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HS Code |
244962 |
| Cas Number | 120-57-0 |
| Molecular Formula | C8H6O3 |
| Molecular Weight | 150.13 g/mol |
| Iupac Name | 1,3-benzodioxole-5-carbaldehyde |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 145-147°C at 20 mmHg |
| Density | 1.22 g/cm³ |
| Solubility In Water | Slightly soluble |
| Synonyms | Heliotropin, Piperonal aldehyde |
| Refractive Index | 1.594 |
| Flash Point | 146°C (closed cup) |
As an accredited 2,3-(Methylenedioxy)Benzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, screw cap sealed, labeled with hazard symbols and product details, containing 100 grams of 2,3-(Methylenedioxy)Benzaldehyde. |
| Shipping | 2,3-(Methylenedioxy)Benzaldehyde is shipped in tightly sealed containers to prevent leakage or contamination. It should be stored in a cool, dry, well-ventilated area, away from heat and ignition sources. Packaging complies with applicable transport regulations for hazardous chemicals, including labeling and documentation, to ensure safe handling during transit. |
| Storage | 2,3-(Methylenedioxy)benzaldehyde should be stored in a tightly sealed container, away from light, heat, and moisture. Keep it in a cool, dry, and well-ventilated area, separate from incompatible substances such as strong oxidizers and acids. Properly label the container and use chemical-resistant storage equipment. Ensure spill containment and access to safety equipment, such as eyewash stations and fire extinguishers. |
Applications of 2,3-(Methylenedioxy)Benzaldehyde in Industrial Manufacturing2,3-(Methylenedioxy)Benzaldehyde serves as a crucial intermediate for select downstream industries. Our manufacturing expertise centers on consistent quality and compliance, ensuring reliable supply for advanced synthesis processes. This section highlights key value-added industrial applications supported by real-world standards and formulation practices. 1. Pharmaceutical Intermediates: Active API SynthesisThe compound plays a specific role in stepwise synthesis of therapeutic molecules, particularly for psychoactive and CNS drug classes. Pharmaceutical manufacturers integrate it during early-stage condensation reactions, forming structural frameworks used in patented medications. Quality control teams monitor impurity profiles to comply with stringent drug regulatory standards. The compound's reactive aldehyde group allows for targeted modification, producing high-value intermediates with minimal side reactions. Industry compliance standards
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2. Agrochemical Intermediate ManufacturingProducers of high-performance fungicides and insecticides utilize this aromatic aldehyde as a building block for synthons in agricultural actives. Stable processing under controlled reaction conditions enables downstream developers to achieve target crop protection functionalities. Material traceability ensures full batch documentation for regulatory filings, with QA testing focused on chemical purity and absence of restricted contaminants relevant to agricultural applications. Industry compliance standards
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3. Fragrance and Aroma Ingredient SynthesisAldehyde-based perfumery compounds incorporate this material in the production of benzodioxole-fragranced bases. Fine fragrance formulators and aroma-chemical producers value the purity and reactivity for customized aroma molecule production. The compound undergoes condensation and reduction steps, defining scent profiles used in high-volume perfumery and home care additives. Traceability to IFRA guidelines governs raw material quality control during the blending of aroma intermediates. Industry compliance standards
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4. Dye Intermediate ProcessingManufacturers producing specialty dyes apply this building block for constructing chromophore frameworks in organic dye molecules, particularly for applications demanding stability in textiles and plastics. The compound's structure allows for later-stage modification via oxidative coupling or cyclization, building intense and stable color properties. Safety teams monitor reaction completeness to align with relevant occupational and environmental standards for colorant manufacture. Industry compliance standards
Typical usage ratio
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At the core of our chemical operations, we've worked up a deep familiarity with 2,3-(Methylenedioxy)Benzaldehyde through years of hands-on production. Many have heard this name in connection with fragrance manufacturing, specialized pharmaceutical synthesis, or in the realm of research chemicals. We focus on producing this compound consistently and safely, using tested methods and rigorous raw material controls, because only strict standards can give consistent performance in downstream applications.
