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HS Code |
175561 |
| Product Name | 3-(4-Ethoxybenzoyl)Propionic Acid |
| Cas Number | 30841-19-7 |
| Molecular Formula | C12H14O4 |
| Molecular Weight | 222.24 g/mol |
| Appearance | White to off-white powder |
| Melting Point | 94-98°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water; soluble in organic solvents (e.g., ethanol, DMSO) |
| Storage Conditions | Store at room temperature, away from moisture and light |
| Smiles | CCOC1=CC=C(C=C1)C(=O)CCC(=O)O |
| Inchikey | MNQHWOABFZKQCG-UHFFFAOYSA-N |
As an accredited 3-(4-Ethoxybenzoyl)Propionic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 3-(4-Ethoxybenzoyl)propionic acid, tightly sealed, with hazard and identification labels. |
| Shipping | **Shipping Description:** 3-(4-Ethoxybenzoyl)Propionic Acid is shipped in a tightly sealed container, protected from light, heat, and moisture. It is labeled according to chemical safety regulations and packed to prevent leakage or damage during transit. Usually shipped as non-hazardous, but always check local regulations for specific shipping requirements. |
| Storage | Store **3-(4-Ethoxybenzoyl)propionic acid** in a tightly sealed container in a cool, dry, and well-ventilated place. Keep away from incompatible materials such as strong oxidizing agents. Protect from light and moisture. Label the container clearly and avoid exposure to heat or direct sunlight. Use appropriate personal protective equipment when handling, and always follow laboratory safety guidelines. |
Applications of 3-(4-Ethoxybenzoyl)Propionic Acid in Industrial Manufacturing3-(4-Ethoxybenzoyl)Propionic Acid serves as a critical intermediate for a select number of mature, volume-driven industrial processes. As an original chemical manufacturer with extensive process know-how, we supply this raw material in strict accordance with national and international regulations to downstream users specializing in high-value API synthesis, UV absorber development, specialty agrochemical preparation, and liquid crystal monomer production. Below, we detail specific industrial application scenarios, regulatory interfaces, formula ratios, integration steps, and resulting product types—ensuring reliable downstream performance and compliance. 1. Pharmaceutical Intermediate for Nonsteroidal Anti-Inflammatory Drug (NSAID) SynthesisDownstream API manufacturers use 3-(4-Ethoxybenzoyl)Propionic Acid as a key synthetic intermediate in producing certain NSAIDs such as etodolac. During multi-step synthesis, our material ensures structural specificity for the target compound, minimizing byproducts according to validated process pathways. Accurate dosing and QC, aligned with pharmacopoeial monograph requirements, remain essential to ensure global finished drug release. Industry compliance standards
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2. UV Absorber Manufacture for Industrial CoatingsFormulators in the coatings sector incorporate 3-(4-Ethoxybenzoyl)Propionic Acid to synthesize benzophenone-derivative UV absorbers. These downstream products require precise integration of our material to achieve the desired chromophore structure for polymer protection, particularly in automotive clear coats, plastic films, and wood varnish. Proper adherence to international chemical control standards and correct batching against resin weights determine photo-stabilizer performance and user safety. Industry compliance standards
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3. Intermediate for Agrochemical Active Ingredient SynthesisSpecialty crop protection companies use 3-(4-Ethoxybenzoyl)Propionic Acid as a building block for selective herbicide and fungicide molecules requiring aromatic substitution. Regulatory traceability of raw material origin and downstream integration in controlled batch synthesis are crucial for meeting product registration standards and residue regulations in various global markets. Industry compliance standards
Typical usage ratio
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4. Precursor in Liquid Crystal Monomer DevelopmentProducers of advanced display materials select 3-(4-Ethoxybenzoyl)Propionic Acid for synthesizing monomers with finely-tuned mesogenic cores. Strict contamination control and precise reagent ratio are essential for maintaining electro-optical properties and phase stability in adaptive display and advanced optical films. Materials handling and clean synthetic protocols follow sector-leading standards for purity. Industry compliance standards
Typical usage ratio
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Producing specialty chemicals demands consistency, especially when users depend on each batch to act predictably in high-stakes applications. Drawing from years of hands-on work in synthesis, 3-(4-Ethoxybenzoyl)Propionic Acid stands out to us as a robust intermediate favored in pharmaceutical research and advanced material projects. Our line, specifically under model EBPA-03, reflects hard work refining each step, from raw material sourcing to solvent removal and the final purification stages. Routine testing across all stages has given us an appreciation for the product’s crucial benchmarks—color, purity, melting range, solubility—and their impact on downstream results.
