|
HS Code |
893663 |
| Productname | 3-Ethoxysalicylaldehyde |
| Casnumber | 13432-34-7 |
| Molecularformula | C9H10O3 |
| Molecularweight | 166.18 |
| Appearance | Yellow liquid |
| Boilingpoint | 118-120°C at 12 mmHg |
| Density | 1.159 g/cm3 |
| Refractiveindex | 1.553 |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents |
| Smiles | CCOC1=CC(=CC=C1C=O)O |
| Inchikey | JQDKAQYUKUXWMJ-UHFFFAOYSA-N |
| Synonyms | 3-Ethoxy-2-hydroxybenzaldehyde |
| Storagetemperature | Store at 2-8°C |
As an accredited 3-Ethoxysalicylaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle of 3-Ethoxysalicylaldehyde, sealed with a screw cap, labeled with hazard and chemical information. |
| Shipping | 3-Ethoxysalicylaldehyde is shipped in tightly sealed containers to prevent moisture and air exposure. The chemical is labeled according to regulatory standards and handled as a hazardous material. It is transported in compliance with international regulations, ensuring protection from heat, light, and physical damage during transit. Suitable packaging is used to prevent leaks or spills. |
| Storage | **3-Ethoxysalicylaldehyde** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Protect it from light and moisture. Ensure storage conditions prevent exposure to air to avoid degradation. Properly label the container and follow all relevant safety guidelines for handling aromatic aldehydes. |
Applications of 3-Ethoxysalicylaldehyde in Industrial ManufacturingAs a direct manufacturer, we supply 3-Ethoxysalicylaldehyde for advanced synthesis and specialty formulation sectors. Our material is produced under controlled conditions to meet quality, traceability, and consistency demands. The following application scenarios reflect real, validated downstream industries where this intermediate drives value by supporting specific, regulated processing or end-product requirements. 1. Pharmaceutical Intermediate Synthesis for API ManufacturingPharmaceutical companies incorporate 3-Ethoxysalicylaldehyde as a key building block in the synthesis pathway of select active pharmaceutical ingredients (APIs), predominantly those involving salicylaldehyde derivatives or heterocyclic frameworks. Our product finds particular use during the condensation or cyclization stages where purity and traceability impact downstream impurity profiles. API manufacturers adjust reagent quantity in line with stringent batch-to-batch consistency, guided by protocol validation and impurity monitoring for global regulatory submissions. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Active Ingredient SynthesisIn the agrochemical sector, 3-Ethoxysalicylaldehyde is integrated into the synthesis of fungicide and herbicide intermediates that require precision in the formylation of aromatic rings. The controlled introduction in multi-step synthesis supports the development of complex molecules that target resistant crop pests. Agrochemical manufacturers rely on its high assay and low moisture content to stabilize reactive syntheses and minimize side reactions, which is critical for achieving high-yield, high-purity actives in line with crop protection performance requirements. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Synthesis of Functional Dyes and PigmentsDye manufacturers utilize 3-Ethoxysalicylaldehyde for constructing colorant molecules where electron-donating and electron-withdrawing features must be precisely balanced on an aromatic core. Its controlled addition governs desired shade, absorption/emission properties, and stability in final dye structures. Production facilities integrate this intermediate during the condensation or Knoevenagel steps, maintaining strict reaction parameter control to comply with coloring matter legislation and minimize by-product formation. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Synthesis of Aroma and Fragrance IntermediatesThe fragrance industry uses 3-Ethoxysalicylaldehyde in fine-chemical synthesis routes for aromatic aldehyde intermediates that enhance complex fragrance blends, especially for applications demanding high stability and nuanced top notes. Its addition influences olfactory tone and chemical mimicry of natural scents. Producers enforce batch QA with GC and impurity profiling as material feeds into acetalization, reductive amination, or further derivatization units relevant for the composition of premium fragrances and flavor compounds. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 3-Ethoxysalicylaldehyde prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
After years of producing 3-ethoxysalicylaldehyde on an industrial scale, our team knows what it takes to deliver a reliable intermediate for demanding formulation work. We have carried this product through countless seasonal batch runs, re-tuned our protocols for yield and clarity, and helped end users troubleshoot formulations that depend on consistency, predictable reactivity, and low impurity levels. We see aromatic aldehydes in two camps: those that meet strict trace requirements for advanced synthesis and off-the-shelf batches that drift over time. From experience, few intermediates reward close process control and skilled handling as much as this compound does.
