|
HS Code |
561270 |
| Chemical Name | 2,4-Dichloro-6-Hydroxybenzaldehyde |
| Cas Number | 34887-76-6 |
| Molecular Formula | C7H4Cl2O2 |
| Molecular Weight | 191.01 g/mol |
| Appearance | Pale yellow solid |
| Melting Point | 142-146 °C |
| Boiling Point | No data available (decomposes) |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Density | 1.49 g/cm³ (approximate) |
| Smiles | C1=C(C=C(C(=C1Cl)O)Cl)C=O |
| Synonyms | 2,4-Dichloro-6-formylphenol |
| Storage Conditions | Store in a cool, dry, well-ventilated area |
| Refractive Index | No data available |
| Hazard Class | Irritant |
As an accredited 2,4-Dichloro-6-Hydroxybenzaldehyde 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 2,4-Dichloro-6-Hydroxybenzaldehyde, sealed with a screw cap and detailed hazard labeling. |
| Shipping | 2,4-Dichloro-6-Hydroxybenzaldehyde is shipped in tightly sealed containers, protected from light and moisture. It is packed following hazardous material regulations, with clear labeling and safety documentation. Handling precautions are observed to avoid spillage or contamination. Temperature control may be used to ensure product stability during transit. |
| Storage | 2,4-Dichloro-6-Hydroxybenzaldehyde should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect it from light and moisture. Ensure the storage area is free from ignition sources, and always label the container appropriately. Use personal protective equipment when handling to prevent skin and eye contact. |
Applications of 2,4-Dichloro-6-Hydroxybenzaldehyde in Industrial ManufacturingAs a direct manufacturer of 2,4-Dichloro-6-Hydroxybenzaldehyde, we supply this intermediate for advanced synthesis in multiple specialized sectors. Below, we detail its principal applications, compliance frameworks, and integration into downstream processing and end products. 1. Pharmaceutical Intermediate for Anti-Infective AgentsLeading API facilities use this raw material as a key building block in the synthesis of various anti-infective compounds, especially for second-generation antibacterial formulations. It serves both as an electrophilic aromatic precursor and a custom-tailored functional group source for complex ring closures, supporting targeted functionalization in proprietary synthetic routes. Process control ensures full compliance with pharmacopoeial impurity profiles for regulated environments. Industry compliance standards
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2. Agrochemical Synthesis: Herbicide and Fungicide Key IntermediateFormulators in the crop protection industry rely on this compound for step-growth integration into selective herbicide and systemic fungicide actives. Its dichlorinated structure provides a scaffold for subsequent halogen exchange, O-alkylation, and oxidative coupling, allowing for high reaction yields and the creation of products with minimal residual contaminants. Production lines align release specifications with major agrochemical regulatory listings. Industry compliance standards
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3. Dye Intermediates for Performance PigmentsIn the industrial pigments sector, manufacturers incorporate this raw material as a key aromatic aldehyde donor during the synthesis of azo, anthraquinone, and heterocyclic dye classes. It enters high-pressure batch reactors paired with amines, regulating chromogenic properties and fastness in the final pigment. Process validation ensures compliance with global colorant regulations, especially for export-bound functional textiles and plastics. Industry compliance standards
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4. Chemical Reagent for Material Science R&DIn advanced material laboratories, this aldehyde finds use as a precursor in synthesizing tailored functional polymers, metal-organic frameworks, and sensor molecules. Research institutions and in-house pilot plants use it for ligand design, surface modification, and as a controlled aldehyde source in condensation polymerizations for specialty polymers with defined electronic or adsorption behaviors. Full traceability in sourcing is maintained to meet public funding and institutional audit requirements. Industry compliance standards
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Direct hands-on production of 2,4-Dichloro-6-hydroxybenzaldehyde gives a unique perspective on how this compound fits into both daily chemical practice and the broader world of fine chemistry. Synthesizing this benzaldehyde runs beyond pressing a button; there is a definite satisfaction involved in watching high-purity white to light tan crystalline solid emerge from a controlled sequence of chlorination, oxidation, and purification steps. Confidence stems from direct batch analysis, visible yield consistency, and robust control of impurity profiles.
