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HS Code |
826744 |
| Product Name | 3,4-Diethoxyphenylacetic Acid |
| Cas Number | 5693-58-9 |
| Molecular Formula | C12H16O4 |
| Molecular Weight | 224.25 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 95-97°C |
| Solubility | Soluble in organic solvents such as ethanol, DMSO |
| Purity | Typically ≥98% |
| Storage Temperature | Store at 2-8°C |
| Synonyms | 2-(3,4-Diethoxyphenyl)acetic acid |
| Structure | Contains a phenylacetic acid core with ethoxy groups at positions 3 and 4 |
| Smiles | CCOC1=CC(=C(C=C1)OCC)CC(=O)O |
| Inchikey | SHIHHOTMQJGJHU-UHFFFAOYSA-N |
As an accredited 3,4-Diethoxyphenylacetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g 3,4-Diethoxyphenylacetic Acid comes in a sealed, amber glass bottle with a chemical-resistant screw cap and detailed labeling. |
| Shipping | 3,4-Diethoxyphenylacetic Acid is shipped in tightly sealed containers to prevent moisture and contamination, following all relevant chemical transportation regulations. It is typically packed with cushioning material and labeled for chemical contents, requiring documentation and handling by trained personnel. Shipping is carried out via ground or air, depending on destination and urgency. |
| Storage | 3,4-Diethoxyphenylacetic acid should be stored in a tightly sealed container, away from light, moisture, and incompatible materials such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature. Properly label the container and ensure access is restricted to trained personnel. Follow all relevant safety and chemical storage guidelines. |
Applications of 3,4-Diethoxyphenylacetic Acid in Industrial Manufacturing3,4-Diethoxyphenylacetic Acid is a specialized aromatic intermediate produced in compliance with international quality and purity benchmarks. This compound serves as a foundational building block in several high-value industrial sectors due to its distinct reactivity profile and compatibility with multiple downstream synthetic protocols. Detailed below are major application fields, covering their industry-specific requirements, integration procedures, and compliance obligations. 1. Pharmaceutical API SynthesisMajor pharmaceutical manufacturers use 3,4-Diethoxyphenylacetic Acid in multi-step organic synthesis for preparing core intermediates in antihypertensive and anticonvulsant active pharmaceutical ingredients (APIs). Our material enables efficient amidation, esterification, and cyclization reactions, allowing researchers and production chemists to achieve high product purity and yield. The compound enters synthesis routes typically after halogenation or acylation stages, contributing to critical molecular frameworks required for drug registration dossiers. Compliance with trace impurity limits and batch genealogy ensures suitability for regulated GMP production. Industry compliance standards
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2. Agrochemical Active Ingredient ManufacturingProducers of crop protection agents utilize this raw material to construct key acidic subunits in certain novel herbicide and fungicide molecules. The electron-donating ethoxy groups of our acid facilitate nucleophilic substitution reactions essential for generating bioactive ring systems. The product is incorporated in scale-up reactors after prior alkylation steps, where its high purity prevents catalyst fouling and undesired byproduct formation. Adhering to residue regulations is necessary to fulfill downstream supply chain audits. Industry compliance standards
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3. Fragrance and Aroma Chemical SynthesisLeading fragrance compound manufacturers employ 3,4-Diethoxyphenylacetic Acid as an aromatic precursor for the production of ethereal and musky tonalities in specialty aroma compositions. Its structure supports custom esterification to produce fragrant esters used in high-end perfumery and personal care. The acid is introduced following the hedonics-testing integration phase and must pass stringent olfactive stability tests. Compositional consistency and residual solvent controls are vital for IFRA compliance and customer certification. Industry compliance standards
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4. Polymer Additive and Plasticizer IndustryProducers of specialty plastics and flexible materials make use of 3,4-Diethoxyphenylacetic Acid in the modification of polyesters and vinyl copolymers. The compound’s diethoxy moiety imparts flexibility and weather-resistance to the final product. Technical managers introduce it into polymer batch reactors immediately before cross-linking catalysts are added, monitoring the acid number to control mechanical performance in the molded item. Documentation for RoHS and food-contact compliance are provided for end-user validation. Industry compliance standards
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5. Laboratory Reagents and Research Chemical ProductionLaboratory-scale chemical suppliers and research institutions specify 3,4-Diethoxyphenylacetic Acid for its function as a model compound in organic mechanism studies and as a reference standard. Its high purity and narrow melting range support reproducibility in analytical method validations and kinetic experiments. The material is often incorporated after chromatographic fraction collection and needs certified documentation for trace metals, elemental analysis, and lot-specific purity profiles. All shipments are accompanied by full traceability and batch analysis certificates. Industry compliance standards
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Over several decades of producing fine chemicals, we have seen a range of phenylacetic acid derivatives come and go, but few have brought the consistency and performance that 3,4-Diethoxyphenylacetic Acid delivers. Our product, under the model DPA-91, reflects direct experience in controlling purity from the earliest steps of synthesis through final isolation. Each stage in our plant focuses on practical details — moisture levels, temperature kinetics, and solvent condition play real roles in product reliability. We do not rely only on automated systems; senior technicians examine batch results with both chromatography and hands-on analytic work, and this vigilance shapes a final material that meets tight expectations in research and production environments.
