Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

3,4-(Methylenedioxy)Phenylacetonitrile

    • Product Name 3,4-(Methylenedioxy)Phenylacetonitrile
    • Alias MDP2N
    • Einecs 208-972-2
    • 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

    555967

    Chemical Name 3,4-(Methylenedioxy)Phenylacetonitrile
    Cas Number 4468-48-8
    Molecular Formula C9H7NO2
    Molecular Weight 161.16
    Appearance White to off-white crystalline powder
    Melting Point 64-68 °C
    Boiling Point 160-162 °C at 15 mmHg
    Density 1.189 g/cm3
    Solubility Slightly soluble in water; soluble in organic solvents like ethanol and acetone
    Purity Typically ≥98%
    Smiles N#CCc1ccc2OCOc2c1
    Inchi InChI=1S/C9H7NO2/c10-5-6-1-2-8-9(3-6)12-7-11-8/h1-3H,7H2
    Storage Conditions Store in a cool, dry place, tightly closed container
    Synonyms MDP2N, 3,4-Methylenedioxyphenylacetonitrile
    Hazard Class Irritant

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

    Packing & Storage
    Packing A 100g amber glass bottle labeled "3,4-(Methylenedioxy)Phenylacetonitrile," tightly sealed with a screw cap, includes safety and hazard information.
    Shipping 3,4-(Methylenedioxy)phenylacetonitrile is shipped in tightly sealed containers, protected from moisture and light. It should be handled as a hazardous chemical, typically shipped as a solid under UN identification, and may require special documentation and labeling according to local and international transport regulations. Shipping must comply with safety standards for toxic substances.
    Storage 3,4-(Methylenedioxy)phenylacetonitrile should be stored in a tightly sealed container, under an inert atmosphere such as nitrogen or argon, and kept in a cool, dry place away from light and moisture. Store it in a well-ventilated chemical storage area, away from incompatible substances like strong oxidizers and acids. Label containers clearly and handle with appropriate personal protective equipment.
    Application of 3,4-(Methylenedioxy)Phenylacetonitrile

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

    3,4-(Methylenedioxy)Phenylacetonitrile serves as a key intermediate in demanding chemical synthesis environments across select downstream industries. As the actual manufacturer, we focus on supporting large-scale B2B production with strict compliance and finely tuned quality controls. Below, we detail the main application segments based on real industrial integration, process requirements, and market standards observed among certified end-users.

    1. Pharmaceutical Intermediates for API Synthesis

    Pharmaceutical producers rely on this molecule in the multi-step synthesis of active pharmaceutical ingredients, particularly within benzodioxole-based frameworks that underpin several CNS and cardiovascular agents. The compound typically enters during the formation of key amine or acid moieties after selective catalytic hydrogenation and hydrolysis steps, requiring high assay consistency and validated impurity profiles. Site operations integrate this precursor in custom multi-ton batch reactions, usually within GMP-inspected environments where full traceability and regulatory adherence are non-negotiable.

    Industry compliance standards

    • ICH Q7A (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • European Pharmacopoeia (Ph. Eur.) monographs—custom intermediates and APIs
    • 21 CFR 210/211 (FDA cGMP for finished pharmaceuticals)
    • USP General Chapters relevant to processing chemicals

    Typical usage ratio

    • Integrated at 0.8%–2.5% w/w depending on target API molecular yield; adjusted per step conversion efficiency and customer molar requirement.

    Downstream process integration

    • Charged directly into the initial reaction stage post-solubilization, preceding catalytic reduction or Grignard reactions; QC sampling at every critical process point for impurity trending.

    Final product types

    • Central nervous system (CNS) drugs—including select serotonin antagonists
    • Antihypertensive pharmaceutical API intermediates
    • Custom contract-manufactured benzodioxole derivatives

    2. Agrochemical Synthesis: Specialty Pesticide Intermediates

    Agrochemical manufacturing utilizes this intermediate in the synthesis of systemic insecticide and fungicide actives where a methylenedioxyphenyl nucleus imparts environmental stability and selectivity. The compound is most commonly added during nitrile-to-amide conversion stages held under strictly monitored temperature and solvent conditions. Batch traceability and adherence to environmental release protocols govern every tonne consumed by downstream pesticide formulators.

