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HS Code |
905005 |
| Name | 3-Ethoxybenzaldehyde |
| Cas Number | 7127-16-4 |
| Molecular Formula | C9H10O2 |
| Molecular Weight | 150.18 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point C | 234-236 |
| Melting Point C | -18 |
| Density G Ml | 1.051 |
| Refractive Index N20d | 1.536 |
| Flash Point C | 100 |
| Smiles | CCOC1=CC=CC(=C1)C=O |
| Pubchem Cid | 293286 |
| Solubility | Insoluble in water, soluble in organic solvents |
As an accredited 3-Ethoxybenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 3-Ethoxybenzaldehyde is supplied in a 100 mL amber glass bottle with a tamper-evident cap, clearly labeled for laboratory use. |
| Shipping | 3-Ethoxybenzaldehyde is shipped in tightly sealed containers to prevent leakage and contamination. It should be kept in a cool, dry, and well-ventilated area, away from incompatible substances. Protective packaging is used to guard against breakage during transit. Complies with relevant chemical shipping regulations and safety guidelines. |
| Storage | 3-Ethoxybenzaldehyde should be stored in a tightly sealed container, away from direct sunlight, heat, and sources of ignition. Keep it in a cool, dry, and well-ventilated area, separate from oxidizing agents and acids. Ensure containers are clearly labeled and protected from physical damage. Appropriate chemical-resistant storage cabinets or shelves are recommended to prevent accidental spills or exposure. |
Applications of 3-Ethoxybenzaldehyde in Industrial Manufacturing3-Ethoxybenzaldehyde is a high-purity aromatic aldehyde widely incorporated as an intermediate and functional additive across several advanced chemical production sectors. As a direct manufacturer specializing in this compound’s industrial-grade output, we ensure consistent supply and batch quality to meet the formulation, process integration, and safety demands of established manufacturing chains worldwide. Below, we detail key application areas based on credible downstream practices and compliance requirements. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical producers deploy 3-ethoxybenzaldehyde primarily as a building block for synthesis of select antihistamines and anti-inflammatory agents, as well as in the development of heterocyclic core frameworks. The compound’s ethoxy-substituted aromatic ring allows precise introduction into nucleophilic aromatic substitution and condensation reactions, improving overall yield and purity in the final API. Its addition occurs during defined synthesis steps requiring strict environmental and impurity controls, with precise weighing and metering to ensure downstream reaction profile consistency in GMP-compliant environments. Industry compliance standards
Typical usage ratio
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2. Aroma Chemical Precursor in Fine Fragrance and Flavour ManufacturingThe flavor and fragrance industry incorporates this compound as a value-added intermediate for the synthesis of aroma molecules containing ethoxy aromatic motifs, most often through downstream acylation, reductive amination, or Schiff base formation. Its entry point is typically in the formulation of aldehyde-based fragrance accords, where the precise ethoxy substitution modulates scent profile character for designer perfumes, luxury soaps, and food flavorings. Manufacturing environments implement rigorous sensory evaluation and batch traceability protocols to uphold global industry standards. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Agrochemical Intermediate for Selective Herbicide DevelopmentProducers in the crop protection sector utilize 3-ethoxybenzaldehyde to introduce electron-donating functional groups in early-stage synthesis of heterocyclic herbicide actives. The compound undergoes condensation and subsequent ring closure reactions, playing a pivotal role in the selectivity profile and soil mobility of the final product. Integration into the large-scale agrochemical process involves in-line raw material verification and closed-system transfer to minimize exposure and guarantee high-purity batch output for registration under global pesticide regulations. Industry compliance standards
Typical usage ratio
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4. Intermediate for Specialty Benzylamine and Benzyl Alcohol DerivativesManufacturers engaging in custom synthesis of specialty chemicals use 3-ethoxybenzaldehyde as a core aldehyde precursor in reductive amination or Grignard addition to yield tailored benzylamine and benzyl alcohol compounds. These intermediates form the basis for downstream monomer, stabilizer, or crosslinker production targeting rubber, plastic, and coating applications. The precision in the ethoxy group’s positioning enables downstream processors to fine-tune the chemical reactivity, achieve high selectivity, and reduce byproduct formation under closely monitored plant conditions. Industry compliance standards
Typical usage ratio
Downstream process integration
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3-Ethoxybenzaldehyde stands out in the chemical industry for its unique aldehyde group directly bonded to an ethoxy-substituted benzene ring. For those working in pharmaceutical development, fragrance compounding, or specialty chemicals, this molecule keeps showing up for good reasons. We have been manufacturing aromatic aldehydes for a long time, and this one always seems to earn repeat demand—not just for what it can achieve, but for its reliable chemistry and versatility in demanding synthesis routes.
