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HS Code |
504289 |
| Chemical Name | 2-Bromoethylbenzene |
| Molecular Formula | C8H9Br |
| Molecular Weight | 185.06 g/mol |
| Cas Number | 103-63-9 |
| Appearance | Colorless to pale yellow liquid |
| Density | 1.34 g/cm3 (at 20°C) |
| Boiling Point | 215-218°C |
| Melting Point | -56°C |
| Refractive Index | 1.551 |
| Flash Point | 91°C (closed cup) |
| Solubility In Water | Insoluble |
| Synonyms | Phenethyl bromide |
| Purity | Typically ≥98% |
| Odor | Aromatic |
| Storage Temperature | Store at room temperature, tightly closed |
As an accredited 2-Bromoethylbenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 mL of 2-Bromoethylbenzene, sealed with a screw cap and labeled with hazard and identification details. |
| Shipping | 2-Bromoethylbenzene is shipped in tightly sealed containers under cool, dry conditions to prevent leaks and degradation. It is classified as a hazardous material (flammable liquid), subject to strict labeling, packaging, and documentation requirements. Handle with appropriate safety measures according to regulatory guidelines, such as those specified by DOT, IATA, or IMDG. |
| Storage | 2-Bromoethylbenzene should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers and bases. Store in tightly sealed containers made of compatible materials, and keep away from heat and ignition sources. Use a chemical storage cabinet if possible, and label containers clearly to avoid accidental misuse or mixing. |
Applications of 2-Bromoethylbenzene in Industrial Manufacturing2-Bromoethylbenzene serves as an important synthetic intermediate for diverse industrial sectors, supporting high-value transformation routes in pharmaceuticals, agrochemicals, advanced materials, and specialty polymer manufacture. Below, we present real downstream application segments with detailed compliance, dosage, process position, and finished product listings for each sector. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)2-Bromoethylbenzene enters pharmaceutical synthesis as a key building block for the production of phenethylamine derivatives and other custom-tailored small molecules. Medicinal chemistry teams exploit its reactivity for nucleophilic substitution steps, constructing linkers or introducing aryl-alkyl chains into complex frameworks. This material supports scalable GMP flows, especially in custom API production under strict regulatory oversight. Industry compliance standards
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2. Agrochemical Synthesis for Herbicide and Insecticide IntermediatesDownstream agrochemical manufacturers employ 2-Bromoethylbenzene as a reactive precursor for constructing arylalkyl groups that enhance bioactivity in select herbicides and insecticidal agents. Synthesis processes involve nucleophilic substitution and Grignard-type couplings to enable new proprietary molecule development. Stringent quality and traceability systems support this route, with adjusted ratios to balance efficacy with regulated residue limits in final use formulations. Industry compliance standards
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3. Specialty Polymer Production for High-Performance MaterialsResearch and industrial polymerization teams use 2-Bromoethylbenzene for introducing pendant aromatic groups into polymer backbones, fine-tuning physical properties such as thermal resistance and mechanical strength. Its use in alkylation or “end-capping” reactions enables the synthesis of tailor-made specialty resins and elastomers. Integration into closed-loop systems ensures control of volatility and residual content per application guidelines. Industry compliance standards
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4. Organic Synthesis Intermediate for Fragrance and Flavor ManufacturingAromatics and fine chemical companies integrate 2-Bromoethylbenzene into production of aromatic aldehydes, alcohols, and custom flavor molecules through controlled nucleophilic substitution and reduction steps. Industrial Grignard reactions convert the raw material into complex fragrance ingredients used in perfumery or indirect food contact applications. Quality management ensures residual species remain below detection in compliance with fragrance industry safety standards. Industry compliance standards
Typical usage ratio
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5. Building Block for Advanced Electronic Chemical SynthesisProducers of fine electronic and photographic chemicals incorporate 2-Bromoethylbenzene for the construction of aryl-alkyl compounds that function as photoresist monomers and charge transport agents. Strict traceability and ultra-high purity controls are mandatory to support the electronic grade market, where any trace contamination risks product reliability in end-use settings such as semiconductors or advanced lithography processes. Industry compliance standards
Typical usage ratio
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Working as a chemical manufacturer day in and day out gives a unique perspective on the true nature of core intermediates. 2-Bromoethylbenzene, known by chemists for its direct aromatic bromination and sturdy ethyl chain, stands out among the building blocks flowing through our reactors. Unlike its more reactive halide cousins, this compound brings consistency, reliability, and versatility to a reaction scheme. Let’s walk through what makes this material matter—not just in test tubes, but in lab production lines and industrial synthesis worldwide.