    Industry compliance standards

    • FAO/WHO specifications for technical material (JMPS)
    • ISO 9001:2015 (quality system management for chemical manufacturing)
    • OECD Good Laboratory Practice for pesticide intermediates
    • REACH Regulation (EC) No 1907/2006 for registration, evaluation, and authorization of chemicals

    Typical usage ratio

    • Ranges from 1.2% to 3% of total reactant mass, with adjustments based on evolutionary yield studies and crop protection efficacy calibrations.

    Downstream process integration

    • Fed into amide bond-forming reactors or processed via hydrolysis followed by coupling, as monitored within closed-loop automated batch PCC systems.

    Final product types

    • Specialty systemic insecticides (e.g., acetamiprid analogues)
    • Broad-spectrum fungicidal technical concentrates for formulating EC and SC
    • Seed treatment actives using aromatic nitrile motif

    3. Flavors and Fragrance Ingredient Manufacturing

    Manufacturers supporting the flavors and fragrance industry employ this molecule to construct odorant intermediates featuring benzodioxole rings, integral to recreating spicy, woody, and floral notes at industrial scale. The compound participates in reductive amination and subsequent cyclization protocols under high-purity constraints. Volatile impurity control and allergen management are crucial, with clear documentation required per international additive statutes and supply-chain transparency programs.

    Industry compliance standards

    • IFRA Code of Practice (International Fragrance Association)
    • FDA 21 CFR 172.515 (synthetic flavoring substances adjuncts)
    • EU FCM Regulation No. 1334/2008 (flavoring regulation)
    • Cosmetic Ingredient Review (CIR) guidelines for raw material traceability

    Typical usage ratio

    • Incorporated at levels of 0.5%–1.6% relative to total charge, tailored to target note intensity and batch aroma reproducibility standards.

    Downstream process integration

    • Added during the first-stage synthetic pathway to generate aldehyde or amine derivatives, then subjected to purification (fractional distillation or crystallization) prior to blending in compounding units.

    Final product types

    • Natural-identical fragrance intermediates (e.g., heliotropin analogues)
    • Spicy and floral perfumery bases
    • Synthetic flavoring agents for beverage and confectionery

    4. Fine Chemical Building Block in Research Chemical Synthesis

    Academic institutes and contract research organizations order this fine chemical as a tailored building block for multi-gram to kilogram scale syntheses enabling structure–activity relationship (SAR) exploration and new material discovery. Researchers require full disclosure on analytical characterization (NMR, HPLC, GC-MS) and demand uncontaminated material that withstands a variety of nucleophilic substitution, reduction, and cross-coupling procedures in standard Schlenk and flow reactors.

    Industry compliance standards

    • ISO 17025:2017 (laboratory testing competence for chemical purity validation)
    • ACROS/Alfa Aesar/TCI internal quality specifications (when custom supplied)
    • Material Safety Data Sheet (GHS-compliant) disclosure for laboratory handling
    • OECD Test Guidelines for chemical method validation

    Typical usage ratio

    • Dosed from 1 mmol scale up to 5% w/w of total substrate input, based on synthetic route length and target library member count.

    Downstream process integration

    • Serves as a starting material or intermediate, introduced in the first or second step of custom organic synthesis; included in one-pot and telescoped process development.

    Final product types

    • Targeted small-molecule research intermediates
    • New heterocyclic motif development
    • SAR probe compounds supplied to discovery teams

    5. Specialty Polymerization Initiators in Advanced Material Science

    Chemical engineers and material scientists harness this compound in synthesizing specialty copolymers that demand controlled aromatic functionality. The compound undergoes polymer-anchoring reactions, often via nitrile-modified aromatic monomers, to impart flexibility, durability, or selective permeability in high-value polymer systems. Downstream users critically evaluate the purity to avoid chain-transfer inhibition and maintain batch-to-batch uniformity suited for precision coating and membrane applications.

    Industry compliance standards

    • ISO 9001:2015 for specialty polymer production
    • ASTM D3641-21 (standard practices for manufacturing plastic materials)
    • RoHS Directive (2011/65/EU) for restricted substance content
    • REACH SVHC compliance (for monomer and polymer safety)

    Typical usage ratio

    • Applied at 0.3%–1.5% total monomer weight, adjusted per formulation viscosity and target molecular weight specifications.

