Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing sales7@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2,2-Dimethoxyethylamine

    • Product Name 2,2-Dimethoxyethylamine
    • Alias Aminoacetaldehyde dimethyl acetal
    • Einecs 'EINECS 223-996-0'
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    741505

    Cas Number 22483-09-6
    Molecular Formula C4H11NO2
    Molecular Weight 105.14
    Iupac Name 2,2-Dimethoxyethan-1-amine
    Appearance Colorless to pale yellow liquid
    Boiling Point 103-105°C at 35 mmHg
    Density 0.936 g/mL at 25°C
    Refractive Index 1.4140-1.4160
    Solubility In Water Miscible
    Flash Point 70°C
    Smiles CNCC(OC)OC
    Storage Temperature Store at 2-8°C

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

    Packing & Storage
    Packing 500 mL amber glass bottle with secure screw cap, chemical-resistant labeling displays "2,2-Dimethoxyethylamine" and hazard warnings.
    Shipping 2,2-Dimethoxyethylamine is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It should be kept away from heat, flames, and incompatible substances. The package is clearly labeled with hazard information and handled according to local, national, and international regulations for chemical transport. Transport in well-ventilated conditions is recommended.
    Storage 2,2-Dimethoxyethylamine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of heat, ignition, and incompatible materials such as strong oxidizers and acids. Protect from moisture and direct sunlight. Use appropriate chemical-resistant materials for containers and avoid prolonged exposure to air. Always follow relevant safety and regulatory guidelines when handling and storing.
    Application of 2,2-Dimethoxyethylamine

    Applications of 2,2-Dimethoxyethylamine in Industrial Manufacturing

    As a specialist manufacturer of 2,2-Dimethoxyethylamine, we supply this intermediate to industrial partners in specialized downstream sectors. Below, we present detailed application fields, unique integration pathways, and corresponding compliance points relevant to global industrial manufacturing operations.

    1. Pharmaceutical Intermediate Synthesis

    2,2-Dimethoxyethylamine serves as a highly functional building block for the synthesis of complex pharmaceutical intermediates. Its reactivity profile supports the production of active pharmaceutical ingredient (API) precursors such as beta-amino ethers used in central nervous system and cardiovascular therapeutics. Process engineers utilize this compound during N-alkylation and amidation steps, optimizing reaction pathways for high-purity output while minimizing by-products to meet ICH and pharmacopoeial requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) purity requirements for API intermediates
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice for finished pharmaceuticals)

    Typical usage ratio

    • 0.8–1.3 molar equivalents per target intermediate, adjusted according to stoichiometry and required yield in synthesis protocols

    Downstream process integration

    • Charged at controlled temperature during multi-step batch or continuous flow reactions; often introduced after initial condensation for specific N-functionalization procedures

    Final product types

    • Central nervous system API intermediates
    • Beta-amino alcohols for antiarrhythmic drugs
    • Pro-drug intermediates for oncology compounds

    2. Crop Protection Active Ingredient Manufacturing

    Agrochemical manufacturers employ 2,2-Dimethoxyethylamine in the synthesis of selective herbicides and fungicide active ingredients. The amine function facilitates the construction of oxygenated side chains crucial for target-specific activity. Production lines incorporate this intermediate in core alkylation or etherification steps, complying with strict impurity profiles and batch traceability required for high-value active substance registration.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) for pesticide actives
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • US EPA Pesticide Registration requirements

    Typical usage ratio

    • 5–12% by weight relative to total reaction mass, modified according to desired alkylation level and product form (emulsifiable concentrate, suspension concentrate, etc.)

    Downstream process integration

    • Introduced during key condensation phases; amine reacts with halo- or epoxide-functionalized substrates to generate the targeted side chain within plant protection active molecules

    Final product types

    • Selective herbicide technical concentrates
    • Systemic fungicide technical actives
    • Intermediate pre-products for insecticide synthesis

    3. Advanced Organic Coating Formulation

    Manufacturers in the specialty coatings sector use 2,2-Dimethoxyethylamine for the creation of ether-functionalized curing agents in epoxy and polyurethane systems. The amine's structure enhances crosslinking density and improves flexibility in solvent-borne and water-reducible resin dispersions. Strict VOC and reach-compliant formulations rely on precise dosing and reactivity control of this intermediate to achieve application-specific performance in automotive and industrial coatings.

