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HS Code |
930318 |
| Chemical Name | N-Methylhomoveratrylamine |
| Cas Number | 13189-14-9 |
| Molecular Formula | C11H17NO2 |
| Molecular Weight | 195.26 |
| Iupac Name | 1-(3,4-dimethoxyphenyl)-N-methylpropan-2-amine |
| Synonyms | 3,4-Dimethoxy-N-methyl-2-phenylpropan-1-amine |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 332.7°C at 760 mmHg |
| Density | 1.04 g/cm3 |
| Solubility | Soluble in organic solvents |
| Smiles | CC(CC1=CC(=C(C=C1)OC)OC)NC |
| Inchi | InChI=1S/C11H17NO2/c1-8(12-2)7-9-5-6-10(13-3)11(4)14-9/h5-6,8,12H,7H2,1-4H3 |
As an accredited N-Methylhomoveratrylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of N-Methylhomoveratrylamine, sealed with a screw cap, labeled with hazard information and CAS number. |
| Shipping | N-Methylhomoveratrylamine is shipped in secure, tightly sealed containers, protected from light, moisture, and incompatible substances. The chemical is transported according to applicable regulations for laboratory chemicals, with appropriate labeling and documentation. Shipping may require temperature control, hazard labeling, and adherence to local, national, and international regulations for safe handling and transit. |
| Storage | N-Methylhomoveratrylamine should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep the container tightly sealed and store under an inert atmosphere, such as nitrogen, if possible. Avoid incompatible substances, especially strong oxidizers and acids. Ensure the storage area is secure and clearly labeled, following all relevant chemical safety regulations. |
Applications of N-Methylhomoveratrylamine in Industrial ManufacturingN-Methylhomoveratrylamine serves as a critical synthesis intermediate for a range of advanced organic compounds. As a manufacturer, we supply this raw material to highly specialized downstream sectors that require stringent process controls and compliance with industry standards. Below are the principal industrial application paths and technical integrations for N-Methylhomoveratrylamine. 1. Pharmaceutical Intermediates for CNS Drug SynthesisLeading pharmaceutical manufacturers use N-Methylhomoveratrylamine as an intermediate in the multi-step synthesis of central nervous system (CNS) therapeutics, notably selective monoamine oxidase inhibitors and related neuroactive compounds. The product is introduced after primary amine protection stages, acting as a methylated amine donor before downstream condensation, cyclization, or alkylation reactions. This application adheres strictly to pharmacopeial-grade material quality, validated by regulatory filings. Finished products include prescription CNS medications and alkaloid derivatives. Industry compliance standards
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2. Agrochemical Active Ingredient SynthesisMajor agrochemical producers apply N-Methylhomoveratrylamine for the tailored synthesis of pesticide and herbicide building blocks. The methylated amine structure affords targeted functional group introduction, optimizing the physicochemical properties of select active pesticide ingredients. Entry into the synthetic route typically occurs post-halogenation or aromatic ring substitution, ensuring compatibility with controlled-pressure organic synthesis systems. The process requires documented material traceability and impurity control. Industry compliance standards
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3. Fragrance and Aroma Chemical DevelopmentLeading aroma and specialty chemical firms utilize N-Methylhomoveratrylamine for the manufacture of musk analogues and fragrance compounds, exploiting its methylated aromatic backbone to impart distinct olfactory notes. Controlled reaction sequences—such as Mannich or reductive amination—integrate the amine during late-stage synthesis, enabling precision tuning of volatility and tenacity. Downstream QC laboratories verify residual solvents and amine content as per global fragrance safety protocols. Industry compliance standards
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4. Fine Chemical Synthesis for Fluorescent Dye ProductionProducers of high-purity fluorescent and luminescent dyes employ N-Methylhomoveratrylamine for the formation of complex heterocyclic cores. This raw material advances integration during cyclization or amide formation steps within multi-stage batch systems. The resulting compounds exhibit specific absorption spectra, key for analytical and imaging applications. All production runs maintain contamination-free environments to pass optical performance and emission purity criteria. Industry compliance standards
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5. API-Grade Intermediate for Veterinary CompoundsVeterinary pharmaceutical manufacturers incorporate N-Methylhomoveratrylamine as a key intermediate in the synthesis of antiemetic and sedative agents for animal healthcare. The material is charged during controlled, closed-system reactions under GMP-certified facilities. Processes closely monitor impurity profiles and retention samples, ensuring full traceability for regulatory inspections. Rigorous validation confirms the amine's structure contribution to bioactive veterinary formulations. Industry compliance standards
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6. R&D Use for Specialty Polymer SynthesisPolymer research institutes and advanced material developers use N-Methylhomoveratrylamine as a monomeric functionalizing agent for precision polymer modification projects. The aromatic amine moiety reacts during copolymer grafting or crosslinking stages to alter matrix flexibility and chemical resistance properties. Application-specific projects adhere to proprietary or published polymerization protocols under inert, controlled lab-scale settings, with experimental logs maintained for technology transfer. Industry compliance standards
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Inside a manufacturing facility, each substance we produce builds on years of accumulated know-how, repeated analysis, and constant tinkering to push benchmarks higher. N-Methylhomoveratrylamine stands out due to the care and fine-tuning built into every batch. This amine draws industry attention for its unique chemical profile, which places it in a class of starting materials critical for advanced organic synthesis. We have spent years developing means to stabilize its structure and ensure purity, helping customers achieve consistent results in research and industrial production.
