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HS Code |
650777 |
| Cas Number | 135-02-4 |
| Iupac Name | 2-Methoxybenzaldehyde |
| Molecular Formula | C8H8O2 |
| Molecular Weight | 136.15 g/mol |
| Appearance | Pale yellow liquid |
| Boiling Point | 248-250 °C |
| Melting Point | 1 °C |
| Density | 1.155 g/cm³ |
| Solubility In Water | Slightly soluble |
| Flash Point | 111 °C |
| Synonyms | o-Anisaldehyde, ortho-Anisaldehyde |
| Odor | Sweet, aromatic |
| Refractive Index | 1.573 |
| Pubchem Cid | 12066 |
| Smiles | COC1=CC=CC=C1C=O |
As an accredited 2-Methoxybenzaldehyde 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 "2-Methoxybenzaldehyde," featuring hazard symbols, chemical formula, batch number, and manufacturer details. |
| Shipping | 2-Methoxybenzaldehyde is shipped in sealed, chemical-resistant containers to prevent leaks and contamination. It is classified as a hazardous material and must be handled according to local and international chemical transport regulations, including labeling and documentation. Protective packaging ensures safety during transit, and temperature control may be applied to avoid degradation. |
| Storage | 2-Methoxybenzaldehyde should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. Keep the container tightly closed and protected from light. Store in a dedicated flammable liquid storage cabinet if possible. Ensure the storage area has proper spill containment and is clearly labeled to prevent unauthorized access. |
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Purity 99%: 2-Methoxybenzaldehyde with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency. Stability temperature 40°C: 2-Methoxybenzaldehyde with stability temperature of 40°C is used in flavor and fragrance formulation, where it maintains aromatic integrity during processing. Melting point 34°C: 2-Methoxybenzaldehyde at 34°C melting point is used in specialty chemical manufacturing, where it facilitates efficient handling and blending operations. Molecular weight 136.15 g/mol: 2-Methoxybenzaldehyde with molecular weight of 136.15 g/mol is used in agrochemical R&D, where it enables precise stoichiometric calculations for formulation development. Low impurity level <0.2%: 2-Methoxybenzaldehyde with impurity level below 0.2% is used in analytical standard preparation, where it guarantees accuracy in quantitative assays. Viscosity 1.2 mPa·s: 2-Methoxybenzaldehyde with viscosity of 1.2 mPa·s is used in resin modifier production, where it ensures uniform dispersion and process reliability. UV absorbance 254 nm: 2-Methoxybenzaldehyde with specific UV absorbance at 254 nm is used in chemical detection systems, where it enhances sensitivity in spectrometric analysis. Color index ≤10 APHA: 2-Methoxybenzaldehyde with color index ≤10 APHA is used in flavor compound manufacturing, where it contributes to transparent end-products without visual contamination. |
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2-Methoxybenzaldehyde isn’t something you stumble across at random; you find it when projects demand more than just the basics. This isn’t your off-the-shelf vanilla fragrance—though I’ll admit, its soft, almost almond-like aroma gives it a certain charm that makes it almost more approachable than some other fine chemicals in the lab. Here we’re talking about a compound that brings together consistency, versatility, and purity, making it a favorite for chemists in pharma, research, and specialty manufacturing.
At its core, 2-Methoxybenzaldehyde, known in some circles as ortho-anisaldehyde, carries the molecular formula C8H8O2. If you’ve handled this aromatic aldehyde before, you know that pure, high-quality batches come as a clear or faintly yellow liquid. Its boiling point lands around 248-250°C, which is something to keep in mind if you plan any syntheses that call for a gentle hand with distillation gear. The compound stands apart from its isomers, like 4-methoxybenzaldehyde (para-anisaldehyde), because even though the formula stays the same, the position of that methoxy group makes a big difference in how it reacts and behaves in various environments.
Over the years, I’ve watched colleagues reach for 2-Methoxybenzaldehyde when they need a reliable building block in complex syntheses. It plays an unsung role in making flavors, fragrances, and a surprising array of active pharmaceutical ingredients. One reason for this popularity comes from how it reacts: where other aromatic aldehydes might be sluggish or stubborn, 2-Methoxybenzaldehyde offers reactivity at just the right pace. It handles condensation, reduction, and nucleophilic addition without giving chemists more headaches than necessary.
Every batch of this compound should be taken seriously because not all 2-Methoxybenzaldehyde is created equal. Labs and factories gravitate toward material with high assay (above 98%) and low moisture content, because small impurities can lead to surprises later in a multi-step sequence. I’ve seen someone throw away whole days of work because an unknown contaminant showed up right at the moment they tried to isolate their main product. In research or production, clarity and color are more than cosmetic—they can warn you about changes in purity or degradation.
