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4,5-Methylenedioxy-2-Nitrocinnamic Acid

    • Product Name 4,5-Methylenedioxy-2-Nitrocinnamic Acid
    • Alias MDNC
    • Einecs 224-623-4
    • 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

    516089

    Chemical Name 4,5-Methylenedioxy-2-Nitrocinnamic Acid
    Molecular Formula C10H7NO6
    Molecular Weight 237.17 g/mol
    Cas Number 77095-64-6
    Appearance Yellow crystalline powder
    Melting Point 218-220°C
    Solubility Slightly soluble in water
    Purity Typically >98%
    Storage Conditions Store in a cool, dry place, away from light
    Iupac Name (E)-3-(4,5-methylenedioxy-2-nitrophenyl)acrylic acid
    Smiles O=C(O)/C=C/c1cc2OCOc2cc1[N+](=O)[O-]
    Synonyms E-3-(1,3-Benzodioxol-4-yl)-2-nitro-acrylic acid

    As an accredited 4,5-Methylenedioxy-2-Nitrocinnamic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging contains 25 grams of 4,5-Methylenedioxy-2-Nitrocinnamic Acid in a sealed amber glass bottle with a tamper-evident cap.
    Shipping 4,5-Methylenedioxy-2-Nitrocinnamic Acid is shipped in tightly sealed, chemically-resistant containers, protected from light and moisture. Standard shipping is via ground or air, in compliance with chemical safety regulations. Appropriate hazard labels are affixed, and shipping documents include safety and handling information. Ensure handling by trained personnel during transit and delivery.
    Storage 4,5-Methylenedioxy-2-nitrocinnamic acid should be stored in a tightly sealed container in a cool, dry, well-ventilated area, away from sources of ignition, direct sunlight, and incompatible substances such as strong oxidizing or reducing agents. Protect from moisture and physical damage. The storage area should be clearly labeled, with access limited to trained personnel. Store at room temperature unless otherwise specified.
    Application of 4,5-Methylenedioxy-2-Nitrocinnamic Acid

    Applications of 4,5-Methylenedioxy-2-Nitrocinnamic Acid in Industrial Manufacturing

    As the direct manufacturer of 4,5-Methylenedioxy-2-Nitrocinnamic Acid, we supply this specialty intermediate to multiple sectors where controlled aromatic modification and nitroaromatic chemistry drive the development of high-performance products. The following sections outline real-world downstream adoption, with practical detail for professionals engaged in fine chemicals processing and industrial synthesis.

    1. Pharmaceutical Intermediates in Non-Steroidal Anti-Inflammatory Drug (NSAID) Synthesis

    Many API manufacturers utilize 4,5-methylenedioxy-2-nitrocinnamic acid as a key ring-substituted precursor in the multi-step synthesis of certain non-steroidal anti-inflammatory drugs. Its electron-rich aromatic structure and nitro group facilitate downstream amination or reduction steps, enabling efficient construction of active scaffolds for finished pharmaceutical tablets and capsules.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • United States Pharmacopeia (USP) General Chapters relevant to intermediates
    • European Pharmacopoeia (Ph. Eur.) guidelines for raw materials quality
    • REACH Registration for supply to EU-based drug manufacturers

    Typical usage ratio

    • Employed in 1.5–5.0 molar equivalents relative to core API precursor, adjusted during reaction optimization based on yield and impurity profile

    Downstream process integration

    • Introduced in early-stage nitration or condensation steps, followed by reduction or coupling to form complete NSAID scaffolds, with inline HPLC monitoring for impurity control

    Final product types

    • Anti-inflammatory bulk APIs
    • Oral NSAID finished dosage forms (tablets, capsules, granules)
    • Topical pharmaceutical anti-inflammatory formulations

    2. Advanced Agrochemical Synthesis (Herbicidal Precursors)

    Agrochemical companies apply this compound as a protected aryl intermediate for the preparation of selective herbicidal actives, especially those requiring controlled nitro group reduction and heterocycle construction. Controlled addition ensures desired selectivity and minimal by-product formation in multi-step synthesis.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Certified Quality Management for chemical raw materials
    • Globally Harmonized System (GHS) for Safety Data and Labeling
    • EU REACH Compliance for agro-input regulation

