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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 | 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. |
Applications of 3,4-(Methylenedioxy)Phenylacetonitrile in Industrial Manufacturing3,4-(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 SynthesisPharmaceutical 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
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2. Agrochemical Synthesis: Specialty Pesticide IntermediatesAgrochemical 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
Typical usage ratio
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3. Flavors and Fragrance Ingredient ManufacturingManufacturers 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
Typical usage ratio
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4. Fine Chemical Building Block in Research Chemical SynthesisAcademic 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
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5. Specialty Polymerization Initiators in Advanced Material ScienceChemical 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
Typical usage ratio
Downstream process integration
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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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.