    Industry compliance standards

    • REACH (EC) No 1907/2006 registration and evaluation
    • EU Directive 2004/42/EC (VOC limits for coatings)
    • ISO 9001 quality management for industrial coating processes

    Typical usage ratio

    • 2–6 parts per hundred resin (phr), adjusted for crosslinking requirements and end-use performance targets

    Downstream process integration

    • Inserted during pre-polymer or polyol modification steps; reacts via nucleophilic substitution or amine-epoxy curing to impart flexibility and resistance to chemical stress

    Final product types

    • Automotive clear coats
    • Industrial anti-corrosive primers
    • Protective topcoats for electronics housings

    4. Gas Treatment and Capture Formulations

    Process engineers in oil, gas, and air purification industries deploy 2,2-Dimethoxyethylamine in the formulation of amine-based gas scrubbing solutions. The compound offers increased CO2 and H2S absorption capacity and is compatible with multi-amine systems, enabling site-specific performance tuning. The synthesis of specialty solvents integrates this tertiary amine to improve stability, lower regeneration energy, and align with modern environmental discharge regulations.

    Industry compliance standards

    • US EPA Clean Air Act (for acid gas removal processes)
    • EN 13606:2018 for refinery gas treatment systems
    • API Standard 942 for amine unit corrosion control

    Typical usage ratio

    • 20–45% by volume in amine solvent blends; tailored according to inlet gas composition, target removal efficiency, and solvent management protocols

    Downstream process integration

    • Blended with principal amines in absorber unit charge; integrated during system mixing, followed by thermal regeneration cycles in continuous operation

    Final product types

    • CO2 removal solutions for natural gas processing
    • Tail gas treating solvents for refinery desulfurization
    • Solvent products for biogas upgrading units

    5. Polymer Additive and Modifier Production

    Chemical processers formulate polymer additives from 2,2-Dimethoxyethylamine for use in modifying polyamide and polyurethane performance. The functional group supports molecular weight control and chain termination in the synthesis of specialty block copolymers. Downstream plants integrate the compound at polymerization or compounding stages, where quality control ensures adherence to food contact or automotive regulatory standards as required by the end-use sector.

    Industry compliance standards

    • FDA 21 CFR 177.1500 (Nylon resins for food contact)
    • EU Regulation (EU) No 10/2011 for plastics intended for food contact
    • IATF 16949 for automotive quality management system when used in vehicle component plastics

    Typical usage ratio

    • 0.5–3 phr by polymer mass, determined by desired additive effectiveness, regulatory migration limits, and mechanical property specification

    Downstream process integration

    • Metered into melt polymerization reactors or compounding extruders; acts as chain stopper, molecular weight adjustor, or functional modification agent

    Final product types

    • Food contact compliant polyamide films
    • Impact-modified engineering plastics for automotive use
    • Flexible polyurethane foams with specialty end-group chemistry
    Free Quote

    Competitive 2,2-Dimethoxyethylamine prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    2,2-Dimethoxyethylamine: A Closer Look at a Key Intermediate

    Direct from Our Production Line

    As a manufacturer with decades of experience scaling up fine amine production, let me walk you through our 2,2-Dimethoxyethylamine. This molecule, with the CAS number 22483-09-6, enters the scene most often in the form of a colorless, low-viscosity liquid, easily miscible with water and a range of common solvents. But to understand what makes 2,2-Dimethoxyethylamine valuable or even distinct, it's important to talk about how we’ve learned to handle—and sometimes wrangle—the substance through years on the factory floor.