    Typical usage ratio

    • Generally dosed at 3–7% by weight of total formulation input for herbicide intermediates; actual ratio depends on targeted yield and desired purity for downstream processing

    Downstream process integration

    • Fed into Buchwald–Hartwig amination or Suzuki coupling sequences after initial arylation to create benzodioxole-based herbicide cores before final formulation adjustment

    Final product types

    • Herbicidal active concentrate
    • Ready-to-use selective herbicide formulations
    • Emulsifiable concentrates for crop protection

    3. Fine Chemical Dye and Colorant Intermediate

    Manufacturers of specialty organic dyes and pigments use this material as a direct aromatic building block for functional group insertion, especially in the synthesis of nitro-substituted and methylenedioxy-containing chromophores. The compound's defined substitution pattern improves batch reproducibility and chromatic stability in custom colorant systems.

    Industry compliance standards

    • OEKO-TEX® Eco Passport for chemical safety in textile dyes
    • EN 71-3:2019 (Toy Safety for colorants)
    • ISO 9001:2015 for quality control in fine chemical manufacturing
    • EU REACH pre-registration as a dye intermediate

    Typical usage ratio

    • Typically used at 0.5–2% by mass in dye precursor mixtures; dosage refined via color intensity and hue requirement for target color palette

    Downstream process integration

    • Introduced in the initial condensation stage with downstream diazotization or coupling, followed by controlled crystallization and filtration to isolate the desired dye intermediate

    Final product types

    • Disperse dyes for polyester fibers
    • Solvent-based pigments for inks and coatings
    • High-performance organic colorants for plastics

    4. Synthesis of Optical Brighteners and UV Absorbers

    Producers of polymer additives and specialty coatings rely on this compound for constructing methylenedioxy-aromatic frameworks used in optical brightening agents and selective UV absorbers. Its chemical stability and reactive nitro group allow high-efficiency coupling during additive assembly, raising performance consistency in end applications.

    Industry compliance standards

    • ASTM D3426 for testing optical brighteners
    • ISO 17234-1 (Leather — Chemical tests for UV absorbers)
    • GMP for Food Contact Materials (EC) No 2023/2006 where used in packaging
    • REACH and TSCA inventory listing for additive supply

    Typical usage ratio

    • Dosed at levels from 0.2–1.5% weight basis in additive synthesizing batches, proportion adjusted depending on required UV absorbance or fluorescence strength in end product

    Downstream process integration

    • Combined with linking agents in high-temperature condensation or amidation, then purified to high optical purity before being blended into polymer matrices or coating emulsions

    Final product types

    • Optical brightener masterbatches for polyethylene and polypropylene
    • UV stabilizers for synthetic leathers
    • Coating additives for paper and textile finishing

    5. Fragrance Chemistry (Precursor for Musk Synthesis)

    The specialty fragrance sector selectively incorporates this chemical as an intermediate for producing nitro-musk bases. Its defined aromatic substitution supports targeted transformations, such as catalytic nitration and ring closure, leading to musky aromatic notes for deployment in personal care blends and household fragrances.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards for nitro musks
    • ISO 9001:2015 for specialty fragrance chemicals
    • EU Cosmetics Regulation (EC) No 1223/2009 for substances used in cosmetic fragrances
    • REACH dossier requirements on aromatic intermediates

    Typical usage ratio

    • Applied at 0.3–1.2% of synthetic batch mass; concentration tailored by targeted musk note intensity and formulation stability

    Downstream process integration

    • Integrated during staged etherification and nitration processes, followed by heat-induced cyclization and vacuum distillation for purity enhancement ahead of blending in fragrance bases

    Final product types

    • Nitro musk aromatic concentrates
    • Compound fragrances for detergents
    • Personal care fragrance oil blends

    6. Electronic Materials Intermediate (OLED and Photoreactive Polymers)

    Manufacturers active in advanced material sectors are utilizing this compound as a precursor for synthesizing photoreactive components in organic electronic materials. The electron-rich methylenedioxy and nitro groups support pi-conjugation in OLED and photoresist applications, promoting desirable charge-transport properties and improved film uniformity.