Our typical batch offers a purity above 99% by HPLC, verified using an independent reference standard. Melting point routinely lands in the 83–87°C interval. We keep water content under 0.3% as measured by Karl Fischer titration. A white to off-white crystalline appearance reflects both its purity and careful drying procedures. We avoid inorganic contaminants by selecting high-grade starting reagents and running thorough wash procedures. The final product is typically packed and stored in airtight, light-resistant containers that guard against slow hydrolysis and discoloration — problems we have documented when storage conditions lapse below standard practice.
3,4-Diethoxyphenylacetic Acid offers a unique blend of chemical features, making it a reliable intermediate for downstream synthesis. Most commonly, it appears on benches in the pharmaceutical sector, where chemists describe its electron-rich aromatic ring and ether groups as especially useful design elements. These groups enable selective coupling and functionalization steps; many who have attempted multi-step syntheses value its reduced tendency toward side reactions, compared to analogues with fewer or more reactive substituents.
In our years supplying both small and bulk lots, we have observed that clients working in medicinal chemistry request this compound for producing molecules where both steric and electronic modulation are key. For example, the dual ethoxy groups confer increased lipophilicity and flexibility in tuning molecular properties versus monoethoxy or halogenated phenylacetic acids. Our chemical engineers have tested its compatibility with a variety of reaction partners: acylating agents, oxidative conditions, and halogenations. It withstands routine handling during multi-step synthesis without significant by-product build-up, in part due to the high control we keep on trace metal and water contamination.
Some customers ask why a specialty manufacturer invests effort in a derivative that sees less commodity-scale demand than unsubstituted phenylacetic acid. Our answer starts at the bench: chemically, the 3,4-diethoxy substitution pattern creates a molecule harder to oxidize under standard laboratory conditions than its mono-ether cousins, an effect seen in lower by-product formation in oxidative coupling reactions. This detail may not matter to every synthesis, but labs aiming for demanding selectivity sometimes find that an inspired substitution can turn a half-yielding step into one that performs consistently near completion.
Among standard options, monoethoxy and dimethoxy derivatives serve in many fine chemical contexts, but the diethoxy variant expands solubility in organic solvents — a difference our clients in materials and pigment research report improves processing. Its melting point profile is narrow, which helps formulation chemists avoid unplanned phase changes in solid-state reagents and tablets. Analytically, we supply extensive certificate of analysis data, not only because customers request it, but also because our own experience shows even minor deviations can disrupt product development. We run each batch through spectroscopic and chromatographic scrutiny, yielding a data file that includes not only purity and identity, but also insight into trace levels of related substances, as per ICH Q3A and Q3B requirements in drug substance production.
Experience has taught us that no two labs use a reagent in quite the same way. Our material often passes through batch reactors, glass vials, Schlenk lines, and automated parallel reactors. In our view, a manufacturer’s job includes delivering a predictable product that supports all these uses. Some formulation chemists work with highly moisture-sensitive derivatives; our approach keeps 3,4-Diethoxyphenylacetic Acid dry, but not so hygroscopic that atmospheric exposure during weighing means immediate waste. We design packaging with feedback from field chemists, aiming for vessel openings that fit standard scooping spatulas and minimize static that could scatter fine crystals.
Over time, clients who scale from milligram to multi-kg production highlight a stable supply as a serious concern. We hedge these scenarios by keeping secondary lots of key upstream chemicals and running parallel synthesis lines during periods of high demand. Batch-to-batch reproducibility counts — not only for routine synthesis but for the publication of patents and regulatory filings involving the compound. We maintain archives of each lot produced, including raw data from moisture, purity, and spectral analyses, so that chemists with process questions years later have access to the full history.
Years of making both standard and specialty phenylacetic acid derivatives teach lessons textbooks skip. For example, when early-career technicians observe color drift in bulk product, we discuss not only purity data but also supplier history, glassware cleaning cycles, and storage oxygen content. We learned the hard way that even brief exposure to atmospheric moisture during packaging can seed acid-catalyzed hydrolysis, so now use inert-gas gloveboxes for longer-term storage-ready material.
We pay close attention to customer reports on reaction outcomes. Sometimes, process chemists share details about crystallization or solvent compatibility that prompt us to adjust rinse solvents or final drying cycles. One client in agrochemical development showed improved downstream yields with our material produced using a slight temperature cut in the recrystallization process — a reminder that even small changes in manufacturing cascade through a supply chain. Regular discussions with formulation and analytical teams outside our plant reveal details about chromatographic baseline drift, low-level impurity challenges, and sample heterogeneity, all of which feed into our ongoing adjustments.
We recognize that consistency counts more than marketing claims. Manufacturing specialty chemicals works best with a team approach to raw material sourcing, in-process control, and logistics. Sometimes international events disrupt chemical supply chains; from our perspective, resilience means qualifying backup suppliers, investing in on-site lab testing for both incoming and outgoing streams, and keeping open channels with freight and warehouse partners.
