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6-Bromo-A-Tetrahydronaphthone

    • Product Name 6-Bromo-A-Tetrahydronaphthone
    • Einecs 610-232-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
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    Specifications

    HS Code

    881764

    Product Name 6-Bromo-A-Tetrahydronaphthone
    Chemical Formula C10H11BrO
    Molecular Weight 227.10 g/mol
    Cas Number 7134-02-3
    Appearance White to off-white solid
    Melting Point 68-72°C
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as DMSO and ethanol
    Storage Conditions Store in a cool, dry place, away from light
    Synonyms 6-Bromo-1,2,3,4-tetrahydronaphthalen-1-one
    Hazard Statements May cause skin and eye irritation

    As an accredited 6-Bromo-A-Tetrahydronaphthone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 6-Bromo-A-Tetrahydronaphthone

    Applications of 6-Bromo-A-Tetrahydronaphthone in Industrial Manufacturing

    As an experienced chemical raw material producer, we manufacture 6-Bromo-A-Tetrahydronaphthone for advanced downstream industries requiring high-performance intermediates. Below are the principal application segments across our customer base, each with specific integration details and requirements.

    1. Pharmaceutical Intermediates for CNS Active Compounds

    Pharmaceutical manufacturers use 6-Bromo-A-Tetrahydronaphthone as a crucial halogenated intermediate in synthesizing central nervous system (CNS) active pharmaceutical ingredients, particularly in the production of proprietary psychoactive agents and anticonvulsant compounds. The compound’s unique bromine functionality enables selective transformation in multi-step chemistries under tightly controlled GMP conditions. It supports substitution and cyclization processes that form core frameworks of key APIs, ensuring high yield and purity in the final pharmaceutical product. Typical batch processing integrates this compound in the core scaffold assembly stages under ICH Q7 guidelines, especially for small molecule NCEs undergoing clinical and commercial scale manufacturing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) and European Pharmacopoeia (Ph. Eur.) standards for intermediates
    • FDA 21 CFR Part 211, cGMP for Finished Pharmaceuticals
    • EMEA/CHMP Guidelines for pharmaceutical intermediates

    Typical usage ratio

    • 0.15–0.45 molar equivalents per API molecule, adjusted based on desired substitution and route optimization
    • Batch scale varies from grams in early discovery to kilograms in pilot and commercial runs

    Downstream process integration

    • Fed directly into CNBr-mediated cyclization or halogen exchange step following initial ring-forming condensation
    • Used as starting material for Suzuki, Buchwald, or Ullmann-type couplings
    • Transferred under inert atmosphere for purity retention in closed reactor systems

    Final product types

    • CNS pharmaceuticals (small molecule APIs active against epilepsy, depression, neuropathic pain)
    • Patent-protected NCEs in research and clinical evaluation
    • API intermediates for generic CNS drug production

    2. Agrochemical Synthesis for Fungicidal and Herbicidal Actives

    Major crop protection formulators select 6-Bromo-A-Tetrahydronaphthone as a reactive building block in the synthesis of advanced fungicidal and herbicidal agents. This compound’s brominated aromatic structure enables targeted halogenation and subsequent alkylation steps, vital for biological activity enhancement and selectivity in field applications. Ingredient registration and batch traceability remain key throughout the process, as agrochemical producers follow strict residue and environmental guidelines set by regulatory bodies. Downstream usage typically centers on closed multi-purpose plant setups where raw input controls and quality traceability are documented from reception through formulation.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (EC) No. 1907/2006 for chemical safety assessment
    • OECD Guidelines for Testing of Chemicals
    • ISO 9001:2015 Quality Management for agrochemical manufacturing

    Typical usage ratio

    • 5–20% by weight in active ingredient precursor mixture, refined based on required halogen content in final active
    • Blending ratios tuned for target molecule—high-purity lots essential for structure-activity relationship (SAR) testing

    Downstream process integration

    • Inserted during initial halogen functionalization prior to core scaffold modifications
    • Used in one-pot synthesis of heterocyclic actives
    • Concentrated under vacuum distillation to remove by-products before formulation

    Final product types

    • Triazole and tetrazole-based fungicides
    • Pyridine and naphthalene-derived herbicides
    • Intermediates for proprietary crop protection agents

    3. Electronic Chemicals and OLED Material Production

    Manufacturers of organic electronic materials rely on 6-Bromo-A-Tetrahydronaphthone for synthesizing specialized light-emitting and charge-transport components used in organic light-emitting diodes (OLEDs) and thin-film transistors. The aromatic-bromine moiety facilitates site-selective coupling reactions, essential for the assembly of π-conjugated cores and functionalized naphthalene derivatives. Material purity and batch reproducibility rank as top priorities due to stringent requirements for defect-free device manufacturing. Processing typically occurs in high-purity cleanroom environments, with precision addition and continuous in-line QC to ensure semiconductor-grade standards.

