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HS Code |
314147 |
| Cas Number | 621-23-8 |
| Iupac Name | 2-bromoethyl phenyl ether |
| Molecular Formula | C8H9BrO |
| Molar Mass | 201.06 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 268-271°C |
| Melting Point | -35°C |
| Density | 1.396 g/cm³ |
| Refractive Index | 1.552 |
| Flash Point | 122°C |
| Solubility In Water | Insoluble |
| Vapor Pressure | 0.012 mmHg at 25°C |
As an accredited 2-Phenoxyethylbromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g amber glass bottle with screw cap, labeled “2-Phenoxyethylbromide,” includes hazard warnings, manufacturer’s logo, and batch number. |
| Shipping | 2-Phenoxyethylbromide is shipped in tightly sealed containers made of compatible materials, typically amber glass bottles or drums, to prevent moisture and light exposure. It is classified as a hazardous material and must be transported in accordance with relevant regulations, including proper labeling, documentation, and handling precautions to ensure safety during transit. |
| Storage | 2-Phenoxyethylbromide should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of ignition. Protect it from moisture and direct sunlight. Store separately from oxidizing agents, acids, and bases. Clearly label the container and follow all relevant safety guidelines and local regulations for hazardous organic chemicals. |
Applications of 2-Phenoxyethylbromide in Industrial ManufacturingAs an experienced manufacturer of 2-Phenoxyethylbromide, we supply global clients engaged in specialized chemical synthesis. Our production supports well-established downstream industries that integrate this compound into refined processes. The following sections detail genuine industrial applications, processing conditions, and compliance considerations for major commercial users. 1. Pharmaceutical Intermediate for CNS Active CompoundsPharmaceutical manufacturers utilize 2-Phenoxyethylbromide as a key alkylating agent in the synthesis of central nervous system (CNS) actives, particularly for selective serotonin reuptake inhibitors and related compounds. Its high reactivity in nucleophilic substitution enables efficient attachment of phenoxyethyl moieties during active pharmaceutical ingredient (API) manufacture. The material’s profile supports consistent batch purity and compliance with stringent impurity management protocols, especially where residual bromide content affects final API quality. Industry compliance standards
Typical usage ratio
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2. Advanced Agrochemical SynthesisMajor agrochemical producers employ this brominated ether in organic syntheses for selective herbicide and fungicide actives. Its capacity to introduce the phenoxyethyl group with high yield improves the efficiency of constructing complex agroactive molecules—especially where ether linkage stability under field conditions is mandatory. Control of trace impurities during scale-up production safeguards compliance with residue and toxicity thresholds imposed by regulatory authorities. Industry compliance standards
Typical usage ratio
Downstream process integration
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3. Synthesis of Functional Polymers and AdditivesSpecialty polymer resin manufacturers incorporate 2-Phenoxyethylbromide to modify backbone structures during copolymer or grafting processes. The introduction of phenoxyethyl units enhances solubility, flexibility, and compatibility in high-performance coatings or engineering resin systems. Its use in precision polymerization provides tunable end-use functionality while manufacturers maintain strict tracking of halogenated raw material inputs in compliance with both process and environmental standards. Industry compliance standards
Typical usage ratio
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4. Synthesis of Liquid Crystal PrecursorsProducers in the liquid crystal and display industries use this compound to craft phenoxyethyl-functionalized aromatic intermediates. These intermediates contribute to precise phase transition and alignment characteristics in liquid crystal formulations, affecting both display resolution and energy efficiency. Precise dosing is monitored to minimize impurities that can disrupt nematic or smectic phase stability in LCD panels, and downstream processes require tight analytical verification routines. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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As a manufacturer who has spent decades refining the production of specialty chemicals, I find 2-Phenoxyethylbromide stands out for those in search of reliability and versatility on both laboratory benches and industrial assembly lines. Our team takes each batch from raw materials to finished reagent with close attention to process control, because those who depend on consistent results cannot afford any surprises. This compound, known by the molecular formula C8H9BrO, offers practical answers to challenges that arise during alkylation, etherification, and the construction of heterocyclic architectures.
In our facility, 2-Phenoxyethylbromide leaves the reactor as a pale yellow liquid, typically with an assay of no less than 99%. Trace impurities, including phenol and dibromide, are systematically monitored through gas chromatography. These steps are often overlooked by outside observers, but anyone who relies on this reagent for scale-up knows how important tight purity control can be. Moisture content is held below 0.05%, as too much water can catalyze hydrolysis and reduce yield in subsequent reactions. Every drum, whether destined for a kilogram-scale pharma trial or a multi-ton fine chemicals process, is checked against these specifications. This is not just a paperwork exercise; claims in brochures do not match what happens if testing is skipped, as even a minor contaminant can derail the entire downstream synthetic route.
