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3,4-Diethoxyphenethylamine

    • Product Name 3,4-Diethoxyphenethylamine
    • Alias 3,4-DEPEA
    • Einecs 841-659-8
    • 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
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    Specifications

    HS Code

    333090

    Chemical Name 3,4-Diethoxyphenethylamine
    Molecular Formula C12H19NO2
    Molar Mass 209.28 g/mol
    Cas Number 120602-76-4
    Smiles CCOCC1=CC=C(C=C1OCC)CCN
    Solubility Unknown; likely soluble in organic solvents
    Pubchem Cid 3446547

    As an accredited 3,4-Diethoxyphenethylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle, securely sealed, labeled “3,4-Diethoxyphenethylamine” with hazard warnings, purity, and batch number displayed.
    Shipping 3,4-Diethoxyphenethylamine is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Packaging complies with chemical safety regulations, using durable materials to prevent leaks or contamination. Shipping follows hazardous material protocols, including proper labeling, documentation, and handling instructions to ensure safe and secure transit to the destination.
    Storage 3,4-Diethoxyphenethylamine should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers and acids. Ensure proper labeling and restrict access to trained personnel. Follow all local regulations for storage of chemical reagents and maintain good laboratory practices.
    Application of 3,4-Diethoxyphenethylamine

    Applications of 3,4-Diethoxyphenethylamine in Industrial Manufacturing

    3,4-Diethoxyphenethylamine serves as a specialized intermediate in several advanced chemical industries. As the direct manufacturer, we support customers in expanding production capacity, enhancing consistency, and meeting stringent regulatory criteria across selected downstream applications. Below, we detail key industry segments with practical usage, process integration, and compliance specifics for this raw material.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) Synthesis

    We supply this compound for use in the early-stage synthesis of complex pharmaceutical APIs, particularly in the development of analgesic and central nervous system drug candidates. Formulators incorporate it during multi-step organic syntheses requiring strict control of feedstock purity and trace contaminant levels. Customers adjust input ratios in response to reaction kinetics and desired conversion rate, monitored under validated laboratory protocols and full batch records. Downstream operations include controlled alkylation, coupling, and subsequent purification before API isolation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) for raw material specifications
    • U.S. FDA CFR Title 21—Part 211 (current Good Manufacturing Practice)
    • REACH registration for European market handling

    Typical usage ratio

    • Employed at 0.2–1.5 molar equivalents per target API batch
    • Adjust based on molar yield, precursor purity, and downstream reactivity
    • Lab trials confirm specific stoichiometry for scale-up
    • Strict input/output documentation for regulatory audits

    Downstream process integration

    • Feedstock in initial amination or condensation reaction sequence
    • Precursor for protected intermediate in multi-step synthesis routes
    • Batch or continuous processing lines with inline purity verification
    • Integration with automated dosing and closed reactor systems

    Final product types

    • Bulk pharmaceutical intermediates
    • Active pharmaceutical ingredients (APIs)
    • Research-grade reference standards
    • Clinical candidate compounds for drug development trials

    2. Custom Agrochemical Synthesis

    Major agrochemical producers use this compound in the synthesis of selective herbicide and pesticide molecules. The ethoxy substitution pattern provides key electronic features for target compound design, supporting reaction pathways such as ether cleavage, halogenation, or Mannich-type condensation. Manufacturers require detailed control of batch-to-batch impurity profiles to meet agricultural product registration and operator safety guidelines.

    Industry compliance standards

    • ISO 9001:2015 certified quality management systems
    • OECD Guidelines for the Testing of Chemicals
    • Global GAP (Good Agricultural Practice) substance traceability
    • National agrochemical registration (e.g., US EPA FIFRA)

    Typical usage ratio

    • Standard input: 1–5% w/w of the initial agrochemical precursor charge
    • Exact dosage set by active compound synthesis route
    • Adjusted for co-reactant purity, target crop specificity, and downstream regulatory residue limits
    • Process yields typically maximized at the lower end of this range

    Downstream process integration

    • Introduced in early-stage aromatic amine derivatization
    • Continuously supplied to reaction vessels for large-batch production
    • Inline GC/HPLC used to monitor conversion and minimize side products
    • Direct link to final formulation or encapsulation units

