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2-Ethoxybenzylamine

    • Product Name 2-Ethoxybenzylamine
    • Alias 2-Ethoxybenzenemethanamine
    • Einecs 249-662-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    407506

    Cas Number 619-76-7
    Molecular Formula C9H13NO
    Molecular Weight 151.21 g/mol
    Iupac Name 2-ethoxybenzylamine
    Appearance Colorless to pale yellow liquid
    Boiling Point 256-258 °C
    Density 1.02 g/mL at 25 °C
    Purity Typically ≥ 98%
    Solubility Soluble in organic solvents; slightly soluble in water
    Smiles CCOC1=CC=CC=C1CN
    Refractive Index 1.5390 (lit.)

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

    Packing & Storage
    Packing Amber glass bottle containing 100 grams of 2-Ethoxybenzylamine, sealed with a screw cap and labeled with hazard and identification details.
    Shipping 2-Ethoxybenzylamine is shipped in tightly sealed containers under appropriate temperature and ventilation conditions to prevent contamination and degradation. It is packaged according to regulatory guidelines for hazardous chemicals, with clear labeling and documentation. Transport should comply with local and international chemical safety regulations to ensure safe handling and delivery.
    Storage 2-Ethoxybenzylamine should be stored in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible materials such as strong oxidizers. Keep the container tightly closed when not in use. Store in a chemically resistant container, preferably amber or opaque, to protect from light. Label the storage vessel clearly and follow all relevant chemical safety protocols.
    Application of 2-Ethoxybenzylamine

    Applications of 2-Ethoxybenzylamine in Industrial Manufacturing

    2-Ethoxybenzylamine is employed as a specialized intermediate in several advanced manufacturing sectors, valued for its chemical reactivity and functional-group compatibility. As an original manufacturer, we supply this raw material to downstream producers who incorporate it into regulated and highly controlled production environments, optimizing synthesis processes and ensuring specification conformity from batch to batch. Below, we outline major application segments where 2-ethoxybenzylamine plays an integral and irreplaceable role.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    This amine offers selective reactivity in key amide coupling, reductive amination, and aromatic substitution reactions involved in the multi-step synthesis of regulated drug molecules. Its controlled profile enables reliable yield and purity targets required in pharmaceutical production. Our manufacturing partners rely on consistent assay and impurity levels to comply with global pharmaceutical standards and to achieve strict target molecular structures in small-molecule API production.

    Industry compliance standards

    • United States Pharmacopeia (USP)
    • European Pharmacopoeia (Ph. Eur.)
    • Japan Pharmacopoeia (JP)
    • ICH Q7 Good Manufacturing Practice Guidance for APIs

    Typical usage ratio

    • 0.5–1.5 molar equivalents relative to target functional group in the synthesis step; adjusted based on process chemist’s optimization for conversion and impurity control

    Downstream process integration

    • Introduced during key amination or N-alkylation steps in API synthetic routes, where reaction stoichiometry and order of addition ensure selectivity and limit byproduct formation

    Final product types

    • Small-molecule pharmaceutical APIs for cardiovascular, CNS, and anti-infective drug families
    • Drug intermediates requiring further synthetic transformations or formulation

    2. Agrochemical Synthesis (Herbicides and Pesticides)

    Downstream agrochemical producers utilize this intermediate for the amination and side-chain modification of select aromatic scaffolds found in advanced crop protection agents. Its low impurity profile and defined reactivity make it suitable for stringent manufacturing setups that must meet agricultural and environmental safety standards in multiple regulatory zones.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EPA Pesticide Registration Guidelines (40 CFR Part 158, FIFRA)
    • REACH Registration, Evaluation, Authorization and Restriction of Chemicals (EU)
    • ISO 9001 for quality management systems in chemical synthesis

    Typical usage ratio

    • 0.2–1.0 molar equivalents as a chain extender or amine source, typically fine-tuned for reaction performance and minimization of residual amine in the finished product

    Downstream process integration

    • Charged during intermediate formation and coupling steps in multi-stage synthesis, often under batch or continuous flow conditions to ensure traceability and consistency

    Final product types

    • Post-emergence herbicides for cereal and broadleaf crops
    • Insect growth regulators and fungicidal actives

    3. Fine Chemical & Specialty Amine Manufacturing

    Producers of specialty amines and downstream fine chemicals use this material for targeted N-functionalization reactions, where maintaining precise electronic and steric requirements is essential for downstream reactivity and stability. Its controlled purity and specified byproduct limits support high-yield syntheses of value-added downstream amines and auxiliaries for further conversion.

