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2-(2-Methoxyphenoxy)Ethylamine

    • Product Name 2-(2-Methoxyphenoxy)Ethylamine
    • Alias 2-(2-methoxyphenoxy)ethylamine
    • Einecs 629-725-0
    • 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

    824167

    Chemical Name 2-(2-Methoxyphenoxy)ethylamine
    Molecular Formula C9H13NO2
    Molecular Weight 167.21 g/mol
    Cas Number 26222-43-5
    Appearance Colorless to pale yellow liquid
    Boiling Point 140-144°C at 10 mmHg
    Density 1.123 g/cm3
    Solubility In Water Slightly soluble
    Refractive Index n20/D 1.539
    Flash Point 118.5°C
    Smiles COC1=CC=CC=C1OCCN
    Synonyms 2-(2-Methoxyphenoxy)ethanamine

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

    Packing & Storage
    Packing A 100g amber glass bottle labeled “2-(2-Methoxyphenoxy)ethylamine,” featuring hazard symbols, lot number, and safety handling instructions.
    Shipping 2-(2-Methoxyphenoxy)Ethylamine is shipped in tightly sealed containers to prevent moisture and contamination. It should be packaged in accordance with local and international regulations for chemical substances, labeled correctly, and protected from physical damage during transport. Ensure transportation in cool, dry conditions and compliance with safety guidelines for handling chemicals.
    Storage 2-(2-Methoxyphenoxy)ethylamine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. Protect from moisture and direct sunlight. Clearly label the container and keep it in a designated chemical storage cabinet, following all relevant safety and regulatory guidelines.
    Application of 2-(2-Methoxyphenoxy)Ethylamine

    Applications of 2-(2-Methoxyphenoxy)Ethylamine in Industrial Manufacturing

    2-(2-Methoxyphenoxy)Ethylamine serves as a specialized intermediate in sectors prioritizing fine chemical synthesis, high-value polymer modification, and advanced agrochemicals. As the original manufacturer, we supply this intermediate to certified enterprises in a controlled value chain. Below, we detail prominent industrial application scenarios, including regulatory context, technical process roles, and end-product categories.

    1. Advanced Epoxy Resin Curing Agents

    Epoxy system formulators utilize 2-(2-Methoxyphenoxy)Ethylamine as a reactive amine hardener for tailored resin performance. Its aromatic-ether group improves flexibility and chemical resistance compared to basic aliphatic amines. Large-scale composite producers integrate this amine for electrical encapsulants, adhesives, and specialty coatings where regulated content and reactivity profiles are critical. Intake occurs at the blending stage, followed by strict in-process monitoring of stoichiometry and post-cure characteristics. Finished products meet rigorous tracking from QC batch records through to final application testing.

    Industry compliance standards

    • REACH Annex XVII (Europe, for epoxy derivatives)
    • RoHS Directive 2011/65/EU (electronics encapsulation)
    • ISO 9001:2015 quality management system (process and documentation)
    • OSHA 29 CFR 1910 Subpart Z (worker exposure in U.S. manufacturing)

    Typical usage ratio

    • Used at 15%–35% weight-of-resin; adjusted for epoxy functionality and target glass transition temperature. Lower ratios reduce crosslink density for flexible systems.

    Downstream process integration

    • Introduced during pre-cure mixing with epoxy prepolymers; amine content directly controls cure rate and final mechanical strength. QC checks for stoichiometry, viscosity, and free amine content prior to casting or coating application.

    Final product types

    • Electrical potting resins
    • Automotive adhesive systems
    • Pipeline and vessel coatings
    • High-performance electronics encapsulants

    2. Agrochemical Synthesis Intermediate

    Agrochemical manufacturers use 2-(2-Methoxyphenoxy)Ethylamine as a building block for active herbicide and pesticide ingredients containing phenoxyalkyl motifs. Controlled addition occurs in amidation and coupling reactions, enabling precise molecular design for selectivity and environmental safety. Production lines observe tight GMP traceability during multi-step synthesis to avoid cross-contamination with other AI (active ingredient) streams. Analytical validation aligns with regulatory submission batches and export certificates.

    Industry compliance standards

    • FAO/WHO pesticide specifications (technical material quality)
    • ISO 17025 for analytical method validation
    • Directive 91/414/EEC (EU plant protection product approval)
    • China ICAMA certification for pesticide manufacture

    Typical usage ratio

    • Blended at 5%–22% molar ratio in stepwise synthesis, tailored to target molecule backbone and batch size. Variation depends on downstream functionalization and side-product controls.

    Downstream process integration

    • Introduced during nucleophilic substitution with acid chlorides or activated esters; integrated under nitrogen with careful temperature control. Residual amine levels checked post-reaction to ensure complete conversion.

