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HS Code |
154057 |
| Iupac Name | 2-(1,2-dibromo-2-phenylethyl)pyridine |
| Molecular Formula | C13H11Br2N |
| Molecular Weight | 357.04 g/mol |
| Cas Number | 160602-29-5 |
| Appearance | White to off-white solid |
| Density | Approx. 1.6 g/cm³ (estimated) |
| Solubility | Soluble in organic solvents such as dichloromethane, chloroform |
| Smiles | BRC(Cc1ccccc1)(c2ccccn2)Br |
| Inchi | InChI=1S/C13H11Br2N/c14-11(13(15)10-6-2-1-3-7-10)12-8-4-5-9-16-12/h1-9,11,13H |
| Storage Conditions | Store in cool, dry place, tightly closed |
| Hazard Statements | May cause skin and eye irritation |
| Chemical Class | Pyridine derivative |
As an accredited 2-(1,2-dibromo-2-phenylethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 5-gram amber glass bottle with a secure screw cap, featuring a white hazard-labeled sticker stating "2-(1,2-dibromo-2-phenylethyl)pyridine." |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 8–10 metric tons packed in 200 kg HDPE drums, securely palletized and loaded for safe transport. |
| Shipping | 2-(1,2-Dibromo-2-phenylethyl)pyridine is shipped in tightly sealed, chemical-resistant containers, compliant with relevant chemical safety and transport regulations. It should be kept protected from light, moisture, and extreme temperatures. Appropriate labeling and shipping documentation must accompany the package, and handling should follow all hazardous material protocols to ensure safe and secure transit. |
| Storage | Store 2-(1,2-dibromo-2-phenylethyl)pyridine in a cool, dry, and well-ventilated area, tightly sealed in a compatible, clearly labeled container. Keep away from strong oxidizers, heat, and direct sunlight. Use secondary containment to prevent leaks or spills. Follow all local regulations and use personal protective equipment when handling. Store in a designated area for hazardous organic chemicals. |
| Shelf Life | **Shelf Life:** 2-(1,2-dibromo-2-phenylethyl)pyridine is stable for at least 2 years when stored tightly closed in a cool, dry place. |
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Purity 98%: 2-(1,2-dibromo-2-phenylethyl)pyridine with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product consistency. Melting Point 72°C: 2-(1,2-dibromo-2-phenylethyl)pyridine with a melting point of 72°C is used in organic catalysis, where it enables controlled processing and optimal crystalline separation. Molecular Weight 370.05 g/mol: 2-(1,2-dibromo-2-phenylethyl)pyridine at a molecular weight of 370.05 g/mol is applied in medicinal chemistry research, where accurate dosing and molecular modeling studies are facilitated. Particle Size <50 µm: 2-(1,2-dibromo-2-phenylethyl)pyridine with particle size less than 50 µm is utilized in fine chemical formulation, where it promotes homogeneous blending and efficient dissolution. Stability Temperature 120°C: 2-(1,2-dibromo-2-phenylethyl)pyridine with stability up to 120°C is employed in polymer modification reactions, where it provides reliable performance under elevated temperature conditions. |
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Working with organic bromides and pyridine derivatives in our production facility has built deep respect for what it takes to create consistency in specialty chemicals. Among the many molecules we handle, 2-(1,2-dibromo-2-phenylethyl)pyridine stands out for both its chemical complexity and the value it delivers across advanced synthesis projects. Over the years, we have committed to refining our batch and quality management processes for every run, because reliability means everything to end users who stake reputation and downstream workflows on our materials.
2-(1,2-dibromo-2-phenylethyl)pyridine sits among a group of pyridine-based compounds where halogenated side chains allow for targeted reactivity and selectivity. Models of this compound typically reference its substitution pattern: the pyridine ring attached at the 2-position to a dibromo-phenylethyl moiety, resulting in a molecular structure that brings both aromatic stability and the unique reactivity of vicinal bromides. Over time, we have noticed that this dual nature makes it a preferred intermediate in research settings where tailored halogenation provides strategic value.
