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HS Code |
366844 |
| Productname | Methyl 6-Bromo-2-Naphthoate |
| Chemicalformula | C12H9BrO2 |
| Molecularweight | 265.10 g/mol |
| Casnumber | 63469-45-2 |
| Appearance | Off-white to light yellow solid |
| Meltingpoint | 100-104°C |
| Purity | Typically ≥98% |
| Boilingpoint | 402.2°C at 760 mmHg |
| Solubility | Soluble in organic solvents (e.g., dichloromethane, ethanol) |
| Storagetemperature | Store at 2-8°C |
| Smiles | COC(=O)c1ccc2cc(Br)ccc2c1 |
| Hscode | 29144090 |
| Synonyms | 6-Bromo-2-naphthoic acid methyl ester |
As an accredited Methyl 6-Bromo-2-Naphthoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical, Methyl 6-Bromo-2-Naphthoate, is supplied in a sealed amber glass bottle, 25 grams, labeled with hazard and handling instructions. |
| Shipping | Methyl 6-Bromo-2-Naphthoate is shipped in tightly sealed containers to prevent contamination and moisture exposure. The package is clearly labeled, stored in a cool, dry environment, and handled as a hazardous chemical. Appropriate documentation accompanies the shipment, following all regulations for transport of laboratory reagents and brominated aromatic compounds. |
| Storage | Methyl 6-Bromo-2-Naphthoate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep it away from incompatible substances such as strong oxidizers. Store at room temperature and avoid excessive heat or moisture. Use appropriate chemical storage protocols, including proper labeling and secondary containment if necessary. |
Applications of Methyl 6-Bromo-2-Naphthoate in Industrial ManufacturingAs a chemical raw material manufacturer, we supply Methyl 6-Bromo-2-Naphthoate for specialized industrial applications that require advanced naphthalene derivatives. The material serves as a precision intermediate in several tightly regulated sectors, each with its own compliance, technical, and production nuances. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisMethyl 6-Bromo-2-Naphthoate is essential for the preparation of naphthyl-based intermediates in the synthesis of antihypertensives and antifungal APIs. Process chemists use this compound in bromination and subsequent substitution reactions, especially where regioselective modification of the naphthalene ring is critical for molecular activity and patent scope. Downstream, this material supports scale-up to batch or continuous synthesis under cGMP conditions. Industry compliance standards
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2. Agrochemical Intermediate for Fungicide SynthesisThis naphthalene ester is a key intermediate in the synthesis of systemically acting fungicides. It supports multi-step synthesis for broad-spectrum crop protection chemicals. Formulation chemists rely on the reactivity of the 6-bromo position for incorporation into naphthalene-carboxylate and related agrochemical structures, especially within manufacturing protocols that demand high conversion rates and purity profiles for regulatory approval in food applications. Industry compliance standards
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3. Electronic Chemicals: Precursor in Organic Semiconductor ManufacturingMethyl 6-Bromo-2-Naphthoate is used by electronic material producers as a building block for developing naphthalene-based conjugated molecules in organic light-emitting diodes (OLED) and organic field-effect transistors (OFETs). Its controlled reactivity provides precise halogen functionality for cross-coupling reactions, enabling high-purity electronic grade products essential for device performance and lifetime. Industry compliance standards
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4. Dye and Pigment Synthesis for Specialty ColorantsProducers of high-performance dyes and specialty pigments use Methyl 6-Bromo-2-Naphthoate for the targeted synthesis of naphthalene-based chromophores. The compound provides brominated aromatic functionality for introducing vivid hues, especially where high thermal and light stability are required in automotive coatings, high-end plastics, or printing inks. QC labs require precise tracking of side products and conformance to migration or heavy metal regulations in finished goods. Industry compliance standards
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We manufacture methyl 6-bromo-2-naphthoate as a specialized organic compound, engineered through years of hands-on chemical synthesis experience. With a bromine atom substituted at the sixth position of the naphthalene ring and a methyl ester at the second, this molecule belongs to a unique family of naphthalene derivatives prized for selectivity in downstream reactions. We’ve produced this molecule with careful batch controls and rigorous process monitoring, focusing on reliability and consistent output, because too many research programs and production lines stall on unreliable intermediates. Unlike more linear esters or less functionalized naphthalenes, methyl 6-bromo-2-naphthoate often delivers cleaner, more predictable reactivity in bromination-driven pathways and ester-centered syntheses.