    Industry compliance standards

    • ISO 9001 for quality management in chemical manufacturing
    • Responsible Care® global chemical safety initiative
    • REACH (EU) registration and safety dossiers
    • Chemical Manufacturers Association (CMA) process safety requirements

    Typical usage ratio

    • 1.0 molar equivalent where used as a primary reactant; lower ratios in catalytic or auxiliary roles, depending on specific synthetic campaign

    Downstream process integration

    • Dosed as a primary or secondary amine input in controlled condensation, reductive amination, or ring-formation steps, with direct connection to in-line QC and real-time monitoring systems

    Final product types

    • Substituted benzylamines with defined substitution patterns
    • Specialty nitrogen-containing building blocks for advanced organic synthesis

    4. Dye and Pigment Intermediate Synthesis

    Industrial dye and pigment producers incorporate 2-ethoxybenzylamine for synthesizing highly specific aromatic amine intermediates required in the creation of functional dyes. Its amine group enhances chromophore attachment and provides controlled substitution, essential for reproducible color profiles in regulated textile, plastics, and printing applications.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for textile dyes)
    • REACH Annex XVII restrictions (on aromatic amines in dyes)
    • ISO 9001 and 14001 for production and environmental management
    • GHS/CLP Regulation EC No 1272/2008 for chemical labeling and safety

    Typical usage ratio

    • 0.3–0.8 molar equivalents relative to diazotized coupling partner, fitting target chromophore requirements and waste minimization objectives

    Downstream process integration

    • Added during key amination or N-alkylation phases of azo, anthraquinone, or benzidine dye precursor synthesis, with strict process control on temperature and reaction pH

    Final product types

    • Dye intermediates for textile coloration and printing inks
    • Functional pigments for plastics and polymer applications
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    Certification & Compliance
    More Introduction

    2-Ethoxybenzylamine: Practical Experience from the Manufacturer's Perspective

    Understanding 2-Ethoxybenzylamine in Daily Production

    Over the years, countless conversations with researchers, product engineers, and procurement teams have turned up a familiar question: what sets 2-Ethoxybenzylamine apart from alternatives? From experience in manufacturing and scaling this product in dedicated workshop lines, a few realities always jump out. This is not just another benzylamine derivative. As a chemical manufacturer, every batch starts with a clear commitment to purity, reliability, and downstream performance. Laboratories and industrial processes rely on our products to work as expected, and failures mean real costs, so there is no room for compromise.

    2-Ethoxybenzylamine, bearing the molecular structure C9H13NO, with a CAS number of 3730-78-1, opens up unique pathways in both pharmaceutical research and organic synthesis. What initially drew our attention more than a decade ago was how the ethoxy substitution at the ortho position brings about distinct reactivity, as compared to regular benzylamine or the methoxy analogues. The nuanced balance between polarity and lipophilicity supports specific reaction mechanisms and intermediate stability. Over multiple pilot phases, we noticed the improved selectivity when this compound acts as a nucleophile or intermediate. We routinely analyze every lot for color, clarity, and amine value, knowing that even trace levels of impurities can introduce side reactions or lower yields in your process.

    Model, Specifications, and Real-World Usage

    Our standard production line delivers 2-Ethoxybenzylamine as a clear, colorless to pale yellow liquid. Our usual specification targets a minimum purity of 99%, determined by GC analysis with verified reference standards. We test for water content (Karl Fischer), ensure residual solvents do not exceed 500 ppm, and confirm single-component profiles by NMR. Our in-house technical staff designed the handling and packaging process to prevent contamination; we fill material under inert nitrogen to suppress oxygen-driven degradation. All material ships in high-density polyethylene drums or amber glass bottles, depending on the size, and tamper-evident seals go on every cap.

    In our long-term partnerships, pharmaceutical teams most frequently use 2-Ethoxybenzylamine as a precursor for heterocyclic scaffolds and novel active pharmaceutical ingredients. During production scale-up phases, this compound appears as a key nucleophile or as a building block in reductive amination and amidation reactions. Our team learned that its solubility profile gives an operational advantage for work-up and purification steps. Medchem groups have reported smoother condensations compared to plain benzylamine, especially where delicate aryl-amine couplings need to minimize side product formation. We have seen our compound used in new kinase inhibitor research, and we support product documentation for regulatory submissions.

