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2-(2-Bromoethoxy)Anisole

    • Product Name 2-(2-Bromoethoxy)Anisole
    • Alias 2-(2-Bromoethoxy)-1-methoxybenzene
    • Einecs 629-029-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    575629

    Product Name 2-(2-Bromoethoxy)Anisole
    Cas Number 34404-58-9
    Molecular Formula C9H11BrO2
    Molecular Weight 231.09 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 143-145 °C (at 20 mmHg)
    Density 1.429 g/cm³
    Melting Point N/A (typically a liquid at room temperature)
    Purity ≥98%
    Refractive Index n20/D 1.538
    Storage Temperature Store at 2-8°C
    Solubility Insoluble in water; soluble in organic solvents
    Smiles COC1=CC=CC=C1OCCBr
    Ec Number 251-985-5

    As an accredited 2-(2-Bromoethoxy)Anisole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 2-(2-Bromoethoxy)anisole, sealed with a screw cap and labeled with hazard warnings.
    Shipping 2-(2-Bromoethoxy)anisole is shipped in compliance with relevant chemical transport regulations. It is securely packed in sealed containers to prevent leaks or contamination, and appropriate labeling indicates its hazardous nature. The shipment includes safety documentation, and temperature control may be applied if necessary to ensure product stability during transit.
    Storage 2-(2-Bromoethoxy)anisole should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep the chemical away from sources of heat, ignition, and incompatible substances such as strong oxidizing agents. Store at room temperature or lower as recommended by the supplier, and ensure proper labeling and secure storage to prevent unauthorized access.
    Application of 2-(2-Bromoethoxy)Anisole

    Applications of 2-(2-Bromoethoxy)Anisole in Industrial Manufacturing

    2-(2-Bromoethoxy)Anisole serves as an essential intermediate in specialized chemical manufacturing industries. Our facility provides this product directly to producers with exacting process requirements, ensuring traceability, reliable supply, and strict compliance with global regulatory expectations. Here, we present its main industrial application scenarios, highlighting exclusive technical details relevant to downstream users.

    1. Pharmaceutical Intermediates for Anti-inflammatory APIs

    Our material is a critical building block during multi-step active pharmaceutical ingredient (API) synthesis, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs) that require selective etherification and alkylation reactions under anhydrous conditions. The use of this intermediate is tightly controlled, with batch documentation for process validation and impurity profiling. Each stage is monitored for residual bromide and anisole derivatives, impacting both yield and pharmacopoeial compliance.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • 21 CFR Part 211 (US FDA cGMP for Finished Pharmaceuticals)
    • Chinese Pharmacopoeia (ChP)
    • European Pharmacopoeia (Ph. Eur.) monograph requirements on API impurities

    Typical usage ratio

    • Added at 0.75–1.8 molar equivalents to the target aromatic core per synthetic batch; ratio adjusted based on alkylation route selectivity, reaction stoichiometry, and scale-up impurity thresholds

    Downstream process integration

    • Introduced during the third or fourth step of the API multi-stage synthesis route, entering the reaction at the etherification or bromoalkyl addition stage; downstream, the crude is further refined by solvent extraction and crystallization

    Final product types

    • Key intermediates for etoricoxib, naproxen, and similar advanced anti-inflammatory agents
    • High-purity bulk API substances exported to licensed pharmaceutical formulators

    2. Synthesis of Performance Polymers with Aromatic Ether Linkages

    Producers of specialty polymers employ our raw material to introduce controlled aromatic ether side chains, modifying thermal and mechanical properties in high-value engineering plastics. The fine-tuning of substitution patterns enables custom polymer backbones for demanding automotive and electronics applications. We support users with consistent boiling range and reactivity profiles, crucial for reproducible process throughput.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • REACH Annex XVII compliance (restricted substance control for plastics)
    • RoHS Directive 2011/65/EU (for polymer-based electrical/electronic components)
    • ASTM D4000 (Standard Classification System for Plastics)

    Typical usage ratio

    • Incorporated at 3–10 wt% of monomer feed, adapting to desired aromaticity and ether content for tailor-made polymer grades; final dosage depends on molecular weight targets and glass transition specifications