    Downstream process integration

    • Introduced during pre-polymer mixing or chain-initiation phase in batch or continuous reactors; followed by in situ monitoring of conversion and molecular distribution prior to extrusion or curing.

    Final product types

    • Custom copolymers for membrane and coating technology
    • Functionalized specialty plastics used in electronics encapsulation
    • Performance films for controlled-release devices
    Free Quote

    Competitive 3,4-(Methylenedioxy)Phenylacetonitrile prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    3,4-(Methylenedioxy)Phenylacetonitrile: A Closer Look from the Manufacturing Floor

    In the world of fine chemicals, not every compound gets the same attention, yet every step in their journey matters. At our manufacturing site, 3,4-(Methylenedioxy)Phenylacetonitrile attracts skilled hands and sharp eyes because of its critical role as an intermediate. Over years, we’ve seen how subtle differences in its preparation can ripple across downstream syntheses, and we’ve learned there’s no shortcut to consistency and purity here.

    Understanding 3,4-(Methylenedioxy)Phenylacetonitrile

    Manufacturing this compound calls for precision. Its structure—anchored by the methylenedioxy bridge on a benzene ring and a nitrile group—makes it a favorite in the synthesis of pharmaceuticals, agrochemicals, and performance materials. Every batch demands accurate control of temperature, pH, moisture, and purification steps to achieve a product that consistently meets demanding applications.

    The product usually comes as a pale yellow to off-white crystalline solid, a result of carefully monitored conditions that favor high purity and minimal by-products. We target a purity of 98% or higher, as even small contaminants create headaches for reaction yields downstream. Customers in high-value synthesis count on this level without having to run extra purification cycles themselves. From experience, fighting for those extra percentiles in purity takes more than upgraded equipment—it depends on experience at the operator level, knowing exactly when a distillation or recrystallization has crossed the line between sufficient and exceptional.

    Model and Specifications

    We base specifications on years of feedback from customers, performance data in different syntheses, and lessons learned in our own reactor halls. Our most sought-after grade features:

    Every batch, before we pack it, passes GC, HPLC, and Karl Fischer analysis. Beyond numbers, the real test sits with process engineers who understand downstream needs. In practice, nobody wants a beautiful spec sheet that doesn’t match reality—so we do regular cross-checks using customer-supplied protocols in our lab.

    Where the Product Fits Best

    Our 3,4-(Methylenedioxy)Phenylacetonitrile finds itself at home in organic synthesis shops focused on building complex molecules. Its methylenedioxy ring often opens the way for selective transformations, especially useful during phenethylamine or benzodioxole derivative synthesis. Custom API synthesis outfits look for our material when they want to avoid unexpected side products that can pop up during reductive amination or Grignard additions.

    From our end, controlling trace metallic and aromatic impurities is non-negotiable. Once, a poorly filtered batch introduced nickel traces that killed a downstream hydrogenation for a customer. That lesson stuck, driving us to double up material handling SOPs and invest in fresh filtration lines. Today, even stubborn compounds that hide at parts per million rarely make it through our detection methods.

    How Our Product Stands Apart

    We’ve handled numerous substituted phenylacetonitriles, and subtle chemical tweaks can turn a straightforward synthesis into a bottleneck. 3,4-(Methylenedioxy)Phenylacetonitrile brings an extra layer of challenge because the methylenedioxy grouping is susceptible to over-oxidation if a process step slips. We’ve built safeguards into every scale-up batch, from glass-lining to atmospheric monitoring, avoiding oxidative by-products that can lower yields or force extra washes.

    Some suppliers try to push products with less attention to contaminant profiles—traces of ortho- and para-isomers, for example, can scramble carefully designed synthetic steps. Our facility focuses on maintaining a clean product without the aromatic by-products that can sneak in during uncontrolled side reactions. Years of working alongside R&D teams have shown us that shortcuts at the intermediate stage almost always translate to lost material or rework down the road.

    As we keep refining, we notice that what matters most isn’t only reported purity, but whether the compound performs predictably in customers’ hands. For high-throughput API work, a single out-of-spec impurity can set a timeline back by weeks. We’ve narrowed in on how trace impurities can sometimes evade detection in typical assay methods, so we've added orthogonal screening like NMR and mass spec for each lot headed to pharmaceutical customers.

