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HS Code |
465121 |
| Cas Number | 940-17-6 |
| Molecular Formula | C9H11NO2 |
| Molecular Weight | 165.19 g/mol |
| Iupac Name | 2-ethoxybenzamide |
| Appearance | White to off-white solid |
| Melting Point | 81-84°C |
| Solubility In Water | Slightly soluble |
| Smiles | CCOC1=CC=CC=C1C(=O)N |
| Inchi | InChI=1S/C9H11NO2/c1-2-12-8-5-3-4-7(6-8)9(11)10/h3-6H,2H2,1H3,(H2,10,11) |
| Pubchem Cid | 31343 |
As an accredited 2-Ethoxybenzamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Ethoxybenzamide is supplied in a tightly sealed 100-gram amber glass bottle with a secure screw cap and chemical hazard labeling. |
| Shipping | 2-Ethoxybenzamide is typically shipped in tightly sealed containers made of compatible materials, such as HDPE or glass, to prevent moisture and contamination. Packages are labeled according to regulatory guidelines and transported as non-hazardous chemical freight. Store and handle in a cool, dry place, away from direct sunlight and incompatible substances. |
| Storage | 2-Ethoxybenzamide should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect the chemical from moisture and direct sunlight. Ensure appropriate labeling and secure access to authorized personnel only. Always follow standard laboratory safety and storage protocols. |
Applications of 2-Ethoxybenzamide in Industrial ManufacturingAs a core raw material manufacturer with decades of formulation and technical support experience, we supply 2-Ethoxybenzamide to support specialized, high-value industrial applications. Below, we outline the most established downstream use cases, with process-specific supply guidelines for safety, quality, and performance. 1. UV Absorber Intermediate for Plastics AdditivesLeading plastics compounders use 2-Ethoxybenzamide as a critical intermediate to synthesize benzamide-based UV absorbers for engineered polyolefins, PVC, and transparent polymers. Multi-stage organic synthesis incorporates this amide to enhance UV stability in outdoor and automotive component manufacturing. Regulatory controls focus on migration limits and residue purity, especially for exposed consumer goods. Manufacturers typically adjust the additive loading based on resin type and optical exposure demands. Industry compliance standards
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2. High-Performance Organic Pigment SynthesisSpecialty pigment producers utilize this compound for the creation of nuanced, lightfast arylamide and benzamide pigments. These are deployed in demanding industrial paints, high-end printing inks, and plastics coloration. Stringent oversight exists on byproduct removal and environmental discharge throughout pigment synthesis and finishing. Usage rates depend on target shade intensity and solvent/medium compatibility in each downstream formulation. Industry compliance standards
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3. Agricultural Chemical Formulation (Herbicide Synthesis Intermediate)Research-driven agrochemical manufacturers adopt 2-Ethoxybenzamide as a tailored intermediate in the synthesis of specific amide-class herbicide actives—such as selective broadleaf weed controls. Purity and trace impurity controls are vital for downstream pesticide registration and field application safety. Actual loading rates in active ingredient synthesis are reaction-specific, monitored via real-time analytical QC to meet agronomic performance and residue thresholds. Industry compliance standards
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4. Pharmaceutical Impurities Reference Standard SynthesisAPI quality control laboratories and certified reference suppliers use this chemical as a precursor for producing precise impurity reference substances. These references, adhering to pharmacopeial monograph specifications, allow accurate quantitation of process-related and degradation impurities during finished drug batch release and stability evaluations. Handling calls for batch-specific documentation and impurity profiling to align with international pharmacopoeia registration. Industry compliance standards
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5. Functional Additive in Specialty Lubricant Grease FormulationSpecialty lubricant manufacturers add this amide as a functional additive to advanced grease and chain oil blends targeting friction reduction and heat stability in demanding applications such as automotive or aerospace assemblies. Additive performance depends on particle dispersion, high-temperature stability, and synergistic effects with base oils and metal protectors. Sector regulations limit unidentified residues and demand full formulation traceability for safety audits and downstream OEM acceptance. Industry compliance standards
Typical usage ratio
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From years standing behind reactors, monitoring batches, and finessing crystallization steps, making 2-Ethoxybenzamide is an exercise in applied chemistry, not paperwork or theoretical optimization. Every shift on the plant floor brings a new lesson about controlling purity, preventing cross-contamination, and keeping consistency batch after batch. Here, product stewardship doesn’t end with a shipping label; it extends from raw material selection straight through to the final QC signoff.
The parent structure, benzamide, is well known—widely used, straightforward, and stable. Introducing the ethoxy group at the ortho position creates 2-Ethoxybenzamide, unlocking distinctive properties that shift its performance and applications in ways regular benzamide simply cannot match. Attaching the ethoxy group is more than a paper swap in a synthesis textbook; it really changes the way the molecule behaves, starting in the reaction vessel and extending right into customer applications.
We begin manufacturing with carefully screened, high-purity 2-ethoxyaniline, selecting only material free of reducible impurities or trace metals. Such defects get magnified downstream, especially in condensation steps that don’t tolerate ambiguity.
