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3,4-(Methylenedioxy)Cinnamic Acid

    • Product Name 3,4-(Methylenedioxy)Cinnamic Acid
    • Alias MDCA
    • Einecs 214-296-6
    • 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

    949233

    Chemical Name 3,4-(Methylenedioxy)Cinnamic Acid
    Synonyms 3,4-Methylenedioxycinnamic acid, MDCA, Piperonylic acid
    Cas Number 94-53-1
    Molecular Formula C10H8O4
    Molecular Weight 192.17 g/mol
    Appearance White to light yellow crystalline powder
    Melting Point 142-145°C
    Solubility Slightly soluble in water, soluble in ethanol and acetone
    Density 1.3 g/cm³ (approximate)
    Smiles O=C(O)/C=C/C1=COC2=CC=CC2=C1
    Inchi InChI=1S/C10H8O4/c11-10(12)5-6-13-7-1-3-8-9(2-7)14-4-8/h1-6H,(H,11,12)/b6-5+
    Storage Conditions Store at room temperature, tightly closed, in a dry place
    Purity Typically ≥98% (varies by supplier)

    As an accredited 3,4-(Methylenedioxy)Cinnamic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle labeled "3,4-(Methylenedioxy)Cinnamic Acid," tightly sealed, with safety and handling instructions provided.
    Shipping **Shipping Description:** 3,4-(Methylenedioxy)Cinnamic Acid is securely packaged in sealed, clearly labeled chemical containers to prevent leaks and contamination. It is shipped according to applicable chemical safety regulations, usually via ground or air transport, with safety data sheets included. Temperature and handling instructions are provided to ensure product stability and personnel safety.
    Storage 3,4-(Methylenedioxy)Cinnamic Acid should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. The container should be tightly closed and protected from moisture and direct sunlight. Properly label the storage container and keep it away from heat and open flames to maintain the compound’s stability and purity.
    Application of 3,4-(Methylenedioxy)Cinnamic Acid

    Applications of 3,4-(Methylenedioxy)Cinnamic Acid in Industrial Manufacturing

    As a specialized chemical raw material supplier, we deliver 3,4-(Methylenedioxy)Cinnamic Acid (MDCA) to global industries with a focus on advanced downstream applications. The following application scenarios present verified industrial sectors where MDCA enters production chains as a high-value additive or intermediate. Each scenario outlines compliance frameworks, recommended usage ratios, typical process integration points, and expected end products.

    1. Pharmaceutical Synthesis of Antimicrobial Agents

    MDCA serves as a critical intermediate in the synthesis of certain antimicrobial active pharmaceutical ingredients (APIs), particularly those targeting resistant Gram-positive bacteria. Medicinal chemists introduce MDCA moieties via amide or ester bond formation during multi-step organic syntheses of candidate drug molecules. Its aromatic methylenedioxy ring provides enhanced molecular stability and lipophilicity, contributing to improved bioavailability and target affinity in final APIs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) for APIs
    • European Pharmacopoeia (EP) monographs relating to antimicrobial agents
    • FDA 21 CFR Part 210/211 for finished pharmaceuticals

    Typical usage ratio

    • Generally 0.5–2.5 molar equivalents per synthesis batch, depending on target API yield and step sequence; chemists adjust input based on molecular weight and stoichiometric requirements.

    Downstream process integration

    • MDCA enters as a raw intermediate during early or mid-stage condensation or acylation reactions, depending on the target antimicrobial compound. Purified API typically undergoes crystallization, drying, and quality testing.

    Final product types

    • Bulk antimicrobial APIs (e.g., β-lactam derivatives, phenolic antimicrobials)
    • Finished pharmaceutical forms such as tablets, capsules, topical gels

    2. UV-Absorbing Monomer for Polymer Modification

    MDCA is manufactured as a UV-absorbing functional monomer used by specialty polymer producers to engineer plastics with improved light stability for automotive and architectural applications. It integrates into resin polymerization (notably polyesters and acrylates) by covalent bonding via its carboxylic acid group, imparting UV-filtering characteristics and contributing to the long-term photostability of the molded parts or films.

