|
HS Code |
133661 |
| Chemicalname | 2-Bromo-6-Methoxynaphthalene |
| Casnumber | 3500-58-7 |
| Molecularformula | C11H9BrO |
| Molecularweight | 237.10 |
| Appearance | White to off-white solid |
| Meltingpoint | 85-88°C |
| Boilingpoint | 346°C at 760 mmHg |
| Density | 1.53 g/cm3 |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents like chloroform and dichloromethane |
| Smiles | COc1ccc2c(c1)ccc(Br)c2 |
| Inchi | InChI=1S/C11H9BrO/c1-13-10-5-4-8-6-9(12)2-3-11(8)7-10/h2-7H,1H3 |
| Refractiveindex | 1.650 (Predicted) |
| Storage | Store at room temperature, keep container tightly closed |
As an accredited 2-Bromo-6-Methoxynaphthalene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, sealed with a plastic cap, labeled with "2-Bromo-6-Methoxynaphthalene, 25g" and safety information, securely packaged. |
| Shipping | 2-Bromo-6-Methoxynaphthalene is shipped in tightly sealed containers to prevent moisture and contamination. It is handled as a hazardous material, with proper labeling and documentation as per regulatory guidelines. The product is transported under controlled conditions, avoiding extreme temperatures and physical shocks to maintain integrity and safety during transit. |
| Storage | 2-Bromo-6-methoxynaphthalene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from light, heat, and moisture. Ensure storage in a secure location out of reach of unauthorized personnel. Proper chemical labeling and adherence to safety data sheet (SDS) recommendations are essential. |
Applications of 2-Bromo-6-Methoxynaphthalene in Industrial ManufacturingOur proprietary production of 2-Bromo-6-Methoxynaphthalene serves advanced sectors demanding precise structural intermediates. Below are leading industrial use cases with dedicated regulatory, formulation, processing, and end-product requirements reflected in the actual practices of large-scale manufacturers and contract synthesis customers worldwide. 1. Pharmaceutical Intermediate SynthesisMajor pharmaceutical producers apply this compound for coupling and derivatization across oncology, anti-infective, and CNS drug syntheses. Its brominated aromatic structure enables directed substitution and key ring formation, supporting high-value active ingredient development. The raw material quality, traceability, and uniformity remain critical for scale validation and downstream regulatory compliance. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Active Compound ManufacturingLeading crop protection and agrochemical companies use this material to build specialty naphthalene frameworks in selective herbicides, fungicides, and pest control agents. The reactivity profile supports selective halogenation and methoxy substitution for targeted biological activity. Downstream customers rely on supply consistency and defined impurity profiles for their regulatory filings. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Specialty Dye and Pigment Precursor ProductionDye manufacturers utilize this compound as a key bridging unit for synthesizing high-performance naphthalene-based chromophores. Its chemical profile supports subsequent substitution for custom hues and light-fastness properties. Strict feedstock identity and performance data inform quality control and downstream blending processes. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Advanced Materials and Electronic Chemicals SynthesisProducers of specialty polymers and advanced electronic materials employ this compound in building blocks for OLEDs, liquid crystal alignment layers, and high-performance polyaromatic polymers. Its substitution profile and electronic properties support precise molecular engineering and enable miniaturized device fabrication. The raw material purity and low trace metal content are specified in electronics supply agreements. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2-Bromo-6-Methoxynaphthalene prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Producing specialty aromatic compounds can be both a science and an art. Our journey with 2-Bromo-6-Methoxynaphthalene reflects this reality daily in our facility. This molecule, known structurally as a brominated methoxynaphthalene, has developed a quiet but consistent reputation in the research and pharmaceutical sectors. Years of painstaking work in process optimization, purification, and scale-up have taught us how every decision during production—solvent choice, temperature control, reaction atmosphere—directly influences the final product’s consistency and usability.
The structure: one bromo atom and one methoxy group sit on the naphthalene backbone in precisely arranged positions, offering unique reactivity. At the most basic level, these substitutions create electronic environments that allow chemists to push the molecule into valuable transformations not so easily performed on plain naphthalene or even other bromo-naphthalenes. This feature is precisely what drove demand among organic synthesis specialists seeking to build more complex frameworks starting from this scaffold.
Consistency defines reliability in the specialty chemicals world. Many chemists have expressed frustration with small differences in color, purity, or particle size when sourcing from traders or resellers cutting corners to maximize short-term gain. Our plant’s workflow is built around minimizing these variables. Every batch of 2-Bromo-6-Methoxynaphthalene passes through repeated crystallization, vacuum drying, and sometimes even post-synthetic re-milling, simply because we have found that downstream reactivity improves when these steps are handled by experienced hands familiar with aromatic halides.
