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6-Methoxytetralone

    • Product Name 6-Methoxytetralone
    • Einecs 219-123-1
    • 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
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    930624

    Chemical Name 6-Methoxytetralone
    Molecular Formula C11H12O2
    Molecular Weight 176.21 g/mol
    Cas Number 16819-11-5
    Iupac Name 6-Methoxy-3,4-dihydro-2H-naphthalen-1-one
    Appearance White to off-white solid
    Melting Point 63-65°C
    Boiling Point 332.7°C at 760 mmHg
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles COC1=CC2=C(C=CC1)C(=O)CC2
    Inchi InChI=1S/C11H12O2/c1-13-9-4-2-3-8-10(9)5-6-11(12)7-8/h2-4H,5-7H2,1H3

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

    Packing & Storage
    Packing A 25-gram amber glass bottle labeled "6-Methoxytetralone, CAS 14114-72-2," tightly sealed, with hazard and storage precautions.
    Shipping 6-Methoxytetralone is shipped in tightly sealed, chemically-resistant containers to protect against moisture and light. Packaging adheres to regulatory standards for safe handling and transportation. All shipments are accompanied by appropriate safety documentation, including Material Safety Data Sheets (MSDS), and comply with local, national, and international shipping regulations for laboratory chemicals.
    Storage 6-Methoxytetralone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, moisture, and incompatible substances such as strong oxidizers. Protect the chemical from light and store it at room temperature, unless otherwise specified by the manufacturer. Always follow appropriate chemical safety and local regulatory guidelines for storage.
    Application of 6-Methoxytetralone

    Applications of 6-Methoxytetralone in Industrial Manufacturing

    As the direct producer of 6-Methoxytetralone, we partner with downstream manufacturers operating in stringent technical environments. Our material supports targeted applications in the synthesis of specialty chemicals, fragrance intermediates, advanced pharmaceuticals, and agrochemical R&D. Below, we provide an in-depth industrial perspective for each sector, covering regulatory expectations, formulation guidelines, process stages, and commercial end products.

    1. Pharmaceutical Intermediate Synthesis

    6-Methoxytetralone is an established key building block for the synthesis of specific CNS-active pharmaceutical substances, including several antidepressant and antipsychotic APIs. Formulation chemists incorporate this raw material during advanced-stage intermediate synthesis due to its functionalized tetralone ring—which enables precise introduction of methoxy groups under controlled conditions. Manufacturers must ensure compliance with rigorous trace impurity controls and validated cleaning verification at this process stage, as dictated by global regulatory frameworks.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA CFR 21 Parts 210/211: cGMP for Drug Manufacturing
    • European Pharmacopoeia (Ph. Eur.) Residual Solvents Specification
    • China Pharmacopoeia, relevant API monographs

    Typical usage ratio

    • Usually loaded at 5–25% w/w relative to main precursor mass, depending on the targeted intermediate; stoichiometry adjusted for substitution yield and isolation efficiency.

    Downstream process integration

    • Introduced during the specific condensation or cyclization step within the multi-stage synthesis route for tetralone-based pharmaceutical intermediates; followed by reduction, amination, or further functional group modification.

    Final product types

    • Active pharmaceutical ingredients (e.g., Sertraline intermediates)
    • Regulated CNS therapeutic precursor substances
    • Research-grade API intermediates for pilot and clinical trials

    2. Fragrance and Aroma Intermediate Production

    Specialty fragrance houses and industrial perfumeries employ 6-Methoxytetralone as a core lactone precursor for high-value musk analogues and floral base notes. Its methoxy functionality imparts a distinctively nuanced odor profile, facilitating signature compound development for luxury scents and office air-care products. Downstream blending operations must comply with international fragrance regulations, including purity specifications and allergen traceability.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards
    • EU Regulation (EC) No 1223/2009 for Cosmetic Products
    • ISO 9235: Aromatic Natural Raw Materials Vocabulary
    • Good Manufacturing Practice for Fragrance Materials (IFRA/IOFI GMP)

    Typical usage ratio

    • Formulators typically dose at 1–10% of the aroma concentrate base, adjusted per olfactive intensity trials and compatibility with carrier solvents.

    Downstream process integration

    • Reactors blend 6-Methoxytetralone with macrocyclic lactone precursors for esterification, followed by top-note balancing in blending vessels and post-synthesis vacuum stripping to achieve fragrance grade.

