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2,4-Dimethoxycinnamic Acid

    • Product Name 2,4-Dimethoxycinnamic Acid
    • Alias o-Anisic acid
    • Einecs 210-382-5
    • 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
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    Specifications

    HS Code

    248880

    Cas Number 2217-00-9
    Molecular Formula C11H12O4
    Molecular Weight 208.21 g/mol
    Iupac Name 2,4-dimethoxy-3-phenylprop-2-enoic acid
    Synonyms 2,4-Dimethoxycinnamic acid; 2,4-Dimethoxy-trans-cinnamic acid
    Appearance White to off-white solid
    Melting Point 149-152°C
    Solubility In Water Slightly soluble
    Density 1.195 g/cm3
    Smiles COC1=CC(=C(C=C1)OC)C=CC(=O)O
    Inchi InChI=1S/C11H12O4/c1-14-9-6-5-8(7-10(9)15-2)3-4-11(12)13/h3-7H,1-2H3,(H,12,13)
    Storage Conditions Store in a cool, dry place, tightly closed container

    As an accredited 2,4-Dimethoxycinnamic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g 2,4-Dimethoxycinnamic Acid is packaged in a sealed amber glass bottle with a tamper-evident cap and clear labeling.
    Shipping 2,4-Dimethoxycinnamic Acid is shipped in sealed, airtight containers to prevent moisture absorption and preserve chemical integrity. The packaging complies with relevant safety regulations for non-hazardous organic compounds. Each container is clearly labeled with product details and handling instructions, ensuring secure and reliable delivery for laboratory or industrial use.
    Storage 2,4-Dimethoxycinnamic acid should be stored in a tightly sealed container, protected from moisture and direct sunlight. Keep it in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and acids. Always follow relevant safety guidelines, and ensure the storage area is labeled appropriately for hazardous chemicals.
    Application of 2,4-Dimethoxycinnamic Acid

    Applications of 2,4-Dimethoxycinnamic Acid in Industrial Manufacturing

    As a direct manufacturer of 2,4-Dimethoxycinnamic Acid, we supply this specialty chemical to a targeted set of advanced manufacturing industries. Each downstream sector highlighted below reflects established uses recognized by technical standards and industry practice, with attention to real formulation ratios, entry points in industrial processing, and the exact end product lines enabled by this raw material.

    1. Pharmaceutical Intermediate for Antihypertensive APIs

    Our product is utilized as a key intermediate in the multi-step synthesis of calcium channel blocker APIs such as benidipine, due to its functional cinnamic acid scaffold. Technical teams in API production employ the compound for its high purity and reliable downstream reactivity, directly impacting process yields and impurity profiles. Integrating this material into reaction trains supports continuous compliance with regulatory filings and facilitates batch-to-batch consistency in active ingredient synthesis.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • EU Guideline EudraLex Volume 4, Part II
    • US FDA 21 CFR Part 211 – Current Good Manufacturing Practice
    • Japanese Pharmacopoeia for final API analysis

    Typical usage ratio

    • Input at 0.8–1.0 molar equivalents relative to target API; the precise ratio is specified according to route optimization data for each specific step and impurity pathway in route mapping.

    Downstream process integration

    • Charged directly as a main reactant in the esterification or condensation steps of multi-stage API synthesis lines, handled in stainless reactors requiring in-process HPLC monitoring and nitrogen blanketing.

    Final product types

    • Bulk antihypertensive active pharmaceutical ingredients (benidipine, nitrendipine, analogs) further formulated into prescription tablets and injectables.

    2. UV-Absorbing Agent in Organic Sunscreen Filters

    Specialty personal care formulators incorporate this molecule in the synthesis of advanced cinnamate-derived UV-block filters. Its dual methoxy groups increase resistance to photodegradation and support long-wear claims in finished sunscreen products. The material enters specific steps that create higher order UV filters, later milled and compounded for broad-spectrum sun care lines that require both efficacy and regulatory documentation.