    Industry compliance standards

    • ISO 4892-2:2013 Plastics—Methods of exposure to laboratory light sources
    • ASTM D2565 Standard Practice for Xenon-Arc Exposure of Plastics Intended for Outdoor Applications
    • REACH Regulation (EC 1907/2006) for polymer and additive registration
    • RoHS Directive 2011/65/EU (where applicable for electrical components)

    Typical usage ratio

    • 0.1–1.0 wt% of total monomer feed in resin formulations; polymer engineers optimize the ratio depending on the desired UV-transmittance cutoff and secondary property trade-offs.

    Downstream process integration

    • MDCA is charged during resin or copolymerization feed preparation as a co-monomer or modifier before bulk, suspension, or solution polymerization. The resulting copolymers are extruded, molded, or film-cast in typical downstream plastics operations.

    Final product types

    • UV-resistant polyesters (e.g., PET for outdoor signage)
    • Architectural and automotive glazing films
    • Plastic housings for electronics exposed to sunlight

    3. Fragrance and Flavor Ingredient in Fine Chemicals

    MDCA’s aromatic structure makes it a valued precursor in the synthesis of specific fragrance compounds with a sweet, balsamic scent profile. Downstream manufacturers in the aroma chemicals sector esterify or reduce MDCA to yield unique flavoring molecules and fragrance lactones used in high-end perfumes and specialty food flavors. Its controlled reactivity and olfactory signature support tailored blend formulations not achievable with simpler cinnamic acid derivatives.

    Industry compliance standards

    • IFRA Standards for Fragrance Ingredient Safety
    • EU Council Directive 88/388/EEC for flavorings used in foods
    • US FDA 21 CFR 172.515—Synthetic flavoring substances
    • ISO 9235:2013—Aromatic natural raw materials for perfumes—Vocabulary

    Typical usage ratio

    • Concentration varies by application: typically 0.05–0.5% in perfume compound bases and below 10 ppm in food flavoring preparations, based on finalized aromatic strength and solubility constraints.

    Downstream process integration

    • MDCA is esterified, hydrogenated, or otherwise derivatized in batch reactors to yield alcohol or lactone intermediates, which are then blended into either fragrance oils or flavor concentrates. Post-processing includes filtration and sensory QC checks.

    Final product types

    • Luxury parfum concentrates for fine fragrance houses
    • Specialty lactone ingredients for food flavors
    • High-value aroma chemicals for blended essential oils

    4. Photoinitiator Precursor for Specialty Coatings

    MDCA acts as a molecular backbone in the synthesis of certain photoinitiator compounds used in UV-curable coating formulations for electronics and printed circuit boards. Its conjugated system increases the efficacy of photoactive moieties, enabling precise crosslinking and hardening under UV light in fast-moving, automated production lines. This application relies on MDCA’s ability to provide chemical stability while allowing rapid energy transfer during photopolymerization events.

    Industry compliance standards

    • IEC 61086: Coatings for electrical and electronic plastics
    • ISO 12944 – Corrosion protection of steel structures by protective paint systems
    • RoHS compliance for final electronic products
    • ISO 9001:2015 Quality Management Systems for specialty chemical manufacturing

    Typical usage ratio

    • Photoinitiator syntheses typically use MDCA at 0.2–1.5 molar equivalents, regulated by the targeted molar absorption coefficient and final formulation requirements of the photoreactive system.

    Downstream process integration

    • Producers synthesize the photoinitiator from MDCA in a controlled reaction, purify, then blend the resulting compound into UV-cured resin systems using high-shear mixers pre-application. In-line quality control ensures stability before application to substrates.

