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3,4-Dimethoxyphenethylamine

    • Product Name 3,4-Dimethoxyphenethylamine
    • Alias 3,4-DMPEA
    • Einecs 208-962-2
    • 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
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    Specifications

    HS Code

    239190

    Chemical Name 3,4-Dimethoxyphenethylamine
    Molecular Formula C10H15NO2
    Molecular Weight 181.23 g/mol
    Cas Number 120-20-7
    Appearance Colorless to pale yellow liquid or crystals
    Melting Point 38-40°C
    Boiling Point 270-274°C
    Density 1.098 g/cm³
    Solubility In Water Slightly soluble
    Iupac Name 2-(3,4-dimethoxyphenyl)ethan-1-amine
    Pubchem Cid 61248
    Smiles COC1=CC=C(CCN)C=C1OC

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

    Packing & Storage
    Packing Amber glass bottle labeled "3,4-Dimethoxyphenethylamine, 25g" with hazard symbols, lot number, CAS: 1204-89-9, and storage instructions.
    Shipping 3,4-Dimethoxyphenethylamine is shipped in tightly sealed containers, protected from light and moisture, and clearly labeled according to regulatory guidelines. Shipping follows all relevant laws regarding hazardous chemical transport, with appropriate safety documentation provided. Packages are cushioned to prevent breakage and handled by certified carriers to ensure safe and compliant delivery.
    Storage 3,4-Dimethoxyphenethylamine should be stored in a tightly sealed container, protected from light, moisture, and heat. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Proper labeling and secure storage are essential to prevent unauthorized access. Follow all relevant safety regulations and institutional guidelines for storing laboratory chemicals.
    Application of 3,4-Dimethoxyphenethylamine

    Applications of 3,4-Dimethoxyphenethylamine in Industrial Manufacturing

    3,4-Dimethoxyphenethylamine serves as a key intermediate in several industrial manufacturing segments, supporting value-added formulations, specialty compound synthesis, and advanced material development. As a primary manufacturer, we supply this raw material to verified sectors with rigorously documented end-uses. The following application scenarios detail downstream use cases where strict industry standards, rational dosages, and repeatable process integration lead to stable finished product quality.

    1. Pharmaceutical Intermediate for Antidepressant Compound Synthesis

    Our material is widely used as an intermediate precursor in the synthesis of active pharmaceutical ingredients, especially within manufacturing routes for specific serotonin receptor modulators and related antidepressant classes. Downstream pharmaceutical compounders employ controlled alkylation, methylation, and cyclization techniques to produce the final APIs, demanding narrow control of trace impurities and consistent batch reproducibility. These processes require transparent tracking of raw material input and alignment with regulatory documentation for EVERY batch release.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP for Intermediates & APIs (EudraLex, Vol. 4, Part II)
    • US FDA 21 CFR Part 211 (CGMP for Finished Pharmaceuticals)
    • USP, EP, JP pharmacopoeial standards (when API is monographed)

    Typical usage ratio

    • 0.8–1.2 mole equivalents per target API molecule; adjusted per specific synthesis route and impurity formation risk assessments. Reactant stoichiometry must be validated via pilot-lot experiments before process scale-up.

    Downstream process integration

    • Added at the initial condensation or reductive amination step, or as a protected amine for subsequent demethylation/cyclization. Introduced into closed-vessel reactor, with process monitoring at each intermediate isolation phase.

    Final product types

    • Bulk antidepressant APIs (e.g., certain phenethylamine derivatives approved by health authorities)
    • Pharmaceutical grade fine chemicals for further formulation
    • Registered API intermediates for CMOs and CDMOs
    • Reference standards for analytical methods

    2. Advanced Dye and Pigment Intermediate in Specialty Colorants

    We supply 3,4-dimethoxyphenethylamine to pigment and dye manufacturers requiring high-purity aromatic precursors for synthesizing specialty colorants. The secondary amine functionality permits ring substitution, diazotization, or further methylation, generating custom chromophores used in technical inks, textile dyes, and industrial coatings. Regulatory alignment protects worker exposure and environmental emissions at pigment production sites.

