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HS Code |
830914 |
| Product Name | 3,6-Dichloro-2-Hydroxy Benzoic Acid |
| Cas Number | 3330-14-3 |
| Molecular Formula | C7H4Cl2O3 |
| Molecular Weight | 207.02 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 225-230°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Boiling Point | Decomposes before boiling |
| Density | 1.71 g/cm³ |
| Synonyms | 2-Hydroxy-3,6-dichlorobenzoic acid |
| Pka | 2.9 (Carboxylic acid group) |
| Smiles | C1=CC(=C(C(=C1Cl)O)C(=O)O)Cl |
As an accredited 3,6-Dichloro-2-Hydroxy Benzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White HDPE bottle, 100 g, labeled "3,6-Dichloro-2-Hydroxy Benzoic Acid"; hazard symbols, batch number, and safety information printed clearly. |
| Shipping | 3,6-Dichloro-2-Hydroxy Benzoic Acid is shipped in tightly sealed, chemically resistant containers to prevent moisture and contamination. It is labeled with appropriate hazard symbols and handled according to relevant safety guidelines. The package is cushioned, compliant with international regulations, and accompanied by a Safety Data Sheet (SDS) for safe transportation. |
| Storage | Store 3,6-Dichloro-2-Hydroxy Benzoic Acid in a tightly sealed container, away from direct sunlight, moisture, and incompatible substances such as strong oxidizers and bases. Keep it in a cool, dry, and well-ventilated area. Label containers clearly and handle with appropriate protective equipment to avoid skin and eye contact. Dispose of residues according to local environmental regulations. |
Applications of 3,6-Dichloro-2-Hydroxy Benzoic Acid in Industrial ManufacturingAs a direct manufacturer specializing in high-purity 3,6-Dichloro-2-Hydroxy Benzoic Acid, we serve core sectors that depend on this chemical for synthesis and functional transformation. The following application scenarios reflect our ongoing collaboration with industrial customers who require tight control over formulation, regulatory compliance, and integration into established process lines. 1. Pharmaceutical Intermediate for Anti-Inflammatory Drug SynthesisPharmaceutical processors utilize this compound as a building block in synthesizing certain non-steroidal anti-inflammatory drugs (NSAIDs). Our product enters proprietary synthesis routes where stringent impurity control supports both finished drug quality and compliance with regional regulations. The process often requires exacting stoichiometry, as downstream transformation efficiency relies heavily on feedstock purity and particle size. Industry compliance standards
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2. Herbicide Intermediate for Agrochemical SynthesisAgrochemical manufacturers rely on 3,6-Dichloro-2-Hydroxy Benzoic Acid for the production of select benzoic acid-based herbicides. Purity and consistent chlorination patterns remain critical for downstream esterification and formulation with adjuvants. Our product integrates into crop protection chemical lines that require certification and traceability. Industry compliance standards
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3. Dye and Pigment IntermediateThe dyestuff industry sources our product as a chlorinated aromatic intermediate for synthesizing specialty azo and anthraquinone dyes. Our materials must display low residual solvent content and batch consistency to ensure predictable color yield and performance in end-use applications that demand consistent fastness and stability. Industry compliance standards
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4. Specialty Polymer Additive SynthesisPlastic and specialty polymer formulators employ this raw material as a chain-modifying intermediate to create halogenated monomers and functionalized polymers. Our fully traceable batches support stringent physical and analytical requirements integral to downstream processing. Applications focus on performance additives and polymer modification. Industry compliance standards
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5. Fine Chemicals Synthesis for Flavors and FragrancesCertain fine chemical producers use 3,6-Dichloro-2-Hydroxy Benzoic Acid as a precursor to aromatic esters and aldehydes involved in the formulation of scent and flavor ingredients. Our product ensures batch-to-batch uniformity and low trace impurities, supporting high reproducibility in complex perfume and food additive development processes. Industry compliance standards
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Competitive 3,6-Dichloro-2-Hydroxy Benzoic Acid prices that fit your budget—flexible terms and customized quotes for every order.
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Every manufacturer who spends years working with chemicals develops an appreciation for compounds that offer both versatility and consistency. 3,6-Dichloro-2-Hydroxy Benzoic Acid is one of those compounds we find ourselves relying on each season, not only because of its sharp reactivity profile but also for the reliability it brings to our processes. Over decades, improvements in raw materials and batch control have helped us refine output, improve purity, and ensure that each shipment meets demanding downstream requirements. It's far from a commodity; it’s a building block central to many specialized reactions.
The compound structure, bearing two chlorine atoms at the meta and para positions and a hydroxyl group in the ortho position to the carboxylic acid, creates selective reactivity that opens doors in organic synthesis. Differences lie in the details. Products that appear similar on paper behave quite differently in reactors. Substitution pattern, for example, directly shapes both electronic character and solubility. Over time, we've learned just how sensitive some applications can be to even small shifts in purity and trace contaminants. Customers require real chemical insight, not just bulk shipments, because industrial processes depend on repeatable results and minimal process upset.