The end result: a batch of 2,4-Dichloro-6-hydroxybenzaldehyde, typically offered in purity upwards of 98%. Melting point ranges sit tightly within controlled limits. Each lot delivers full traceability from raw material origin through every filtration and crystallization. There’s no ambiguity about what is in the drum or the bottle, and that precision translates directly into reliability when customers place their orders.
Experience with this aldehyde teaches a lot about practical applications. The most frequent requests come from companies synthesizing advanced pharmaceutical intermediates, specialty pigments, or agrochemical building blocks. 2,4-Dichloro-6-hydroxybenzaldehyde carries two tightly positioned chlorines and a phenolic hydroxyl, flanking the aldehyde group at precise ortho and para locations. This structure is no accident—it underpins the molecule’s success as a foundation for downstream reactions, particularly coupling and condensation, often through the hydroxyl and formyl functionalities.
Long-standing clients appreciate the viability of this compound as a platform for building more complex heterocyclic rings—get the placement of the functional groups right, and the difference in reaction rates or product yields quickly becomes apparent. Working directly with the compound day after day, one learns to spot slight variations in powder color or faint changes in aroma that point to differences from other isomers or from analogues bearing methyl or acetyl substituents in place of halogens.
Real assurance only happens because of repeated, daily quality checks: melting points align batch to batch within the 100–102 °C range. TLC and HPLC methods keep trace impurities well below 1%, with most batches providing even higher standards than typical benchmarks for specialty chemicals. Moisture is kept low, checked by Karl Fischer titration, especially for sensitive applications; this extra step saves headaches for downstream catalysis and Grignard reactions.
Packing can vary—our drums or bags are driven by customer preference as much as logistics. No elaborate packaging stories. The focus always rests on keeping the product dry, shielded from sunlight, and secure in sealed liners for transit. Years in the warehouse have shown how moisture or ambient temperatures can stress quality, so shipments leave our facility only after multiple checks. Direct feedback from end-users drives continual tweaks in packing materials, with each small change adding up to clearer, drier, and more manageable product on a chemist’s bench.
Manufacturing 2,4-Dichloro-6-hydroxybenzaldehyde does not run on autopilot. The process begins with selecting the right grade of phenol derivative, using only sources with proven track records. Every shift involves direct oversight—temperature control at the chlorination step becomes a matter of timing and teamwork. Even a few degrees of fluctuation during oxidation lead to impurity drift, and purification decisions impact both yield and downstream usability.
Direct knowledge of the process teaches how every step matters for the final purity. Flushing the last traces of acidic byproducts before recrystallization prevents tough-to-remove discolorations later. Tweaking filtration speed, based on particle size observations, tightens the required specification window and shaves hours off the plant’s weekly workload. Years spent watching batches roll through crystalline and powdery phases have shown how to tune conditions for maximum recovery with minimum rework.
Market shelves fill quickly with structurally similar benzaldehydes. Close analogues such as 2,4-dichlorobenzaldehyde or 2,6-dichloro-4-hydroxybenzaldehyde emerge from other makers, but subtle differences matter when it comes to actual performance in the next synthesis step.
Working directly in a plant highlights these differences. The placement of chlorines at the 2 and 4 positions and a single hydroxyl at 6 creates distinctive electronic effects, driving faster reactivity in electrophilic aromatic substitution. Formyl group position ensures better alignment in Mannich or Knoevenagel condensations. Feedback from partners in the pigment and pharmaceutical fields consistently points to the value of having chlorines and the phenol in the correct relationship—yield, color formation, or final bioactivity all depend on this correct skeleton.