    Final product types

    • Musk fragrance intermediates
    • Perfumery base notes for fine fragrances
    • Scented household air fresheners and laundry softeners

    3. Specialty Dye and Pigment Precursor Manufacturing

    Advanced dye and pigment formulators recognize the value of 6-Methoxytetralone in the tailored creation of functionalized anthraquinone and naphthalimide chromophores. Its handled methylation and oxidative potential allow precise color tuning in lightfast textile or ink applications. Tight process control at this stage enables color chemists to comply with textile and food contact dye regulations, reducing off-tone batches and improving end-user acceptance.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (textile dye safety)
    • REACH (EC No. 1907/2006) Registration, Evaluation, Authorisation and Restriction of Chemicals
    • US FDA 21 CFR Parts 73 and 74 (color additive regulations)
    • ISO 105 (Textile color fastness testing)

    Typical usage ratio

    • Included at 2–8% by mass in precursor charge, determined by target molar extinction coefficient and hue uniformity requirements of the finished pigment.

    Downstream process integration

    • Dosed during the oxidative coupling or cyclization stage in dye intermediate syntheses, prior to salt formation and filtration; followed by solvent phase separation and particle size control processing.

    Final product types

    • Lightfast textile dyes
    • Industrial colorants for plastics or coatings
    • High-purity ink pigments

    4. Agrochemical Discovery and Hybridization

    Agrochemical R&D divisions utilize 6-Methoxytetralone as a reactant in the development of new plant growth regulators and selective fungicides. The methoxy-tetralone core supports molecular hybridization strategies for trialing new bioactive agents. Here, raw material handling and documentation must conform to GLP and environmental safety assessment frameworks, ensuring all downstream screening batches retain complete traceability for regulatory filings and field testing.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • US EPA FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act) Regulatory Compliance
    • ISO 17025: Testing and Calibration Laboratories
    • European Commission Regulation (EC) No 1107/2009—Plant Protection Products

    Typical usage ratio

    • Typically incorporated at 1–12% depending on laboratory scale synthesis and targeted scaffold diversity for library generation in bioassay studies.

    Downstream process integration

    • Charged into the combinatorial synthesis step with other lead fragments; follows purification and in vitro activity screening prior to pilot-scale formulation blending (wettable powders or EC concentrates).

    Final product types

    • Plant growth regulator candidate compounds
    • Trial batch fungicide actives
    • Pipeline agrochemical prototypes for regulatory field trials
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    Certification & Compliance
    More Introduction

    Introducing 6-Methoxytetralone: Quality from the Manufacturer’s Line

    Real-World Experience with 6-Methoxytetralone

    Walking through our production facility, the steady hum of reactors and the familiar scent of aromatic intermediates always signal a batch of 6-Methoxytetralone in progress. This compound has become a key player for researchers and formulators who understand both its unique profile and its limitations. Through years of synthesis and process refinement, we've shaped our 6-Methoxytetralone output to meet real laboratory and plant needs, not just a generic list of specifications.

    Model and Specifications: Built on Consistency

    Our batches typically feature the 6-Methoxytetralone base structure, a methoxy group sitting on the aromatic ring, and a fused tetralone backbone. Each unit passes strict in-house HPLC testing, IR spectroscopy, and melting point analysis. Chemists in our lab painstakingly run purity checks exceeding 98%. This isn’t about chasing lab stats — it’s about being able to hand a customer a jar and know the compound inside will work as designed, batch after batch.

    Crystal form, color, and melt characteristics might not be exciting outside the lab, but every time one of our technicians scoops out a sample, those visible differences mean something. Too pale or off-tone signals an impurity, a change in crystal habit sometimes hints at a mixing issue. So we watch those details closely. We do not send out batches unless those signals line up with years of past experience, which cuts down on wildcards when you're running a process where every variable matters.

    From the Manufacturer’s Bench: Handling and Usage

    Over two decades, we’ve witnessed all sorts of applications for 6-Methoxytetralone in our clients’ hands. This compound has pulled its weight in medicinal chemistry projects, pigment synthesis, and special flavoring ingredient studies. In our own R&D experiments, it often acts as a core intermediate when building more elaborate molecular scaffolds. The methoxy group has a notable impact: it changes the electronic environment in the aromatic ring, affecting both reactivity and solubility.

    Each time we scale up a synthesis, engineers run safety reviews. Liquid handling routines, filtration steps, and bulk crystallization have all been tweaked for real-world usage. Storage gets plenty of attention. Our warehouse consistently logs in a 4–8 °C ambient control for bulk inventories; these controls aren’t just for shelf life, but to prevent the minor degradations that can dog downstream reactions.

    There’s a particular sweet spot where 6-Methoxytetralone outperforms less-modified tetralinones. Many pharmaceutical teams look for it as a starting point for later ring closures, methylations, or halogenations. That isn’t accidental — it’s a product of both our close monitoring of side product levels and careful protection against over-oxidation during production. Each intervention means less troubleshooting on the customer side, quicker process validation, fewer odd odors or out-of-spec NMR traces.