    Specifications and Material Purity

    Producing high-purity 2,2-Dimethoxyethylamine doesn’t happen by accident. Within our facilities, we focus on controlling the water content because amines can attract moisture from the air. Consistent drying in a nitrogen atmosphere helps minimize hydrolysis risk. Purity levels above 99% (by GC) have proved necessary for advanced pharmaceutical synthesis, since even small contaminants can interfere with catalytic or enzymatic reactions downstream. To achieve this, we don’t rely on a single distillation run—we employ multi-step distillation and in-process verification using gas chromatography, making sure the final product meets not just our specs, but the process sensitivities of our customers. Even after years in the business, we don’t skip leak-testing our reactors and storage tanks, because trace oxygen can trigger formation of formamides and decomposition products.

    On a practical note, viscosity stays low enough at room temperature for drum and intermediate bulk container transfers, which keeps supply chains flexible. Temperature stability also means storage doesn’t become an engineering headache, even in summer—a real concern for many amines in our portfolio that tend to form solid byproducts or need cooling jackets.

    How Our Customers Use It

    The most frequent users of 2,2-Dimethoxyethylamine are found in pharmaceutical R&D, agrochemical synthesis, and fine chemical research. Medicinal chemists turn to this amine for introducing a protected amino group onto various backbones. Its dialkoxyethyl motif makes it a reliable precursor for molecules requiring an eventual conversion to aldehydes or for building more elaborate side chains through Mannich-type reactions. The two methoxy groups offer more hydrolytic resilience than their ethoxy counterparts, enabling more selective post-reaction deprotection steps—a difference that matters during iterative library synthesis.

    Formulators in agricultural chemistry have reported better rate control during subsequent functional group installations compared to shorter chain analogs or monoalkoxyethylamines. Our batch records show this isn’t just anecdotal: tighter boiling range, fewer peroxides, and no solid residue on thermal cycling. These practical details come directly from combing through years of stability data and working alongside our customers when the unexpected crops up in pilot plants.

    What Sets 2,2-Dimethoxyethylamine Apart?

    Among its structural isomers and relatives, 2,2-Dimethoxyethylamine stands out by virtue of its double methoxy substitution. Single-methoxyethylamines, such as 2-methoxyethylamine, often hydrolyze too easily or lend themselves to side reactions under mild acidic or basic conditions. For us in manufacturing, that means higher risk of unstable end-products when customers push their syntheses hard. We’ve seen more than one project derailed by reliance on a less protected amine, resulting in unwanted aldehyde formation mid-reaction—and lost weeks of costly R&D time.

    In contrast, longer chain dialkoxyamines, like 3,3-dimethoxypropylamine, come with higher boiling points and increased handling challenges (including greater odor and lower volatility) on the industrial scale. From worker comfort and environmental controls to drum venting, every extra carbon on an amine can introduce real-world headaches. Sticking with two carbons and two methoxy groups allows 2,2-Dimethoxyethylamine to split the difference: high enough boiling point for safe handling, low enough for easy recovery and purification.

    Practical Insights from Production

    One of the lesser-known facts about 2,2-Dimethoxyethylamine is its propensity for slow degradation if stored in open containers or exposed to light for prolonged periods. While these reactions proceed slowly, going unmonitored can cause the amine number to drop by a few percent per year. We addressed this over a decade ago by switching from metal drums with poorly fitted seals to lined containers equipped with one-way valves, sharply cutting any contamination and discoloration.

    Manufacturers like us benefit from observing the subtle batch-to-batch differences that pop up from seemingly minor plant changes. For example, batch failures from mixing impeller friction can spike local heat above 90°C, causing demethylation and color body formation, which in turn gives rise to off-odors. Through hard-won troubleshooting—sometimes on a weekend night—we established stirring schedules and temperature monitors beyond basic spec sheets. Because 2,2-Dimethoxyethylamine can modestly absorb water, even a short exposure to humid air during a transfer can nudge the material above the depot’s published moisture thresholds.

    Quality Challenges and Solutions

    A lot of stories circulate about how a little inattention during distillation ruins entire lots of amine. In our own experience, refining 2,2-Dimethoxyethylamine involves walking a line: too much heat, and by-products form; too little, and product comes off with persistently high impurity tails. Years ago, a switch to vacuum distillation let us drop the working temperature, sharply cutting formation of thermally-induced tars.