Our regular customers tell us 2-Phenoxyethylbromide is often selected as a key intermediate for the production of β-phenoxyethyl derivatives, including anti-inflammatory agents and specific agrochemicals that require high selectivity during synthesis. In fine chemical custom synthesis, its reactivity profile gives medicinal chemists an edge when they install complex side chains onto aromatic rings. The benzyl bromide moiety activates the ethyl chain toward nucleophilic substitution, but with less aggressive leaving group behavior than benzyl chloride derivatives. This distinction means greater control—fewer side-products, easier downstream purification, higher confidence in reproducibility.
During process development, we have seen customers streamline multi-step syntheses by swapping previous halogenating agents for our 2-Phenoxyethylbromide, because the cleaner reactions reduce both waste and rework. The outcome often shifts project timelines, especially for companies balancing green chemistry objectives with pressure for rapid delivery. In our own pilot projects, a switch to this compound resulted in over 30% reduction in by-product formation in nucleophilic substitutions, allowing easier chromatographic purifications and decreased solvent use.
Every team member in the plant knows that handling precision chemicals like 2-Phenoxyethylbromide requires a level head and respect for proper protocols. The liquid’s moderate vapor pressure calls for careful transfer and closed systems to prevent uncontrolled emissions. Some customers ask about personal protective equipment, sharing stories about previous suppliers whose bulk product created fumes or residue; that is not an issue with batches produced under well-ventilated, closed conditions and when containers remain properly sealed. We guide partners through risk assessments based on years of hands-on experience—not generic advice—so safe, efficient operations remain standard practice.
A key difference between 2-Phenoxyethylbromide and more conventional benzyl halide reagents shows itself in selectivity. The phenoxyethyl moiety shifts the electron density of the molecule, making it less reactive than primary alkyl bromides. In practice, this translates into slower but more controlled substitutions, compared with common alkylating agents like benzyl bromide or benzyl chloride. We have witnessed firsthand how this property benefits those seeking to minimize side reactions, especially in high-value pharmaceutical and specialty material syntheses. Our process improvements have been built on this observation: by reducing “overalkylation,” we extend catalyst life and improve atom economy, which is becoming increasingly important as sustainability pressures mount.
Chloride analogs, although a popular low-cost option, introduce some headaches that chemists on the ground must handle. The bromide ion leaves more readily, making the substitution process more efficient and resulting in a faster conversion. Fewer by-products mean simpler purification and fewer downstream headaches for process engineers tasked with material recovery. This has allowed us to streamline plant operations during multi-ton production runs, freeing up resources otherwise tied up in rework or disposal management. Customers typically cite time savings of up to two days per batch when switching to well-formulated 2-Phenoxyethylbromide, which makes a real difference in competitive timelines.
Years in the trenches have shown us how minor adjustments make a major difference in 2-Phenoxyethylbromide manufacturing. Precise temperature profiles during bromination are not just theoretical—they influence purity, color, and reproducibility in a measurable way. We operate with automated, sequenced batch reactors, which enables tight control of temperature and stirring, so the risk of localized overheating or incomplete reaction is minimized. Our operators track progress by in-process NMR and GC checks, because we’ve seen the costly fallout that comes from failing to spot subtle deviations during long reaction cycles.
Once the crude reaction mixture is ready, our purification teams use fractional distillation under reduced pressure. At this point, the human element matters most: knowing when to cut fractions and being able to smell or spot minute traces of carryover. It’s not a step that can be reliably automated, as experienced staff recognize off-notes or color drifts far sooner than a sensor set alone. By retaining this hands-on oversight, we consistently deliver lots with the bright, pale yellow character of a well-made batch—signaling both purity and freshness.
We have resisted the push for universal “one-size-fits-all” processes. Instead, our team tailors each run for customer requirements, whether it be for ultra-high purity pharmaceutical applications or industrial formulations that prioritize batch-to-batch consistency over extreme grades of refinement. Receiving honest feedback from end-users—sometimes voicing concerns over minor residue or unexpected olfactory notes—drives our continuous improvement. The conversations we’ve had with R&D customers and plant technicians have changed specific steps as much as any academic literature or regulatory guidance.
One lesson stands clear in the specialty chemical field: not all 2-Phenoxyethylbromide suppliers produce the same standard of product. In our experience, customers who move from trading houses or resellers to direct-from-manufacturer procurement report a notable reduction in shipment delays, product variability, and unplanned technical queries. We don’t rely on what is printed in an external compliance certificate; our internal labs verify each batch prior to shipment, using high-resolution spectroscopy and chromatography to check for potential interference compounds that may never show up in routine assays.