    Final product types

    • Selective broadleaf herbicides
    • Systemic insecticides with phenoxyalkyl moieties
    • Environmental degradation studies reference substances
    • Agrochemical intermediate isolates for contracted synthesis

    3. Modified Polyurethane Systems

    Producers develop high-resilience polyurethane elastomers and foams by incorporating 2-(2-Methoxyphenoxy)Ethylamine as a chain extender or functional group modifier. The aryl ether linkage provides enhanced hydrolytic stability and UV resistance compared to standard extenders. System integrators must balance reactivity with isocyanates to control cure profiles and final material flexibility. Production lines monitor amine indices and batch homogenization through automated dosing systems, supporting detailed traceability from raw material receipt to final product testing.

    Industry compliance standards

    • ISO 9001:2015 (quality assurance for polymer production)
    • ISO 178 (flexural properties of plastics)
    • EN 71-3 (migration of certain elements in toy safety if used in relevant goods)
    • Technical Regulation TR CU 007/2011 (product safety for polyurethane goods in the Eurasian Economic Union)

    Typical usage ratio

    • Employed at 5–12 parts per hundred polyol (php); ratio tuned by required crosslink density and end-use flexibility. Higher loadings for durable foams and lower for elastic sealants.

    Downstream process integration

    • Added to the polyol blend prior to prepolymer formation; direct in-line mixing with monitoring for gel time, viscosity, and amine/isocyanate balance. QC assessment includes IR-spectra analysis to confirm incorporation.

    Final product types

    • Sealants and gaskets for industrial equipment
    • High-performance flexible foams
    • Automotive NVH (noise, vibration, harshness) control elements
    • Furniture grade cast elastomers

    4. API Intermediate for CNS-Active Compounds (Contract Manufacturing Only)

    Pharmaceutical manufacturers employ 2-(2-Methoxyphenoxy)Ethylamine as a synthetic intermediate for certain CNS-active active pharmaceutical ingredients, often those containing aryl ether-alkylamine structures. Strict segregation and documentation align with cGMP and global pharmacopoeia standards. Integration occurs in early solid-phase or liquid-phase synthetic steps, followed by extensive purification and analytical assays. End-use batches receive full regulatory dossiers for each shipment to support clinical trial or finished drug registration.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF monographs (where applicable for specific APIs)
    • EDQM CEP certification (for EU supply)
    • China CDE DMF filing for pharmaceutical raw materials

    Typical usage ratio

    • Molar ratio typically 1:1 with aryl halide/carbamate in key synthetic steps; excess limited to 10–15% to minimize mother liquor residuals. Batch-to-batch variation minimized by in-process HPLC and NMR tracking.

    Downstream process integration

    • Charged at initial coupling or alkylamination step under inert conditions; sequence followed by phase transfer, extraction, and chromatography to isolate pure intermediates. Analytical release precedes any further derivatization toward the API.

    Final product types

    • Pharmaceutical intermediates for CNS drug classes
    • Reference standards for process validation
    • cGMP-compliant drug substance supply chains
    • API building blocks for licensed finished formulations
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    Certification & Compliance
    More Introduction

    2-(2-Methoxyphenoxy)Ethylamine: A Manufacturer’s Perspective

    Introduction to 2-(2-Methoxyphenoxy)Ethylamine

    Shaping molecules isn’t just chemistry—it’s a craft, and 2-(2-Methoxyphenoxy)ethylamine stands as a good example of this attention to detail. We produce this compound in-house, making sure that not just the end product, but every part of the journey, matches the changing demand from specialty chemicals, pharmaceuticals, and advanced materials fields. Our teams follow the process directly, so purity and consistency go well beyond the numbers printed on a typical spec sheet.

    Why This Compound Earns Its Place

    2-(2-Methoxyphenoxy)ethylamine offers a unique combination: a methoxy phenyl ring coupled to an ethylamine, separated by an ether bridge. This particular structure gives it an edge in both reactivity and selectivity. Chemists prefer it for constructing intermediates that demand straightforward transformations without the tangle of unwanted byproducts. The compound’s design supports coupling reactions, nucleophilic substitutions, and formation of amide linkages with remarkable reliability. Years operating reactors and cleaning glassware after failed syntheses have taught us to appreciate intermediates that behave as predicted.

    In comparison to simpler aromatic amines or ethers, this molecule provides added control over reactivity—less prone to oxidation and not as susceptible to unwanted polymerization. Chemists gain the latitude to design stepwise functionalization processes, since the methoxy group stabilizes the aromatic ring, and the ethylamine opens doors for tailored end groups. In our experience, that means fewer headaches for production chemists and more successful scale-ups.