Our plant workers and technical staff handle bulk 2,3-(Methylenedioxy)Benzaldehyde daily. The best product comes from a careful process—beginning with handpicking high-purity starting materials, carefully controlling temperature and reaction durations, and not cutting corners on solvent recovery or distillation. Our best batches reach a purity upwards of 99% GC, as measured by our own in-house labs using calibrated reference standards. Even small fluctuations—like a marginal change in water content or a contaminant spike—can mean the difference between a smooth reaction downstream and a headache full of waste. That’s a reality we don’t take lightly.
Most chemists who use our 2,3-(Methylenedioxy)Benzaldehyde want reproducible results. They rely on specific melting points, tight vapor pressure ranges, and reliable stability under shipping and storage conditions. The aldehyde has a clear, pale-yellow appearance, but its subtlety belies a sharp, spicy aroma—the sign that the methylenedioxy ring holds its integrity. When synthesized properly, it does not darken quickly and avoids trace-level byproducts that can disrupt key downstream catalytic steps.
It attracts those looking for both yield and processability. Our compound's relatively high boiling point helps users control volatilization losses even when processes require some heat. Because we maintain strict impurity benchmarks, users avoid headaches from problematic side-reactions or the addition of unwanted complexity during product purification—even at scale. Even after transport or months of shelf time, our customers find their product the same as the day it left us, as long as it stays sealed from air and moisture.
Chemically, 2,3-(Methylenedioxy)Benzaldehyde belongs to a broader group of methylenedioxy-benzaldehydes and related aromatic aldehydes. Often, purchasing teams or formulators confuse it with 3,4-(Methylenedioxy)Benzaldehyde or the well-known 4-hydroxy derivatives. As production chemists, we see day in and day out how these differences play out in process chemistry: the position of the methylenedioxy bridge not only shapes the physical characteristics of the molecule, but also alters its reactivity and suitability for further reactions.
For example, in synthetic campaigns aimed at benzofuran development or in exploring regulatory-compliant drug intermediate processes, 2,3-linkage stands out for producing fewer polymerization issues compared to its 3,4 counterpart. The nuanced electronic effects of our compound’s aromatic system render it slightly less prone to side oxidation, which pleases both our own purification staff and customers scaling up production lines. When chemists ask about using 2,3-(Methylenedioxy)Benzaldehyde over similar chemicals, our most objective response remains: it supports cleaner conversions and gives manufacturers the edge in yield and separation simplicity.
Many in the field recognize the subtle differences only after running side-by-side processes multiple times. For example, someone running a condensation might expect similar yields and color profiles across a range of substituted benzaldehydes, only to notice the downstream mixture cleans up easier when using our 2,3 isomer. Such stories circulate among technical teams, fueling preferences for our material above generic alternatives.
Aldehyde chemistry always brings challenges, whether making a flavor compound, an intermediate for life sciences work, or a research tool for structural analysis. The knack for choosing the right aldehyde—especially a nuanced one like 2,3-(Methylenedioxy)Benzaldehyde—shows up most in the actual workflow. In perfume bases, our compound brings a certain intensity and fullness, without the heaviness or resinous tailing found in other aromatic aldehydes. Niche fragrance creators—some of whom regularly share their observations—tell us the product can serve as either a punchy heart note or drop into supporting roles with orange flower, vetiver, or benzoin.
Scientists in pharmaceuticals or crop protection chase another quality: reliability through scale. Early-stage discovery chemistry might tolerate a deviation in purity or isomer distribution, but by pilot scale, process unforgiveness sets in. Starting from a solid batch of our 2,3-(Methylenedioxy)Benzaldehyde, chemists routinely synthesize complex heterocycles, acetal-protected intermediates, and other benzene-fused structures without the hassle of late-stage chromatographic purification. That edge—in time saved and labor avoided—translates to better throughput and easier regulatory compliance.
