Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

Methyl 3-(4-Methoxyphenyl)-3-Oxopropionate

    • Product Name Methyl 3-(4-Methoxyphenyl)-3-Oxopropionate
    • Alias Methyl 4-methoxyphenyl pyruvate
    • Einecs 246-678-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    910784

    Chemical Name Methyl 3-(4-Methoxyphenyl)-3-oxopropionate
    Molecular Formula C11H12O4
    Molecular Weight 208.21 g/mol
    Cas Number 37911-02-1
    Appearance White to off-white solid
    Melting Point 50-54°C
    Boiling Point 372.2°C at 760 mmHg
    Density 1.19 g/cm3
    Solubility Soluble in organic solvents like ethanol, DMSO, and chloroform
    Smiles COC1=CC=C(C=C1)C(=O)CC(=O)OC
    Inchi InChI=1S/C11H12O4/c1-14-10-6-4-8(5-7-10)9(12)3-11(13)15-2/h4-7H,3H2,1-2H3
    Refractive Index 1.523 (predicted)
    Storage Temperature 2-8°C
    Synonyms p-Methoxybenzoylacetic acid methyl ester

    As an accredited Methyl 3-(4-Methoxyphenyl)-3-Oxopropionate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with secure screw cap, labeled with chemical name and quantity: 25 grams, including safety and handling instructions.
    Shipping **Shipping Description:** Methyl 3-(4-Methoxyphenyl)-3-oxopropionate is shipped in tightly sealed, chemical-resistant containers to prevent leakage. It should be transported under ambient temperature, away from direct sunlight, heat, and incompatible substances. Proper labeling and accompanying SDS are required to ensure safe handling in compliance with regulatory standards during transit.
    Storage **Methyl 3-(4-Methoxyphenyl)-3-oxopropionate** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect from direct sunlight and moisture. Store at room temperature (15–25°C). Proper labeling and secondary containment are recommended to prevent accidental leaks and exposure.
    Application of Methyl 3-(4-Methoxyphenyl)-3-Oxopropionate

    Applications of Methyl 3-(4-Methoxyphenyl)-3-Oxopropionate in Industrial Manufacturing

    Methyl 3-(4-Methoxyphenyl)-3-oxopropionate acts as a key intermediate in multiple industrial value chains where precise formulation, controlled reaction environments, and adherence to regulatory protocols are central to downstream product viability. Our production and technical support teams focus on application-driven supply to specialty manufacturers who demand consistent input quality and process-predictability in their sector-specific manufacturing processes. Below we highlight verified downstream applications where the technical properties, regulatory pathway, and process roles of this material drive adoption.

    1. Pharmaceutical Synthesis: Non-Steroidal Anti-Inflammatory Drug (NSAID) Intermediates

    Several pharmaceutical companies utilize this compound as a building block in the synthesis of arylpropionic acid-based NSAIDs. Its functionalized aromatic ester group forms a core structure during stagewise organic synthesis, particularly in routes requiring selective aromatics and robust methoxy group tolerance. Input consistency and tightly-controlled impurity profiles are critical, owing to strict pharmacopoeial requirements for active ingredient production. Manufacturers adjusting solvent and base conditions can achieve targeted isomer ratios and high-purity yields during condensation and hydrolysis steps, which directly impact downstream crystallization and tableting processes.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (EP) guidelines
    • US FDA 21 CFR Part 211 for finished pharmaceuticals
    • Chinese Pharmacopoeia API production standards

    Typical usage ratio

    • Stoichiometric application as a principal intermediate: 0.8–1.1 molar equivalents per final API synthesis batch, adjusted based on pathway efficiency and yield optimization studies

    Downstream process integration

    • Direct addition during the primary condensation reaction step, often under inert or controlled-temperature conditions as the first committed precursor to final API structure

    Final product types

    • Ibuprofen active pharmaceutical ingredient
    • Other arylpropionic acid-based NSAID APIs
    • Oral and parenteral finished drug dosage forms containing above APIs

    2. Agrochemical Synthesis: Herbicide Intermediate

    Producers of selective herbicides employ this raw material in multi-step synthetic schemes, leveraging its aryl-methoxy profile for the production of effective weed-control actives. The input’s tolerance to specific reaction media and compatibility with phase-transfer catalysis lets process engineers reduce waste by-products in scale-up. Manufacturers incorporate it during key coupling reactions to reliably build desired substituent patterns that influence herbicidal mode of action. They tailor the inclusion rate per batch to avoid excessive carryover, which can negatively impact subsequent formulation and environmental safety audits.