Our controlled reaction runs draw upon precision dosing and temperature management. Experience shows that trying to rush the coupling process leads to unwanted side reactions—over-condensation, N,N-di-substitution, and even ring-closure events under alkaline stress. We use a proprietary mix of solvents which support even heat distribution and easy phase separation, and we deploy exhaustive inline monitoring. Chromatograms tell us not just what’s in the vessel but how to tweak the process to hit that sweet spot: sharp melting point, colorless-to-pale yellow appearance, and zero residual acidity.
The process route steers clear of heavy metals and chlorinated solvents to meet both regulatory trends and end-user compliance expectations. Final product passes, on average, 99.5% purity by HPLC, with moisture content capped at 0.3% and no detectable heavy metals. Granule size falls in the 200–400 μm range. These numbers might seem mundane to those reading after the fact, but in daily plant operations, hitting them reflects hands-on vigilance. Deviate by a single degree or overextend a step, and these guidelines slip quickly, with consequences for both downstream synthesis and environmental compliance.
2-Ethoxybenzamide carves out a niche that other substituted benzamides can’t fill. The ethoxy group at the ortho position increases electron density, which creates a less reactive but much more hydrolytically stable amide bond. In our own solvent-solubility testing and stability trials, it tolerates alkaline washes that would cleave regular benzamides. And this makes a world of difference for customers integrating it into synthetic schemes with variable pH swings.
We have studied its behavior across several reaction types, from pharmaceutical intermediates to specialty resin modifications. From the vantage of the plant floor, 2-Ethoxybenzamide keeps formation of impurities—such as ortho-aminophenol or hydroxybenzamides—at bay during scale-up. This purification edge reduces solvent use and waste, cutting down remediation cost and supporting a cleaner process workflow.
There is a sharp contrast between the behavior of 2-Ethoxybenzamide and that of unsubstituted benzamide or even 4-ethoxybenzamide analogs. The ortho orientation hampers catalytic hydrogenation and restricts specific N-acylation routes, making it a more selective building block. Experienced synthetic chemists will spot reduced side-product formation and less sensitivity to ambient moisture or acid fumes, simplifying storage and handling in the real-world plant environment.
Customers in pharmaceuticals, dyestuffs, and polymer additive fields return to this compound for reason of repeatability and reliability. It acts as a versatile intermediate, taking part in step-growth polymerization, offering targeted modification to chain ends, and providing a platform for N-substitution or further functionalization. Process chemists value it chiefly for its resilience against base-catalyzed hydrolysis, allowing preps that might destroy competing intermediates.
The compound sees routine use in the synthesis of specific psychoactive agents, analgesics, and anti-inflammatory targets where ortho-substitution alters pharmacodynamic behavior. Its ability to act as a masking group or transient intermediate stands out in multi-stage synthetic routes. The pharmaceutical industry routinely leans on its solubility in common polar aprotic solvents—such as DMF, DMSO, and even hot acetone—accelerating purification and downstream workups.
Polymer chemists already know about 2-Ethoxybenzamide’s compatibility with acrylic, epoxy, and urethane systems. The ortho-ethoxy group confers steric resistance to oxidation without leaving the compound inert; this effect helps tailor degradation timelines in specialty coatings and controlled-release films. Paint and pigment manufacturers have tested it for stable color development, with fewer batch-to-batch deviations and lower levels of undesirable tars compared to more reactive amides.
Quality assurance is neither outsourced nor detached from our day-to-day synthesis. Every batch undergoes a full set of pre-release tests: spectral identification using IR and NMR, HPLC for purity, Karl Fischer analysis for moisture, and melting point determination at a controlled ramp rate. Our documentation integrates synthetic log entries, analytical graphs, and batch-specific deviations—often annotated by the very chemists who stirred the reactors. Over years, we’ve found that connecting QC outcomes with real processing notes brings rich feedback loops, giving us a foot up on troubleshooting faster than many desk-driven operations.
Every request from a downstream R&D team, whether pharmaceutical, agrochemical, or polymeric, feeds into an ongoing quality and process improvement program. Customers grappling with residue problems, crystallization grain size issues, or filtration difficulties receive direct technical support anchored in conditions we observe in our own plant runs. True process troubleshooters know grounding advice in practical floor experiences makes for faster and more reliable solutions.
Since 2010, regulatory pressures have nudged us to reduce residual solvent loads, eliminate trace chlorides, and document every origin of supply. It’s not simply a box-checking exercise; these changes align more with the values customers expect from a modern chemical manufacturer—traceability, reproducibility, and environmental consideration. Adapting older process steps for modern expectations involved rethinking condensation vessels and solvent systems and reducing reliance on energy-intensive purification units. In tackling these, valuable operational experience accumulates year by year.
From a manufacturer’s standpoint, maintaining a reliable supply chain for 2-Ethoxybenzamide pivots on long-term relationships with tried-and-tested upstream suppliers. Volatility in the market for ethoxyaniline intermediates, unexpected port closures, and regulatory changes in precursor handling have each affected raw material availability at one time or another.
