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HS Code |
340834 |
| Chemicalname | 2-Bromo-6-Chlorobenzoic Acid |
| Casnumber | 20432-14-6 |
| Molecularformula | C7H4BrClO2 |
| Molecularweight | 235.46 |
| Appearance | White to off-white solid |
| Meltingpoint | 185-189°C |
| Purity | Typically >98% |
| Solubility | Slightly soluble in water, soluble in organic solvents (e.g., ethanol, DMSO) |
| Density | 1.8 g/cm³ (approximate) |
| Synonyms | 2-Bromo-6-chlorobenzoic acid, 6-Chloro-2-bromobenzoic acid |
| Smiles | C1=CC(=C(C(=C1)Cl)C(=O)O)Br |
As an accredited 2-Bromo-6-Chlorobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25g of 2-Bromo-6-Chlorobenzoic Acid, tightly sealed with a screw cap, labeled with hazard warnings. |
| Shipping | 2-Bromo-6-Chlorobenzoic Acid is shipped in tightly sealed containers, protected from moisture and light. It is transported in compliance with relevant hazardous material regulations, with clear labeling for chemical identification. Appropriate safety measures, including use of secondary containment and accompanying safety documentation, ensure safe handling and delivery during transit. |
| Storage | 2-Bromo-6-Chlorobenzoic Acid 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 moisture, direct sunlight, and sources of ignition. Proper chemical labeling and secure storage are essential to prevent accidental release or exposure. Use personal protective equipment when handling the compound. |
Applications of 2-Bromo-6-Chlorobenzoic Acid in Industrial ManufacturingAs a direct manufacturer, we supply 2-Bromo-6-Chlorobenzoic Acid to strategic markets where strict quality, process control, and regulatory compliance are required. Our plant supplies this intermediate for advanced pharmaceutical synthesis, agrochemical active manufacturing, liquid crystal material development, and electronic chemical production. Below, we detail each downstream segment based on real sector demand, regulatory environment, and in-plant application. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisPharmaceutical companies regularly utilize this compound as a building block for specific heterocyclic APIs, especially in anti-inflammatory agents and kinase inhibitors. Reacting in ortho-condensation and acylation steps, it serves as an irreplaceable aromatic precursor for regulated drug portfolios. Extensive ingredient traceability and batch consistency underpin all usage in this vertical. Industry compliance standards
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2. Agrochemical Active Ingredient SynthesisMajor agrochemical producers use this material for constructing multi-substituted benzene rings essential in pesticide actives and herbicide intermediates. The halogen functionalities favor targeted halogenation and condensation reactions, streamlining production of modern sulfonylureas and phenoxy carboxylic acids. Process safety and trace impurity control are strictly monitored throughout contract manufacturing. Industry compliance standards
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3. Liquid Crystal Material SynthesisLCD and OLED material manufacturers deploy this raw material in the tailored synthesis of highly-conjugated aromatic cores. It acts as a critical structure-directing unit in custom halogenated biphenyl, terphenyl, and benzoic acid derivatives, enabling the fine-tuning of display switching speed and thermal stability. Manufacturing adheres to rigorous electronic and photonic raw material purity specifications, with continuous analytical monitoring. Industry compliance standards
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4. Electronic Chemical Manufacturing (Fine Electronic Intermediates)High-end semiconductor and specialty electronics chemical firms demand this aromatic acid as a halogen-substituted intermediate for etching-resistant polymer backbones and photoresist resins. Its controlled halogen pattern ensures precise crosslinking or block copolymerization behavior, vital for microfabrication lithography. Full batch traceability, halide analysis, and residual solvent testing underpin supply to logic chip and micro-display factory integration. Industry compliance standards
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Producing specialty halogenated benzoic acid compounds gives us a front row seat to the kind of work that underpins modern chemistry. We’ve worked hands-on with 2-Bromo-6-Chlorobenzoic Acid, fine-tuning both its synthesis and its quality from batch to batch. Over years of technical practice, we have learned not just the formula and reaction conditions, but also the quirks of this molecule, the critical role of careful purification, and the importance of sound analytical verification. Our focus rests on delivering a reliable product with consistent performance for downstream users.
2-Bromo-6-Chlorobenzoic Acid brings together two halogen atoms on a benzoic acid backbone: a bromine at the 2-position, a chlorine at the 6-position. This molecular arrangement creates a substrate that offers interesting reactivity for various chemistries. The acid’s white to pale off-white crystalline appearance, together with a defined melting range and stability, has proven attractive for synthetic and formulation work. In the lab, you can expect sharp spot TLCs and a manageable handling profile, not the unpredictable behavior seen with some multi-halogenated analogs.