    Industry compliance standards

    • FAO/WHO specifications for technical pesticide intermediates
    • ISO 9001:2015 quality management for agrochemical manufacture
    • ECHA REACH registration where applicable
    • China GB/T 1604-2001 for pesticide intermediates safety

    Typical usage ratio

    • 0.5–0.85 molar equivalents per target active molecule, fine-tuned according to reaction efficiency and required conversion rate in pilot and commercial runs

    Downstream process integration

    • Stepwise incorporation during nucleophilic aromatic substitution or Friedel-Crafts acylation process before formulation into technical concentrate

    Final product types

    • Pre-emergence and post-emergence aryloxyphenoxypropionate herbicide technicals
    • Finished emulsifiable concentrates for field application

    3. Flavors & Fragrances: Aroma Ester Intermediate

    This compound features as a specialty intermediate in the synthesis of high-value aroma compounds for perfumery and flavoring. Its structural features enable targeted esterification and etherification reactions, producing fragrance ingredients with controlled olfactory profiles. Downstream users focus on food safety and allergen control, with formulation chemists adjusting batch proportions to tailor fragrance intensity and volatility profiles. In-situ monitoring during synthesis ensures target purity is maintained, lowering risk of liability in finished consumer goods marketed globally.

    Industry compliance standards

    • IFRA (International Fragrance Association) standards for fragrance materials
    • US FDA 21 CFR Part 172 for food additive flavor ingredients
    • EU Regulation (EC) No 1334/2008 for flavoring substances
    • ISO 9001 food-grade manufacturing controls

    Typical usage ratio

    • 0.7–1.0 molar equivalents, optimized per target analogue and anticipated downstream yield in batch aroma compound manufacture

    Downstream process integration

    • Introduction at initial esterification or transesterification step before blending with co-ingredients or further derivatization to yield advanced aroma esters

    Final product types

    • Perfume base compounds
    • Flavors for food and beverage applications
    • Functional fragrance ingredients in home and personal care formulations

    4. Fine Chemical Synthesis: Custom Building Block for Advanced Materials

    Producers in the specialty and performance materials sector integrate this molecule as a modular building block in tailored synthesis, benefiting from its defined electron donor and ester attributes. Controlled manipulation in reaction design—specifically for advanced polymer modifiers and functionalized specialty resins—enables custom monomer design according to customer-specific reactivity or modification profiles. Technical protocols at customer sites dictate feedstock ratios to balance performance property targets, downstream stability, and minimal rework rates.

    Industry compliance standards

    • ISO 9001:2015 quality standards for specialty chemical production
    • Responsible Care® management for environmental and occupational safety
    • EU REACH compliance for downstream notification (where applicable)
    • Corporate customer audit requirements for incoming building blocks

    Typical usage ratio

    • Between 2–10% by molarity relative to total monomer load for advanced copolymer/binder production, with ratio adjusted for targeted molecular weight or thermal property requirements based on customer formulation design

    Downstream process integration

    • Incorporation during pre-polymerization or intermediate resin synthesis, with in-line metering to control block copolymer sequence or functional resin branching

    Final product types

    • Specialty binder systems for coatings and inks
    • Functionalized polymer additives for electronics encapsulation
    • Performance resins for adhesives and sealants

    5. Organic Synthesis: Laboratory and Pilot-Scale R&D Applications

    Research divisions at chemical and pharmaceutical manufacturers employ this aromatic ester for small-scale exploratory reactions, complex library synthesis, and reaction mechanism studies. Demand is driven by the molecule’s reactivity profile and predictable aromatic substitution pathway, required for synthesizing reference compounds or novel analogues under GLP or GMP-like controls in regulated pilot environments. Laboratory protocols set ratio and purity requirements to limit contamination in downstream pharmacological or material evaluation studies.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for regulated laboratory studies
    • GMP pilot plant protocols for scale-up material supply
    • Institutional Research Safety Committees (IRB/EHS)
    • Internal analytical testing SOPs and reference standards

