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HS Code |
772549 |
| Chemical Name | 3,4-(Methylenedioxy)Butyrophenone |
| Cas Number | 14251-72-4 |
| Molecular Formula | C10H10O3 |
| Molecular Weight | 178.19 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 329.5 °C at 760 mmHg |
| Density | 1.17 g/cm³ |
| Synonyms | 3,4-Methylenedioxybutyrophenone; 1-(3,4-Methylenedioxyphenyl)butan-1-one |
| Smiles | CCCC(=O)C1=CC2=C(C=C1)OCO2 |
| Inchi | InChI=1S/C10H10O3/c1-2-3-10(11)7-4-5-8-9(6-7)13-6-12-8/h4-6H,2-3H2,1H3 |
| Refractive Index | 1.561 |
| Storage Conditions | Store at room temperature, tightly closed, away from light |
As an accredited 3,4-(Methylenedioxy)Butyrophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 3,4-(Methylenedioxy)butyrophenone is packaged in a sealed 100g amber glass bottle, labeled with hazard and handling information. |
| Shipping | 3,4-(Methylenedioxy)butyrophenone is shipped in tightly sealed, chemical-resistant containers to prevent leaks or contamination. Packaging complies with local and international regulations for chemical transport. Handle with proper labeling and documentation, and ship via authorized carriers equipped for hazardous material, ensuring secure storage and prompt delivery to prevent exposure or degradation. |
| Storage | 3,4-(Methylenedioxy)butyrophenone should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances (such as strong oxidizing agents). Store at room temperature and avoid moisture. All containers should be clearly labeled, and access should be restricted to trained personnel. Use appropriate secondary containment to prevent leaks or spills. |
Applications of 3,4-(Methylenedioxy)butyrophenone in Industrial Manufacturing3,4-(Methylenedioxy)butyrophenone supports multiple fine and specialty chemical production streams due to its unique aromatic structure, controlled reactivity, and compatibility with regulated synthesis environments. Below are key real-world industrial applications, their compliance requirements, incorporation ratios, production process interfaces, and tangible final products. 1. Pharmaceutical Intermediate for Piperonal-Based APIsThis compound acts as a key intermediate in the multistep synthesis of certain piperonal-derived pharmaceuticals, including antihypertensive and anticonvulsant agents. Manufacturers utilize its reactive core for nucleophilic or reductive functionalizations, forming part of the API backbone in cGMP environments. Customers require tight impurity profiles and traceability from the intermediate stage to the finished drug substance. Industry compliance standards
Typical usage ratio
Downstream process integration
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2. Synthesis of Fragrance and Aroma IngredientsThis chemical is incorporated in the synthesis route of complex aromatic compounds, notably those with a methylenedioxyphenyl motif found in fine fragrances and food-safe aroma chemicals. Downstream processors execute controlled oxidation or reduction, employing established flavor industry protocols and meeting global consumer safety compliance for trace impurities and prohibited substances. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Agrochemical Intermediate for Select HerbicidesSelected agrochemical companies use this building block to construct specialty herbicide molecules featuring a methylenedioxy core. Its controlled electrophilicity benefits halogenation or aminomethylation sequences. Application protocols stress controlled reaction parameters and strict handling procedures, as downstream users require traceability and validated impurity controls for use in crop management. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Dye and Colorant Intermediate for Technical PigmentsProducers of technical dyes and high-stability pigments employ this material in the formation of advanced methylenedioxy-bridged chromophores. Controlled synthesis enables vibrant and lightfast properties in high-performance pigment and ink production, crucial for industrial printing and plastics coloration. Each batch undergoes rigorous QC and conforms to appropriate industrial grade toxicological and purity standards. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Decades spent synthesizing specialty chemicals have taught us the value in tracking every detail from raw material sourcing to final application. 3,4-(Methylenedioxy)Butyrophenone stands out in our catalogue because this compound demonstrates both reliable performance and versatility in several downstream industries. Over the years, we’ve refined its production, faced real-world process challenges, and responded to our laboratory partners’ priorities with every cycle of feedback. This gives our understanding of the product practical depth that’s hard to find among generic resellers or catalog suppliers.
Producing 3,4-(Methylenedioxy)Butyrophenone means paying close attention to the quality of starting materials and the conditions in every reaction step. The molecular structure—built from a butyrophenone backbone fused with a methylenedioxy functional group at the 3 and 4 positions on the aromatic ring—does not tolerate shortcuts. From experience, lax purification leads to undesirable byproducts, which can compromise both yield and downstream synthetic reliability.
Our batches bear the internal model reference MDCB-01, which marks a material offered at a minimum purity of 98% by GC. By keeping moisture and related ketone impurities well below 0.5%, we prevent complications for clients’ subsequent catalytic or condensation reactions. Most requests come for white crystalline powder, packed in HDPE drum liners to prevent contamination and water ingress. We regularly audit our production lines to maintain lot-to-lot consistency, which is often overlooked by bulk traders.
