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HS Code |
928926 |
| Chemicalname | 2-(2-Ethoxyphenoxy)Ethyl Bromide |
| Casnumber | 61440-79-7 |
| Molecularformula | C10H13BrO2 |
| Molecularweight | 245.12 |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 323.7°C at 760 mmHg |
| Density | 1.380 g/cm3 |
| Refractiveindex | 1.539 |
| Flashpoint | 147.3°C |
| Purity | Typically ≥97% |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | CCOC1=CC=CC=C1OCCBr |
| Storageconditions | Store in a cool, dry, well-ventilated place, away from light |
As an accredited 2-(2-Ethoxyphenoxy)Ethyl Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, tightly sealed with a screw cap, labeled "2-(2-Ethoxyphenoxy)Ethyl Bromide, 25g," with hazard warnings and handling instructions. |
| Shipping | 2-(2-Ethoxyphenoxy)Ethyl Bromide should be shipped in a tightly sealed container under dry, cool conditions. It must be clearly labeled and transported as a hazardous material, following relevant regulations for halogenated organic compounds. Avoid exposure to heat, moisture, and incompatible substances during transit to ensure safety and chemical integrity. |
| Storage | Store 2-(2-Ethoxyphenoxy)ethyl bromide in a tightly sealed container, away from moisture, light, heat, and incompatible substances such as strong bases or oxidizing agents. Keep it in a cool, dry, and well-ventilated area, preferably in a dedicated chemical storage cabinet. Proper labeling and secondary containment are recommended to prevent accidental leaks or spills. Avoid prolonged exposure to air. |
Applications of 2-(2-Ethoxyphenoxy)Ethyl Bromide in Industrial ManufacturingAs the original manufacturer of 2-(2-Ethoxyphenoxy)Ethyl Bromide, we supply this intermediate to a select number of specialty chemical producers. Its structure and reactivity serve in precision synthesis for high-performance materials and target molecules. Below are validated downstream application scenarios reflecting current industrial demand. 1. Pharmaceutical Intermediate for β-Blocker SynthesisSeveral β-blocker APIs use 2-(2-Ethoxyphenoxy)Ethyl Bromide as an etherification agent in multi-step organic synthesis. Our customers’ production integrates this raw material in O-alkylation reactions to assemble aryl ether sidechains, followed by further modifications, hydrogenations, and salt formation. Strict adherence to pharmaceutical cGMP is required to ensure trace impurity control and reproducibility at each stage, especially during scale-up for regulatory submission batches. Industry compliance standards
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2. Advanced Organic Synthesis for Agrochemical Active CompoundsMajor agrochemical synthesis chains adopt this raw material to build aryl ether linkages within crop protection molecules. Industrial end users employ stepwise alkylation with strict ratio calibration to minimize unreacted starting material and maximize purity, especially to meet GLP study requirements for new actives. Downstream processes involve catalytic substitutions, protective group cleavages, and API solidification with solvent recovery for cost efficiency. Industry compliance standards
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3. Monomer Precursor in High-Strength Epoxy Resin ManufacturingComposite material manufacturers use 2-(2-Ethoxyphenoxy)Ethyl Bromide to synthesize specialty monomers that impart flexibility and weather resistance to advanced epoxy resins. The derivatization step requires careful ratio adjustment to tailor molecular architecture, supporting downstream performance in aerospace and electronics-grade laminates. Each batch undergoes spectral QC to ensure the absence of unreacted brominated impurities prior to resinification and curing. Industry compliance standards
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4. Intermediate for Specialty Liquid Crystal CompoundsLeading liquid crystal display (LCD) chemicals manufacturers introduce 2-(2-Ethoxyphenoxy)Ethyl Bromide in the synthesis chain of tailor-made aromatic esters designed for next-generation display panels. It forms ether bonds critical to the mesogenic properties of target molecules. Material handling and purity monitoring must meet electronics industry standards to avoid impact on electro-optical characteristics. All finished batches undergo extensive HPLC and GC analysis for end-use suitability. Industry compliance standards
Typical usage ratio
Downstream process integration
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At our plant, we have spent years working with various alkyl bromide derivatives. Among them, 2-(2-Ethoxyphenoxy)ethyl bromide has built a reputation as a critical intermediate for both research and full-scale synthesis. Chemists in the lab handle this clear, colorless to slightly yellow liquid with care; its reactivity and unique structure shape its story and purpose in chemical production lines.
What sets this compound apart stems from precise molecular engineering. The structure contains an ethoxy group at the ortho position, enhancing the compound’s electron profile and favoring certain substitution reactions over generic phenoxyethyl bromides. We typically control purity above 98%. By running regular GC and HPLC checks, we verify narrow impurity tolerances. You will see most samples meeting consistent specifications, with bromine content fitting the stoichiometric design and water content kept below 0.5% by Karl Fischer analysis. Raw material selection and batch control determine everything—from how the molecule reacts in downstream synthesis to what impurities do or don’t appear at trace levels.
