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HS Code |
111765 |
| Name | 3-(2-Methoxyphenyl)Propionic Acid |
| Chemical Formula | C10H12O3 |
| Cas Number | 6740-65-8 |
| Appearance | White to off-white crystalline powder |
| Melting Point | 62-65°C |
| Solubility In Water | Slightly soluble |
| Density | 1.17 g/cm³ (approximate) |
| Purity | Typically >98% |
| Storage Temperature | Room temperature |
| Synonyms | 2-Methoxyhydrocinnamic acid |
| Smiles | COC1=CC=CC=C1CCC(=O)O |
| Inchi | InChI=1S/C10H12O3/c1-13-10-6-4-2-3-5-9(10)7-8-11/h2-6H,7-8H2,1H3,(H,11,12) |
As an accredited 3-(2-Methoxyphenyl)Propionic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 3-(2-Methoxyphenyl)Propionic Acid is supplied in a 100g amber glass bottle with a sealed screw cap and clear labeling. |
| Shipping | 3-(2-Methoxyphenyl)Propionic Acid is shipped in tightly sealed containers, protected from moisture and light, and labeled according to safety regulations. The package complies with local and international transport guidelines to ensure safe delivery. Temperature-sensitive shipping may be required, typically under ambient conditions, with handling and documentation per relevant chemical safety standards. |
| Storage | Store 3-(2-Methoxyphenyl)propionic acid in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of heat, ignition, and incompatible substances such as strong oxidizing agents. Protect from excessive moisture and direct sunlight. Clearly label the container and keep it out of reach of unauthorized personnel. Follow standard chemical storage protocols. |
Applications of 3-(2-Methoxyphenyl)Propionic Acid in Industrial Manufacturing3-(2-Methoxyphenyl)Propionic Acid finds targeted use across several advanced industrial sectors. Below, we detail its practical roles, compliance requirements, dosages, processing pathways, and resulting end-products in genuine downstream applications. All information reflects direct feedback from OEM partners and proprietary process expertise. 1. Pharmaceutical Intermediate for Non-Steroidal Anti-Inflammatory Drugs (NSAIDs)Originating from controlled esterification and hydrolysis steps, 3-(2-Methoxyphenyl)Propionic Acid serves as a key pharmaceutical intermediate in the synthesis of selective NSAIDs. Formulators value its clean conversion rates and predictable impurity profiles in multi-step reactions. This material enters amidation or acylation routes, supporting scalable batch synthesis for major API manufacturers. Strict change control and documented GMP handling apply throughout shipment, storage, and charge-in stages, helping innovators and generics producers meet audit requirements in regulated markets. Industry compliance standards
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2. Aromatic Ester Synthesis for Fragrance IndustryPerfumery chemical specialists use 3-(2-Methoxyphenyl)Propionic Acid for high-value aromatic ester synthesis. Its methoxy-phenyl structure supports the formation of esters offering long-lasting odor notes and thermally stable profiles in fine fragrance bases. Scale-up involves acid-catalyzed Fischer esterification or enzyme-catalyzed routes. Feedstock purity, minimized sulfur carryover, and reproducible acid value support manufacturer QC release and IFRA-compliant usage in finished scents. Material flows tightly from chemical warehouse into batch-controlled reactors under validated standard operating procedures. Industry compliance standards
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3. Advanced Polymer Additive in Specialty CoatingsProducers of engineered coatings adopt 3-(2-Methoxyphenyl)Propionic Acid as a reactive chain-modifier in select polyester and polyamide resins. This reagent helps tailor flexibility, adhesion, and heat stability in thermoset film and automotive topcoats. The acid group participates in melt condensation or solution polymerization, enabling precise integration into the backbone rather than as a mere blend additive. Material specification, particle size, and residual solvent content require strict monitoring according to downstream customer product approval. Finished polymer lots undergo accelerated aging and chemical soak tests before certification release. Industry compliance standards
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4. Synthesis of Pesticide Intermediates for Agrochemical ProductionLeading agrochemical formulators utilize this material as an intermediate for manufacturing selective herbicide and fungicide active ingredients. The electron-rich aromatic ring and propionic acid side chain enable key C–C and C–N bond-forming transformations under controlled halogenation, nitration, or amination conditions. Material acceptance depends on transparency over trace contaminants, robust COA support, and full regulatory compliance. Downstream QC teams demand thorough documentation to underpin safe field applications and seasonal batch traceability. Industry compliance standards
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Working in chemical manufacturing, I have seen how targeted molecules can shape real outcomes in fields as diverse as pharmaceuticals, crop protection, and materials science. Our 3-(2-Methoxyphenyl)propionic acid is a standout in our line of aromatic building blocks, produced in-house under strict quality controls. This compound, often recognized by its CAS number 586-38-9, features a methoxy group positioned at the 2-spot on the phenyl ring, bonded to a three-carbon propionic acid backbone. Our synthesis routes have been optimized over the years, and that hard-won experience allows us to offer material that meets the daily demands of experienced researchers, formulators, and process engineers.