    Why 6-Methoxytetralone Stands Apart

    Years of floor time tell us where generic N-tetralones or basic tetralins drop the ball. Customers regularly ask why they can’t substitute another tetralone or a demethoxy analog. Every time we steer them back. Electrophilic substitution at the aromatic ring proceeds differently when a methoxy group sits at position 6. Chemoselectivity improves in downstream alkylations. Some legacy syntheses that languished with other tetralones find new legs when fed the methoxy analog.

    Our customers measure actual chemical outcomes on pilot lines, not just theory. A pharmaceutical chemist once described the unique reactivity as “razor-edged” when using our 6-Methoxytetralone in a stepwise build toward a target heterocycle. That’s the kind of feedback we lean on — results documented in spectra and process yields, not just copy in a brochure.

    Color and purity differences stand out to a practiced eye. A standard tetralone without the methoxy group usually gives slightly lower solubility in several organic solvents, which can bog down some procedures. In contrast, our 6-Methoxytetralone, thanks to the electron-rich aromatic system, dissolves more readily in acetone, methanol, and even some less-common solvents used for recrystallization and downstream coupling. That added handle isn’t trivial; process engineers use it to bump up yields or ease product isolation. Trouble-free dissolving directly cuts filtration headaches and cuts batch-to-batch variation down.

    Production, Purity, and Process Learnings

    Consistently hitting high-purity marks calls for more than automated reactors. Over the years, our production team overhauled the purification process twice, specifically after tracking down off-odors and browning in finished lots. Investment in larger rotary evaporators, a new suite of filters, and extra rounds of column chromatography weren’t cheap — but after seeing the effect on purity, nobody wanted to go back. Stable, pale crystals every time keep our QC team focused on improvement, not damage control.

    Handling of spent solvents became a bigger piece of the puzzle. Every liter of side-stream solvent gets routed to dedicated recovery tanks, keeping the main product line clean and reducing environmental impact. Moving away from the old plate-and-frame filtration also helped. Staff used to spend hours cleaning downtime pipeline blockages, usually because of “gel-like” byproducts that come from pushing impure feedstocks too hard. After retooling our sequence and putting in extra safety checks, those interruptions dropped off sharply.

    Lately, our in-process analytics shifted toward more NMR quick-scans and less reliance on wet chemistry. Instead of waiting on endpoint confirmation, a technician picks up a mini sample, runs the test, and flags irregularities instantly. This sort of real-time process control rarely shows up in sales literature, but for those making things at scale, it means a great deal less rework, and more reliability for every downstream chemist.

    Tackling Real Process Issues

    Switching from a non-methylated analog to our 6-Methoxytetralone highlighted tangible process gains. Our regular clients have reported fewer side products in subsequent acylation and Michael addition reactions. Downstream cleanup takes less solvent, especially when compared to lower-grade material purchased from traders, which sometimes comes with trace levels of unreacted starting material or unwanted isomers.

    Our technical team gets calls about off-spec physical appearance or unexpected reactivity from chemists who sourced material from less-controlled providers. They’ll describe cloudy suspensions or inconsistent melting points. Experience taught us that moisture contamination and incomplete purification cause these headaches. Early on, we learned to prioritize thorough drying — not just heat, but actual vacuum oven cycles after every crystallization. It’s details like these, grounded in physical lab practice, that keep the product true to its chemical potential.

    We’ve also prioritized trace impurity tracking. GC-MS analyses run for each batch highlight potential late-eluting hydrocarbon signals or residual alkoxy fragments. These often escape notice in standard vendor supplies. By keeping impurity levels low, our customers regularly avoid downstream blockages in continuous flow reactors or fine-filtration cues that can surge costs and delay pilot batches.

    Listening to Customer Projects: Real Uses, Real Feedback

    A flavoring company reached out last year, attempting to isolate a new compound suite based on our 6-Methoxytetralone. Their R&D director called after switching sourcing to our batches, noting improved yield and better control over final product aroma. These small, statistically supported outcomes not only build us a silent reputation, but they reinforce how direct quality from manufacturer hands makes a difference.

    From the pharmaceutical side, one team working on CNS-active agents connected with us regarding prolonged stability studies. They tracked decomposition patterns over time, uncovering less byproduct formation with material banked from our factory. Their reports relied on LC-MS comparison, and our higher-purity lots produced fewer false signals during their analytical runs. Results like these shape our continuous improvement.