Our methyl 6-bromo-2-naphthoate carries an exact molecular structure—C12H9BrO2—backed by routine NMR, LC-MS, and GC testing. Years of production have sharpened our understanding of what makes this compound acceptable for medicinal chemistry, pigment work, or advanced materials research. Laboratories ask us for low-residue, highly pure lots. We prepare it as an odorless, off-white solid, melting between 94 and 97°C by DSC measurement, and it resists aerial oxidation during storage. Moisture content runs below 0.2% by Karl Fischer titration. Typical batch purity by HPLC comes in above 99%.
You won’t find unnecessary fillers or additives. Every time analysts trace an outlier, we dig into reagent history, glassware residue, or environmental controls to find the source. Customers often comment on how our product flows—powdered firmly, not lumpy or stuck, so lab techs waste less time on handling or sample dividing. As chemists ourselves, we keep the particle sizing and crystallization step under a watchful eye, since stubborn clumping can slow down filtration and downstream reactions.
Much of the world’s research into functional naphthalene derivatives depends on access to intermediates like methyl 6-bromo-2-naphthoate. Medicinal chemists design new kinase inhibitors, antitumor agents, and advanced fluorophores off this core. We have supported clients building candidate pharmaceutical scaffolds, compound libraries, and even custom probes based on modified naphthalene units. Our product finds regular use as a coupling agent in Suzuki, Stille, and Buchwald reactions, where the electron-withdrawing methyl ester and the strategic bromo position steer reactivity.
Users in pigment and materials science work with our molecule for dye precursors, liquid crystal displays, and polymer additives. Industrial testing has shown this compound can function as an efficient synthon for larger, multi-ring structures by offering both nucleophilic ester and electrophilic aryl bromide reactivity. As we keep hearing from R&D teams, such bifunctional handles can compress multi-step sequences into fewer reaction pots—saving time, waste, and lost yield.
Ask anyone synthesizing naphthalene analogs: methyl 6-bromo-2-naphthoate does things unsubstituted naphthalenes or para-brominated naphthalenes can’t manage. The 6-position bromo group reads as more selective towards coupling at C-6, reducing side reactions that tend to pop up with other bromonaphthalene isomers. Our own bench-scale tests have shown methyl 2-bromo-1-naphthoate or 1-bromo-2-naphthoate run less smoothly under cross-coupling, often yielding more tarry byproducts or suffering from lower isolated yields.
On the ester side, the methyl group blocks aggressive hydrolysis, giving chemical stability across warehouses and shipping lanes. We’ve seen ethyl or bulkier esters hydrolyze or lose homogeneity in long-term storage, especially in regions with humidity swings. By sticking to methyl, the product transports better, weighs out more precisely, and tolerates fluctuating climate conditions from European winters to subtropical Asian monsoon zones.
In comparison to acid analogs, the methyl ester delivers better solubility in medium-polarity solvents, making workups and purifications faster. Chemists get crystalline fractions during isolation instead of sticky residues that slow down filter funnels and gum up chromatographic columns.
Over years of refining 6-bromo-2-naphthoate synthesis, our team has faced the many headaches found in aromatic bromination and esterification chemistry. Bromine handling raises obvious safety issues, made sharper by global regulatory shifts and tighter workplace exposure limits. We’ve invested in contained reaction modules with overhead scrubbers—not only for staff safety, but to prevent contamination and errant reagent losses.