    Industry compliance standards

    • OEKO-TEX Standard 100 (textile dyes)
    • REACH Annex XVII restrictions (aromatic amines and colorants)
    • ETAD (Ecological and Toxicological Association of Dyes and Pigments Manufacturers) recommendations
    • ISO 9001:2015 Quality Management System

    Typical usage ratio

    • 3–10% total pigment mass (w/w) as ring modifier for chromophore synthesis in batch processes; precise ratio determined by target hue specificity and color strength targets

    Downstream process integration

    • Employed during the azo coupling or phenolic ring substitution phase, typically after the primary diazotization step. Reagent added to reaction vessel under inert atmosphere, with subsequent separation, washing, and drying of pigment mass.

    Final product types

    • Specialty azo and anthraquinone dyes for textiles and plastics
    • Colorfast technical inks for industrial and security applications
    • Custom pigment dispersions for automotive paint systems
    • Printing inks for high-definition packaging and labels

    3. Intermediate for Synthesis of Performance Polymer Additives

    Our 3,4-dimethoxyphenethylamine enables the synthesis of high-performance polymer additives in the specialty materials industry. The amino aromatics are essential for constructing light stabilizers, thermal antioxidants, and UV-absorbing agents via further condensation and functional group transformation. End-users prioritize trace analysis of residual amine and consistent color yield in downstream compounding for polymers used in demanding technical environments.

    Industry compliance standards

    • ISO 14001 Environmental Management for chemical blending
    • FDA 21 CFR 177 (Polymers intended for food contact, if used for such grades)
    • RoHS 2015/863/EU (Restriction of Hazardous Substances in electrical/electronics)
    • ASTM D2565 (Xenon-Arc Light Stability, plastics coatings)

    Typical usage ratio

    • 0.5–2.5% by weight in additive synthesis reactions; actual proportion set based on polymer host matrix, targeted function (e.g., UV absorption vs. antioxidant activity), and absorption spectrum matching in final QC.

    Downstream process integration

    • Amine introduced at initial batch charge during condensation to obtain functionalized stabilizer. Resulting additive is isolated and milled before incorporation into masterbatch or compounder lines for extrusion or molding.

    Final product types

    • Hindered amine light stabilizers (HALS) for polypropylene, polyethylene
    • Thermally stable antioxidants for engineering plastics
    • UV absorbers for outdoor coatings and films
    • Specialty masterbatches for compounding houses

    4. Research-Grade Reagent in Bulk Organic Synthesis Laboratories

    We provide 3,4-dimethoxyphenethylamine under analytical-grade specifications to pilot and contract synthesis laboratories focused on medicinal chemistry, process optimization, and pathway development. Researchers apply the compound in proof-of-concept routes for both academic projects and scale-up preparation of new phenethylamine derivatives. Documentation of impurity profiles and batch consistency are supplied for full traceability in project protocols and regulatory filings.

    Industry compliance standards

    • GLP (Good Laboratory Practice) OECD Principles
    • ISO/IEC 17025 (Testing and calibration laboratories)
    • Certificate of Analysis (CoA) and Material Safety Data Sheet (MSDS) endorsement for every lot
    • Local transport and handling safety requirements, including IATA and IMDG (for international lab supply)

    Typical usage ratio

    • 1–5 mmol per reaction set-up in small scale; larger pilot batches use 10–100 g depending on protocol and target yield. Usage optimized for minimum waste and maximum conversion during method development.

    Downstream process integration

    • Loaded at initial synthetic step for library generation or structure–activity relationship (SAR) studies; frequently paired with other functional groups in varied condensation, reductive amination, or ring-closure pathways before scale-up.