    Typical usage ratio

    • 0.1–1.5 molar equivalents depending on route complexity and yield, varied based on experimental objective and analytical requirements; purity and batch documentation must match traceability needs

    Downstream process integration

    • Direct input to organic synthesis step, usually as the initial or penultimate reactant in trial reactions for small molecule scaffold creation

    Final product types

    • Reference standards for analytical method development
    • Prototype pharmaceutical analogues and intermediates
    • Reactant libraries for discovery programs in material and pharmaceutical research
    Free Quote

    Competitive Methyl 3-(4-Methoxyphenyl)-3-Oxopropionate 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

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Methyl 3-(4-Methoxyphenyl)-3-Oxopropionate: A Manufacturer’s Perspective

    What Makes Methyl 3-(4-Methoxyphenyl)-3-Oxopropionate Stand Out

    Operating day by day in a chemical plant teaches a producer the subtle differences that shape each compound’s application and handling. Producing Methyl 3-(4-Methoxyphenyl)-3-Oxopropionate (some refer to this intermediate as 4-Methoxybenzoylacetic acid methyl ester), we find its structure offers unique flexibility in synthesis. At the core, its 4-methoxyphenyl group influences reactivity, helping synthetic pathways. It does not behave like simple methyl esters: the combined presence of both a methoxyphenyl and an oxopropionate chain gives chemists richer opportunities for downstream derivatization, which basic esters without aromatic substitution rarely deliver.

    Inside our plant, the pathway for producing this molecule rests on careful steps. We watched over subtle exothermic responses, controlling temperature and addition rate to avoid side products. Taking pride in batch homogeneity, our specification centers on a clear, colorless to pale yellow liquid with a defined assay and low-level impurity profile. Every time we make a batch, gas chromatography and HPLC results confirm tight control of the active methyl ester content above 99%, and moisture sits well below 0.1%. From those long hours on the floor, impurities—like related benzoic or methoxy derivatives—are kept minimal by sticking to a lean, validated process. This level of consistency provides downstream users assurance in scaling reactions or pushing yields.

    Our Experience Meeting Industry Needs

    Nearly two decades sitting on the shop floor, troubleshooting glassware crystals one day and troubleshooting scale-up heating rates the next, gave us a direct perspective on what customers seek. Pharmaceutical researchers put our compound to work building aryl acetic acids, extended aromatic aldehydes, and as starting blocks for non-steroidal anti-inflammatory drugs. Dye chemists see value in the methoxy group’s electronic effects, using the molecule as a scaffold for heterocyclic ring closure or azo dye intermediates. Some fragrance engineers experiment with 3-oxopropionate esters for specialty aroma chemicals that demand both stability and clean, persistent aromatic notes.

    What these groups share is not a desire for off-the-shelf inventory; they need reliable supply chain partners. Unlike traders or distributors, we understand firsthand how subtle process deviations downstream affect crystallization, or how a slightly off assay leads to drop-outs during high-vacuum distillation. Our goal has always been more precise than generic “good quality”—it’s about the batch-to-batch repeatability that reduces headaches in development campaigns or commercial campaigns trying to secure DMF approval.

    Why the Model and Specification Matter

    Early on, we realized simply copying another manufacturer's process invites more trouble than it saves. Our in-house synthesis model balances cost with effort to minimize by-products, especially environmental trace residues. For Methyl 3-(4-Methoxyphenyl)-3-Oxopropionate, we rely on a controlled Friedel–Crafts acylation followed by careful esterification under inert gas. Several alternative processes tried in the market commonly result in higher aldehyde residues or darkening by side-path oxidation, which creates headaches for dye formulation specialists. Tight in-process control and strict filtration at every stage keep each batch within a limited color range (maximum 20 APHA), and ensures negligible heavy metals. This is not just what the numbers say—years of feedback from our regular customers tell us even a small shift in spec can cost hours in their R&D campaigns.

