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2,4,6-Trimethoxybenzylamine Hydrochloride

    • Product Name 2,4,6-Trimethoxybenzylamine Hydrochloride
    • Alias 2,4,6-TMBA·HCl
    • Einecs 68430-17-1
    • 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

    786263

    Product Name 2,4,6-Trimethoxybenzylamine Hydrochloride
    Cas Number 36557-92-3
    Molecular Formula C10H16ClNO3
    Molecular Weight 233.69 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 134-138°C
    Solubility Soluble in water
    Purity Typically ≥98%
    Storage Temperature 2-8°C (Refrigerated)
    Synonyms 2,4,6-Trimethoxybenzenemethanamine hydrochloride
    Smiles COC1=CC(=C(C(=C1)OC)CN)OC.Cl
    Inchi InChI=1S/C10H15NO3.ClH/c1-12-7-4-8(13-2)10(6-11)9(5-7)14-3;/h4-5H,6,11H2,1-3H3;1H

    As an accredited 2,4,6-Trimethoxybenzylamine Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g quantity of 2,4,6-Trimethoxybenzylamine Hydrochloride is packaged in a sealed amber glass bottle with a secure screw cap.
    Shipping 2,4,6-Trimethoxybenzylamine Hydrochloride is shipped in tightly sealed containers to prevent moisture absorption and contamination. It is packaged according to regulatory guidelines for chemicals, labeled with product identification and hazard information, and transported under ambient conditions. Appropriate documentation and safety data sheets accompany each shipment to ensure safe handling and compliance.
    Storage 2,4,6-Trimethoxybenzylamine Hydrochloride should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature (15–25°C). Ensure the storage area is compatible with hydrochloride salts, away from incompatible substances, and clearly labeled. Follow relevant safety and chemical handling guidelines.
    Application of 2,4,6-Trimethoxybenzylamine Hydrochloride

    Applications of 2,4,6-Trimethoxybenzylamine Hydrochloride in Industrial Manufacturing

    As a manufacturer focused on 2,4,6-Trimethoxybenzylamine Hydrochloride, we supply this compound in high purity grades suitable for critical downstream processes. The compound serves specialized roles across pharmaceutical, agrochemical, dye synthesis, and fine chemical industries. Below, we highlight specific use cases, process details, and applicable compliance requirements for industrial partners.

    1. Pharmaceutical Intermediate for CNS-Active Molecule Synthesis

    In pharmaceutical active ingredient manufacturing, our compound’s electron-rich aromatic amine core supports benzylation steps in CNS (central nervous system) drug synthesis. This role includes serving as a key intermediate for developing dopamine receptor modulators and serotonergic agents. Manufacturers rely on this material for strictly regulated GMP routes where consistent impurity profiles directly link to regulatory filings and batch release.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 US cGMP for finished pharmaceuticals
    • EU GMP Annex 8 and 15 for process validation and documentation
    • Ph. Eur. and USP monograph reference when applicable for final APIs

    Typical usage ratio

    • 1.0–1.5 molar equivalent per theoretical drug intermediate batch
    • Adjusted based on target yield and stoichiometry optimization during route development

    Downstream process integration

    • Introduced during reductive amination or nucleophilic substitution stages
    • Filtered and analyzed for residual solvents and byproducts post-coupling
    • Serves as direct building block in high-purity batch or continuous flow reactors

    Final product types

    • Neuropsychiatric drug substances
    • Serotonin–dopamine modulator APIs
    • Precursor entities for CNS ANDA/DMF submissions

    2. Key Building Block in Agrochemical Active Ingredient Synthesis

    Agrochemical manufacturers apply 2,4,6-trimethoxybenzylamine hydrochloride in the assembly of herbicidal and fungicidal active ingredients. The methoxylated aromatic ring enhances molecular stability and environmental compatibility for select crop protection agents. Our strict traceability and batch uniformity support multi-ton custom synthesis agreements for large-scale pesticide production.

