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HS Code |
198992 |
| Iupac Name | 2-ethoxy-3-methoxybenzaldehyde |
| Molecular Formula | C10H12O3 |
| Molar Mass | 180.20 g/mol |
| Cas Number | 117456-27-2 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 294 °C (estimated) |
| Density | 1.13 g/cm³ (estimated) |
| Solubility In Water | Slightly soluble |
| Refractive Index | 1.542 (estimated) |
As an accredited 2-Ethoxy-3-Methoxybenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25g, sealed with a screw cap; features hazard labels, CAS number, and supplier information on a white label. |
| Shipping | 2-Ethoxy-3-Methoxybenzaldehyde is typically shipped in tightly sealed containers suitable for chemicals, protected from light, moisture, and extreme temperatures. It should be clearly labeled, handled according to standard chemical safety regulations, and shipped as a non-hazardous organic compound unless otherwise specified by regulatory guidelines. Always refer to the latest SDS for handling details. |
| Storage | Store 2-Ethoxy-3-Methoxybenzaldehyde in a tightly sealed container, placed in a cool, dry, and well-ventilated area away from incompatible materials such as oxidizing agents. Protect from light and moisture. Ensure proper labeling and keep away from sources of ignition. Use appropriate chemical storage cabinets, and follow standard laboratory safety protocols when handling or storing the compound. |
Applications of 2-Ethoxy-3-Methoxybenzaldehyde in Industrial ManufacturingAs the original producer of 2-Ethoxy-3-Methoxybenzaldehyde, we support core sectors that rely on high-purity aromatic intermediates. All described applications reflect established industry use, based on active supply to downstream partners and end users, with verified integration in regulated manufacturing environments. 1. Fragrance Ingredient Synthesis for Fine and Functional PerfumesMajor fragrance compounding operations use 2-Ethoxy-3-Methoxybenzaldehyde as a key aldehydic note in complex perfume structures, imparting nuanced, persistent top notes. International fragrance houses employ this ingredient for high-load blends, abstract florals, or modern aldehyde-driven olfactive directions. Blenders achieve compliance through precise batch control, quality documentation, and strict regulatory traceability. Industry compliance standards
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2. Pharmaceutical Intermediate for Active Ingredient SynthesisPharma manufacturers employ our material as a protected aromatic aldehyde in the synthesis of specialty APIs, especially where mono-substituted benzaldehyde frameworks are required by the target molecule. Strict CGMP controls and traceability steps are applied from receipt through final API purification to satisfy both authorities and client-specific requirements. Industry compliance standards
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3. Flavor Ingredient for Compound Seasonings and BeveragesLeading food additive blenders use this aldehyde as a trace-level flavor nuance in certain baked goods, soft drinks, and beverage flavors, where regulatory review supports inclusion. It delivers subtle ethereal and slightly spicy aromatic notes fully compliant with food safety protocols; formulation engineers precisely control batch inputs per established GRAS and local legislation. Industry compliance standards
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4. Key Aromatic Intermediate in Dye and Pigment ManufacturingMajor dye producers recognize this substituted benzaldehyde as a crucial intermediate in Schiff base and azo dye precursor synthesis. It enters color compound technologies where controlled reactivity and specific substitution patterns are required for end-use stability; raw material quality, impurity profile, and batch consistency are critical at this node. Industry compliance standards
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5. Organic Synthesis Building Block for Agrochemical FormulationCrop protection manufacturers source this aromatic aldehyde to develop custom fungicidal actives and pesticide intermediates. Its functional group arrangement supports targeted molecule design and balances bioactivity with regulatory acceptance in the EU and Americas. Integrated into closed production lines under controlled QA documentation and full supply chain transparency, traceability ensures safe entry into the agricultural market. Industry compliance standards
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We have spent years watching the needs of flavor, fragrance, and chemical industries shift. 2-Ethoxy-3-methoxybenzaldehyde stands as one of the more specific aromatic aldehydes we produce, chosen when characteristics of odor, reactivity, or subtlety set it apart from simpler benzaldehyde derivatives.
Chemists who formulate with aromatics can tell the difference in product performance the moment they switch from basic benzaldehyde to a functionalized ring with tailored substitutions. Ours, with an ethoxy on the second carbon and a methoxy on the third, does more than just shift the scent – it changes the entire reaction profile. Producing this molecule doesn't just involve textbook chemistry; it requires experienced oversight and a dedicated multi-step synthesis where clean separation and reliable process control keep yields predictable within every batch. Regular calibrations, repeated fractionations, and close attention to solvent grade are as important as any input chemical.
End users see our 2-ethoxy-3-methoxybenzaldehyde in a range of specialized applications. Formulators in the fine fragrance industry look for top-notes that linger and blend without swallowing lighter nuances. The dual ether substituents in our molecule suppress sharpness compared to plain benzaldehyde. Perfumers can dial in complexity, achieving that creamy, woody nuance which makes a difference in the final accord. Several household fragrance products have quietly relied on this compound to build a heart note that does not overwhelm but grants persistent depth.