    Purity and Quality Control

    Quality sets the foundation for every batch. Even one part per thousand of unreacted starting material or side product can affect downstream outcomes. Our process targets purities of at least 99%, verified by GC and NMR. It doesn’t stop at numbers. We track byproducts developed at every stage, identify volatile impurities in the crude fractions, and tune our purification process using knowledge gained from years of processing both small and large lots. With each cycle, we listen to feedback from those working on the plant floor—adjusting distillation curves or fine-tuning solvent ratios after seeing what collects in the traps.

    Comparing our own samples side by side with competitors has made a big difference. We’ve noticed some suppliers cut corners at the work-up stage and leave traces of phenolic impurities—traces that disrupt downstream coupling or generate color on standing. In contrast, our batches typically stay clear and colorless in storage for extended periods, which we attribute to dedicated air and moisture exclusion steps.

    Application Areas: Insights from Real Manufacturing Use

    Most of the product heads toward synthetic intermediates for pharma targets, specialty resins, and sometimes as starting material for custom polymers. Chemists get a handle on the amine and the ether oxygen’s contrasting behaviors, exploiting the former for attachment and the latter for electronic modification. This duality finds uses in selective derivatization steps that other amines and ethers can’t achieve with the same precision. For example, one project we supported involved linking the compound into a multi-step active pharmaceutical ingredient, where no other substitution pattern would match the flexibility required for late-stage modifications.

    We’ve regularly received requests for alternative packaging, which often signals back-end usage that requires very low contamination. The compound’s behavior in solution, whether in polar or non-polar solvents, also gives it an edge—soluble enough for practical pipetting but not so hydrophilic as to complicate phases during extraction. Our feedback channels with both industrial and research chemists have helped us keep the product line relevant by offering solutions at standard concentrations or custom dilutions for direct reactor charging.

    Differences From Other Building Blocks

    Direct comparison with more common ethylamines and phenoxy derivatives reveals a number of strengths. Monoalkylamines sometimes generate volatile or malodorous fumes—2-(2-Methoxyphenoxy)ethylamine, in contrast, has proven far easier to handle even at elevated temperatures. Storage stability sets it apart. Simple arylamines can darken or oxidize even when sealed, but the ether linkage and para-methoxy substitution check that tendency, providing greater shelf stability and reducing the need for nitrogen-blanketed storage in all but the hottest months.

    We’ve also run side-by-side compatibility checks in polymerization setups. Traditional amines with similar chain lengths can trigger chain termination or branching unpredictably. Our compound’s aromatic core and controlled side groups channel the reaction more reliably, generating cleaner polymers with less post-processing needed.

    Comparing it to analogues with hydroxy, methyl, or longer-chain ether substituents shows important distinctions. Those compounds may boost solubility or processability in specific systems, but in direct coupling reactions and multi-step syntheses, our product achieves more selective transformations, minimizing messy side reactions. The presence of both methoxy and ether groups tunes the electron density on the phenyl ring and side chain, a balance we’ve seen reflected in direct feedback from partners scaling gram tests up to metric tons.

    Supporting Product Development and Customization

    Today’s research labs and production lines rely on speed and predictability. On our side, we have tracked the progression from small bottle shipments for bench-scale optimizations all the way to bulk deliveries for continuous production processes. Making things easier for researchers working under tight deadlines led us to set up rapid response protocols and pre-tested product lots—no more week-long delays for new batches to be approved.

    Some of the tougher projects involve adapting the molecule for conjugation to specialty scaffolds, such as PEGylation for biotech intermediates or linking to chromophores for diagnostics. We work alongside partners, adjusting parameters at our site to avoid side product build-up that can interfere with critical final steps. In these cases, it helps to draw on practical understanding—years seeing which filtration aids actually speed up versus slow down throughput, or which pH ranges drag down yield for subtle side reactions.

    Tailoring product flow doesn’t always involve fancy chemistry. It sometimes means catering to the realities of the shop floor: drum sizes that match the actual pump rates, and labeling that spells out exactly what’s inside, not just a code number. If a customer’s process line depends on viscosity or pourability, we run real-life pouring and mixing tests ourselves to see what works before we commit to process changes.

    Worker Safety and Environmental Responsibility

    Operating reactors and monitoring batch runs brings a close-up view of potential risks. 2-(2-Methoxyphenoxy)ethylamine, compared to many conventional amines, brings improved handling safety. It lacks the aggressive vapor and skin reactivity found in methylamine or ethylenediamine, so exposure incidents are rare across our sites. We designed ventilation and containment safeguards around actual working conditions, based on years of incident logs, rather than idealized lab test setups.

    On the environmental front, we minimize waste by recycling unused raw material back into the process wherever purity allows. Any spent solvent passes through on-site recovery, not just for cost savings but as a measure against needless disposal. Only a small volume of genuinely unusable waste heads out to certified destruction, making both regulatory compliance and community relations easier. Our team keeps an eye on emissions and adheres closely to limits set by local environmental authorities, tracking actual ambient concentrations and feeding results back into process improvements.