Our teams regularly handle customer feedback and track usage trends, allowing us to respond not by guessing, but by implementing real improvements. It’s not uncommon for a process chemist or research director to raise a query about minor impurities or an unexpected shift in chromatographic behavior. We've seen how small, overlooked variances can derail a synthesis or reduce output yield, so every step in our process aims for control and predictability. In our work, N-Methylhomoveratrylamine arrived as a challenging but rewarding molecule to tame, given its sensitivity to moisture and certain transition metals. Verification methods, from GC-MS to NMR, form the backbone of our assurance strategy.
Years ago, we recognized that off-the-shelf standards couldn't keep up with the rising standards of pharmaceutical and fine chemical sectors. Instead of generalizing, we honed practices for targeted purification. Material produced in our reactors regularly exceeds purity requirements—meeting or exceeding 98% assay as tested by both our own protocol and independent labs. Our process minimizes side products, especially any that can interfere with the next steps in a customer's synthetic pathway.
We go beyond minimum compliance for heavy metal content, water, and residual solvents. For example, the limit of water by Karl Fischer titration is kept below 0.3%, a threshold based on what end-users report as critical for downstream chemistry. It's common for contract partners to submit their own microanalysis audits; being open to third-party scrutiny keeps our own teams motivated and focused on measurable outcomes.
End users, whether academic or industrial, draw value from N-Methylhomoveratrylamine due to its role as a methylated amine building block with the electron-rich veratryl motif. We’ve witnessed increased demand from labs working on alkaloid synthesis, where this molecule provides a reliable handle for C-N bond construction. Some groups focus on central nervous system drug candidates, exploring the 3,4-dimethoxybenzyl pattern as part of their structure-activity studies.
Teams that adopt this molecule in custom synthesis or scale-up programs notice both its atom efficiency and responsiveness to reductive amination protocols. If the target compound involves a dimethoxybenzyl unit, choosing the N-methyl derivative often trims down the protection-deprotection steps required elsewhere. These are lessons learned through joint projects with customers: we’ve sat in meetings listening to process chemists air frustrations about hard-to-handle intermediates and shared in the relief when a well-made batch proves dependable.
Unlike general alkylamines or benzylamines, N-Methylhomoveratrylamine’s electron-donating aromatic system boosts nucleophilic strength at nitrogen, which affects not just yield, but also selectivity in cyclization and functionalization reactions. Our on-site production team reviews each customer’s use case to refine packaging protocols, ensuring inert atmosphere fill and HDPE containers maintain product stability. We have come across scenarios where even a few hours in the wrong container led to product degradation—a costly lesson that fuels our diligence.
On paper, the difference between N-Methylhomoveratrylamine and the broader category of homologous amines might seem subtle; in reality, it’s significant. Even a few extra methyl groups or methoxy substitutions shift the electronic environment around the amine group. This adjustment translates into sharper reactivity profiles and alternate selectivity in standard coupling reactions. In our hands, substituting a regular benzylamine for N-Methylhomoveratrylamine never gives identical conversion or ease of purification, particularly when working with sensitive aromatic halides.
Industry trends show a marked shift away from plain benzylamines in medicinal chemistry due to metabolic lability. The veratryl frame found in this compound resists enzymatic modification, which appeals to groups tuning their molecules for improved pharmacokinetics. We watch for these signals—not just in published literature but in real-time requests and purchasing spikes. When our production planners see upticks, they alert R&D to double-check related synthetic steps for any needed upgrades.
Unlike tertiary amines or fully protected variants, the secondary nature and methyl group on N-Methylhomoveratrylamine strike a balance between reactivity and stability. Shelf life consistently surpasses 18 months under proper storage, based on long-term lot testing in our environmental stability chambers. We avoid adding unnecessary stabilizers or diluents. Nearly all feedback confirms that users see no residue after evaporation—a crucial requirement in pharmaceutical research.
Our factory doesn't run on assumptions. We invite chemists to tour, audit our lines, and look over our production logs. Trust comes from transparency, and chemical manufacturing today faces rising scrutiny, both from regulatory bodies and clients. E-E-A-T principles—especially the "Experience" part—play out at ground level, where batch consistency means more than just a checkmark on a specification sheet. It means chemistry teams can commit to long-term projects confidently, knowing their inputs won’t change unexpectedly.