Tracking trace iron and heavy metal contamination matters too, since transition metal catalysis underpins most coupling and derivatization steps downstream. Many manufacturers overlook these trace impurities, but repeatedly, we’ve found even a fraction of a percent can poison future reaction steps or skew biological assays. All our stock passes through chelation and careful filtration before drying and packaging, because these nuances translate into fewer headaches for the end user—and we know how often troubleshooting an unexpected orange spot on a TLC plate leads right back to contaminated starting material.
Environmental compliance has risen over the last decade. By switching our main bromination route to greener, solvent-minimized systems, we’ve cut generated halogen waste streams, keeping discharge within local standards and avoiding petrochemical cleanup surcharges. Chemist-managers still need to manage the inevitable halide loading of wastewater carefully, since even ppm levels of free bromide can trigger shutdowns in older municipal wastewater systems. We hold every batch’s waste logs for auditing and invite customer compliance teams to site visits whenever requested.
Chemists use methyl 6-bromo-2-naphthoate across a broad spectrum of industries. Synthetic organic chemists in drug discovery, dyestuff development, and materials innovation rely on predictable performance. We respond fastest to large-batch researchers and university labs working on new analogs, offering flexible container sizes and prompt technical advice. Every so often, we field requests for ton-scale supply to pilot plants, and thanks to modular reactors, we can scale-up without introducing cross-contamination from unrelated syntheses.
We recognize the pressures faced at the bench—tight timelines, shifting grant requirements, or sudden program pivots. Product support goes beyond shipping a bottle out the door; we help with analytical documentation, impurity profiling, and on-request COAs delivered within hours. Several start-up projects credit us for helping them fine-tune their initial hydrolysis or coupling protocols using real-world data from our plant, not just textbook synthesis steps.
Technical queries often target solubility, purity, trace side-product identification, and best-use scenarios. Over the years, we have compiled an FAQ and knowledge base drawn from actual customer feedback and in-house troubleshooting logs. This keeps our team nimble when researchers reach out with niche requirements or run-into trouble with scale or time constraints.
Quality doesn’t exist on a certificate; it starts back at raw material selection. Our bromine arrives in isotainer loads with full QC and supply chain traceability; methyl naphthoate sources stay consistent, partnered with established upstream chemical companies. We log every vessel wash, weigh-in, and labeling run—because a missed input or incorrect cleaning step creates problems down the line.
Packing the finished product requires its own attention. We’ve witnessed poor or inconsistent packing in the industry—powder caking, exposure to atmospheric moisture, label smearing, or worse, leaking containers. We rely on fully sealed HDPE containers with vacuum-snap inserts for laboratory portion sizes, scaling to UN-rated fiber drums for large-scale manufacturing partners. Vacuum packing before container closure limits oxygen and humidity ingress, preserving the product from origin to customer.
Labels feature both batch ID and full synthetic route tracking, so if a customer identifies a concern, we backtrack and pin down the root cause. Few things matter more than actionable traceability in chemical manufacturing, particularly because scientific work often hinges on a single key starting material.
While specifications alone don’t tell the story, some technical benchmarks set our product apart. A high melting range and clean NMR spectrum (proton and carbon) indicate minimal isomeric content and low residual solvent. Bromide content falls in line with predictive stoichiometry. Analytical methods—GC, HPLC, mass spectrometry—show consistent batch reversibility when checked against authenticated standards.
Routine spot checks during blending and filling catch off-spec lots before they ever ship. By insisting on batch sub-sampling, we keep true to representative impurity data, instead of relying on single “golden sample” testing. Over the years, this focus on QA-QC integration has reduced customer complaints and improved acceptance testing rates for our largest buyers.
Scaling involves predictable engineering adjustments. Pilot to plant-scale runs maintain reactivity and isolation profiles, because plate-out losses of naphthalene aren’t acceptable at ton quantities. Recovery steps include in-line fractionation and triple-stage filtration to guarantee a crisp, free-flowing product.
Users working through challenging synthetic routes know how limiting some halogenated naphthalene materials can be. Many competitors focus on common 1- or 2-substituted derivatives, but the 6-bromo group lets chemists access substitution patterns otherwise cumbersome or impossible through traditional routes. Bromo-naphthoates with methyl ester at the second ring offer access to more complex arylation and cross-coupling endpoints.