Buffer inventories and diversified sourcing help sidestep most hiccups, but periodic market tightening tests the strength of any partnership. Our approach keeps production at a scale above short-run pilot batches but below the inertia of massive commodity lines. This flexibility lets us meet both steady monthly releases and urgent, unforeseen demands—a balance that, in practice, can only be maintained by monitoring global shipments and keeping open lines with our suppliers. No process lives in a vacuum, and this is doubly true for specialty chemicals with such targeted uses as 2-Ethoxybenzamide.
We run regular stability trials in real-world storage conditions, logging everything from container integrity at different humidity points to the impact of minor temperature cycling over seasons. By simulating shipping steps—road vibration, stacking weights, warehouse delays—we align claims about shelf life with observations on fresh stock from other continents. These data points, tied together with customer feedback from different climates, drive small changes in packaging type or container safeguards. Such practical experience, collected across a span of production years, forms the backbone of what we deliver, not just batch records and spec sheets.
Every year, the demands on product and process only ratchet up. Most improvements come from the shop floor: a piped steam line to reduce reaction times by half an hour, a change in stirring paddle profile trimming down foaming and solvent evaporation, and real-world analytic tweaks that speed up QC bottlenecks. Plant technicians and shift leads, working shifts at midnight and in summer heat, shape these process changes through practical engagement. They notice subtle color changes, filter rate slowdowns, or shifts in solvent odor long before a deviation appears on a digital monitor.
We give feedback not just to lab managers but also to synth chemists looking to integrate 2-Ethoxybenzamide into new syntheses. For example, one customer’s trouble with unsatisfactory crystallization yields on a downstream heterocycle prompted a joint troubleshooting effort that led to both plant and lab-side adjustments: swapping in a new grade of anti-solvent, revisiting cooling profile, and retraining filter operators on optimal vacuum rates. Collaboration became a means to advancing both routine output and flexible, creative solutions for new market needs.
Instead of relying on static recipes or legacy process instructions, our approach blends tradition—hard-won knowledge from earlier operators—with insights gained from current analytics and external research. It’s not uncommon to revisit a previous failed method and, after five or ten attempts, make it work through subtle modifications, debugging one variable at a time. Engaging directly with customer feedback, we see the ripple effect of each change far downstream.
Every bottle of 2-Ethoxybenzamide leaving our plant reflects decisions made by people who understand their own equipment and constraints deeply. There is no substitute for walking the line, inspecting particle size distribution visually, and reviewing chromatograms with an eye for the unexpected. We rely on people who are willing to adjust parameters on the fly—willing to halt a batch after catching an off-odor at 2 a.m. Facility standards and documentation back this up, but experience teaches that personal judgment and accountability at the bench remain at the heart of consistently delivering a premium product.
Veteran process supervisors emphasize continual skill-building—training new hires not only on hazard response and process steps but also on the subtle signals that precede a failed batch or a product deviation. It’s in this transmission of workplace-only knowledge that our plant sets itself apart. We're driven not by faceless specifications, but by the pride that comes with improving yield, quality, and cost control through shared experience and trust.
From what we've seen, other benzamide derivatives—such as 4-ethoxy or N-alkyl analogs—don’t achieve the same balance between reactivity and selectivity. For process engineers, these alternatives often bring improved reactivity but at the cost of storage sensitivity or lower yields in certain pharmaceutical applications. On the other hand, unsubstituted benzamide, while cheaper and more accessible, lacks the same hydrolytic stability and often requires extra purification steps if targeted at fine chemical or medical-grade specifications.
Across industries, 2-Ethoxybenzamide builds a practical bridge for downstream users wanting to streamline complicated syntheses or avoid common pitfalls linked with active-substitution patterns. Users who started with other compounds tend to revert to our product when scale-up challenges arise. Cost per kilogram only matters when the product performs every time, lowering total operational expense across multiple stages. Over years of batch feedback, we have seen fewer complaints and more positive returns from customers who value its measured stability and straightforward application.
Regulations push everyone in the industry towards safer, greener, and more thoroughly documented processes. Our route to 2-Ethoxybenzamide responds directly to these pressures—every technical modification aims to reduce exposure risks, minimize emissions, and document actual step-by-step provenance. We forged our current process in response to existing customer needs and careful observation of product performance in application, not in theoretical isolation. By listening to the real-world stories, both good and bad, we maintain a product that responds to more than just ticking boxes on a compliance form.
Shifts in raw material costs, tightening compliance expectations, and a constant drumbeat for process improvements mark every year we’ve spent in this business. Change rarely arises from a single innovation or managerial mandate—it grows on the back of shared daily effort. 2-Ethoxybenzamide serves as both a staple and as a platform for new applications, relying on a robust manufacturing discipline to remain competitive and adaptable.
We focus on ongoing education, transparent collaboration, and continual validation of every improvement before institutionalizing it across the plant. Market forecasts and academic research only go so far; real progress emerges from blended perspectives—operators, chemists, engineers, and technical customers facing deadlines and trying to hit their own specs. This backyard approach drives us to keep questioning every aspect of our process in pursuit of a safer, cleaner, and more responsive way to create 2-Ethoxybenzamide now and in the years ahead.