    Final product types

    • UV-cure coatings for electronic components
    • Solder mask resins for PCBs
    • Specialty UV-printing inks
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    Certification & Compliance
    More Introduction

    Introducing 3,4-(Methylenedioxy)Cinnamic Acid: Direct Insights from the Manufacturer

    Our Approach to 3,4-(Methylenedioxy)Cinnamic Acid

    Years on the factory floor teach lessons you won’t find in catalog descriptions. Every batch of 3,4-(Methylenedioxy)Cinnamic Acid we make carries a story — from the selection of raw materials to the final checks before shipment leaves our facility. The model we most commonly supply fits the needs of research labs, specialty chemical formulators, and fine chemical producers. Our team has developed processes that keep the purity steady and the batches reproducible, so each lot supports reliable results in downstream projects.

    Quality of raw resources drives the outcome. We take a hands-on approach with our vendors, sourcing the most consistent starting materials. Oversight like this guarantees an acid that meets or exceeds the bar set by analytical standards. Each batch comes with a clear, off-white to pale yellow crystalline appearance — a telltale sign of its good health. The signature methylenedioxy group on the cinnamic backbone defines its chemical profile, setting apart its performance in synthesis applications and specialty formulations.

    Technical Details That Matter in Practice

    From a manufacturing standpoint, specs aren’t just numbers. Purity usually hits above 99% by HPLC analysis. Melting points remain tight in the 156–159°C range, eliminating doubts about product drift. Moisture sits low, typically under 0.5%, because water can spark side reactions in sensitive syntheses — a fact any bench chemist knows too well. By tightening up the drying stage, we keep unwanted variables out, batch after batch.

    Packaging never sits on automatic pilot either. The powders travel sealed in light-blocking, moisture-proof containers. We overwrap to avoid light-catalyzed decomposition, which is a real threat with aromatic acids, particularly those bearing functional groups like methylenedioxy that might be sensitive to both moisture and airborne oxidants. These are lessons learned the hard way in years past, prompted by real shipping mishaps and feedback from cautious customers.

    Applications in Synthesis and Beyond

    For those working in organic synthesis or research, 3,4-(Methylenedioxy)Cinnamic Acid stands out by providing a fused benzodioxole ring on the cinnamic scaffold. Unlike generic cinnamic acid or 3,4-dimethoxycinnamic acid, this compound brings distinct reactivity. The methylenedioxy group alters electron distribution across the aromatic system, meaning it behaves differently in electrophilic and nucleophilic substitution reactions. Medicinal chemists value this distinction because it unlocks substitution patterns you can’t access with unsubstituted or methoxy-derivatized analogs.

    In pharmaceutical development, our customers use it as both an intermediate and a reference compound. The presence of the fused heterocycle enables exploration of structure-activity relationships in benzodioxole-containing therapeutics. Some labs explore it as a building block in anti-inflammatory and antioxidant research, citing the unique scaffold as a core feature in natural product analog work. We’ve equipped contract partners with kilogram batches for pilot-scale transformations, supporting their move from benchtop curiosity to scale-up feasibility.

    Outside the pharmaceutical sector, fine chemical producers turn to our 3,4-(Methylenedioxy)Cinnamic Acid for making specialty polymers and resins. The rigid, conjugated system translates mechanical stability and tailored properties into the final product. In fragrance and flavor chemistry, its aromatic structure allows the design of niche compounds that aren’t accessible through more common cinnamic variants. Sometimes, it supports pesticide or fungicide R&D, allowing agrochemical formulators to probe activity-persistent scaffolds.

    Comparing to Other Cinnamic Derivatives

    The world of cinnamic derivatives includes a crowd of options, but few match the functional diversity of the methylenedioxy-substituted version. Regular cinnamic acid offers a simpler backbone and lower molecular weight, making it a staple for basic coupling and esterification steps. Add a methoxy group at positions 3 and 4, and you get different solubility and reactivity profiles — the dimethoxy methylation pattern shifts electron density, affecting how the molecule takes part in catalytic cycles or bioactive assays.

    The methylenedioxy group, by contrast, introduces a fused dioxole ring, not a simple alkoxy. This architectural choice makes the molecule more sterically demanding, influencing both the rate and regioselectivity of many reactions. In oxidative coupling or cycloaddition studies, researchers report significant differences in yields and product profiles compared to using dimethoxy analogs. Our experience supplying both versions to research groups over the years confirms these distinctions in practice.