    Industry compliance standards

    • IEC 62679-3-1:2015 for testing organic semiconductor performance
    • RoHS Directive 2011/65/EU for hazardous substance control
    • ISO 9001:2015 for raw material traceability in electronics
    • REACH authorization for advanced electronic intermediates

    Typical usage ratio

    • Blended at 1–4% w/w in functional polymer matrix precursor; loading rate determined based on desired photoreactivity and film properties under device fabrication conditions

    Downstream process integration

    • Mixed with monomer precursors prior to polymerization or direct deposition (spin coating), followed by post-cure and photophysical testing to ensure material consistency

    Final product types

    • OLED emitting layer compounds
    • Photodefinable resist polymers
    • Conductive coatings for flexible displays
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    Certification & Compliance
    More Introduction

    4,5-Methylenedioxy-2-Nitrocinnamic Acid: A Direct Manufacturer’s Insight

    Origins and Chemistry Rooted in Real Production

    Stepping onto our plant floor, the distinct aroma from a freshly drawn batch marks another day working with 4,5-Methylenedioxy-2-Nitrocinnamic Acid. Every gram in our facility goes through carefully controlled synthesis pathways that minimize impurity build-up, setting our process apart from makeshift labs or facilities that cut corners to boost volume over purity. Our hands-on approach means we fine-tune each step, from initial solvent selection to controlled temperature management at the nitration stage. Over more than a decade, tweaks in our set-up have consistently helped us reach a purity grade well above 98% without reliance on excessive post-reaction purification, a common pitfall for those chasing yield at the expense of stability.

    Product Models and Material Characteristics

    Through our direct production, we deliver 4,5-Methylenedioxy-2-Nitrocinnamic Acid as a fine, pale-yellow crystalline powder. We manufacture several model grades based on end-use requirements, whether high-purity batches for research, or a production grade tuned to the rigorous protocols of industrial synthesis. Our typical product comes tailored at a mesh size of 80–100, which allows for easy dispersion in organic solvents favored by pharmaceutical and agrochemical intermediate producers.

    Other producers often rely on standard extraction and isolation methods, delivering material that may look similar but carries higher residual solvents or color impurities. Across the years, we encountered shipments from outside vendors with faint brown or greenish hues, a clear marker of side-reaction byproducts. These can cripple reaction yields during downstream hydrogenation or coupling steps, a frustration all too familiar for process chemists. A key difference in our product stems from our strict chromatography and crystallization controls—visible not just in the powder’s color but in its performance during extended storage and in robust reproducibility during later transformations.

    Why Purity and Consistency Matter Down the Chain

    Every user hoping to build complex molecules knows the frustration when a key intermediate shows unexpected behavior at scale. Our technical support team fields questions from direct users nearly every week, ranging from reaction compatibility to solubility quirks. We’ve gathered years of data not just from in-house QC but from collaborative feedback with university labs and industrial partners. Customers regularly come back impressed after side-by-side trials: Our cinnamic acid derivative consistently resists oxidative color change and holds up under both short and long-term storage between 2–8°C, a direct result of batch consistency rather than simple product repacking.

    We do not filter or “blend in” off-spec material to meet shipment deadlines. Instead, strict batch segregation avoids cross-lot mixing, a practice that sometimes happens when intermediates are simply sourced and relabeled by non-manufacturing companies. Even under dry air, we observe that our material keeps structural fidelity for years, which matters deeply when scale-up is on the line—every wasted reactor hour or failed crystallization represents major loss for formulators.

    Primary Applications and Downstream Flexibility

    Years spent working with pharmaceutical innovators and agrochemical developers have given us a clear picture: During the early lead optimization stage, medicinal chemists value intermediates that offer clean reactivity, supporting both esterification and amide coupling routes. Our 4,5-Methylenedioxy-2-Nitrocinnamic Acid supports both, thanks to the strategic placement of the nitro and methylenedioxy groups on the aromatic ring.

