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HS Code |
414225 |
| Chemical Name | 3,5-Dimethoxyphenylpropionic Acid |
| Cas Number | 830-88-6 |
| Molecular Formula | C11H14O4 |
| Molecular Weight | 210.23 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 93-97°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically ≥98% |
| Smiles | COC1=CC(=CC(=C1)OC)CCC(=O)O |
| Inchi | InChI=1S/C11H14O4/c1-14-9-6-8(4-3-7-12)5-10(15-2)11(9)13/h5-6H,3-4,7H2,1-2H3,(H,12,13) |
| Storage Conditions | Store at 2-8°C, keep container tightly closed |
| Synonyms | 3,5-Dimethoxy-β-phenylpropionic acid |
As an accredited 3,5-Dimethoxyphenylpropionic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g quantity of 3,5-Dimethoxyphenylpropionic Acid is packaged in a sealed amber glass bottle with a tamper-evident cap. |
| Shipping | 3,5-Dimethoxyphenylpropionic Acid is shipped in tightly sealed, chemical-resistant containers to prevent contamination and moisture absorption. Packaging complies with relevant chemical transport regulations. Product is labeled with hazard information and handling instructions, and is typically shipped via ground or air freight, depending on destination, to ensure safe and prompt delivery. |
| Storage | 3,5-Dimethoxyphenylpropionic Acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from light and moisture to maintain stability. It is recommended to keep the chemical at room temperature and labeled clearly. Avoid exposure to excessive heat and direct sunlight during storage. |
Applications of 3,5-Dimethoxyphenylpropionic Acid in Industrial ManufacturingAs an established producer of 3,5-Dimethoxyphenylpropionic Acid, we support a focused group of downstream manufacturers in regulated sectors. Below we outline key industrial scenarios where this raw material demonstrates proven value, offering technical details about compliance, formulation, integration, and end-use types based on real-world practice. 1. Pharmaceutical Intermediates for Antihypertensive APIsDownstream pharmaceutical firms employ 3,5-Dimethoxyphenylpropionic Acid as a key side-chain building block in the multi-step synthesis of select antihypertensive active pharmaceutical ingredients, notably within the sartans and related drug classes. Our material’s high purity enables integration in precise reaction stages where functional group compatibility and chiral integrity strongly affect yield. QC teams evaluate every lot against strict trace impurity and heavy metal requirements to maintain process integrity. Industry compliance standards
Typical usage ratio
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2. Synthesis of Flavonoid Derivatives in Fine ChemicalsOur customers in the fine chemical sector utilize 3,5-Dimethoxyphenylpropionic Acid for synthesis of customized flavonoid analogues, mainly for supply to research and pre-commercial projects in the nutraceutical and specialty ingredient markets. The material’s methoxy substitution ensures controlled aromatic substitution reactions and reproducible product profiles, crucial for batch-to-batch standardization and downstream characterization. Industry compliance standards
Typical usage ratio
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3. Aroma & Fragrance Ingredient Precursor ManufacturingA major use for 3,5-Dimethoxyphenylpropionic Acid lies in the aroma and fragrance sector, especially in the production of custom aromatic aldehydes and phenols sought after for fine perfumery and flavor enhancement blends. Its structure supports Friedel–Crafts acylation and oxidative conversion processes focused on clean, low-tar impurity profiles. Technical departments prioritize traceability and absence of phthalate contaminations through validated batch protocols. Industry compliance standards
Typical usage ratio
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4. Synthesis of Specialty Polyester Resins for CoatingsWithin the specialty coatings and resin modification sector, formulators use 3,5-Dimethoxyphenylpropionic Acid as a monomeric feedstock in the design of modified polyesters. Its methoxy-substituted aromatic core offers improved UV stability and modified glass transition temperatures, which helps resin manufacturers meet advanced performance criteria in high-durability, weather-resistant coating systems. Quality assurance relies on tight control of residual acid content and homogeneous mixing at the pre-polymerization stage. Industry compliance standards
Typical usage ratio
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Every batch we manufacture tells a story of research, testing, and meeting high expectations from partners who work in pharmaceuticals, fine chemicals, and specialty applications. This compound, 3,5-Dimethoxyphenylpropionic Acid, has drawn attention among researchers due to its structure: an aromatic ring substituted with two methoxy groups at the 3 and 5 positions and linked by a three-carbon chain terminating in a carboxylic acid. Put simply, our team produces this compound with a focus on delivering clear advantages in reactivity and purity crucial to both research and wider-scale synthesis.
Most inquiries we see from R&D teams relate to consistent purity. We typically provide 3,5-Dimethoxyphenylpropionic Acid above 98% purity by HPLC, and pack it in moisture-resistant bottles to ensure quality is preserved on arrival. Typical batches have a fine, free-flowing appearance, off-white in color, with a melting point close to 80–82°C. This matches with the needs of labs and synthesis teams who look to avoid unexpected side products, which can slow down projects or muddy downstream transformations.
