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HS Code |
581393 |
| Cas Number | 608-32-2 |
| Molecular Formula | C10H6Br2O2 |
| Molecular Weight | 334.97 g/mol |
| Iupac Name | 2,6-dibromonaphthalene-1,5-diol |
| Appearance | Light brown to tan crystalline powder |
| Melting Point | 242-245 °C |
| Solubility | Slightly soluble in water, soluble in organic solvents like ethanol and acetone |
| Density | 2.25 g/cm³ (approximate) |
| Pubchem Cid | 100629 |
| Smiles | C1=CC2=C(C(=C1O)Br)C(=CC=C2O)Br |
| Synonyms | 1,5-Dihydroxy-2,6-dibromonaphthalene |
| Storage Conditions | Store at 2-8°C, in a dry and tightly sealed container |
| Ec Number | 210-150-7 |
As an accredited 2,6-Dibromo-1,5-Dihydroxynaphthalene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle with a secure screw cap and hazard labeling, clearly marked as 2,6-Dibromo-1,5-Dihydroxynaphthalene. |
| Shipping | 2,6-Dibromo-1,5-dihydroxynaphthalene is shipped in sealed, chemical-resistant containers. Packaging complies with international regulations for hazardous materials. The substance should be stored and transported in a cool, dry place, away from incompatible materials. Ensure proper labeling and documentation. Handle with care—use appropriate personal protective equipment during all shipping and handling procedures. |
| Storage | 2,6-Dibromo-1,5-Dihydroxynaphthalene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition. Protect from direct sunlight, moisture, and incompatible substances such as strong oxidizers. Ensure the container is properly labeled, and handle using appropriate protective equipment to prevent skin and eye contact. Store according to local regulations. |
Applications of 2,6-Dibromo-1,5-Dihydroxynaphthalene in Industrial ManufacturingAs the direct manufacturer of 2,6-Dibromo-1,5-Dihydroxynaphthalene, we support customers in multiple downstream sectors where this intermediate offers unique molecular functionalities. The following application areas represent core industries with distinct formulation, quality, and regulatory requirements. 1. Synthesis of Vat Dyes for Textile IndustriesIn vat dye production, 2,6-Dibromo-1,5-Dihydroxynaphthalene serves as a principal building block for high-performance anthraquinone-based colorants. Dye manufacturers introduce this compound during condensation reactions with chlorinated anthraquinone derivatives, thereby modulating hue stability and wash fastness essential for denim and industrial fabric applications. End-users target deep, long-lasting shades in both natural and synthetic fiber products, demanding precise bromination patterns and high-purity intermediates from raw material suppliers. Industry compliance standards
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2. Pharmaceutical Intermediate for Anti-Infective APIsPharmaceutical manufacturers rely on 2,6-Dibromo-1,5-Dihydroxynaphthalene as a key intermediate in multi-step syntheses for certain naphthalene-derived active pharmaceutical ingredients, particularly in the anti-infective segment. Synthesis typically involves oxidative coupling with additional halogenated components under controlled temperature and pH, precise to ICH Q7 GMP guidelines. Accurate process validation and impurity control at this stage are critical for producing drug substances that meet international pharmacopoeia standards. Industry compliance standards
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3. Monomer Precursor in High-Temperature Polymer ChemistryHigh-end polymer manufacturers use 2,6-Dibromo-1,5-Dihydroxynaphthalene as a specialist dihydroxylated aromatic monomer for condensation polymerizations yielding resins with enhanced thermal stability and flame resistance. The compound enters the process at the pre-polymerization stage, reacting with isocyanate or diacid monomers. Stringent control of substituent distribution supports production of aerospace-grade composites and high-performance laminates where mechanical and temperature specifications must be certifiable. Industry compliance standards
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4. Specialty Ligand Synthesis in Agrochemical ResearchR&D units in the agrochemical sector deploy 2,6-Dibromo-1,5-Dihydroxynaphthalene as a modular ligand precursor when synthesizing metal-chelate pesticides and herbicide actives. The material’s stable dihydroxy and dibromo positions allow custom coordination with transition metals, affording unique selectivity in chelate complexation reactions. Accurate stoichiometric dosing and reaction monitoring help ensure reproducibility in lab-to-pilot scale translation, crucial for active ingredient development under evolving agrochemical regulations. Industry compliance standards
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2,6-Dibromo-1,5-dihydroxynaphthalene has shaped the way specialty chemicals lay the groundwork for advanced manufacturing across a wide landscape of sectors. As a chemical producer with decades spent perfecting naphthalene derivatives, the real-world performance and practical value of each batch speak louder than technical jargon. Our direct experience in handling, refining, and supplying this compound brings forward a perspective built on consistency, deep process knowledge, and the challenges met on the chemical plant floor.