    Production in Practice: Lessons on the Line

    Producing a fine chemical at scale rarely goes by the book. 3,4-(Methylenedioxy)Phenylacetonitrile requires careful sourcing of starting materials, as the quality of the substituted benzaldehyde directly impacts by-product formation. Over time, we've worked closely with a select group of upstream partners, building strong relationships to address issues before they chain into our reactors. Trust, in this case, has become a two-way street, where feedback and prompt corrective action prevent disruptions.

    Our plant runs continuous process control, not just end-point batch reviews, which allows real-time adjustments. Operators logging hourly reactor readings and visually inspecting crystallization offer checkpoints computers miss. The ability to pause, adjust, and re-check before the material leaves the reactor ensures consistency more than retroactive fixes ever could.

    Safety, Handling, and the Human Side of Chemistry

    A nitrile group isn’t just another functional handle—it brings toxicity concerns that demand careful handling. Plant teams get thorough briefings on personal protective equipment, proper loading, and best practices for air handling. Years ago, we updated our extraction and ventilation systems after one incident where localized fumes made it into an adjacent work area. This led to stepped-up monitoring and dedicated nitrile-handling bays, emphasizing that protocol is never just paperwork.

    We partner with experienced logistics companies to move finished lots, after fully confirming packaging compatibility through prolonged stability trials. Our shipping partners ensure secure documentation and traceability, reducing the risk of misrouting or exposure along the way. Taking shortcuts with packaging or carriers only raises the likelihood of costly delays and potential regulatory headaches.

    Traceability and Accountability—A Manufacturer’s Commitment

    Every container tagged on our floor ties back to full traceability records, from raw material lots to operator signatures. If a customer’s feedback points to a strange odor or color, our QC team can pull line data, sample retainers, and batch history for investigation. In one case, post-shipment customer feedback highlighted an off-spec melting point, leading us to a root-cause in solvent residue. We then adjusted solvent stripping parameters, and since then, those issues haven’t returned.

    That internal transparency builds trust with downstream partners, who know they can challenge a lot or request analytical data without pushback. Having teams with years of plant experience proves invaluable in tracking subtle shifts in product profiles that automated alerts sometimes overlook—a difference especially important in regulated applications where even minute inconsistencies risk triggering regulatory audits.

    Regulatory and Compliance—No Corners to Cut

    Sticking to compliance isn’t optional, especially with nitrile intermediates like this. Local and international regulations grow more detailed with each year, so our documentation process starts at intake and moves through every processing step. Internal audits and routine refresher training sit side by side with third-party assessments, girding every specification and practice so they line up with global standards.

    We heard from API clients that some suppliers let compliance slip, especially between markets. Our approach holds every batch to the highest regulatory expectations, sending regulatory documentation alongside COAs so nobody is left guessing about provenance and standards.

    Improving with Industry Shifts

    As green chemistry advancements expand, the sector increasingly expects lower waste, safer reagents, and more energy-efficient synthesis routes. For our 3,4-(Methylenedioxy)Phenylacetonitrile, we’ve shifted processes toward solvent recovery and recycling, lowering both costs and environmental impact. The move to closed process loops in purification steps came from in-house brainstorming and listening to customers eager for greener supply chains.

    A few years back, we faced a challenge sourcing greener oxidants that didn’t add unwanted by-products while cutting environmental discharge. After pilot testing a range of options, we settled on one that balanced high yields with fewer downstream pollutants, and upgraded our effluent treatment system to keep up with stricter discharge norms. Each improvement drew on feedback from both our own sustainability team and customers under pressure to document carbon footprints and waste streams.

    The Real Differences vs. Other Intermediates

    Comparing 3,4-(Methylenedioxy)Phenylacetonitrile with close relatives like unsubstituted phenylacetonitriles or those with different ring substitutions, you notice more than just the analytical data. The methylenedioxy moiety shifts reactivity, impacting overall yields, selectivity, and end-product profiles. Where the parent phenylacetonitrile may pass through certain transformations smoothly, the dioxole group sometimes demands different catalysts, or calls for stricter exclusion of acid or base traces to prevent unwanted side reactions.

    As a manufacturer, another notable variation comes from physical handling. Our staff has found the 3,4-methylenedioxy variant more air- and light-sensitive compared to simpler analogs. In response, process enclosures and amber containment have become standard here, reducing photodegradation risks throughout storage and transit. Product stability tests after adjusting these measures revealed a significant drop in minor decomposition products—a small adjustment with outsized impact for our partners building complex libraries off this core structure.