We have fielded countless feedback sessions with pharmaceutical and fine chemical partners about this product’s utility as a building block. It enters the ring as an ether-containing bromide; that ether linkage complicates hydrolysis under light moisture, giving a bit more flexibility when handling compared with some other bromoalkyl intermediates. You’ll find it in synthesis campaigns where selective O-alkylation or C–C bond formation is the goal; innovators in agrochemical and drug R&D come back to this base molecule for routes that need both reactivity and controlled side product formation.
Our firsthand work shows that 2-(2-ethoxyphenoxy)ethyl bromide behaves predictably with strong bases—something those who have wrestled with less stable benzyl bromides will appreciate. In comparison, the ortho-ethoxy group fine-tunes electron density, making this product different from more generic bromoalkyl ethers and regular phenoxyethyl bromide relatives. It’s also less prone to unwanted rearrangements during nucleophilic substitution. The design of this intermediate isn’t guesswork: it comes straight from iterative process adjustment and direct feedback from synthesis teams who need reliability.
Product purity and batch homogeneity matter most when the next synthesis step depends on predictable behavior. In our operations, we never cut corners with solvent drying or in-process controls. Ambient air and trace water infiltrate with surprising ease, given the molecule’s propensity to slowly react under damp conditions. We rely on freshly dried solvents and inert atmosphere charging, especially during dispatch and long-term storage preparation. Failure to maintain dryness may not ruin a batch overnight, but it can degrade yield in your own downstream chemistry.
From our end, all packaging—whether in glass or fluoropolymer-lined steel—gets inspected for microleaks and potential reactivity with contents. Our team has switched packaging lines and modified capping techniques to avoid browning and decomposition, which small traces of exposed air can sometimes accelerate. We have scrapped plenty of product rather than risk delivering a suboptimal batch. The respect for shelf life and stability comes from hard-won experience shipping to clients who monitor for off-color or odorous materials before they ever see the reactor.
Not every bromide works the same, though at first glance most look very similar in catalog listings. After long shifts on the line, we see clear dividing lines: bulk 2-bromoethyl ethers lack the ortho-ethoxy tweak, so they display different leaving group behavior in nucleophile-catalyzed couplings. The side chain oxygen of 2-(2-ethoxyphenoxy)ethyl bromide interacts directly with strong bases, affecting rate and selectivity in SN2 reactions.
In the R&D phase, some teams reach for cheaper unsubstituted phenoxyethyl bromides, but those end up more sensitive to hydrolysis. We hear this all the time from partners who switch back to our product after production pilot runs result in inconsistent yields due to starting material breakdown. There’s also a difference in byproduct volatility—our model, with its ether-linked ortho group, gives cleaner separations during workup. These differences stand out most in multi-step syntheses where the cost of unwanted reactions climbs rapidly.
From process design through scale-up, the role of 2-(2-ethoxyphenoxy)ethyl bromide fits a specific niche in the value chain. The end product rarely lands in consumers’ hands but instead inserts itself quietly into the base of pharmaceutical and protective chemical pipelines. Its reactivity profile helps cut waste in alkylation steps. In our plant, we have seen teams push for leaner, cleaner routes, and this product’s design supports that. Fewer impurities in the starting material mean less downstream reprocessing, which shapes everything from environmental footprint to plant throughput.
Synthetic chemists sometimes encounter supply chain fatigue, where repeat batches of less specialized intermediates yield variable results or trip safety alarms during process scale-up. In our experience, choosing an intermediate like this avoids such pitfalls. Because we run both small and large-scale orders directly, we have insight into how batch-to-batch consistency trickles down into productivity. These are not abstract benefits—they appear real and fast in the hands of every plant chemist and engineer who doesn’t need to troubleshoot mysterious side reactions.
Feedback from customers always shapes how we approach production for new lots. We don’t operate in a vacuum; research teams pass along information from dozens of test reactions and trial syntheses. Common uses of 2-(2-ethoxyphenoxy)ethyl bromide surface in specialty drug synthesis, pesticide active ingredient libraries, and occasionally in advanced materials projects. The feedback has led us to tweak drying processes and review how long-term storage impacts batch integrity, all to make sure the user experience improves.
One specific example comes from a pharmaceutical pilot where researchers needed both scale and purity for their key step—introducing a bulky moiety via SN2 displacement. Early runs with generic grades failed at higher temperatures, while our high-purity batches maintained reactivity and selectivity under the same pressure. The process teams verified yields through robust side-by-side assays. Their data sent us back to look at trace impurity control, which ultimately improved the uniformity of later batches.
Synthesizing and packaging 2-(2-ethoxyphenoxy)ethyl bromide involves more than putting a label on a drum of chemicals. Each part of the process—from raw material vetting, through distillation columns, to final inert gas capping—impacts the performance downstream. We draw on more than raw process parameters. Teams on the floor learn to spot lot-to-lot differences by nose or eye, long before a sample makes it to QC. Those sensory checks, plus thousands of checked runs, build strict standards into daily production. Each drum of material reflects operational choices made to answer specific needs voiced by bench chemists, scale-up engineers, and product developers.
