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HS Code |
896309 |
| Chemical Name | 2-Hydroxy-4-Methoxybenzaldehyde |
| Molecular Formula | C8H8O3 |
| Molar Mass | 152.15 g/mol |
| Cas Number | 673-22-3 |
| Appearance | White to pale yellow solid |
| Melting Point | 110-113°C |
| Boiling Point | 317°C |
| Density | 1.24 g/cm³ |
| Solubility | Soluble in ethanol, ether; slightly soluble in water |
| Pubchem Cid | 6926 |
As an accredited 2-Hydroxy-4-Methoxybenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle labeled "2-Hydroxy-4-Methoxybenzaldehyde" with hazard symbols, batch number, and tightly sealed screw cap. |
| Shipping | 2-Hydroxy-4-Methoxybenzaldehyde is typically shipped in tightly sealed containers to prevent contamination and moisture absorption. It should be packed according to chemical safety regulations, labeled appropriately, and kept away from incompatible substances. Transport conditions should avoid extremes of temperature, ensuring stability and safety during transit. Always refer to the relevant MSDS for detailed handling instructions. |
| Storage | 2-Hydroxy-4-Methoxybenzaldehyde should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature. Proper labeling and adherence to standard chemical storage protocols are recommended to ensure safety and maintain the compound’s stability and purity. |
Applications of 2-Hydroxy-4-Methoxybenzaldehyde in Industrial ManufacturingOur factory-grade 2-Hydroxy-4-Methoxybenzaldehyde directly supports demanding industrial production in sectors where its unique aldehyde and phenolic structure delivers critical performance characteristics. As a primary manufacturer, we enable consistent supply at strict quality benchmarks to customers who integrate this raw material across several well-established downstream applications. Below are the most relevant, real-world use cases, broken down by end-market with key regulatory, formulation, processing, and finished product details. 1. Fragrance Ingredient in Fine PerfumerySpecialty fragrance houses use this compound to introduce a delicate floral-vanillin nuance into high-end perfume bases, especially targeting feminine and oriental scents. Our product’s stability and moderate volatility suit both concentrate and finished format production, with its addition generally occurring during the compounded oil phase. Compliance with international perfume regulations is essential for market access. Industry compliance standards
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2. Pharmaceutical Intermediate for Antihypertensive APIsAPI manufacturers utilize this selective aldehyde as a protected aromatic building block in the synthesis route for certain antihypertensive agents, including some angiotensin-converting enzyme (ACE) inhibitors. The material’s purity and controlled reactivity are crucial during condensation and cyclization steps in the plant’s multi-step API production flows. Entry into regulated markets requires adherence to pharmacopoeia and GMP benchmarks. Industry compliance standards
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3. UV Absorber Precursor in Sunscreen ManufactureSunscreen manufacturers leverage this compound as a key starting material in the synthesis of methoxysalicylate-based UV filters. Its functional group arrangement provides an essential intermediate block in the formation of long-lasting, photostable UVB absorbers. All processing follows cosmetic ingredient regulations and phototesting protocols to ensure safety in sun care finished goods. Industry compliance standards
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4. Synthetic Flavor Intermediate in Food Additives ProductionFood additive producers employ this aldehyde as an essential aromatic intermediate in the synthesis of vanilla and spicy-floral flavoring agents for beverages, confectionery, and bakery products. Batch formulation must ensure compliance with strict food additive identity and safety standards, with full traceability throughout production and downstream blending before finalized into consumer-ready goods. Industry compliance standards
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5. Specialty Dye Intermediate for Textile ColorantsColorant manufacturers source our material as a critical intermediate in the synthesis of selective azo and anthraquinone dyes. Its chemical behavior supports condensed-phase reactions for stable, high-purity dye molecule generation, which textile processors then apply through either exhaust or continuous dyeing systems. Regulatory frameworks govern both the dye’s chemical composition and the absence of prohibited impurities in garment-grade products. Industry compliance standards
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Decades of hands-on work with aromatic aldehydes have shown us that subtle changes in molecule structure transform not just performance, but the very attitude of the raw material in application. 2-Hydroxy-4-Methoxybenzaldehyde tells this story better than most. Its molecular formula—C8H8O3—sets it apart right from the start. A simple shift of functional groups opens paths for manufacturers who value reliability and chemical integrity. The product known in labs and by seasoned chemists as “para-anisaldehyde” may look like a cousin, but once on the production line, the distinction stands out. Our daily manufacturing experience has shown this difference can mark success or failure in downstream reactions.