Every gram of 3-(4-Ethoxybenzoyl)Propionic Acid coming off our reactor aligns with rigorous guidelines. During purification, we see the melt-point stay steady in a reliable window, an outcome linked to both precise temperature programming and removal of color bodies and trace by-products. Analytical work—particularly HPLC, TLC, and nuclear magnetic resonance—corroborates the purity levels, typically surpassing 99%. Finished powder has a faint off-white color, with the ethoxyphenyl signal presenting crisp and distinct on proton NMR. We pack our batches with an eye to keeping out light and moisture, as those factors can influence shelf stability, and we keep a close watch on any low-level impurities, ensuring they remain far below typical thresholds so as not to cause interference in catalytic or enzymatic studies.
In daily work, researchers and process chemists seek reliable intermediates that perform predictably. 3-(4-Ethoxybenzoyl)Propionic Acid bridges key transformations—particularly for designing compounds that require a benzoyl core extended by an aliphatic chain. We have seen chemists turn to this molecule for creating heterocycles, via cyclization reactions, and for providing essential linkers in complex molecule assembly. Its carboxylic acid group invites esterification and amidation, while the ethoxy substituent on the benzene ring subtly modulates electronic properties, giving rise to selective reactivity under varied conditions. Our clients in medicinal chemistry often comment on the ease with which it integrates into multi-step syntheses, leveraging the ethoxy handle as a site for further functionalization or as a means to affect pharmacokinetics in target compounds.
Not all propionic acid derivatives serve the same needs. The specific 4-ethoxy substitution on the benzoyl ring influences both solubility in organic solvents and the rate of electron withdrawal during key reactions. Compared to the more common 4-methoxy or unsubstituted benzoylpropionic acids, our product tends to dissolve more readily in solvents like dichloromethane, ethyl acetate, and even toluene, which has helped our partners run cleaner work-ups and extractions. The reactant’s electron-donating properties, brought by the ethoxy group, tune reactivity during condensation or ring formation steps, especially when forming complex aromatic systems where selectivity cannot be compromised. Our in-house tests reveal less by-product formation in Friedel-Crafts acylation when using 3-(4-Ethoxybenzoyl)Propionic Acid compared to the methoxy equivalent, a reflection of direct experience with both molecules under otherwise identical conditions.
From the manufacturing floor, several trends influence how specialty acids like this must be produced. Customers often request flexibility in batch size—sometimes pilot, sometimes full production. Running our system in both kilo-lab and commercial reactors has been educational: It’s easier to maintain consistency when feeding and agitating conditions match experience from scale-up trials. Crystallization—always a make-or-break step—shows distinct behaviors for 3-(4-Ethoxybenzoyl)Propionic Acid compared to other analogues: It forms dense needles, and if cooled too quickly, occluded solvent can get trapped, raising purity concerns. Over time, we have refined filtration and washing steps, switching between cold isopropanol and water or tweaking the pH during the acidification, to ensure the mother liquor contains nothing problematic.
Customers tell us that the compound’s robust performance as a building block saves them both time and cost in downstream processing, especially since clean reactions reduce the burden on final purifications. Documented cases show the use of our product in non-steroidal anti-inflammatory drug R&D and as a coupling intermediate in polymer chemistry, pointing toward versatility that goes beyond single-project demands.
The strength of every batch starts with the inputs. Sourcing high-grade 4-ethoxybenzoic acid and assuring propionyl chloride stocks meet exacting GC and water content specs keep our process in control from the outset. The choice of catalyst—whether switching between Lewis acids or acid anhydrides—gives us different yield and impurity profiles; years of testing have led us to a preferred combination, one that maximizes conversion and cuts down on heavy residues. Each run sees a verification step where we check for residual starting acid by HPLC, since any leftover precursor can compromise subsequent steps in pharmaceutical and pigment applications.
Packing the product also gets hands-on attention. We learned early that headspace humidity and oxygen exposure, especially on hot days or during long shipments, can shorten the shelf life. Our plant switched to using laminated, opaque packaging that offers a vapor-barrier, and we often flush the headspace with inert gas to minimize oxidation risk. This might matter less for immediate-use batches, but our customers focused on long-term storage consistently reported fewer issues since we changed procedures.
Handling 3-(4-Ethoxybenzoyl)Propionic Acid requires practical steps to manage both dust and the mild irritant properties seen in bench and pilot trials. Unlike more hazardous benzoylchloride derivatives, this acid doesn’t release corrosive fumes, and it remains stable under recommended storage conditions, typically between 2 and 8°C. Everyone who interacts with it on our floor wears gloves and dust masks, not because of acute dangers, but to keep allergic skin reactions and mild respiratory irritation at bay. Our logistics team packs the product in double-lined bags inside leak-proof, heavy-wall drums which stack securely, lowering the odds of leaks or spills in transit.