    Industry compliance standards

    • FAO/WHO pesticide specification guidelines
    • ISO 9001:2015 quality management system
    • REACH Regulation (EC) No 1907/2006 for European agrochemical registration
    • Chemical safety assessment per CLP Regulation (EC) No 1272/2008

    Typical usage ratio

    • 0.85–1.2 equivalents relative to chlorinated raw substrate per batch
    • Optimized based on purification needs and target conversion rate in multi-step synthesis

    Downstream process integration

    • Charged into condensation or alkylation reactors with stringent moisture controls
    • Monitored for conversion by HPLC or GC-MS in intermediate stage QC
    • Follow-up steps include protective group manipulations before final product isolation

    Final product types

    • Selective herbicide actives for cereal and vegetable crops
    • Systemic fungicide intermediates
    • Plant growth regulator precursors

    3. Fine Chemical Synthesis for Functional Dyes and Pigments

    Specialty dye manufacturers select 2,4,6-trimethoxybenzylamine hydrochloride for assembling chromophore segments in high-performance colorants. The compound’s aromatic reactivity allows for precise diazotization, coupling, and nucleophilic aromatic substitution steps. Its Methoxy groups improve solubility and lightfastness in engineered pigment systems used in plastics and coatings.

    Industry compliance standards

    • ISO 9001:2015 for fine chemical production
    • REACH pre-registration for dye intermediates
    • OEKO-TEX Eco-Passport compliance for textile and polymer dyes
    • Quality documentation per relevant EN 71 or ASTM standards for colorants, as required

    Typical usage ratio

    • Variable: 0.5–1.3 molar ratio, determined by the dye’s desired hue intensity and target batch size
    • Loadings adjusted to maintain consistent chroma and yield in multi-site operations

    Downstream process integration

    • Fed into reaction mixtures for diazonium salt formation and aromatic coupling
    • Employed in closed-loop reactors with automated pH and temperature control
    • Post-coupling filtration and purification required for pigment-grade output

    Final product types

    • High-purity azo and anthraquinone dyes
    • Polymer-compatible pigments for plastics
    • Stable colorant dispersions for ink and masterbatch applications

    4. Custom Intermediate for Flavor and Fragrance Molecule Production

    Aromatic chemistry specialists utilize this raw material for constructing complex core structures in synthetic flavors and perfumery compounds. Its amine functionality and steric profile enable selective alkylation and formylation steps necessary for odorant and taste active molecules, under controlled, food-grade processing conditions.

    Industry compliance standards

    • IFRA (International Fragrance Association) compliance for final blends
    • FSSC 22000 certification for food-related intermediate supply
    • FDA CFR 21 Part 172 indirect food additive regulations
    • Hazard Analysis and Critical Control Point (HACCP) system in plant operations

    Typical usage ratio

    • Typically 1.1–1.3 equivalents per target molecule, reviewed during formula scale-up trials
    • Usage rate refined to optimize downstream yield and reduce byproduct formation

    Downstream process integration

    • Applied in in situ amination or reductive alkylation within jacketed, stainless steel reactors
    • Monitored for complete reaction via HPLC and GC-FID methods
    • Pilot and full-scale batches segregated to prevent cross-contamination as per food safety SOPs

    Final product types

    • Synthetic musk and floral intermediate derivatives
    • Flavor precursors for beverages, confectionery, and bakery end users
    • Alkylated aromatics for fine fragrance compounding

    5. Specialty Polymer and Resin Modifier Synthesis

    In advanced materials manufacturing, formulators integrate this compound as a functional group donor in resin and specialty polymer modification. The trimethoxybenzylamine moiety reacts during resin curing or post-modification, imparting specific solubility or flexibility traits for end-use in adhesives, coatings, and engineered plastics.

