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HS Code |
853690 |
| Iupac Name | 1-(4-Bromophenyl)-2,5-dimethyl-1H-pyrrole |
| Cas Number | 187463-70-9 |
| Molecular Formula | C12H12BrN |
| Molecular Weight | 250.14 |
| Appearance | Off-white to light brown solid |
| Melting Point | 76-80 °C |
| Purity | Typically >98% |
| Solubility | Soluble in organic solvents like DMSO and chloroform |
| Smiles | CC1=CC=C(N1C2=CC=C(C=C2)Br)C |
| Inchi | InChI=1S/C12H12BrN/c1-9-5-6-13(10(2)7-9)12-4-3-11(14)8-12/h3-8H,1-2H3 |
| Storage Temperature | Store at 2-8 °C |
| Synonyms | 4-Bromophenyl-2,5-dimethylpyrrole |
As an accredited 1-(4-Bromophenyl)-2,5-Dimethyl-1H-Pyrrole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle containing 10 grams of 1-(4-Bromophenyl)-2,5-Dimethyl-1H-Pyrrole, labeled with hazard warnings and purity details. |
| Shipping | 1-(4-Bromophenyl)-2,5-Dimethyl-1H-Pyrrole is securely packaged in airtight containers to prevent moisture and contamination. It is shipped in compliance with relevant chemical transport regulations, often via ground or air freight, ensuring temperature stability and safety. Full documentation, including safety data sheets, accompanies each shipment for regulatory and handling purposes. |
| Storage | **1-(4-Bromophenyl)-2,5-dimethyl-1H-pyrrole** should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent moisture or air exposure. Keep in a cool, dry, well-ventilated area, away from heat, open flames, and incompatible substances such as strong oxidizers. Store at room temperature and protect from direct sunlight. Use appropriate personal protective equipment when handling. |
Applications of 1-(4-Bromophenyl)-2,5-Dimethyl-1H-Pyrrole in Industrial ManufacturingAs a specialist manufacturer, we supply 1-(4-Bromophenyl)-2,5-dimethyl-1H-pyrrole to several established downstream industrial sectors where this intermediate plays a pivotal role in synthesis and transformation processes. Our material consistently supports precise formulation and meets traceability demands across fine chemicals, pharmaceuticals, agrochemicals, specialty dye production, and advanced electronic materials. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisAPI manufacturers utilize 1-(4-Bromophenyl)-2,5-dimethyl-1H-pyrrole in targeted pyrrole-based scaffold construction. The brominated phenyl group and methyl positions provide a stable yet reactive moiety, essential for Suzuki and Stille cross-coupling to build complex pharmaceutical molecules. Downstream chemists demand batch consistency and strict impurity profiles to facilitate regulatory submissions and simplify purification during final API synthesis. Industry compliance standards
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2. Agrochemical Active Ingredient SynthesisLeading agrochemical producers adopt this compound for constructing pyrazole and pyrrole-derived pesticides and herbicide actives. The bromophenyl substitution offers useful reactivity during halogen exchange and cyclization, which is crucial for designing systemic crop protection agents. This intermediate must meet agricultural regulations on residual metals and halide content, supporting smooth registration in regulated markets. Industry compliance standards
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3. Advanced Electronic Material PrecursorsFabricators of functional electronic materials use this pyrrole derivative to produce molecular wires, organic semiconductors, and low-band-gap polymer blocks. Bromine functionality is crucial for controlled polymerization through cross-coupling, affecting conductivity and stability in finished circuits. This application requires extremely tight control of ionic contamination and consistent particle morphology to prevent film defects. Industry compliance standards
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4. Specialty Dye and Pigment ManufacturingProducers of high-performance dyes and pigments integrate this compound into specialty purple, blue, and near-IR sensitive colorants. The bromophenyl-pyrrole structure enables specific chromophore modification and enhanced photostability, essential for textile, inkjet, and photographic applications. Consistency of the starting material directly impacts tone precision and lightfastness in downstream blends. Industry compliance standards
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5. Fine Chemical Synthesis for Research and DevelopmentLeading contract research organizations and chemical innovation labs require 1-(4-bromophenyl)-2,5-dimethyl-1H-pyrrole as a high-value building block in ligand design, catalyst development, and synthesis of heterocyclic test molecules. Here, demand for reproducible reactivity, extended shelf stability, and detailed lot documentation supports high-throughput screening and publication-quality compound generation. Industry compliance standards
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Our facility has spent years working with advanced heterocyclic compounds, and among those, 1-(4-Bromophenyl)-2,5-dimethyl-1H-pyrrole stands out due to its balance of performance and consistency. This molecule, known within chemical research as an arylated pyrrole, offers practical attributes in a world of specialty intermediates. From our experience, an aryl bromide on a pyrrole ring doesn't simply add a functional moiety; it opens tuning possibilities in electronic properties and allows for efficient downstream chemistry in pharmaceutical, polymer, and organic electronics applications.