With the molecular formula C9H10O3, 3-ethoxysalicylaldehyde contains an ethoxy group substituted at the 3-position on the salicylaldehyde backbone. The material arrives as a pale-yellow liquid in its purest form. Over the years, we have refined each stage—starting with phenolic etherification, then controlled oxidation, followed by careful distillation—to keep every lot within typical specifications. Our routine GC analysis shows our product maintaining an assay above 99% by area normalization. Water levels and color are also tightly monitored, since both can complicate downstream reactions.
Some manufacturers focus attention on throughput. We directed our investment at batch uniformity and isolation techniques to reduce congeners, since most of our clients ask about low byproduct levels. We regularly hear from R&D chemists across the pharmaceutical sector and fine chemical houses who cannot afford variability in key intermediates: an off-spec lot can set a campaign back by weeks. By adhering to narrow process windows, we give our users what they’ve come to expect—no hidden surprises at the work-up stage.
In real-world practice, most of our output finds its way into fine organic synthesis, especially as a precursor for more elaborate molecules. Our 3-ethoxysalicylaldehyde often travels from our reactors directly to pharma and agrochemical R&D lines. Synthetic chemists value the ethoxy substitution at the meta position because it changes both reactivity profile and steric environment. It gives better control during subsequent condensation and cyclization stages, opening up routes not accessible with unsubstituted salicylaldehydes or other positional isomers.
One common use involves Schiff base formation. Customers report smoother, higher-yielding reactions with our material compared to unrelated aromatic aldehydes or certain ortho/para variants. Choice of substitution on the aromatic ring governs not only product yield but also downstream analytical characteristics—especially when screening for novel ligands or running combinatorial syntheses. We have observed that minor shifts in the position of the ethoxy group alter spectroscopic signatures and separation behavior in chromatography. Each of these differences matters downstream, and every lab move upstream can ripple through an innovation pipeline.
Besides ligand synthesis, another key area lies in advanced material development. This includes dendrimer anchors, specialty polymers, and dye intermediates. Bench chemists often point out how electron-donating groups like ethoxy at the meta position affect not only nucleophilicity but also solution stability. Many specialty applications, from photoinitiators to advanced chelating agents, require starting materials with specific aromatic substitution patterns and minimum trace contaminants. As manufacturers, we have worked through iterative cleaning and drying steps so that the impurity profile does not drift between lots or through extended storage.
Aromatic chemistry offers a host of salicylaldehyde derivatives. Over the past decade, requests have shifted from simple salicylaldehyde to a spectrum of ethoxy, methoxy, and halogenated variants. Side-by-side, clients notice tangible differences between each. For example, o-ethoxysalicylaldehyde and p-ethoxysalicylaldehyde both differ in reactivity and hydrogen bonding, which translates into changes in final product solubility and color.
Unsubstituted salicylaldehyde, though easy to source, lacks the fine-tuned reactivity for certain condensation or cyclization steps—a fact many find only after repeat runs and chromatographic work. Here, the structural features of 3-ethoxysalicylaldehyde—particularly the meta ethoxy group—moderate electronic effects without introducing the kind of steric hindrance seen in the ortho variant. This creates slightly higher selectivity and improved yields, especially in aza-heterocycle synthesis. Many researchers have shown us kinetic data or handed in spectra and TLC plates after trialing multiple salicylaldehyde isomers. 3-ethoxysalicylaldehyde appears to hit a balance: enhanced reactivity over unsubstituted material, cleaner separation than the ortho isomer, and less solubility headaches than para analogues.
We also see clear differences in odor and handling. The 3-ethoxy variant emits significantly less pungency than salicylaldehyde itself, and chemists working long hours in fume hoods appreciate the reduced volatility and improved work environment. Proper packaging minimizes degradation, so we match bottle size and lining to specific storage needs. In high-throughput settings—where precision outpaces speed—reproducibility sets a premium. Over the years, clients have shared stories about contaminated or slow-reacting samples from general chemical traders, which disrupts not just R&D but also planning in pilot lots. Direct supply from a dedicated reactor line, with ongoing analytical support, brings both peace of mind and a tangible return for the applications that lean on close tolerances.
In chemical manufacturing, the best process improvements grow from problem-solving. We have faced polymerization trouble during distillation and stubborn discoloration during product isolation. Each time a customer provides feedback—sometimes a change in odor, yield, or color—we track it to the root and tweak parameters in the next run. Beyond simple specs, we learned a lesson familiar in the pharmaceutical industry: full traceability and documentation provide value long before inspectors ask for paperwork.
