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2,5-Dimethoxycinnamic Acid

    • Product Name 2,5-Dimethoxycinnamic Acid
    • Alias NSC 3452
    • Einecs 223-638-3
    • 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

    633950

    Name 2,5-Dimethoxycinnamic Acid
    Cas Number 22227-20-1
    Molecular Formula C11H12O4
    Molecular Weight 208.21 g/mol
    Appearance White to off-white solid
    Melting Point 191-194 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles COC1=CC(=C(C=C1)OC)C=CC(=O)O
    Iupac Name 3-(2,5-dimethoxyphenyl)prop-2-enoic acid
    Purity Typically ≥98%
    Storage Temperature Store at 2-8 °C

    As an accredited 2,5-Dimethoxycinnamic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2,5-Dimethoxycinnamic Acid is supplied in a 25g amber glass bottle with a secure screw cap and detailed safety labeling.
    Shipping 2,5-Dimethoxycinnamic Acid is shipped in tightly sealed containers to prevent contamination and moisture exposure. Packaging complies with chemical safety standards, and labeling includes identification, hazard warnings, and handling instructions. During transit, the product is protected from extreme temperatures and physical damage to maintain quality and ensure safe delivery.
    Storage 2,5-Dimethoxycinnamic acid should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep it in a cool, dry, and well-ventilated area, ideally in a dedicated chemical storage cabinet. Avoid exposure to incompatible substances such as strong oxidizing agents. Properly label the container to ensure safe identification and handling.
    Application of 2,5-Dimethoxycinnamic Acid

    Applications of 2,5-Dimethoxycinnamic Acid in Industrial Manufacturing

    As an experienced chemical raw material producer, we supply 2,5-Dimethoxycinnamic Acid to established sectors requiring precise intermediates, advanced synthesis pathways, and regulatory-compliant formulations. Our product’s consistent purity and precise performance characteristics support a range of demanding industrial applications, from active pharmaceutical ingredient synthesis to specialty polymer and advanced UV absorber manufacturing.

    1. Pharmaceutical Intermediate for Antifungal Drug Synthesis

    In the pharmaceutical sector, downstream manufacturers employ our material as a targeted intermediate during the synthesis of azole-based antifungal actives. The product participates in selective condensation and acylation steps, introducing methoxy groups to frameworks central for triazole derivatives. Strict process controls during these transformations ensure consistent isomeric purity, which directly impacts the safety and efficacy testing phases required for regulatory submissions.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • European Pharmacopoeia (Ph. Eur.) monographs on intermediates
    • US FDA DMF guidelines for key starting materials
    • ICH Q3A Residual Solvents requirements

    Typical usage ratio

    • Batchwise input 0.8-1.2 mmol per target API equivalent; adjusted for molecular yield to 1–5% of final drug mass, depending on step conversion efficiency

    Downstream process integration

    • Enters as a foundational raw intermediate in early synthetic stages of azole drugs like fluconazole or voriconazole; typically undergoes esterification, reduction, and coupling reactions in pilot plant reactors

    Final product types

    • Bulk pharmaceutical intermediates (BPIs)
    • Registered antifungal active pharmaceutical ingredients (APIs)
    • Hospital-grade generic tablets and injectables containing azole actives
    • Custom intermediates for clinical research batches

    2. Precursor in UV-Absorber Manufacturing for High-Performance Coatings

    The coatings industry integrates this compound as a customizable feedstock for the development of benzophenone-type UV stabilizers. By introducing 2,5-dimethoxy groups, formulators enhance photo-absorption and migration resistance in clearcoat polymers. Control of reactor temperature, catalyst identity, and solvent polarity critically influences the efficiency of methylation and coupling during the absorber’s construction, ensuring downstream compliance with emission and migration limits in consumer and automotive finishes.

    Industry compliance standards

    • REACH (EC 1907/2006) Annex XVII for UV additives
    • EN 71-3 (Safety of toys—migration of certain elements including stabilizers)
    • EU Directive 2004/42/CE (VOC in paints and varnishes)
    • ISO 10685-2 (Ophthalmic optics—UV filters for lenses)

    Typical usage ratio

    • 0.3–2.5% w/w of total stabilizer precursor input for UV absorbers; usage determined by the type and exposure criteria of the final coating

    Downstream process integration

    • Introduced in condensation and cyclization steps during the synthesis of UV stabilizer molecules, then compounded into resin premixes using high-shear dispersers or continuous blending reactors for mass-market clearcoats

    Final product types

    • Industrial clearcoats for automotive and aerospace finishes
    • Architectural UV-blocking coatings
    • Transparent UV-stabilized plastics and films
    • Performance sunglasses lenses and polycarbonate sheets

    3. Monomer Modifier in High-Temperature Specialty Polyesters

    In advanced polymer synthesis, downstream processors select this acid as a functional chain modifier to incorporate methoxy-functionalized aromatic units into engineering polyesters. The distinct electron density provided by the 2,5-methoxy substitution improves thermal stability and alters crystallization behavior, which is critical for extrusion and injection molding of films and technical parts. Reactors require inert gas blanketing and tightly controlled monomer feed ratios for consistent molecular weight distribution and minimal cross-contamination.