    Beyond the pharmaceutical space, industrial users take advantage of the ethoxy group for applications in electronic material processing, UV absorbers, and custom surfactant design. The compound’s modest basicity and aromatic core offer specific performance in selective extraction systems. The consistency of our batches has enabled multiple customers to scale from 100-gram pilots to multi-metric ton output, without process re-optimization or purification headaches.

    Hands-On Differences vs. Other Benzylamines

    Years of batch testing and customer feedback keep pointing out how 2-Ethoxybenzylamine stands apart from unsubstituted benzylamine, 2-methoxybenzylamine, and other substituted analogues. During routine product qualification, we compare the stability under storage, reactivity in SN2 and reductive aminations, and potential for hazardous byproduct formation under reaction conditions.

    Unsubstituted benzylamine, a workhorse for basic amination, cannot offer the same selectivity. Customers trying to access particular aryl amide frameworks quickly see how the ortho ethoxy group facilitates milder conditions – less acid or base is needed, often improving safety and cutting utility costs. Compared directly to 2-methoxybenzylamine, the ethoxy variant resists hydrolysis better under extended storage and wet conditions. We have tracked peroxide formation and demonstrated lower rates for the ethoxy form. This makes it particularly valued in processes that require multi-month shelf life for intermediates or where temperature fluctuations are unavoidable. Its broader solubility range supports ease of formulation, particularly for nonpolar or intermediate polarity solvents.

    Dealing with strongly electron-withdrawing or donating substituents can change basicity or provoke unwanted side reactions. Our team ran pilot syntheses with a range of aromatics and noticed improved yields with fewer chromatographic purifications required. That difference translates to real productivity for lab and plant operators.

    Quality Assurance as a Core Principle

    Every order of 2-Ethoxybenzylamine we release carries the assurance of rigorous in-process and final QC. As a manufacturer, we do not depend on co-packers or outside consultants to run these controls; our technical and QC teams work side-by-side, using validated analytical methods tailored to the peculiarities of this chemical. Customers often request full traceability on raw materials and process auxiliaries, and we have invested in digital systems to provide that. Most days, this is less about paperwork and more about quickly answering the phone when a process step goes sideways at your location.

    In years past, we have fielded calls about batch-to-batch variation. One problem we encountered during a scale-up job involved minor color changes that hinted at amine oxidation. Our production staff traced the issue to excess oxygen in the headspace before filling. Modifying the filling protocol and inerting the storage drums eliminated this, and we shared the findings in our customer newsletters. By keeping the process hands-on, we are ready to implement changes on the fly, based on process data and field troubleshooting.

    For regulatory-sensitive applications, we supply full impurity profiles and can provide stability data upon request. Our documentation covers material origin, storage recommendations, recommended shelf-life under different storage conditions, and full analytical support for your tech transfer, validation, and scale-up needs. Our familiarity with evolving analytical requirements allows us to quickly adapt certificates of analysis to novel regulatory demands, such as ICH Q3A/B impurity thresholds or requirements for genotoxic impurity tracking. Our labs routinely archive reserve samples in case downstream deviations need investigation.

    Supporting Innovation and Addressing User Challenges

    The most rewarding moments occur when conversations with technical users lead to new product tweaks. By sharing case studies about how 2-Ethoxybenzylamine was used as a bench-mark compound in new process methodologies or green chemistry protocols, we learn about shifting priorities in different sectors. A few years ago, a project required a non-standard impurity threshold due to a new synthetic route downstream. Our approach was to adapt the crystallization and drying steps, implementing new in-process controls to suppress hydrolysis and limit trace tertiary amines.

    We have faced recurring inquiries about safe handling guidelines, storage recommendations in high-humidity plants, and best practices for larger-scale solvent recovery. Knowing that 2-Ethoxybenzylamine possesses moderate volatility, we designed closed filling and dedicated vapor extraction in the main handling area. Our client site visits focus on training for safe decanting, vapor detection, and disposal. In some markets, our technical outreach programs include webinars on “root cause” analysis for unexpected out-of-spec events related to aminated intermediates. Our in-house technical team has run benchtop tests to validate customer protocols for clean-in-place, confirming the product leaves negligible residue after standard aqueous and organic washes.

    Resource constraints press users to minimize hazardous waste and optimize yields. The relatively clean reactivity profile of 2-Ethoxybenzylamine, with its absence of problematic leaving groups, supports more straightforward mother liquor recycling. That saves time in purification and allows for reduced solvent use across multiple batches. This compounded saving becomes significant at scale; many clients have slashed their process waste disposal costs thanks to this cleaner reactivity.