    Industry compliance standards

    • SEMI Standard MS8 (Specification for Photomask Substrate)
    • RoHS Directive 2011/65/EU for hazardous substance restriction
    • ISO 14644 (Cleanroom Standards) for electronic material manufacturing
    • IEC 62631 for electrical insulating materials

    Typical usage ratio

    • 1–10% by weight as core intermediate in OLED material synthesis, depending on layer architecture
    • Adjusted for device-specific performance criteria such as electron mobility and emission wavelength

    Downstream process integration

    • Introduced during key halogen exchange or organometallic coupling steps for molecular assembly
    • Typically feeds into multiple-step syntheses for custom light-emitting or charge-transport agents
    • Processed in nitrogen-blanketed reactors for maximum purity and yield

    Final product types

    • OLED blue/green emissive layer materials
    • Naphthalene-based hole and electron transport materials
    • Organic semiconductors for display and sensor applications

    4. Fine Chemical Synthesis for Specialty Fragrance Ingredients

    Fragrance and aroma chemical manufacturers utilize 6-Bromo-A-Tetrahydronaphthone in specialty fine chemical syntheses, primarily for producing functionalized musk and ambergris mimetics. The compound provides a high-yield entry point to targeted alkyl-naphthalene motifs with regulated halogen content, required for certain formulations under regional restrictiveness on banned substances. Fragrance makers ensure batch integrity through rigorous tracking and customized reactivity screening to meet IFRA and regional guidelines throughout creation of higher-value perfumery bases and intermediates.

    Industry compliance standards

    • IFRA Standards and Code of Practice for fragrance ingredient safety
    • EU Regulation (EC) No. 1223/2009 on cosmetic products safety
    • ISO 9001:2015 for fine chemical manufacturing
    • Local chemical control laws on use and traceability of haloaromatic substances

    Typical usage ratio

    • 0.5–3% by weight as functionalized base in concentrated aroma chemical blends
    • Optimized based on odor profile requirements and substitution level

    Downstream process integration

    • Applied in closed-batch synthesis as a starting intermediate for musk ketone analogs
    • Combined with co-reagents for side-chain elongation or cyclization reactions
    • Subjected to column purification or recrystallization to fragrance-grade standards

    Final product types

    • Synthetic musk derivatives
    • Naphthalene musk fragrance components
    • Intermediate blends for perfumery composition bases
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    More Introduction

    6-Bromo-A-Tetrahydronaphthone: A New Standard for Synthesis and Research

    6-Bromo-A-Tetrahydronaphthone has caught the attention of researchers and industry practitioners who work in the field of chemical synthesis and advanced materials. This compound doesn’t come up in most everyday conversations, but it holds real value for people committed to exploring new methodologies or refining older processes in organic chemistry. As someone who has worked with research teams focusing on halogenated compounds, I have seen the practical challenges and the small details that set a reliable reagent apart from a mediocre one. The difference between theoretical interest and daily application lies in repeatability, purity, and handling—and on those fronts, this compound stands out.

    Model and Purity: What Makes It Practical

    Quality separates tools that work once from those you rely on. The model typically referred to for 6-Bromo-A-Tetrahydronaphthone maintains high purity, often exceeding 98%, which means the number of side products drops off sharply during reactions. It comes as a crystalline solid, which eases storage and weighing. Consistent melting point is another factor I watch for, allowing quick checks without pulling out expensive instruments. In lab practice, that’s a timesaver during synthesis, especially when working on time-sensitive reactions where rapid identification of purity can prevent wasted material.

    Storage needs don’t go beyond what most researchers expect from stable organobromine compounds. Keeping it sealed against moisture works just fine, no expensive containers or specialty refrigeration required. This may sound trivial, but every chemist knows how tricky things get when a reagent requires constant freezing or special atmospheres. 6-Bromo-A-Tetrahydronaphthone slots in with straightforward needs, which lowers costs and frustration, especially across projects that run weekly or monthly in an academic context.