Based on customer feedback, our product shows higher conversion yields and reduced side reactions under most Pd- or Ni-catalyzed coupling conditions compared to standard 1-bromo or 2-bromo naphthalene reagents. The electron-withdrawing properties of the methyl ester stabilize intermediates, providing improved chemoselectivity and fewer byproducts after workup.
We also see dye and pigment manufacturers push this product ahead of alternatives because it creates cleaner, more reproducible hues after final oxidation and condensation steps. In liquid crystal work, the physical properties and substitution pattern lend themselves to forming elongated, anisotropic molecules essential for display and photonic applications.
Chemists often face delays or uncertainty with high-value intermediates. Supply chain reliability determines project timing more than almost any reagent property. We address this by keeping strategic inventory—rotating large and medium lot sizes to accommodate both regular and one-time orders.
We’ve encountered disruptions from raw material shortages, changing regulatory import–export controls, and shipping bottlenecks, especially for temperature-sensitive products. Over time, we’ve built dual-source arrangements and maintain audit logs to verify continuous supply, not just spot availability. Advanced forecasting, aided by close customer communication, means we adjust lead time projections to help buyers plan seasonal projects and meet grant, bid, or process deadlines.
We understand that researchers don’t always have time to chase down analytical data or hunt for obscure certificates. Full analytical datasets—NMR, HPLC, GC, purity profiles—are readily available for every lot, delivered electronically within hours if requested. Chemists at the bench benefit from direct access to our technical team, often getting synthesis or troubleshooting support on the same day.
Feedback loops work in both directions. We collect stories, suggestions, and incident reports from our buyers, using them to tweak process controls, introduce safer packaging, or clarify batch specs. Product support means actual synthetic insight and readiness to help interpret anomalous reaction outcomes, not just boilerplate MSDS documents.
We’ve hosted joint review calls with biotech startups, pharma research teams, and academic groups to sort out issues all the way from solution prep to analytical quantitation. Building and maintaining trust in specialty chemicals depends on this level of technical communication and accountability.
Over recent years, chemical producers faced rising scrutiny and obligation to track impurities and emissions—not just at the plant, but across the supply chain. Our experience complying with global regulations—from European REACH to Asian environmental codes—means buyers can get documentation free from missing fields or vague provenance. We invest in periodic third-party audits, using their feedback to build toward best-in-class standards.
Handling bromine and aromatic esters underpins an array of regulatory controls. Organic synthesis always holds risk; we mitigate these by using closed processing, equipped environmental monitoring, and continuous staff safety coaching. Auditable logs capture all hazardous stream handling, while product-specific MSDS documents stay up-to-date with legislative changes. Customers benefit from supply chain confidence, knowing our product will not derail compliance at their sites.
We treat every run as a learning experience. Production methods adapt using real-world feedback: if problems emerge with shelf life or flowability, our team responds by tweaking crystallization conditions or adjusting anti-caking agents. We set up regular review cycles to benchmark our batches against international reference standards, ensuring every production shift learns from the last.
Capital investment goes into automation—precision weighing, online analytics, and envelope tracking—to reduce human error and speed up release cycles. This technology backbone ensures even tight deadlines or unusual customization requests can be filled without a dip in quality.
We built our methyl 6-bromo-2-naphthoate practice on a foundation of technical agility and close-knit client partnerships. Every bottle we ship reflects hard-earned lessons on process safety, environmental stewardship, responsive customer service, and a relentless drive to improve batch quality. While other structures and substitutions yield their own utility, the carefully chosen 6-bromo and 2-methyl ester arrangement offers standout reactivity, stability, and reliability for modern synthetic chemistry.
In the end, chemists need more than specifications—they want tested support, batch-to-batch performance, and real-world insight. That’s why, after years of listening to the needs of the scientific community, we back our product with a focus on solutions, not just molecules. Those who rely on methyl 6-bromo-2-naphthoate as a key intermediate can count on us to provide value at every stage from purchase to project completion.