    Final product types

    • Active ingredient concentrates for herbicide formulations
    • Pesticide technical materials
    • Custom agrochemical intermediates
    • Research crop protection target scaffolds

    3. High-Performance Polymer Additives

    Advanced plastics manufacturers employ this amine derivative as a functional monomer modifier in specialty polymers, particularly where enhanced flexibility and dielectric properties are required. The compound is co-polymerized or grafted onto base polymer chains in solvent or melt-phase processes. Industrial blending protocols stipulate pre-drying and precise metering, ensuring uniform dispersion through twin-screw extruders or sealed reactors. Resulting finished goods must meet sector-specific thermal, electrical, and mechanical test panels.

    Industry compliance standards

    • UL 94 (plastics flammability standard)
    • ISO 11357-1:2016 (Differential Scanning Calorimetry for polymers)
    • RoHS Directive (EU Restriction of Hazardous Substances)
    • ASTM D638 (Tensile properties of plastics)

    Typical usage ratio

    • 0.5–2.5% by weight of the total polymer charge
    • Increased loading for high-modulus or antistatic formulations
    • Lower dosages for thin-film or coating applications
    • Dosage validated by end-use performance testing

    Downstream process integration

    • Direct compounding with resin pellets or powders
    • Fed into extruders or reactors post-initial polymerization
    • Molecular-level incorporation in co-monomer addition steps
    • Integrated in masterbatches for easier downstream application

    Final product types

    • Specialty polymer compounds
    • Insulative cable coatings for electronics
    • Flexible industrial films
    • High-impact molded parts

    4. Organic Electronic Material Precursors

    Producers of organic semiconductors and electronic inks source this intermediate for fine chemical routes constructing advanced arylamine-based electronic materials. Purity and moisture content are tightly controlled, as trace contaminants can dramatically affect carrier mobility and device stability. Input levels depend on molecule complexity and structural function within the target conjugated system, with precise adjustments made after evaluating spectroscopic batch analyses. Materials scientists design integration steps in conjunction with device fabrication schedules to minimize degradation and optimize yield.

    Industry compliance standards

    • ISO 14644-1 for cleanroom environmental controls
    • IEC 61249-2-21 (halogen-free electronic materials)
    • IPC-4101 for laminate and prepreg materials
    • RoHS/REACH-compliant substance management

    Typical usage ratio

    • 0.1–0.8 equiv. relative to conjugated core synthetized
    • Input scaled to desired conduction level and polymer backbone length
    • Varies for substrate versus functional thin-film use
    • Adjusted post-pilot for charge storage retention or optical benchmarking

    Downstream process integration

    • Fed into controlled organic coupling reactions in nitrogen-purged reactors
    • Grignard or Suzuki coupling steps for extended conjugation systems
    • Transferred to thin-film deposition or ink formulation post-purification
    • Logistics coordinated for synchronized device fabrication workflows

    Final product types

    • OLED and photovoltaic active layers
    • Organic field-effect transistor (OFET) precursors
    • Electronic ink additives
    • Specialty conductive polymers for flexible displays

    5. Fine Fragrance & Aroma Intermediate Production

    Manufacturers of fine aroma chemicals select this amine as a tailored building block for the synthesis of high-value ethereal and floral aroma compounds. It enters processes like selective oxidation, acetylation, or cyclization, all requiring low-odor, high-purity input verified by GC-MS. Strict batch control is implemented, as even minor impurities can impact fragrance profiles in final perfumery concentrates, compounded with IFRA guideline adherence.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • EU Regulation (EC) No 1223/2009 (Cosmetics Regulation)
    • Good Manufacturing Practice for Flavors and Fragrances (ISO 22716)
    • JECFA/FEMA GRAS status tracking as applicable

    Typical usage ratio

    • Ranges from 0.2–2% of batch mass for target aroma intermediate
    • Adjusted to impact fragrance strength and compound yield
    • Determined by analytical comparison versus standard profiles
    • Batches sampled to ensure consistent olfactory output

    Downstream process integration

    • Integration in ring-closing or ether formation steps
    • Upstream input for multi-step aroma scaffold construction
    • Inline purity and odor assessment before final distillation
    • Coordination with downstream compound blending teams