Producing chemicals like 2-(1,2-dibromo-2-phenylethyl)pyridine demands more than a formula on paper. Success in this business means precise sourcing, timely processes, and an unwavering focus on impurities, especially with compounds containing multiple bromine atoms. We maintain strict oversight of raw bromine and phenylethyl sources, ensuring suppliers provide consistent input material that meets our pre-approved specs. In the bromination step, bench chemists monitor reaction courses daily to avoid over-bromination or incomplete conversion, as traces of mono-bromo or unreacted phenylethyl intermediates can disrupt further synthesis steps for downstream chemical engineers and lab scientists.
Quality analysis includes NMR, GC-MS, and HPLC, calibrated against both in-house and external standards. Our analysts spend time understanding the signal patterns for this molecule, focusing on purity levels, possible side-products, and bromine content. With each run, feedback from the quality department goes straight to process engineers, letting us adjust conditions in real time. This has kept product rejection rates down and upheld the standards expected by the pharmaceutical and specialty material R&D teams who trust our supply.
Over the past decade, customer feedback and our own pilot campaigns have taught us what details make the biggest difference with this molecule. Researchers frequently mention the importance of single-batch traceability and consistent bromination, because fluctuations—just a few tenths of a percent in bromine content—compromise sensitive synthetic routes. Every lot leaves our tank with a well-documented specification, including melting point range, HPLC purity (typically exceeding 98%), and a transparent impurity profile. From an industrial manufacturer’s point of view, specifications are not just about ticking boxes. They dictate how smoothly our material can transition into the next step of a synthesis—whether for pharmaceuticals, agrochemicals, or specialty dyes.
2-(1,2-dibromo-2-phenylethyl)pyridine sometimes draws comparison with similar halogenated pyridine derivatives, which can include 2-bromo, 2,6-dibromo, or other biphenyl-pyridine compounds. Direct experience working with these alternatives shows each has its place. For example, mono-brominated or mixed halide-phenylethylpyridines tend to deliver less control in selective downstream substitutions, often requiring more purification or leading to lower overall yields. The di-bromo compound, in contrast, offers both reactivity and selectivity, which can simplify process design and save time in multi-stage organic syntheses.
Many of our recurring customers use 2-(1,2-dibromo-2-phenylethyl)pyridine as a key building block for further elaboration—usually in organometallic coupling, C–N or C–C bond formations, and cross-coupling reactions that bring together aromatic rings. Our engagement with academic partners and formulation chemists has provided unique insight into its practical behaviors in actual bench-scale runs. Chemists mention reliable activation points at the brominated sites allow for selectivity in Suzuki and related palladium-catalyzed couplings. The phenylethyl side chain, meanwhile, serves as a robust backbone when constructing larger, more complex molecules, supporting firm ring or chain orientations even in the face of challenging synthetic conditions.
Compared to other pyridine-based intermediates, this molecule’s symmetrical dibrominated side chain offers more predictable outcomes during reaction optimization and scale-up. Over the years, demand has shown a trend where R&D teams move away from complex, less predictable multi-halogenated aromatics in favor of cleaner, well-characterized substrates that cut down on byproduct formation and facilitate isolation. In feedback sessions, chemists frequently attribute smooth scale-up, fewer purification cycles, and higher yields to the consistent supply and quality that our production systems enable.
Manufacturing organobromides at scale rarely unfolds in linear fashion. We have worked through episodes of batch-to-batch inconsistency, sometimes prompted by subtle changes in raw bromine or even barrel storage conditions. One season, a batch delivered by a new logistics contractor exposed us to a prolonged odor from residual epichlorohydrin in a minor precursor—traced back to a cracked seal during transit. For some suppliers, this kind of issue might slip through to the customer. Our QA team traced the problem early, worked directly with the shipper, and adjusted our supplier chain before product reached a single lab bench. It became a vivid case study in the realities of chemical logistics, and reinforced our view that direct manufacturer oversight at every step remains non-negotiable.