    Industry compliance standards

    • UL 94 (Flammability test for plastics)
    • ISO 9001:2015 (Quality Management Systems for polymer plants)
    • ASTM D3418 (Polymer transition temperature characterization)
    • FDA 21 CFR 177.1630 (Indirect food additives: polyesters in food contact)

    Typical usage ratio

    • 0.5–3.0 mol% chain modifier relative to main polyester monomers; adjusted per mechanical and thermal performance specifications demanded by the final product

    Downstream process integration

    • Fed continuously or by batch into esterification and polycondensation reactors alongside main monomers such as ethylene glycol and terephthalic acid; chain length and modification degree are monitored via in-process NMR and GPC

    Final product types

    • High-performance polyester films for packaging electronics
    • Technical molded parts for automotive applications
    • Specialty fibers for filtration membranes
    • Coengineered food packaging sheets with modified migration profiles

    4. Synthetic Building Block for Flavors and Fragrance Formulation

    In flavor and fragrance synthesis, formulators apply our product as a starting esterifiable acid in pathways to methoxylated cinnamic esters. These intermediates deliver nuanced spicy-woody notes and extend shelf stability in high-temperature processing of fragrance oils and compounded flavors. Process engineers and perfumers achieve consistent olfactory signatures by controlling stoichiometry and reaction time in Fischer esterification or transesterification units running GMP-compliant protocols.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards & QRA
    • FDA GRAS regulations (21 CFR Part 182, Flavors)
    • Flavor and Extract Manufacturers Association (FEMA) GRAS lists
    • ISO 9235 (Natural aromatic raw materials)

    Typical usage ratio

    • 0.5–5% w/w of esterifiable acid source in synthetic flavor base or perfume accord; ratio dialed by target aroma threshold and stability profile

    Downstream process integration

    • Reacted with selected alcohols under catalytic conditions to produce methoxylated cinnamic esters, subsequently formulated into fragrance oils or flavor bases prior to blending or encapsulation

    Final product types

    • Perfumed fine chemicals for detergent and personal care products
    • Compound flavors for beverage and confection industries
    • Essential oil blends with high oxidative and UV stability
    • Microencapsulated flavor or fragrance microbeads
    Free Quote

    Competitive 2,5-Dimethoxycinnamic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2,5-Dimethoxycinnamic Acid: From Laboratory Synthesis to Scalable Application

    A Closer Look at 2,5-Dimethoxycinnamic Acid

    After years of precision work with aromatic acids, our team recognizes certain molecules attract chemists for good reason. 2,5-Dimethoxycinnamic acid stands out in several research circles thanks to its flexible methoxy substitution, accessible carboxylic functional group, and compatibility with various downstream chemistries. Once, this compound sat hidden in specialty libraries mostly reserved for academic studies, but practical manufacturing has changed this. Now, regular large-scale synthesis makes it available for innovators wanting proven reliability and quality.

    Our facility employs decades-old strategies fine-tuned by hands-on experience. The acid emerges white and crystalline, usually melting above 150°C, odorless and stably stored under standard conditions. Purity reaches high levels as verified by HPLC and NMR, and we've consistently refined isolation protocols so that batches remain reproducible over long production runs. Whether labs need milligrams or processors require kilograms, such infrastructure handles both with assurance.

    Product Model and Typical Characteristics

    We prepare 2,5-Dimethoxycinnamic acid under one core model, keeping key characteristics stable for repeat orders. The molecule, C11H12O4, offers methoxy groups at the 2 and 5 positions, anchored on the cinnamic backbone. For every batch, we check that the melting point, spectral data, and moisture content fall within strict internal ranges. HPLC purity always exceeds 98%, and common impurities remain tightly controlled, since even minor contamination complicates downstream work.