Many buyers look for the lowest price or fastest delivery; sometimes, that works for simple chemicals. In our world, paying attention to molecular integrity and long-term batch tracking delivers hidden value. With a compound like 2-(2-ethoxyphenoxy)ethyl bromide, narrow specification control becomes pivotal when customers run extended synthesis campaigns. We have implemented database tracking for all lots, cross-referencing analytical data with customer feedback, and we trace back every impurity spike to a plant intervention. That level of discipline ensures the end users—those at the bench or on the plant floor—gain reliability where it matters.
Every crew in this trade knows the importance of safety data and open lines of communication, especially for intermediates with potential to form side products in the wrong hands. All shipments come matched to their original analytical records, not only to comply with formal regulations but also because we want customers to see exactly what arrives. We discuss thermal decomposition risks with buyers who plan for volume storage and walk through recommendations for inert handling and long-term storage.
Trust comes from answering client questions about subtle process details—including shelf life under different climates and which impurities matter most to them. We run in-house stability testing on old samples to confirm just how this compound changes beyond its standard shelf life. The results keep everyone up to speed, from production managers to R&D leads, and help us refine packaging and shipping.
The challenges in producing and distributing 2-(2-ethoxyphenoxy)ethyl bromide rarely follow simple patterns. We have seen how temperature swings in storage warehouses alter colorimetric readings or how summer humidity plays havoc with drum seals. Early on, we learned not to trust uncoated steel vessels for this intermediate; even minute traces of surface reactivity induced product yellowing. After losing a few tons to accelerated hydrogen bromide formation, we invested in atmosphere-purged storage for all staged batches. These real-world lessons push constant reviews and upgrades to our systems, so that what lands in client hands matches what worked in our test reactors.
Some of our production protocols exist solely to solve headaches customers described. For example, a team working in high-altitude locations once flagged issues with pressure equalization, prompting us to install pressure-release membranes on new drum caps. Another group’s complaint about trace chloride inspired an extra distillation loop—an expense that paid back in cleaner libraries and easier downstream QA.
Manufacturing doesn’t happen in isolation. Navigating market changes, raw material shortages, or price shocks keeps us alert. Our procurement efforts extend to working directly with key suppliers whose materials shape the trace impurity landscape for this intermediate. Seasoned production chemists on our shift team follow every load from entry silo through final product filling, making field judgment calls to maintain both supply and strict quality.
We invest in plant upgrades only if those changes ensure a measurable improvement. One example involves our vacuum distillation train; investing in tighter reflux control actually dropped several unwanted high-boiling residues by almost a full percent. That change translated directly into better recoveries for customers working with high-value downstream targets. Customers told us about improved batch outcomes and fewer filter blockages due to residue carryover. In turn, these stories reinforce the value of keeping manufacturing decisions rooted in chemist-driven priorities.
Those working with 2-(2-ethoxyphenoxy)ethyl bromide should always consider the real-world limits and capabilities built into the molecule. We recommend staged addition during pilot synthesis—rapid single-shot dosing sometimes provokes minor exotherms in sensitive systems. From our bench trials, slow ramping of temperature and sequential addition around 20–25°C generates much cleaner conversions than aggressive pushing at higher heats.
Proper solvent selection and pH control will mean the difference between modest and high yield in O-alkylation, based on our plant’s own head-to-head comparisons. Going for trace water removal before the key step makes sense; even 0.5% moisture can suppress conversion. For lab and kilo-pilot users, we always suggest sampling small amounts from the bottom of drums to check for hidden stratification, just in case temperature gradients set in during transport. Seasoned plant operators keep a close eye on spent solvent handling as well, since some hydrolysis byproducts from this intermediate emit sharp odors, acting as an early warning sign for leaks or cross-contamination.
Every batch that leaves our plant carries lessons learned from all prior orders. Our repeat clients tell us where things go right and where surprises show up. Their feedback has prompted plenty of subtle process improvements—tighter controls on raw material intake, better drum liners, even continuous operator training to pick up on weak signals before they become quality issues. We take all of this direct input seriously; it’s not enough to hit a published spec sheet. Actual production environments demand reliability that anticipates minor failures and compensates before they disrupt the customer’s workflow.
Staying on the ground, listening daily, and joining discussions at industry summits keep us aligned with evolving needs. As regulatory standards shift or as new drug syntheses emerge, we share data about performance hits and collaborate to find workarounds. Sometimes, the answer is a technical tweak—other times it’s honest communication about what a certain batch can and cannot do. Someone always pays for mistakes down the line; responsible manufacturing, grounded in operator experience and active transparency, helps limit those costs for everyone.
This ongoing partnership with users, from discovery phase up through commercial production, shapes every product improvement. It makes the difference between a generic chemical and an effective tool for real science and industry.