Customers planning GMP synthesis or later-stage clinical trials press for more than purity numbers. They expect records showing temperature, pressure, and analytical signatures at each stage. Many production campaigns draw from multiple drum lots, stretching across months. This means every unit must trace back to its reactor, with full retention of spectra and chromatograms. Starting materials like 3-ethoxysalicylaldehyde often make up a small share of total cost, but they sit in the critical path. As the manufacturer, we found the up-front work on documentation, enterprise-level batch records, and authenticated sample retention adds reliability to the entire supply chain. Some new clients call after experiencing sudden IMF or FDA attention triggered by missing or incomplete audit trails. Our decision to invest early in digital QA tracking and standardized lot referencing now saves both time and headaches—often at the very point it matters most.
Environmental responsibility has changed how everyone runs aromatic chemical synthesis. Gone are the days of unchecked disposal or loose emission standards. Each batch of 3-ethoxysalicylaldehyde now requires a clear report of solvent recovery percentage, effluent treatment, and byproduct tracing. Stakeholders in pharmaceutical, agrochemical, and advanced materials demand not only technical results but also assurance that upstream chemicals meet modern production codes. Regulatory pressure increases every year, not just from agencies but also from internal procurement teams guided by ESG audits. So, we changed our work too.
A few years ago, we swapped out halogenated solvents and pooled significant resources into solvent distillation systems that recycle streams through multi-stage recovery. Real-time emissions sensors and periodic third-party wastewater audits moved from “nice to have” to required operating procedure. Our teams shifted to batch-record software that captures not only product outcomes but also each step’s environmental footprint. We found clients pay attention, especially those with European or North American end users, who must map the entire sourcing chain when submitting regulatory files. In one recent case, our documentation on recycled solvent sources and low-emission heating allowed a client’s product to clear EU REACH review without secondary data requests.
Whether a customer needs a single research-scale bottle or a long-term bulk contract, producing 3-ethoxysalicylaldehyde at scale means more than filling containers with yellow liquid. Every batch reflects thousands of hours spent optimizing reaction times, tuning distillation columns, and double-checking clean-in-place procedures so that no trace contamination creeps in. Over time, feedback cycles between chemists at the bench and operators at the plant shape best practices for drying, storage, and even vessel selection. In our lab, a shift in ambient temperature or a slightly out-of-spec drum taught us how fragile aromatic aldehydes can be—not just to heat or moisture but also to oxygen exposure and transportation vibration. With each lesson, we improved storage, packaging, and shipment practices to preserve the product’s characteristics.
Some end-users in specialty chemicals and fine organic synthesis have reported dramatic improvement in process throughput simply by switching to a 3-ethoxysalicylaldehyde with a more consistent impurity profile and lower chromophoric residues. A dye manufacturer once traced a recurring color shift in product batches back to a trace contaminant—one we now test for and spike below critical levels. The difference lay not in headline assay figures but in regular analytical surveillance and the direct relationship between synthesis-scale feedback and production scale.
Our approach now centers on direct dialogue with users. Scaling up is routine, but translating bench results to reliable bulk output demands full attention to process detail and risk management. Whether shipping drums overseas for a multinational pharmaceutical or supplying kitted bottles for research, we know that supporting innovation at our customers’ sites starts by respecting every step inside our own. Our ongoing investments in analytical chemists, digital QC monitoring, and close client interaction set the foundation for chemistry that performs predictably and safely, wherever it ends up.
We have weathered boom and bust cycles in bulk aromatic intermediates, from the scarcity of reliable starting materials to the glut that occasionally follows a market craze. Through each, the strongest principle remains unchanged: measured improvements over time matter more than any marketing line. By auditing supply chain steps, refining purification, and holding finished goods to demanding standards, we have built not just a product shelf but a production culture. This approach protects both our clients and our own people. In an industry where a stray contaminant or inconsistent reagent can cascade through entire syntheses, the most important tool at our disposal remains the continuous, open channel between process technology and the needs of experienced scientists at the bench.
These insights shaped every improvement, from a humble pressure gauge upgrade to full-on SCADA automation and deeper statistical analysis of final purity. Customers depend on us to flag any blip and act decisively. By working closely with academic and industrial partners, we actively participate in protocol development and product trials, always open about both successes and setbacks. When we identify a new degradation product or fail a batch, lessons get passed down the entire chain. This results in a higher baseline of trust, one that shows up in reliable project outcomes rather than the prospect of piecing together answers from anonymous traders.
We take pride in our 3-ethoxysalicylaldehyde, but not for any superficial reason. Its true value emerges through the hard-won lessons of consistent, attentive manufacturing. We produce this aromatic aldehyde for practical chemists who insist on trustworthy inputs, minimizing unexplained results at their bench and catching regulatory challenges before they cost real time and money. Every batch that leaves our facility carries the legacy of thousands of reactions on winding synthetic pathways, and each drum or bottle marks a commitment to both your output and our shared standards in modern chemistry.