We start with the purest feedstock. Our plants operate with continuous monitoring for moisture and residual solvents, because even tiny residues can twist a customer’s run, particularly in pharmaceutical or crop protection manufacturing. Each batch follows a controlled reaction, leveraging chlorination and hydrolysis under conditions that optimize yield while minimizing byproduct. Final product undergoes thorough filtration and multiple rounds of drying. Analytical equipment—HPLC, NMR, and ICP-MS—monitors purity, not just on paper, but in practice during and after production. We document each lot for trace metals and organochlorine residuals since years of feedback have taught us how even high-ppm traces can affect coupling reactions or polymerization outcomes.
In the last decade, we raised our minimum assay standards to above 99%. We also hold a tight line on known impurities including monochlorinated and trichlorinated benzoic acids, as they tend to interfere in select transformations. Consistency from batch to batch comes from technical expertise and relentless troubleshooting, not just equipment upgrades. Our own lab chemists run pilot lots before we scale, ensuring minor tweaks at the kilo scale don’t spiral into headaches at the tonne scale.
There are a few common lines of benzoic acid derivatives; some manufacturers offer ortho- or para-substituted products. The 3,6-dichloro pattern brings a unique balance of halogenation and hydrogen bonding, setting it apart from better-known isomers. Its electronic effects favor certain electrophilic aromatic substitutions and facilitate selective coupling in heterocycle synthesis. Compared to mono-chlorinated benzoic acids, the extra chlorine directs reactions more predictably—important for anyone designing a stepwise synthesis or planning for minimal side product generation.
Methylation, etherification, and esterification with our 3,6-dichloro-2-hydroxy benzoic acid rarely demand excessive purification. We keep an eye on any trace methyl salicylate, sometimes encountered during hydrolysis; our protocol strips this out over a multi-step wash. When comparing to the 3,5-dichloro analog, solubility in common polar-aprotic solvents comes up in discussions with formulation chemists, especially those working on dispersed systems or specialty pigments. The difference may sound subtle, but the chain of synthetic utility, from salts to esters, depends on these minute distinctions.
Practicality counts. Our customers use 3,6-dichloro-2-hydroxy benzoic acid in diverse sectors from pharmaceutical intermediates, herbicide precursors, dye chemistry, and even high-end polymer additives. It’s a favorite precursor for certain non-steroidal anti-inflammatory compounds, where the steric and electronic control of the dichloro substitution speeds up final coupling and reduces off-pathway oxidation. In agricultural chemistry, the molecule participates in the creation of active ingredients designed to survive sunlight and oxidative conditions. The residual hydroxyl group offers a functional handle, making it a ready substrate for ether or ester formation.
Over the years, technical teams visiting our facility have brought new challenges. One year, a team required a variant with extra tight control on sulfonate content, as their catalyst was sensitive to anionic trace contaminants. Another client in advanced electron transport materials sought batches with sub-ppm levels of iron and copper, both because final conductivities suffered otherwise. Habits like these—achieved through rigorous process design and close communication between production and analysis—underline why process design at manufacturing scale matters just as much as at small scale. For all the regulatory paperwork, what matters most remains: does the product do what is says, every time?
Once, a downstream partner ran into yield drops they traced back to residual monochloro material. It hadn’t shown up at the typical analysis levels, but their process, uniquely sensitive, caught the difference. Tweaking our recrystallization regime ironed out the contamination. Those kinds of feedback loops matter. We encourage conversation beyond the purchase order. People on the formulation, R&D, and QA sides want more than a certificate—they want a dialogue. Sometimes, a manufacturing chemist or a quality manager will spot issues not even we predict; we value that feedback because each correction improves us for everyone else as well.
There’s always the temptation in industry to buy to a minimum price, especially as external markets push for cost reduction. We’ve seen what happens when shortcuts get taken or when less-experienced producers rush product to ship. Off-color lots, batch-to-batch drift, or compromised stability can shut down a customer’s process for weeks. Confidence builds over repeated cycles; no lab test can fully substitute for months or years of uninterrupted process flow in real production plants.
Runoff, waste stream management, and emissions are not afterthoughts; they’re part of the process. Our facility reclaims most of the solvents used in synthesis, thanks to an integrated distillation system. Boron and halide management means regular monitoring, and byproduct separation is designed not only to reclaim value but to keep our regulatory profile clean. The fact that 3,6-dichloro-2-hydroxy benzoic acid shows minimal volatility simplifies some environmental controls while putting the focus on aqueous disposal. We carry out pilot runs on alternative work-up steps, often in parallel with main production, so improvements travel quickly from lab to plant floor.
