and funding secured.

    The difference in outcome usually starts with simple details: a guaranteed dryness level, zero extraneous dust, or a melt point matching published literature. Although basic, getting the right physical properties often separates an efficient workflow from days spent in troubleshooting. Every story we receive feeds back into our training and QC protocols, so next time the bar is set a bit higher and process improvements come a bit faster.

    Differences from Other Brominated Pyrroles: Practical Realities

    Not all bromophenyl pyrroles are alike, and direct competitors often overlook the subtle chemical and physical details affecting downstream results. The 3-bromo variant doesn’t just offer a unique substitution pattern; real differences emerge in how it interacts during cross-couplings, ring closures, and other key transformations. Para- or ortho- isomers may introduce less steric hindrance or result in different electron distributions along the aromatic ring, leading to challenges or shortcuts in advanced synthetic work.

    Our production chemists highlight that the staple 4-bromophenyl-1H-pyrrole tends to favor more rapid but sometimes less selective reactivity, whereas the meta configuration sometimes slows things down but delivers increased control and cleaner target products. End users in academic, pigment, and pharmaceutical research settings have shared comparative data showing that our 3-bromo isomer can bypass side reactions and cut down on labor-intensive purifications. Through these hard-won findings, we’re able to offer not just another CAS-listed compound, but a choice that matters to the synthetic chemist’s workflow.

    Real-World Solutions and Improvements

    Continuous learning sets the pace. Wherever industry standards lag, our team turns to customer feedback and internal tinkering to raise the quality bar. In the early days, a handful of returns prompted process upgrades that resulted in cleaner, more manageable product. Since then, we have built in additional in-process controls and invested in better drying technology. Every new procedural tweak or equipment enhancement came directly from either findings on the lab bench or suggestions from end users who hit real obstacles in application.

    With advanced analytical support on hand, challenges around trace metals, particle sizing, and even minor byproduct formation now resolve more quickly. Our technical support regularly fields questions from customers working at the interface of organic synthesis and materials science, helping them troubleshoot reaction conditions or streamline their solvent systems based on our manufacturing and analytical insights.

    Usage: Turning Raw Material Into Research Value

    Demand for 1-(3-bromophenyl)-1H-pyrrole keeps climbing as the need for advanced heterocycles touches on new research frontiers. Experienced users tap its versatility not only in Suzuki or Stille couplings, but also in creating precursors for nitrogen-rich frameworks in functionalized materials and pharmaceuticals. Because reproducibility matters at every scale, we’ve refined both our plant process and batch reporting so academic and industrial users can leverage every gram produced with confidence.

    Those running exploratory medicinal chemistry campaigns, assembling bi-heteroaromatic motifs, or prototyping optoelectronic devices all seek the same things: reliability, purity, and proven compatibility. Regular shipments to academic labs and research start-ups demonstrate that, with steady supply honoring changing project demands—sometimes within days, sometimes for long-term programs. The underlying lesson is that success in synthesis traces back to the subtle performance details of each input, which stem from every decision made by our production and quality teams.

    Supporting Discovery at Every Step

    Being the manufacturer means seeing projects through from base chemicals to breakthrough molecules. Raw material handling, scale-ups, and method optimization all mean little if compound quality doesn’t translate into real results for the end user. Whether a customer is working in fundamental organic chemistry or pushing the envelope in functional materials, our commitment is grounded in practical know-how and a willingness to adjust until the right solution emerges.

    It’s the blend of analytical discipline, lived problem-solving, and day-to-day communication with chemists and engineers that keeps us invested. Every metric tracked, complaint addressed, and batch improved moves us forward. Trusted suppliers don’t just meet standards—they evolve them based on what customers and lab partners actually see at the bench.

    Beyond the Product: Manufacturing Trust

    People come to us for the compound, but they stay for the partnership. By manufacturing 1-(3-bromophenyl)-1H-pyrrole in-house, every stage, from the initial raw input to the final packaged product, stays tightly controlled and adaptable. The feedback that guides our product evolution comes directly from the chemists and technicians who use it every week, allowing us to anticipate trends and common pain points before they reach the laboratory.

    Our work rarely ends with a single shipment. Ongoing collaborations lead to tailored grades, large-batch fulfillment, and sometimes even custom documentation for regulatory endpoints. Decades of hands-on time with customers and projects has given us a unique outlook on how innovation happens—not in isolation but through open dialogue and continual improvement.

    Staying Ahead: Innovation Rooted in Experience

    We don’t settle for ‘good enough’ because process optimization and chemistry never stand still. Whether it’s integrating new reactor technology, improving drying efficiency, or simply making ordering and delivery seamless, our operations reflect a willingness to learn by doing. Every change, however small, passes through the lens of real-world use, not just regulatory checkboxes or abstract quality goals.

    The real drivers of innovation aren’t only at large conferences or in regulatory filings. They’re in the bench notes of research chemists and the post-run logs of plant supervisors. We put those voices first, ensuring that every lot of 1-(3-bromophenyl)-1H-pyrrole leaves our facility better aligned with today’s demanding chemistry environments.

    Delivering Value Through Expertise

    Decades spent on the manufacturing side make one key fact clear: product quality is as much a function of human expertise as it is of raw material and machinery. Every process improvement, customer technical call, and minor tweak to method or packaging carries a signature of lived knowledge, built up run after run.

    Whether 1-(3-bromophenyl)-1H-pyrrole proves useful in a new cross-coupling protocol or as a precursor in sophisticated material design, its real value stems from how reliably it bridges the path from conceptual design to tangible progress. Each customer challenge, every round of feedback, and ongoing technical problem-solving further raises our manufacturing standards, providing the industry with both a dependable tool and a trusted resource in pursuit of advanced chemistry.