Through real-world production runs, we have become familiar with the specific conditions and requirements this compound puts on both our reactors and our people. We have refined our process to yield a crystalline product with high purity and consistency. By focusing on batch quality and thorough process monitoring, we guard against the kind of variability that ruins larger batches or leads to rejections down the line. Laboratory chemists and industrial formulators require that when they source 2-Hydroxy-4-Methoxybenzaldehyde from a manufacturer, they see the same melting point, purity, and performance time and again. Experience with variable, outsourced input materials in the past taught us that sticking to well-tuned synthesis parameters reduces headaches for everyone downstream.
We see a clear distinction between this aromatic aldehyde and others in its family. The addition of a methoxy group at the para-position relative to the hydroxyl transforms how the molecule behaves in both organic synthesis and product outcomes. During experimental trials, research teams found that the specificity of reactivity—especially in condensation and coupling reactions—creates avenues for new possibilities in complex molecule design. Compared to simple vanillin or salicylaldehyde, 2-Hydroxy-4-Methoxybenzaldehyde introduces a unique electron distribution, which, as we’ve observed, helps to moderate reactivity, making it a more controllable intermediate.
We have settled on a model that delivers the material as a fine, free-flowing crystalline powder, with a typical purity greater than 99% as measured by HPLC and NMR. Every batch goes through on-site testing; trained specialists analyze melting point, water content by Karl Fischer, and color index. Extended work with customers in the pharmaceutical and flavor industries has made us attentive to even minor impurities—trace isomer formation or residual solvents found in lower-grade materials can throw off both synthesis yields and product quality. Through systematized quality control and continual investment in our analytical facilities, we’ve been able to address this shared pain point.
You learn quickly in this business—few raw materials actually “just go anywhere.” 2-Hydroxy-4-Methoxybenzaldehyde’s structural features enable nuanced performance, especially in industries focusing on fine fragrance, advanced pharmaceuticals, and analytical chemistry. In the laboratory, its dual functional groups make it a reliable building block for complex synthesis. Synthetic chemists, not content with broad-strokes characterization, repeatedly highlight the molecule’s impact on reaction selectivity—its ability to push a reaction “just right” when stronger or less predictable aldehydes cannot. Several major aromatic compounds in both pharma intermediates and flavoring chemicals derive their backbone from its selective reactivity.
Our work with fragrance and flavor manufacturers has underscored the difference between this product and more common benzaldehyde derivatives. At low concentrations, 2-Hydroxy-4-Methoxybenzaldehyde imparts a sweet, warm odor profile—useful for perfumers seeking complexity beyond the basic notes of vanillin. The phenolic undertone, mellowed by the methoxy group, opens up space for fresh accords without drowning out delicate top notes. Over time, we have seen the appreciation for this compound grow among formulators aiming for signature profiles not possible with standard aldehydes.
Pharmaceutical processors and R&D centers value this product for a different reason. The molecule enables the preparation of heterocycles under mild conditions. Over the past five years, we have seen a surge in requests from researchers looking for reliable materials to support new antitumor and antimicrobial agent development. The ortho-hydroxy and para-methoxy substitutions favor selective reactions, especially in Knoevenagel condensations and Mannich-type reactions, giving rise to a broader palette of possible ligands and scaffolds.
