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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 | 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. |
Applications of 3,4-Dimethoxyphenethylamine in Industrial Manufacturing3,4-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 SynthesisOur 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
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2. Advanced Dye and Pigment Intermediate in Specialty ColorantsWe 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
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3. Intermediate for Synthesis of Performance Polymer AdditivesOur 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
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4. Research-Grade Reagent in Bulk Organic Synthesis LaboratoriesWe 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
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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.
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.
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.
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.
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.
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.
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.
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.
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.
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 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.
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.
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.
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.
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.