    Sometimes, a synthetic organic chemist will ring up the technical line to run through a challenging hydrogenation or coupling procedure. We walk through the lot data together, often referencing in-house notes from similar projects we’ve supported in the past. It’s a relationship grounded in feedback and shared technical know-how — not a sales brochure promise.

    Comparing 6-Methoxytetralone with Other Materials

    Sourcing chemical intermediates isn’t just about ticking off a purity percentage. Chemists who have run head-to-head synthesis comparisons know the subtle differences. Our 6-Methoxytetralone delivers different kinetic profiles in a Friedel-Crafts acylation, for instance, than what results from using unsubstituted 1-tetralone. Customers notice better selectivity, reduced tar formation, and a shorter workup cycle.

    These differences stem from molecular structure. The methoxy group at position 6 funnels electron density into the aromatic ring, shifting reactivity in ways that generic suppliers don’t always account for. Instead of “acceptable” impurity profiles, customers get material where byproducts don’t mask important functional groups or slow down later stage chemistry. We’ve seen scale-ups reach higher yields — and more reliable quality control numbers — just by choosing this specific intermediate.

    Supply chain interruptions present another real-world contrast. A global shortage of tetralin derivatives last year forced some project leaders to scramble. Loyal clients weathered those months without disruption, while others risked switching sources — only to deal with lost time, extra purification, and disappointing end products. The years we’ve invested in ensuring raw material stability and in-house process flexibility means deliveries do not slip, and grade never slides.

    Addressing Challenges and Charting Solutions

    Production isn’t without hurdles. Over the years, we’ve grappled with environmental compliance as regulatory limits shifted. Waste solvent recovery, air emissions, and equipment cleaning took real investment. We pivoted, moving to closed-loop recycling on certain cleaning streams and capturing all emissions through upgraded scrubbing units. These shifts weren’t abstract policy moves. They meant tangible downtime hits and new monitoring routines, but in the end, plant emissions data trended downward, and product consistency saw another bump up.

    Staff training presents another important piece. New process workers shadow veterans, learning not just the “how” but the “why” behind every synthesis stage. Documentation fills gaps, but lived experience still governs critical decisions — whether adjusting stir speed to avoid frothing, or recognizing the right endpoint by eye before a crystalline slurry turns too opaque. A consistent training schedule and rotating roles sharpen both process discipline and troubleshooting instincts.

    Digitization offered another opportunity. Our digital lot-history system now lets us pull up detailed batch data within minutes of a customer call. Troubleshooting a quality deviation or confirming a COA just means checking a scan, not chasing after a paper record buried in a desk stack. Turnaround on queries sped up, accountability tightened, and customers noticed the difference right away.

    Focusing on Chemistry That Works for People

    Our decision to keep 6-Methoxytetralone production in-house rather than outsource it to third-party processors roots in quality and reliability. Doing the chemistry ourselves gives full line-of-sight into every raw material, every vessel, every output. It keeps problems local, solvable, and often faster to fix. When a technician spots an anomaly, it doesn’t take a global chain of emails to diagnose and solve the issue. Instead, experienced hands gather, check the batch, and run whatever corrections experience dictates.

    Supply chain events of the last few years highlighted cracks in global outsourcing. Chemists we work with need stability not just in delivery times, but chemical consistency they can tie back to a single set of hands and eyes. Our work never promises more than the chemistry shows is possible — but our process improvements mean steady progress in output, waste reduction, and product quality, year on year.

    Clients who look for lowest-price lots may shave cents off a kilo, yet see costs return through extra purification, wasted project time, and lost yields. There’s a real cost to cutting corners that manufacturers understand. Giving out a sample or a kilo means something — we know our name runs with every shipment, and that every time a project moves ahead based on our material, trust is either built or lost.

    A Manufacturer’s Final Word on 6-Methoxytetralone

    All the talk about products, specs, and process comes down to a straightforward goal: empowering real chemists to do their work, solve their synthesis challenges, and move projects forward without the friction of unpredictable materials. Making 6-Methoxytetralone here — in our own plant, by the hands of our people — means fewer surprises and faster progress for every process that touches it.

    Some might say any source of this intermediate could work, that the basic chemistry isn’t so complex. Years of watching failed reactions, lost batch work, and frustrated development teams say otherwise. So we keep after process control, invest in equipment upgrades, retrain teams, and listen to tough feedback. It’s the only way this business makes sense — not by filling order books, but by building a foundation where customers know exactly what they’re getting, every single batch.

    For every formulation, pilot trial, or full-scale run where difference, reliability, and deep chemistry knowledge make or break a project, we’re ready to help ensure you get the best from 6-Methoxytetralone. We keep it simple: exceptional quality, full transparency, and commitment to every batch that leaves our floor.