Our 2,6-Dibromo-1,5-dihydroxynaphthalene, commonly known in the specialty chemical circuit as a key naphthalene derivative, typically arrives to formulators and R&D teams as an off-white to faintly colored crystalline solid. The stability and reactivity fill a crucial niche — this molecule’s structure, featuring two robust bromine atoms at the 2- and 6-positions flanking a pair of hydroxyl groups, means it operates as both a versatile intermediate and a platform for more complex substitutions. The technical nuances behind this specific substitution pattern — two electron-withdrawing bromines and two activating hydroxyls — push its reactivity further than what you’d find in simple, unsubstituted naphthalenes or mono-halogenated variants. Our teams observe these distinctions each production cycle; the differences go far beyond what textbook diagrams can convey.
Producing this compound calls for careful management of bromination and subsequent hydrolysis steps. Over the years, our process engineers have tackled not only the challenges of regioselectivity but also the elimination of unwanted polybrominated by-products. These unwanted variations can stunt yield, impede downstream reactions, and, if unchecked, contaminate what should be a sharp, high-purity intermediate. As seasoned manufacturers, the ability to tune reaction conditions — everything from temperature modulation in the bromination reactor to strict timing at each stage of purification — underpins consistent quality. Analytical checks built into the workflow go beyond point-of-sale specs; they focus on repeatable performance in application, batch after batch.
Our in-house systems handle not just raw synthesis but end-to-end logistics — from containment of corrosive bromine in closed-loop setups to dedicated solvents that maximize conversion and minimize waste. This hands-on experience speaks volumes about real-world safety, low trace impurity profiles, and overall reliability. What sets our approach apart isn’t an abstract claim to purity or quality. It’s about maintaining those levels over hundreds of batches, over years of shifting customer needs, and the deep process memory captured in every iteration of plant operation.
From the earliest days making this compound, customer focus came down to more than paper specs. Chemists and technical directors from dye plants, pharmaceutics R&D, and electronic materials have challenged us to adapt particle size, batch volume, and impurity limits. Most of the time, laboratories want product at a purity exceeding 98% by HPLC, with water content and trace halide residues at the lowest practical level. The melting range provides insight into isomeric purity and preparation quality — we target a consistent bracket that reflects a controlled, repeatable synthesis and drying stage.
Differences from related products leap to the foreground in practice. Compared to mono-brominated or unsubstituted 1,5-dihydroxynaphthalenes, the dibromo analog retains higher electron density at key positions, which chemists exploit for further substitution. In downstream synthesis of dyes, pigments, or specialty polymers, our customers note the unique reactivity profile of this compound: it promotes selective coupling, introduces controlled halogenation into advanced molecules, and enables access to color spaces or property windows that remain out of reach for more common intermediates.
Markets for naphthalene-based compounds don’t hold still. Changes in regulatory landscape, environmental standards, and customer R&D priorities all flow back into our factory floor. For example, brominated intermediates have come under close scrutiny in some sectors for their environmental persistence. Our own commitment to responsible manufacturing, solvent recovery, and strict minimization of fugitive emissions respond directly to those concerns. While regulations shape permissible impurity levels and guide us toward best manufacturing practices, our own data-driven approach seeks more — reducing process waste, maximizing product isolation yields, and ensuring waste disposal matches current environmental protocols.