    Supply Reliability and Real-World Logistics

    Every plant manager has fielded anxious calls when a critical intermediate suddenly turns scarce. To head off those headaches, we combine on-site storage with flexible batch production scheduling, giving our partners supply assurance even during times of global raw material volatility. We avoid dependency on any single upstream supplier. Our stock management team adjusts inventory targets not based on projections, but on real consumption data sent by customers and historical trends.

    Quick turnaround comes down to location and experience—our plant’s proximity to both major roadways and key ports helps products reach international customers on deadline. We learned early that it’s not enough just to ship on time. It matters to make sure drums, cans, or bottles don’t ride rough or face temperature swings en route. That means custom packing and good tracking—not just paperwork, but phone calls and actual follow-up if a pallet winds up stuck in customs.

    Customer Partnerships and Technical Support

    Working with researchers and production chemists directly means gaining insight that seldom shows up in formal reports. Every time we get feedback on a sticking point—say, a shift in byproduct profile or a haze showing up unexpectedly—we involve the same people who oversaw original process development. This direct loop helps us troubleshoot and resolve issues fast, sharing lessons back to other clients facing similar challenges.

    We maintain a practice of offering technical details only when they directly help customers resolve problems. For example, providing not only analytical data, but also tips from our lab technicians about mixing order, dilution strategies, and batch charging rates that reduce foaming or clumping. When customers face unexpectedly stubborn emulsions or trouble with miscibility, our in-house chemists and plant operators pool their field-tested solutions and share those insights as part of our ongoing support.

    Regulatory Context and Compliance

    Complying with regulation isn’t just a matter of ticking boxes. Our products undergo careful review at every stage, including raw material assessment and batch release. We monitor changing global chemical controls for key starting materials and finished compounds, revisiting documentation and ensuring there won’t be shipment bottlenecks after customers have staked progress on our supply.

    Because 2-(2-Methoxyphenoxy)ethylamine touches many pharmaceutical and material R&D chains, we participate actively in sectoral bodies and return feedback from audits into our system. We’ve found that supporting customer regulatory filings with high-detail batch records and impurity profiles makes project approvals less nerve-wracking for everyone down the line. Delivering a reliable, document-backed product means fewer compliance surprises and smoother collaboration with both domestic and overseas partners.

    Process Improvements and Innovation In Practice

    No synthesis route stays unchanged forever. Continuous small-scale trials at our site let us improve reaction efficiency and reduce bottlenecks whenever materials or customer volumes change. Recent years have seen us fine-tune conditions for greater energy efficiency, yielding higher output per reactor day and less waste to manage. Often, line operators spot areas where automated controls or in-line monitoring reduce the risk of batch misses—insights drawn from running night shifts as much as from formal lab reviews.

    On a molecular level, periodic review of reaction profiles and product analyses uncovers subtle changes—perhaps triggered by shifts in raw material source or updates in water treatment protocols. By catching these early, we keep batch-to-batch consistency steady. Drawing on practical know-how, such as adjusting quench rates or rotating tank usage, builds a margin of safety for both process stability and on-time delivery.

    Efforts to lower energy and resource footprints don’t rely solely on abstract pledges. We’ve rebuilt condenser arrays, updated reaction vessel insulation, and installed higher-efficiency solvent recovery units. These updates directly cut fuel and hazardous waste bills, while environmental reports reflect measurable drops in emissions. As a manufacturing team, we share results internally and set targets based on real performance, not just paperwork.

    Customer Collaboration and Future Challenges

    Markets for both niche chemicals and widely-used intermediates keep evolving. Demand can spike unexpectedly, especially after breakthroughs in medicine, coatings, or electronics. The only way to stay ahead is ongoing collaboration with innovators and manufacturers pushing boundaries in their own industries. Our ongoing partnerships have steered us into new territory, for example by adapting purification for ultra-low color specification or changing process timing to fit into continuous production models.

    Managing change means staying alert to customer forecasts, global supply trends, and regulatory developments. Experience tells us that flexibility—backed by practical knowledge and prompt action—keeps relationships on track even through unexpected setbacks. When urgent pivots become necessary, having a team that mixes technical experience with operational savvy ensures both quality and reliability can scale along with the newest demands.

    Conclusion: Why Our Experience Matters

    Our years spent producing, packaging, and supporting users of 2-(2-Methoxyphenoxy)ethylamine have shaped our approach to supply and service. Each improvement, tweak, and direct interaction provides lessons. We take pride not just in the purity numbers but in the relationships and practical knowledge built over the years—this sets both the product and our service apart. Supporting the development and manufacture of critical chemicals calls for more than technical data: it takes transparent communication, plain hard work, and a constant drive to make things better for the next batch, the next customer, and every new challenge still to come.