On our production line, careful batch control always receives priority. Details matter: from selection of chlorination reagents, stepwise temperature ramping, and anhydrous environments, to glass-lining of reactors and correct stirring speeds. These decisions stem from a history of monitoring reactions and watching for signs of degradation or impurity formation. For most clients, we supply this product as a technical grade powder or crystalline mass. Our specification for 2-Bromo-6-Chlorobenzoic Acid keeps impurity levels below 1%. Residual solvents come in under 500 ppm, confirmed via GC and NMR, with moisture content less than 0.5%. The product meets a minimum purity level of 98% by HPLC, and every batch receives full COA documentation, including HNMR confirmation of substitution pattern. This sort of spec is vital in complex syntheses—traces of unreacted halogenated anilines or benzoic acid byproducts can foul catalysts or distort downstream reactions.
We see 2-Bromo-6-Chlorobenzoic Acid serve as a building block in pharmaceutical and agrochemical development pipelines. Researchers often look for compounds that can be selectively transformed by Suzuki, Buchwald-Hartwig, or Ullmann-type couplings. The double halogenation at ortho positions makes this acid a valuable starting point for regioselective introduction of further groups, such as amines, ethers, or heterocycles. Medicinal chemists use the molecule’s electron-withdrawing nature to fine-tune bioactivity, improving metabolic stability or refining target selectivity.
Beyond drug intermediates, application spreads through dye manufacture and polymer modification. The acid moiety allows for attachment to diverse substrates, including resins or advanced polymer backbones. Researchers working in the field of materials chemistry have used 2-Bromo-6-Chlorobenzoic Acid for constructing custom monomers with halogen-functionalized aromatic rings. Sometimes, it supports the design of fluorescent tags or tailored ligands used in advanced imaging or sensing.
Several clients shared results from scale-up runs in pilot plants or kilo labs. They report smooth incorporation into palladium-catalyzed reactions and manageable filtration and crystallization steps. Feedback focused on reproducible yield and clarity of NMR spectra, not only from the acid itself but also from diverse follow-up products—evidence that tight control of batch consistency pays off long after the original shipment has left our facility.
Benzoic acid halogenation reactions have never been as straightforward as textbook diagrams suggest. The fine distinction between ortho, meta, and para substitution requires selective conditions, patient monitoring, and good separation. Multiple runs and much scrutiny went into our optimization of the chlorination and bromination steps—simple over-reflux reactions fail to deliver clean product in the quantity our clients expect. During scale-up, issues like exothermic handling, solubility limits, and precipitation rates came to the fore. Each of these factors influences the impurity profile.
We learned early on to avoid recycled solvents for this particular process—trace contamination from previous runs brought discontinuity in product color and compromised NMR standards. The approach we settled on uses high-purity raw materials in fresh solvents, with staged addition of halogenating reagents and continual sampling until endpoint. Filtration through tight-mesh stainless steel avoids introduction of fiber residue, a small but significant detail. We store bulk product in cool, dry environments and ship it in double-lined containers to keep moisture and contaminants at bay.
Those who work with halogenated benzoic acids recognize that each substitution pattern serves a unique function. Customers sometimes ask why not just work with either mono-chlorinated or mono-brominated benzoic acid. From practical experience, 2-Bromo-6-Chlorobenzoic Acid establishes a distinct place in the toolbox: it delivers orthogonal reactivity, especially in multi-step syntheses where stepwise activation is required. The sequence of halogen displacement or metalation can be fine-tuned, reducing side reactions common with fully brominated or fully chlorinated variants.
Compounds like 2-Chlorobenzoic Acid or 2-Bromobenzoic Acid offer single-halogen handles; they will react, but the versatility and downstream selectivity are more limited. If one seeks to build complexity on a single aromatic ring, dual-halogenated acids like ours provide flexibility. Functionalizing just one position, then leveraging the other for subsequent steps, saves time, reagents, and often avoids over-reaction or ring degradation.
Another angle comes from physical properties. Mono-substituted acids may have easier crystallization and melting profiles, but the introduction of the second halogen atom noticeably shifts both solubility and thermal behavior. We see slightly higher melting points and somewhat lower solubility in non-polar solvents, which can aid or complicate purification, depending on the next synthetic step.
Some clients have tested their own purifications with other benzoic acid derivatives, such as 2-Chloro-5-Nitrobenzoic Acid or 3-Bromo-5-Chlorobenzoic Acid. In these cases, the substitution pattern changes reactivity in metal-catalyzed couplings. Rates, yields, and even the color of reaction solutions shift accordingly. Our experience tells us that 2-Bromo-6-Chlorobenzoic Acid delivers high chemoselectivity, making it preferable when stepwise transformation is called for.