We remember a period years ago when we struggled with trace moisture in packaged product, causing problems in sensitive Grignard and coupling reactions reported back from a key customer’s lab. The solution involved equipment upgrades and a shift to argon blanketing. Most plants avoid this due to added cost, but waste less time troubleshooting avoidable issues. Customers report fewer unexpected side-reactions during Suzuki-Miyaura or Buchwald-Hartwig coupling when they begin with our material, a fact we attribute to relentless process troubleshooting and attention to handling.
Each lot comes as a solid white to off-white crystalline powder. The bromo and methoxy substitutions make this molecule substantially more versatile than plain naphthalene derivatives. Aromatic chemistry often comes down to functional handles—where can you add on, where can you pull off electrons, how can you direct further reactions? Technicians and chemists frequently choose this material because its bromine atom provides a reactive site for cross-coupling, and its methoxy group can steer regioselectivity in downstream reactions. This is not the case with unsubstituted naphthalene, which lacks such directional guides or activation.
Our standard material sits comfortably at high assay values, confirmed by independent third-party analysis. Many users struggle to verify exact regioisomeric content when sourcing through casual channels. Over years, we have honed analytical methods, not just GC and HPLC, but in-depth NMR control, ensuring no surprise isomers persist in the lot—an issue that can torpedo research or lead to expensive setbacks in scale-up. By controlling entire process chains from raw bromine and naphthol forward, we eliminate contamination that creeps in when multiple middlemen hide behind paperwork.
Physical properties match standard literature: a melting point that matches independently published values, a clear spectrum without residual starting material, and no detectable color bodies on TLC. Each of these quality markers serves a practical purpose. We have seen labs stalled by oily, off-spec bromonaphthalenes, while a clean crystallized product on the other hand dissolves readily and reacts predictably under standard coupling protocols.
Research groups and process development units working in pharmaceutical discovery turn to 2-Bromo-6-Methoxynaphthalene as an important intermediate. The bromo handle is perfect for palladium and nickel mediated cross-couplings, opening the molecule to subsequent complexity-building steps. The methoxy group influences both reactivity and the electronic character of products, which is useful in the synthesis of certain heterocycles and fused ring systems. Companies exploring custom dye molecules, or advanced materials for electronic prototypes, have also approached us, excited by the selectivity offered by this substitution pattern.
We have assisted R&D teams encountering trouble transferring reactions from bench to kilo scale. Granulometry, batch moisture, and purity consistency all become acute problems during scale-up that rarely matter on 100 mg scale. Our team’s input, born from decades of real plant experience, often helps partners navigate these bottlenecks. Where off-the-shelf bromoaromatics from traders often require hours of extra filtration or route-changing purification, customers consistently report faster optimization and lower development risk with our tightly controlled material. It's rewarding to see their projects move from flask to pilot unit without downtime spent hunting obscure contaminants or chasing down ill-characterized isomers.
Every producer makes claims about “high purity” and “batch consistency.” For years, we have proven these differences in practice, not just on paper. Our 2-Bromo-6-Methoxynaphthalene stands out in how reliably chemists achieve high yields in their key transformations. In cross-coupling chemistry, even trace levels of incorrectly substituted naphthalenes or unreacted starting material can derail long, expensive synthesis campaigns. We’ve tested competitive samples: common findings include persistent yellowish tint (often a sign of polybromo impurities or oxidation products), wider melting range, or inconsistent reaction rates when put through Suzuki coupling screens.
By contrast, we’ve documented smoother reaction profiles, less need for excess catalyst, and improved reproducibility with our batches. Years ago, a partner working on agrochemical intermediates compared our product head-to-head with three commercial alternatives. Their results showed not only faster coupling but less fouling of palladium catalyst beds and easier removal of by-products at workup. No single purity number on a certificate can explain these benefits; they come from tight upstream process control and experience with the chemistry’s quirks.
The methoxy group’s position on the naphthalene ring plays a subtle but powerful role. Its electron-donating effect influences not just reactivity, but also downstream chemical behavior—something we see reflected when R&D partners feed our product into multi-step syntheses for bioactive core structures. Several times, customers have come back after trying cheaper, off-brand bromo-naphthalenes, only to complain about unpredictable yields and color impurities in final products. Our process results in batches that keep projects moving forward.