Customized particle size distribution rarely gets requested for this compound, since solution reactions make use simple. But our team still monitors this factor during quality control to nip handling issues before they reach customers. Solubility tests show that 3,5-Dimethoxyphenylpropionic Acid dissolves readily in common polar organic solvents, like methanol and dimethyl sulfoxide, and has sufficient compatibility with weak bases for salt formation steps.
Across hundreds of shipments, common uses have emerged from direct customer feedback. Medicinal chemistry teams use this material when they want the 3,5-dimethoxy motif as a building block—often for making analogues of bioactive molecules seen in literature. These methoxy groups tend to boost metabolic stability and can shift the electronic environment of the aromatic system, leading to new chemical behavior in the final compound. We see several projects where it enters coupling reactions, such as Suzuki or amidation steps, thanks to the activated aromatic ring and the protic acid group at the end.
The flavor and fragrance sector occasionally approaches us about using it as a precursor or modulator, but more often demand comes from innovators developing small-molecule APIs or agrochemicals. Those teams want a starting material that reliably introduces the 3,5-dimethoxyphenyl motif at the right stage, which can mean surface reactions, forming esters, or extended chain modifications.
Beyond creative synthesis, some customers use this compound as a reference standard in analytics, or as an intermediate in process scale-up studies. They rely on tight batch-to-batch reproducibility—something we’ve invested in with automated reaction controls and advanced analytical instrumentation.
Not all phenylpropionic acids behave alike, and subtle structure tweaks can reshape how a molecule performs. The dual methoxy pattern on the ring of this compound creates a distinct electronic character, which sometimes allows for cleaner coupling reactions or different solubility properties compared to unsubstituted or monosubstituted analogues. More hydrophobic than simple phenylpropionic acids, it commonly dissolves in less polar environments, letting chemists push certain reactions under milder or more selective conditions.
There’s another practical angle: methoxy groups protect the aromatic ring from oxidation under certain reaction conditions, so teams developing multi-step syntheses can move forward without detours to re-protect aromatics or clean up byproducts. This feature alone saves weeks for some of our partners in medicinal chemistry, especially when timelines run tight between lead identification and optimization.
We manufacture straight from the core raw materials, without relying on tollers or outside processors. This means drawing from high-grade anisole derivatives, strict temperature control during methylation, and in-house acidification steps. Over time, this vertical pathway has helped us trim impurities—like residual halides or low-level aromatic byproducts—that can show up when shortcuts get taken.
Customers who’ve used both 3,5-Dimethoxyphenylpropionic Acid and its 2,4-dimethoxy or 3,4,5-trimethoxy counterparts often comment on two things: yields in downstream steps and solubility profiles. The 3,5-arrangement seems to offer the right balance for Suzuki or Buchwald–Hartwig couplings, delivering higher isolated yields, especially when working under less-than-ideal solvent choices. With 3,4,5-trimethoxyphenylpropionic acid, for instance, extra bulk can complicate purification and sometimes reduces final product solubility in water. Our product stands out by keeping functional groups precisely positioned for both ease of work and reliability in scale-ups.
We’ve spent years refining upstream processes to avoid the headaches our clients sometimes reported in the past: inconsistent batch profiles, trace inorganic contamination, or unpredictable color. Our facility brings together automated solid–liquid separation technology, precise in-line pH controls, and rigorous endpoint testing of both functional group content and organoleptic properties. For end users, this means starting each reaction with confidence the input quality matches specs—without delays from recharacterization or pre-purification.
This acid falls into a niche that usually demands both versatility and higher reliability than the typical off-the-shelf building block. Larger distributors may focus on basic commodity phenylpropionic acids, but our facility scales from pilot to metric-ton orders without crossing over into third-party handling, which can risk contamination. That’s been our edge—total inward tracing from precursor to drum.
Research teams in academic groups tend to use smaller sample sizes, often under a gram. Industrial clients running continuous synthesis order much greater volumes packaged in controlled-atmosphere drums. Each receives the same documentation and lot characteristics, because we know how crucial it is to maintain consistent data for regulatory filings or pilot validation work. From order to shipment, our on-site chemists and QC specialists double-check all documentation and analytical profiles, ensuring no mismatch between what ships and what the initial request specified.
Several process innovators use this compound to enable more modular approaches to complex molecule assembly. By providing a core scaffold that’s both electron-rich and easy to derivatize, 3,5-Dimethoxyphenylpropionic Acid serves as a springboard substrate for building up key bioisosteres. Some customers take advantage of its side-chain acid in amide coupling, producing peptide-like structures or mimetics for target screening. Others modify the aromatic ring further, using electrophilic substitutions or aromatic halogenation to produce a palette of advanced intermediates.