In the early years of supplying 3,4-Diethoxyphenylacetic Acid, process interruptions resulted from solvent grade shortages and customs holdups. Each incident forced us to look at contingency planning, from setting up in-house purification for solvents, to expanding finished goods warehousing. Today, we keep inventory buffers and monitor shelf-life with regular stability tests, including stress exposure to light, oxygen, and heat. The data we gather translates into revised recommendations for customers on best handling practice — sometimes a small reminder on avoiding plastic scoops vs. stainless steel leads to more reproducible laboratory results.
Having made and supplied a spread of phenylacetic acid derivatives, we see distinctions in downstream functionalization potential, handling stability, and regulatory compliance. The 3,4-diethoxy version stands apart in ease of purification after synthesis; typical batches offer high acetonitrile and DMSO solubility, giving formulation chemists cleaner access to high-concentration solutions. Laboratories that need rapid material dissolution see fewer clumping or agglomeration issues than with monoethoxy or plain phenylacetic acids.
Regulatory expectations influence choice for active pharmaceutical ingredients and testing standards. Dimethoxy and diethoxy compounds differ in regulatory familiarity, but our data show that the diethoxy version can reach desired impurity thresholds with less reprocessing. Value comes from not having to rework a batch because of late-stage discovery of hydrolysable or extractable impurities. The product’s defined melting point helps tableting and granulation engineers predict consistency in finished tablets, with less risk of unplanned softening.
Every specialty chemical faces hurdles, often outside strict chemical purity. Packaging strength matters. In our experience, traditional LDPE bottles sometimes allow slow oxygen ingress, so we switched to multi-layer barrier containers, extending shelf life for distribution across climates. We found bulk pack users prefer wide-mouth glass jars, and our research teams monitor for particulate matter shed from caps or liners.
Shipping restrictions on aromatic acids create headaches. We adapted by designing labels and documentation compatible with international codes, so customs delays do not tie up shipments longer than necessary — a lesson learned from early setbacks with batch holds at foreign ports. For temperature control, we offer data loggers that track the journey, and can intervene using emergency restocking within days from regional warehouses.
Waste management comes into play at the user end. Each customer site has different incineration, solvent disposal, and wastewater requirements. Our process chemists ensure materials meet local regulations by running environmental tests before shipment. After seeing several pilot scale projects encounter delays while waiting on compliance documentation, we now prepare environmental impact statements for large orders at the time of manufacture.
Insight from end-users often drives improvements we did not initially anticipate. As one example, multiple feedback cycles brought to our attention subtleties in particle size distribution that affected not only filtration rates in the customer’s lab, but also wetting properties and transfer losses. Minor tweaks in milling and sifting during our crystallization process produced a product better suited to automated pipetting and solid handling systems.
Some research partners publish reaction details that hint at batch variations or alternate by-product profiles when using 3,4-diethoxy- vs. dimethoxyphenylacetic acids. We collaborate with clients to refine approaches and troubleshoot, using joint data reviews or even side-by-side laboratory trials. Our team values this two-way street; often, a phone conversation with a process engineer uncovers details missed in a formal QA document.
Our reputation grows with the reliability of each delivery. When researchers report clear HPLC traces and reproducible yield, it confirms upstream control. Part of this equation involves transparency — our batch records, analyst notes, and method development SOPs are open to review by customer QA teams and regulators. We offer both technical and practical support: from sharing chromatograms to demonstrating sample weighing techniques for viscous crystallized forms.
Feedback from pilot plant managers and university groups suggests that real-world usability matters as much as published specifications. Subtle differences in particle morphology, dust generation, and static charge behavior can influence weighing, transfer, and dissolution. We monitor these details during every run, making small adjustments to improve user experience across the board.
For us, quality is rooted in daily operations: careful selection of starting materials, control of every parameter in synthesis, and real attention to detail in storage. We perform accelerated aging studies and monitor for low-level impurity formation over time. Each production cycle concludes with rigorous batch review meetings, where chemists, production managers, and quality assurance teams review every anomaly and pattern in the data. This commitment means we catch trends before they become problems for our customers.
We have invested in both continuous-flow and batch synthesis options, to bridge demand spikes and ensure flexibility. All analysis happens in-house, with third-party audits scheduled quarterly. These controls mean less worry about lab-to-lab differences, so customers can focus on pushing research forward, confident in the stability and reactivity of each order.
Making and supplying 3,4-Diethoxyphenylacetic Acid involves much more than preparing a fine powder to specification. We follow the trail from upstream reagent choice, through process tweaks and packaging innovations, to the fine details that shape real-world results in sector after sector: pharmaceutical, material science, analytical chemistry, and more. Our efforts in stability testing, process flexibility, trace analysis, and transparent support systems draw on hard experience as well as ongoing communication with scientists at every level.
For labs needing a phenylacetic acid derivative with high purity, stability, and adaptability, our approach favors controlled, measured, and continually improved manufacturing — a path forged on years of learning from the ground up. We push for a future where specialty chemicals support creativity and precision, grounded in real relationships and tested know-how.