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HS Code |
455249 |
| Iupac Name | 2-hydroxy-5-methoxy-3-nitrobenzaldehyde |
| Molecular Formula | C8H7NO5 |
| Molar Mass | 197.15 g/mol |
| Cas Number | 50816-92-3 |
| Appearance | Yellow crystalline powder |
| Melting Point | 143-146°C |
| Solubility In Water | Slightly soluble |
| Smiles | COC1=CC(=CC(=C1O)[N+](=O)[O-])C=O |
| Storage Temperature | 2-8°C (cool, dry place) |
| Purity | Typically >98% |
| Synonyms | 5-Methoxy-2-hydroxy-3-nitrobenzaldehyde |
As an accredited 2-Hydroxy-5-Methoxy-3-Nitro-Benzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2-Hydroxy-5-Methoxy-3-Nitro-Benzaldehyde, sealed with a secure cap and labeled for laboratory use. |
| Shipping | **Shipping Description for 2-Hydroxy-5-Methoxy-3-Nitro-Benzaldehyde:** Ship in tightly sealed containers, protected from light and moisture. Store at room temperature. Handle following standard chemical safety protocols. Ensure compliance with local, national, and international chemical transport regulations. Include appropriate hazard labeling and documentation. Avoid shipping with incompatible substances such as strong oxidizers or reducing agents. |
| Storage | 2-Hydroxy-5-Methoxy-3-Nitro-Benzaldehyde should be stored in a cool, dry, well-ventilated area away from direct sunlight, moisture, and sources of ignition. Store the chemical in a tightly sealed container, clearly labeled, and compatible with organic compounds. Avoid contact with strong oxidizing agents and acids. Follow all relevant safety protocols and consult the safety data sheet (SDS) for specific instructions. |
Applications of 2-Hydroxy-5-Methoxy-3-Nitro-Benzaldehyde in Industrial ManufacturingOur production facilities supply 2-Hydroxy-5-Methoxy-3-Nitro-Benzaldehyde to specialist industries demanding precision building blocks for advanced synthesis. We service formulations and processors with consistent grade, ensuring process compatibility and regulatory alignment in multiple high-value segments. 1. Pharmaceutical Intermediate SynthesisLeading pharmaceutical manufacturers use this compound as a crucial intermediate in the synthesis of selective active pharmaceutical ingredients, particularly within anti-inflammatory and antimicrobial agent families. Its functional groups enable introduction at defined condensation or cyclization stages, where purity and isomeric stability are critical for the downstream production of validated APIs. Industry compliance standards
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2. Agrochemical SynthesisMajor agrochemical companies adopt our product for use as an advanced intermediate in the production of complex herbicide and fungicide molecules, especially those requiring specific nitrobenzaldehyde scaffolds. The controlled methoxy and hydroxy substitution enables robust performance in nitration-coupled synthesis, facilitating scalable batch consistency and process troubleshooting. Industry compliance standards
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3. Dye Intermediate ProductionColorants and specialty dyes producers utilize this molecule as a key intermediate in the synthesis of select azo and anthraquinone derivatives. Its unique substitution pattern enables targeted electrophilic aromatic substitution, critical for pigment and dye matrix assembly with precise chromatic output. Industry compliance standards
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4. Specialty Chemical and Fragrance Building BlockResearchers and manufacturers within flavor and fragrance intermediates utilize this aromatic aldehyde for controlled synthesis of complex aromatic motifs. Its defined substitution allows incorporation into fragrance precursor chains or as a masking note within specialty blends, following rigorous purity and character validation for downstream olfactory attributes. Industry compliance standards
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Standing in the daily bustle of our manufacturing plant, we come across specialty benzaldehydes in all forms, but few draw the hands-on attention like 2-Hydroxy-5-Methoxy-3-Nitro-Benzaldehyde. Each batch we produce, from raw materials to packed drums, reflects the careful chemistry and practical knowledge shaped by decades in our field. Many in the lab know it by its structure: a benzaldehyde core, decorated with a nitro group, hydroxy, and methoxy substituents. We recognize it first for its value as a versatile intermediate, but real appreciation grows from direct experience. End-users will often ask about the details or what sets this aldehyde apart—we find the answers lie in both the structure and in its consistent performance in day-to-day production.
