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HS Code |
792781 |
| Iupac Name | Ethyl 3-(3,4-dimethoxyphenyl)-3-oxopropanoate |
| Molecular Formula | C13H16O5 |
| Molecular Weight | 252.26 g/mol |
| Cas Number | 19147-16-1 |
| Appearance | White to off-white solid |
| Melting Point | 63-67°C |
| Boiling Point | 372.6°C at 760 mmHg |
| Solubility | Soluble in organic solvents like methanol, ethanol, and DMSO |
| Density | 1.18 g/cm³ |
| Smiles | CCOC(=O)CC(=O)C1=CC(=C(C=C1)OC)OC |
| Purity | Typically >98% |
| Storage Temperature | Store at 2-8°C |
| Refractive Index | 1.522 |
As an accredited 3-(3,4-Dimethoxy-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester 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, sealed with a screw cap, labeled with the chemical name, concentration, CAS number, and hazard symbols. |
| Shipping | This chemical, 3-(3,4-Dimethoxy-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester, is shipped in tightly sealed containers, protected from moisture and light. It is packed according to regulations for non-hazardous laboratory chemicals, with labeling for identification and handling instructions. Standard delivery options and temperature controls are available upon request. |
| Storage | 3-(3,4-Dimethoxy-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated location. Store away from incompatible substances such as strong oxidizing agents. Keep at room temperature or as recommended by the supplier, and avoid excessive heat to maintain chemical stability and prevent decomposition. |
Applications of 3-(3,4-Dimethoxy-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester in Industrial Manufacturing3-(3,4-Dimethoxy-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester is a core intermediate for advanced organic synthesis. Our direct synthesis and quality control enable precise integration into specialized workflows across pharmaceutical, agrochemical, and material science domains. Below, we outline key downstream application tracks with their technical requirements and industrial fabrication pathways. 1. API Precursor in Non-Steroidal Anti-Inflammatory Drugs (NSAIDs)This compound plays a critical role as a building block in the multi-step synthesis of specific NSAIDs, particularly where dimethoxyphenyl substitutions influence pharmacological profiles. Manufacturers use it in acylation and condensation reactions during the upstream stages of active pharmaceutical ingredient (API) development, ensuring target molecule purity and batch uniformity. Industry compliance standards
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2. Intermediate for Agrochemical Synthesis (Herbicide and Fungicide Actives)Agrochemical formulation companies select this ester for fabricating block molecules central to the production of selective herbicides and systemic fungicides. Its unique substitution pattern optimizes binding affinity in actives targeting resistant weed and fungal strains through advanced synthetic routes. Industry compliance standards
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3. Chemical Intermediate in Specialty Polymer AdditivesPolymer manufacturers employ this compound as a monomeric precursor in the tailored synthesis of additives imparting UV protection and oxidative stability for coatings and plastics. The dimethoxy groups facilitate integration into polycondensation workflows used in specialty films and engineered resins. Industry compliance standards
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4. Building Block for Bioactive Flavonoid Derivatives in Nutraceutical ManufacturingNutraceutical and botanical firms utilize this ethyl ester as a precursor for semi-synthetic modification of core flavonoid structures, enhancing solubility and biological activity in dietary supplement actives. Its defined aromatic substitution allows precise enzymatic or chemical elaboration without uncontrolled side reactions. Industry compliance standards
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5. Starting Material in Research Scale Synthesis of Novel Organic CompoundsScientific and R&D laboratories source this ester for early-stage synthesis of structurally modified bioactives, dyes, and advanced materials. Its defined functionality supports robust route scouting and structure-property relationship studies for subsequent upscaling. Industry compliance standards
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Year after year, specialty chemicals like 3-(3,4-Dimethoxy-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester have played a defining role in downstream development for a surprisingly diverse array of applications. As a manufacturer, our approach doesn’t start with the chemistry itself but rather with the needs of experienced R&D professionals and process engineers. We work side-by-side with teams who expect not just purity—measured by GC or HPLC—but by robust supply chains and lot-to-lot reproducibility that shave days and errors off large batch production.