Beyond lab benchtops or pilot plants, industrial-scale downstream players insert our material into continuous flow operations. The aldehyde’s predictable melting and boiling behavior aligns with automated dosing systems, while its low residual moisture supports moisture-sensitive additions. One of our partners in Eastern Europe runs daily lots of 2,3-(Methylenedioxy)Benzaldehyde through a four-step route to a specialty active, rarely reporting concern about off-odors, discolorations, or batch-to-batch drift. We attribute this outcome to our investment in in-process analytical controls and batch segregation, not just finished-goods testing.
Too often, this market sees low-ball offers from traders eager to flip unexamined material between regions. We’ve had customers burned by earlier suppliers, who shipped product unfit for demanding syntheses. Complaints — dark oil instead of solid, acidic tinge, unpredictable boiling points — always point back to process shortcuts or inattentive packaging. As actual producers, we know the implications are more than inconvenience; unstable product throws off entire months of inventory planning, leads to loss of client confidence, and causes real regulatory headaches.
We do not take shortcuts on solvent removals or purification cycles. Every kilogram of 2,3-(Methylenedioxy)Benzaldehyde gets tracked and charted for color, GC trace contaminants, and water titration. These technical checks underscore a commitment that outlasts a shipment: our name and reputation ride on every container, whether drum or bulk tank. We coach our operators through best practices in inert gas blanketing, ultra-clean drum sealing, and quick-response packing.
Logistics teams know how poorly-stored aldehydes can degrade in transit. We work closely with shippers, often specifying conditions above generic cargo requirements, because inexpensive decisions in the warehouse or on the truck can undo weeks of proper synthesis—adding color, forming unwanted peroxides, or simply rendering the product unstable before it arrives. Over time, one sees marked differences between a product manufactured with “just good enough” attention and one delivered with meticulous stewardship.
Real-world handling experience trumps theoretical advice every day. We use stainless and glass-lined vessels in all direct contact points, steer clear of copper or iron that can accelerate auto-oxidation, and keep drum fills under nitrogen. Temperature-controlled storage helps avoid aldehyde dimerization. Each drum shipment moves with internal silica gel desiccants, keeping water pickup at bay. Outgoing lots meet a simple standard: if our own internal plant processes would suffer, it doesn’t leave our warehouse.
Users sometimes ask why their older stock—whether purchased from us or another vendor—looks darker or smells different months after storage. Usually, continuous air ingress, persistent humidity, or slight packaging punctures have caused silent degradation. In our facilities, we use predictive shelf-life studies to adjust resin coatings and cap liner choices, evolving our drum selection year after year. Every season’s lessons—whether from a humid summer batch or a winter logistics grind—feed into guidance we provide to new customers, streamlining their own warehousing and QA routines.
We collaborate with customers scaling up, who rely on our advice about mixing rates, solvent compatibility, and reaction times. Lab recipes rarely translate seamlessly to kiloliter vessels. Running this aldehyde at scale, we have firsthand stories of exotherm control, batch-to-batch reproducibility, and key metrics like color hold after extended reflux. We’ve advised multi-site clients who wanted to switch from older glassware to stainless reactors. A change in reactor geometry or heating method can alter product appearance and trace impurity, unless upstream chemistry and downstream collection both get adjusted.
In some plants—especially those producing flavors and fragrances at volume—key batch issues stem not from synthesis itself, but filtration, drum decanting, or temperature cycling during storage and transfer. We encourage on-site sampling, not just at dispatch but again before internal transfer, to nip issues in the bud. If an obscure impurity or off-spec color emerges, we pull historical records—batch logs, analytic runs, and warehouse conditions—until root causes reveal themselves. This deep engagement, made possible by direct manufacturing control, centers quality over short-term cost.
Other groups using our 2,3-(Methylenedioxy)Benzaldehyde outright seek novel process routes, such as greener solvents, catalytic flow reactors, or step-reducing coupling methods. Our engagement focuses less on buzzwords and more on nitration risk profiles, contamination control, or trace element compatibility. If a new route means updated impurity profiles, we validate our own product’s fit before customers invest in scale. That hands-on problem-solving saves time—and trust.
