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HS Code |
594983 |
| Product Name | 4-Bromo-2,6-Dichlorobenzaldehyde |
| Cas Number | 77098-07-8 |
| Molecular Formula | C7H3BrCl2O |
| Molecular Weight | 269.91 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 124-128 °C |
| Purity | Typically ≥97% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Density | 1.86 g/cm³ (estimated) |
| Smiles | O=Cc1c(Br)cc(Cl)cc1Cl |
| Inchi | InChI=1S/C7H3BrCl2O/c8-5-1-4(3-11)2-6(9)7(5)10 |
| Storage Conditions | Store at room temperature, keep container tightly closed |
As an accredited 4-Bromo-2,6-Dichlorobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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Too often, specialty chemicals slide under the radar, but for those who spend their days at the bench or plan out sourcing for synthesis, products like 4-Bromo-2,6-Dichlorobenzaldehyde carry real meaning. This aromatic compound shows up in advanced research labs, quality control departments, and even in industrial innovation meetings, which tells a story about how subtle differences in chemical structure can shape everything from pharmaceutical pipelines to forensic screens.
I've worked with many chemicals in the lab, and 4-Bromo-2,6-Dichlorobenzaldehyde stands out for its distinctive skeletal structure: a benzaldehyde ring with bromine at position four and chlorine atoms at positions two and six. The chemical formula is C7H3BrCl2O, with a molecular weight that hovers just above 256 g/mol. Its crystalline form typically runs pale yellow to white, and I've found it doesn't dissolve that easily in water—a usual trait for halogenated benzenes—but shows good solubility in ethanol, chloroform, and many ethers.
Though catalog numbers and model references differ from supplier to supplier, the main identifiers—CAS number 16945-39-4 and the IUPAC name—don’t change, which helps anyone double-check purity or tracking across global inventories. In practice, labs often demand at least 98% purity, based on high-performance liquid chromatography or gas chromatography results. Glass-bottled batches arrive tightly sealed, often with nitrogen to protect from moisture, since exposure to air can gradually degrade sensitive samples. Proper storage at room temperature, away from light and damp conditions, keeps the material reliable for months if not years.
From my experience, small changes in ring substitution make a night-and-day difference in reactivity. This particular arrangement—bromine and two chlorines on the benzene ring—gives the molecule a tricky balance of electron-withdrawing power and steric bulk. Such factors aren't academic details; they directly set how this intermediate behaves once you start running acylations, couplings, or reductions. Many researchers choose 4-Bromo-2,6-Dichlorobenzaldehyde for its unique platform for further derivatization, whether the next step calls for forging a C-N bond or introducing heterocycles in drug candidates.
With other benzaldehydes, you can run into unpredictable reactivity. Too many electron donors can cause a runaway reduction, and insufficient selectivity can muddy your product mix. In contrast, the twin chlorines on this scaffold moderate the benzaldehyde group, while the para-bromo lets chemists target cross-coupling reactions that benefit from bromo’s reactivity—Suzuki and Heck reactions come to mind. These features don't just add up to an academic footnote; they're why process chemists keep returning to this compound for certain analog synthesis routes, particularly when looking for selective halogenated patterns that confer metabolic stability on drug candidates.
In my line of work, I often see 4-Bromo-2,6-Dichlorobenzaldehyde discussed in project meetings with medicinal chemists as well as in the patents of agrochemical giants. This molecule doesn't pretend to be a blockbuster on its own—rather, chemists value it as a stepping stone to more complex molecules. Its use as an intermediate fills a gap where other aldehydes prove less adaptable. I’ve watched teams try to make unusual benzylamines from substituted benzaldehydes for CNS-targeted drug candidates, and this molecule comes up often since the halogen pattern controls the compound’s electronic and metabolic fate.
Beyond pharma, the paint and coating industry occasionally taps into unique halogenated intermediates like this one for pigment modifications or as crosslinking agents, since the substituent pattern packs some resistance against UV and oxidative degradation. Organic synthesis groups value the way the trial-halogen ring supports the formation of specialty ligands, functional polymers, and bespoke reactants for niche markets. In environmental or forensic science, halogenated benzaldehydes form benchmarks or internal standards during analytical method development. The reason is simple: the molecule’s halogen content makes it easy to track via mass spectrometry or X-ray crystallography.
Having ordered this compound for synthetic runs, I've seen first-hand what high-purity batches mean for productivity. Impurities, even in trace amounts, can tank yields and skew analytical readouts. A batch with subpar HPLC specs or broad melting points isn’t worth risking a reaction that might spiral into a sticky mess—especially when scale-up costs keep managers up at night. Rigorous suppliers always provide analytical data sheets, and established supply chains run repeated checks for heavy metal content, residual solvents, or unwanted side products, ensuring that the core chemical performs as billed from flask to pilot reactor.