    Downstream process integration

    • Charged during initial monomer blending for polycondensation or step-growth polymerization, often co-fed with bisphenols or diacid esters; enters workflow before polymer chain extension and extrusion

    Final product types

    • Thermoplastics for precision automotive connectors
    • Electronic encapsulation compounds
    • Heat-resistant films and laminates

    3. Agrochemical Synthesis for Herbicide and Fungicide Actives

    Leading agrochemical manufacturers utilize 2-(2-Bromoethoxy)Anisole as a functional intermediate during synthesis of selective herbicidal agents and fungicidal compounds, especially those relying on substituted anisole pharmacophores. Our material’s purity minimizes by-product contamination in final formulations, which is critical for biological activity claims and environmental registration. Stringent raw material traceability supports full downstream audit trails for global supply chains.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products)
    • ISO 17025 (Testing and Calibration Laboratories for pesticide formulation)
    • China GB 4839-2009 (Quality Standard for Agrochemicals)

    Typical usage ratio

    • 0.35–1.2 molar equivalents relative to the primary substrate, depending on targeted crop selectivity spectrum and final loading in commercial formulations

    Downstream process integration

    • Fed into mid-stage alkylation or etherification steps in heterocyclic herbicide or fungicide synthesis, offering scalable routes for production batches exceeding tens of metric tons per year

    Final product types

    • Post-patent selective herbicides (e.g., specific anisole-based triarylpyrimidines)
    • Systemic fungicide concentrates
    • Agrochemical technical grade bulk for formulation houses

    4. Fine Chemical Intermediates for Liquid Crystal Precursors

    The high selectivity and purity specification of our product make it particularly suited for liquid crystal (LC) material synthesis, where precise substitution patterns define the electro-optical performance of final LC displays. Downstream producers rely on consistent halogen content and minimal isomeric impurities, as even trace contaminants can compromise alignment layer compatibility or thermal stability in display modules for automotive, medical, and consumer devices.

    Industry compliance standards

    • IEC 61340-5-1 (ESD Protection for Sensitive Electronics)
    • ISO 9001 and IATF 16949 (Automotive sector LC materials supply chain)
    • RoHS-compliant raw material sourcing
    • Internal customer-specific LC material purity standards (≤30 ppm halide content)

    Typical usage ratio

    • Ranges from 1–5 mol% as a key precursor input to LC core structure synthesis; adjusted based on required birefringence, viscosity, and dielectric anisotropy of the final LC blend

    Downstream process integration

    • Integrated during early-phase coupling reactions yielding anisole-substituted esters or ethers, prior to final fluorination or extended ring-closure processes; downstream, intermediates undergo high-vacuum distillation and chromatic purification for display-quality grades

    Final product types

    • Core LC materials for TFT-LCD panel backplanes
    • Specialty nematic and chiral dopants
    • Liquid crystal mixture masterbatches for device assembly
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    Certification & Compliance
    More Introduction

    2-(2-Bromoethoxy)Anisole: An Insider’s Look from the Manufacturer’s Bench

    Anyone who has spent time in the development or production halls of custom chemicals knows a few things about specialty intermediates. It takes steady focus to meet needs in pharmaceuticals, agrochemicals, and fine chemicals. One molecule where we see this play out clearly is 2-(2-Bromoethoxy)anisole, a compound we produce with care, using experience honed over years of hands-on synthesis at scale.

    Molecular Insight: Structure with Purpose

    The structure of 2-(2-Bromoethoxy)anisole has earned its way into project pipelines across different sectors. Chemists recognize the logical layout: an anisole core connected through an ethoxy linker, capped with a reactive bromo group. With a formula of C9H11BrO2, you won’t find unnecessary complexity. This gives the compound several practical touches:

    As a manufacturer, we appreciate how these features let our partners build elaborate molecules without starting from scratch every time. 2-(2-Bromoethoxy)anisole offers a springboard for many valuable transformations.