Stability under storage varies between derivatives. We watched 2-Bromo-6-Chlorobenzoic Acid hold up well even under months of storage, given reasonable control of temperature and humidity. Mono-brominated analogs seemed more prone to slow decomposition under similar circumstances, especially in humid climates.
Production of halogenated aromatic acids brings occupational and environmental responsibilities. Personnel safety always stands as a daily priority. In our operations, exhaust scrubbing and careful containment keep exposure levels far under published thresholds. We provide extensive safety training, and our team has direct experience with the importance of personal protective equipment and vigilant process monitoring. Aromatic acid dust and halogenated volatiles present risks; we address both in reactor setup and process scheduling.
Waste minimization has taken considerable effort. Implementing solvent recovery for low-toxicity organics, segregating halogenated waste streams, and operating at low excess of halogenating reagents each contribute to improved environmental outcomes. We collect audit data for every campaign, part of an ongoing process to limit our chemical footprint. For shipments to clients, we furnish detailed SDS documents and packaging that limits accidental exposure or leaks.
Because we handle the process from raw material up through finished product, we’re often the first to spot when something odd appears on a chromatogram or elemental analysis. That level of direct technical oversight allows smoother troubleshooting and a responsive update cycle. We’ve collaborated with R&D teams at both startups and established firms, offering input on solubility or reactivity in custom formulations. In several instances, our chemists advised on protocol modifications that boosted yields or reduced byproduct formation. Access to hands-on batch records means we can answer detailed technical queries, or suggest alternative procedures should a synthesis not proceed as planned.
We see steady demand from medicinal chemistry discovery groups, combinatorial chemistry pitches, and process development labs. Typical customers mention the usefulness of gram to kilogram quantities, depending on research stage. Our ability to supply multi-kilo lots without deviation in specification has enabled our product to bridge research trials and pilot plant campaigns with confidence.
Markets, requirements, and regulatory context never stand still. We regularly engage in critical reevaluation of our synthesis routes and analytical standards. New catalytic systems or greener halogenating agents receive early evaluation in our laboratory. We actively minimize hazardous side streams and have replaced some legacy solvents with safer, less persistent alternatives. Close dialogue with end-users guides these improvements—feedback loops spur us to raise our purity standards and reduce impurity profiles as new downstream applications arise.
We store and analyze long-term stability samples, watching for subtle changes in content or structure over time. Any anomaly gets reviewed for root cause—storage, packaging, or changes in raw material supply chain. Twice yearly, we update our analytical methods in line with best industry practices, implementing more sensitive quantitation when achievable. Our technical staff regularly attends symposia and brings back new methods or troubleshooting insights.
In one notable project, collaboration with a research institute led to integration of real-time process analytics, cutting down production cycle times and reducing off-spec output by nearly 40%. Beyond metrics, this sort of investment creates a culture of direct engagement—everyone from plant operators to QC analysts knows the importance of detail and consistency for our customers.
Expansion into new application spaces drives some of our ongoing investment in 2-Bromo-6-Chlorobenzoic Acid. We fielded requests for use in high-throughput screening libraries, fragment-based drug discovery, and custom ligands. Each new field brings technical challenges: special purity needs for pharma, low-metal content for catalysts, or documentation requirements for regulated industries. We field questions at all hours from partners who just want to confirm a spectral signal or need advice on optimizing a coupling protocol.
Nobody working in specialty chemicals is immune to fluctuating raw material costs or regulatory shifts. We’ve seen sudden spikes in halogen supply or unexpected freight bottlenecks slow production. Advanced planning and diversified supply sourcing help, but unpredictabilities remain. In more than one instance, short runs of out-of-spec product required full reprocessing—scrapping material isn’t fun or cheap, but we learned that strict adherence to process parameters prevents bigger headaches for our clients.
Sometimes we have to field requests for chemicals that look similar but behave quite differently. Our technical team routinely checks every molecular structure submitted via purchase request, making sure we’re matching product to intended use. Mislabeling or mix-ups at the scale of grams can throw an entire route into confusion. We keep our lab and customer support informed and proactive.
Our direct manufacturing approach lets us share practical perspective beyond datasheets or spec tables. We support chemists, engineers, and formulators through collaborative conversation, troubleshooting, and honest feedback. We always aim to adjust as new requirements arise—whether that means custom packing, rush orders, or a tweak in impurity profile to match a new analytical standard.
Everything we produce—every drum or high-purity pack of 2-Bromo-6-Chlorobenzoic Acid—comes with direct experience in synthesis, real-world application, and a culture of craft. We have seen firsthand how a reliable supply of these building blocks shapes the speed and success of diverse scientific endeavors. As markets evolve, we continue to improve, grounded in a clear understanding of what quality means not just to us, but to colleagues across the chemical industry.