    Final product types

    • High-grade aroma intermediates
    • Fine fragrance base notes
    • Perfume accords for luxury blends
    • Flavor and fragrance concentrate batches
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    More Introduction

    3,4-Diethoxyphenethylamine: An Insight from the Manufacturer's Bench

    Understanding the Compound

    Over the years, industrial chemistry has seen its share of workhorse molecules. Some catch on and become household names, while others thrive quietly behind the scenes, enabling breakthroughs in fields ranging from pharmaceuticals to specialty coatings. 3,4-Diethoxyphenethylamine belongs firmly in the second category. With a chemical formula of C12H19NO2, it features a phenethylamine backbone bonded to diethoxy groups at the 3 and 4 positions of the aromatic ring.

    As manufacturers, we spend a lot of time with this compound from raw material sourcing through to the last batch out of the reactor. It stands out in our catalogue not for sheer volume but for versatility and utility in specific, high-value applications. Let’s dig into what makes it distinct and why customers in research, development, and production settings keep coming back for it.

    Molecular Nature and Variants

    The phenethylamine framework starts simple: a benzene ring joined to a two-carbon chain with an amine group at the end. The placement of two ethoxy groups at the 3 and 4 positions might seem minor to the untrained eye, but we see the impact every day in the lab—these modifications change solubility, reactivity, and downstream synthesis possibilities. It’s a marked difference from related compounds with methoxy groups, as the ethoxy variant generally confers greater hydrophobic character and subtle electronic effects on the ring, factors that chemical process engineers rely on while building custom molecules for their objectives.

    Currently, our production lines support 3,4-Diethoxyphenethylamine in purities suitable for standard organic synthesis—routinely above 98%, with options for finer purification where the end-use merits that investment. Each batch comes off the line with consistent melting point and NMR signatures, giving teams confidence in their own formulation steps.

    Applications that Make a Difference

    Most inquiries for 3,4-Diethoxyphenethylamine come from innovation hubs—university labs, pharmaceutical development companies, and R&D centers. Frequently, it serves as a precursor in the synthesis of more complex molecules, particularly pharmaceutical intermediates and ligands for research. Over decades of conversations with chemists and engineers, we’ve seen it support several directions:

    Our direct experience has shown researchers appreciate the reliability of the ethoxy modification. Compared to methoxy or unsubstituted phenethylamines, the diethoxy version often produces materials with increased lipophilicity, which can help chemical probes partition between phases in biological assays or materials applications. This property sometimes opens new paths for delivery vehicles, membrane permeability, or binding in enzyme active sites.

    In one recent pharmaceutical pilot, a customer developing enzyme inhibitors encountered a wall with more common phenethylamine derivatives—they couldn’t optimize the compound’s cellular uptake. Once they shifted to our diethoxy variant, the increased hydrophobicity helped clear that roadblock. We can’t take credit for their medicinal chemistry insight, but it’s satisfying to know we helped supply a tool that made a direct impact.

    How We Make It—and Why It Matters

    Production at our plant runs through standard aromatic substitution and alkylation methodologies, relying on phenethylamine as a base. Precise selection of ethoxylation reagents and reaction temperatures ensures the 3,4 substitution pattern without stray isomers. Our team has tuned yields over time, tweaking catalysts and quenching steps to minimize by-products. That devotion isn’t just academic—low-impurity batches cut down on headaches for our partners at the next step, saving days or weeks in downstream purification and analytical work.

    Every time a new order lands, we know people are counting on the reliability of our process. Subtle differences in starting material grade can turn a batch from ordinary to exceptional. For example, trace metals in base chemicals show up as problems during high-resolution NMR or mass spec analysis on the customer’s end. We maintain a tight grip on incoming quality, running our own checks before anything enters the reactor.

    A few years back, an uptick in demand allowed us to scale up batch sizes. Scaling changes a lot, not least in thermal management and solvent recovery, but our operators and lab analysts kept a close feedback loop, ensuring the product emerging from larger reactors matched what labs got from the pilot line. It’s the sort of consistency that builds partnerships over time, not just transactions.

    Regulatory and Safety Realities

    With its placement on the market, 3,4-Diethoxyphenethylamine draws scrutiny not just from our QC but also from compliance teams. Like many amine derivatives, proper storage and transportation become critical. Over the years, we’ve adapted our packaging—moving from simple HDPE bottles to tamper-evident, inert-lined drums that guard against both oxidation and leaching.

