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3,4,5-Trimethoxybenzylamine

    • Product Name 3,4,5-Trimethoxybenzylamine
    • Alias Benzenemethanamine, 3,4,5-trimethoxy-
    • Einecs 211-575-2
    • 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
    VTB
    Specifications

    HS Code

    208432

    Chemical Name 3,4,5-Trimethoxybenzylamine
    Cas Number 3604-57-3
    Molecular Formula C10H15NO3
    Molecular Weight 197.23
    Appearance Off-white to pale yellow solid
    Melting Point 71-73°C
    Boiling Point 310.9°C at 760 mmHg
    Density 1.15 g/cm3
    Solubility Soluble in water, ethanol, and methanol
    Purity Typically >98%
    Synonyms 3,4,5-Trimethoxybenzenemethanamine
    Storage Conditions Store at 2-8°C, tightly closed
    Smiles COC1=CC(=CC(=C1OC)OC)CN
    Inchi Key JQJUAARNKHDHHB-UHFFFAOYSA-N
    Refractive Index 1.563

    As an accredited 3,4,5-Trimethoxybenzylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 3,4,5-Trimethoxybenzylamine, 25g, is packaged in a sealed amber glass bottle with a secure screw cap and clear labeling.
    Shipping 3,4,5-Trimethoxybenzylamine is shipped in tightly sealed containers to prevent contamination and moisture exposure. It is typically packaged according to hazardous material guidelines, with labeling for proper identification and safety. Transport is carried out by certified carriers, complying with local and international regulations, ensuring safe and secure delivery.
    Storage 3,4,5-Trimethoxybenzylamine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Store at room temperature and protect from light and moisture. Proper labeling and secure storage are essential to prevent accidental exposure or spillage. Use appropriate safety precautions while handling the chemical.
    Application of 3,4,5-Trimethoxybenzylamine

    Applications of 3,4,5-Trimethoxybenzylamine in Industrial Manufacturing

    3,4,5-Trimethoxybenzylamine serves as a specialized intermediate within regulated chemical synthesis industries, contributing to multiple high-value end products. The following application overview clarifies its unique role in selected downstream sectors, outlining regulatory compliance, practical formulation ratios, integration within process flows, and the resulting finished product types.

    1. Active Pharmaceutical Ingredient (API) Synthesis in Small-Molecule Drug Manufacturing

    API manufacturers utilize this compound as a core building block during the synthesis of certain small-molecule therapeutic candidates, particularly within the oncology and central nervous system (CNS) drug classes. It participates in key alkylation and reductive amination reactions where its aromatic amine structure imparts essential functional groups to the final molecule. Its use requires strict oversight to align with regulatory expectations surrounding material traceability and impurity profiles for GMP-compliant drug substance production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Annex 1 and 13
    • United States Pharmacopeia (USP) General Chapters <797>, <1078>
    • EDQM CEP Certification (where applicable)

    Typical usage ratio

    • 0.2 – 1.0 molar equivalent, determined by target API synthetic route and stoichiometry in key coupling or amination steps. Amount adapts to minimize residual starting material and control impurity levels as per process validation data.

    Downstream process integration

    • Introduced during solution-phase synthesis following activation of a carboxylic acid or halide functional intermediate; incorporated via nucleophilic substitution or reductive amination, followed by workup and chromatographic purification prior to finishing and isolation of API.

    Final product types

    • Pharmaceutical actives including certain anti-tumor agents, antidepressants, and receptor modulators as specified in DMF/CEP submissions

    2. Advanced Chemical Intermediate for Agrochemical Active Ingredient Production

    Specialty agrochemical processing facilities employ the material to deliver unique substitution patterns on benzylamine derivatives, enabling synthesis of herbicide and fungicide content molecules. In these cases, the product undergoes condensation, acylation, and selective methylation reactions to form core ring systems or sidechains of crop protection agents, underscoring the importance of control over purity and consistency in supporting regulated field deployment.