In a chemical plant, even small impurities can stall development projects or lead to lost batches. Countless users have learned the difference between laboratory-grade samples and truly reliable process chemicals. Because we manufacture from raw benzene derivatives under closed-loop conditions, we minimize side-products and degradation. Typical purity exceeds 98%, verified by multiple runs of HPLC and GC, with documentation to match. We learned early that batch-to-batch consistency matters just as much as top-tier purity: one drum must match the next. As a result, our customers report fewer surprises scaling up from the bench to full pilot plant trials.
Our teams often get questions about the best contexts for 3-(2-Methoxyphenyl)propionic acid. Most often, it takes center stage in pharmaceutical research, such as in the synthesis of non-steroidal anti-inflammatory intermediates and other aromatic compounds. We have supplied this molecule to groups developing prodrugs, and several industrial clients rely on it as a backbone for custom ligand libraries. Out in the field, some agrochemical innovators use it as a key intermediate for herbicide analogs. Synthetic flexibility proved valuable through years of process refinement. Whether clients opt for direct acylation, amidation, or more complex functionalization, this acid offers a predictable reactivity thanks to its selectively placed methoxy substituent. That para-directing group guides reactions toward the right products with fewer unexpected byproducts—a lesson learned over multiple pilot projects.
We publish a robust certificate of analysis with each lot that ships from our facilities. We focus on more than just the headline purity. Water content and heavy metals receive close attention given their downstream impact; we set our internal maxima below levels typically accepted in the market, based on our own process experience. For example, chloride and sulfate levels fall well within pharmacopeial expectations, giving downstream chemistry a much cleaner start.
Melting point is checked regularly, not just for confirmation but as an early indicator of shifts in process control. Our 3-(2-Methoxyphenyl)propionic acid typically demonstrates a melting point from 64–66°C, correlating tightly with spectroscopic analysis. For those working on tight timelines, solubility—in both polar and nonpolar solvents—is predictable, meaning formulation trials tend to run more smoothly. We measure and report particle size for each lot, knowing from feedback that handling and dosing into reactors can hinge on getting this factor right.
Decades of production data tell us that consistency comes from deep process understanding, not luck or shortcuts. Each chemist in our team knows the quirks of the methylation step, and we have refined our oxidation approach to reduce byproduct formation even at scale. Repeatability depends on monitoring key temperatures and residence times in our reactors; even a few degrees can affect final product acidity and overall appearance. Early on, batches revealed wider color shifts and lingering odors—lessons that pushed us to perfect our washing and filtration steps.
No less important is the process of acidification and crystallization. We cool at precise rates, favoring controlled nucleation and steady crystal growth. This step makes handling more reliable for anyone repackaging, reformulating, or converting the compound downstream. Doing the job right—without short-term fixes—means more predictable yield and fewer runbacks. Such operational discipline often determines whether a customer’s project launches on schedule.
Some buyers ask why this molecule matters compared to related structures, such as unsubstituted phenylpropionic acid or the isomeric alternatives. Through sustained technical collaboration, we’ve seen that the methoxy group at the ortho position does more than modify reactivity. It shifts electron density, making ring substitutions more selective—an edge in medicinal chemistry where controlling side-product formation speeds up purification and validation. In certain screens, ortho methoxy enhances bioactive potential, distinguishing it from the less functionalized equivalents. We notice this particularly in projects aiming for enzyme modulation or altered pharmacokinetics.