Since 4-Bromo-2,6-Dichlorobenzaldehyde rarely serves as the endpoint, every minor impurity can sneak into downstream steps. I’ve witnessed teams spend hours, if not days, on purification protocols to pull out a single failing byproduct that traced back to a contaminated raw intermediate. Sourcing from trusted vendors or requesting a new Certificate of Analysis is less about bureaucracy and more about keeping entire project timelines manageable.
I remember the first time I compared this product directly with 2,4-dichlorobenzaldehyde or 3,5-dibromobenzaldehyde. The changes might sound minor to those outside the field, but they morph the compound’s properties significantly. Both melting point and volatility can vary by several degrees, and that throws off crystallization strategies or even solvent choices. Reactivity flips, too: swap out one halogen, and the pace of nucleophilic addition or reduction can shift in ways that textbooks don’t always predict. For synthetic planning, such nuance isn’t luxury—it’s survival.
Another compound like 4-Bromo-3,5-Dichlorobenzaldehyde, similar in formula, diverges in action under certain catalytic conditions. Bromine’s placement can tip off selectivity during cross-coupling, and dual chlorination at ortho-positions gives 2,6-dichloro patterns more rigidity, guiding the entire molecule’s functionality. Sourcing mistakes happen if purchasing teams or new chemists overlook the structural differences. Each variant comes with its quirks, which explains why suppliers must commit to clear labeling and full documentation. An early mistake here can cost both time and money in R&D, sometimes jeopardizing intellectual property filings or regulatory compliance.
Over the years, demand for high-quality 4-Bromo-2,6-Dichlorobenzaldehyde has climbed, partly in response to contract research organizations ramping up their capacities. While working with a start-up, I once watched purchasing scrabble to find a steady source. Bottlenecks don’t just disrupt one lab—they ripple all the way through to multinational production lines. The market periodically faces shortages, especially when upstream suppliers face regulatory hurdles or raw-material scarcities. This is another reason researchers and supply chain specialists keep a roster of backup vendors and check prices across global markets.
Pricing rides on purity, packaging, and quantity. Smaller bottles suit bench-scale evaluation, while in-house kilo production demands bulk, often with custom packaging and specific transportation arrangements. Logistics teams juggle international regulations on halogenated organics, sometimes requiring special declarations under REACH or TSCA depending on region. Having sat in on compliance calls, I know firsthand how seemingly minor paperwork details turn into lynchpins for timely delivery.
Safety officers and environmental specialists often bring their own lens to this molecule. With twin chlorines and a bromo substituent, 4-Bromo-2,6-Dichlorobenzaldehyde requires careful handling and disposal. Unintentional release can lead to environmental persistence; halogenated aromatics do not break down rapidly in soil or water. Working in regulated labs, I learned how important it is to log every milligram used, store spent solvents properly, and secure leftover compound in locked waste containers destined for specialized incineration. It’s easy to overlook the waste stream for intermediates, believing the real risk lies with final products, but diligent stewardship here keeps operations in line with today’s sustainability commitments and prepares organizations for tightening regulations.
Proper personal protective equipment is not optional—and that means gloves resistant not only to organic solvents, but also halogenated agents. Inhalation or skin contact risks exist if spills or splashes occur during open handling or weighing. Modern fume hoods and careful workflows, combined with regular safety briefings, keep risks low. Transport crews must label containers correctly and use hazardous goods protocols even for small volumes. Eyes glaze over during safety videos, but anyone who has experienced an unplanned chemical exposure knows how fast a quiet morning can unravel.
One recurring theme in the chemical industry is clear traceability. As regulatory and customer expectations mount, 4-Bromo-2,6-Dichlorobenzaldehyde’s origin and processing history need to be well-documented. Analysts like me rely on certificate of analysis files to check not just purity but residual solvent content and batch-to-batch consistency. Large buyers look for validated quality management processes—auditable supply chains and full documentation back up each delivery.
Scandals and recalls resulting from mislabeling or accidental contamination drive home why traceability can't just be lip service. In practice, QA/QC officers periodically reanalyze both archived and incoming lots, randomly sampling for unexpected signals. This push for constant quality reflects not only business interests, but also ethical responsibilities to downstream partners and end-users. Customers working at the frontier of drug research or agricultural chemistry don't get second chances; their innovation depends on raw materials meeting agreed specs, free from unknown or unlisted contaminants.
Some of the best advice I ever received about specialty chemical sourcing came from a veteran procurement agent: “Know your vendor, and keep a running log of real-world performance, not just what’s on paper.” In the case of 4-Bromo-2,6-Dichlorobenzaldehyde, that extra diligence pays off with each project. Feedback from staff working in both synthesis and analysis tells a richer story than catalog specs alone. Actual results—reaction yields, side-product profiles, and handling notes—help companies adjust protocols and avoid repetition of preventable mistakes.