    Industry compliance standards

    • FAO/WHO Specification for Pesticides (JMPS Guidelines)
    • OECD Principles of Good Laboratory Practice (GLP)
    • European Union Regulation EC 1107/2009 on Plant Protection Products
    • ISO 9001:2015 Quality Management certified production

    Typical usage ratio

    • 3–8% w/w in intermediate batch charge, depending on target molecule and required substitution position. Labs adjust within this range based on reaction yield and chemistry of the downstream product being prepared.

    Downstream process integration

    • Charged during early- and mid-stage synthesis as a coupling partner for carboxylic or sulfonic acid derivatives, typically in solvent reflux conditions, followed by purification steps leading to active ingredient isolation, then technical concentrate formulation.

    Final product types

    • Technical grade herbicides (e.g., methylated aromatic amine-based)
    • Fungicide intermediates for further derivatization

    3. Fine Chemical Manufacturing: Intermediate for Liquid Crystal Display (LCD) Material Synthesis

    Producers of high-performance liquid crystal chemicals apply the compound in constructing tailored aromatic intermediates, particularly when engineering mesogenic cores or sidechains requiring defined substitution with multiple methoxy functionalities. Such use demands rigorous quality agreements since impurities can directly impact display performance metrics and compliance with technical electronics standards.

    Industry compliance standards

    • IEC 61249-2-41:2012 (Halogen-Free Materials for Electronic Components)
    • Restriction of Hazardous Substances Directive (RoHS) – 2011/65/EU
    • ISO 9001:2015 Certified QC Processes
    • Customer-specific technical agreements for display-grade purity (typically >99.0%)

    Typical usage ratio

    • 5–12% by intermediate mass, based on molecular design of the final liquid crystal compound. Adjusted depending on target viscosity, clearing point, and miscibility attributes in the downstream formulation.

    Downstream process integration

    • Added at the arylation or amination stage via nucleophilic substitution, followed by workup under inert atmosphere; incorporated into repeated crystallization and distillation steps to achieve electronic-industry grade material prior to mixing into LC formulations.

    Final product types

    • High-purity liquid crystal intermediates used for active matrix LCD panels
    • Component monomers for further reaction into copolymeric LC hosts

    4. Fragrance and Aroma Chemical Intermediate Synthesis

    Specialized aroma chemical manufacturers employ this benzylamine derivative in the synthesis of complex ether and ester fragrance molecules demanding high specificity in ring substitution. Its function as a nucleophilic agent and precursor allows formation of aroma-active scaffolds with desirable olfactory notes. Manufacturers routinely monitor residual solvent and amine content to meet IFRA and global fragrance safety norms.

    Industry compliance standards

    • International Fragrance Association (IFRA) Global Fragrance Standards
    • REACH Regulation (EC) No 1907/2006
    • IFRA/IOFI Labelling Manual
    • ISO 9001 and FSSC 22000 for food-contact aromas

    Typical usage ratio

    • 1–4% by batch mass for aroma chemicals synthesis, varied according to desired concentration and reaction efficiency of specific odorant scaffold formation. Parameters set based on aldehyde or acid partner used in coupling reactions.

    Downstream process integration

    • Fed into condensation or reductive amination sequence with aldehydes, then separated via vacuum distillation. Isolation and purification ensure compliance with residual amine thresholds for perfumery and cosmetic aroma ingredient standards.

    Final product types

    • Musk and spicy ether aroma compounds for fine fragrances
    • Substituted aromatic esters for food flavorings and personal care aroma systems
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    Certification & Compliance
    More Introduction

    3,4,5-Trimethoxybenzylamine: Refining the Standards of Specialty Chemicals

    What Sets 3,4,5-Trimethoxybenzylamine Apart from Common Benzylamine Derivatives

    Working in chemical synthesis day after day teaches you there’s a world of difference between “good enough” and truly reliable intermediates. 3,4,5-Trimethoxybenzylamine delivers consistency and purity where generic benzylamines run into trouble. Its structure—three methoxy groups neatly perched on the aromatic ring—offers key handling and reactivity benefits, making it a favorite for teams focused on complex molecular design. During nitration or further alkylation, this arrangement buffers the ring, stabilizes intermediates, and saves time spent troubleshooting.

