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HS Code |
893946 |
| Chemical Name | 3-(2,5-Dimethoxyphenyl)propionic acid |
| Cas Number | 83851-23-6 |
| Molecular Formula | C11H14O4 |
| Molecular Weight | 210.23 |
| Appearance | White to off-white solid |
| Melting Point | 95-98 °C |
| Solubility | Soluble in organic solvents |
| Purity | Typically ≥98% |
| Storage Temperature | 2-8 °C |
| Smiles | COC1=CC(CCC(=O)O)=CC=C1OC |
| Inchi | InChI=1S/C11H14O4/c1-14-9-5-8(4-3-11(12)13)6-10(7-9)15-2 |
| Usage | Intermediate in organic synthesis |
| Synonyms | 2,5-Dimethoxyhydrocinnamic acid |
As an accredited 3-(2,5-Dimethoxyphenyl)Propionic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a 25g amber glass bottle with a secure screw cap, labeled with the chemical name, purity, hazard, and supplier details. |
| Shipping | 3-(2,5-Dimethoxyphenyl)propionic acid is shipped in tightly sealed containers to prevent contamination and moisture absorption. The packaging complies with relevant chemical transport regulations, ensuring safety during transit. It is typically transported by air or ground courier, accompanied by appropriate documentation, and stored under cool, dry conditions away from incompatible substances. |
| Storage | 3-(2,5-Dimethoxyphenyl)propionic acid should be stored in a cool, dry, well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizing agents. Keep the container tightly closed to avoid moisture absorption and contamination. Store at room temperature, ideally between 2–8°C, and ensure proper labeling. Use appropriate chemical safety procedures and personal protective equipment when handling. |
Applications of 3-(2,5-Dimethoxyphenyl)Propionic Acid in Industrial Manufacturing3-(2,5-Dimethoxyphenyl)Propionic Acid serves as a specialty chemical intermediate in several precise industrial processes. Direct manufacturers incorporate this raw material in targeted synthesis workflows where aromatic substitutions are essential, supporting scalable production of specific compound classes in regulated downstream sectors. 1. Pharmaceutical Intermediate SynthesisManufacturers use this compound as a key building block for the synthesis of selective serotonin receptor ligands and catecholamine derivatives. The aromatic methoxy substitution pattern enables regioselective transformations for APIs (Active Pharmaceutical Ingredients) in advanced medicinal chemistry. Downstream pharma companies require tight control on isomeric purity and use stepwise coupling and reduction protocols in GMP-compliant environments. Industry compliance standards
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2. Agrochemical Active Ingredient DevelopmentThis intermediate finds use as a core aromatic unit in the research and pilot-scale synthesis of certain herbicide analogues and growth control agents. R&D divisions incorporate the compound in structure-activity relationship studies for new bioactive molecules targeting weed or pest resistance, utilizing its specific substitution framework for improved selectivity and metabolic stability. Industry compliance standards
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3. Specialty Fragrance and Flavor Intermediate ProductionAromatic acid derivatives like this compound play a controlled role in the manufacture of bespoke fragrance ingredients and modified flavoring agents, mainly for industry-limited research and regulatory-approved trial products. Professionals in aroma chemistry leverage the methoxy-protected structure for oxidative coupling, producing stable intermediates for floral, woody, or spicy notes in downstream compounding. Industry compliance standards
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4. Advanced Polymer Modifier R&DThe compound serves as a niche monomer modifier in specialty polymer research and development, especially for creating custom aromatic functionalities within polyesters or polyamides. Polymer scientists introduce it to adjust glass transition temperatures and mechanical flexibility for innovative film-forming or coating materials, producing small batches for coating or advanced plastic applications under pilot-scale assessment. Industry compliance standards
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Working at the intersection of organic synthesis and practical production, we see trends shift quickly, and the pace at which researchers develop new catalysts, derivatives, and building blocks means each molecule starts to tell its own story. 3-(2,5-Dimethoxyphenyl)propionic acid has, over time, shifted from an obscure intermediate to a mainstay in the toolkit of many pharmaceutical and materials chemists. Our team dedicates much of our daily work to ensuring the purity and reproducibility of our output because we understand how a small impurity ripple in this molecule can upset complicated syntheses downstream.
Our material generally leaves our facility at a purity upwards of 99%, HPLC verified, crystalline, and with a melting point that matches the literature values closely. We aren’t a broker moving inventory from warehouse to warehouse. Our lines start with downstream derivatization strategies in mind. In daily practice, most requests for this molecule call for tight control over isomeric purity. That’s reasonable: downstream steps like reductions or oxidations suffer significantly from even slight variations. Our in-house QC keeps track of any deviation, and our production chemists notice even minor aberrations when scaling.