    Colleagues in logistics learned to flag regulatory changes in target markets early. Since the molecule has appeared from time to time in literature related to psychoactive research, certain jurisdictions watch shipments carefully. We work closely with our clients to clarify intended use and complete any supporting documentation, which saves time and avoids customs delays. Looking back, this proactive stance has resolved countless regulatory bottlenecks and built trust with first-time and repeat buyers.

    As for worker safety, our plant engineers designed synthesis and packaging areas with air handling and splash control—simple precautions because the compound, like many amines, doesn’t play nicely with mucous membranes and skin. Gloves and goggles have always been standard, and in some seasons, we’ve gone further with negative pressure hoods to deal with fumes.

    To manufacturers, small details in procedure make an outsized difference. Over years of audits, we’ve adopted a “right the first time” attitude: document everything, double-check scales, and if a drum looks suspect, don’t fill it. Our foreman says this approach probably saved us headaches more often than any single reactor upgrade.

    What Sets It Apart from Other Substituted Phenethylamines?

    In conversations with synthetic organic chemists, a recurring subject is the practical impact of slightly different aromatic substitutions. The methoxy analogues, like 3,4-dimethoxyphenethylamine, have been common in research and synthesis for decades—they’re straightforward to access and tend to dissolve easily in polar solvents. The switch to ethoxy groups is less routine, but it rewards those who pursue particular properties.

    The longer alkoxy chains on the ethoxy version give higher lipophilicity than their methoxy cousins. That shows up in everything from solubility testing in organic solvents to structure-docking studies on hydrophobic protein pockets. Grad students and postdocs have told us they swapped in diethoxy analogues to break solubility bottlenecks or to shake up non-covalent binding interactions in target compounds.

    From a manufacturing standpoint, the difference also means more attention on raw material purity and slightly higher handling costs—ethoxylating agents have their own quirks, and runs sometimes require additional post-reaction cleanup to hit high analytical purity. We tackle this with in-process checks, running aliquots by HPLC or GC before shipping final product. In practical terms, buyers get material that goes straight into their next step, rather than spending days removing trace side-products.

    We often compare the performance in pilot syntheses for advanced intermediates or testing new catalysts. Many teams now avoid the more traditional 3,4-dimethoxy option when tackling non-aqueous formulations, preferring the handling characteristics and downstream reactivity of the diethoxy compound.

    A few years ago, one production client reported success stabilizing a specialty catalyst with 3,4-diethoxyphenethylamine as the ligand. The extra electron-donating effect of ethoxy helped maintain catalytic activity over more cycles than the methoxy version. That isn’t a one-size-fits-all anecdote, but it’s typical of how niche shifts in molecular structure can open up distinctive chemistry.

    Challenges We Encounter and How We Address Them

    It’s not all smooth sailing. One enduring challenge involves waste stream management. Organic amine processes often generate amine-laden waters and organic solvent byproducts. About a decade ago, new discharge regulations forced us to overhaul our wastewater treatment—building out a two-stage distillation and carbon capture system. The upfront investment stung, but it resulted in lower plant emissions and higher recovery of useable solvents. Over time, those changes paid off in cleaner records with local regulators and gave us material for solvent credits.

    Supply chain wobbles also rear up now and then, especially for finely specified reagents like high-purity ethyl bromide or specialty catalysts. Our procurement team makes early commitments to multi-year supplier contracts, keeping buffer stocks where possible. During the pandemic, delivery times for glassware and even drums stretched from weeks to months, so we increased on-site inventory for vital consumables.

    We also deal with cyclical shifts in demand. Some quarters, our standard batches are enough; other times, a university research project or new pharmaceutical contract eats up inventory in a flash. To handle these swings, production lines keep flexible schedules, and the team knows how to scale quickly without trading away product integrity.

    Raw material costs climb year to year too. Instead of passing on every price increase, we work to lock in longer-term deals with partners and review our own process for savings. For instance, we switched to a catalytic continuous-flow system for a key alkylation step—a decision that cut energy use and waste per kilo produced. These incremental tweaks matter over the long haul.