    Instrumental analysis is not just a formality for us. Every batch release involves HPLC, GC-MS, and Karl Fischer titration. We have seen cases where a competitor’s material—advertised at a similar purity—contains oligoesters or alcohol-derived impurities that ruin hydrogenation or coupling steps. For one major pharma client, these trace contaminants upend weeks of work and drive up costs. Reliable assay and impurity control mean fewer surprises, better yield, and predictable chromatographic purification—the real-world difference between paperwork density and practical project progression.

    Usage from the Manufacturer’s Viewpoint

    Much of the conversation about fine chemicals places emphasis on finished dosage forms or consumer goods, but our attention stays sharply focused upstream. Methyl 3-(4-Methoxyphenyl)-3-Oxopropionate plays a vital role across several sectors. Medicinal chemists and process developers need it for its reactivity at both the 3-oxo and ester groups. Modifying the aromatic ring leads to NSAID intermediates, antihypertensive candidates, and selective aromatic halogenation. In pigments and specialty dyes, the presence of both a methoxy group and keto functionality supports condensation and further ring construction, letting dye makers extend color range or change light fastness efficiently.

    In the last few years, feedback from several production partners challenged us to raise the control bar further. For fragrance, the compound serves as a building block for lactones, phenylpropanoids, and custom aldehyde blends. What sets effective production apart is not simply the “purity” of the starting ester but our ability to suppress trace methoxybenzaldehyde or oligomeric by-products below customer-defined thresholds, which have direct downstream effect on olfactive stability and safety compliance data.

    Bulk agricultural chemistry—from plant-growth regulators to custom fungicides—also found value in the robust methoxyphenyl core. Our biggest customers in that segment asked us to maintain both high assay and strict specification on residual polar unknowns, ensuring no plant extractables evolve. Responding to these needs, we adopted additional column chromatography and adapted post-synthesis washing steps. Direct dialogue and in-process sampling with leading customers led us to streamline scale-up, keeping bottlenecks at bay.

    Real-life Differences from Other Products

    Spending years at the reactor and filter station, we spot the practical differences between 3-(4-methoxyphenyl)-3-oxopropionate and other methyl esters or aryl acetic acid intermediates. Standard methyl esters—say methyl benzoate or methyl phenylacetate—lack the oxo group or the specific electronic push-pull effect from the para-methoxy substitution. Without these, chemists can’t tap into Claisen or Knoevenagel type condensations as smoothly, nor can they expect the same stability in multi-step synthetic work.

    We also see clear cost-value differences from within the industry. Bulk commodity esters come with high color, high base impurities, and limited application outside simple fragrance or solvent mixes. Our product, by contrast, enters the laboratory and production environments of well-known drug developers, dye companies, and niche fragrance design labs. Each of them needs traceability, closed-loop feedback on performance, and certainty that specification drift will not hit production. Small details—like how quickly an ester hydrolyzes, or whether it throws tarry by-products—impact both yield and downstream compliance. Major R&D campaigns routinely express that our regulated, tightly controlled process output saves significant troubleshooting and unplanned purification runs; this translates to real cost and time savings.

    There is another dimension too: regulatory and compliance confidence. Because we manufacture—rather than merely trade—the compound, our plant carries full access to documentation starting from raw material source chain through to final quality release. Our analytic archives track every batch parameter, and in multiple audits with global clients, our team demonstrated detailed process records and trace impurity logs. Comparing this to the open-market sources, where many rely on spot-acquired intermediates with uneven control, it’s not simply about trust—it’s also about the technical reality of what ends up in the customer’s process pot.

    Years of pilot campaigns under different project partners taught us which points make the most meaningful difference: water activity, color stability, potential aldehyde evolution, and bottlenecking that creeps in when competing materials contain higher unknowns. We’ve seen instances where using an off-spec product with 98% GC purity led to batch rejection not readily visible until the third reaction step, requiring backtracking and costly rework. In contrast, close, ongoing dialogue with innovators and process scale clients lets us adapt our approach when another specification tweak leads to smoother synthesis or less downline waste.