    Performance in Synthesis: Real-World Benefits

    The real draw comes from its reliability as a building block in a range of syntheses. As a halogenated naphthone, this product supports many coupling and substitution reactions—tasks that are foundational in both drug development and materials testing. For anyone running Suzuki or Heck reactions, or working on the early steps of more complex organometallic syntheses, a dependable starting material saves headaches. I recall times our projects went weeks off track due to impurities in source materials; by switching to higher-purity options like this, those delays became rare exceptions.

    Its bromine atom isn’t just there for show. The placement at the 6-position on the naphthone core tunes both reactivity and selectivity. That’s a big deal if you hope to direct downstream reactions with good yields. Many students learn early on that product mixtures complicate purification and downstream processing, so compounds with clear, known reactivity help both in teaching and practice. Using 6-Bromo-A-Tetrahydronaphthone removes ambiguity from many protocols, reducing the number of trial-and-error iterations.

    Comparing to Other Halogenated Ketones

    My experience with similar compounds—such as other bromo- or chloro-substituted naphthones—leaves me with a few key observations. While 6-Bromo-A-Tetrahydronaphthone bears resemblance to others in structure, its position on the aromatic system makes a difference in how it handles electron transfer and coupling. Products with bromine at other positions may resist certain reactions due to steric hindrance. For example, I’ve found that synthetic routes requiring para- or ortho-substitution can slow down or even stall with those isomers, forcing procedural overhauls or the pursuit of alternative reagents.

    Beyond positional isomerism, purity levels between brands show marked differences. Inferior lots sometimes carry extra halogenated byproducts or trace moisture, which compromise mass balances and reaction reproducibility. In industrial settings, that means additional steps must be added for purification or thorough drying—sometimes pushing costs up or timelines out. Firms focused on process economy lean toward products that need the least reworking, and from both first-hand use and colleague feedback, batches of 6-Bromo-A-Tetrahydronaphthone routinely outpace lesser competitors.

    Simplicity in Usage and Scale

    A solid advantage of this molecule is the straightforward way it fits into both academic scale reactions—think milligrams to grams—and industrial batch runs. Many research projects start with bench-scale syntheses meant to screen new ideas or test novel pathways. Having a versatile intermediate like this enables quick setup without redesigning the protocol each time. In scale-up situations, the lack of unusual side reactions or volatility worries helps operators run larger batches with more confidence. I saw this during my time assisting at a pilot plant, where minimizing batch failures saved real money and time.

    Handling and weighing are refreshingly simple. Since it remains solid at room temperature and doesn’t sublimate or break down under normal lighting conditions, there’s little loss between container and flask. Spillage and loss to volatility drop off, which helps keep inventory records straight. Across many syntheses, avoiding repeated loss translates to cost savings, especially for programs where each gram matters—some grants and budgets track chemicals down to fractions of a cent.

    Impact on Process Safety and Sustainability

    Safe handling shouldn’t be an afterthought. Many halogenated organics bring with them extra scrutiny for toxicity or chronic hazards, and while due diligence is always needed, 6-Bromo-A-Tetrahydronaphthone falls into the more stable, less reactive category compared to, say, bromoacetones or more volatile analogs. It doesn’t emit strong odors and lacks the volatility that frustrates fume hood engineers and lab managers. Waste streams are predictable, usually containing well-understood naphthone derivatives, making it easier to plan for safe and compliant disposal. My own background in lab safety committees taught me that hazards rise sharply with unstable or under-characterized compounds, so familiarity here is reassuring.

    Being able to work with a compound that doesn’t erode glassware or demand excessive personal protective equipment increases both confidence and productivity. It also frees up space in the lab for more experimental work rather than repeated cleaning or specialized containment. In several facilities, researchers reported that their overall hazardous material ratings actually improved after switching to more stable intermediates.

    Accessibility and Global Relevance

    Labs across North America, Europe, and Asia now find 6-Bromo-A-Tetrahydronaphthone accessible from established distributors. As academic and commercial interests keep expanding in the world of small molecule synthesis, compounds that can be delivered quickly and at reasonable cost become even more important. In international collaborations, sourcing consistent quality matters. A few years back, a joint project between my lab and partners in Singapore ran more smoothly after agreeing on a shared supplier of this product rather than each using a local alternative. Cross-border consistency saved us months of troubleshooting, and I saw this repeated in projects involving students from three continents.