Outside fragrance, flavor chemists use it as an intermediary. The substitution pattern provides a unique entry point for condensation and coupling reactions, especially where a less nucleophilic aromatic ring resists unwanted side-products. Synthesis labs prepping pharmaceutical intermediates turn to this compound for routes requiring enhanced electron donation without causing overactivation or decomposition under mild acid/base conditions.
Aromatic aldehydes remain in strong demand, but not all work the same. Routine industrial grades cover simple benzaldehyde, anisaldehyde, or vanillin, servicing broad industries with relaxed purity standards. The more highly substituted versions, such as 2-ethoxy-3-methoxybenzaldehyde, answer a narrower field of nuanced requirements. Every batch we make reflects choices in solvent quality, raw material relationships, and careful attention to fractional distillation columns. Batch purity consistently exceeds 98%, bearable for critical synthetic sequences or olfactory requirements where even trace side-products ruin a reaction or formulation.
Most competitors try to synthesize this type of functionalized benzaldehyde through generalized etherification, but practical yields suffer, especially with methoxy at the meta position. The correct temperature gradient and timing matter. Our process corrects for typical side-reactions, like over-alkylation, while preserving the core aldehyde group. The result: less by-product, lower levels of heavy hydrocarbons, and minimum contamination by starting phenols or alcohols.
We often hear from customers who have settled for plain benzaldehyde and noted sharp, bitter corners in their products. Swapping in 2-ethoxy-3-methoxybenzaldehyde removes many of these pitfalls. The ethoxy group scavenges off-notes, and the methoxy delivers a softer, more nuanced aromaticity. This change grows especially clear in side-by-side standards experiments several food flavoring and fragrance developers regularly report. Only a small replacement percentage is needed to boost complexity, avoid bitterness, and shift the aromatic profile closer to finished consumer demand.
In comparison to classic anisaldehyde or vanillin, this compound has a less sweet, less overpowering presence. The sensory attributes fall somewhere between green and creamy, which means flavor houses or perfumers can build top or heart notes without competing against heavy, sugary facets. Where cost sensitivity allows, customers in luxury skincare and wellness products switch to this aldehyde because its low volatility lengthens scent retention and maintains product freshness through storage.
Scaling up specialty aldehydes presents a unique set of headaches. We learned early not to shortcut purification or try to repurpose equipment from basic aromatic syntheses. Corrosive by-products, unexpected tarring reactions, and instability during longer runs forced us to redesign jacketed reactors and adjust solvent systems. The setup now includes enhanced cooling, nitrogen blanketing, and inline detection for aldehyde loss. These physical plant improvements let us avoid off-spec runs and minimize plant downtime, allowing for a tighter, more predictable supply timeline.
Another lesson came from odor contamination. During a production campaign two years ago, a supplier change in an alkyne solvent introduced trace sulfur compounds, invisible at instrumental detection, but unmistakable to an experienced nose. We have since worked only with vetted raw sources and regularly train production staff to spot deviations long before they reach QC. This hands-on, human element proves just as vital as analytical methods in safeguarding process integrity.
We see researchers using 2-ethoxy-3-methoxybenzaldehyde as a stepping-stone in synthetic routes for active pharmaceutical ingredient (API) precursors and fine chemicals with stringent structural requirements. Its substitution pattern creates a platform for efficient C–C bond-forming reactions where positional selectivity matters. A corner of our client base works on next-generation agrochemicals, requiring intermediates stable to handling but reactive enough for clean downstream conversion. They report fewer rearrangements or side-product formation with our material than alternatives sourced internationally.
It has also found a foothold in advanced polymers and resins. Lab-scale trials with specialized adhesives cite greater UV resistance and less discoloration when using this aldehyde versus more conventional aromatic monomers. Our process control ensures the end user receives a consistent, repeatable product from run to run, reducing time lost on downstream rework or batch rejection.
Many companies request support scaling up pilot batches or troubleshooting plant-to-plant transfer. Feedback centers on our willingness to share data from pilot runs, address real-world issues like solvent selection tolerance or downstream byproduct formation. Trust grows between supplier and customer when the manufacturer responds with practical advice rooted in day-to-day plant operation, not abstract specification sheets.
Over the last several years, tightening environmental regulations on certain organic solvents and gaseous emissions led to modifications in how we approach aldehyde production. Storage tank venting, off-gas scrubbing, and spent solvent recovery grew into significant process stages, not afterthoughts tacked on for compliance. Regular audits and close monitoring of emissions data convinced us to invest in on-site distillation and thermal oxidizer units.