Feedback from actual downstream users — not just sales data — provides our sharpest sense of what’s working and where improvements should land next. That could be a finding that a new class of naphthyl-derived building blocks launch more smoothly with lower chloride contamination, or that pigment mills operating in high-humidity regions benefit from reduced water-of-crystallization content. In our view, every challenge is charted and addressed within the real constraints and possibilities of a large-scale, real-world chemical plant.
Over a generation in this business, we’ve tracked the spread of 2,6-dibromo-1,5-dihydroxynaphthalene far beyond its early niches. Dyes and pigments formed the first clear market, where the molecule moved directly into the heart of chromophore synthesis. Its role as a precursor for bright, lightfast reds, violets, and sophisticated specialty shades relies on the controlled dihalogenation point, which resists overreaction and preserves the planned color development.
Pharmaceutical and agrochemical researchers value the molecule for the way it combines chemical robustness with modifiable positions. The dibromo unit stays put through condensation and cyclization steps, while the hydroxyl groups can drive further elaboration: etherification, esterification, or coupling to more advanced frameworks. Each property gained through these modifications tracks back to the exact placement of the bromo and hydroxy groups — our attention to positional purity preserves every benefit downstream.
Organic electronics research, including advanced polymer chemistry and thin film materials, has opened new paths for this intermediate. The bromines serve as coupling handles for cross-coupling and Suzuki-type reactions, producing materials with tightly controlled optoelectronic properties. We’ve seen real-world results as our partners in these fields achieve target band gaps, stability profiles, and processability thanks, in part, to a clean, reliable starting material batch after batch.
Debates over which intermediate best suits a target molecule rarely get settled by theoretical reactivity alone. On the factory floor, mono-brominated or other positional isomers can cause issues in both yield and selectivity. For customers who need high reproducibility, trace isomer contamination can translate to lower batch yields, extra purification steps, or even failed regulatory submissions due to unidentified impurities. The two bromines situated at 2 and 6 on the naphthalene ring put our product in a league of its own, allowing much more controlled reaction pathways and making it a favorite for complex architectures.
We’ve tested many variants ourselves before settling on this one as our flagship dual-brominated naphthalene. Consistent results in next-step coupling reactions, predictable crystallization patterns, and clean melt behavior matter to our process partners. Other materials, such as mixtures of mono- and di-bromo naphthalenes, tend to fall short — more elaborate purification is needed, and downstream users face unexpected losses. Our compound’s repeatable, high-yielding synthesis steps give a confidence and economy that generalized mixtures or less controlled alternatives simply don’t provide.
For users accustomed to batch-to-batch irregularity or fluctuating impurity levels, our approach built on rigorous in-process monitoring pays off in both ease of use and regulatory compliance. We’ve heard from multiple partners that switching to our product streamlines not just lab work, but documentation and QA in line with ISO and environmental frameworks.
Every innovation in specialty chemicals, dyes, electronic materials, and pharmaceuticals builds on reliable intermediates. Our product plays a vital role in those supply chains. By focusing on raw material stability, narrow impurity profiles, and transparent traceability, we help customers unlock new routes in their own research. Reliable 2,6-dibromo-1,5-dihydroxynaphthalene shipment after shipment — matching specs with tested, lived-in experience — keeps production lines and R&D projects moving ahead.
Changes in demand signal shifts in end-user priorities. As customers move toward greener, safer, and more specialized processes, we respond by investing in better solvent systems, process automation that improves isolation and drying, and regular retraining on handling of brominated and hydroxy-aromatic intermediates. Our goal is grounded in sustained partnership: adjusting specs, shipment volumes, or supportive documentation so the work at the user’s end runs smoothly every time.