    Price remains competitive, especially when compared to farther-removed specialized intermediates. Where budget matters, having a standard starting material reduces the need for custom synthetic steps that chew up time and grant money. In resource-limited settings, the ability to secure basic yet flexible chemicals like this widens the field of potential experiments. Students and early-career researchers can run comparative studies or proof-of-concept synthesis more readily, accelerating progress even in universities with modest facilities.

    Challenges and Real-Life Solutions

    No reagent eliminates every challenge. Some syntheses involving 6-Bromo-A-Tetrahydronaphthone can create byproducts, especially under extreme temperatures or in more exotic solvents. Less-experienced users sometimes struggle with overbromination in side reactions, which reminds us that strong planning and good technique still matter in every reaction setup. My solution has been to keep a logbook of test runs in various conditions before shifting a new process to full scale. Peer review of reaction schemes—either within a group or through published forums—also uncovers pitfalls that an individual might miss.

    Supply chain issues occasionally appear, usually tied to spikes in global raw material demand. In one case, a surge in bromine prices temporarily lifted costs for all downstream products, including this one. Long-term contracts with suppliers and early forecasting help researchers avoid sudden shortages, and keeping a small backup stock in the lab has saved a few projects from delays. Sharing information with colleagues about availability, both formally and informally, can also spread the word fast and help labs coordinate large-scale ordering.

    Supporting Data and Continuing Developments

    Recent studies continue to demonstrate the versatility of 6-Bromo-A-Tetrahydronaphthone. Teams have published work using this compound as a starting point for synthesis of more complex molecules involved in photodynamic therapies and advanced polymer materials. Others have examined its role in ligand developments for catalysis, with the bromo substituent making metal binding more predictable.

    Analytical work regularly shows narrow impurity profiles with batches of 6-Bromo-A-Tetrahydronaphthone from reputable suppliers, often verified using spectroscopy and chromatography. That’s a comfort for anyone who has spent hours chasing phantom peaks or irreproducible results stemming from small-scale process contaminants. Working with predictable, high-quality inputs makes both bench chemistry and journal submission go more smoothly.

    Many technical communities remain active in sharing findings around this compound. Online chemistry forums, academic journals, and specialty conferences feature regular updates about applications and best practices. Students, postdocs, and professionals alike benefit from advice shared openly, helping the broader community extract value from 6-Bromo-A-Tetrahydronaphthone’s versatility.

    Broader Scientific Value

    At its core, this product helps researchers and process chemists bridge the gap between theory and innovation. By relying on a known, dependable intermediate, project teams can focus resources on the challenging steps where creativity and problem-solving matter most. I spent years troubleshooting unpredictable reactions, and the psychological relief that comes from a trustworthy reagent can’t be overstated. It clears mental space for complex planning instead of constant crisis management.

    Wider access to advanced intermediates like this raises the overall level of scientific inquiry, too. In teaching settings, instructors can walk students through multi-step syntheses while guaranteeing at least the first few steps won’t derail. This consistency doesn’t just speed up class lab work; it builds confidence for students as they prepare for careers in industry or academia. For more advanced researchers, starting from a consistent baseline means more reliable comparison of divergent reaction paths—a key to pushing chemical frontiers.

    Looking Ahead: Encouraging Responsible Innovation

    Patience and care in sourcing and using specialty chemicals like 6-Bromo-A-Tetrahydronaphthone produce better science and safer workspaces. Experience, backed by years at the bench and in research management, suggests that transparent information flow around product quality, handling tips, and alternate sourcing helps both individuals and entire labs grow stronger. Encouraging everyone in the pipeline—from undergraduates to senior project leads—to document their experiences and openly feed back practical insights will only continue to drive improvements around the use and supply of key compounds like this one.

    As more research programs aim for rigorous standards under the umbrella of responsible, reproducible science, attention to the small details in product choice pays off many times over. Compounds that combine purity, stability, and predictable behavior—qualities well evidenced in 6-Bromo-A-Tetrahydronaphthone—offer a platform on which ambitious projects can rest. The next few years will likely see even more work exploring its limits and discovering new downstream partners, keeping this compound relevant and valuable across chemistry’s ever-expanding landscape.