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HS Code |
699821 |
| Cas Number | 13301-35-8 |
| Molecular Formula | C10H6Br2O |
| Molecular Weight | 314.97 g/mol |
| Appearance | Yellow to orange crystalline powder |
| Melting Point | 193-196 °C |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in ethanol, ether, and chloroform |
| Purity | Typically ≥98% |
| Iupac Name | 2,4-dibromonaphthalen-1-ol |
| Synonyms | 2,4-Dibromo-1-hydroxynaphthalene |
| Storage Conditions | Store at room temperature, protect from light and moisture |
| Hazard Statements | Irritant |
As an accredited 2,4-Dibromo-1-Naphthol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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Life in the chemical industry moves fast, and every component counts whether you're working in dyes, pharmaceuticals, or pushing for new breakthroughs in research. Out on the shop floor, we're always looking for products that bring both reliability and flexibility to the table. I have spent years tracking specialty chemicals as they shape everyday products—sometimes in ways we hardly notice. One compound that keeps showing up where innovation matters is 2,4-Dibromo-1-Naphthol.
Some might see it as just another name on a spec sheet. I see it as one of those unsung contributors in chemical labs and production lines alike. Tucked into the chemical structure of 2,4-Dibromo-1-Naphthol is a part that holds value for people working to make things more colorful, more effective, safer, or more precise. I’ve watched chemists reach for this compound because of its dependable performance and the specific benefits it can provide, depending on the needs at hand.
Think about the models and variants that people deal with in chemical sourcing. 2,4-Dibromo-1-Naphthol typically turns up as an off-white to light brown crystalline powder. The most trusted suppliers keep purity levels tight—often above 98% when measured by HPLC. Impurities matter in sensitive applications. I remember more than one team sidestepping headaches because they insisted on cleaner batches and solid documentation.
On a technical side, 2,4-Dibromo-1-Naphthol carries the CAS number 2925-19-5 and lines up with a molecular formula of C10H6Br2O. It boasts a molecular weight of about 314.97 g/mol. The two bromine atoms at the 2 and 4 positions shape this compound’s unique set of chemical responses. These details guide decisions for people behind the scenes, whether they’re matching a dye’s colorfastness or troubleshooting a batch synthesis in a pharmaceutical pipeline.
Nobody orders a specialized compound like this unless they have a good reason. You’ll find 2,4-Dibromo-1-Naphthol packed in airtight, light-resistant containers, often in small to medium lots to match lab-scale or pilot-scale production—not bulk industrial quantities. Reliable handling and packaging protect both stability and user safety.
Chemical specialists keep this compound on hand for a reason. I’ve talked with colleagues who trust it in synthetic dye manufacture. Its brominated naphthol structure makes it a useful intermediate in developing specialty colorants, especially where heat stability or resistance to fading is essential. The difference this makes to the end result isn’t something you can always spot at first glance, but it matters to the people making and using these dyes.
In pharmaceutical synthesis, it can step in as a building block. That means someone crafting advanced molecules may count on its reactivity at key steps in a multi-stage process, leveraging the naphthol’s oxygen and bromine positions for selectivity. Anyone with experience in organic chemistry knows that a dependable intermediate can save time, money, and raw materials in a complex synthesis. It pays off in higher yields and less troubleshooting down the production line.
Once in a while, I get questions from people developing specialty materials—polymers, high-performance additives, and research materials—who want a brominated aromatic nucleus for their work, and this compound fits the bill. The predictable behavior under reaction conditions brings peace of mind to busy researchers and production staff.
The naphthol family is broad, with many isomers and derivatives. Small tweaks in the position of substituents can lead to meaningful shifts in chemical behavior. In the case of 2,4-Dibromo-1-Naphthol, the positioning of the two bromine atoms brings unique advantages. Compared to its cousin, 1-Naphthol, or even 2,4-dibromophenol, the extra weight and electron effects added by bromine at the 2 and 4 slots alter its solubility, reactivity, and selectivity in cross-coupling and substitution reactions.