    Handling in the plant also differs. Methylenedioxy-containing intermediates can demand extra attention during oxidation and purification. By investing early in robust air handling and humidity control, we protect the molecule from the atmospheric variables that more tolerant derivatives might shrug off. These protocols come from decades of operational tweaks, each adjustment triggered by real events — not hypothetical risks.

    Meeting Real-World Manufacturing Challenges

    Manufacturing a substituted cinnamic acid with a fused dioxole needs more than precise chemistry. It requires a plant layout that keeps reactive intermediates separated, containment systems that avoid cross-contamination with more volatile or hygroscopic products, and a workforce versed in the quirks of aromatic acid processing. Over the years, we’ve re-engineered our synthesis lines to run these acids offline from sensitive aminos, because we’ve seen first-hand how even trace migration between batches can throw product quality off course.

    Impurity profiles in 3,4-(Methylenedioxy)Cinnamic Acid batches aren’t always visible in a standard QC report. Some come from subtle byproducts formed during bromination or selective oxidation stages. Recognizing these requires running deeper NMR and LC-MS analyses at regular intervals. Reworking a single batch costs more in time and energy than running extra analytics upfront. Every team member understands this, because struggling to rescue a shipment from a marginal batch once teaches lessons they never forget.

    Customers occasionally ask for bespoke particle sizes or solvent-wetted forms. Meeting these requests means shifting downstream processes, sometimes on short notice. Our facility keeps modular milling and wetting lines, which helps us intercept these niche requirements without holding up larger projects. All changes get logged and tracked on a per-batch basis, maintaining full traceability. The factory floor leans on robust digital batch records, with operators trained to spot deviations early rather than trusting automation alone.

    Reliability Built on Experience

    A manufacturer’s reputation depends on keeping surprises out of customer hands. Over the years, we’ve seen competitors cut corners with drying or packaging, only to see customers deal with clumpy powders or off-smelling solids. Each defective batch triggers expensive returns, lab clean-ups, and process revalidations. Our team has built feedback loops with R&D customers and production formulators, which means we adjust procedures based on real application feedback. This connection to the application side keeps the product relevant, and it means every improvement we make shows up in the results.

    We support ongoing research collaborations with direct shipment samples for pilot trials and follow-up support. Chemical properties drive many choices in synthesis, but so does real conversation between labs and the people who make their starting materials. This back-and-forth encourages method development and lets us optimize process conditions for end users, from bench chemists scaling up oxidative couplings to process engineers integrating new intermediates into flow reactors.

    The trust that grows from consistently high purity and reliability leads to new project requests, custom runs, and joint troubleshooting when scale-up issues arise. That two-way trust stands as the backbone of any long-term partnership in the fine chemical world, and we invest time and resources in keeping it strong.

    Physical Handling and Storage Know-How

    Handling substituted cinnamic acids presents challenges over time. The methylenedioxy ring can undergo slow hydrolysis or rearrangement if stored under the wrong conditions. Beyond designing better packaging, we offer straightforward advice for users to store materials in cool, dry, and dark environments. Extended observations from our own shelf-life stability testing provide practical shelf life estimates, which beats the guesswork many customers are used to.

    Product recalls are rare here. Problems are resolved at the preventive stage instead, with regular pull samples and accelerated aging programs. By keeping internal communications flowing between QA and production, out-of-spec material gets intercepted long before it leaves our loading dock. These routines make a difference for researchers running sensitive transformation reactions, where microimpurities or subtle degradation can spoil days of work.

    Waste management matters as well. We treat every byproduct, rinse waste, and packaging residue per local regulatory standards. Employees cycle through ongoing training on handling and disposal, staying up to date on compliance rules and best practices. This goes beyond environmental responsibility; it safeguards our team and our neighbors, maintaining community trust and our operating license.