This ethyl ester, often referenced by the model DMPEE-03, is more than a list of chemical attributes. Drawing from years of continuous synthesis, we emphasize parameters like minimum assay, residual solvents, isomer ratios, and color by APHA, all backed by batch-centered quality control. Every tank, every blend, and every shipment draws from analytical data supported by in-process controls. Stability—even in the face of long-haul logistics cycles or shifts in raw material quality—always sits at the core of our manufacturing strategy.
Sourcing intermediates with a finely tuned structure like DMPEE-03 often presents non-obvious challenges. It isn’t just about a simple one-pot reaction. As we’ve learned, selecting the right grade of starting reagents sets the trajectory for downstream chromatographic impurities and yield curves. It’s a mistake to think of this as a routine esterification. Each production run starts by verifying the integrity of our phenolic precursors and ensuring the catalysts haven’t drifted in effectiveness across consumption cycles.
Many customers come to us seeking materials for critical synthetic building blocks—pharmaceutical intermediates, specialty polymers, advanced agrochemical candidates. We’ve seen that while catalog vendors may deliver a lab-scale quantity, reproducibly scaling those syntheses for an industrial process introduces unique hurdles. Foam control, exothermicity at scale, and recycling solvents without cross-contamination turn “cookie-cutter” processes into sources of risk. Over the past decade, our in-house teams have refined continuous processes with strict controls on temperatures, reagent addition times, and in situ monitoring. These details block up unwanted side products and cut down on costly reprocessing.
In a world flush with similar-sounding esters and ketone-bearing acid derivatives, buyers quickly spot the subtle factors marking the difference between a commodity-grade input and a pharmaceutical-ready intermediate. Our DMPEE-03 avoids excess residual acidity or broad impurity profiles. We monitor trace decomposition products using validated analytical methods, preventing batch-to-batch surprises that disrupt synthesis downstream.
As manufacturers, we address more than just yield and purity on a spec sheet. The two methoxy groups on the aromatic ring bring improved solubility characteristics, especially in polar and aprotic solvents. We tailor isolation and drying steps to avoid water ingress, which can trigger unwanted hydrolysis or transesterification, deteriorating the material for downstream uses. A process that succeeded for one aromatic ester might not translate to this molecule. After dozens of scale-ups and late-night troubleshooting, our team corrected subtle process drifts, ensuring the color and odor sit within tight bounds, and the profile matches up across years.
Years of hands-on feedback from formulators and chemists confirm what the books don’t always stress: specifications sometimes mask what truly matters on the plant floor or benchtop. For DMPEE-03, trace solvent residues—let’s say, ethanol from the esterification—can tip off an entire campaign if not controlled under low ppm. We measure and report all volatiles down to relevant thresholds, not just at the time of packing but throughout storage stability checks. Stability studies under ultraviolet exposure, different pH stores, and temperature cycles guarantee consistent performance regardless of warehousing conditions.
Production methods at scale have forced us to confront certain persistent problems. For instance, solvent recovery from aromatic esterifications leaves small but crucial quantities of side byproducts. Rather than leave those for downstream purification steps, our plant uses multi-stage distillation and chromatographic filtration, shaped by years of incremental improvements. The result? Downstream processors don’t run into off-spec reactions, color shifts, or unexplained losses.
DMPEE-03 frequently ends up at the heart of synthetic routes for more complex molecules. Many of our clients—multinational pharma companies and R&D-focused startups—require this intermediate for constructing protected phenolic units, heterocyclic frameworks, or as a substitute in peptidomimetic chemistry. For high-throughput screening, even a slight deviation in purity or melting point leads to batch failures and schedule risks. By structuring our production plans to chase down known bottlenecks before scale-up, we give our clients predictability rarely matched by low-volume repackagers.
We also account for varying procedural demands: customers working with metal catalysts in cross-coupling reactions see different impurity vulnerabilities compared to those into biosynthetic hybrid methods. Adjusting the process for a higher degree of hydrogenation control or downstream deprotection makes a real difference in yields and side product profiles. With DMPEE-03, we dig into granular questions—trace ion content, particle fines, filterability—to minimize knock-on effects at customer sites.
Sustainability and environmental stewardship no longer come as afterthoughts to process optimization. Chemical manufacturing of aromatic esters historically relied on halogenated solvents and heavy metals. From our first pilot runs, our teams focused on greener alternatives: reusable solvent loops, reduced aqueous waste, and non-tin-based catalysts. Over time, small choices around process solvents or catalyst loading have cut our waste stream footprint without compromising the consistency of DMPEE-03.