Chemicals destined for regulated markets create their own paperwork trail. Our manufacturing documentation stands ready, detailing raw material lots, Certificate of Analysis results, and stability data as required by law and client SOPs. We believe transparency in batch records and repeatable analytics underpins every legitimate pharma or food-grade audit. That depth—sometimes a slog, always worth it—separates manufacturers from traders who hope the next scan won’t ask deeper traceability questions. Customers regularly ask for extended impurity cut sheets, heavy-metal checks, or breakdowns of trace residuals from raw materials. Everything we certify comes from actual analytical work, not third-hand summaries.
Some clients need additional assurances about trace allergen content, residual solvents, or potential byproducts. We open our testing data without reservation, and if an uncommon contaminant arises in an end-use process, we review upstream and downstream chemistry to propose mitigation. That ongoing dialogue with formulators—especially in high-spec application fields—turns batch delivery into a real partnership, minimizing compliance risk and showing our ongoing investment in the client’s project success as much as our own.
We hear from labs and factories confronting practical frustrations: a shipment from a trader arrives off-color or with musty aroma; an “equivalent” material from a faraway source produces more side-products and needs multiple re-crystallizations, eating away time and margin. Our product isn’t chosen solely on price, but for the consistent experience from small pilot runs through thousands of liters, shipment after shipment. By fielding both complaints and praise directly, we constantly shift our internal QC focus to the points that matter to working chemists, not the ones that look good on a marketing sheet.
It is a badge of pride around our site that returning users recognize both the product and the voice on the other end: inquiries aren’t funneled through anonymous resellers, but handled by people involved in the very synthesis run being shipped or repeated. This responsiveness means we catch oddities before they spiral. We don’t just listen to customer anecdotes, we act: a report of longer dissolution in certain solvents pushed us to review particle profile and led to an update in crystallizer operation. A request for more robust packaging for tropical export made us retool drum linings and recreate QA breakpoints in shipping.
End-market demands never freeze. Sustainability requirements, pressure for milder processes, and customer focus on lifecycle analysis all reshape today’s manufacturing landscape. We’re seeing an uptick in inquiries about renewable-source precursors, lower-carbon utilities, and closed-loop solvent systems. Rather than resting on a decades-old synthesis, we continue to adapt, running test lots through alternative oxygen sources and adjusting workup procedures to cut waste. The result isn’t a “greenwashed” product, but one with lower overall campaign footprint and smaller effluent streams.
On the compliance side, market divergence grows: some regions require exhaustive batch-level disclosures, while others prioritize performance and delivery times. Manufacturers sit at the intersection. We balance local regulatory expectations with smooth international delivery, all while never relaxing the technical discipline underlying trustworthy product.
A final trend involves supporting digital traceability—a newer demand we are embracing. Modern customers want more than a stamped CoA; they expect electronic lot tracking, digital signature analytics, and integrated recall contingency plans. We deploy both internal and third-party software to make every batch’s life cycle transparent. Field teams love the reduction in paperwork; customers benefit from confidence in traceable, recall-ready product.
Our reputation with 2,3-(Methylenedioxy)Benzaldehyde flows from a blend of hard, hands-on experience and responsiveness to shifting needs. As the industry cycles through fads, regulation, or new market entrants, our approach rests on the simple principle that manufacturing quality determines all else. We do not rely on appearance or market talk; we engage in detailed chemical stewardship, batch after batch.
We’ll continue adapting synthesis routes, investing in better people training, and raising the bar for what “good” material means. Every improvement in process returns value to those using our product on the factory floor or in the R&D bench. For clients, this translates to robust supply chains, lower waste, fewer batch recalls, and easier regulatory audits. For us, it strengthens the reason we make chemicals in the first place: transforming molecules into value, supported by knowledge earned from actually running the reactions, day in and day out.
2,3-(Methylenedioxy)Benzaldehyde isn’t just another item on a chemical list for us. It’s a compound we know inside and out, able to deliver not only on the properties that matter in your process today but evolving as needs change year on year. Our door stays open to feedback, and our lines remain busy with the next batch, ready for today’s chemical challenges.