Temperature, batch concentration, and stirring rate matter tremendously in the bromination step, especially because competing side reactions produce isomers and byproducts. Early on, we tried scaling one pilot batch too fast, leading to unexpected exotherms and a spike in unwanted side-products. Process engineers went back, retooled agitation speed, and put in extra sampling intervals. From that hard lesson, today’s practice includes scheduled stops and quality checks at intervals that match the reaction kinetics of this specific molecule. Skilled operators remain in tune with the chemistry, knowing from experience when subtle discoloration or viscosity changes flag a problem.
This kind of continuous vigilance is what builds trust with technical clients in pharmaceutical research. They need assurances, not just on a data sheet, but in real-world supply over years—not months. A batch out of specification risks halting entire R&D programs where every lost day has financial and reputational costs. That’s why we view every contract not as an order, but as a commitment that starts in our sourcing and ends only when our customer’s own projects deliver the results they expect.
Halogenated organics—especially those with multiple bromine atoms—raise specific challenges in both environment and worker safety. In our plant, these concerns shaped the investment in fume extraction, sealed batch reactors, and solvent recycling systems designed to handle brominated process streams. Operators don full PPE, double gloves, and maintain strict shower-in, shower-out procedures for all synthesis areas handling this compound. As a manufacturer, acknowledging and addressing potential exposure isn’t just about compliance—it’s about our commitment to each employee’s well-being.
Our effluent treatment runs through multi-stage activated carbon systems, and bromine recovery allows us to minimize waste and cut direct emissions. By collaborating with regulatory and environmental experts, we have refined waste management protocols, aiming for annual reductions in halogenated organic residue. Incidents like unexpected emission spikes have driven further updates in our monitoring systems, so that both ambient and process air remain within international safety limits. Customers now inquire about lifecycle impacts—from feedstock to waste—and expect precise answers about the total ecological footprint of specialty chemicals. We share our learnings, both good and bad, because progress relies on open, honest engagement across the supply chain.
Intermediates like 2-(1,2-dibromo-2-phenylethyl)pyridine often enter projects at the research or kilo-lab phase, but successful adoption depends on our ability to support scale-up. Over the past few years, we’ve supported several transitions from gram to multi-ton production by partnering closely with customer engineers and chemists. As projects move out of the lab, the tolerance for inconsistency narrows. For our customers developing pharmaceuticals, electronics, or novel materials, even a minor batch deviation or unexpected impurity profile can halt progress. We treat early technical exchanges as collaborative problem-solving sessions, not just order processing. These partnerships have allowed our staff to suggest practical steps—adjusting solvent blends, modifying workup conditions, or selecting the optimal temperature program—to de-risk scale-up and unlock multi-ton capacity without sacrificing product quality.
By sharing technical data and opening our site to customer audits, we help build confidence in our processes. Real-life challenges, including raw material shortages or process troubleshooting, work best when tackled in the open. Over the past year, we helped a development team navigate a global bromine supply crunch by substituting suitable alternative lots, conducting joint analytical validation, and adjusting schedules to match changing timelines. That agility—drawing on firsthand experience, flexible logistics, and open lines of communication—continues to set manufacturers like us apart from mere traders or resellers.
A close-up view of how 2-(1,2-dibromo-2-phenylethyl)pyridine performs compared to similar molecules underscores why users return to this specific material. Mono-bromo phenylethylpyridines, for example, can be useful in select cases but tend to produce lower yields during aryl-aryl couplings, as incomplete halogenation or unexpected byproducts complicate downstream separation. For higher reactivity customers, especially those in materials R&D working on polymer-linked systems, di-bromination not only ensures more efficient coupling but also supports the creation of architecturally predictable chain structures. Many early users switched from mixed halide analogs after extended purification cycles and solvent loads drove up both costs and emissions—a shift visible not only on the balance sheet, but in the day-to-day workload for their chemists.