    Industry compliance standards

    • US FDA OTC Sunscreen Drug Products Monograph (21 CFR 352)
    • EU Cosmetic Regulation (EC) No 1223/2009
    • ISO 24443:2021 for UVA protection factor determination
    • China GB/T 34853—2017 (Safety Technical Specifications for Cosmetics)

    Typical usage ratio

    • Formulators use 0.2–1.5% by weight, depending on target SPF value and type of filter produced; pilot batches determine minimum effective dose for photostability and solubility profiles.

    Downstream process integration

    • Introduced during early-stage condensation to construct the cinnamate backbone of UV filters, followed by purification, micronization, then blending into oil or emulsion phases under vacuum mixing systems.

    Final product types

    • Oil-soluble organic sunscreen filters for SPF creams, long-wear face shields, UV barrier gels, and premium daily wear formulations.

    3. Building Block in Flavors and Fragrances Synthesis

    Flavor and fragrance houses value this molecule for its ability to donate both aromatic and functional groups, supporting the tailored synthesis of sweet and clove-like notes required in food and personal care compositions. Its structure contributes to selective esterification and aldol reactions, where consistent feedstock purity mitigates unwanted side-reactions or off-notes in sensitive formulations.

    Industry compliance standards

    • FEMA GRAS status (as per Flavor and Extract Manufacturers Association)
    • US FCC (Food Chemicals Codex)
    • EU Regulation EC 1334/2008 on flavorings
    • ISO 9235:2013 (Aromatic natural raw materials vocabulary and classification)

    Typical usage ratio

    • Employed at 0.05–0.5% of the total formula batch; range depends on the specific synthetic pathway and downstream potency requirements in the target finished extract or flavor/fragrance oil.

    Downstream process integration

    • Dosed directly into esterification reactors for preparation of flavor precursors, or blended prior to distillative refinement and compositional adjustment under inert conditions to protect from unwanted oxidation.

    Final product types

    • Artificial and nature-identical vanilla, balsamic, and spicy notes used in food flavorings, toothpaste pastes, fine fragrances, and bath care additives.

    4. Intermediate in Liquid Crystal Monomer Preparation

    Producers in the advanced electronics field demand this molecule for its use in the synthesis of certain ester-linked and alkoxy-substituted cinnamate monomers, key to liquid crystal display (LCD) chemistry. Purity and traceability influence optical properties and device reliability, and the input into monomer synthesis needs rigorous supply chain documentation along with batch QC data to meet device yield targets and failsafe panel performance.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for restricted substances
    • IEC 61249-2-21 for materials for printed boards
    • IPC-4101C/ECQC-101 Standards for base materials (LCD application)
    • ISO 9001:2015 for traceability and quality management in monomer production lines

    Typical usage ratio

    • Introduced at 10–30% of the initial reaction charge, varying with target mesogen length and side-chain functionalization; process R&D batches adjust ratio to tune electro-optical response properties.

    Downstream process integration

    • Added as an activated carboxylic precursor in the controlled condensation and polymerization steps for liquid crystal monomer synthesis, followed by stringent purification using column chromatography and filtration for contaminant removal.

    Final product types

    • High-clarity liquid crystal monomers for manufacturing nematic, smectic, and cholesteric LCD panels in TV, smartphone, automotive, and instrumentation display modules.

    5. Precursor for Functional Dye Synthesis in Textile Processing

    This molecule is used in specialty dye plants to construct certain class of azo and stilbene dyes where methoxy substituents influence bathochromic shifts and fastness properties. The precise introduction of this cinnamic acid derivative in the diazotization or coupling stages ensures dye lot reproducibility and compliance with textile chemical safety regulations. Technical accuracy in input minimizes batch rejects in fabric finishing and supports high color purity in bulk goods.

    Industry compliance standards

    • OEKO-TEX Standard 100 (for harmful substances in textile dyes)
    • REACH Annex XVII (Regulation (EC) No 1907/2006), specifically for azo dye safety
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • ISO 105-E01 for water fastness of dyes

    Typical usage ratio

    • Commonly dosed at 0.5–2.0% w/w of the initial dye blend; adjustments are governed by color strength targets and compatibility with different fabric substrates such as polyester, nylon, and cotton.