Some suppliers try to pass off low-grade or poorly stored product with little thought about shelf life or stability. That’s why responsible teams pay attention to storage and work above room temperature only with good ventilation. Handling 2-Methoxybenzaldehyde may not demand a hazmat suit, but keeping the compound tightly sealed, away from light and heat, goes a long way to avoiding headaches both literal and chemical. Proper labeling and organized storage don’t just prevent mix-ups—they serve as a line of defense against costly mistakes down the road.
I remember the first time I saw a new route for a promising agrochemical intermediate that hinged on this compound. With the right expertise, 2-Methoxybenzaldehyde opens doors to robust reactions. Its electron-donating methoxy group makes the aromatic ring more active in electrophilic substitution, offering a gentle push that can simplify reaction planning. People often come across this attribute when looking to branch off from the old reliable methods based on benzaldehyde itself, especially if something more selective is the goal.
Compare it to its para- or meta-isomers, and the distinction pops up quickly. Ortho-anisaldehyde is more than another flavor molecule; it brings a different set of reactivity and selectivity to the table. Pharma researchers seem to appreciate that in fine synthesis, where even a small boost in reaction rate or change in byproducts can cut down on time, waste, and expense. And that’s no small feat in the era of green chemistry and cost control.
Across the broader landscape, you’ll spot 2-Methoxybenzaldehyde cropping up in reactions like the Perkin, Knoevenagel, and Wittig. Anyone who’s spent time troubleshooting why a reaction won’t go to completion after switching from para- to ortho-anisaldehyde understands the significance. That little shift changes both the electron density and the accessibility of the functional group, which translates into a new set of possibilities for downstream reactions. This difference matters more than people think—until it trips someone up in project planning.
While major chemistry advances tend to grab headlines, it’s worth noticing how often 2-Methoxybenzaldehyde pops up closer to daily life. In flavors and fragrances, its subtle spicy-sweet character underpins some notes in soaps and perfumes. The reason people don’t talk about it as much as vanilla or benzaldehyde is almost because of its reliability—it blends so smoothly, and works behind the scenes to balance out bolder scents.
Modern consumer products benefit from having predictable, safe building blocks, and here’s where 2-Methoxybenzaldehyde again shines. Safety data supports careful and responsible use, as it can cause irritation if handled clumsily. Regulatory bodies like the FDA and ECHA have evaluated it, and the key is using educated best practices instead of taking shortcuts. The clear labeling of containers, clean handling, and explicit instructions during any mixing or transfer help avoid the types of accidents that can undermine trust in supply chains.
Demand for fine chemicals ebbs and flows, sometimes in response to new pharmaceutical launches, sometimes because of changes in consumer trends. No matter the shifts, consistent quality remains a backbone for anyone building complex molecules from scratch. High assay, reliable odor profile, and low levels of associative impurities are all traits that separate dependable 2-Methoxybenzaldehyde from low-tier alternatives.
Any manufacturer working with this compound learns quickly that shortcuts in supply chain transparency don’t pay off. Batch-to-batch consistency helps both big and small teams streamline research, avoid surprise revalidation, and keep their overheads predictable. It pays in the long term to buy from sources with systems for traceability, documentation, and certifications like ISO or GMP. Colleagues in QA would often stress that they could tell when the procurement process paid extra care to the audit trail—problems went down, rework plummeted, and teams stopped dreading routine inspections.
Down through the years, public attention toward chemical safety has only tightened. In sectors that use 2-Methoxybenzaldehyde as a stepping stone, there’s no room for outdated processes or poor record-keeping. Developing alternative synthesis pathways that waste less solvent or avoid toxic reagents serves everyone—producers, workers, consumers, and the planet. Progress isn’t about cutting costs for its own sake; it’s about coupling efficiency with responsibility and accountability.
Some organizations have pioneered greener routes to 2-Methoxybenzaldehyde, including catalytic oxidation of 2-methoxytoluene or optimized direct formylation of anisole. These advancements aren’t just academic—they mean safer working environments and fewer emissions of unpleasant byproducts. The move toward renewable stock or reduced pressure methods is gaining traction as organizations face stronger regulations and more scrutiny from stakeholders.
Safety data often scares newcomers, but practiced hands know that with gloves, goggles, and respect, 2-Methoxybenzaldehyde causes few problems. Makers and users take extra steps to contain vapors, avoid spills, and ensure good air flow in workshops and labs. Waste should always go through proper collection and treatment routes—never down the drain or into regular trash—because the cost of cleanup outweighs the savings from any “short and quick” disposal.
Not every project with 2-Methoxybenzaldehyde goes off without a hitch. I’ve seen researchers run into shelf life issues from careless storage or see yields drop due to unnoticed impurities. These aren’t rare or freak events—they’re the small slip-ups that come from distractions, cut corners, or unclear communication. Teams that invest in steady, clear protocols and periodic retraining see fewer of these setbacks. Good habits form the invisible scaffolding that holds up any lab or production floor with a regular need for specialty aldehydes.