Many associate purity with marketing claims; in the plant, the stakes are much higher. We manufacture 2-Bromoethylbenzene to a minimum GC purity of 99.5%, with isomer content closely controlled by fine-tuning process conditions. Even small traces of byproducts such as dibromoethane can destabilize downstream yields. By tightening our purification and using in-line analytics, we ensure that each batch delivers the reliability medicinal and agrochemical manufacturers expect in complex syntheses. Impurities don’t just add unwanted cost or paperwork—they can ruin a multi-step pharmaceutical run or lead to out-of-spec resin batches. Years of iteration have taught our team that hands-on quality control and veteran process engineers produce better outcomes than simply playing catch-up after the fact.
Comparisons crop up between 2-Bromoethylbenzene and similar chemicals, such as 4-bromotoluene, benzyl bromide, or ethylbenzene derivatives acting in electrophilic substitution. The aryl-ethyl skeleton of 2-Bromoethylbenzene acts differently due to the stability of its benzylic position; it resists overreaction and lends itself well to selective coupling and chain extension reactions. Chemists chasing specific chain lengths or aiming to avoid benzyl fragmentation find fewer surprises with this intermediate. Production teams notice the difference: reflux behavior, volatility, and shelf-life all track back to small structural variations, which ripple through shipping and storage. Our R&D department frequently works with formulation chemists to explore why a subtle change—moving a bromine or methyl group—leads to totally different performance in organometallic or polymer synthesis.
Across our customer base, most demand comes from sectors involved in complex molecule construction. This includes not just custom synthesis labs but bulk pharmaceuticals and advanced polymers relying on high-purity brominated intermediates. 2-Bromoethylbenzene acts as an alkylating agent, a handle for Suzuki and Heck couplings, and a source for extended aromatic systems. In our own pilot trials, scale-up engineers demonstrate how its reactivity profile makes it valuable for introducing ethyl branches without overbromination or troublesome side-reactions.
Some of the more innovative uses tap into its role as a linker or precursor for new ligands, surface modifiers, or specialized monomers. Instead of chasing after generic solvent-like properties, end-users look for intermediates that resist degradation in harsh conditions or that provide stable attachment points for catalysis. This is how the day-to-day performance of batches, not just the theoretical molecule, makes a difference. Repeat customers often share feedback about cleaner workups and fewer process interruptions, which tie back directly to the compound’s physical characteristics—high purity, low moisture, and minimized residual acidity.
Inside our facility, long-chain aryl bromides do not forgive shortcuts. We learned years ago to tune storage protocols around the material’s moderate volatility and susceptibility to light-induced decomposition. Using dark glass and inert-atmosphere packaging, we minimize byproduct formation; analytical teams check for trace peroxide or discoloration that might creep up in less-controlled processes. The difference between fresh 2-Bromoethylbenzene and slightly degraded material shows up in NMR readings and, ultimately, in final product performance—especially in pharmaceuticals where impurity thresholds keep tightening each year.
Shipping logistics also shape how we prepare orders for global delivery. Local customers often request bulk drums, with temperature-monitored shipping to prevent off-spec arrivals. International clients cite our track record with sealed ampoule samples for method development before scaling up large purchases. Communicating clearly about shelf life, packaging materials, and shipment best practices keeps everyone on the same page, reducing costly surprises.
Over years of operation, input materials and process design have changed considerably. We prioritize selecting verified suppliers for precursor chemicals, because even slight inconsistencies echo down the line into finished material quality. Early on, we relied on off-the-shelf bromine and ethylbenzene sources—the resulting batch-to-batch variability triggered several rounds of investigation. Since then, qualified starting materials combined with robust in-line QA have allowed us to set specifications that remain achievable and reliable.
One frequent challenge: controlling exothermic reactions during bromination. Temperature spikes, sometimes triggered by weather or unpredictable heat exchange, risk undesired di-brominated byproducts. Our onsite engineers developed custom reactor jackets and continuous monitoring to avoid runaway reactions and deliver steadier product. It’s not a theoretical risk—these experiences underline why the practical aspects of process control and reactor design mean more to real output than any literature value. Customers may only see the clear, colorless liquid in their vials, but every shipment represents thousands of carefully tuned process variables, each logged and analyzed by hands familiar with more than just screens and spreadsheets.
Industrial chemists face tough choices in selecting the right aryl halide for their workflow. The decision often comes down to factors beyond mere theoretical compatibility. Bromobenzene and benzyl bromide, common benchmarks, differ from 2-Bromoethylbenzene in both reactivity and handling. Bromobenzene, for example, offers broad substitutability, but lacks the ethyl chain essential in certain ligand synthesis and advanced pharmaceutical intermediates. Benzyl bromide delivers higher reactivity, which sometimes undermines selectivity or leads to unwanted side-chains.
Our feedback from development chemists highlights why 2-Bromoethylbenzene gets repeat use in routes where selectivity and chain integrity matter more than aggressive functionalization. In peptide synthesis, for instance, an unplanned reaction can derail entire sequences. The ethyl group in our product acts as both a physical and electronic buffer, preventing overreaction in sensitive assemblies. Scale-up teams also report notably fewer byproducts during process intensification, translating directly to higher overall efficiency and less waste.