On our lines, the typical specification for 2-Hydroxy-5-Methoxy-3-Nitro-Benzaldehyde tightly controls for moisture, color, and purity—always a minimum of 98% by HPLC. The off-white to light yellow crystalline powder signals a successful synthesis, while unwanted tints act as red flags for us in quality control. Trace metals or color impurities have ruined many potential syntheses in our pilot runs, so our team maintains rigorous attention to purification. Every lot is packed under dry, inert atmosphere to limit oxidation, and we ensure stability during shipment through lined fiber drums. Many buyers request particle size distribution, but for most syntheses downstream, the focus rests on purity and the absence of residual solvents. Finished product carries a faint, sharp aromatic odor, a telltale sign that prompts anyone familiar to give it a nod of recognition.
We’ve experimented with various synthetic pathways for target molecules like this one. Our chemists long since moved away from inefficient nitration sequences with unpredictable regioselectivity or byproduct profiles. Today, strict in-house control over starting phenols and ortho-para directing groups keeps each run on target. Even subtle changes in sodium nitrite addition or methoxylation temperature reveal themselves later, sometimes visibly, sometimes only as shifts in analytical chromatograms. We’ve learned that minimization of byproducts such as dinitro-compounds not only streamlines our own filtering process but gives downstream users fewer headaches during later-stage functionalizations. Less clean-up afterwards means improved overall yields for everyone in the supply chain.
The largest share of our product doesn’t stay with us. We supply several national and international customers, ranging from research institutions working on new active pharmaceutical ingredients, to fine chemical companies developing specialty dyes or antioxidants. This nitro-benzaldehyde is a privileged intermediate in many lines of work. Its specific substitution pattern enables direct engagement of both nucleophiles and electrophiles, providing a scaffold to build out a wide variety of downstream products. Our partners have used it as a valuable building block in the synthesis of heterocycles, including benzoxazoles, which emerge from condensation with o-aminophenols. In our own test runs, we’ve seen the hydroxy and methoxy groups activate the ring toward such ring-closing reactions, and the position of the nitro group modulates both electronic and solubility profiles of new molecules grown from this scaffold.
Our most frequent feedback comes from R&D teams working in early-stage drug discovery. Medicinal chemists exploit the ortho-hydroxy and methoxy moieties, knowing that these functional groups provide direct opportunities for coupling and derivatization. The nitro group, at the meta position relative to the formyl, makes it possible to introduce amine functionality by reduction, inserting new diversity points in SAR campaigns. In-house, we’ve seen clean reductions to amines under mild conditions, opening new routes to Schiff bases and other analogues. Several research groups have published on the use of this compound in aromatic amination and ligand elaboration work. Across our own bench experiments, we observe low byproducts and dependable reactivity, two points our chemical engineers value in every campaign.
There’s no shortage of benzaldehyde derivatives in the catalogues, but the combination of hydroxy, methoxy, and nitro at carefully chosen sites sets this product apart. A starting point like plain vanillin or even ortho-hydroxy-benzaldehyde cannot substitute for the unique combination of reactivity. The placement of the methoxy group at the 5-position, hydroxy at 2-position, and nitro at 3-position creates a scaffold with pronounced electron demand in specific locations—something basic salicylaldehydes lack. In practical runs, we watch downstream functionalizations snap into place quickly where classical substrates drag or suffer from overreaction. Our QA team regularly compares spectra with other industry standards; shifts in NMR and IR validate the influence these substituents provide to the aromatic ring.
Any chemist working at kilo scale quickly learns which products present trouble. We handle this benzaldehyde with standard personal protection—gloves, goggles, and fume hoods. Its crystalline nature favors straightforward weighing and transfer without the airborne dust problems some fine powders create. Over the years we’ve catalogued our own observations on thermal stability; once past 110°C, decomposition begins, stressing the need for moderate processing conditions. The nitro group bestows both utility and a caution flag: while not shock-sensitive, we never treat nitro aromatics lightly. Safe solvent choices—typically dichloromethane or ethyl acetate—have made all the difference in minimizing exposure and ensuring batch-to-batch reproducibility.
Colleagues in the industry can share tales of trouble from poorly defined sources. Some market offerings, especially those sourced from resellers or unverified traders, arrive with a shadowy impurity profile—not always a deliberate problem, sometimes just a symptom of short-cuts in originating factories. Direct-from-manufacturer procurement avoids these pitfalls. By producing in-house, we close every loop from starting materials to finished goods, catching subtle deviations in melting point, color, or assay well before the product reaches downstream partners. A few cost-cutters dilute or adulterate with less expensive aldehyde derivatives, but our process-focused approach overcomes these temptations. The end-use feedback we receive provides a real-world test bench for what we ship.