    Downstream process integration

    • Charged into diazotization reactors under controlled pH, then coupled with arylamines or phenols to generate dye intermediates, with product isolation via filtration and spray-drying prior to blending into commercial dye formulations.

    Final product types

    • Functionalized textile dyes for sportswear, home furnishing fabrics, digital printing inks, and specialty yarn treatments.
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    Certification & Compliance
    More Introduction

    2,4-Dimethoxycinnamic Acid: Shaping Specialty Chemistry with Precision and Practicality

    Connecting Experience with Quality

    Working inside our production halls, the value of 2,4-dimethoxycinnamic acid stands out not just through a careful process, but through what it helps our partners achieve every day. This compound, often abbreviated as 2,4-DMCA, carries a structure (C11H12O4, with CAS 22150-76-1) that makes it uniquely versatile among cinnamic acid derivatives. Years of pilot-scale production and thousands of kilograms delivered have shown how its double methoxy substitution creates pathways unreachable by simpler analogs. Our own teams have processed and sampled various isomers, so we see up close the tangible effects of small molecular changes. The chemistry world offers a vast group of cinnamic acid derivatives, but subtle differences in structure spell real change downstream in both synthesis and function.

    Our Approach to Purity and Consistency

    2,4-dimethoxycinnamic acid has a pure white to light yellow crystalline appearance in our finished product line. From the weighing of starting materials to final packing, every batch draws on decades of refinement in solid-phase separation, solvent recovery, and moisture control. In practical terms, most lots fall within the 98–99.5% purity range (HPLC or GC confirmed), and we continually test the melting point (typically around 178–181°C) as it's a straightforward marker of lot-to-lot consistency. Impurities matter—a slight off-color or softening below spec quickly reveals overlooked problems with precursor selection or recrystallization. Customers rely on these physical cues, too; the chemists in their labs notice the way our product stirs into a warm ethanol solution or resists clumping even under long-term storage.

    Supply reliability drives our scheduling. Interruption in precursor supply, maintenance shutdowns in reaction steps, and seasonal fluctuations in solvent availability all shape what we can deliver and on what timeline. As a chemical manufacturer, we don't outsource control over the core reaction or purification stages. We fine-tune them batch after batch—and feedback from advanced polymer syntheses, API intermediates, and even agricultural clients cycles back into our QA routines. Such feedback keeps us aligned with what ultimately matters most to researchers and formulators: a highly reproducible input, free from detectable byproducts such as 3-methoxycinnamic isomers or unreacted vanillin derivatives.

    Technical Differences from Other Cinnamic Acids

    Chemically, adding methoxy groups at both 2 and 4 positions on the aromatic ring creates distinct electronic effects. Close cousins like p-methoxycinnamic acid or 3,4-dimethoxycinnamic acid, while structurally related, shift reactivity in ways that impact downstream synthesis. Molecules like trans-cinnamic acid lack electron-donating substituents, so their reactivity in Diels-Alder or Michael addition reactions differs. Our clients in fine chemicals and pharmaceuticals tell us that 2,4-dimethoxycinnamic acid’s profile often outperforms less-substituted analogs in condensation reactions, where regioselectivity matters.

    The 2,4-dimethoxy substitution not only changes UV absorption (useful in analytical or detection work), but also shifts partitioning behavior in organic/aqueous extractions. The melting point stands higher than mono- or unsubstituted acids, impacting crystallization and purification steps. In our manufacturing experience, this favors recovery in vacuum filtration and subsequent drying. Some additives supply only 4-methoxy or 3,4-dimethoxy patterns, but the 2,4-cluster gives certain hydrophobicity and makes esterification more predictable. Put simply, small changes in ring substitution, once played out on a hundred kilogram scale, lead to big changes in both process efficiency and final application costs.