    Environmental Responsibility and Safety

    Our team recognizes the growing scrutiny around chemical manufacturing waste and occupational hazards. With 2-Ethoxybenzylamine, we made conscious decisions years ago to only use raw material suppliers that comply with both local and international chemical safety standards. All wastewater streams get direct in-line monitoring for amine content before treatment. Solvent vapor collection captures emissions, cutting down on environmental releases, and all spent drums return to a certified reprocessing facility.

    Based on operator feedback, we improved ventilation in the drums-handling section after a few staff experienced mild amine exposure symptoms one summer. After that experience, refresher safety training became standard in our facility, and next-generation vapor detectors were added. We treat PPE and safety improvements as an ongoing process, not a static requirement. Our material safety data sheets summarize practical exposure situations for both plant workers and users on the receiving end.

    Ongoing Improvements and Listening to Real-World Feedback

    Real progress with specialty amines comes not from complacency but from challenging old standards. Whether addressing questions about particle filtration for high-purity reactors, handling special request packaging formats, or running joint pilot projects to qualify our product for new processes, our team treats every scenario as an opportunity to learn. That philosophy has directly shaped our 2-Ethoxybenzylamine product. We keep a continuous improvement log based on customer audits and the feedback collected after every campaign run. Small tweaks in heater control, new cleaning procedures for filling lines, and attention to detail in drum labelling have all translated to a smoother experience for end-users.

    A recent customer partnership involved rigorous LC-MS screening for trace byproducts not previously relevant. We worked side-by-side with their analytical chemists, using our own pilot reactors to mirror their conditions. By synchronizing our QC checkpoints, we reduced requalification downtime for our client and improved the shelf stability for their finished product. None of these results came just by writing protocols; they grew from practical engagement and shared problem-solving.

    Why 2-Ethoxybenzylamine Earns Trust from Chemical Users

    Newcomers often enter the amines market believing that price or worksheet data can tell the whole story. Real-world performance tells a different story. Our product wins loyalty not just by offering typical purity but by providing consistency, batch after batch, in ways that allow chemists and production technicians to do their jobs with confidence. Reproducible reactions, low residue, and hassle-free clean-up—these outcomes matter far more than generic data sheets can illustrate.

    From troubleshooting novel heterocycle synthesis in academic pharmaceutical labs to supporting ISO-driven quality documentation for exacting electronic materials, our direct work with users informs all product development. New regulatory demands and changing environmental standards only sharpen our focus on maintaining accountability and transparency. If you have faced frustration with variable batches, unlisted impurities, or unexpected hazard control gaps, know that these are the realities we address every production day.

    Practical Guidance for Integration

    We encourage technical users to reach out with process requirements, even those that lie outside the normal run of specifications. Our years manufacturing 2-Ethoxybenzylamine showed that technical integration rarely succeeds with a “one size fits all” mindset. Nearly every scale-up or formulation change involves a direct conversation about process temperatures, reaction catalysts, and solvent systems. By working directly with research and scale-up teams, our product development cycles continuously evolve and respond to emerging needs.

    Our advisory team frequently assists with solvent selection for initial dissolutions, offers guidance on storage temperature ranges for longer-term lot stability, and supports impurity threshold discussions for novel therapeutic uses. For sectors pursuing green chemistry awards or working towards ISO 14001 certification, the clean downstream recovery of our product aligns well with those goals. Documentation support, access to archived production data, and flexible batch production scheduling remain part of our commitment to facilitating real progress.

    Moving Forward Together

    Those purchasing or relying on 2-Ethoxybenzylamine measure its value by the time saved, yields preserved, and safety gains protected on the plant or lab floor. Our direct experience as the manufacturer, working without middlemen, grounds every technical response and every improvement we make. Feedback from both seasoned formulation specialists and chemists carrying out their first large-scale batch matters and has shaped the product evolution from early proof-of-concept to full commercial maturity.

    We invite technical and procurement professionals who rely on quality, transparency, and proven consistency to discover how our team’s manufacturing experience with 2-Ethoxybenzylamine translates into fewer surprises, higher reliability, and stronger project outcomes. The door is always open for dialogue, troubleshooting, or process optimization partnership. Our team remains ready to support technical advances and remain accountable for every batch we produce.