    Final product types

    • Lead compound libraries for pharmaceutical R&D
    • Synthetic building blocks for advanced organic chemistry
    • Patent-protected research molecules for licensing deals
    • Analytical standards for chromatographic calibration
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    Certification & Compliance
    More Introduction

    3,4-Dimethoxyphenethylamine: Precision from the Source

    Experience Shaping Every Batch

    Decades spent in aromatic amine synthesis give us unique insight into both the consistency and potential of 3,4-Dimethoxyphenethylamine. Chemists often refer to it as “DMPEA.” For those shaping new research or scaling existing applications, a reliable stream of DMPEA can mean the difference between a stalled project and progress. Contract manufacturers who depend on a well-defined amine profile often reach out to producers with hard-earned reputations because they know unexplained variations in isomer ratio or residual solvents can cost weeks, sometimes months, of lost development effort.

    Chemical Identity that Opens Doors

    This compound stands out with the formula C10H15NO2. The structure features two methoxy groups at the 3- and 4-positions of the phenyl ring, linked to a two-carbon ethylamine chain. That arrangement sets it apart in reactivity and downstream performance from its relatives, like 2,4-dimethoxyphenethylamine, 2-phenylethylamine, or 3-methoxy derivatives. The difference in substitution pattern means noticeable shifts in melting point, solubility, and both electronic and steric influences on subsequent reactions. Across pharmacological and fine chemical research labs, feedback often remarks on how DMPEA carries an edge in purity, giving sharper chromatographic profiles compared to less purified material from less stringent routes.

    Key Specifications that Matter in Practice

    We isolate the hydrochloride salt in crystalline form—favored by most research clients—using direct precipitation and a sequence of washes, never relying on recycled solvents during key purification steps. Our average melting point sits between 198 and 202 °C, and residual water content consistently meets strict moisture controls. NMR spectra are clear, showing no extraneous aromatic impurities, and gas chromatography confirms the absence of typical synthetic side-products. After years of feedback, inspections, and thousands of analytical runs, we’ve learned the best conditions to keep lot-to-lot variation below 0.3% for content by weight.

    From our experience, the nuances of the manufacturing setup—choice of reaction vessel, temperature ramp, addition rates—have outsized impacts on color and organoleptic profile. Early years of operation involved trial after trial to eliminate trace tars, a process made possible by the absence of time pressure from external stockists or third-party buyers. Our internal quality system grew directly out of the lessons learned from pilot scale mishaps and finished batch bottlenecks, not top-down procedure copies.

    The Shaping of Applications

    A steady supply of high-purity DMPEA supports both discovery chemistry and scale-up projects. In pharma research, teams demand it as an intermediate for novel psychoactive compounds and ligand scaffolds—because the electron-donating methoxy groups change both receptor activity and synthetic “handles” for further derivatization. Those working in dye chemistry appreciate its ability to bridge aromatic frameworks for new colorants. In some custom polymer applications, research groups describe how careful control over amine functionality determines the integrity or hue of the final material.

    We have seen academic groups request lots with purposely tailored impurity profiles to probe their own catalytic systems. Process chemists sometimes ask for microbatches with intentionally adjusted water content for solubility screening. Such demands only make sense with manufacturers directly controlling each step, not intermediaries juggling third-party stocks. Over orders spanning years, consistency in spectroscopic profiles and residue analysis has built trust that “stockroom surprises” will not disrupt ongoing work.

    Differences from Other Phenethylamines

    From a chemist’s vantage point, substitution pattern matters more than almost any other factor. Side-by-side, 3,4-dimethoxyphenethylamine delivers better shelf stability than several o-methoxy or unsubstituted analogues. The ortho substitution, as found in 2,4-derivatives, often complicates purification—producing sticky oils instead of packable crystals.

    Analytical teams often report that 3,4-DMPEA provides cleaner, faster HPLC separation from by-product amines than the 2,3- or mixed-methoxy variants. Where 2-phenylethylamine oxidizes rapidly in air, 3,4-dimethoxy resist such degradation—an advantage that means no need to repeat analysis after a weekend left in the open. We see repeat business from process chemists whose stack reactors benefit from the clean melting and solution behavior offered by our version of this molecule.