Other benzaldehyde derivatives may mimic some features, but the unique arrangement in 2,4-dichloro-6-hydroxybenzaldehyde delivers more consistent performance during the scale-up phases of complex synthesis. As manufacturers, it becomes clear that quality variation in precursors rapidly snowballs into larger downstream issues—impurity delays in chromatography, extra recrystallizations, or unwanted byproducts. Each carefully checked lot reduces these headaches on the customer end, something we take seriously with every release.
Conversations with chemists around the world have shown diverse uses for this compound, but a few strands come up again and again. Pharmaceutical teams use 2,4-dichloro-6-hydroxybenzaldehyde to build up heterocycles that are tough to reach by other synthetic paths. Custom dye houses rely on its specificity in forming bright, stable coloration across multiple substrates. Even small research labs appreciate its robustness in synthesizing reference compounds for analytical method development.
On the plant floor, time after time, the feedback loop shows how small tweaks in crystal habit or granularity significantly change the ease of handling, weighing, or dissolving. Our direct control—from bulk charging to final sieving—keeps particle size in the range preferred by real-world users, not just meeting arbitrary catalog descriptions.
Long before regulatory compliance became bogged down in paperwork, plant experience drove home the importance of keeping emissions low, both for worker well-being and neighborhood safety. Handling the hydroxybenzaldehyde’s dust and volatile residues, and recording direct exposure levels built the foundation for careful engineering controls.
Routine monitoring remains part of daily process checks. All batches receive full traceability reflected not just in internal paperwork, but in real sample retention and cross-batch analysis. Waste, even down to the rinse waters and spent filter cakes, gets neutralized and recorded, with disposal following technical guidelines drawn from practical, hard-won experience, not just paper rules. Clean production lines and minimum batch cross-talk, achieved by thorough cleaning between syntheses, keep contamination out of future lots and in turn, out of our clients’ products as well.
As a manufacturer, the demand for a reliable, stable supply of specialty aldehydes is clear. Over the years, direct conversations with purchasing managers and R&D teams have shown how interruptions in raw material flow hit production schedules hard. Fluctuations in precursor pricing or quality stall entire projects, and last-minute changes from third-party suppliers burn trust.
Our approach prioritizes direct sourcing from partner plants with long-term agreements. By keeping raw materials in-house, and not depending on unpredictable outside brokers, production lines stay active and consistent. Inventory management, built on decades of market experience, balances the pressures of “just-in-time” demands against the very real need for emergency reserves. Regular plant audits and daily batch records mean problems don’t snowball unnoticed. When supply dips in the broader market, it becomes possible to adapt—shifting batch scheduling, retooling purification, or drawing from reserve stores to deliver exactly what has been ordered.
No system runs perfectly forever, but experience has taught the value of open communication with end-users—confirming delivery schedules, clarifying packaging needs, or cooperating on documentation. Many product improvements to our 2,4-dichloro-6-hydroxybenzaldehyde come straight from feedback loops: how quickly drums open, whether labeling with batch numbers matches each client’s system, or if having a technical file with the main shipment reduces onboarding bottlenecks.
Every few years, customer requirements shift—a new downstream application opens up, environmental protocols tighten, or a new synthetic route becomes popular. Direct involvement in production enables adaptation. Tweaks in purification to remove colored side-products, or implementing energy-efficient reaction setups, all come from plant-level suggestions, not distant corporate plans.
Working with formulation specialists means collaborating on solutions to real handling problems: product clumping in humid sites, static during powder transfer, or controlling outgassing in sealed vessels. Fixes, like adding inert gas blankets or switching up drying protocols, save downstream time and cut costs. Some solutions are as straightforward as regular technical check-ins, offering advice on pH adjustment in users’ own facilities, or sending a “best practices” guide along with samples for first-time buyers.