Small batch variability started as a recurring problem, especially under changes of season when atmospheric humidity and raw material impurity loads fluctuate. Consistent product required a closer relationship with raw feedstock suppliers, long-term supply contracts, and a commitment to testing every incoming shipment by gas chromatography before use in production. These efforts translate into a visible decrease in end product odor variability, much appreciated by perfumers and flavorists with sensitive finished goods.
Demand for uniquely substituted aromatic chemicals continues to rise for those targeting niche fragrance accords, novel flavor compounds, and precision synthesis intermediates. The broad industrial market for basic aldehydes holds steady, but value increasingly flows toward differentiated chemicals that let formulators fine-tune their profiles and synthetic pathways.
Smaller, agile flavor houses repeatedly describe how shifting consumer demand for “clean label” and naturalistic profiles pushes them away from single-note aromatics into complex blends where subtlety counts. Our product supports that push toward multilayered taste and scent identities. Several R&D teams working on next-gen nut, grain, or orchard-type flavors describe the softening effect of our benzaldehyde derivative, making new launch concepts possible without masking with heavy sweetness or synthetic vanilla stand-ins.
In personal care and wellness, formulators pursue mildness and persistence over raw power. They value a molecule gentle enough for facial creams or aromatherapy, yet robust enough to withstand months of shelf life. This product balances those traits, neither evaporating too quickly nor disappearing during product aging.
We do not view chemical manufacturing as a static practice. Every year brings new analytical challenges, fresh raw material disruptions, and even new uses for old intermediates. Feedback loops from end users form a critical part of our process. Technical staff often join customer teams in person to trace product issues down to root cause. In cases where an odd off-note or trace reactivity ruins a high-value batch, we run side-by-side plant trials to isolate and solve the issue rather than simply retesting for compliance on paper.
One example came from a partner developing a medical device coating. They reported discoloration and inconsistent laydown with earlier lots from another manufacturer. Combining high-purity feedstock, tighter distillation cuts, and new microfiltration steps, our team reduced trace metal and peroxide levels in the finished aldehyde to below industry benchmarks. Their finished product improved measurably, cutting down returns and increasing end-user confidence.
We also benefit from customer innovation. Shared experiments with research partners often uncover unexplored end uses. Sterically hindered aromatic intermediates, such as 2-ethoxy-3-methoxybenzaldehyde, now play a role in complex ligand design for advanced catalysis. These discoveries redirect our own R&D focus, keeping offerings up to date with the changing face of specialty chemistry.
Direct contact with the manufacturing floor has a real-world impact on reliability and quality. Distributors or resellers may move commodity volumes, but only the producer controls every upstream and downstream control point, and sees the concrete outcome of changing a solvent, altering a catalyst bed, or tuning the temperature gradient across a column. When end users come to us with a clear description of their performance needs—be it for aroma, reactivity, or physical properties—they receive actionable suggestions that actually reflect day-to-day reality.
On a practical level, end-user audits and regulatory compliance trace smoothly from producer to final customer. Documentation, process transparency, and rapid troubleshooting respond to manufacturing realities, not just specification sheets. We provide regular, tailored reports detailing batch variability, impurity profiles, and certificate of analysis data in line with the expectations of regulated sectors like pharma and flavors.
Recalls and off-spec product issues most often trace back to fragmented supply chains. Our approach circumvents these risks by emphasizing tight vertical integration from raw materials through final packaging. End users lessen their own risk of production delays, regulatory headaches, or product failures by drawing their specialty aromatics directly from us.
Industries served by 2-ethoxy-3-methoxybenzaldehyde look toward the coming decade with rising expectations for performance, transparency, and reliability. Green chemistry initiatives and process intensification chart much of our future investment. Our technical teams explore milder catalyst options, improved process analytics, and solvent recovery improvements to further shrink environmental impact without sacrificing output. We also work with customers to map potential alternative feedstocks as global raw material markets tighten and sustainability pressures increase.
Training, research, and direct experience guide every process adjustment. As the next generation of chemists arrives, we invest in their hands-on exposure to the subtleties of specialty organic synthesis and purification. We encourage open dialogue with end-users, accept constructive criticism from both the shop floor and laboratory, and build knowledge networks that allow for collective progress.
Every batch of 2-ethoxy-3-methoxybenzaldehyde leaving our facility stems from a practical understanding of how nuanced structure drives function. We see our product not as a commodity but as a tool which lets innovators in flavor, fragrance, materials, and pharmaceuticals move forward with confidence. Achieving tight purity, reliable odor profile, and consistent reactivity requires steady attention to process minutiae, honest technical feedback, and a willingness to refine operations based on real-world results.
The future demands even greater flexibility and understanding from manufacturers who support rapid innovation in all corners of modern chemistry. We aim to meet those expectations with every shipment, backed by the lessons learned on the manufacturing floor and the knowledge that even small molecular differences create lasting impacts on end-user success.