This compound's structure—distinctive for its 4-bromophenyl group at the N-1 position and double methylation at the 2,5-ring sites—would not deliver value if purity went overlooked. Our in-house synthetic process focuses on a reproducible method starting from elementary building blocks, leveraging column chromatography and controlled crystallization. Typical batch checks report purity exceeding 98% by HPLC, with trace side-products characterized and minimized through direct process optimization. Each run demonstrates the effect of incremental improvements like solvent choice and reagent grade—not just in numbers, but in the ease our partners report during downstream reactions.
As a manufacturer, actual usability starts at the bench. We’ve seen how 1-(4-Bromophenyl)-2,5-dimethyl-1H-pyrrole behaves when compared to similar heterocycles: it presents as a faintly colored to off-white solid—no fussy oils or unstable pastes. Handling benefits from this important physical property, enabling precise weighing and secure transfer in both research and larger production settings. This physical stability, paired with low hygroscopicity, permits storage at standard ambient conditions without special atmosphere or refrigeration.
For industrial orders, we pack in airtight, chemical-resistant containers to shield the material from light and moisture. Every filled drum or smaller jar is lot-traceable; we chose this protocol after seeing how traceability simplified troubleshooting for both us and our clients. The packaging itself passes tests for compatibility and minimizes static and contamination risk.
Our laboratories have shipped material for a range of work including pharmaceutical intermediate synthesis, organic light-emitting diode (OLED) development, and specialty polymers. In drug discovery, the pyrrole core remains an attractive motif for bioactivity, and our compound has enabled chemists to explore new routes to anti-cancer and anti-inflammatory scaffolds. The electron-rich pyrrole ring, combined with an electron-withdrawing bromophenyl group, sets the stage for Suzuki and Buchwald-Hartwig couplings—a valuable feature for expanding molecular libraries efficiently.
Polymer chemists turn to this product for its ability to introduce rigidity and tunable optoelectronic features into conjugated backbones. Some customers target high-mobility thin-film transistors, where crystalline order and dispersibility matter. The dimethyl groups at the 2,5 positions inhibit over-oxidation and improve thermal stability, directly impacting both process reliability and device longevity.
Those working with OLEDs use this intermediate to tune charge transport layers. Its bromophenyl substituent allows post-condensation functionalization for unique aryl or heteroaryl derivatives, which we’ve seen make a difference in color and efficiency tuning in display technology. The selective reactivity at the bromine position also enables attaching solubilizing groups, boosting processability in both spin-coating and vapor deposition.
We’ve synthesized a spectrum of pyrrole-containing intermediates over the years. Minor structural tweaks often yield pronounced differences in application results. The presence of the 4-bromophenyl group distinguishes our product from unfunctionalized 2,5-dimethylpyrrole—a factor that grants access to further functional group introduction via standard aryl halide cross-coupling strategies. By contrast, non-halogenated pyrroles often require pre-functionalization steps, slowing throughput for rapid library synthesis or scale-up.
In comparison to para-chlorophenyl or iodophenyl analogs, the brominated variant shows a balance: more reactive than the chloro version in Pd-catalyzed couplings and easier to isolate than the iodo counterpart, which tends to be less stable and decomposes more quickly under similar conditions. These handling details, learned through dozens of kilogram-scale campaigns, translate into less downtime and higher success rates in customer workflows.
Structure-activity investigations in both organic electronics and medicinal chemistry have shown that subtle changes impact both device performance and biological affinity. Our product’s pattern of substitution often results in higher selectivity during secondary modifications and cleaner downstream purification. Researchers who start with this pyrrole frequently report more straightforward NMR and LC-MS analysis owing to its symmetrical dimethyl framework.
Synthesis of this compound does not run on autopilot. We discovered early that metal contamination could arise from traditional halogenation routes, complicating analytical compliance for sensitive end uses. Our team switched to a higher grade of catalysts and improved post-reaction work-ups, implementing atomic absorption spectroscopy to routinely check residual metal levels. Customer feedback helped us refine crystallization parameters to prevent solvent entrapment and reduce batch-to-batch variability.