    These groups open up synthetic avenues not present in simpler cinnamic acid derivatives. The electron-withdrawing nitro moiety slows unwanted Michael additions while boosting para-selective hydrogenation options. The methylenedioxy ring lends unique properties to the resulting molecules, relevant for anti-infective and neuroactive compound scaffolds. In agrochemical research, users report that this compound provides a tractable backbone for the rapid screening of new crop protection agents: The two distinct functional groups encourage inventive substitution patterns that keep resistance at bay.

    Manufacturing at Scale: Lessons Learned on the Floor

    Having scaled up in incremental steps—kilo to hundreds of kilos annually—we learned that small things matter immensely. Just a few degrees’ deviation in the condensation reaction can drag down conversion rates, a fact not obvious from bench-scale runs. Diligent process monitoring means our senior chemists adjust crystallization pH and mother liquor removal on the fly, preventing retention of low-level tars or colored impurities.

    Older, less refined processes often yield variable particle shapes, which leads to unpredictable filtration rates—an issue for anyone hoping to incorporate the acid directly using automated powder handling or slurry dosing systems. After years of trial, we now standardize to a narrow particle distribution, so our material pours and dissolves with minimal dust. Packaging in moisture-barrier, food-grade PE bags locked inside steel drums, we block out contamination that often sneaks in during long export journeys, especially in humid climates.

    True Differences From Competing Products

    A head-to-head analysis against regional and international samples paints a clear picture: Purity alone does not tell the full story. Many competing versions, even those advertised at 98% or above, lag on batch reproducibility. We run FT-IR and NMR checks beyond standard HPLC tests, because our long-term collaborators ask for more than a certificate of analysis—they want assurance rooted in hands-on experience and clear peak overlays, not just a paperwork metric.

    We routinely observe “ghost peaks” from residual starting materials or byproducts (often nitrobenzaldehyde or related derivatives), showing up only when detailed spectral scrutiny is applied. These compounds disrupt precision reactions, especially during Pd-catalyzed coupling or chiral reduction steps pursued by advanced pharmaceutical R&D. Our process washes and recrystallizations knock these contaminants well below one percent, supporting complex transformations without side-track loss. End-users report tighter end-point masses, higher yields, and less scrap, translating to both financial savings and fewer reruns.

    Supporting the R&D Edge: Beyond the Sale

    A major frustration for chemists lies in bridging lab-scale discoveries with pilot or production scale confidence. We address these concerns on a daily basis, offering direct access to our technical and QA talent who speak the same language as the scientists working at the bench. We don’t just cite “compatibility with Grignard or Suzuki conditions”—we hold in-depth troubleshooting sessions, sometimes involving overnight pre-trials, to help researchers adjust solvent systems or pH, tuning reactions for their specific work-up and isolation steps.

    By openly sharing both successful routes and past failures, we help others avoid wasteful detours, and our partners often build proprietary IP without shouldering all the risk alone. Working with academia and startups, we have supported novel heterocycle construction, custom isolation methods, and purification process tweaks, directly feeding back into our own manufacturing improvements. This mutually beneficial cycle is what keeps the field advancing: Direct touchpoints, field visits, and solution-driven support, not just email-based ticket responses.

    Regulatory and Documentation: Meeting Today’s Standards

    With growing regulation across regions, especially in pharmaceuticals and fine chemicals, the paperwork behind a chemical now travels as far as the product itself. Straight from our facility, each shipment carries full traceability from incoming raw materials to finished product, complete with batch production records and impurity profiles tracked for over ten years. A key feature for customers undergoing registration or regulatory filing is knowing that the compound they tested in early trials matches exactly what goes into production scale. Lot-to-lot QA, supported by physical retains and retained documentation, builds confidence during audits and small molecule registration.

