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HS Code |
993112 |
| Chemicalname | 3-Bromo-2-Naphthol |
| Casnumber | 144-32-7 |
| Molecularformula | C10H7BrO |
| Molecularweight | 223.07 |
| Appearance | Light yellow to beige solid |
| Meltingpoint | 110-113°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Density | 1.68 g/cm³ |
| Purity | Typically >98% |
| Synonyms | 3-Bromo-2-hydroxynaphthalene |
| Storagetemperature | Store at 2-8°C |
| Smiles | Brc1cc2ccccc2c(O)c1 |
| Inchi | InChI=1S/C10H7BrO/c11-8-5-7-3-1-2-4-9(7)10(12)6-8/h1-6,12H |
As an accredited 3-Bromo-2-Naphthol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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In the world of organic synthesis, a few compounds make life easier for both industrial chemists and researchers forging new ground. 3-Bromo-2-Naphthol sits among these unsung heroes. Its formula, C10H7BrO, may seem modest, yet it opens doors to a range of downstream chemicals and advanced materials. With a white to pale yellow solid appearance and a molecular weight of 223.07 g/mol, this compound stands out in labs that value versatility. Whether it’s about building blocks for pharmaceuticals or creating specialty dyes, 3-Bromo-2-Naphthol proves itself time and time again.
Let’s consider how it’s put to use. Organic chemists use 3-Bromo-2-Naphthol as a starting point for more complicated molecules. The bromine atom at the 3-position creates reactive sites, so it enters cross-coupling reactions smoothly. Suzuki-Miyaura and Buchwald-Hartwig reactions, which are foundational tools for assembling drug candidates, often rely on this molecule. At the same time, its naphthol structure gives it unique electronic properties. This comes into play for dye and pigment synthesis, leading to robust colors. Some of these end up in materials science applications, like organic light-emitting diodes. The chemical’s versatility means that users frequently value not just what it is, but what it enables.
Chemists know that consistency counts for a lot. Supply chains have seen plenty of uncertainty, but users of 3-Bromo-2-Naphthol seek qualities they can trust. The best batches arrive as well-defined crystals, with purity levels that reduce background noise in research or production. Look for melting points in the 100-105°C range, crisp and sharp melting profiles, and quick solvency in popular lab solvents—this eases process integration for both research and scale-up. In my own experience, solid handling and straightforward solubility go a long way when projects run on tight deadlines. You don’t want surprises or delays from raw materials.
Safety deserves attention as well. 3-Bromo-2-Naphthol is classified as an irritant in many regions, requiring responsible handling and proper PPE. Industry standards call for storage in cool, dry places, away from incompatible agents. With smart practices and well-trained staff, risks remain manageable. There’s peace of mind in knowing a product’s hazards upfront—nobody likes learning about reactivity or toxicity in the middle of a batch run.
It’s easy to lump 3-Bromo-2-Naphthol together with other naphthol compounds, but experienced chemists soon notice its unique character. Compare it to 1-Naphthol, for example. 1-Naphthol lacks the bromine substitution, resulting in a completely different profile in synthetic routes. The bromine group on the third carbon isn’t a minor tweak—it turns a relatively non-reactive ring into a lively participant in reactions prized by many industries. Chemists cherish this because it streamlines pathways to arylated products or advanced ligands. For researchers focusing on material science, this means more latitude in introducing functional groups and exploring new properties.
Let’s look at a more common counterpart: 2-Naphthol. While it shares the hydroxyl group at the 2-position, the absence of bromine points it in divergent directions. Its applications focus more on dye manufacture and antioxidant studies, not advanced cross-coupling or late-stage functionalization. Introducing the bromine atom at the 3-position changes both the electronic nature and subsequent reactivity of the molecule, giving chemists a reliable tool for selective substitution. In my own lab work, the difference between reaction efficiency and unwanted byproducts often boiled down to these subtle structural choices.
This all comes alive outside journal articles. In pharmaceutical research, where time pressures run high and failure rates eclipse 90%, a reagent that can introduce complex groups reliably gives a much-needed edge. For example, using 3-Bromo-2-Naphthol as a coupling partner accelerates the discovery of kinase inhibitors, antifungals, or anti-cancer molecules. Its predictable behavior cuts down on late-stage surprises. From startups to large companies, this reliability can mean the difference between a shelved project and a patent application.
For materials scientists, the story continues. Research into organic semiconductors leans on robust aromatic compounds. The bromine in 3-Bromo-2-Naphthol can support the fine-tuning of conjugated polymers, leading to useful properties like increased charge mobility or tunable photoluminescence. Some of these polymers turn up in flexible electronics—a field where innovation moves fast and the materials library keeps expanding. Actual end-users see benefits in faster displays, thinner device profiles, or longer-lasting OLED lights. None of this happens without the right building blocks.
Over the years, labs and companies have seen ups and downs in the supply of specialized reagents. Trade realities and global disruptions made it clear that not all molecules are created equal. Those working with 3-Bromo-2-Naphthol report variable availability, as this is not a mass-market commodity. The best sources provide analytical data including NMR, IR spectra, and HPLC traces—these help confirm that what arrives matches what’s promised. Buyers tend to scrutinize each lot’s certification of analysis, not just as a box-ticking step, but as insurance for their downstream work. From my own experience, a well-documented supply beats a mystery container every time, especially when the next step in your synthesis can cost thousands of dollars in resources.