The dual bromine groups on 2-(1,2-dibromo-2-phenylethyl)pyridine add synthetic versatility, creating multiple positions for functionalization or cross-linking steps. Teams working on new pharmaceuticals or functional polymers consistently tell us that these features save weeks, sometimes months, by reducing the need for parallel process development. As a manufacturer, we measure our success not just by bulk sales, but by how our material helps our customers scale up new reactions faster with higher reliability.
Our technical support staff work from the practical end, reviewing how tweaks to bromine substitution patterns—or switching to alternative side chains—impact customer outcomes. While some industrial customers find value in more exotic pyridine derivatives, for mainstream applications in regulated markets, simplicity and reproducibility often trump complexity. Experience has shown that supporting core demand for well-characterized, predictable intermediates like 2-(1,2-dibromo-2-phenylethyl)pyridine helps advance more new chemistry than chasing every novel substitute.
An often-overlooked part of specialty chemical supply lies in packaging and delivery. Some specialty compounds arrive in containers unsuited to long-term storage, leading to caking, cross-contamination, or decomposition. Early on, we faced challenges—old high-density drums sometimes leaked or absorbed solvent vapors, causing minor quality dips. To address this, we shifted to inert-lined, airtight containers designed for brominated compounds, combining capacity and protection for both small batches and large-scale shipments. Workers update container labels with real batch codes, not just generic stickers, allowing customers to track the full supply chain chain for regulatory compliance and proprietary project records.
Order fulfillment means more than dispatching goods. In the rare event of a logistics disruption—such as customs holdups, port closures, or local weather events—our policy prioritizes direct, timely communication with customers and reroutes through alternate logistics partners where possible. Small details, like integrating barcoded tracking with real-time inventory systems, keep our shipments aligned with project schedules, even in volatile supply chain environments.
Long-term partnerships have brought home the reality that the value of a chemical lies in what it enables, not just how it’s made. In one case, a pharma client working on oncology drug candidates provided us samples after early medicinal chemistry stages faltered using a competitor’s less pure intermediate. Analytical feedback isolated the problem to trace byproducts, which our process control had eliminated through modified workup conditions. Their subsequent success in late-stage animal trials showed the downstream consequences of technical rigor at the manufacturing stage.
Elsewhere, advanced materials customers have explored the use of our 2-(1,2-dibromo-2-phenylethyl)pyridine in novel OLED and photovoltaic precursor research, citing high conversion yields and reduced waste streams. Our willingness to engage in iterative technical dialogue, reviewing both our analyses and data from their own labs, has accelerated several project timelines.
End-user success stories reinforce a core lesson: specialty chemical manufacturing thrives where technical excellence, candid communication, and real hands-on engagement intersect. Every project that moves from the lab to commercial scale with fewer stoppages—from pure batch chemistry to safe, on-schedule delivery—cements the manufacturer’s role as a cornerstone in the value chain.
As the specialty chemicals market shifts toward greener practices and closed-loop sourcing, manufacturers bear growing expectations for transparency, lifecycle assessment, and innovation. Over the past two years, we have piloted greener bromination protocols seeking to cut reagent and solvent consumption, and are testing recyclable process aids tailored for this class of pyridine derivatives. Early trials indicate modest improvements in waste reduction and process energy, but industry transition remains a gradual, collective process. Customers investing in new chemistry and sustainable materials now ask for lifecycle data and prefer supply partners willing to collaborate on pilot demonstration runs, joint waste audits, or reuse trials.
Participating in industry groups and technical consortia helps us anticipate which molecules—like 2-(1,2-dibromo-2-phenylethyl)pyridine—might find future value in emerging markets such as functional coatings, organometallic catalysis, or specialty resins. These next steps rely as much on transparent relationships and technical capability as they do on molecular design. Our story as a manufacturer is not just about the chemistry itself, but about listening to our customers, investing in rigorous production, and driving toward process improvements that make advanced synthesis accessible and reliable for every project.
By anchoring product development and technical support in our direct experience—not simply on market trends or abstract claims—we reinforce our commitment to science-driven, trustworthy partnerships. Whether supporting a single research project or supplying bulk intermediates across industries, our work keeps evolving alongside both the molecules we make and the people who put them to use.