    We also respond to custom documentation needs, such as detailed impurity breakdowns, ICH stability data under forced conditions, or residual solvent reporting in compliance with ICH Q3C. Our regulatory experts track evolving standards in each customer’s market, whether working to comply with REACH, K-REACH, US TSCA, or emerging inventory norms in fast-moving innovation hubs in Asia.

    Safety and Handling: Lessons From Long-Term Practice

    Many intermediates can prove tricky in scale-up, with risks unnoticed at the gram bench scale. Our team has watched small spills of similar nitro aromatics oxidize unexpectedly when exposed to the wrong wiping cloth or solvent. Through repeated hazard and operability studies, we set strict limits on allowable heat, static, and moisture exposure, training operators well beyond manual “read and react” routines. We caution against practices like vacuum drying above 50°C unless purging is rapid and oxygen-controlled—key tips that seem second nature after years on the line but often get lost in dry safety sheets.

    All bulk containers ship with double protection, not only to block ambient moisture but also to deter friction ignition during transport—a rare but real possibility for certain specialty aromatics. Frequent refresher drills in our handling areas build a culture of respect around what seems like “just another solid intermediate.” The nuances of nitro group reactivity, potential for exotherm, and static management cannot be overemphasized—each lesson earned through years of safe, incident-free manufacturing.

    Environmental Responsibility Built Into Manufacturing

    Today’s buyers and regulators pay sharp attention to more than just lab purity or regulatory files—the source of each molecule and its environmental context increasingly dictate procurement decisions. Our facility’s closed-cycle solvent recovery system means that over 90% of organic solvent can be recycled on-site, slashing not just our own waste output, but also the risk that escaped solvent could enter local water or air. Routine audits by both internal EHS teams and external parties have helped us tune process effluent and minimize chemical oxygen demand in the waste stream.

    We relaunched our intermediate wash stations last year with more efficient activated carbon capture, reducing even trace nitrated organics below strict discharge thresholds. Regular data sharing with our neighbors upstream and downstream forces transparency, and community-level engagement has led to improved safety standards up and down the valley. Such work leaves a traceable difference on both the company and the local environment, reinforcing a duty of care that runs parallel to product innovation.

    Perspectives on Emerging Uses and Research Trends

    Over recent years, the utility of 4,5-Methylenedioxy-2-Nitrocinnamic Acid has moved well beyond bootstrapped pharmaceutical candidates. The number of research projects harnessing this compound for advanced material development, such as new photoactive polymers or organic semiconductors, has grown. Strong electron-donating/electron-withdrawing resonance in this structure produces molecules with desirable light absorption properties, which engineers and scientists look to capitalize on in everything from solar cell substrates to biosensor platforms.

    Even in established fields, curiosity-driven inquiries push the boundaries of what’s possible. Our in-house R&D continues to test new routes that lengthen the utility of this intermediate, such as late-stage functionalization and cross-coupling procedures that unlock branched or fused-ring architectures. By keeping a finger on the pulse of this evolving landscape, our technical staff help customers spot opportunities and tackle roadblocks early, before scale-up makes adjustments costly.

    Looking Ahead: Practical Solutions for User Challenges

    Customers rarely face issues that are purely academic; most arise from the realities of putting a compound to work under industrial conditions. Questions around solubility in non-standard solvents, batch-to-batch reaction reproducibility, or safe waste treatment drive our ongoing improvements. Through these decades, the most impactful advances came not from flashy “breakthroughs” but from a relentless focus on stability, supply chain robustness, and operational transparency.

    We openly share our in-process control plans, not because it’s a sales pitch, but because we have seen firsthand how companies struggle after trial-scale delivery, only to be let down by unpredictable quality or vague documentation. By holding regular feedback sessions with our customers, we continue to learn and improve, pursuing leaner production cycles while expanding the process window for new synthetic approaches.

    Manufacturing 4,5-Methylenedioxy-2-Nitrocinnamic Acid remains as much an ongoing craft as it is a science. The batch records, material certificates, and quality assurances mean more after years of practical test and experience than any templated description or brochure. Through every stage of its production and application, our commitment is to clarity, reliability, and hands-on problem-solving—qualities forged on the factory floor, not just in the boardroom.