Sustainability has started to take priority as well. The traditional synthesis of 3-Bromo-2-Naphthol requires halogenation and a careful balancing of yields, waste, and hazards. Researchers in green chemistry now seek routes that generate less hazardous waste and make better use of solvents or catalysts. Some suppliers now adopt newer techniques, using flow chemistry or recyclable reagents. These approaches won’t just tick environmental boxes—they often reduce cost and boost efficiency over time. Still, more industry collaboration and willingness to try new routes could strengthen long-term resilience, cut down on waste, and support both regulatory compliance and public image.
No modern commentary can skip over the increasing role of safety and regulation in chemical supply chains. 3-Bromo-2-Naphthol, given its structure, avoids the kind of spotlight reserved for controlled substances, but manufacturers and end-users still track compliance with local and international standards. REACH, GHS, and other frameworks determine labeling and transport requirements; no one can afford to ignore these if they want their products to move efficiently across borders.
On the factory or research floor, this means investing in hazard training and response plans. Spills or accidental contact need to be managed with solid protocols. In the mid-2010s, incidents involving basic naphthol handling underlined the value of robust safety procedures in preventing exposure and minimizing disruption. Whether it’s as simple as a well-stocked eyewash station or as robust as a remote access chemical inventory system, these investments in safety infrastructure keep chemists out of emergency rooms and projects on track.
Some people see specialty chemicals as arcane or marginal, but anyone working at the intersection of research and commercialization knows better. Every established process started as a wild idea in a lab, powered by the availability of the right compounds. For undergraduate students, handling a reagent like 3-Bromo-2-Naphthol can spark curiosity, leading to new ideas and deeper understanding. In graduate research, its role in functionalizing aromatic compounds often determines the feasibility of ambitious synthetic strategies and the depth of collaboration with partners in pharmacology or advanced materials.
As more research groups focus on molecular design, demand for specialty intermediates like 3-Bromo-2-Naphthol will likely increase. Computational chemists run virtual screens that point toward unexplored derivatives, but these models need real-world compounds to test and validate predictions. The compound’s track record in generating analogs with novel activity keeps it firmly in the toolbox of innovators, not just bench chemists but also those working to automate and digitize drug development.
Sourcing and making complex aromatics is rarely a simple task, especially at scale or when purity requirements push into the decimals. Researchers continue to develop new ways to prepare 3-Bromo-2-Naphthol, seeking better yields and greener processes. Traditional methods often rely on elemental bromine—a substance that brings its own hazards and regulatory headaches. The drive to replace these with catalytic bromination, or in-situ bromine generation, shows up in recent conference presentations and in the patent literature.
Some groups now use modern catalysts that selectively deliver bromine only where it’s wanted, slashing byproduct levels. Switch to continuous-flow setups, and the process gains both speed and safety, as smaller reaction volumes reduce the hazard profile. Yet, these benefits need buy-in from plant staff and decision-makers who may prefer older, proven recipes. Academia, consulting with industry, has a real shot at bridging this gap. It’s not just about being greener—it’s about responding to real supply volatility and cost pressures. Small advances in method or materials can ripple out, improving reliability in research-driven fields.
Cost always figures into planning for chemical synthesis, whether the order is a few grams for a thesis project or several kilograms for a pilot line. The price of specialty compounds like 3-Bromo-2-Naphthol can shift sharply. Raw material availability, logistics, and complexity in synthesis contribute to regular swings. Companies able to forecast demand and secure long-term suppliers ride out turbulence, while those who buy on the spot market risk missing critical timelines. Chemical supply chain resilience means more than contracts; it’s built on trust, transparency in sourcing, and shared incentives between buyer and seller.
For educators thinking ahead, this landscape calls for more training in procurement, not just reaction mechanisms. The next generation of chemists will need not just technical skill at the bench but also the practical know-how to ask the right questions before they order a crucial reagent. The best programs now blend lab skills with modules on supply chain and compliance. Those who can navigate this new landscape will feed smoothly into either research or industry, better prepared for both breakthrough discoveries and the day-to-day realities of modern labs.
Every chemical in the storeroom carries a story, but only a select few unlock so many opportunities across disciplines. 3-Bromo-2-Naphthol isn’t just a molecule on a shelf; it’s a flexible partner for those working at the border of discovery and application. Whether your focus lies in the fine-structure of pharmaceuticals or the rapid evolution of new materials, this compound deserves a place in your toolkit. My own experience with naphthol derivatives has shown that small details in molecular structure often spell the difference between success and wasted effort. Discussing, planning, and troubleshooting synthesis often comes down to access to smart reagents like this one.
As research pushes toward more tailored syntheses and scalable, eco-conscious manufacturing, the demand for versatile intermediates remains strong. Producing and using 3-Bromo-2-Naphthol highlights a blend of traditional chemistry and forward-looking innovation. Working together—chemists, suppliers, and regulators—there’s a good chance to keep improving both the science and the practice behind these indispensable compounds.
The future for 3-Bromo-2-Naphthol, like so many specialty compounds, grows brighter with collective efforts. Open communication between those producing, using, and regulating chemicals supports both progress and safety. Researchers gain by sharing not just data, but practical notes about real-world performance. Manufacturers respond by improving consistency, investing in safer, greener synthesis, and offering better documentation. Regulators, in turn, continue to refine frameworks that keep people and environments safe while supporting innovation.
Building on this culture of transparency, the value derived from intermediates like 3-Bromo-2-Naphthol spreads out, touching not just labs and factories but the lives of patients, consumers, and students. As a writer and a chemist, I see real meaning in this web of relationships. Every insight gained at the bench or in a production line becomes a resource, growing the global knowledge base and supporting smarter science in years to come.