    Industry compliance standards

    • ISO 14001:2015 for environmental management in chemical industries
    • RoHS Directive 2015/863/EU for electronics-grade polymer additives
    • REACH Annex XVII for restricted substance protocols in final polymer matrices
    • ISO 9001:2015 documentation for resin additive batch tracing

    Typical usage ratio

    • Low dosing: 0.2–0.6% weight/weight, tailored for specific polymer matrix reactivity
    • Adjusted after performance lab-trials to meet end-use mechanical or thermal properties

    Downstream process integration

    • Charged into batch reactors during polymerization or post-polymer modification
    • In-line addition compatible in solvent-borne and waterborne resin systems
    • Blend stability and dispersal quality assured via QC sample pulls every processing shift

    Final product types

    • UV-resistant polymer coatings
    • Industrial adhesives for electronics and automotive applications
    • Thermoplastic masterbatches with customized solubility or flexibility profiles
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 2,4,6-Trimethoxybenzylamine Hydrochloride in the Lab and Beyond

    Product Overview and the Manufacturer’S Perspective

    Producing 2,4,6-Trimethoxybenzylamine Hydrochloride isn’t just about churning out another catalog line. This compound reflects countless hours invested in reaction optimization, purification steps, and careful batch testing. In our facility, every process—from raw material sourcing to the controlled crystallization that forms this product—has been shaped by feedback from medicinal chemists and academic researchers who continually push for improved reliability and quality.

    We label it as Model: 2,4,6-Trimethoxybenzylamine Hydrochloride, keeping things straightforward for traceability. With a molar mass of 245.7 g/mol and an appearance that ranges consistently as a white to off-white crystalline powder, this compound fits into a specific niche that demands high purity. Over the years, customers have asked for different mesh sizes and solubility profiles, so we’ve steadily improved our process to remove trace impurities and moisture that would otherwise interfere with sensitive reactions.

    Seeing the Compound in Action: Usage and Application Fields

    Our process suits the demands of those performing synthetic steps in pharmaceutical development. When we started producing 2,4,6-Trimethoxybenzylamine Hydrochloride, most requests came from teams working on active compounds for target delivery in CNS research. The compound, built around a trimethoxyphenyl moiety, serves as a reliable amine protecting group and a versatile building block in heterocycle synthesis. In our own experience supporting multistep pharma projects, we have seen orders spike for pilot and full-scale batches—sometimes with turnaround times as tight as two weeks—because customers realized the substitutes didn’t behave as reliably under hydrogenation, reductive amination, or condensation steps.

    For those doing small molecule development, the stability in both anhydrous conditions and during exposure to air offers a practical edge. Storage at room temperature suffices for several months, provided the container stays sealed. Shelf-life requests led us to batch stability studies: analysis shows no significant breakdown over the typical research timeline. Chemical engineers using automated reaction set-ups comment that our product dissolves quickly in standard solvents like methanol and ethanol, with no visible residue—a requirement for those who can’t afford downtime during scale-up.

    Where 2,4,6-Trimethoxybenzylamine Hydrochloride Outpaces Alternate Compounds

    A few years ago, researchers tried to swap this hydrochloride for the free base or even other substituted benzylamines to cut costs. The outcome often involved unexpected by-products or persistence of starting materials. We saw several customers return, frustrated by heavy workup and purification headaches with competitors’ lots. Differences often lie in the small details: the hydrochloride salt exhibits greater stability and easier handling, eliminating volatility issues seen in the free amine. The hydrochloride form doesn’t discolor as fast, either—a telltale sign of oxidation or impurity formation—so chemists spend less time troubleshooting bench results.

    A number of differentiated alkoxy benzylamine salts float around the marketplace. Our product stands apart in its degree of controlled crystallization and rigorous salt formation processes. The result: batches show minimal polymorphism and offer tight reproducibility between syntheses. Unsurprisingly, this reduces variability during key intermediates’ formation, saving both time and costly purification efforts downstream for our partners in small molecule and pharmaceutical synthesis.