This attention to process details matters since trace contaminants like aldehydes, dichloromethane, or unreacted starting phenols can interfere with palladium-catalyzed couplings. Several years ago, a research partner in pharmaceutical intermediates noted that our consistent impurity profile reduced troubleshooting time compared to “mix-batch” imports. Their product development timeline benefited directly.
3,4-(Methylenedioxy)Butyrophenone acts as an anchor compound in the creation of new API intermediates (Active Pharmaceutical Ingredients), aroma chemicals, and, in rarer contexts, specialty dyes. The methylenedioxy ring lends itself as a synthetic handle, especially in medicinal chemistry routes requiring selective functionalization at para- and ortho-positions. Research teams using our product often explore it as a precursor to substituted phenethylamines or as a building block in heterocyclic ligand synthesis.
One of our long-term clients in the fragrance sector chooses our grade because it gives them predictable carbonyl reactivity during their ketone condensation steps. Poorly controlled butyrophenone sources lead to aromatization or tar byproducts, which ruin batch purity in expensive syntheses. Laboratory feedback, supported by return-of-experience data, has shown our process keeps contamination at bay, saving weeks of downstream chromatography.
For those interested in scale-up, our production experience also covers larger kilogram lots for pilot plants. During a transition from bench-scale to multi-kilo reactors, engineers adjust reagent equivalents to coax cleaner crystallization from the reaction mixture. Minor variations in pH and reaction time influence the resulting color and melting point of the product. These tweaks, gained from running dozens of pilot batches, aren’t always detailed in literature but make or break reliability in industrial settings.
Chemically speaking, 3,4-(Methylenedioxy)Butyrophenone shares foundational traits with plain butyrophenone and other methylenedioxy-substituted aromatics. Yet the introduction of the dioxole ring at the 3,4-positions creates stark differences in solubility, electronic effects, and handling properties. Some clients ask why not just use 4-methoxybutyrophenone (or a non-dioxy analogue) for their applications. From repeated tests, we’ve found those variants fail in specific cross-coupling or Friedel–Crafts alkylation procedures common to advanced pharmaceutical synthesis.
The methylenedioxy moiety delivers greater electron-donating character compared to single methoxy or hydroxy phenyl ketones. This alters rates of nucleophilic addition and makes it more suitable for constructing certain bioactive heterocycles. A few years back, a partner attempted to substitute with a simple dihydroxy derivative. It resulted in unwanted oxidative polymerization and inconsistent yields until switching to our 3,4-methylenedioxy variant, resolving nearly all reactivity issues.
From a handling viewpoint, our product also resists moisture pickup better than closely related hydroxy or carboxylate substituted analogues, which tend to clump or discolor if exposed to ambient humidity for more than a day. We designed our packaging and recommended storage conditions from years of watching these minor degradative changes damage process reproducibility.
It’s easy to underestimate the challenge in maintaining high quality standards run after run. Many smaller operations lean on third-party tollers without full oversight, risking introduction of uncontrolled impurities. Having in-house process control not only improves traceability for compliance, it allows us to catch subtle shifts in byproduct profile or shift in specific rotation—details that downstream R&D teams depend on for high-stakes reactions.
The evolution of quality systems in our shop followed customer pushback and unexpected setbacks. Early on, we fielded complaints from a medicinal chemistry client who traced synthetic failures to minor fluorenone byproducts in a competing supplier’s shipment. Using an in-line HPLC set-up allowed us to spot this problem early in our own batches and improve post-synthesis vacuum distillation steps. Today, tracking each lot through the process means supporting partners who want regulatory traceability and aren’t willing to roll the dice on anonymous sources.
Our plant operators feed feedback from each day’s run to process supervisors, who then adjust purification protocols on the fly. One adjustment in crystallizer cooling rates improved not only yield, but the product’s filterability, shaving hours off drying rotations. These sorts of practical, in-the-trenches tweaks cannot be found in generic product descriptions or handed down by intermediaries. They're only earned by closely watching what each cycle produces—and learning what customers report works for them in production.
Supply chain stability has grown more important as regulatory scrutiny increases and logistics interruptions grow more common. A customer using 3,4-(Methylenedioxy)Butyrophenone as an active building block for clinical candidates needs reassurance the next order will match the last—down to the impurity fingerprint. Our receiving technicians rigorously blend and sample every inbound drum of key raw materials, using NMR and IR screens to reject out-of-spec shipments. Quality managers cross-reference these readings with historical chromatograms, maintaining a database going back several years to detect any creeping drift in profile.
Even under the pressures of rising global demand and logistical bottlenecks, we invested in materials tracking and local warehousing. These steps buffer against supply shocks and keep critical projects from stalling at the downstream synthetic phase. Our clients benefit because they have a single accountable source for both technical dialogue and actual material fulfillment. This feedback loop lets us anticipate industry needs ahead of the market.