Strong vendor relationships allow for more than just good pricing. They let buyers request customizations when unique batch characteristics or packaging needs arrive. Establishing real partnerships with producers sometimes solves issues before they can disrupt production schedules or new project launches. After years in the field, I know the value of accessible technical support, prompt shipment notifications, and honest dialogue whenever supply hiccups—or even big mistakes—occur. Real organizations thrive on trust and clear communication, something too many overlook in the race to cut costs or speed timelines.
As someone who has sat through many cross-functional meetings, I can say the biggest headaches often stem from unstable markets and shifting regulatory ground. 4-Bromo-2,6-Dichlorobenzaldehyde falls under increasing scrutiny in trade regions that monitor persistent organic pollutants and emissions from chemical processes. European buyers, for instance, must cross-verify shipments against REACH provisions and update site documentation for every halogenated delivery. Similar paperwork surges affect shipments to the United States and parts of Asia, where customs officers double-check bills for proper declaration of hazardous materials.
Cost pressures don’t always stem from the molecule itself. Swings in bromine or chlorine prices quickly pass through the production chain. Global supply links magnify delays; a temporary closure at an Asian synthesis plant can leave European firms scrambling. These issues underline the importance of agile purchasing strategies and broader supplier diversification.
Shipping restrictions on hazmat-labeled containers, evolving WTO trade codes, and supply chain disruptions caused by global events have all impacted reliable sourcing. I’ve watched colleagues pivot overnight, shifting from one vendor to another because a customs holdup pushed delivery times from days to weeks. Building in lead time, running test orders before large projects, and securing backup approval lines help teams navigate the uncertainty.
Despite regulatory and supply-chain hurdles, 4-Bromo-2,6-Dichlorobenzaldehyde keeps finding new adopters. This is no accident; its substitution pattern aligns with rising interest in halogenated scaffolds for next-gen pharmaceutical and agricultural solutions. The molecule’s combination of stability and targeted reactivity provides creative synthetic chemists with a versatile building block, supporting not only drug design but also advanced materials science. I’ve seen research groups adapt procedures to leverage this compound for imaging agent design and advanced diagnostics platforms, suggesting there’s more utility to uncover.
One exciting area involves targeted molecular library generation, where unique halogen arrangements facilitate combinatorial synthesis approaches. This flexibility can streamline discovery pipelines, save time, and minimize waste. The environmental persistence of halogenated intermediates could drive companies to adapt greener chemistry solutions—higher efficiency routes, less hazardous reagents, or cleaner downstream purification techniques. The trend towards sustainability in fine chemicals doesn’t mean dropping useful tools; it requires smart adaptation so researchers can keep up with evolving standards without sacrificing performance.
Success in sourcing and using 4-Bromo-2,6-Dichlorobenzaldehyde ties back to preparation. Teams should maintain up-to-date supplier assessments, robust internal documentation, and real-world feedback channels—not just rely on what looks good in a spreadsheet. In practice, that means running small pilot reactions to confirm supplier purity, regularly auditing inventory, and fostering good relationships not only with primary vendors but also with niche distributors able to offer quick-turn shipments when markets tighten.
Strategic purchasing involves balancing price with quality, emphasizing documented batch history, and keeping up-to-date certifications. Environmental health and safety officers should stay informed about shifting regulatory rules so that compliance does not lag behind innovation. Companies can further strengthen resilience by engaging in joint quality improvement projects, sharing feedback, and supporting supplier investments in greener production techniques. Labs building in-house expertise in purification, analytical verification, and proper waste handling stay ready for expected—and unexpected—market shifts.
Working with halogenated benzaldehydes like 4-Bromo-2,6-Dichlorobenzaldehyde teaches lessons about the value of precision, transparency, and adaptability. The compound’s robust performance is not just a matter of molecular structure, but also reliable delivery, trustworthy sourcing, ongoing communication between supplier and user, and a persistent focus on safety and environmental responsibility. The best teams I’ve met approach specialty chemicals not only as tools or commodities but also as collaborative partners in discovery.
Staying ahead in today’s chemical landscape means keeping up with evolving technical standards, regulatory rules, and supply chain realities. Success doesn’t just look like a perfect analytic readout—it means orders arrive on time, analysts know what’s in each drum or bottle, and researchers push their projects forward without sleepless nights over unexpected contaminants or shortages. Over decades of applied research, collaboration, and troubleshooting, it becomes clear: reliable chemistry takes both rigor and relationships.
4-Bromo-2,6-Dichlorobenzaldehyde may not get headlines outside technical circles, but its real-world impact is felt daily across labs, supply chains, and innovation teams. For all who count on chemistry to unlock possibilities, this compound offers both challenges and opportunities—demanding care, rewarding diligence, and showing, once more, that every detail in a reaction or transaction truly matters.