    Variations in the aminoalkyl side chain—such as β-methyl or α-substituted ethylamines—give rise to different boiling points and toxicity concerns. We have focused production on the parent 3,4-dimethoxy version because, over time, feedback pointed to a sweet spot: adequate reactivity for synthetic elaboration, without the increased regulatory scrutiny found with certain higher-homologue amines.

    Real-World Feedback and Adjustments

    Interactions with hundreds of clients, including quality assurance officers and research leads, generated not just technical data but valuable working knowledge. Requests for improved solubility in water led to a refinement of our final isolation phase ten years ago—dropping an outdated filtration step that had limited access to finely crystalline material. Environmental regulators inspected our site twice during the past five years, leading to tighter control limits on residual solvents. None of those site improvements would have happened if we only responded to market trends or catalog inquiries.

    One issue observed in earlier years: end-users unhappy with dust levels. Feedback made it clear that high-static, fluffy material often contaminated vial seals and analytical balances, especially in small-scale labs. Our solution, based on real consultation with floor staff, involved switching the final sizing equipment to a low-shear granulator. Since making that change, both bulk and research customers have expressed appreciation for consistently manageable flow.

    Process Hazards and Responsible Handling

    Observing daily chemical operations shapes a realistic sense of risk and responsibility. 3,4-dimethoxyphenethylamine synthesis, particularly on the pilot scale, presents hazards unique to exothermic amination and controlled crystallization. Off-gassing during reductive amination and rapid temperature swings have resulted in foaming or splashing; new batch runs always start with a safety briefing, as dose-maximized phenethylamines demand proper controls.

    Facilities committed to ongoing training fare better with compounds like this. Close relationships with solvent suppliers reduce the chance that minor contaminants slip through and impact batch purity. Even with all protocols, unexpected reactivity sometimes appears—the learning here is to build extra capacity for physical separation and waste processing, instead of hoping minor accidents will simply vanish. Teams that handle the entire process in-house react quickly to both standard and unusual process upsets, fine-tuning humidity levels or changing filtration media in response to the demands of the compound, rather than contractual arrangements.

    Quality Assurance Grounded in Practice

    Our on-site laboratory performs not just standard titrations or basic chromatography, but regular “unknown spot” checks on both raw materials and finished product. Over the years, incidents involving low-level catalyst residues led to reinforced metal ion testing as a standard checkpoint. Downstream, EPR and NMR testing frequently detect trace oxidation that would elude color comparison alone. Partners from demanding industries learned to request certificates with attached spectra, not just the typical numeric readout.

    Regulatory compliance means more than ticking boxes—a lesson driven home by the necessity of rapid response to evolving standards. Roughly twelve years ago, an accidental leak on the packaging line demonstrated the value of hard-won process controls. Tight physical security and staged documentation for this family of chemicals arises not from theoretical concern, but from the lived reality of changes to chemical regulations and public safety consciousness worldwide.

    Beyond Simple Supply: Collaboration and Long-Term Thinking

    Collaboration with end-users distinguishes a true manufacturing relationship from commodity trading. We rely on two-way feedback—to streamline drying or blending stages, match the scale of preparation to real market needs, and minimize waste through informed process adjustments. Large R&D projects benefit from co-planning production parameters, as targeted modifications to stoichiometry or purification routes help support unique synthetic goals.

    One example—years ago, a major academic consortium requested periodic reports not just on batch completion, but on waste minimization. They used our monthly analytics to optimize their own workup and disposal, closing the loop between production and application. Input from users of 3,4-dimethoxyphenethylamine doesn’t just improve our own practices; it often shapes the standards for those following in industry and academia.

    Addressing Core Challenges in Supply and Storage

    Bench chemists often mention the frustration of receiving photodegraded or off-odor samples. To reduce that risk, we designed new packaging options—opaque, nitrogen-flushed, and in some cases pre-weighed for sensitive handling. The feedback since making this shift has been overwhelmingly positive, especially from research teams requiring reproducible results over long synthetic campaigns.