    Practical Advice from a Manufacturer’s Lens

    From our vantage point, getting consistent, reliable results with 3,4-Diethoxyphenethylamine boils down to a few essentials: start with high-purity feedstocks, enforce tight process controls, and stay vigilant for shifts in both regulation and customer requirement. Every chemist who’s ever been burned by an off-spec batch knows why that matters.

    We see that direct, open feedback with clients helps everyone. Over the years, we’ve benefited from scientists sharing data back—what’s working in their syntheses, what causes hiccups at the next stage. More than a few times, a tweak in recrystallization or an extra-day drying cycle solved recurring issues, and it’s this dialogue that steers manufacturing improvement.

    On the documentation side, prepared paperwork speeds orders. Custom clearance can turn into a maze for specialty chemicals, especially with varying regulations on amines by country and end use, so upfront preparation makes everyone’s life easier.

    Finally, we learned not to underestimate scale-up challenges. What works in a round-bottom flask on a hot plate might misbehave in a 500-liter jacketed tank. Heat transfer, stirring regime, reagent order—all the details need revalidation in real-world production. Training the team to expect the unexpected helps us stay resilient.

    Why Direct Manufacturing Matters

    The discussion around chemical supply has changed dramatically since the pandemic. More customers want certainty—a direct line from the shop floor to their loading dock. As actual manufacturers, we have firsthand control over material quality, documentation, and traceability. Unlike traders or resellers, there’s no guesswork about the origin of each kilo or what happened at each step. One phone call, and we can trace a reference sample all the way back through batch records and raw material lots.

    Customers appreciate that level of traceability, especially in regulated industries or grant-funded research, where data trails and reproducibility are everything. It’s no longer enough to promise a COA (Certificate of Analysis); labs need to trust there are real process controls and human oversight behind the paper.

    The spirit of continuous improvement comes from being closest to the chemistry. Every time a filtration proves trickier or a new analytical instrument flags a contaminant, the team learns and improves the next run. The feedback loop between production, R&D, and QC is tighter here than it could ever be for a pure reseller model.

    We see our job as more than synthesis and packaging. Partners rely on honest assessment—if lead times stretch or raw material quality dips, a direct manufacturer addresses that without spin. This resilience and transparency drives many of our longest customer relationships.

    Looking Forward: What’s Next for 3,4-Diethoxyphenethylamine

    Demand for advanced building blocks only seems to grow as industries push for more nuanced, complex molecules—especially in pharmaceuticals, chemical biology, and high-performance materials. 3,4-Diethoxyphenethylamine remains on the radar of forward-thinking teams for its adaptability and unique property set. Even now, collaborations on new families of aromatic ethers and amine derivatives keep our R&D group hunting for the next improvement in synthesis methods and purity profiles.

    Environmental stewardship will shape production at every stage, from greener solvents and waste recovery to minimizing the energy footprint per kilogram shipped. Years ago, most of these discussions happened only after neighbors or regulators raised alarms. Now, it’s a core part of every new project planning session.

    Feedback loops between manufacturer and users continue to speed up. Customers no longer wait a quarter to report successes or problems; digital channels mean we get data as fast as it’s generated. This helps us address production tweaks much sooner, whether it’s a change in crystallization temperature or new filtration media.

    We see continued value in fostering direct customer relationships—not just to secure orders, but to expand shared understanding of how subtle chemical modifications play out in the real world. 3,4-Diethoxyphenethylamine serves as a case study in the value of collaborative progress, built by the people making, testing, and transforming the molecule every day.

    Conclusion: Experience Drives Results

    For those of us making chemicals, actual hands-on experience counts for more than any glossy brochure or digital catalogue. The team here knows every nuance of 3,4-Diethoxyphenethylamine production, from sourcing the cleanest feedstocks to packaging the final drum with the right documentation. The goal is to deliver chemistry that works—not just on paper, but in every beaker, flask, and process vessel our clients use.

    It’s a rewarding challenge to support innovations that rely on precise, consistent molecules. Each order, each batch, tells the story of hundreds of daily decisions made by the people who actually work with the chemistry. For researchers and manufacturers using 3,4-diethoxyphenethylamine, direct access to that expertise—and a willingness to share lessons learned—remains the real difference-maker.