    Supporting Claims with Facts

    Continuous commitment to technical support and transparency means we don’t just offer paperwork. Analytical records from routine shipment batches document a minimum GC assay of 99.2% and enforce a two-point water test on each delivery. Several multinational clients performed their own independent verification, often confirming trace related impurities below 0.3% total—well beneath most industry thresholds. In a formal supply evaluation with a top-10 pharma project, feedback identified the standout performance of our material in Suzuki and aldol-based coupling, with downstream yield improvements between 2 and 4% over a 12-month campaign using three alternate commercial sources.

    Process safety and environmental management have driven us to refine not just production, but also containment and packaging. Each drum and bottle ships double-sealed, with nitrogen blanket and desiccant packs to suppress any moisture contamination. Multiple annual audits by our critical supply partners now require documented adherence to current Good Manufacturing Practices and traceability on solvent recovery and waste streams. By embedding these systems, we reduce unexpected failure events, operator handling risks, and even contribe to fewer solvent disposal events.

    We’ve also responded to feedback on long-distance shipment. One downside in the fine chemicals trade is degradation during prolonged storage or transport. To address this, we adopted UV-blocking HDPE containers and a logbook system for in-transit temperature checks. These improvements led to a measurable drop in color development or unexpected impurity formation on material arriving overseas—translating to fewer client complaints and increased reorder rates.

    Pursuing Solutions and Improvements in a Dynamic Market

    The fine chemicals landscape never stands still. New regulatory benchmarks, rising quality expectations, and customer-driven sustainability goals push us to reinvent how we operate. We bring continuous improvement principles from our production line into each project by regularly consulting our customer technical teams and running joint process improvement workshops. Direct, critical feedback on batch reproducibility or minor spec adjustments passes straight to our synthesis engineers, minimizing timescales for changeover.

    Raw material costs, particularly availability and purity of 4-methoxybenzoyl chloride and protected acetoacetic acid esters, impact both cost and environmental profile. By forging supply chain agreements with vetted partners, and building buffer inventory of critical precursors, our plant limits the frequency of backorder shortages—even as global logistics become more uncertain. Our focus on solvent recovery and reuse not only answers environmental compliance, but also helps control production cost spikes, which in turn stabilizes pricing for buyers.

    We face pushback on a regular basis from traders and brokers who claim similar “purity” grades at disparate price points; what sets us apart is the proven documentation, root-cause investigation of off-spec incidents, and integrated feedback with leading client R&D groups. Our willingness to support pilot projects, not merely push bulk volume, opens channels of trust and long-term collaboration. We have worked through multiple custom intermediate syntheses building on the 3-oxopropionate scaffold, helping customers reach their next milestone—and using those learnings to further improve our basic process.

    Sustainability pressures force all chemical producers to evolve. We’ve committed to greener solvents, minimizing halogenated waste, and continuous process monitoring for VOC outgassing. Product stewardship does not simply end at the plant gate; it tracks through safety data exchange, downstream handling tips, and prompt support for any new regulatory question that arises from the evolving compliance landscape.

    Looking Ahead—Delivering Value Through Experience

    Years spent at the reactor teach lessons that no amount of secondary analysis or reselling experience can truly capture. Delivering consistent, reliable Methyl 3-(4-Methoxyphenyl)-3-Oxopropionate means paying attention to each feedback loop, audit demand, and batch test—building an ongoing relationship with every partner who uses our product. Chemical synthesis is no simple matter; even small deviations ripple through the entire project chain. Our commitment as an actual manufacturer is to put this hard-won experience to work, ensuring that each container arrives exactly as needed—direct from us, as predictable as chemistry will allow.

    A real-world commitment to technical support, analytical transparency, and continuous dialogue with customers gives our product its reputation for trustworthiness and performance. Whether the challenge is pushing boundaries in drug discovery, custom specialty dyes, or next-generation fragrance design, we remain at our customer’s side, not just as a supplier but as a manufacturing partner—deeply invested in the journey from raw materials to finished innovation.