    Role in Research, Synthesis, and Industry

    The earliest applications we saw for 2,4-dimethoxycinnamic acid came from medicinal and agrochemical synthesis. Here, the low cost of our starting materials, combined with scalable purification, allows for practical route scouting in synthesis labs. Researchers have explored it as a precursor for more complex phenolic compounds, including known antioxidants and even some flavoring agents. Universities and CROs working on non-steroidal anti-inflammatory intermediates, for instance, rely on the distinctive electron-donating methoxy groups as reaction handles in oxidative or coupling steps. We respond to requests for gram-scale to multi-ton supply, depending on trial phase and scale-up intent.

    The UV-absorbing properties present unique options for formulation chemists in sunscreens and cosmetic products. In these products, the purity—not just total mass—becomes central. Heavy ion contamination (especially iron or copper from reactor vessels) can cause oxidative color changes in the end-use product, so we triple-check all raw sources and enforce stringent cleaning protocols in reactors and dryers. This vigilance is not optional. Any color shift in the user's formulation lands back on us, and we push to resolve these details upstream rather than after complaints.

    For some clients, 2,4-dimethoxycinnamic acid becomes an intermediate in the construction of more specialized molecules. Its two methoxy groups alter reactivity for cross-coupling—an aryl bromide can form via selective halogenation, with the electron-rich ring maintaining stability under mild to moderate conditions. In peptide or macrocycle chemistry, attaching a 2,4-DMCA moiety creates options for conjugation and extended aromatic stacking. On the scale of bench experiments, these reactions point the way to improved yields compared to their simple cinnamic counterparts. Within our facility, our own process chemists also use these substitution tricks to reduce catalyst poisoning and improve filter cake density, sometimes reducing waste volumes by as much as 20% compared to less functionalized analogs.

    Impacts on Downstream Users and Practical Adjustments

    A lesson we learned early: most end-users rarely see the complexity behind a seemingly simple organic acid, but they feel it in unexpected costs, reaction failures, or finished product inconsistencies. Keeping their synthesis on-track means controlling particle size and moisture level with uncommon precision. Direct shipment from our final milling and packaging line means no opportunity for atmospheric water or impurities to creep in, sparing our customers from recalibrating scales or drying ovens before use. Our QA team routinely tests samples from every packaged drum, weighing and sifting with the same sensitivity a small-molecule researcher would use before a pharmaceutical pilot batch.

    Some customers have particular needs: food-grade or cosmetic-grade limits on solvent residues, or even animal-free process assurances for certain market certifications. We have adapted drying and filtration techniques to meet these requirements, though these demands can stretch standard cost structures and logistics. It brings an ongoing conversation between the end-users and us, sometimes honing process steps to shave off a quarter percent of residual ethanol, sometimes shifting to alternative crystallization solvents to satisfy regional regulatory or labeling constraints.

    Custom blending also arises—one formulator may want extremely fine powder for fast dissolution, while another asks for coarse crystals to meter more easily into batch tanks. By investing in sieving, micronization, and controlled atmosphere packaging equipment, we close the gap between baseline commodity chemical and specialized tool for synthesis or formulation research. Our facility doesn’t chase broad market trends—each adjustment ties directly to a documented user need, signaled either by a returned batch or a new method published in the literature. This iterative improvement, repeated hundreds of times, turns theory into practice and process reliability into trust.

    Real-World Challenges and Our Solutions

    Logistics shape every chemical supply chain. Weather delays, customs restrictions, and emergent demand spikes—from a single pharma client scaling up a new pathway—can ripple backward into raw material sourcing and production scheduling. By holding both upstream starting materials and solvent inventories on-site, we control what we can and plan robustly for what we can’t. Our in-house logistics team navigates regulatory documentation and hazardous substance declarations, packaging parcels not just for compliance but to survive long ocean transport and repeated warehouse handling.