Many compounds play just a small role in the grand scheme; 2-Bromoethylbenzene’s influence far exceeds its volume. As an intermediate, its integrity and predictability affect late-stage pharmaceutical intermediates, specialty polymer backbones, and even agrochemical actives. We regularly observe how traces of unreacted halide or unexpected conversion byproducts in this step compromise the next few links in a synthetic chain. This means every improvement in our quality translates directly into better yields and regulatory compliance for our clients.
Engineers working with phenylethyl derivatives, for example, rely on the preservation of the benzene ring and predictable ethyl chain placement to maintain downstream activity. Any deviation prompts painstaking troubleshooting, especially for actives bound for stringent regulatory review. Years of audit feedback and shared technical troubleshooting reports showed us the long-term savings and strategic advantages that come with consistent, high-grade supply. We don’t view purity as a statistic but as a lived expectation—one checked at every drum, not just on paper or export documentation.
Experience has proven theories only go so far—what works brilliantly in a 250 mL flask rarely translates with zero adjustments to 500-liter production runs. During our initial expansion, several process variables highlighted just how well 2-Bromoethylbenzene behaves under scale pressure compared to its more problematic analogs. Reaction selectivity held fast, solvent loss remained manageable, and quenching steps ran cleanly, producing manageable aqueous and organic waste.
One persistent issue stemmed from the variable exotherm in different seasons—summer runs risked overheating, which led to formation of stubborn side-products in early QA checks. Tighter process control, including integrating digital feedback loops between the synthesis and purification steps, closed the gap and leveled out seasonal effects. That kind of operational learning shapes how we both make and recommend using 2-Bromoethylbenzene in third-party scale-ups. Many R&D managers contact us for hands-on advice, sharing process diagrams and yield data to optimize their own flows. We see these hands-on exchanges as part of our job, not an afterthought.
Handling aryl bromides involves environmental and staff welfare considerations. Regulations governing hazardous intermediates keep tightening, with more focus each year on bromine handling, emissions, and waste minimization. We have invested in on-site scrubbing and recycling options that capture and reprocess bromine vapors, reducing loss and local environmental impact. Every kilo of recycled reagent reduces both raw material costs and the carbon burden of our operations.
Staff training matters just as much as equipment. In our facility, everyone from shift operators to analytical chemists receives practical, scenario-based safety training: spills, vapor containment, PPE standards, and rapid neutralization protocols for accidental releases. It’s not about ticking regulatory boxes—it’s about building muscle memory and a safety culture. The benefits show in our incident records and the confidence of visiting auditors. Labs downstream of us often seek similar support, knowing the safe and careful production of a reactive intermediate gives them a head start in their own environmental audits.
As regulations worldwide shift and new synthetic techniques edge into mainstream adoption, the role of well-controlled, high-purity halogenated intermediates has only become more central. We see rapid growth in demand from fields such as advanced medicinal chemistry and high-performance materials, both hungry for reliable sources of aryl alkyl bromides. The drive for greener chemistry places more weight on intermediates that deliver maximum selectivity and use fewer additives—traits that direct development work on our 2-Bromoethylbenzene line.
We’re increasingly involved in custom synthesis partnerships for bespoke aryl and alkyl halides. Experience tells us that every molecular tweak customers demand brings new production challenges, but also creates learning opportunities. For instance, users seeking non-traditional substituents lean on our knowledge of substitution patterns and habitability, cutting down development time and optimizing their processes without compromise.
Prompt order fulfillment only marks the start of a professional handshake. Ongoing technical support shapes most customer relationships. Our application chemists field questions about reaction conditions, solubility, and waste management—not all of which ever appear in the literature. Sometimes, feedback loops take unexpected turns: a customer comes back with a chromatogram showing an unexplained split-peak. Our technical services team works with them, sharing in-house diagnostics and troubleshooting the whole synthetic sequence. Over time, these conversations crystallize into process guides, FAQs, and shared learnings that improve outcomes for the next wave of users.
Many customers use our product as the foundation for more elaborate scaffolds or as a staging point in multi-step syntheses. They need practicality—not just theoretical compatibility. By tracking real-world reaction failures and mapping them to intermediate impurity profiles, we’re able to offer more than just product, but insight that shapes future project chemistry.
Making 2-Bromoethylbenzene is as much about people and practical details as molecular diagrams. Every kilogram reflects hard-won production know-how, effective teamwork, and constant communication between process, analytical, and safety teams. Over time, our understanding of physical properties and real-world impacts has deepened, driven by close collaboration with customers tackling ambitious projects. As the demand for reliable intermediates rises, the lessons learned on the manufacturing floor—about purity, storage, troubleshooting, and customer support—become the backbone of long-term partnerships and technical advancement. That’s what continues to set 2-Bromoethylbenzene apart in a lab and across the global marketplace.