    Another topic that surfaces is shelf-life extension. Early lots suffered reduced potency when temperature and humidity guidelines went unheeded. By investing in local climate control—not just relying on shipper recommendations—we ensure that every outgoing lot meets both current application requirements and offers reliable storage for months after receipt.

    Environmental Impact and Process Evolution

    Environmental stewardship comes from the ground up. Many plants in our sector pursue simple compliance, but lessons learned during scale-up taught us otherwise. Reviewing process waste ten years ago prompted us to invest in solvent recycling, not just to save cost, but because waste acid and organic contaminants once limited both yield and team morale. Ongoing emissions monitoring allows us to stay ahead of expected standards; we schedule regular reviews with engineers to ensure not only regulatory approval, but practical improvements to air and water quality around the site.

    We shifted to greener, less hazardous reagents wherever possible. Older protocols demanded the use of large volumes of chlorinated solvents; the phasing out in favor of cleaner, more recoverable materials now eliminates an old headache—a shift our operators welcomed, knowing the risk and fatigue associated with legacy methods. The result has been both a safer work environment and cleaner product, evident in supplier reports and routine analytical summaries.

    Learning from Unexpected Outcomes

    Every manufacturer faces unexpected situations. Once, a rare double-crystallization event led to a small batch testing outside the target melting range. Immediate investigation uncovered an upstream pH fluctuation that only first-hand, hands-on oversight could detect. Far from a setback, this event led to an adjustment in our continuous monitoring system, ensuring similar issues got caught before they impacted further production.

    Another case: a well-regarded research institute once received a lot that developed faint yellowing during long-term storage. Our team identified a trace air ingress; the packaging plant changed the sealing method, and such yellowing vanished from later shipments. Experiences like these shape our understanding that reliable quality means staying vigilant, not assuming early success translates to all conditions.

    Supporting Advanced Research

    3,4-Dimethoxyphenethylamine serves synthetic chemistry teams who explore new ligands, functional materials, and advanced small-molecule scaffolds. Direct application in analytical standards underlines a need for trace consistency. For custom applications in fragrance and flavor chemistry, this amine forms a valuable structural motif, building on both its aromatic stability and reactivity. The same properties that favor downstream electrophilic substitution in one setting support cyclization and condensation in another. With input from diverse collaborators, our specifications balance needs across industries—matching academic requirements for high-resolution spectral purity, while also supplying larger volumes for pilot-scale industrial routes.

    Through ongoing dialogue, we update handling practices and batch sizes in step with requirements for both human and environmental safety, not just because of regulation, but because of direct questions and insights from users relying on repeated, reliable results.

    Responsiveness that Shapes the Industry

    Direct manufacturing relationships reveal common patterns—requests for lower peroxide levels in certain applications, or demands for particle size optimization in automated dispensation systems. Advanced users share downstream analytic data, giving us a chance to recalibrate processes in real time, sometimes scheduling new pilot runs within days to meet urgent deadlines. This shared momentum stands apart from slower, less-informed supply chains where no direct chemistry dialogue occurs.

    While logistics constraints always bring pressure, manufacturing transparency and flexibility spring from direct feedback and responsible scaling, not abstract supply chain optimization. Lessons learned and improvements implemented here reflect the shared knowledge of chemists, operators, and end-users working side by side.

    Why Direct Manufacturing Matters

    The advantage of working directly with a chemical producer becomes obvious to those who have spent time troubleshooting unexpected impurity peaks or inconsistent reactivity. By controlling all stages—raw material selection, reaction optimization, purification, and packaging—we ensure that every lot of 3,4-dimethoxyphenethylamine leaves the facility with an unbroken chain of knowledge behind it. For advanced synthesis, insightful research, and responsible chemical stewardship, those links create reliability where it matters: in real-world progress, not just on paper.