    Many requests focus on standard mesh powders, since that form weighs and dissolves predictably. Granulation only rarely comes up, usually when clients need to minimize dust or prefer faster dispersion. Our shifts adjust drying, sieving, and packaging methods according to these preferences—experience has taught us that small details here bring up fewer headaches in downstream steps.

    Knowledge Earned from Manufacturing Experience

    Each compound has quirks that become obvious only through handling thousands of batches. We see less caking and clumping with 2,5-dimethoxycinnamic acid compared to some hydroxy analogues, likely a result of its dual ether protection. Humidity remains the biggest threat, so double packaging and fast bagging after crystallization have nearly eliminated stickiness and powder agglomeration on the warehouse shelf.

    Atmospheric oxygen does not noticeably impact shelf life, contrasting with compounds where color changes betray oxidation within months. Here, our own storage studies showed properly closed drums maintain full quality for over two years at room temperature. Customers benefit from this stability, speeding up procurement schedules since they do not need to rush through entire lots after delivery.

    Applications: Where 2,5-Dimethoxycinnamic Acid Shines

    This molecule enters a surprising variety of synthetic routes. Our biggest commercial demand currently comes from the pharmaceutical and advanced material sectors. Many downstream transformations, including esterification, amidation, and cross-coupling, take advantage of the orthogonally protected acid structure. Chemists often choose it for designing intermediates that require eventual deprotection or targeted substitutions, since its dimethoxy substitution map offers both regioselectivity and tunable reactivity.

    Over the last five years, several groups have adopted 2,5-dimethoxycinnamic acid for early-phase kinase inhibitor syntheses and crop protection libraries. The acid’s backbone allows cyclization and condensation strategies that yield skeletons impossible to build from more basic cinnamic acids. In fragrance chemistry, our partners note that methoxy substitutions improve the volatility and odor profile of certain esters—again, direct experiences shared between our site and our most demanding industrial partners drive formulation tweaks and process improvements.

    Comparing to Other Related Compounds

    Within the family of cinnamic acids, substitution patterns change everything. Simple trans-cinnamic acid, which sees broad commodity use, costs less and is easier to source, but lacks the steric and electronic features introduced by dual methoxy groups. In our hands, 2,5-dimethoxycinnamic acid delivers better yields in selected aldol-type condensations and Diels-Alder reactions, where aromatic electron density matters.

    Narrowing the comparison further, mono-methoxy cinnamic acids (such as p-methoxycinnamic acid) behave somewhat differently in coupling reactions; controlling regioisomer ratios proves harder, especially in oxidative steps. Our customers relay this regularly—having worked with mono- and tri-methoxy analogues in parallel projects, they appreciate the predictable reactivity and selectivity of the 2,5-pattern.

    In bulk pharmaceutical work, the methoxy configuration dictates everything from solubility to product purification. Other manufacturers sometimes ship off-grade or unevenly substituted materials; those bring unnecessary drama to a process that already demands precision at every turn. Our own in-process checks guarantee the right isomer with each lot.

    Challenges Faced and How We’ve Solved Them

    Nearly every synthetic sequence encounters pressure from three sides: supply consistency, impurity management, and regulatory compliance. 2,5-dimethoxycinnamic acid once posed supply issues because of the limited upstream availability of 1,4-dimethoxybenzaldehyde. Relentless sourcing and qualifying multiple suppliers finally stabilized this risk. Maintaining a steady line of the key starting material lets us promise uninterrupted shipments, an edge that wins trust among purchasing managers burned by shortages elsewhere.

    Impurity management takes patience and persistent fine-tuning. On one occasion, a small impurity at roughly 0.1% triggered challenges in a client’s end reaction. After several deep dives into the chromatograms and upstream purification columns, we identified a byproduct from raw aldehyde oxidation. Process tweaks—better inert gas blanketing and solvent degassing—dropped this impurity below detection.

    Environmental safety standards keep tightening worldwide. From day one, we committed to closed reaction vessels, solvent recycling, and capturing trace emissions at each purification step. This infrastructure pays for itself in smoother regulatory audits and cleaner annual inspections. The shift to greener chemistry is not a marketing pitch but a pragmatic necessity; handling phenolic solvents only works long-term when emission controls run round the clock.

    Quality Assurance, Batch Control, and Lessons from Scale-Up

    Batch consistency rarely receives the attention it deserves until variability surfaces in R&D or production. In our early years, scale-up from 500 g to 20 kg introduced minor crystallization differences, leading to some unexpected polymorphism. Sometimes, subtle temperature drifts produced crystals that filtered poorly, wasting operator time. Getting this under control involved both hardware (precise jacketed reactors, rapid cooling) and software (refined SOPs that force slow, staged addition).