    Supporting Innovation in R&D and Scale-Up

    We join innovation efforts by running custom syntheses, troubleshooting tough purification steps, and sharing analytical data on request. Our technical team partners with R&D customers, running pilot batch manipulations that mirror customer protocols as closely as possible. Researchers count on this type of technical support, especially on tight project timelines where downtime means missed grant deadlines or delayed launches.

    Sometimes discovery hits a stumbling block with a challenging intermediate or formulation step. Our team runs side-by-side with lab partners to pinpoint root causes, using our in-house knowledge base. Adjustments to crystallization, solvent swaps, or in-process quality checks spring up from these collaborations. With each new learning, we add to our in-house process notes, building a knowledge reservoir that sets us apart from traders who focus only on balance sheets and shipping routes.

    Scale-up brings another set of hurdles. Reaction exothermicity, filtration bottlenecks, and powder flowability issues rarely show up in the literature but always reveal themselves in the pilot plant. Our engineers stay in the trenches for pilot runs, logging detailed process parameters, and capturing “small” adjustments that stabilize yields and purity as volumes increase. When surprises hit, experience helps. Adjustments take minutes, not weeks, and shrink the timeline from pilot to production.

    Real-World Differences Drive Product Choice

    In fine chemicals, similar molecules can deliver very different results in application. The 3,4-(Methylenedioxy)Cinnamic Acid we provide supports synthesis routes not accessible with regular cinnamic acid. The aromatic ring modification gives both reactivity and selectivity shifts for key transformations. For example, this difference has enabled contract partners to access novel heterocyclic compounds via Diels-Alder and cyclization pathways. Flavor or agrochemical formulators have leveraged the robust methylenedioxy core for enhanced stability in aggressive processing conditions.

    We see demand rise from researchers interested in rare scaffolds for bioactive small molecule design. As parallel synthesis platforms become more commonplace, the need for reliable, well-characterized building blocks grows. Feedback from these teams has improved our impurity profiling and sparked changes to drying and packaging stages, which brings real-world advantages in shelf life and usability. By acting directly on user feedback, we keep our product aligned with changing needs.

    Customers who have switched from third-party or imported sources have flagged differences in batch consistency, shelf stability, and trace impurity levels. Direct control over every stage — from raw input to finished packaging — shows up in fewer recalls, tighter quality specifications, and higher confidence when customers put the product into their processes.

    Building a Future for Specialty Cinnamic Acids

    The continued demand for advanced building blocks like 3,4-(Methylenedioxy)Cinnamic Acid ties into broader shifts in pharmaceutical and specialty chemical innovation. As new reaction methodologies and screening techniques expand compound libraries, chemists pursue structures with unique substitution patterns. Our facility responds by investing in versatile reactor systems, tighter analytical workflows, and staff development focused on specialty chemical synthesis.

    We keep investing in sustainability and process intensification. Internally, we develop greener oxidation routes and more efficient work-up steps, which bring both cost savings and a smaller environmental footprint. Process improvements translate directly to cleaner products, less waste, and better long-term viability — benefits that don’t make splashy headlines but matter on the shop floor, in the shipping yard, and at the customer’s bench.

    Long relationships with end users drive innovation. Regular check-ins, site visits, and transparent reporting align customer expectations with our capabilities. This collaboration benefits both sides, delivering better research outcomes and fewer interrupted projects. As regulatory standards evolve, we adapt — whether through updated documentation, stricter impurity thresholds, or improved labeling for safe and secure transport.

    Looking Ahead

    Our experience manufacturing 3,4-(Methylenedioxy)Cinnamic Acid teaches the value of diligence, attention to detail, and flexibility in production. Each improvement we make, every challenge we overcome, feeds back into the next batch. Our reputation grows strongest not from advertising, but from real-world performance and user trust. As new fields open up in drug discovery, materials science, and specialty industries, we stay ready — not by following trends, but by listening to the needs of the people running the reactions and relying on the results. This cycle of production, feedback, learning, and improvement defines the path forward for specialty manufacturing in chemicals large and small.