    Production Experience and Learning from the Lab Floor

    For new production runs, we draw from inline monitoring technologies and run systematic quality checkpoints rooted in industry best practices, not just batch records for compliance. Over a decade in the field has shown us that just meeting a 98% purity spec isn’t enough. Impurities such as unreacted starting materials or trace alkali must drop below the detection threshold. The sharpest researchers often spot subtle batch variances by TLC or NMR, prompting in-depth rechecks on our end. Whenever process engineers or process development teams send additional characterization requests, our response comes from facing similar hurdles internally. Each request sharpens the focus of our crystallization parameters or narrows our solvent selection window for optimal salt isolation.

    Our method combines methoxylation and benzylamine substitution under strictly maintained temperature and pH windows. Nitrogen-purged reactors and closed-system transfers ensure we keep out contaminants. Solvents receive additional filtration, with in-line monitoring for unwanted ions or moisture. Our batch records track each lot from the raw trimethoxybenzaldehyde to the isolated hydrochloride salt, so repeat customers line up analytical data spanning years—something we encourage for ongoing transparency.

    Responding to Shifts in Market Demand and End-Use Innovation

    Product requests used to come mainly from specialty drug research outfits in North America and Europe. That changed as manufacturing hubs in Asia started working on green process innovations, emphasizing clean, high-yield conversion with minimal waste. Several years ago, we faced pressure to prune back residual solvents and transition to more sustainable, closed-loop purification stages. We answered by upgrading to higher capacity rotary evaporators and custom solid-phase filtrations. Now, batches meet tighter residual solvent levels and carry certificates of analysis detailing every tested parameter, not just a one-line purity value.

    Similar compounds, such as mono- or di-methoxy analogs, lack the precise electronic or steric profile that 2,4,6-Trimethoxybenzylamine Hydrochloride offers. In our facility, yield differences become obvious after scaling reactions above 10 kilograms. These seemingly minor changes dramatically impact process safety, especially in larger-scale pressure reactors. Day-to-day, we've learned such distinctions matter less on paper than in practice, where every minute of rework adds up.

    Facing Supply Chain and Quality Challenges Head-On

    No chemical line escapes the impact of raw material shortages or transport disruptions. Recent years forced us to reevaluate our supplier base, qualifying each source of trimethoxy precursors and confirming the reliability of route partners with hands-on audits. Shifting to dual sourcing paid off during recent global shipping delays, with orders delivered on time even as nearby producers ran short. The cost benefits of long-term stable partner relationships regularly outweigh the savings from simply chasing the lowest priced lot off the spot market.

    End users care about what they see at the bench: consistency vial-to-vial and order-to-order. We invest in third-party verifications and routine reanalysis of retained samples after shipment. Reports always list actual test values—HPLC, melting point, moisture content—so research chemists can troubleshoot processes with full context. Industry colleagues know that transparency on lot records can mean the difference between a stalled project and a completed set of experiments.

    Supporting Research and Innovation Through Feedback

    Direct feedback from experienced chemists has proven more valuable than any marketing claim. Teams conducting multi-step syntheses often flag issues that only emerge at higher concentration or during specific workup procedures—things that rarely show up in standard lab modeling or literature reports. By opening a direct channel to production managers, we've resolved bottlenecks by adjusting batch aging times or stovepiping specialty packaging for those needing air/moisture protection.

    Over time, we've learned that pairing analytical support with every order builds a cycle of improvement. Customers receive detailed spectra and batch notes; in return, they flag subtle quirks or successes in their workflows. This kind of firsthand reporting helps us zero in on unexpected interactions in next-generation synthetic routes. These lessons, gathered from hundreds of real-world projects, now guide every production run.