Some producers have told me they choose this molecule exactly because it steers reactions down a known path when exploring new synthesis approaches. For me, seeing a research chemist select this over simpler naphthol analogues is a sign they need that blend of stability and targeted reactivity. Others have mentioned that the bromine atoms allow for further modifications; these groups can act as handles for Suzuki, Stille, or Heck reactions that broaden a chemist’s toolkit when building up complex molecules.
There’s another angle, too: safety and environmental impact. I’ve experienced stricter rules around dangerous byproducts and waste disposal, especially with halogenated compounds. But compared to some older brominated naphthalene derivatives, 2,4-Dibromo-1-Naphthol tends to show a favorable profile in controllable lab and production environments, where proper waste management is already in place.
Anyone who’s handled procurement knows the frustration of inconsistent quality, delivery delays, or unclear documentation. I can recall several cases in which a poorly characterized or contaminated batch of specialized chemicals brought an entire lab project to a standstill. So, for 2,4-Dibromo-1-Naphthol, the consistent message from experienced colleagues and procurement pros remains: prioritize stable suppliers and full batch traceability.
In my experience, those who work directly with this compound in the lab respect its reactivity and take proper gear seriously—ventilation, gloves, and eye protection come standard. The crystal structure is less prone to dusting than some powders, but spills or airborne exposure still risk irritation. Most teams keep a clear records of storage temperatures and expiration dates to avoid unpredictable results or downtime.
It’s easy to get caught up in catalog numbers and batch certifications, but every purchase comes back to people making decisions with limited time and incomplete information. I’ve worked alongside researchers who have switched suppliers or formulas halfway through a project, always trying to balance performance demands, cost pressure, and logistical realities. Strong relationships with chemical providers mean a better shot at getting the right bottle to the right bench, with the data to back it up.
Choosing 2,4-Dibromo-1-Naphthol boils down to experience. I’ve come to trust the product from suppliers with a track record of clear COAs and who answer questions fast. That’s not just a matter of convenience. For teams burning through research budgets or facing regulatory reviews, speedy access to well-documented, consistently pure material makes a real difference.
There’s never just one route to the same synthesis goal. I’ve seen teams weigh options: maybe swap for a monobromo naphthol to cut costs or use a different isomer to try a new coupling route. Sometimes, that gamble pays off. But often, the advantages that 2,4-Dibromo-1-Naphthol brings in selectivity and post-synthetic modification simply can’t be matched, especially in moderate-scale or pilot research.
Some large-scale operations gravitate to other intermediates because of price or availability. From my seat, that makes sense when volume is everything and the chemistry allows it. For researchers targeting more precise or specialty needs, sticking with 2,4-Dibromo-1-Naphthol avoids wasted time re-optimizing reaction conditions or seeing yields drop below a project’s target. I recall one pharmaceutical team who tested cheaper naphthol alternatives but circled back because the added work to clean up impurities cost more in the end.
Another group I spoke with shared that, for some dye applications, they tried different halogenated aromatics after a supplier backlog, only to see performance on colorfastness and shelf life degrade. As with so many specialty chemicals, the well-established track record carries real value.
As someone who’s seen the chemical industry push through tighter regulations and shifting safety expectations, I’ve noticed that users of 2,4-Dibromo-1-Naphthol increasingly ask how the compound fits with sustainability goals. The brominated structure requires thoughtful handling and disposal. But new approaches in waste management, including solvent recovery and engineered containment systems, allow for safer, cleaner use of halogenated intermediates.
Teams adopting green chemistry best practices look for options to recycle or neutralize side streams. I’ve seen success stories where investment in scrubbers and in-line waste monitoring paid back quickly by reducing fines and process interruptions. It's heartening to see newer labs get built with these systems from the ground up, inspired by a mix of regulation and new staff who expect more from their employers.
Training also makes a difference. Where I’ve worked, refresher courses and clear communication around hazardous chemicals lead to fewer incidents and quicker responses if something does go wrong. Embedding safety into routine work builds a culture where nobody wants to cut corners just to save a few minutes.