Many customers, particularly those in pharma and agchem, come with increasingly demanding downstream regulatory requirements. Trace analysis for REACH, EPA, or Food and Drug regulations can spin up unexpectedly. With every change in legislation, we modify our analysis screening regime, sometimes even creating new test methods to preempt potential compliance issues. This adds some complexity, but it also pushes us to engineer a cleaner process from the outset. Experience shows that companies investing ahead of the curve save time, money, and reputation in the long run.
The purity of 3,6-dichloro-2-hydroxy benzoic acid carries implications at every next synthetic step. If a customer’s next step involves a Grignard or palladium-catalyzed cross-coupling, for instance, any halide or metal ion content outside spec spells extra cleaning and sometimes costly downtime. Even minor levels of sulfated ash appear as unwanted residues in sensitive formulations. Few spec sheets talk in detail about how process solvents from the original plant can find their way, as micro-residuals, into the finished product. Our analytics team, through years of batch data, tracks these problems and designs countermeasures—a housekeeping protocol here, a secondary drying column there—to keep final output cleaner than the minimum required.
Choosing the right synthesis route early makes a difference. A process that looks efficient on paper—but leaves mineral acids or trace ethereal solvents—will cause more problems downstream when the product finds its way into formulations. Many customers face annual or biannual requalification with their own end users, particularly in pharma and electronics. A supply chain that can’t deliver consistent performance causes ripple effects far beyond missed deadlines. That’s why our teams focus on process integration, where upstream and downstream steps aren’t just sequenced, but coordinated to anticipate and minimize batch drift.
More than a few clients want custom lots: slightly modified drying, a different particle profile, or even customized packaging to prevent moisture uptake. These requests come from real production pain points. In one case, a major client lost two weeks’ output due to caking from inadvertent moisture ingress during transit. That led to a full-scale review of our bulk-packaging options, desiccant loading, and container linings. Collaboration doesn’t mean just responding to a punch list—it means anticipating pain points and adapting upstream.
While the core molecule follows a strict process, minor variations can carry significant downstream advantages. Some users in dye or pigment applications, for example, prefer a different crystal morphology to ensure homogeneous dispersion. Our R&D team, drawing on years of bench experience, can tweak recrystallization or employ anti-solvent processing for these needs, always tracking impact on purity and cost efficiency. These details, invisible in standard datasheets, matter deeply at the customer’s application scale. We see our job as starting with the molecule and ending with a solution that works smoothly in real production, not just under idealized lab conditions.
Today’s markets thrive on just-in-time inventory, but chemicals don’t always fit cleanly into timelines. Weather, logistics, and supply chain disruptions still exist. Our own schedules plan for buffer stock at each stage—not just for emergencies, but because production always brings the unexpected. Detailed tracking lets us spot trends: which customers are scaling up, which lots needed rework, where process improvements have paid dividends. Real-world experience with 3,6-dichloro-2-hydroxy benzoic acid comes not only from laboratory skill but from cumulative years getting material to customers who depend on it for product launches, regulatory filings, and routine operations.
Long-term partnerships develop through shared experience. If a spec changes due to upstream raw material variation, we reach out, often working with our customer’s own technical staff to pinpoint and solve any hiccups. That responsiveness, honed by years of working on tight deadlines and demanding application requirements, defines trust more deeply than any third-party audit or external certification.
Chemistry never stands still. New applications for 3,6-dichloro-2-hydroxy benzoic acid arise every year—novel reactivities, updated regulatory controls, more demanding process needs. We support technical exchanges with long-standing customers and attend industry symposia to stay current. Such engagement keeps our production staff and R&D aware of shifting standards and predictive about potential hurdles. Whether it is crystal habit modification, refining the removal of specific trace contaminants, or tweaking packaging logistics for improved shelf live, proactive adaptation ensures we don’t just meet existing needs but anticipate what’s around the corner.
Every improvement turns into a competitive advantage for both us and our partners. Keeping lines of communication open isn’t just a value—it’s the engine of chemical manufacturing progress. As customers’ expectations rise, manufacturers have to step up, not just with documentation and product but by thinking ahead on the scientific and practical details that lead to trouble-free application.
We have built our approach to 3,6-dichloro-2-hydroxy benzoic acid around three pillars: scientific understanding, manufacturing excellence, and genuine partnership with our customers. Our knowledge comes from thousands of batches, each teaching something new. Manufacturing excellence comes from an obsessive attention to detail—materials tracking, in-line analysis, and closed feedback loops with real world users. And partnership means listening carefully, adapting quickly, and standing behind the molecule whether the order is a drum or a container lot.
The right 3,6-dichloro-2-hydroxy benzoic acid delivers measurable gains in yield, process reliability, and cost containment. It’s tempting to view it as another commodity chemical, but those who work with it realize the difference between supplier and manufacturing partner comes in these details. We keep our eyes on both the molecule and those who rely on it, so that every lot, every shipment, supports the next round of innovation across all the fields our partners serve.