    Any manufacturer will tell you, lab-scale technique doesn’t always scale up neatly. On our largest reactors, ensuring rapid cooling at fraction cut points took retrofitting pre-cooled condensers and adjusting solvent charge rates. The most noticeable improvement came in terms of peroxides and color stability; clear, almost water-white product meant fewer rejected drums at the customer’s receiving dock. This isn’t just about visual appeal: those rejecting volatile contaminants or troubleshooting yield drops later on will track the root cause to early material handling.

    Every so often we encounter off-feedstock or minor process contamination. Dedicated upstream monitoring—infrared and GC-Mass Spec—lets us catch these before they can sabotage a campaign. Regular cross-checks with downstream users ensure that subtle shifts in chromatographic profile don’t translate to reactivity changes.

    Handling and Safety Considerations

    2,2-Dimethoxyethylamine comes with the same safety responsibilities as other small, volatile amines, but we defend its low vapor pressure as a real-world safety asset. Plant operators thank us for picking compounds less likely to overwhelm site ventilation systems. We’ve invested in closed-loop pump and fill systems, in part because small exposures can lead to irritation. Setting up a good odor abatement system also keeps local air quality complaints down—this is an amine, after all, and folks working nearby will notice if we slack on carbon scrubber maintenance.

    Tank cleaning and system purges require specific procedures at our site to prevent build-up of residues that lead to exothermic decompositions. Over years of operation, we’ve developed detailed checklists and rotating crew patrols to keep storage areas within narrow temperature and humidity bands. It’s not uncommon to get a call from a customer whose own trials are showing slow yellowing or trace cloudiness—often tied to overlooked exposure to air or residual cleaning agents. We take these notes back to our QA team for routine process review, integrating customer feedback directly into our protocols.

    Supply Reliability and Traceability

    Speed and dependability matter, especially to customers waiting on intermediate shipments to keep their plants running. Our experience tells us that pinch points aren’t only about last-mile logistics; upstream hiccups like raw material shortages or a balky filtration system can short an entire week’s output. That’s why we maintain buffer stocks and provision raw materials from multiple, vetted sources. By keeping traceability intact from batch to batch, down to reactor logs and operator shift notes, we’ve been able to track and eliminate sources of recurring contamination or color drift.

    Within the past year, for example, we traced an unexpected surge of high-peroxide batches to an upstream solvent refill that had changed without advance notice. With real-time spectroscopic analysis and rapid communication between our incoming inspection and main production crews, we adapted onsite and resolved the matter before customer lines felt the impact. Subtle process shifts—like changing vacuum pump oil or adjusting inerting gas purity—become more important as customer applications demand ever-tighter consistency.

    The Role in Modern Synthetic Chemistry

    Chemical teams today want reagents that can simplify their step counts, reduce purification labor, and deliver ultimate flexibility for downstream derivatization. 2,2-Dimethoxyethylamine checks these boxes for scientists engineering new active pharmaceutical ingredients, catalysts, and monomers. The di-methoxy protection allows the introduction of amine groups in synthetically friendly form. Once incorporated, subsequent hydrolysis can unveil masked aldehydes, unlocking functional transformations not accessible using more reactive or fragile intermediates.

    Compared to traditional alkylamines, 2,2-Dimethoxyethylamine crafts a unique balance between stability during handling and versatility during synthesis. In contrast to bulk commodity amines, which often serve as simple acid scavengers, this molecule plays an active, creative role in target molecule assembly.

    Fine chemical and pharmaceutical firms have told us how employing this amine can effectively gatekeep side-reaction pathways in multi-step syntheses, reducing the cost and time needed for purification. Combining this amine with selective catalytic or enzymatic systems has revealed impressive boosts in regioselectivity, supporting the rapid development of new candidate compounds. Likewise, agrochemical innovators report that leveraging 2,2-Dimethoxyethylamine lets them achieve sharper functionalization at points where typical alkylamines fall short, all while meeting stability benchmarks set by international regulators.