    Why Chemists Request It

    Almost every discussion about new product development revolves around workable handles for molecular construction. The bromoethoxy function in this molecule is a favorite tool among organic chemists. After seeing projects in both pharma and materials science, the appeal is clear:

    Our direct conversations with development chemists highlighted how much time a reliable, clean bromoethoxy intermediate can save, compared to older multi-step options that leave too much debris. Purity matters, and the design of this molecule simplifies purification.

    Unpacking Specifications: Details that Influence Results

    Industrial buyers often care about more than a simple CAS number or molecular weight. What matters as much as the core formula is the consistency and process knowledge that shapes each batch.

    Years of monitoring reaction conditions in the factory have taught us that temperature spikes during bromination can lead to unwanted dibromo byproducts. Tight control at every turn, from solvent concentration to light exposure, keeps each shipment of 2-(2-Bromoethoxy)anisole on target.

    Finished batches head for quality checks against reference samples. When the NMR spectra show clean signals at the expected positions—without echoes of raw materials or side products—then we know the batch deserves a place on our outgoing shelves. GC-MS analysis confirms it. Meeting sub-1% impurity content isn’t optional; it’s our standard. If off-target peaks appear, the lot stays put. That’s a promise driven by operational experience, not just paperwork.

    In terms of physical properties, customers value this compound’s moderate melting range and its status as a liquid or pale solid, depending on temperature. We’ve dialed in drying and purification routines to avoid occluded solvents or trace inorganic salts. Customers told us about clumping and caking in earlier commercial samples from other suppliers. By switching to antistatic packaging and using new sealing techniques, these concerns have faded.

    Usage Scenarios: Real-World Projects

    We see the requests coming from a few major directions. One of the earliest orders we filled went to a research lab focused on heterocycle synthesis for new kinase inhibitors. The methylated oxygen on the ring fended off side reactions, while the bromoethoxy arm installed as a linker opened a route to kinase-binding scaffolds.

    Agrochemical customers have also knocked on our door. In their arena, rapid assembly of large chemical libraries for field testing means each intermediate must work smoothly in combinatorial settings. Our 2-(2-Bromoethoxy)anisole lets teams multiply new lead candidates swiftly, using either solution-phase or solid-phase methods.

    Material scientists experimenting with custom polymers take advantage of the ethoxy linker to connect 2-(2-Bromoethoxy)anisole onto core units for block copolymer formation. The bromo leaving group helps these assembly steps proceed under mild conditions, sparing sensitive functionalities elsewhere in their molecules.

    From feedback and our own technical support, we know that not every run ends with a breakthrough. Even so, nobody wants to track down an obscure impurity from a contaminated intermediate. This expectation for batch-to-batch reliability has pushed our factory team to maintain high in-process controls, above what many generic suppliers offer.

    Standing Apart: Against Other Bromoethoxy Reagents

    Chemical markets overflow with lookalikes, so what sets 2-(2-Bromoethoxy)anisole apart? Our team often fields questions about subtle differences among bromoethoxy reagents, so let’s address what has come out of years hands-on at the plant and in customer projects.

    Compared to simple bromoethoxybenzenes, the methoxy at position 1 changes both reactivity and selectivity. In cross-coupling or alkylation work, customers find that standard bromoethoxybenzene undergoes side reactions more often, leading to mixtures that burn time and solvent during separation. With 2-(2-Bromoethoxy)anisole, the added resonance from the anisole motif protects more delicate partner molecules. Yields stay stronger, with fewer purification headaches.

    There’s temptation to use cheaper o-bromoethoxyphenols, but their free hydroxyl group can scramble delicate reactions and forms intractable salts with bases. We’ve had multiple project leads report polymerization and deactivation issues that never come up with our well-protected anisole variant.

    Our consistent batch color, low moisture content, and trace metals below a few ppm have all been fully traceable. Many end users chasing high throughput—where a failed run means more than lost material—have pivoted to our version to save repeated troubleshooting.

    Production Philosophy: Why Manufacturing Matters

    Synthetic chemistry rewards patience more than shortcuts. From decades in the field, our team has seen what happens when upstream yields drop, or purification steps pile up near the finish line. We built our internal controls not out of theory, but from decades of reworking failed processes.