We’ve seen firsthand how quality lapses cost time and money. A pharmaceutical firm looking to scale up a new pain management compound once received a contaminated batch from an unverified supplier; the result was an entire week lost remediating reactor fouling—an entirely preventable setback had they worked with a manufacturer that tracks each production lot from raw material to shipment. This is not an isolated tale; such stories drive our commitment to in-house quality, because the cost of scrapping a kilo of product is trivial compared to the downtime and lost credibility when a bulk campaign stalls.
Compliance is not just about ticking boxes; real-world handling of halogenated compounds requires vigilance, proactive risk management, and a willingness to invest in effluent and atmospheric monitoring. Our plant abides by continuous air and water discharge tracking, recognizing that releases of bromine-containing by-products impact both the environment and our license to operate. Our team has adopted solvent-recycling strategies and closed-circuit scrubbers for off-gas, drastically reducing the potential for accidental exposures.
Feedback from environmental compliance auditors drives us to develop greener process pathways. By limiting use of auxiliary bromine sources and reusing process solvents, not only do we improve our environmental footprint, but we also reduce raw material consumption—aligning with new regulatory guidance and customer expectations. These steps are not optional extras, but everyday priorities that influence how much value we provide and how much trust we command from safety-oriented partners.
After years supplying bulk quantities to heavy industry and smaller volumes to academic innovators, we’ve learned how vital just-in-time logistics and stable material quality are to project success. Market volatility, transport disruptions, and surges in downstream demand cause frequent headaches for buyers when sourcing less common intermediates. Because we manage inventory from precursor to finished product, customers benefit from short lead times and rapid resupply. During global supply chain disruptions, time and again this level of control made possible a steady flow of raw materials for plants and pilot projects. People counting on us for uninterrupted synthesis coordination depend on reliability, and our focus remains squarely on eliminating preventable shortages.
Direct collaboration often unlocks solutions that no specification sheet provides. In one project, a custom polymer synthesis required altering our purification regime to address an unforeseen downstream reactivity. The project team shared their analytical data and concerns, and our process chemists adapted the workflow to achieve the required selectivity and purity—without disrupting the customer’s timeline. Expanding beyond the minimum technical standard, we see our role as troubleshooting partners, drawing on every relevant experience to turn new challenges into opportunities for improvement.
Researchers developing next-generation pesticides brought us a challenge: they faced inconsistent results with generic grades and frequent batch-to-batch variability. Together, we ran a short production campaign targeting enhanced traceability, including tighter impurity tracking and custom packaging to shield the sensitive molecule from light and air. The end result was a robust supply chain that allowed their development work to proceed smoothly through field trials and into early commercialization. The project reminds us why it pays to seek a manufacturer whose approach is built on hands-on understanding, rather than the lowest price per kilo.
Switching to well-controlled batches of 2-Phenoxyethylbromide reshapes reaction schemes, bringing practical improvements to everyday process development. Some clients in the specialty polymer industry have told us that yields rise simply because the batch-to-batch control eliminates the guesswork from scale-up. Pharmaceutical customers often point out another benefit: their technical teams spend less time troubleshooting unexplained chromatographic peaks, and more time optimizing new synthetic steps. Time and cost savings gained through improved starting material quality seldom appear on a procurement spreadsheet, but make all the difference during struggling discovery or process optimization campaigns.
Our plant operators and development chemists notice the difference, too. Process safety risks drop, waste reduction goals become more attainable, and equipment utilization rates rise when reagents behave predictably. These operational improvements scale up the economic and environmental value delivered, supporting both bottom lines and sustainability goals in a single move.
No chemical factory remains static, and we invest consistently in both equipment upgrades and staff expertise. Our teams participate in regular cross-training sessions, not just for compliance but because hands-on know-how is irreplaceable in this field. The ever-evolving demands from advanced materials science, pharmaceuticals, and crop protection industries spur ongoing innovation in both product refinement and logistics. Continual dialogue with our customers, regulatory agencies, and technical partners ensures that practices evolve alongside new research and market needs.
Looking out over the next decade, we see demand for specialty reagents rising, driven by both the rapid growth in biopharma research and broader adoption of green chemistry. As regulatory scrutiny increases, customers rightly expect tighter guarantees and deeper technical support from manufacturers. We built our reputation not on broad claims, but on every accurately weighed drum, every expertly filtered fraction, every honest conversation about what works and what could go wrong. In the messy reality of chemical manufacturing, trust is not conferred by a certificate but earned one production lot at a time.
Choosing 2-Phenoxyethylbromide from a manufacturer who combines technical discipline with deep experience delivers advantages that go far beyond what is written on a specification sheet. Reliable quality, customer partnership, and relentless pursuit of better process outcomes make the difference when stakes are high and timelines tight. This is the standard we strive for with every batch, and the commitment that has carried our partners’ projects from idea to market. For those investing in new syntheses, scale-up, or discovery, dependable supply and technical integrity continue to unlock possibilities in chemistry that matter.