Producing specialty aromatics brings real-life complexity every single cycle. Factors like precise temperature ramping or solvent sequence can swing yield and purity significantly. Over time, we’ve tackled fine points like in-process atmospheric control, solvent recovery to avoid cross-contamination, and tailored filtration. Unlike what some might think, bromination reactions demand serious expertise—halides can run wild without precise addition and mixing. Our crew has avoided countless batch losses by adjusting process parameters in real time, based not just on readings but on cumulative experience.
We’ve also invested heavily in real-time monitoring and in-house analytical capability. Sometimes, even small-scale reactivity screens under practical conditions serve as the best final test. In one instance, a barely perceptible yellow shift tipped us off to an upstream impurity that HPLC missed, and this troubleshooting saved a pharmaceutical customer enormous headache downstream. We’ve often trained partners in how subtle material quality differences impact their synthesis outcomes; those lessons pay dividends for both sides long-term.
Shipping specialty chemicals isn’t just logistics. The moment lots leave our plant, we recognize how sensitive materials can degrade under the wrong conditions, so we’ve developed both packaging and handling protocols using input from our team and end users. Every year, practical field feedback returns into our production loop, refining everything from fill weights to packaging seal strength for moisture-sensitive intermediates like this one.
Many customers have told stories of delays and confusion from working through international trading layers or unclear provenance. No matter the market pressure to cut corners, we believe in direct traceability—each batch can be traced back to our precise reactor history, reagent lot, drying cycle, and QC record. Open transparency keeps everything grounded; we welcome audits and joint investigations of challenges. Some companies try to mask poor material under paperwork, but we stand behind the actual molecules in each drum or jar sent out.
Throughout our time making 2-Bromo-6-Methoxynaphthalene, we have chosen to highlight hands-on process insight. Whether working with small biotech startups or major multinational chemistry teams, we prioritize ongoing technical exchange. Sometimes, this means custom tweaks to batch scale, physical form, or even special sieving to match unique process constraints in customer protocols. We don’t see this as a burden—each adjustment deepens mutual trust and improves everyone’s results.
Countless synthetic successes and failures start with the input quality. From medicinal chemistry teams racing to build libraries, to engineering groups designing luminescent polymers, reliable, reproducible starting materials reduce cost, trim dead time, and, above all, make new discoveries achievable. For many, specialty halogenated aromatics like 2-Bromo-6-Methoxynaphthalene represent one ingredient among dozens, but gaining control over results often starts with who actually makes the molecules at the plant level.
We have lost count of the number of times research groups found themselves stuck after purchasing through anonymous brokers, only to discover compromised product and no recourse. Our direct relationships enable fast turnaround: if a customer encounters a problem, we trace, test, and advise in real time—there’s no stalling behind call centers or paperwork backlogs. For a product as specialized and reactive as this, access to the manufacturing source creates an insurance policy that generic resellers simply cannot offer.
2-Bromo-6-Methoxynaphthalene isn’t the most famous molecule on any chemist’s shelf, but it occupies a vital spot in the toolkit of those building up more complex aromatic scaffolds, tailored pharmaceuticals, or high-performance materials. We understand exactly what goes into every jar and take pride in knowing each gram can anchor a dozen or a hundred further steps in someone else’s synthesis campaign.
The specialty chemicals landscape never stands still. As regulatory demands evolve and customers push for ever more robust supply chains, we press forward with investment in both process automation and staff training. Our latest upgrades integrate predictive analytics, reducing risk and waste before it makes a mark on the lot. Feedback from seasoned chemists facing unexpected bottlenecks pushes us to innovate, while our laboratory team constantly explores new purification techniques, greener solvents, and safer process modifications.
Close contact with research partners has shown us gaps in availability for related structures or for even greater batch-to-batch precision. We don’t rest on current process specifications but constantly re-examine how tweaks can cut downtime, improve selectivity, or smooth scale-up. That insight drives steady, sustainable gains in purity, consistency, and supply reliability.
Our experience has proven that attention to detail transforms specialty chemical manufacturing from a commodity business into a collaborative innovation engine. Each drum, each batch, reflects hands-on expertise, not generic paperwork. As we continue refining our production of 2-Bromo-6-Methoxynaphthalene, customers can count on the depth of support, traceable quality, and real problem-solving that come only from those who manufacture, not simply sell, specialty aromatics.
The path from raw material to finished chemical teaches us new lessons with every campaign. Starting from reliable inputs like high-purity 2-Bromo-6-Methoxynaphthalene, chemical innovators build everything from candidate drugs to advanced coatings and electronics. On-the-floor insight combined with open technical exchange keeps projects on track and launches discoveries beyond the limitations of inconsistent starting materials. We remain as committed as ever to advancing that progress, supporting every customer with the experience and reliability only a true manufacturing source can provide.