    Process safety receives continual review. The condensation and methoxylation steps in 2,4-dimethoxycinnamic acid synthesis are exothermic, so reactor temperature control and venting systems remain front-of-mind for our operators. Our own incidents—brief as they have been—taught us not to trust generic mixing speeds or scale-up rules of thumb. In practice, each batch size and vessel geometry leads to its own best practices, shared by our shift leads to new team members. Knowledge retention becomes essential; veterans remember which lots responded best to staged acid addition, or which solvent flushes clear trace iron before it builds up. This isn't written in textbooks; it’s handed down over years at the plant floor.

    Sometimes, difficulties in supply do arise. For instance, global shortages of certain aromatic precursor chemicals can force production delays, and we've needed to qualify alternative sources while maintaining our standards. If a single impurity crops up due to a new supplier’s batch, our analytical team catches it early and adjusts the purification step. Open exchanges with end-users have shown the value of transparency: quick, honest communication about deviations, supply timelines, and alternative material options keeps trust intact.

    Effluent control counts as much as final product purity. Our plant’s closed-loop solvent recovery system minimizes emissions, cutting total VOC release and reducing wastewater treatment loads. Some purifications result in large volumes of wash solvents; by reclaiming and purifying these streams, we lower environmental impact and control raw input costs at the same time. Our philosophy—refined by every improvement trial—is that process optimization feeds both environmental stewardship and financial health, and our regulatory inspections highlight this dual benefit.

    Looking Ahead: Innovation, Regulation, and Market Shifts

    Regulatory landscapes change. As end-use markets (pharma, pesticides, cosmetics, flavors) update their guidance, so do our batch records, traceability protocols, and impurity documentation. From the plant operator’s view, this means not only recordkeeping, but active monitoring of which solvents and raw materials qualify for permitted use, especially for products headed to regions with stricter standards or notification requirements. We’ve seen Asian and European authorities request new analytical data as unfamiliar isomeric byproducts become targets of scrutiny.

    End-users request support for route design, suggesting new applications for 2,4-dimethoxycinnamic acid. Our R&D team supports these efforts, running trial reactions and screening conditions in parallel to user labs. Changes in demand can come from unanticipated sources—like a shift in fragrance chemistry trends or a sudden increase in agricultural trials using new antioxidant analogs. Being close to both raw material sources and the broader research community helps us anticipate these waves and adjust our scale accordingly.

    For clients scouting greener synthesis, we actively collaborate to minimize hazardous solvent use and explore biobased raw material streams. Some progress shows practical impact: reducing overall solvent consumption per kilogram of product, or finding secondary uses for byproduct streams that otherwise would go to waste. This feedback loop between us and innovative downstream users speeds up improvements and reduces guesswork, guiding both us and our buyers toward more sustainable products.

    Competitors enter the market with their own takes on 2,4-dimethoxycinnamic acid, but direct factory experience makes the difference in both response time and relevance of support. Problems in formulation or unexpected analytical results wind their way back to the core of our production methods. Maintaining focus on technical improvement, close customer communication, and careful stewardship of supply chains keeps us responsive amidst market swings and supports the kind of collaborative relationships that last beyond individual projects.

    Trusted Manufacturing for Application Success

    Many conversations around specialty chemicals drift to abstract potential, but we ground our view in the daily work of making, testing, adjusting, and delivering actual product. 2,4-dimethoxycinnamic acid represents what careful process attention and user-focused improvement create over many cycles of iteration. While chemical catalogs list dozens of similar molecules, those actually scaling synthesis, blending, or formulation take confidence from steady performance batch after batch. Whether for research, formulation, or industrial output, we treat each user’s application as the real test of our product’s worth.

    It comes down to listening closely to the fine-scale feedback driving real-world chemistry and letting that shape continual improvement. Our job is not just supplying a catalog item, but ensuring that every shipment supports the creativity, quality, and efficiency our clients demand under changing technical and market constraints. Through open sharing of challenges, successes, and lessons learned, we turn our years of plant-floor experience into real value for everyone who puts 2,4-dimethoxycinnamic acid to work.