We’ve seen real momentum in combinatorial chemistry, where rapid parallel synthesis wins projects. Here, reliability of each input counts—variation in melting point, moisture content, or even minimal trace organics can throw off a whole library’s analysis. By focusing on low residual solvent levels, less than 0.2% on routine batches, we eliminate much of the “noise” that can creep into mass spectral or chromatographic studies. This consistency enables teams to focus on their innovations, not backtracking to verify what actually went into a failed batch.
The same goes for synthetic route scouting: teams looking to replace legacy ingredients, like less environmentally friendly halogenated aromatics, find this acid offers a greener profile—our synthesis process minimizes waste to levels well below current regulatory thresholds, and much of our solvent and aqueous waste is rigorously reclaimed on-site.
The propionic acid moiety also lays the groundwork for ester or amide linkages, giving process chemists more options for downstream modifications without complex protection or deprotection steps. Our technical support is rooted in direct process experience; we routinely advise partners on which solvent systems deliver highest yields, or how subtle changes in acid/base ratio can swing a reaction outcome. The best results always come when there’s a two-way conversation rather than a one-size-fits-all approach.
Many manufacturers advertise high purity but overlook the importance of trace level profiling. We act differently because our lab teams track every histogram right down to sub-ppm by LC-MS and NMR. Common impurities, like remnant methylating agents or aromatic tars, are almost undetectable in our final product. We verify this both through batch-to-batch tracking and long-term stability studies, ensuring downstream users are never surprised by a sudden change in chromatogram peaks.
Quality matters most during scale-ups. The last thing a process chemist wants is to discover that what works in a flask fails in a reactor due to unreported contaminants or unpredictable byproducts. By choosing raw materials based on strict certification, running parallel stability and stress tests, and sampling across multiple reactors, our QA department closes each production lot only when satisfied—sometimes going beyond customer-requested documentation. Feedback from contract research and manufacturing partners drives our process improvement; their process data, alongside our own, guides incremental upgrades to achieve even tighter impurity thresholds.
Our shipments come with complete spectra and traceability data. This detail reassures partners who need to submit supporting information for regulatory filings and helps speed up qualification processes in large scale manufacturing. Clean, reproducible product not only keeps your synthesis on track but can shave weeks off tech transfer timelines by reducing the need for incoming material requalification. Over the years, users have highlighted this as a defining benefit that sets us apart from less vertically integrated suppliers.
As a manufacturer, we carry full responsibility not just for product quality but for how our operations affect communities and the environment. We have adopted solvent recycling units in our main production lines, and now send a large proportion of aqueous waste through biological treatment before final discharge. For 3,5-Dimethoxyphenylpropionic Acid, we developed a process that eliminates the need for halogenated intermediates, reducing both air and water emissions compared to legacy methods.
We draw on green chemistry principles where possible—for example, by choosing milder reaction conditions that lower overall energy usage, or by selecting catalytic processes that limit salt build-up. Our environmental monitoring teams report quarterly to internal review boards, which feeds into a continuous improvement loop for safer and more responsible manufacturing. Our partners repeatedly mention how this focus mirrors the demands they face in their own regions for cleaner processes and transparent tracking of environmental impact.
Details like energy use, emissions, and waste handling might seem abstract, but they show up in the bottom line when customers need lifecycle data or regulatory assurance. Our in-plant technology upgrades have let us keep costs competitive while preserving long-term viability, something more clients have come to expect as part of doing business with us.
We have seen 3,5-Dimethoxyphenylpropionic Acid play roles we never expected at the outset—from its adoption in advanced pharmaceutical intermediates to work in flavor science and specialty polymers. This trajectory only reinforces our belief in the strength of consistent production processes, smart chemistry, and close customer partnerships. With each new feedback cycle, we learn about emerging requirements: lower metal content, unique crystal forms, custom packing for specific solvent compatibility. Our actions adapt accordingly, with product development informed by what works—and what fails—in the hands of real end users.
Our path forward relies as much on technical proficiency as on honest, ongoing conversations with the laboratories and innovators who choose our products. It’s not enough to offer a high-purity chemical; support, documentation, and transparency underpin the relationships that keep projects moving through every phase, from bench to pilot to plant. As we continue to invest in both facility upgrades and chemist training, our goal is always the same: to provide the kind of material and back-up support that not only gets the job done but actually accelerates what’s possible for our clients.
Knowing how important each synthesis is to an organization’s research or production aim, we keep refining our approach—adding efficiencies, improving impurity controls, and building technical resources that help our customers make the leap from the drawing board to delivered product. Every day’s work reminds us the best chemicals are only as good as the team, the systems, and the commitment behind them. For 3,5-Dimethoxyphenylpropionic Acid, that commitment stays steadfast, driven by our hands-on manufacturing experience and the trust of those who rely on what we make.