    We have years of feedback from labs and plants alike: this amine stands up to tougher process demands and scales smoothly. Compared to plain benzylamine, 3,4,5-trimethoxy substitution keeps side reactions at bay, allowing for cleaner end products and reduced purification. Without these substitutions, many multi-step reactions stumble from byproducts or harsh conditions that this product simply shrugs off. Simple amines may suit bulk commodity work, but once selectivity or downstream complexity rise, this molecule shines.

    Specifications and Purity: Meeting High Expectations

    Performance hinges on purity—ours typically runs above 98%, confirmed by advanced HPLC testing on each batch. Under close inspection, residue levels and trace contaminants can drag an entire synthesis off course, so we devote resources towards careful crystal formation and thorough drying. Typical batches come as fine white to slightly off-white powder or crystals, with melting points falling in the verified range. Residual solvents and starting materials are pushed far below industry acceptance thresholds.

    Over years investing in better reactor control, real-time monitoring, and intensive washing steps, we have dialed in a process that repeats, batch after batch. Every customer application—whether in pharmaceuticals, agrochemicals, or fine fragrance precursors—draws benefits from tighter purity standards. Consistent crystal morphology minimizes caking, improves transfer, and speeds up downstream processing. Even trace bench impurities can influence chiral reactions or produce unpredictable colors in functional end-products, so we chase the details.

    What Real-World Applications Rely on This Compound

    Our production teams have seen chemists in pharmaceutical R&D and API manufacturing flock to 3,4,5-Trimethoxybenzylamine. This amine’s unique pattern underpins synthesis of various cardiovascular drugs, CNS-active molecules, and precursors for natural product synthesis. The methoxy groups permit more predictable substitution and coupling—key for building molecular scaffolds where failure rates are costly.

    Downstream in the plant, teams blend it into batch runs making advanced intermediates—those that eventually give rise to active drug substances, or even to ultrafine dyes and pigments. Much of today’s research in bioactive molecule discovery demands building blocks like ours, where precise placement of electron-donating groups pays off in yield and selectivity. From process development pilots to kilo-scale production, supervisors and technicians report smoother crystalline isolation and fewer surprises.

    We have also collaborated with fragrance and flavor manufacturers. Where reliability matters most, our product minimizes risk of off-notes or unwanted reactivity in aroma intermediates. The product’s compatibility with a range of protective group strategies opens options for peptide and small molecule design—especially where stepwise modifications build in complexity.

    Addressing Industry Challenges: Batch Uniformity and Reliability

    It’s one thing to synthesize a complex organic molecule once, at bench scale. It’s quite another to deliver that compound, at high purity, time after time, at the ton scale. Laboratories relying on standard benzylamines report frustration at batch-to-batch inconsistencies, particularly when it comes to side-chain reactivity or purification. Subpar lots require labor-intensive reprocessing, eating into both time and cost budgets.

    Our plant tackles this problem at the root: through in-process controls. Laser-based spectroscopic monitoring, high-shear agitation, and temperature management fight lot-to-lot drift. The result is tight control, not just at the starting point but all the way through drying, isolating, and packaging. Many of our competitors cut corners, shipping materials with detectable levels of sodium, halides, or aromatic contaminants. We monitor for these, determined to eliminate hidden process headaches. For pharmaceutical use, teams consistently report minimal deviations—an achievement built from investment, iteration, and critical feedback.

    Reactivity: Electronic Effects and Process Simplicity

    Aromatic amines all share some properties, but the trimethoxy arrangement of this compound changes the game. Three methoxy groups push electron density into the ring, activating specific positions for further manipulation or providing protection from harsh oxidative conditions. This means more selectivity in standard reactions—fewer useless side products, less time in column chromatography, and more predictable endpoints.

    Without these methoxy groups, chemists often struggle to direct reactivity or achieve the yields industrial processes demand. During reductive aminations, for instance, the product’s enhanced electron-donating pattern speeds reaction, even under tougher conditions. In cross-coupling reactions, substitution proceeds concisely, enabling direct scale-up without constant need for revalidation. Colleagues in medicinal chemistry tell us the difference this makes: smoother route scouting, less debugging, and more reliable downstream analog production.