Keeping an open door to formulators and synthetic chemists means learning what serves actual process goals, not just what looks good on a COA. In one case, a large-scale developer asked for tailored particle size to suit their continuous manufacturing line. Working directly with their process team, our operators ran pH and solvent variation experiments to provide a product that poured freely and integrated smoothly onto their feed line.
Running modern synthesis lines for specialty aromatics brings environmental stewardship front and center. We’ve updated the process for 3,4-(Methylenedioxy)Butyrophenone, shifting away from old halogenated solvents where possible and adopting closed-loop recovery systems for reagents. Our R&D team trialed greener oxidants and streamlined work-ups to generate less chlorinated waste. These initiatives came after frank discussions with partners who demanded improved EHS compliance—not just on paper, but evident in lower effluent test results.
Discharge volumes and emission controls are tracked with third-party audits. We installed in-line carbon filtration to keep vent air losses under mandated local thresholds. Plant staff receive regular training on safe handling and spill mitigation—folding in lessons directly from past incidents within our site and in the sector at large. These hands-on measures show our commitment to both workplace safety and environmental responsibility in chemical production.
Actual implementation of these systems allowed us to secure acceptance with international customers subject to more rigorous standards. This opens the door for industry partnerships that go beyond an arm’s-length transaction and ensures that our material holds up to regulatory review worldwide.
We built reliability into every aspect of our offering over many years, not by accident or marketing, but by responding to the needs of formulators, process chemists, and technical managers in changing sectors. That attitude extends into how we track market shifts or regulatory changes. An uptick in regulatory review for precursor chemicals prompted us to implement advanced lot tracking and rapid-response testing protocols. These upgrades reassured our largest clients, who must demonstrate full supply-chain transparency during audits or regulatory submissions.
Changes in application trends drive process adjustments as well. Increased demand in aroma chemicals caused our engineers to review batch temperature profiles, improving the selectivity of methylenedioxy group formation and lowering residual phenol carryover. We keep experimental feedback loops open with R&D users, modifying our process or packing protocols based on firsthand application reports, not just in-house analytics.
Access to real-world performance data enables faster troubleshooting of new formulation blends. We worked with a research group which faced recurring tar formation during catalytic reductions. Side experiments in our in-house kilo lab allowed us to isolate a trace byproduct, then share both analytical findings and purification advice, weaving technical partnership into material fulfilment.
Transparency about origin, process route, and impurity profile matters especially for specialty intermediates like 3,4-(Methylenedioxy)Butyrophenone. Our technical sheets include full spectral verifications, not pared-down summaries. Purity readings incorporate both GC and HPLC data. We openly share analytical traces so that technical managers can benchmark incoming lots against their own standards.
During international regulatory reviews, this level of documentation difference sets clients at ease and builds trust in the supply relationship. Our willingness to provide supporting batch data or facilitate on-site audits comes straight out of our belief in open, accountable manufacturing—a philosophy forged from years of serving advanced synthetic labs and industrial partners with demanding requirements.
We openly discuss process limitations and challenges alongside successes. Not every batch has gone perfectly, but working through setbacks and retooling the process adds depth to the knowledge and capability embedded in every package that leaves our factory. This openness supports strong working relationships with clients who value integrity and seek long-term technical partners rather than faceless vendors.
The world of specialty intermediates does not stand still. Applications for 3,4-(Methylenedioxy)Butyrophenone continue to move beyond traditional synthesis. Our development team watches the latest literature for emerging applications, from functional materials to next-generation ligands for transition metal catalysis. Each inquiry triggers a cycle of technical review and production adaptation, connecting academic discovery to full-scale industrial use.
Clients in changing sectors—whether working in life sciences, fine fragrance, or advanced materials—have unique process demands. We flex process parameters in response, not just to secure an order, but to ensure their end products gain the reliability and quality that only experienced hands can deliver. Our process improvements come directly out of feedback from these sectors, whether it’s better impurity rejection, improved storage stability, or tailored pack sizes for seamless logistics.
As end-user requirements evolve and regulatory standards tighten, our role as actual manufacturers gives us both responsibility and opportunity. We stay proactive by retaining technical expertise in-house, keeping dialog lines open, and embedding lessons learned from every run into future protocols. These grounded practices drive our approach, shaping a product line that serves not merely as a catalogue entry but as an enabler of innovation and progress in client laboratories and industrial plants alike.
Supplying 3,4-(Methylenedioxy)Butyrophenone is about more than meeting a purity target. Each kilogram fulfills hard-earned customer trust in our integrity and capability. The daily practice of careful reaction control, robust QA, and open dialogue ensures materials that support research, scale-up, and commercial manufacture in dynamic markets. Where traders chase the next deal, we invest in building up our processes and partner relationships year after year.
Clients, whether new or established, experience the difference this perspective brings: prompt technical response, transparency on process capabilities, and a genuine willingness to incorporate feedback into continuous improvement. The compound’s unique performance traits are inseparable from the hands and knowledge guiding its synthesis—a reality understood only from years on the production floor and in the laboratory.