    Our analytical team runs every lot against a library of NMR and HPLC fingerprints built up over hundreds of batches. They check not just stated impurity limits but also appearance (grain size, clumping), moisture levels, and even trickier variables like filterability. Only then does any raw material or finished product move from QA into a customer’s hands.

    Clients once flagged a rare lot for off-white dust, a sign of slight thermal degradation. This taught us to batch smaller amounts during peak summer heat. Learning from our own decades-long operation required humility—no imported specification sheet can replace on-the-floor troubleshooting. Today, we spend more hours in-process checking than documentation would ever strictly require. The outcome is low incident rates, fewer rejected lots, and happier downstream operators.

    Packing, Shipping, and Handling Insights

    Customers value reliable shipping as much as chemistry. Our operators, having loaded everything from 1 kg tins for R&D to 500 kg drums for major API programs, know that tedium kills accuracy. Each lot receives clear batch labeling, double-sealed liners, and tamper-evident closures. Before any drum leaves our door, loading supervisors confirm air-tight seals and accurate labeling—this grows from years of field calls about “dusty bags” or “mislabelled cases” that slow down client production chains.

    Overseas customers in humid regions often call for added desiccants. Our logistics crew, seasoned by tropical summers and monsoon disruptions, doubles up on desiccant packs and uses thicker liners as a matter of practice. Too many years of regional complaints about powder caking and carton collapse taught us that investing a few cents more on packaging prevents headaches and lost business.

    Practical Uses Across Industries

    2,5-Dimethoxycinnamic acid once looked like a specialty for a handful of chemists, but it now sees consistent use in both established and emerging sectors. Pharmaceutical process teams often start with it when working toward advanced intermediates—those groups building macrocyclic peptides or designing protected scaffolds for subsequent deprotection. Aromatic esters formed from this acid go into performance coatings and niche fragrance compounds. The same methoxy pattern that stabilizes intermediates in drug chemistry enhances binding in certain enzyme models, a useful trick picked up by many medicinal chemistry groups hunting for lead molecules.

    Another field, polymer modification, has lately explored this acid for use in specialty resins. The dimethoxy structure incorporates easily, granting flexibility to copolymer backbones and affecting thermal behaviors. This current is still growing, but we already see more incoming requests from R&D teams running feasibility studies in lightweight, heat-resistant materials.

    What Sets Our 2,5-Dimethoxycinnamic Acid Apart

    Spending years perfecting one molecule sounds repetitive, but that single-minded focus pays off in small but important differences. Chemists enjoy closer technical support, rapid turnaround times, and a willingness to adapt packaging or batch sizes. Several customers report that material from less meticulous sources occasionally interrupts automation by gumming feeders or causing blockages—these headaches stem from overlooked particle size or moisture issues, pitfalls our plant avoids because each batch is checked for such traits.

    We have faced every possible challenge: sourcing blips in the chemical feedstock market, unexpected chromatography peaks, and ever-rising standards from both regulators and the clients themselves. Instead of cutting corners, our response always consists of tightening controls and investing in better training and equipment. In the end, our experience, focus, and oversized respect for detail become the reasons customers keep coming back for this raw material, whether their application lands in pharmaceuticals, coatings, or new material prototyping.

    Summary of Ongoing Developments and Industry Insights

    2,5-Dimethoxycinnamic acid has shifted from a niche research curiosity to an indispensable building block in rigorous synthetic chemistry, trusted both for its reactivity and stability. The lessons learned manufacturing this compound—every improvement in yield, purity, and handling—feed into broader knowledge that circulates throughout the chemical community. Clients now expect a premium, repeatable product that fits straight into both bench-level experimentation and full-scale manufacturing campaigns. We see new research every month: more complex small molecules, more ambitious material targets, and a persistently tricky regulatory environment keeping everyone on their toes.

    Process knowledge keeps evolving. As better reactor controls and greener chemistries develop, our shop floor adapts them toward this and similar products. We maintain open channels with our biggest users, absorbing field feedback and sending our own troubleshooting tips and lessons learned back into the pipeline. For many, our 2,5-dimethoxycinnamic acid now represents not just a chemical, but proof that careful process design and hands-on manufacturing experience still matter in a world eager for speed and scale.

    Ultimately, our story with this compound shows how a single well-made aromatic acid can support entire chains of discovery and innovation. Every drum, bag, and tin that leaves our factory stands behind years of iterative gains: tighter purity, more reliable shipping, smarter hazard management, and thousands of conversations with chemists around the world driving requirements forward.