Experience has shown me that no two labs approach a new project in the same way. Some people tackle projects with established protocols, moving cautiously and relying on tried-and-true chemicals like 2,4-Dibromo-1-Naphthol to give steady results. Others like to experiment—testing new green alternatives or custom derivatives if time and money allow.
This variety gives the industry its edge, fueling progress. But most recognize that safety, reliability, and reproducibility are not just checkboxes—they create the confidence that lets people take creative leaps. For mid-sized producers or scaling startups, a straightforward, well-characterized intermediate can unlock new product lines or speed time-to-market.
I once watched a startup struggle to scale a promising reaction for polymer additives. Their troubleshooting logs eventually showed that switching back to 2,4-Dibromo-1-Naphthol stabilized yields and helped them secure their next round of funding. It’s a pattern I see across sectors: trusted chemical building blocks drive progress, while poor substitutes derail it.
As the industry looks to automate and digitize more of its workflows, the value of clean, reproducible input chemicals will only grow. Software can flag impurities or inventory shortfalls in real time, but only if the materials themselves live up to their specs. That’s been my takeaway from reviewing sites that went digital first.
Trade wars, logistics disruptions, and even natural disasters can ripple through the world of specialty chemicals faster than you expect. I’ve heard purchasing teams recount days lost tracking down shipments for compounds like 2,4-Dibromo-1-Naphthol. Multiple sources—or regional stocking points—cut risk, but not every organization has the scale to line up three or four approved suppliers.
A reliable supplier relationship can smooth these rough patches and lock in priority status for new shipments. Larger customers often negotiate contracts that guarantee minimum stock levels in local warehouses. In my experience, small labs tend to work around spot shortages by partnering with academic groups or leaning on networked procurement services. The willingness to collaborate and share is stronger than most outsiders realize.
Documented shelf life and batch integrity matter more when restocking gets uncertain. Colleagues sometimes over-order or stretch old supplies further than comfortable just to keep projects moving. If you’re running time-sensitive research or regulatory testing, keeping a close eye on inventory and expiration dates can save an enormous amount of stress at the finish line.
The conversation around better chemical sourcing never really ends. I’ve found that regular supplier audits and open channels for feedback push companies to maintain higher standards. Watching industry bodies publish updated recommendations on documentation and traceable lot numbers gives hope that more labs will have what they need to trust the chemicals on their shelves.
As automation and digital documentation become standard, even small discrepancies in chemical identity or purity stand out sooner thanks to analytics software. That cuts down on failed syntheses and wasted time but means every chemical partner has to keep pace. From my own experience, being honest about unexpected impurities or supply interruptions builds a stronger relationship in the long run. Chemical production isn't a perfect science, but transparent communication and a willingness to address problems up front go a long way.
Green chemistry will keep driving the shift, especially for halogenated compounds. Early adopters see the importance of reusing solvents, minimizing solid waste, and switching to closed-loop systems. Those making the transition often find that the upfront work pays dividends in smoother audits, friendlier communities, and fewer workplace incidents.
Every chemical has its own story—how people discovered it, improved its preparation, and decided to rely on it. For 2,4-Dibromo-1-Naphthol, experience shows that it fills an important spot in modern research and production. The balance of purity, availability, and unique chemical behavior make it a consistent value-add for users with demanding needs.
Unlike commodity chemicals, where cost and bulk availability matter most, this compound sits in the zone where reliability and documentation count for more. That’s especially true for organizations bringing new pharmaceuticals to market, testing out advanced materials, or turning out dyes for industries with rigorous specs. Keeping a sharp eye on sourcing, supplier reliability, and regulatory compatibility helps guarantee success.
So much gets built on foundation stones like this one. Even with new alternatives and shifting market forces, the days I see the most progress are the ones where researchers, project managers, and safety officers have the right inputs and the right information. In that setting, 2,4-Dibromo-1-Naphthol still earns its place—not because it’s perfect, but because the people who depend on it make that choice from experience, diligence, and collaboration.