Recycling and solvent recovery have become tangible difference-makers for us, both in economics and in compliance. Batch analytics no longer stop at the final product; we track byproduct profiles with the same detail to anticipate storage, transportation, and eventual disposal needs. Working at industrial scale, this continuous monitoring transforms site audits and certification renewals. Our customers have remarked on how clean supply chain documentation and cradle-to-gate transparency accelerate their regulatory submissions for novel drugs and materials.
Customers frequently reach out with unique hurdles: unanticipated side reactions, storage stability concerns, or even application questions in fields outside our main area of expertise. Our technical specialists don’t just read product data sheets—they assimilate years of plant and QC data, leveraging lessons learned from real problems to quickly diagnose customer challenges.
Perhaps a chromatographer notices a subtle shift in retention time over several months of DMPEE-03 shipments. Rather than offer theoretical causes, we share actual run logs, production parameters, and any equipment maintenance updates that overlap the relevant periods. This history-based approach, rather than defaulting to standard troubleshooting templates, has helped partners in the pharmaceutical sector and specialty materials field avoid unnecessary downtime.
Every kilogram of DMPEE-03 we ship is underpinned by a robust analytical profile. High-performance liquid chromatography, gas chromatography, mass spectrometry—each lot comes with full traceability down to the raw material supply run. Customers working with hazardous chemistry or high-value syntheses count on consistent data because even a minor impurity can introduce outlier results or add risk.
Through feedback from our partners, we’ve expanded our batch analytics far beyond what the general market demands. We actively track color, odor, non-volatile impurity load, and trace elements. We make this information accessible to buyers and process engineers, supporting a move toward open data sharing and a new baseline for accountability in fine chemical manufacturing.
Consistency and timeliness in chemical supply matter as much as single-batch quality. Delays, missed shipments, and inconsistent lots can ripple through entire production timelines, costing real developmental momentum. Through direct control over our logistics—temperature control, secondary containment protocol, and rapid turnover inventory practices—our team helps avoid last-minute surprises in the lab or production facility.
Frequent collaboration between our manufacturing and fulfillment teams means bottlenecks get identified and addressed before finished material reaches customer docks. As demand for this ester grows, especially among global buyers subject to shifting customs or regulatory environments, we maintain redundant supply plans and secondary shipping channels. We’ve supported clients in strategic stockpiling, reduced delivery volatility, and fast response times when unforeseen circumstances strike.
Manufacturing never stands still. Over the past few years, both the technical and market demands for DMPEE-03 have changed. Clients ask for more stringent impurity controls, new packaging to handle sensitive supply chain routes, or specialized batch records for rapid regulatory review. Our development group, looped tightly with production management, evaluates every improvement. Upgraded reactor sensors deliver tighter temperature control, and regular process audits refine scale-up procedure. Simple data like agitation speeds or cooling rates affect analytical results.
We regularly explore new synthetic routes for greater efficiency or environmental advantage. Pilot runs compare different protocol optimizations, such as shifting from mineral acid catalysis to enzymatic or solid-supported techniques where feasible. The goal is keeping product consistency at the highest standard while matching up with evolving standards on both domestic and international levels.
A successful supply relationship in the fine chemical field doesn’t revolve around once-a-year contracts. We engage with partners through every stage of the project lifecycle. Longstanding clients have taught us that the ability to transparently troubleshoot, adapt formulations, and predict supply hiccups delivers more value than just lowering price points.
Each interaction—whether planning a new synthesis campaign, scaling from grams to tons, or supporting analytical method transfer—gives us more insight into how DMPEE-03 meets real-world demands. These conversations spur continuous improvement: whether through better analytical testing, more flexible batch sizes, or new process validation runs tailored to a customer’s specific workflow.
Stepping back from data, specifications, and protocols, producing 3-(3,4-Dimethoxy-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester at commercial scale teaches valuable lessons about the wider responsibilities a manufacturer carries. It’s not just about making the best possible product but about shaping the standards for reliability, transparency, and customer support.
Each drum shipped reflects thousands of decisions made on the plant floor, in QC labs, and in boardroom discussions. Our focus remains: stable quality, agile response, and a commitment to real partnerships with customers who drive the next wave of chemical discovery and innovation.