Every large-scale process generates discussion about sustainability and compliance. This nitro benzaldehyde’s synthesis doesn’t lend itself to zero-waste perfection, but continuous improvement in waste minimization carries real-world benefits. We engineer each reaction step for maximum atom economy, reclaim spent solvents for reuse, and neutralize effluents on-site under precisely monitored conditions. Regulatory scrutiny on aromatic nitro compounds has grown in recent years—not just for export, but for internal responsible care, too. Our compliance team remains in step with local and international statutes, supplying detailed batch and regulatory information to our customers by habit, not by exception. Worker health, effluent standards, and air quality get careful attention during every inspection. We’ve adopted improvements suggested by external audits, adding scrubbers and more nuanced control of process temperatures to mitigate air emissions. We know customers are watching, and likewise, so are our employees and neighbors.
Some materials scale up easily; this one asks for more care. Exothermic steps and hazardous reagents prove manageable in glassware, but new variables appear at 200 kilos. Over time, we’ve remodeled reaction vessels and optimized mixing speeds to prevent hotspots during key additions, especially during the nitration and methylation steps. We track not just yield, but also the energy input and downtime between runs. In upstream procurement, market fluctuations in phenolic starting materials sometimes squeeze margins, meaning process efficiency matters to everyone—not just to management, but to every operator on the plant floor. Few appreciate how a short supply of a single intermediate can ripple through an entire multi-step contract, impacting timelines for pharma and specialty chemical makers. For our part, direct lines of communication with our regular buyers help everyone stay focused and prevent surprises.
We’ve learned the most from direct field feedback. Some customers want the option for custom packaging, down to the net weight and drum lining. Others, focusing on detailed regulatory compliance, request certificates of origin or full traceability to starting materials. A few use this benzaldehyde in syntheses sensitive to residual metal content, so we maintain optional analytical data sets for trace elements, adjusting purification methods as needed. When buyers encounter difficulty in dissolving or transferring the solid, we look for practical fixes—be it modified milling, anti-caking agents, or tailored particle size. The best results stem from collaborative troubleshooting, where we are not merely vendors but partners invested in their manufacturing success.
Chemical manufacturing rarely stands still. The demands of research and specialty product development continue to shift the expectations for purity, handling, and documentation. We’ve begun experimenting with bio-based phenolic sources, not simply as a nod to green chemistry but because supply stability and cost control matter to long-term buyers. Automated real-time analytics are entering our QC workflow, speeding release times and catching deviations more proactively. Feedback from pharmaceutical partners has us exploring additional high-purity grades with even tighter residual solvent and transition metal limits. Down the road, some sectors may require solid state forms or novel co-crystals, which will draw on our existing platform but push us to rethink drying, milling, and storage strategies.
Conversations around aromatic nitro compounds sometimes fixate on regulatory hurdles, but real progress comes from long-term commitment to in-house process improvement and transparent supplier relationships. We listened when customers voiced frustration over mystery impurities or delivery delays; those lessons shape batch scheduling and procurement policies today. In supply routes—especially for pharmaceutical and fine chemical applications—traceability isn’t a luxury, it is a baseline requirement. So, we invested not just in new instrumentation, but in people: training plant operators to troubleshoot not just the equipment but the chemistry and documentation that come with every container produced. We believe every improvement to process reliability ultimately benefits everyone from our own team to end users at R&D labs across the world.
Years of producing and refining 2-Hydroxy-5-Methoxy-3-Nitro-Benzaldehyde have shown us the importance of attention to detail and responsiveness to customer needs. Trackable quality, well-documented process adjustments, and practical handling experience distinguish our material in a global market crowded with offerings that look similar at a glance but diverge on closer use. Teams working downstream rely on the assurance that this nitro benzaldehyde, packed and shipped directly from our line, offers predictable behavior batch after batch. As regulatory requirements, customer applications, and scientific standards evolve, we see our role as continuing to build trust—not just through specification sheets, but by standing behind our product and adapting together with our partners. For us, delivering this compound means delivering on the full promise of our manufacturing experience.