    Handling and Safety

    Our teams know that no matter how elegant a molecule may be on paper, handling it safely is just as important as its chemical properties. 3,4,5-Trimethoxybenzylamine handles cleanly, forming low-dust crystals that reduce airborne exposure. Safe packaging, using moisture-barrier liners and rigid drums, allows the material to withstand transit even between continents. Because the product remains stable under normal storage conditions, our warehouses rarely see losses or reworks due to degradation or caking.

    Operators tasked with charging reactors appreciate the lack of volatile aromatics and the mild, non-pungent odor compared to some lower-grade benzylamines or halogenated derivatives. Customers with sensitive process streams cite reduced headaches arising from fugitive emissions—especially useful in closed-system pharmaceutical environments governed by strict emission controls.

    Environmental Impact and Sustainable Production

    Concerns about sustainability and waste trace deep into modern chemical production. Some benzylamine sources still employ outdated, inefficient processes that generate aggressive solvent waste or uncontrolled emissions. Over several process improvements, we replaced older stoichiometric reduction steps with largely catalytic or hydrogenation-based approaches, reducing both energy consumption and hazardous byproducts.

    Every kilogram shipped reflects not just a synthetic step, but broader choices: renewable feedstocks where possible, closed-loop solvent recovery, and a fully documented waste management stream. Teams at our site track energy, water, and solvent usage on a rolling basis. This focus helps our partners meet their own sustainability goals and shows up in the form of less variable process performance.

    Our analytical chemists regularly study effluent streams and gas phase emissions. Where possible, we recapture, recycle, and reintegrate not just solvent, but also low-level amine residues. Customers increasingly ask about life-cycle analysis—our records and test results prove that reliable specialty chemicals can emerge from a more responsible process.

    Supporting Product Innovation: How Labs and Plants Benefit

    Across three decades in the chemical industry, requests for 3,4,5-Trimethoxybenzylamine have grown as research boundaries expand. Several academic teams publish new reactions every year relying on this molecule for ligand synthesis, natural product mimicry, or new pharmaceutical lead generation. Our site’s proximity to major research hubs gives us a direct feedback channel—you learn fast when researchers bring back real-world problems or ask for lot-specific customizations.

    Process chemists, especially in pharma, report shorter optimization times and faster pathfinding when they switch to our grade of the amine. For small to mid-sized companies that don’t have the resources for endless re-testing, this makes a difference: one less variable, quicker launches, and leaner validation dossiers. In flavors and fragrances, the same properties that benefit synthetic efficiency mean cleaner aroma expression and less risk of regulatory hurdles.

    We maintain both pilot and production-scale reactors, giving us the flexibility to support customers at every stage—from early grams for catalyst screening to multi-ton campaigns. Scale-up teams notice minimal difference in impurity pattern as batch sizes rise, a tangible benefit as process validation and audits increase in frequency and scrutiny.

    Comparison with Alternative Amines

    Engineers and chemists shopping for benzylamine derivatives often ask why not use simpler analogs. The answer traces back to electronic effects and downstream outcomes: non-substituted or mono-substituted benzylamines often give unpredictable results. Lack of sufficient electron-donating groups causes incomplete conversions and sticky side products that gum up the works at scale.

    Attempts to swap in other trimethoxybenzene derivatives lead to other headaches—less manageable amine stability, higher volatility, or incompatibility with desired protective group strategies. Many of these molecules prove fussy in continuous reactors, forming resinous byproducts or evading crystallization entirely. Controlled substitution at the 3,4,5-positions stabilizes the aromatic core, boosting tolerance for process upsets and minimizing runoff of problematic tars or oils.

    When we put samples in the hands of process chemists at trial stage, most notice the difference even before final analysis—the way the product dissolves, its crystal structure, the absence of pelleting or microclumps that complicate dosing. Rather than chasing alternate amines and accepting higher risks, teams have found long-term savings and fewer downstream bottlenecks by sticking with this well-characterized intermediate.