Traceability down to the raw material lot forms the backbone of our in-house quality systems. Each drum carries a unique identifier, linking it to spectroscopic and chromatographic records. This hands-on attention answers a common request from customers: certainty that what arrives next month will match what proved successful in this quarter’s pilot run.
A recent partnership illustrated this approach. A drug development company came to us struggling with reproducibility during late-stage amination. After running diagnostics together, we traced the issue to a non-homogenous supply from a third-party blender. Once we shipped our certified batch, the reported conversion improved by more than 10%, and unwanted byproducts dropped sharply. Stories like this reinforce our belief that high standards on the manufacturing floor ripple through to innovation at the end user.
Manufacturing N-Methylhomoveratrylamine safely demands respect for both human and environmental health. Internal guidelines extend far beyond basic compliance, including extensive air scrubbing, solvent recovery, and procedures that reduce the risk of exposure during handling. Workers receive ongoing education about personal protection and waste segregation, and we conduct routine drills on containment in case of a spill or system malfunction.
We have learned—sometimes the hard way—that minor lapses during scale-up can have outsized consequences. Early pilot batches highlighted this molecule’s exothermic response in certain oxidation steps, prompting redesigns of venting and cooling setups. Our engineers have since implemented in-line monitoring for both pressure and temperature, lessening the likelihood of thermal runaway or vent releases. These measures reflect advice from both international safety bodies and sharp-eyed process safety engineers on our team.
Once the manufacturing stream ends, responsibility shifts to safe shipping and customer education on best handling practices. Our technical support answers questions about storage, shelf life, and suitable diluents, discussing the tradeoffs between cost and safety measures based on project size and urgency. Throughout, we publish environmental impact data for each production run—covering solvent recycling rates, energy consumption, and waste dilution outcomes. Customers share this interest, using supplier data to bolster their own sustainability reports.
We have seen firsthand where problems arise with N-Methylhomoveratrylamine. Moisture contamination crops up most frequently, especially over long-distance shipments or in humid environments. Our team tested a range of desiccants in transit, finally settling on a system that keeps weight and cost low without sacrificing absorption. Batch data now shows less than 0.1% water uptake over 90 days under worst-case logistics conditions.
Other pain points often turn up in downstream use—such as catalytic hydrogenations that falter due to trace oxidants or residual metal ions. We redesigned purification to target these, resulting in amines with heavy metal contents well below accepted industry maxima. Open feedback channels help here: instead of dismissing reported incidents, we encourage users to send back samples for joint investigation. This direct feedback loop drives steady improvement, benefitting both research and large-scale manufacturing partners.
Discussions with research groups and commercial processors reveal another priority—the need for accessible technical documentation. We respond with in-depth COAs, but also field technical calls to walk through analytical signals, optimal reaction conditions, and troubleshooting tips for different scales. Our technical team draws from both the literature and our manufacturing history, so users gain insights grounded in both theory and repeated hands-on trials.
N-Methylhomoveratrylamine's story does not stop at production. It continues in the benches and pilot plants of those who adopt it into their developmental pathways. We encourage open communication; when customers propose new uses or present challenges—unusual impurities, unexpected reactivity, scaling issues—our process scientists engage directly. Sometimes this leads to small tweaks: adjusting a crystallization solvent, swapping container linings, revisiting trace impurity thresholds; always seeking longer shelf life, safer handling, or even a more concentrated form.
Manufacturing doesn’t flourish in a vacuum. We regularly update methodologies, not only to satisfy revised regulatory checklists but because the needs of customers shift as science and technology move forward. N-Methylhomoveratrylamine’s market keeps growing as new applications emerge—each with fresh challenges, whether in drug synthesis, agrochemical development, or advanced materials. Our teams track these, investing in pilot lots and feasibility studies before moving to full production, so that no new application catches us unprepared.
Our company’s role as manufacturer places us at the coalface of both supply and technical advancement. While third-party traders might view this product as just another line item, those who spend day after day refining the chemistry grasp that end-use requirements dictate how each batch is made, authenticated, and delivered.
Supplying N-Methylhomoveratrylamine remains an ongoing education in what chemists want and why smart sourcing pays off. Our approach leans on honesty about capabilities, direct acknowledgment of challenges, and a track record of finding solutions rather than making promises that can’t be substantiated. Each improvement in our process reflects a story: an engineer studying a distillation curve, a quality officer catching a subtle chromatogram shift, a customer’s analytical chemist reporting a trace impurity that could have gone unnoticed.
We draw confidence from this shared pool of effort and discovery, always recognizing that product integrity and technical support matter. In an industry where small differences in quality and responsiveness influence both scientific outcomes and commercial success, we hold ourselves to the standards shaped by both our experience and the evolving landscape of end use.
With N-Methylhomoveratrylamine, the path between raw material and final application is paved by teamwork—our hands-on understanding of both molecule and market dovetailing with the expertise and ambitions of the chemists we serve.