The structure looks simple enough: a three-carbon chain bearing a 2,5-dimethoxyphenyl ring with a carboxyl group on the terminus. This molecule enters the fray frequently in medicinal chemistry, particularly during library expansion exercises. As synthetic chemists look to build new analogues for bioactivity screening, a phenylpropionic acid backbone with 2,5-dimethoxy substitution provides a versatile platform for further modifications. The methoxy groups at the 2 and 5 positions have a significant electronic influence, tuning reactivity for selective functionalization. They also increase solubility in organic solvents, giving researchers flexibility during purification steps.
Materials scientists, too, have found use for this molecule in the development of organic electronic components such as charge transport layers. There, the methoxy substitution pattern on the benzene ring often matters as much as the side-chain configuration. We’ve supplied research teams who described that attempts to swap for 2,4-dimethoxy analogues yielded less predictable reactivity or dropped device performance due to unintended side reactions. Sticking to 2,5-dimethoxy can bring down batch-to-batch variability when scaling up electronic applications.
We started manufacturing 3-(2,5-dimethoxyphenyl)propionic acid when we heard from local universities and startup pharmaceutical labs demanding kilogram-scale lots with quality consistency. They’d struggled with smaller resellers who could provide a gram here or there in variable quality but froze on larger requests. The challenge wasn’t only cost. Many labs spent more time purifying commercial sources than in actual downstream experiments, which forced delays in project deadlines.
On our side, scaling requires careful monitoring of reaction conditions. Exothermic steps, especially during the introduction of the methoxy groups, demand reactors with precise temperature control. These details aren’t visible to most end users. As production chemists, we catch the subtleties—how trace metal contamination in methoxylation steps will show up in NMR or LC-MS three or four steps later, derailing high-purity syntheses. Our operation avoids this pitfall by strict quality control on incoming reagents and by running in small-to-midsize batch reactors with complete traceability.
Across various labs, the use-case for 3-(2,5-dimethoxyphenyl)propionic acid keeps growing. Its robust compatibility with a wide array of functional groups gives medicinal chemists room to push boundaries in structure-activity relationship exploration. The acid moiety can be transformed into amides, esters, or participate in coupling reactions; the dimethoxybenzene skeleton permits further elaborations and acts as a platform for late-stage diversification. Our discussions with synthetic teams confirm that the electron-rich ring handles oxidation and reduction with stability. In contrast, less methoxylated analogues more easily undergo unwanted side reactions, limiting their utility when researchers need consistent intermediates.
Analytics routinely show that crude intermediates, if sourced elsewhere, often mix in positional isomers or unreacted starting materials, both of which complicate isolation and drive up cost and time for research chemists. Our documentation chain follows a batch right through synthesis, purification, drying, and packaging, with detailed spectral data and full transparency. This approach isn’t flashy but it means our clients rarely write to complain about obscure chromatographic peaks or unpredictable melting points.
Many synthetic projects turn to this molecule for Suzuki couplings, amidation, or formation of bioisosteres. Compared with simple phenylpropionic acids, the 2,5-dimethoxy-substituted version opens up new chemistry without excessive reactivity. We’ve seen examples where substituting alternate isomers with 2,3- or 3,4- patterns fails because the electron-donating effects alter the reactivity profile too much for reliable downstream chemistry.
A recurring comment from our customers in discovery chemistry is that scale-up to gram or multi-gram batches preserves consistency across runs. This isn’t by accident; our facility deliberately minimizes batch-to-batch risk by running parallel pilot reactions and constant monitoring of critical parameters. Each vessel, each step, and every processed output is tracked in-house, never offshored or delegated without oversight. The result is a steady supply for customers developing next-generation therapeutics or high-performance materials.
In the chemical supply industry, plenty of catalogues list 3-(2,5-dimethoxyphenyl)propionic acid. Not every process can guarantee the same standards. Some market offerings, especially those funneled through brokers or bottom-dollar bulk suppliers, arrive with vague COAs, barely a nod to impurity profiling, and little detail concerning batch origin. That brings risk for research-dependent operations, where a single failed run can mean weeks lost.
As a manufacturer, our role does not end at the shipping dock. We keep batch samples archived for reference and can supply matching spectral data for any delivery. For larger, multi-kg orders, we handle requests for custom particle size distribution, specialized drying protocols, or modified packaging to suit handling needs. Factories embedding this molecule into polymer frameworks or pharmaceutical final steps have found that even subtle handling changes during drying or milling affect the downstream process. Our process is robust against those sources of variability.
Biotech companies scaling up novel drug candidates frequently start with relatively simple structures, then build in complexity as they confirm bioactivity. Several trusted partners chose our 3-(2,5-dimethoxyphenyl)propionic acid as the substrate for synthesizing CNS-active molecules, leveraging reactivity at the benzylic and carboxylate positions. Organic semiconductors researchers have developed new charge-transport layers using oligomers with this backbone, citing its predictable performance in electron-rich environments and reproducibility at larger scale.