You’ll often see it referenced under the model 3-ethoxybenzaldehyde, with its well-known CAS number 3476-89-3. Its most appreciated characteristic is the strong, pure aromatic note, subtlety balanced between sharp and sweet, thanks to the 3-ethoxy arrangement on the benzene ring. This kind of fine-tuning sets it apart from basic benzaldehyde or other ether-modified analogues. Handling this material daily in our plant, I’ve learned to trust its predictability during both scale-up and small-batch work.
We focus on achieving high purity—typically not less than 98%—with a distinct boiling point, usually in the 240–242°C range. Our team rigorously removes trace amounts of byproducts that can affect downstream reactions, especially for those producing advanced pharmaceuticals or formulating fine fragrances. The liquid remains transparent with a pale yellow tint, and impurities like residual solvents or unreacted starting materials stay well below industry limits.
Odor and appearance offer practical cues in our daily QC routines. 3-Ethoxybenzaldehyde has a nuanced, floral-almond aroma that is both gentler and less bitter than unmodified benzaldehyde. These sensory qualities aren’t just pleasant—they can directly influence the success of a finished formula in the fragrance sector, where off-notes and impurities show up even in tiny traces.
Not every facility achieves a consistent melting or boiling profile, but over the years, we’ve learned that careful temperature control during synthesis and distillation pays off with fewer production headaches for our clients. Our batches consistently pass the GC-MS and HPLC assays demanded by modern pharma and fragrance labs.
In the real world, most lots of 3-Ethoxybenzaldehyde leave our plant destined for two sectors: pharmaceuticals and flavors & fragrances. It serves as a key intermediate in multi-step synthetic reactions, especially where chemists want both reactivity and selectivity. The 3-ethoxy group alters the reactivity compared to standard benzaldehyde, which can help route select catalytic reductions, formylations, or condensation reactions. For pharmaceutical research, it often becomes part of new scaffolds for biologically active molecules. Medicinal chemists appreciate its stability—there’s less risk of uncontrolled side reactions.
In the fragrance world, perfumers incorporate this material to add a nuanced almond note, softer than using straight benzaldehyde. It helps build top- and heart-notes that last longer, with less tendency to overpower other formula ingredients. Compared to the harshness of the unsubstituted aldehyde, the ethoxy substitution rounds out the olfactory profile, allowing perfumers to construct more complex blends. In flavor houses, it gets used at low levels for nutty or floral nuances that can’t be achieved with standard flavor modulators.
Having worked through many customer applications, we've seen how easy it is to mix up positional isomers. 2-Ethoxybenzaldehyde, 4-ethoxybenzaldehyde, and 3-ethoxybenzaldehyde are not interchangeable. Even small differences in structure give rise to differences in odor, reactivity, and solubility. We’ve run head-to-head tests on these variants, using the same downstream chemistry, and results diverge in conversion yields or final product purity. With 3-ethoxy, you get a unique pattern of reactivity and a distinct sensory impact. Make sure the supply chain handles the right isomer—QC with careful NMR or HPLC always helps.
Substituted benzaldehydes sometimes bring hidden risks. We watch for trace residual solvents (like ethyl acetate or toluene from processing steps), which can sneak through crude distillation without tight process control. Over the years, we refined our process to eliminate these impurities below regulatory limits, allowing worry-free use in sensitive formulations. Those who’ve sourced from less attentive producers probably know the headaches that follow in the form of off-odors or reductions in synthetic yield.