    Traceability, Documentation, and Process Transparency

    Quality is only as good as the ability to prove it. Our plant tracks raw materials, process controls, and finished lot data, retaining analytical sheets for each shipment. Customers in regulated industries, especially pharmaceuticals and personal care, ask us to provide traceability back to every step of manufacture. Analytical results, stability profiles, and impurity fingerprints come from in-house QA labs equipped with state-of-the-art instruments—these records not only pass audits, but speed up customer method development.

    We have worked closely with partner labs to troubleshoot, even running side-by-side analyses to confirm batch integrity. This reduces uncertainty, cuts risk of recalls, and builds confidence across supply chains. In an age where every raw material can trigger a weeks-long investigation if a batch runs off spec, full documentation matters more than ever before.

    Listening and Learning: Continuous Improvement from Practical Feedback

    Real-world chemistry throws curveballs no synthetic route can fully anticipate. Every year, our production and technical support teams meet with R&D partners to review new challenges—fresh analytical requirements, unexpected reaction failures, or tightening environmental standards. These conversations feed directly into our manufacturing playbook.

    Suppose a customer reports color issues during nitrosation. Our response doesn’t wait for regulatory push—teams will tweak purification, update standard procedures, and prepare custom documentation if needed. Problem-solving in chemistry means listening as well as making, anticipating what could go wrong, and acting before it does. Production-scale improvement often flows from bench-scale surprises—the hard-won lessons from a stubborn impurity, or a breakage during crystallization, shape our process controls for the next campaign.

    This discipline pays off across applications. It’s not about “tailoring” to second-guess every possibility, but about answering questions with facts, data, and a willingness to adjust instead of hiding behind certifications or blanket assurances.

    Shipping, Storage, and Process Support

    Reliable arrival of 3,4,5-Trimethoxybenzylamine depends on more than just a finished batch—it depends on robust packaging and secure timelines. We seal each drum with inner liners and tamperproof seals. Our customers routinely move materials between temperature ranges, sometimes facing months-long storage or cross-ocean transit. Handling rugged packaging and keeping to real nitrogen-blanketed storage can keep this product within spec for extended periods. Shipments come with full supporting paperwork and a summary sheet of tested parameters for quick intake checks.

    Once delivered, technical support teams stand ready to answer process questions—solubility profiles, re-drying protocols, and guidance on re-purification if needed. Even an established process sometimes needs a tweak based on site conditions; experience has shown that process reliability starts at the chemistry, but is completed on the production floor. Whether a partner needs to switch to continuous addition, address scale-up foaming, or prepare the material for GMP runs, teams familiar with both lab and plant conditions offer guidance because they have seen the shift from beaker to reactor wall up close.

    Future Trends and Where We See Demand Growing

    Industry patterns point toward greater demand for specialty aromatic amines with robust impurity control, not just for blockbuster drugs but for hard-to-source intermediates in niche manufacturing. The toolbox in organic synthesis grows more complex, but so do the standards: process intensification, green chemistry, and continuous manufacturing all mean the raw materials must offer more consistency than in previous decades.

    Data from the past five years—both inside our walls and from sourcing managers across the globe—confirms that repeatability, low impurity burden, and adaptability to new processes grow in value. We see orders shifting toward kilogram and ton scales for novel research APIs, small-molecule agricultural projects, and even advanced battery or surface-treatment chemistry where purity and substitution effects ripple downstream.

    Customers now demand background data—not just “COAs” but actual chromatograms, spectral overlays, and trial dissolution curves. In return, manufacturers who invest early in process transparency and supporting documentation will earn the trust and repeat business of those innovating at the front end of science and technology.

    Closing Thoughts from the Production Floor

    From years spent troubleshooting at the reactor and purifying crystalline lots, it becomes clear: details at every stage feed into results the market and the bench can measure. 3,4,5-Trimethoxybenzylamine gives modern synthesis teams a reliable foundation for demanding projects, backed by documentation, tested protocols, and a long-term commitment to fixing small issues before they turn into production headaches.

    Experience on the ground matters. Colleagues in the plant, in R&D, and in logistics come together to ensure this compound leaves our site ready for high-stakes work. Each batch shipped represents the lessons learned from the last—building on experience, responding to new needs, and refining so those who depend on our products know they can push their projects forward, batch after batch.