Technical conversations take place daily. Chemists and engineers call to talk through reaction pathways—what impurities to expect, how to handle minor byproducts, or even just how best to dissolve the hydroxybenzaldehyde for large-scale runs. These discussions are far from theoretical. Our staff, having used this molecule thousands of times themselves, can address how subtle changes in process parameters impact final yields and what troubleshooting steps actually work under real plant conditions.
Occasionally, a client encounters issues unfamiliar to their R&D team: trouble scaling up from a literature method, or struggling to remove traces of color or tar from the final product. Drawing from our own hours at the bench, troubleshooting becomes practical—advising on simple wash steps or proposing temperature ramps for improved selectivity.
From those hundreds of calls and emails, updated protocols, FAQs, and user guidelines grow, sharpening both product quality and end-user success. Seeing a customer base move past sticking points—whether in fine chemicals or specialty dyes—creates its own reward, and leads in turn to stronger, more collaborative working relationships.
The shifting landscape of global chemistry now demands more sustainable processes in specialty chemical production. Investment in closed-loop solvent recovery, solventless approaches, and minimal-waste workups comes not from external pressure, but from daily plant experience showing cost savings and better worker safety.
Energy use receives the same attention—heat exchangers recover process heat, and batch reactors draw from lower-carbon power sources wherever possible. Each shift toward closed systems and minimized volatile emissions means less risk for staff and local environments. Routine auditing of effluent streams and periodic reviews of reaction byproducts drive real improvements, cutting both regulatory risk and workplace incidents.
On-the-floor changes sometimes do more for safety and sustainability than sweeping corporate pledges. Well-trained teams, practical cleanup routines, and regular training updates create a plant culture where responsibility for product quality and environmental stewardship is real, not just theoretical.
Maintaining open doors means that customers, auditors, and even competitors develop genuine confidence in the quality, purity, and safety of our 2,4-dichloro-6-hydroxybenzaldehyde. Batch records, retained samples, and complete certificates ensure nothing is left to chance. Years of documentation become more than just files on a shelf—each test trend or out-of-spec notification becomes part of continual improvement.
Regular visits by partners and customers keep our processes honest. Getting feedback mid-production or observing bench-level workflows exposes opportunities for improvement that paperwork alone might hide. These continuing, hands-on partnerships ground decision-making where it matters—at the point where chemistry, safety, and reliability collide.
Whether the end use is a specialty pigment, a pharmaceutical ingredient, or an advanced material component, clients stake months or years of project time on the steady quality of 2,4-dichloro-6-hydroxybenzaldehyde. Understanding this pressure from years in production, we have made real investments in technician training, process automation where it helps, and frequent testing.
Spot-checks catch minor issues before they reach the customer. Data from each batch builds trendlines, predicting and addressing blips before they become real problems. Some improvements seem small, but these changes consistently reduce returns, delays, or customer complaints. Consistency at this level creates real business value, not just industry compliance.
No production cycle stands still. Research teams and line operators throw ideas back and forth: refining yields, shortening reaction steps, trimming costs while lifting product purity. Recent efforts to recover more usable product from what was once considered waste not only cut expenses, but also turn out cleaner batches.
Investments in analytical technology at the source—GC, HPLC, and advanced spectroscopy—allow operators to spot and solve deviation at the earliest sign. The learning loop between production staff and application chemists has built a bank of direct knowledge that supports rapid troubleshooting, and keeps process improvements relevant to actual use.
Regular field visits and pilot collaborations help align product features with current real-world application trends. Chemists from our plant sometimes work side by side with client R&D teams, tackling bottlenecks in process scale-up or method validation. These partnerships generate valuable feedback, prompting process changes that help future users.
Direct, practical approaches—open technical discussions, prompt follow-up on unusual impurity patterns, or custom packing runs—keep us directly connected to both the science and the everyday business of chemicals. Years spent at the intersection of plant operation and field support shape everything from reaction protocols to packaging habits, ensuring that our 2,4-dichloro-6-hydroxybenzaldehyde keeps meeting the evolving needs of a diverse and demanding marketplace.