On the logistical front, dealing with transport and compliance continues to throw tricky hurdles. Air or sea shipments must account for the hazardous nature of aldehydes. Paperwork, customs documentation, and labeling all matter. Working with brokers and carriers who know the score keeps transit smooth. Delays mean more than just lost time—they can impact the product’s shelf stability and effectiveness once it finally hits the site. I’ve learned over time that every hour extra in uncontrolled conditions can shave weeks or months off a bottle’s useful life.
One middle path that’s worked for teams I’ve worked with has been to build small safety stocks and to form purchasing partnerships with suppliers invested in transparent communication. These networks, including reputable distributors, not only warn about disruptions but help clients adapt without major losses. In markets prone to price fluctuations, planning ahead with dual sourcing or even local stock production can guard against unpredictable surges that hit small players hardest.
People sometimes ask what sets 2-Methoxybenzaldehyde apart from other benzaldehyde-related options. The answer rarely sits only in the lines of a data sheet. In actual practice, the ortho-isomer’s reactivity, lower toxicity, and more moderate odor profile make it both versatile and less of a headache in everything from bench-top R&D to scaled-up applied manufacturing.
If you’ve ever used benzaldehyde, you quickly realize that while it’s a useful starting point, it lacks the added value that the methoxy group brings. That single oxygen—tucked onto the ring in the two-position—nudges the reactions along, sometimes giving smoother product formation or affording a more direct synthesis. Parallels to other isomers, like para-anisaldehyde, reveal subtle and not-so-subtle differences in both performance and end-use applications. The ortho form tends to be chosen when selectivity is crucial or where steric effects are needed to block side reactions.
Cost, shelf life, and availability matter too. Certain farm chemical manufacturers have told me that even a couple of percent drop in starting material purity can tank downstream yields. They stick to reliable 2-Methoxybenzaldehyde and find the investments worthwhile because headaches from failed batches far outstrip the up-front costs. It’s a story I’ve heard echoed from contract research organizations all the way up to big-name pharma and home-care manufacturers.
Universities and small spin-off startups are always on the hunt for flexible reagents that let them juggle timelines and resources. 2-Methoxybenzaldehyde gets tapped for everything from the synthesis of heterocyclic scaffolds—indoles, benzofurans—through to prodrugs and advanced intermediates. Its ability to steer reactions with moderate direction but strong enough electron-pushing effect works in favor of exploratory chemists working at the frontiers of what’s possible.
Graduate students, under pressure to publish, lean on the reliability of a well-handled bottle shipped with certainty. Professors with more years in the game value how it opens up routes to compounds that show up in nature, as well as non-natural analogs aimed at understanding fundamental mechanism. More than a placeholder, 2-Methoxybenzaldehyde underlies progress in building block chemistry, feeding both basic and applied science.
Several projects over the last decade have taken advantage of its manageable reactivity. For example, its selective reactions with amines to form Schiff bases or imines make it ideal for molecular scaffolds. In organic electronics research, it’s even served as a precursor to certain aromatic polymers and dyes. Here, even the byproducts don’t go to waste, with downstream recovery and recycling possible for advanced workflow operations.
Behind the science, you find stories. Take a specialty fragrance designer searching for a soft, lasting almond note that won’t overpower the rest of the blend. Or a process chemist working on fine-tuning an API for time-release drugs who finds that the ortho-isomer delivers a cleaner route to the desired impurity profile. It’s the kind of tool that ends up at the center of a lot of real-world breakthroughs, yet rarely gets the spotlight—except among those who know what it truly offers.
In my experience, working with students just starting out or teams pushing at the limits of environmental responsibility, 2-Methoxybenzaldehyde has provided a bridge between the practical and the innovative. Having a product that’s stable, easy enough to measure and handle, but powerful in its chemistry opens up new research directions with confidence instead of hesitation. Instead of worrying about repeatability, teams can focus on discovering and refining the solutions that matter most to their work.
Interest in compounds like 2-Methoxybenzaldehyde is only bound to grow. Pressures for cleaner, safer processes mean that reliable, well-understood chemicals will stay in the foreground as regulators, consumers, and innovators all push for greater transparency and better performance. The trend now is to source materials with data packages that include traceability, safety, and carbon footprint, with regular third-party audits. An era where procurement and research labs communicate more openly ensures fewer mistakes and safer, higher-yield projects.
Scaling up new routes for sustainable production could bring down costs and open new markets. As knowledge and best practices spread, expect demand for not only the product itself but more information about where and how it’s made. Fully digitized tracking and open data for purity, supply chain origin, and safety history will set apart premium producers. Consumers of every size will come to expect that buying a bottle means access to everything from synthesis path to full environmental impact disclosure.
Small businesses, educational labs, and big industry players alike will rely on solutions that combine chemical know-how with responsible stewardship. 2-Methoxybenzaldehyde stands ready for the role—tested, trusted, and in steady demand for good reason. Its record as a safe, useful compound is built on real experience, real outcomes, and a widespread willingness to keep improving how we make and manage the chemicals that drive discovery and invention.