Reproducibility counts. Some small factories chase output by sacrificing in-process controls, but our experience has shown that missed steps at scale create headaches, especially for partners running time-sensitive high-throughput screens or quality-driven device prototyping. Our line invests in real-time reaction monitoring and staged sampling to head off deviations before they reach packaging. Every time a new method improves yield or purity, we log the change and update downstream documentation, which has cut our customer support requests in half over the last two years.
As a chemical manufacturer, we face direct pressure from both environmental agencies and conscientious clients to keep all production safe and clean. Handling brominated aromatics brings specific challenges related to waste streams and operator health. By transitioning process steps to closed reactors and adopting targeted extraction techniques, we have both reduced fugitive emissions and improved operator exposure profiles. Disposal of residues involves coordination with licensed incinerators, and we maintain on-site solvent recovery to reduce overall waste.
Our internal audits pay particular attention to both raw material sourcing and downstream transport documentation. During shipments, shock and leak-resistant containers further limit spill risks, and every outgoing order includes barcoded tracking. Audit trails matter not just for compliance, but for instilling trust—a lesson our staff has absorbed over years of regulatory and partner reviews.
Even specialized chemicals are not developed in a vacuum. Demand for 1-(4-Bromophenyl)-2,5-dimethyl-1H-pyrrole responds to R&D cycles in biotech, electronics, and specialty materials. Over the past three years, we’ve watched growth in organic electronics drive bulk demand, prompting us to streamline batch scheduling and raw material procurement. Feedback from pilot projects in Europe and North America helped pinpoint desirable specs and inform quicker, more flexible order fulfillment.
Through direct partnerships, we've collected detailed performance metrics on our pyrrole in various finished products. These insights led us to tune not just purity but also moisture control and residual halogen spec sheets. Some pharma partners needed custom lot sizes or specific impurity profiles for toxicology studies; our production log allowed us to quote and deliver to those requirements. The more we collaborate upstream and downstream, the easier it becomes to anticipate needs and prevent costly rework.
No batch leaves our plant until it has passed a hands-on technical review. Talking with researchers, not just procurement staff, lets us spot trends and troubleshoot. One frequent issue: palladium-catalyzed couplings run into snags when trace water or halide impurities sneak in. We refined our drying step, invested in upgraded filtration, and began providing technical notes with each shipment, not fluff—just what matters in lab or plant transformations. Our product documentation reflects user feedback, collected from labs large and small.
As IP-driven fields grow more competitive, our partners need fast answers on side reaction profiles or expected shelf-life under varying conditions. Our QC team takes pride in direct response times—less “case number” nonsense, more solutions grounded in the day’s real data. Sometimes a fix comes from a chemist recalling a past run, rather than a webmaster regurgitating a manual.
Cost in fine chemicals never boils down to feedstock price alone. Labor, regulatory compliance, and testing overhead add up. Over multiple campaigns, we’ve learned efficiency hinges on solid relationships with reliable suppliers and a willingness to invest in new equipment. Automation in solvent handling shaved days from cycle time. Early-stage pilot feedback highlighted which purification bottlenecks hurt the most, and we responded by scaling up column diameter and re-mapping storage logistics.
Initial investigations required a focus on yield; today, our best efficiencies come from hitting reproducible metrics batch after batch. By investing in analytical training and automation, rejected batches have become rare. These improvements—backed by years of collective expertise—help contain costs and pass tangible savings to collaborators, without resorting to shortcuts that would erode trust or compromise application outcomes.
Changing application landscapes mean technical support and innovation must keep pace. As OLED and conductive polymer technology presses for higher purity and tighter specifications, feedback cycles get shorter. We noticed requests for milligram samples evolving into kilogram orders within months, and this shift shaped our lot-sizing strategies and document turnaround commitments.
Novel coupling techniques, new detection assays, and more sophisticated analytics all put new demands on our product’s consistency. We review literature and customer feedback in real time, adapting our chemistry to work with greener reagents or less hazardous solvents. Our engagement doesn’t end at shipment; it extends to following up on real-world problems researchers encounter, which keeps our team sharp and our product improving.
Every kilogram of 1-(4-Bromophenyl)-2,5-dimethyl-1H-pyrrole draws on our facility’s accumulated expertise: chemical handling, attention to trace impurities, and practical support at every step. Differences matter—our hands-on experience with structure, reactivity, and user needs defines what arrives at the customer's loading dock. We view this compound not as a line item, but as a tool built for productivity and reliability in real-world labs and pilot lines.
Whether destined for a pharmaceutical pipeline, a device R&D program, or a materials showcase, our product earns its place through persistent refinement, transparent communication, and attention to the voices of those using it. Our decades in specialty chemical production remind us: excellence isn’t just theory—it’s borne out one batch, one project, one partnership at a time.