Consistency, from the manufacturer’s perspective, emerges only with commitment to tight process control—something we have built over time through batch logging and rapid-issue troubleshooting. 2-Hydroxy-4-Methoxybenzaldehyde synthesis poses unique purification challenges. Small errors in pH adjustment or timing during extraction steps allow side products or unwanted isomers to slip through. These contaminants bring unpredictability down the value chain, whether in scaled-up pharmaceutical runs or specialized aroma ingredient production.
Continuous improvement in our recrystallization and drying methods has meaningfully impacted the quality and shelf-stability of the product. We rejected the cheaper approach—skip controlled drying, let a bit of moisture remain, and scale up fast—after years of hearing from frustrated formulation specialists who noticed inconsistency. We now ensure that all material is thoroughly dried and stored under inert atmosphere. Moisture control is particularly important for this aldehyde, as even trace water can initiate self-condensation or hydrolysis over months of storage. Real-world trials and feedback from loyal customers have repeatedly confirmed this approach: dry, stable powder makes all the difference in long-term results.
We have fielded many questions from formulators about the difference between 2-Hydroxy-4-Methoxybenzaldehyde and parallel compounds. Unlike vanillin, which also contains a methoxy and hydroxy substitution but at different positions, our product displays markedly different chemical behavior. Take comparative condensation reactions as an example. The ortho relationship between the hydroxy and formyl favors chelation and internal hydrogen bonding, which affects both solubility and reactivity in larger molecule assembly. We have noticed that in developing certain advanced ligands or dye intermediates, only our product delivers the selectivity needed at industrial scale.
Some clients in analytical supply chains have experimented with cheaper ortho- or meta-substituted alternatives. Over time, most return to ask for our product again—typically because the yield or analytical purity of their targets dropped when switching away. The cost savings rarely compensate for the time lost troubleshooting reactions or cleaning up unexpected byproducts. Our experience with repeated scale-up batches supports this: the specific arrangement of groups on the aromatic ring is key, and knock-off or misidentified materials create more problems than they solve.
Part of our responsibility as a manufacturer involves not just making a pure product but also conveying knowledge gained by day-to-day handling. Personnel who directly interact with the product report that, compared to some related aldehydes, this material emits a noticeably less pungent odor and carries lower volatility, making for safer, friendlier processing environments. Dust control becomes more manageable; clumping and caking, issues that crop up with certain similar compounds, have not presented persistent problems, thanks to active focus on moisture management in packaging and logistics. We have learned to supplement our packaging with additional desiccants in humid seasons, which keeps the product free-flowing from our plant to our customers’ sites.
Another point worth sharing from our experience is storage. Our technical teams noticed that minor lapses—incautious exposure to heat, UV, or oxygen—speed up the yellowing of the powder and reduce shelf life. Regular refresher training for warehouse staff and collaborative feedback with long-term buyers have prompted small, critical changes. All containers are now nitrogen-flushed and vacuum-sealed before leaving our doors. This keeps the aldehyde from degrading, improving both the product’s longevity and reliability in your own applications.
Continuous production means continuous learning. In the early years, we encountered some stubborn roadblocks during scale-up. The key challenge lay in controlling side reactions—especially unwanted oxidation and oligomerization, both of which depleted yields and complicated purification. Incremental process refinements served as turning points: adjusting temperature profiles by a few degrees, switching to more robust reaction vessels, and improving the efficiency of downstream washing steps.
Investments in process analytical technology have delivered gains in both safety and efficiency. Sensors positioned throughout our reactors monitor not only temperature, but also pressure and pH in real time. This data-driven approach allows us to respond instantly if any parameter escapes its defined window. Several production runs benefited from this real-time control, especially on high-volume orders where a small slip does not escape detection for hours.
Our technical managers flag solvent selection as a persistent issue. Many routes to 2-Hydroxy-4-Methoxybenzaldehyde rely on environmentally sensitive solvents, and substitutes often impact product yield or downstream waste treatment. In the past several years, sustainability considerations have pushed us to switch to greener solvents and recover solvents onsite for reuse. Although the up-front investment stung at first, the reduced regulatory burden and long-term operational savings have vindicated this decision. Communication with local regulators and a willingness to open our factory for inspections have streamlined our certification processes and built trust in our community.