Manufacturers walk a fine line between efficiency and maintaining integrity in raw material production. In practice, most downstream headaches tie back to poor-quality input. If a producer cuts corners—rushing the synthesis, using recycled solvents, skipping crucial purification steps—the end user pays for it twice: once during initial formulation, and again when failed batches or recalls creep in.
Honest feedback from customers tells us that reliable sourcing often beats cost savings, especially where finished goods enter regulated markets. For pharmaceuticals, impurities like byproducts or unknown residuals can lead to major revalidation costs. In flavors and fragrances, a minute contamination can change how the end product is perceived by a consumer. Experienced formulation chemists quickly spot these differences in chromatograms, and sensory panels catch off-notes even at low ppm levels.
Some new entrants into the market offer lower-cost versions, often with questionable documentation or inconsistent analytical data. Our advice, shaped by decades in aromatic aldehydes, is that consistent process control and full traceability trump minor pricing gaps. Long-term partnerships with formulators and R&D teams only work when suppliers treat material consistency as non-negotiable.
The true performance of a raw material starts with how it gets packaged and shipped. Over the years, we adopted sealed drums and lined containers, as 3-ethoxybenzaldehyde reacts readily with strong oxidizers and light. Older suppliers sometimes ship in poorly protected tanks or barrels, which leads to peroxide formation or color changes over time.
In our facility, storage means cool, dry environments with limited exposure to sunlight—basic steps, but easily overlooked. High humidity or fluctuating temperatures can degrade sensitive aldehydes more quickly than most expect. On the plant floor, operators use chemical splash goggles and gloves rated for aromatic aldehydes. Spills get contained immediately, as inhalation of vapors can irritate the respiratory tract. Proper labeling and safety data are always attached to each drum, minimizing the risk for downstream handlers. Customers needing large-scale shipments often insist on third-party logistics providers with certified chemical handling protocols.
Scaling up aromatic aldehyde production takes more than a recipe—it takes a commitment to slow iterative process development. Uncontrolled side reactions waste time and drive up purification costs. Through years of incremental changes to process parameters like catalyst selection, solvent purity, and fractionation temperature control, the team has found the balance between throughput and product quality.
A stubborn residual often appears during ether formation, if precursors or solvents diverge from spec. We discovered that careful solvent distillation pre-synthesis cuts final purification time dramatically. By changing the order of reagent addition and investing in in-line temperature monitoring, unwanted side-reactions dropped, batch rejection rate fell, and waste streams got easier—and cheaper—to manage.
We’ve also automated bottleneck steps, such as distillation and solvent recovery, allowing fresh lots to ship on schedule with less human error. This stability turns into peace of mind for buyers needing steady, reproducible inputs for their laboratory or factory lines.
Benzaldehyde itself forms the core for many syntheses, but the ethoxy modification truly broadens the molecule’s utility. Alternatives like 4-ethoxybenzaldehyde may look similar on paper, yet show different chemical and sensory patterns. We have supplied both as part of custom projects, but end users rarely substitute one for another without a clear reason in their pathway or formula.
3-Ethoxybenzaldehyde delivers more selectivity in many addition and condensation reactions due to the electron-donating effect of the ethoxy group in the 3-position. This can boost yields for specific intermediates, saving time and cost. For perfumers and flavorists, the position of the ethoxy group changes the aroma from a harsh, bitter almond blast to a smoother, more rounded scent profile—this difference matters at scale, where subtle changes in ingredient notes get magnified in consumer products. We often receive sensory feedback that highlights these distinctions, helping clients dial in their signature scents or flavor profiles.
In resins and specialty polymers, the 3-ethoxy variant displays better compatibility with some backbones due to its steric and electronic features. This results in coatings and polymer additives that maintain properties across broader temperature or environmental ranges. While other aromatic aldehydes can sometimes serve, real-world performance differences show up in stability or process efficiency.
Clients share recurring issues when switching from distributor-supplied lots to direct-from-manufacturer supply. One example: fragrance houses found unexpected color changes or faint off-notes after product launch, traced back to a few ppm impurity in raw 3-ethoxybenzaldehyde. By sharing our GC-MS reports, and sometimes re-running their batch samples through our analytic systems, we helped pinpoint the source and eliminate the problem for the next production round. This level of support comes from deep process knowledge, not from off-the-shelf commodity thinking.