Regulatory compliance remains central to how we approach all shipments. We monitor changing transport regulations—especially those impacting export to the EU, North America, or Japan. Although our acid doesn’t trigger most dangerous goods rules, we attach documentation that identifies potential hazards and points out safe handling requirements based on feedback we have received from importers and regulatory reviewers.
From the bench to plant, several sticking points come up with benzoylpropionic acids: solubility, ease of purification, and compatibility with sensitive reactants. Our technical support draws on real experience troubleshooting these hurdles. For example, scaling up a reaction involving 3-(4-Ethoxybenzoyl)Propionic Acid calls for attention to solvent ratio and order of addition—undissolved acid at the start can generate inconsistent yields. We recommend a pre-mix step, heating gently while stirring to ensure complete dissolution before introducing bases or coupling agents.
Neutralization and washing during work-up also benefit from specific approaches. Too rapid a pH swing can precipitate sticky gums or cause emulsions; we advise controlled, gradual addition of acid or base, followed by phase separation under agitation. Our product’s tendency to crystallize cleanly at lower temperatures, compared to analogues, gives a practical edge—less oiling out and more solid recovery. For those running multistep syntheses, minimizing residual solvent trapped in the cake becomes key; longer vacuum drying and a staged reduction in temperature has improved consistency for several partners, especially in humidity-prone regions.
Laboratory teams and research organizations experimenting with next-generation drugs, agrochemicals, or novel polymers continually press for higher quality standards in chemical building blocks. By producing 3-(4-Ethoxybenzoyl)Propionic Acid to such standards—validating each lot, maintaining clear chain-of-custody documentation, and supporting repeat sampling—we contribute to experimental reproducibility. We know from client collaborations that switching from less pure alternatives to our product can cut down on batch-to-batch variability and unexpected side-products, driving smoother scale-up to pilot or full production.
Some organizations want customization for certain applications—particle size, drying profile, or pre-blending with compatible solvents. We respond directly, not through intermediaries. Because our staff run the same reactors and perform the same crystallizations as our customers do, we recreate and troubleshoot actual conditions faced by labs and factories. We have even paired technical support with ongoing production runs, offering advice on how to integrate 3-(4-Ethoxybenzoyl)Propionic Acid into new or existing synthetic workflows, and sharing bench-level tips that skip the common pitfalls of overgeneralized datasheets.
Cost, performance, and timelines all shape customer requirements. Our perspective as a manufacturer means we track seasonality in raw material prices and transportation delays to secure the best inputs and guarantee continuous supply. Working with 3-(4-Ethoxybenzoyl)Propionic Acid involves more than putting out a specification—it relies on understanding and controlling every variable, from batch scales of a few hundred grams for development work right through to multi-ton campaigns. We balance cost-effectiveness with the integrity of each lot, investing in in-process controls that catch issues before they reach final QA.
Feedback from partnerships has guided several process changes. In response to tighter rejection thresholds for trace impurities seen in biologic R&D, our production lines introduced extra carbon polishing and multiple recrystallization cycles. Where customers flagged problems with slower dissolution during high-throughput screening, we modified drying regimes and improved particle reduction steps, offering finer, more free-flowing acid that disperses quickly and cleanly.
Having worked with various aromatic acids, subtle property shifts become clear. Compared to traditional benzoylpropionics lacking the ethoxy group, our 3-(4-Ethoxybenzoyl)Propionic Acid scores higher in cold solubility tests. That enables lower-temperature reactions, valuable for heat-sensitive assemblies, and means reduced loss to filtration. Compared with the 4-methoxy counterpart, the ethoxy provides a slower, more controlled reactivity in certain condensations and ring closures, which process chemists appreciate when trying to minimize by-products.
We have also seen improved compatibility with common coupling agents—EDC, DCC, and carbodiimides—which contribute to higher yields of amides and esters, day after day. That repeatability comes from both the molecule’s intrinsic properties and the fine-tuning we have invested in manufacturing.
Reliability in specialty chemicals relies not just on scale but on direct oversight, measurable outcomes, and honest answers. Our technical and manufacturing teams work closely, and feedback loops from hundreds of customer projects continually shape each production run. We track every key performance figure—melt point, color, HPLC trace, water content—to avoid guesswork. With 3-(4-Ethoxybenzoyl)Propionic Acid, we strive to balance high performance and regulatory assurance, supporting our users in sectors where precision and innovation define success.
By keeping production in-house, we remain responsive when needs shift or standards change. That means rapid iterations, custom production scales, and consistent transparency throughout each order. Our staff bring together both chemical expertise and a craftsman’s attention to process. With each batch, our goal remains unchanged: deliver a chemical tool our partners trust, informed by practical experience and a genuine belief in the value of rigorous, reliable manufacturing.