    Over years, direct experience highlights that not all substituted phenylacetonitriles offer the same track record for reaction reliability. Evaluating customer feedback and our own synthetic validation shows the methylenedioxy version consistently gives less aromatic by-product when run through selective reductions, provided our controls stay tight. Other variants can introduce higher background noise in analytics, pushing downstream QC labs to chase down spurious peaks that slow approvals and batch release—a clear value-add for buyers who need predictable performance over hundreds of reaction cycles.

    Practical Solutions to Common Issues

    The rare issues we hear most often from users concern deposits in their reactors or color formation during storage. Working with them, we traced many problems to improper dilution solvents or lack of temperature control during initial handling. We now provide application advice based on extensive feedback, not just best guesses. Some labs switched to lower-boiling carriers for dissolving the nitrile, slashing deposit rates and improving reproducibility.

    Occasionally, a customer’s process calls for lower residual moisture than our specification. Our response has been to offer a further-dried grade upon request, using vacuum ovens and in-line desiccation. Years of hands-on work with such requests makes it clear that each application can call for its own tweaks, and manufacturers ignore this reality at their peril.

    Sometimes researchers mention unexpected odor or tint. Here, improved packaging integrity and tighter temperature monitoring during transit has made a clear difference. By assigning a dedicated product manager to each high-volume customer, ongoing QC monitoring and periodic feedback ensure that quality doesn’t degrade from the dock to the lab bench.

    Supporting Sustainable Synthesis

    Industry trends lean toward sustainability, and we’ve made sure our 3,4-(Methylenedioxy)Phenylacetonitrile stands in line with these goals. By closing loops in our solvent systems and choosing greener starting materials, we help our customers tell their own sustainability stories to regulators and boards. Last year, we invested in a process optimization audit, which found new solvent recovery options that cut waste by 20% in three months. Not every step reduced costs, but the gains in environmental impact and customer preference more than justified the upfront effort.

    These improvements add up, particularly for customers moving to larger-scale applications, and our collaborations with leading companies in pharma and materials science underscore the value in long-term thinking. Sharing best practices, open process reviews, and detailed impact reports strengthens trust with buyers whose own customers increasingly demand transparency.

    The Hands-On Differences Manufacturers Bring

    Actively producing 3,4-(Methylenedioxy)Phenylacetonitrile has taught our plant teams to respect the unpredictability of chemistry. No two batches ever feel completely alike. Every production shift builds both confidence and humility. Mistakes—though rare—are treated as the fastest way to get better.

    Consistently delivering the expected product, both in chemical integrity and logistical smoothness, requires commitment across every department. R&D acts as a bridge between customer demands and practical manufacture, regularly looping back to plant operators with ideas for process improvements or tweaks to meet unusual needs. We don’t just ship chemical drums; we stay in touch, ask for process updates, and invite feedback, tweaking routines to better match real-world application.

    Our job never stops at “good enough.” Each step, from sampling to shipping, reflects pride of workmanship shaped by direct experience. The backbone of sustained supply—especially for exacting sectors like pharmaceuticals—remains a mix of technical knowledge, process discipline, and genuine listening. Put simply, excellence at this level comes from walking the manufacturing floor every day, understanding the unique quirks of this molecule, and adapting and learning with each run.

    Looking Forward: Meeting the Challenges of Tomorrow

    As regulations around chemicals and active intermediates evolve, responding fast and proactively matters more each year. We stay ahead by monitoring changes not only in national and regional policy but also in customer expectations. Committing openly to quality, transparency, and sustainable practices doesn’t mean changing course every time the industry shifts; it means embedding those values into everyday decision-making, from the shop floor to the management office.

    Manufacturing 3,4-(Methylenedioxy)Phenylacetonitrile at scale, with an eye on purity, safety, and sustainability, takes more than procedures. It takes a willingness to stay present, to treat each batch and customer challenge as a real opportunity for improvement, and to share insights across the supply chain. By keeping the lines of communication honest and open, we keep raising the standard for ourselves and our partners. For us, the privilege of making this molecule comes with real responsibility—a responsibility we accept each day with care, consistency, and respect for every customer journey that starts here.