    Comparative Perspective: How It Stacks Up Against Alternatives

    On the factory floor, cost, safety, and downstream compatibility set the ground rules for picking one amine over another. We’ve compared 2,2-Dimethoxyethylamine with analogs such as 2-methoxyethylamine, N-methyl-(2-methoxyethyl)amine, or even 2,2-diethoxyethylamine.

    Where shorter chain analogs sacrifice oxidative and hydrolytic stability, longer chain and higher alkoxy versions become more difficult to distill and less pleasant to handle in bulk. The two-methoxy structure manages a middle path: broad compatibility, moderate boiling point, and a lack of fouling yet still robust enough to resist decomposition over several months in closed containers.

    For continuous-flow chemistry setups, the low viscosity and forgiving volatility profile have made it a popular choice. Unlike heavier or branched amines, it doesn’t clog lines or generate pressure spikes in standard dosing pumps. We’ve had inquiries from customers who first tried more basic alkylamines, only to switch to 2,2-Dimethoxyethylamine mid-project after hitting roadblocks with inconsistent conversion rates or intractable downstream purification. Those results reach us as gratitude for making a molecule available that unlocks transformations, rather than bottlenecking them.

    Environmental Considerations and Waste Management

    From long experience with regulatory audits, we know that proper waste capture and treatment are integral for any amine process. 2,2-Dimethoxyethylamine produces hydrolysis products—methanol and formaldehyde—under strongly basic or acidic conditions. Leading customers demand assurances that secondary waste streams don’t exceed permitted levels of volatile organic output. We addressed this by updating our plant scrubber systems and shifting from open transfers to closed loading, thereby slashing the risk of fugitive emissions during hot-loading operations.

    Wastewater profiles also shifted for the better after we incorporated multi-effect evaporators and additional carbon beds onsite. Our data show a significant reduction in residual organics, keeping our operations compliant and ensuring uninterrupted product release. Onsite, continuous-monitoring sensors keep us ahead of release thresholds, with records checked weekly for compliance and five-year trend analysis. In-plant circulation not only keeps the air within limits but also improved the comfort of workers in day-to-day operations—a point that matters at the end of a long shift.

    Customer Partnerships and Transparent Communication

    We’ve learned that the best results for complex organics like 2,2-Dimethoxyethylamine come from steady contact with users. There’s no substitute for real data shared between plant and application scientists. Some of our longest partnerships began with problem-solving phone calls. One multinational pharmaceuticals group, stuck with a recurring instability in their intermediate, shipped us samples for joint testing. Together, we identified a trace by-product—lurking beneath the sensitivity of most rapid assays—that was amplified under their specific storage regime. Adaptations to our phase separation and storage brought their campaign back on track in time for a funding milestone.

    We take these lessons and adapt our production playbook to reflect them. Supplier-to-customer information loops have let us fine-tune process windows, stay ahead of regulatory shifts, and spot best practices before they turn into urgent compliance matters. Details like inerted transfer, container relabeling, and proactive dialog about shelf-life are not corporate slogans—they are actionable habits baked into every shipment cycle.

    Looking Forward: The Place of 2,2-Dimethoxyethylamine Moving Ahead

    Chemical manufacturing is evolving rapidly as demands for complexity, reproducibility, and environmental stewardship intensify. The role for building-block molecules like 2,2-Dimethoxyethylamine only expands in the drive toward more efficient, predictable syntheses. We continue to invest in process automation and in-depth analytics, so shifts in raw material quality or process drift are quickly recognized and corrected long before they show up in the finished product.

    With stricter quality standards, reduced tolerance for process variation, and increasingly sophisticated reaction schemes, there’s a clear need for intermediates that play well with a wide array of transformations. 2,2-Dimethoxyethylamine remains a key contributor—not because it marks the cutting edge of novelty, but because it brings predictability, robust performance, and proven reliability to every project it enters.

    As expectations rise for transparency, traceability, and rapid iteration in R&D pipelines, we remain committed to advancing the quality and accessibility of core amines like this one. By blending decades of factory knowledge, real-time analytics, and proactive customer engagement, we deliver not just a molecule, but the confidence that comes with a fully traceable, production-grade amine built for today’s chemistry challenges.