Academic collaborations enabled us to provide hundreds of grams annually, supporting students optimizing process methodologies. Adjusting temperature ramps and solvent ratios, they reported consistent yields using our acid, a welcome contrast compared to trialing lesser-known sources. We value openness in experimental design; many research teams share feedback and spectral data, helping us identify trends and fine-tune synthesis protocols.
Across the many derivatives of phenylpropionic acids, subtle shifts in substitution deliver dramatically different properties. Adding methoxy groups at the 2 and 5 positions enhances electron donation on the aromatic ring, stabilizing cationic intermediates formed during Friedel-Crafts or related reactions. That effect often isn’t visible on paper, but it becomes evident in the lab, particularly during cyclizations or acylations. We have also seen that the purity of the starting acid drives the selectivity in boronic acid formation, another crucial building block in pharmaceutical development.
Researchers occasionally ask if they can substitute a generic phenylpropionic acid or even a 2,4-dimethoxyphenyl variant. The answer often depends on what behavior downstream they wish to influence. Our years of analytical work show side reactions climb sharply with isomeric variants, most evident during oxidative coupling or when reagents like palladium catalysts are used. Early in our manufacturing journey, we ran controlled trials on these isomers, finding that product purity, yield, and process stability were best served by sticking to the 2,5 pattern. That translates to reproducible kinetics and fewer surprises in process optimization.
It’s worth noting that 3-(2,5-dimethoxyphenyl)propionic acid, like most fine chemicals, demands attention to handling and storage. Our facility controls moisture and temperature, with packaging designed to survive changes in humidity or accidental exposure. On delivery, each batch comes vacuum-sealed in foil or high-barrier containers, with bulk deliveries shifted to lined drums. We store in inert environments; this retains crystalline form and releases the product ready for weighing and direct use.
End-users may not see the spectrum of production challenges as raw material moves from kilo-lot reactors to filtration, drying, and packing. Our team manages each transition, minimizing potential for cross-contamination or degradation. Feedback cycles with customers allow us to rapidly resolve any deviation from standard, whether a milestone analytical result falls out of spec or a new derivative project changes solvent compatibility.
Our customers know the cost of small process hiccups—failed runs in scale-up, unexpected spectral anomalies before submission of regulatory data, or supply interruptions that force project delays. By serving as both manufacturer and long-term partner, we stake our reputation on each delivery. Researchers building on a foundation of reliable raw materials can focus on innovation and results, rather than re-purifying standard chemicals.
This holds true whether teams are doing discovery research on a new CNS-active agent or building a next-generation organic light-emitting diode. We get calls for advice long after initial deliveries—questions on formulation, process improvement, or troubleshooting. Our approach always centers on transparency, reproducibility, and a willingness to learn from every batch run, both internally and in client hands.
Modern manufacturing no longer views waste and sustainability as afterthoughts. In our operation, solvent recovery, efficient purification, and byproduct tracking form part of every scale-up. For 3-(2,5-dimethoxyphenyl)propionic acid, we’ve managed waste stream minimization through real-time monitoring and process optimization. Our chemists evaluate greener alternatives for solvents, work-up, and isolation procedures yearly, always looking to minimize environmental load without compromising purity.
Feedback from progressive research groups often inspires our process upgrades. By documenting and acting on each suggestion—say, a request for alternate solvent residuals or recyclable containers—we close the loop from bench to batch reactor. Trust develops not by promising miracles, but by quietly, continuously improving each stage of supply, and by being honest about limitations and upcoming changes.
Plenty of suppliers offer phenylpropionic acids, but not every product holds up across demanding synthesis routes or large-scale production. Our direct experience shows batch consistency and traceable origin matter most. Laboratories trying alternatives with lower price points or isomeric substitutions often circle back after seeing lower yields, increased purification complexity, or inconsistent spectral matches.
Other acids, such as the unsubstituted or 3,4-dimethoxyphenylpropionic versions, appear similar in chemical structure but introduce unpredictable effects due to altered electron distribution. The 2,5-dimethoxy base reduces these risks, providing a tighter, more selective reaction profile across various coupling and cycloaddition methodologies. Pharmaceutical developers particularly appreciate this aspect for late-stage lead optimization when failure points become unforgiving.
Our business rests on more than a product listing. By manufacturing this molecule in batches aligned with actual demand, overseeing each production run end-to-end, and offering rapid, honest feedback in response to technical questions, we support both global and local research. The role of 3-(2,5-dimethoxyphenyl)propionic acid continues to grow in the medicinal and materials chemistry sectors; our part is to deliver reliability, backed by process knowledge and genuine collaboration.
Not every chemical is a blockbuster, but the dependable ones—built on a platform of known properties and careful manufacturing—underpin the everyday progress of research teams the world over. 3-(2,5-dimethoxyphenyl)propionic acid has quietly earned its spot as a go-to intermediate for reliable, forward-looking synthesis. Our job is to make sure each user receives it at the purity and consistency that modern science demands, with real-world experience standing behind every package sent out our doors.