In pharmaceutical R&D, a failed scale-up using another supplier’s material led to inconsistent downstream intermediates. The root analysis showed a higher-than-normal level of unreacted starting aldehyde and minor isomer content. Supplying a fresh lot from our process restored confidence and finished product purity, saving the client an expensive campaign rework. We believe communication between manufacturer and end user, especially around analytical support, closes quality gaps and accelerates project timelines.
Demand for sophisticated, high-purity aromatic intermediates continues to increase. At the same time, regulatory profiles for trace contaminants, solvent residues, and byproducts have tightened. Our internal audits now follow evolving international standards, from Europe’s REACH to U.S. FDA guidelines. These requirements encourage us to stay precise, but also add cost and scrutiny to every batch. Our position as primary producer means handling this complexity ourselves, not offloading responsibility to unaccountable brokers.
One persistent challenge is balancing process efficiency against environmental responsibility. Waste minimization efforts have prompted us to recover and recycle process solvents, treat emissions at-source, and partner with outside firms for disposal of byproducts outside permitted limits. This effort extends beyond legal obligations. Our teams have found that upfront investment in greener processes pays off through better community relations, reduced risk, and a stronger reputation in sensitive markets like food and pharma.
We’ve had success in developing in-process controls that lessen the generation of hazardous secondary products. By sitting down with our own analytical chemists—people who work on the same plant floors as our production operators—we spot sources of waste and correct them in real time. Third-party certifications confirm this work, but for us, direct daily control keeps surprises to a minimum.
Final product performance starts back at the raw material bin. Keeping 3-ethoxybenzaldehyde contaminant-free demands tight attention to drum handling. Never allow transfer pumps or hoses intended for lower-grade aldehydes to touch high-purity aromatic lots. Even slight cross-contamination leaves a fingerprint detectable all the way to the finished consumer item.
Storing unopened drums in a cool, dry warehouse extends shelf life well past a year, as long as seal integrity gets checked upon arrival. If decanting into smaller containers for batch use, avoid plastics that can leach plasticizers—glass or stainless steel works best. For production managers, keeping a small reference sample from each lot improves traceability down the line, especially for regulatory audits or customer feedback requests.
Waste handling remains an often-overlooked step, but proper disposal of aldehyde-laden residues helps maintain both workplace safety and community standing. Avoid open drains or uncontrolled venting; we recommend sealed waste containers and periodic reviews of local disposal guidelines. Many problems that land at environmental, health, or safety desks start with shortcuts in the drum pit or tank washout sumps.
Supplying 3-ethoxybenzaldehyde directly from the original manufacturing facility places responsibility squarely with us. We do not have the luxury of disclaiming product drawn from some anonymous tank farm. Every drum, every certificate of analysis, and every shipment carries our signature because our team produced, tested, and packed it. Honest, direct dialogue with those who use this compound means problems surface early, when they’re still easy to address.
Over decades at the reactor and in customer meetings, a practical truth emerges: you get what you check, not just what you expect. This material can serve specialists driving fine chemical innovations or large-scale formulators who need bulk tonnage, but the difference between success and recall often comes down to raw material integrity. No amount of clever process engineering downstream can salvage unpredictability at the source.
3-Ethoxybenzaldehyde, though a single tool in the chemist’s kit, represents what disciplined manufacturing enables. From the sound of the reactor heating up before dawn, to the clatter of drums heading out across borders or oceans, this product embodies what a transparent, accountable supplier relationship really means.
Chemistry evolves, and expectations for quality and accountability move with it. We remain focused not just on the performance of one aromatic aldehyde, but on the long-term trust that comes when a customer experiences batch-after-batch reliability. Regulatory landscapes, environmental stewardship, and global supply dynamics add complexity with every season, yet the fundamentals stay simple: process discipline, scientific openness, and pride in genuine manufacturing. For those searching for consistency and partnership, direct engagement with the actual producer continues to make all the difference.