In real synthesis labs, 3-(2-Methoxyphenyl)propionic acid fills the gap between simpler phenyl acids and more elaborate diarylpropionates. It’s less prone to unwanted oxidative dimerization than some para-methoxy derivatives, giving a more reliable throughput in demanding multi-step syntheses. The acid group’s position yields predictable coupling results, making this structure an attractive scaffold for SAR (structure-activity relationship) explorations. Over time, research customers have shifted more attention here for analog workups—driven in part by cleaner NMR spectra and higher isolated yields.
In the daily reality of a chemical plant, abstract metrics mean little without operational impact. We retooled our reactors based on feedback from a pharmaceuticals partner who needed larger lots with tighter particle size control; a simple sieve swap wasn’t enough, so we modified agitation speeds and upgraded jacket cooling for sharper distributions. When one client ran into filtration bottlenecks, we pulled samples from each wash stage and dialed in better solvent mixes—solving a problem that had cost weeks in lost production runs elsewhere. Years on the production floor have shaped how we approach QA processes for this molecule.
Our technical team keeps records not only of each lot’s specifications but also of practical feedback from operators who dose and process the acid every shift. One customer, scaling up to kilogram reactors, ran into unexpected foaming during dissolution; we traced this to a trace peroxide artifact and updated our peroxide testing before release. Across all these adjustments, we filter lessons back to earlier process steps. It’s the small gains in yield and handling that, over repeated cycles, mean projects move from lab curiosity to registered products.
Manufacturing specialty chemicals responsibly requires a continuous focus on solvent recovery, waste minimization, and emission control. Every batch of 3-(2-Methoxyphenyl)propionic acid passes through a rigorously managed waste stream, with spent solvents distilled and reused or safely incinerated. Over the years, we replaced older chlorinated solvents with less hazardous alternatives. Our engineers found that switching to greener oxidants, even at higher cost, saved downtime by simplifying treatment of liquid effluent. The resulting drop in process waste led to higher internal yields—a benefit for both the environment and the bottom line.
Process water receives in-house biological treatment, so trace organics exit well below regulatory thresholds. Years of collaboration with regional authorities have improved not just our footprint but also that of the wider supply chain. Customers working on green chemistry initiatives can count on documented process improvements, supporting their own sustainability narratives and regulatory compliance efforts. What started as an economic decision grew into a key factor in long-term partnerships.
Anyone in chemical manufacturing knows delivery gets complicated if packaging doesn’t fit the user’s scale or storage needs. Our acid ships in fiber drums, sealed pails, or lined bulk bags, matching what customers told us works in real warehouses. Over time, we replaced older lids with tamper-evident designs and introduced smaller-volume packs for teams who run smaller pilot trials or infrequent campaigns. Shipping weight, lot labeling, and sealing protocols all trace back to what we learned from users’ receiving teams, not marketing surveys.
With temperature shifts in transit a real threat, we validated both cold- and warm-chain delivery to prevent clumping or hydrolysis. We adjust packaging in response to specific storage environments or on high-humidity routes. Downstream users might never notice, but stable form on arrival cuts rework and ensures accurate dosing—damage avoided, not just inconvenience.
We notice that successful innovation rarely happens in isolation. Process chemists trying to scale new API intermediates approach us for technical consultations, bringing not just specs but also real questions about handling, storage, and compatibility. We host regular site visits and share upstream data so clients can replicate and predict performance more reliably in their own plants. In several projects, we developed custom grades—lowering residual metals or preparing larger crystals—so a specific downstream step met regulatory or analytical signoffs the very first time.
These partnerships shape what we do next. By collecting process feedback and acting on it, small improvements mount up quickly: a change in drying conditions delivers a tighter melting point range; a tweak in purification chemistry clears up minor off-notes in aroma or residual solvent. Open exchange, not just a finished COA, is the real engine of progress.