    Each kilo starts with a fresh screening of incoming raw materials. We reject any phenol feedstock with off-odor or background peaks in its spectrum. Our solvents run through in-house distillation to guarantee low water and zero halide. During addition of the bromoethoxy chain, temperature and agitation get steady human attention, not just automation.

    Customers who tried sourcing similar molecules from low-cost traders often shared horror stories: lost cycles on contaminated raw materials, and inconsistent delivery schedules that broke research pipelines. As manufacturers, we see our obligation as more than a logistic link—it’s stewardship from the building blocks through every process stage.

    Balancing Environment, Health, and Safety

    Every synthesis of organobromine compounds brings up health and ecological concerns. Our facility runs scrubbing units for vent gases and neutralization setups for waste streams, so downstream users face less scrutiny meeting their own compliance targets. For workers, strict monitoring of airborne organobromine concentrations during production keeps our team safe, and that experience shapes how we advise safe handling downstream.

    Each year, as regulators tighten reporting requirements, customers trust our full material history, SDS transparency, and operational documentation. These elements don’t add to the chemical, but they remake how easily it passes audits and clears customs in different countries.

    Continuous Innovation: Listening and Responding

    Feedback never stops. A pharmaceutical partner recently requested tighter controls on base-sensitive impurity levels. In response, production shifted to using freshly prepared, ultra-dry base and expanded final QC by adding a sensitivity sweep. Shelf life stability grew, and yield losses from unwanted degradation dropped. Those findings now inform every production run.

    One concrete request from biotech partners involved lighter packaging that resisted shock and avoided sweating (moisture condensation) during air freight. With those comments, our shipping team experimented with new composite liners and finally dialed in a wrap that survived all climate zones—something generic vendors rarely even consider.

    This two-way street—feedback from chemists, process tweaks from our side—keeps 2-(2-Bromoethoxy)anisole production from slipping into ruts. By sharing what works and explaining the why behind each adjustment, our factory supports not just a chemical, but a shared progress in chemistry.

    Looking Ahead: Where 2-(2-Bromoethoxy)anisole Fits Next

    Already on the wish list for several late-stage syntheses, the compound has shown its muscle as teams push for scalable methods in API manufacture. Its use in next-generation OLED intermediates appeared in the past few years, taking advantage of its compatibility with palladium cross-coupling. One materials researcher cited our batch’s low chloride levels as the reason for consistent device fabrication—trace impurities disrupt surface chemistry far more than many believe.

    Biotechnology players are now testing it as a linking piece in oligonucleotide antagonists and probe molecules. Unlike older intermediates, 2-(2-Bromoethoxy)anisole can anchor to sugar or nucleobase fragments without risking oxidative damage. These reactions, highly sensitive to metal contaminants, demand batch-readiness that only experienced manufacturing can guarantee.

    What Makes a Product Reliable over the Years?

    A quality intermediate keeps its value by never surprising users. That means rigorous control, accessible technical support, and factory teams who see their impact far beyond the shop floor. Direct customer contact shapes our hours and choices every cycle.

    We see the results not just in sales, but in return messages from teams who made new molecules with our 2-(2-Bromoethoxy)anisole—sometimes a clinical lead, sometimes a pilot-scale breakthrough, sometimes a classroom demo. Making a molecule isn’t the same as competing on price, and every batch that leaves our gates carries the sum of years of craft and adjustment.

    Conclusion: Chemical Manufacturing as a Responsibility

    Every compound we send into the world, including 2-(2-Bromoethoxy)anisole, shapes discoveries in ways we may never see. We owe our customers transparency, attention, and real support—right down to the packaging we use and the documentation we attach. The lesson learned from years standing over reactors and sifting through data: a chemical earns its place in a project when it works, every time, for every user.

    For those charting new synthetic paths, our team welcomes direct questions about fit, application, or process fine-tuning. Meeting tomorrow’s challenges with molecules that empower, not complicate, sets our mission every day. Through dialogue and craft, we expect 2-(2-Bromoethoxy)anisole to open more doors as chemistry evolves.