On a people level, cross-training our operators has had a noticeable impact. Instead of compartmentalizing knowledge about one step or another, operators rotate between tasks and develop a full-picture understanding of the entire synthesis and purification pipeline. They spot potential problems sooner; a small error caught in reaction setup or distillation averts a night’s worth of wasted material. Turnover dropped and pride in the workplace improved—a virtuous cycle that our customers feel through better batch reliability and supply continuity.
Years of conversation with research scientists and industrial engineers continually reinforce the practical appeal of 2-Hydroxy-4-Methoxybenzaldehyde: reactivity, selectivity, and sensory function line up in a single molecule. Many specialty organics demand exactly this, and nowhere more so than in pharmaceuticals and flavors where the cost of rejects or reformulations bites hard. This molecule’s predictable behavior in condensation and cyclization puts power in the hands of synthetic chemists, letting them experiment confidently.
From the perspective of a working manufacturer, we focus not only on chemical structure but also on the lived experience and outcomes. We have seen how careful control of parameters—raw material integrity, process analytics, operator skill, moisture management, and storage best practices—combine to yield an aromatic aldehyde that is more than just a passing entry in a reagent catalog. The product integrates into workflows for fine fragrances, specialty medicines, and labeling agents, each setting distinct requirements which our production lines have become accustomed to meeting.
The differences between products like 2-Hydroxy-4-Methoxybenzaldehyde and similar aldehydes often emerge not on paper, but at the bench or during the shift. Clean synthesis, stable storage, and direct manufacturer support count for more than generic purity specs. Customers rely on our team’s practical advice for integrating the material, minimizing losses, and troubleshooting hiccups—whether it is a purification setback in a pilot plant or an unexpected color change in storage. Our knowledge, earned batch by batch and problem by problem, feeds into every order that leaves our plant.
Throughout the time we have produced and shipped this compound, we’ve witnessed shifting industry needs, from stricter regulatory guidelines to the demand for alternative intermediates for niche therapeutics and to complex fragrances. Our response has been to keep lines of communication open, to listen when something doesn’t work in a customer’s process, and to adapt both our product and service model as needed.
Long-running collaboration with clients—from boutique fragrance houses to multinational pharma R&D—spotlights the importance of rapid troubleshooting and willingness to innovate. Our regular shipments support projects ranging from small-scale synthesis to multi-ton scale-up, yet we stay grounded in the realities of custom needs: sometimes it’s tighter particle size distribution, other times it’s a shift away from certain process solvents, or even advice on optimizing batch filtration. Most questions have answers rooted in everyday production know-how, not marketing promises.
Customers have come to us with requests for documented trace impurities, assistance in regulatory dossier preparation, or even access to reserved production lines for short-turnaround orders. Having direct control over process flows and QC labs allows us to accommodate these requests without the delays or loss of batch traceability often seen with intermediaries. In practical terms, this means problems can be solved quickly and honestly, with feedback loops right back to the manufacturing team.
We expect a steady increase in demand for 2-Hydroxy-4-Methoxybenzaldehyde, driven by advances in medicinal chemistry and growing sophistication in fragrance and flavor development. The demand for technical guidance and consistent supply rarely slows. Our commitment remains to standing by the workhorse values: producing a stable, high-purity batch, confirming every lot’s identity by robust analytical methods, and maintaining open conversations with everyone who relies on what we make.
Though technology continues to advance, it’s the cumulative collection of lessons—what works, what backfires, and what keeps the line moving—that gives manufacturers like us the edge. Every batch of 2-Hydroxy-4-Methoxybenzaldehyde that ships from our facility carries this history, and our customers see it in both product performance and the support that comes bundled with every drum and every technical inquiry.