One of the questions we hear often is how handling and use of 3-(2-Methoxyphenyl)propionic acid stack up to alternatives on the market. The material’s crystalline nature simplifies weighing and dosing, and its mild odor makes lab work more comfortable, especially compared to raw phenolic acids that can irritate operators or taint air-sampling equipment. Unlike free-flowing liquids or sticky pastes, our acid remains workable at standard room temperatures, allowing formulators to pre-blend before active stage chemistry. Dosing accuracy benefits, so there’s less risk of overdosing or slipping outside target stoichiometry.
Not all reactors yield the same results with similar acids. If users switch in a different isomer or a less pure alternative, they sometimes see color shifts or filtration issues—evidence of byproducts that clog or foul equipment. Our in-house quality checks catch minor impurities upstream, keeping the acid consistent from batch to batch. This reliability shortens troubleshooting and supports faster tech validation when specs matter most.
As an experienced team, we have seen the hidden costs when third-party suppliers cut corners—untracked contaminants, unpredictable particle sizes, and the risk of delayed shipments. Owning the production end-to-end means never wondering about trace solvent sources or unknown synthetic routes. In those moments when supply chains tighten or regulatory demands climb, control gives us flexibility, traceability, and peace of mind for every customer.
We keep detailed batch histories, down to small process deviations, and review them after every campaign. Training our staff to spot and correct small changes early gives us the confidence to deliver on tight timelines, even in uncertain markets. Customers get more than a drum—they gain an experienced partner who can adapt and troubleshoot in real time, sharing expertise that’s developed over long campaigns and intensive audits.
Regulatory filings and quality audits have grown more demanding over the years, especially in pharmaceutical and agricultural applications. We built our internal documentation to reflect this reality. Every shipment can be traced back through raw materials, individual operators, and laboratory data. This depth saves days during audits and certifications, and accelerates customer approval processes.
Quality systems evolve as regulations move. Our records extend beyond batch paperwork; we keep spectral archives, calibration logs, and sampling histories. This allows rapid investigations of any deviation and supports ongoing compliance with national and international standards. Process transparency builds real trust, and our repeat customers know we respond with complete data, not just stock answers.
Many of the research teams we supply use 3-(2-Methoxyphenyl)propionic acid to chase ambitious targets—novel drug candidates, efficient synthetic methodologies, or high-performance additives. As projects scale, researchers lean hard on reliability. Unplanned process hiccups hurt development schedules and grant timelines, while unexplained analysis discrepancies risk entire campaigns. Our experience matches these needs, both at screening scale and in the move to multi-kilogram volumes.
Some of our most interesting collaborations saw this molecule serving as a jumping-off point for new SAR exploration. Direct feedback from medicinal chemists pushed us to refine analytical controls and share structure-confirmation spectra with each lot, paving the way for smoother GLP validations. Knowing where small impurities originate helps teams design purification strategies or submit analytical filings. The compound’s unique substitution pattern opens doors for specific arylation and alkylation routes not easily accessible with related acids, guiding innovation toward new lead compounds.
We expect demands for quality, transparency, and responsible manufacturing to only intensify. The lessons learned from refining 3-(2-Methoxyphenyl)propionic acid—how to manage trace contaminants, optimize reaction steps, and minimize environmental footprint—feed directly into our future product launches. We review customer trends, new regulatory proposals, and advances in synthetic chemistry, updating processes as real-world needs shift.
By sharing data and case stories, we help our partners anticipate changes in their own markets. Early access to process improvements or analytical trends allows more agile research and manufacturing. Whether supporting stricter pharmacopeial standards or green chemistry initiatives, the technical depth honed through years of manufacturing this compound empowers both our team and the clients we serve.
We measure our performance not in abstract terms, but in the tight melting point ranges, reproducible particle sizes, and direct results in our customers’ downstream chemistry. Our 3-(2-Methoxyphenyl)propionic acid reflects the lessons and investments of years on the production floor. Those using our products get more than a certificate—they gain a responsive partner driven by technical precision and a genuine investment in their long-term success. Through continuous feedback, constant process improvement, and a focus on practical utility, we do more than fill orders—we help creators turn new possibilities into working reality.