    Why Quality Delivers the Edge in Competitive Sectors

    Small-scale researchers and large pharmaceutical manufacturers alike share common frustrations: unwanted side products, slow reaction kinetics, or physical variability that threatens project timelines. Here, stable salt formation and careful exclusion of both acid and base-catalyzed hydrolysis products shift the calculus away from troubleshooting and back toward productive research. Our facility’s ability to quickly scale custom batches—from gram to commercial scale—means researchers can trust the consistency required for repeat studies and eventual scale-up.

    Solid handling properties also matter for those running automated dosing setups. Our process targets a narrow particle size range to avoid fluidization or clumping in robotic feeders. Skipping these incremental improvements often leads to hours lost to resuspension or cleaning, with productivity losses that add up rapidly over extended campaigns.

    Providing Solutions, Not Just Material

    Many of our customers cite prior frustrations with supply variability: one lot would dissolve well, another would prove stubborn, or they’d find inconsistent reactivity. A rigorous approach—both in the actual chemistry and handling—underlies every batch. If a client faces hurdles during a reaction sequence, our technical team can trace lot certificates and process records to identify root causes or suggest tailored process tweaks—something traders or resellers rarely offer.

    We treat every shipment as a reflection of collaborative progress. Whether supporting a team developing CNS-targeted compounds or assisting molecular scaffold screening for biotech start-ups, we see our work intersecting with breakthroughs at the bench level. By making process data transparent and acting on user input, we help move forward the entire research community relying on 2,4,6-Trimethoxybenzylamine Hydrochloride.

    Seeing Past the Specification Sheet: Real-World Impact

    Much of our motivation comes from partnerships with labs pushing for new drug discoveries or chemical transformations. These teams don't just read the fine print on a certificate—they notice every shift in solubility, every unexpected byproduct spot on TLC, every uptick in NMR impurity signals. Our decision to offer both small and large batch options means research groups of any scale can test, pilot, and eventually move to full production without disruptive materials changes along the way.

    The jump from benchtop feasibility to process reliability often hinges on materials actually matching their specifications, batch after batch. We’ve kept ahead by investing in targeted staff training and formulation upgrades. Our chemists care about subtle markers—moisture, trace catalyst residue, or color shifts—that other suppliers might overlook. In the end, reliability and knowledge-sharing drive everything we do, not just order fulfillment.

    Tackling Technical Hurdles With Practical Experience

    Sourcing this compound is just the start. We've worked shoulder-to-shoulder with project managers handling ambitious timelines and urgent syntheses. From navigating last-minute stability questions to troubleshooting odd particles seen in a filtered solution, our team responds with what we know works—not just textbook answers. These frontline experiences shape every improvement. Many of the workflow upgrades we’ve implemented during the past decade—such as improved solvent drying, precision pH adjustments, or staged addition protocols—come straight from customer pain points and lab results, not industry conferences or case studies.

    As more innovators branch into new reaction types—enzymatic catalysis, high-pressure hydrogenations, or automated multistep flow syntheses—our compound sees wider adoption in areas we never anticipated at launch. Staying responsive to these evolving needs keeps us accountable for ongoing quality and flexibility in production planning.

    Future Outlook and Continuous Advancement

    Advancements in process chemistry and material science keep shifting what customers expect. To stay relevant, we regularly upgrade analytical instrumentation and run targeted impurity profiling on every production campaign. The trend toward automation in synthesis cuts little slack for off-spec batches. That’s why we keep staff involved in production, not apart from it, so feedback loops run directly from customer to lab floor and right back into the workflow. Our goal stays focused: deliver precisely what researchers need to turn bench science into scalable innovation—batch after batch, year after year.

    2,4,6-Trimethoxybenzylamine Hydrochloride will remain a fixture in the synthetic toolkit for one simple reason: it works dependably in challenging applications. Rather than just supplying a reagent, our work helps open new paths to discovery, proof of concept, and ultimately the next generation of breakthrough molecules. Every process change, every customer insight, and every batch improvement grows out of this close connection to real-world chemical manufacturing challenges.