Our own technical service team, drawn from chemical engineering and applied chemistry backgrounds, supports scale-ups and adapts to process changes. They’ve seen — and solved — problems that rarely make it onto datasheets: crystallization issues from unexpected humidity, batch-end color formations that signal oxidation, or plant-scale filtration challenges at high throughput. As a direct producer, the feedback we capture on each incident moves straight into our continuous improvement practices.
Quality assurance in naphthalene derivatives begins well before drums and containers roll out the gate. As a manufacturer, every tankful starts with highly screened starting materials — naphthalene feedstocks with tightly controlled aromatic purity, bromine sourced from audited, consistent pools, and reagents that meet set reactivity and residue criteria. Throughout synthesis, process chemists and plant operators track every drop of reactant, every glycol flow rate, every distillation fraction. Our own operators have spent years learning the subtle cues — shifts in color development, onset of exotherms, or formation of unwanted side fractions — that signal the difference between a successful run and a costly rework.
The purification steps matter as much as the main reactions. Efficient liquid-solid separation, careful solvent switching, and mechanical handling all work together to avoid cross-contamination and maximize product capture. Final drying takes place under conditions fine-tuned to prevent both product dehydration (which can damage crystal integrity) and excessive residual solvent (a risk for sensitive downstream transformations).
Each batch goes through a regimented QC regime, blending classic spot tests (for halide, coloration, and moisture) with state-of-the-art chromatography. The results, logged and trended across years of production, reveal strengths and weak points, informing not just whether a shipment releases, but how to evolve practice for the next batch or plant expansion.
Today’s market demands more than chemistry. Working as the original manufacturer comes with responsibility for traceability, batch-level documentation, and open reporting on safety and environmental impacts. Our records, running from raw material origin to final product shipment, capture not just compliance, but a history of continuous improvement and honest engagement with the realities of industrial chemistry.
All our plant operators and supervisors hold themselves to the same safety and ethical standards, whether dealing directly with hazardous intermediates or adjusting recipes in a climate of changing international expectations. We close the loop with end users, taking questions and feedback as direction for future upgrades, not as simple after-sale service. Honest engagement — admitting a missed specification, acting rapidly on complaints, sharing best-practice protocols — upholds not just regulatory requirements, but a long-standing culture of mutual respect.
Production audits open our doors to customer review teams, letting them see the cleanliness and precise tracking at every production stage. This gives downstream innovators the confidence to build demanding, high-value products on the back of our intermediate. In return, our own teams benefit from understanding new application goals, regulatory trends, and upcoming product areas. This cycle of open communication, transparency, and documented traceability shapes our commitment to both environmental stewardship and technical advancement.
Cutting-edge research programs and day-to-day factory output both depend on reliable sources for key intermediates. 2,6-Dibromo-1,5-dihydroxynaphthalene, as produced through our seasoned, closely-managed processes, forms one critical link in these value chains. We continue adapting synthesis protocols, tightening in-process controls, and expanding ecological safeguards not as a response to passing regulatory trends, but out of grounded experience on what works over years.
Customers pushing the limits of dye chemistry, organic semiconductors, or specialty molecular architectures turn to suppliers with the infrastructure and practical confidence to meet complex requirements — not just today, but over the horizon. Over countless syntheses and product upgrades, we witness firsthand the transformative effect a reliable, clean, high-purity intermediate holds over entire lines of finished goods. Infusing that practical knowledge into every run, and honoring technical feedback from our customers, remains both our day-to-day work and our guiding principle.
Our perspective on 2,6-dibromo-1,5-dihydroxynaphthalene arises from active engagement in its journey from raw chemical building block to the advanced products fueling tomorrow’s industries. The difference isn’t just in a spec sheet or an assay value — it shows in consistency, customer trust, and a history built up batch by batch. We welcome questions, specific requests, and new performance requirements; those challenges have shaped better chemistry, better products, and enduring partnerships throughout our decades of manufacturing.