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5-Methoxy-3,4-Dihydro-2H-Naphthalen-1-One

    • Product Name 5-Methoxy-3,4-Dihydro-2H-Naphthalen-1-One
    • Alias 5-Methoxy-1-tetralone
    • Einecs 642-245-6
    • 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

    314813

    Iupac Name 5-Methoxy-3,4-dihydro-2H-naphthalen-1-one
    Molecular Formula C11H12O2
    Molecular Weight 176.21 g/mol
    Cas Number 37122-52-8
    Appearance White to off-white solid
    Melting Point 65-68 °C
    Boiling Point 135-140 °C at 5 mmHg
    Density 1.16 g/cm³
    Solubility In Water Slightly soluble
    Smiles COC1=CC=CC2=C1CCC(=O)C2
    Inchi InChI=1S/C11H12O2/c1-13-10-4-2-3-8-9(10)5-6-11(8)12/h2-4H,5-7H2,1H3
    Synonyms 5-Methoxy-1-tetralone
    Refractive Index 1.583 (predicted)

    As an accredited 5-Methoxy-3,4-Dihydro-2H-Naphthalen-1-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 50g chemical is securely sealed in an amber glass bottle, labeled with the compound name, CAS number, and hazard information.
    Shipping The chemical **5-Methoxy-3,4-Dihydro-2H-Naphthalen-1-One** is shipped in sealed, chemical-resistant containers to prevent contamination and leakage. Packages are clearly labeled in accordance with regulatory requirements and protected against moisture and light. All shipments comply with local, national, and international transport and safety regulations for chemical substances.
    Storage Store 5-Methoxy-3,4-dihydro-2H-naphthalen-1-one in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from sources of ignition, oxidizers, and incompatible substances. Ensure proper labeling and restrict access to trained personnel. Follow all relevant safety regulations and guidelines for chemical storage.
    Application of 5-Methoxy-3,4-Dihydro-2H-Naphthalen-1-One

    Applications of 5-Methoxy-3,4-Dihydro-2H-Naphthalen-1-One in Industrial Manufacturing

    5-Methoxy-3,4-Dihydro-2H-Naphthalen-1-One serves as a high-purity specialty intermediate across several chemical industries. On this page, we present specific downstream use cases where this material forms a critical component of established manufacturing flows. Our factory delivers this raw material with controlled specifications designed for direct batching or further synthesis in industrial environments.

    1. Fragrance Ester Synthesis for Fine Fragrance Manufacture

    Leading fragrance houses incorporate this material as a key precursor for crafting musky and woody scent bases. Production lines first run selective hydrogenation followed by esterification, yielding macrocyclic musks used in fine perfumes and high-end colognes. Its stable odor profile supports complex blending and sustained sillage in premium finished fragrances.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards
    • EU Cosmetics Regulation (EC) No 1223/2009
    • REACH registration (European Union)
    • ISO 9235 (Aromatic Natural Raw Materials - Terminology)

    Typical usage ratio

    • Employed at 0.5%–2% within the total volume of fragrance oil concentrates, adjustable based on target musk intensity and final IFRA restrictions.

    Downstream process integration

    • Introduced during the early batch stage of esterification reactions to synthesize macrocyclic musk esters.
    • Subjected to multi-step purification prior to blending into perfumer compounding tanks.
    • Homogenization follows with other aldehyde/fixative notes.
    • Incorporated into ethanol or carrier oil matrices for commercial perfume bottling.

    Final product types

    • Fine perfumes
    • Eau de Toilette formulations
    • Personal care scent bases
    • Luxury home fragrance diffusers

    2. Aroma Intermediate in Food Flavor Formulation

    Major food ingredient manufacturers use our product to construct controlled aroma compounds for food-grade flavor bases, especially nutty, creamy, or dairy-mimetic profiles in confectionery and ice cream formulas. The raw material's high purity ensures batch reproducibility, while compliance with food safety regulations is strictly maintained during ingredient synthesis.

    Industry compliance standards

    • Food Chemicals Codex (FCC)
    • US FDA 21 CFR 172.515 (Synthetic Flavoring Substances)
    • EU Regulation (EC) No 1334/2008 (Flavorings and Food Ingredients)
    • ISO 22000 (Food Safety Management System)

    Typical usage ratio

    • 0.01%–0.1% in flavor compound, adjusted per sensory thresholds and legal limits in final food matrix.

    Downstream process integration

    • Used as an upstream intermediate for lactone or cyclic ketone syntheses.
    • Processed within closed reactor systems to yield final GRAS-listed flavor ingredients.
    • Subjected to analytical verification (GC/MS) before addition to food flavor premixes.
    • Blended with other food-grade carriers for liquid or encapsulated flavor systems.

    Final product types

    • Chocolate and praline flavorings
    • Ready-to-eat dessert flavors
    • Dairy analogues and plant-based beverage flavors
    • Bakery application flavors

    3. Pharmaceutical Intermediate for CNS Active Molecules

    Active pharmaceutical ingredient (API) manufacturers deploy this intermediate in the multi-step synthesis of select central nervous system (CNS) compounds. The process involves formal condensation, further functionalization, and purification to yield core scaffolds for investigational or established CNS therapeutics. Stringent quality and trace impurity control underpin the process.

    Industry compliance standards

    • ICH Q7 (GMP for Active Pharmaceutical Ingredients)
    • European Pharmacopoeia (Ph. Eur.) monographs (where applicable)
    • US FDA CFR Title 21 Part 210/211 (cGMP Manufacturing, Processing, and Packing of Drugs)
    • Japanese Pharmacopoeia standards

    Typical usage ratio

    • Typically 1–1.5 equivalents relative to core amine input, fine-tuned by downstream yield requirements and process impurity profiles.

    Downstream process integration

    • Charged as the main backbone forming unit in the initial condensation or ring-expansion stage.
    • Processed under anhydrous, inert atmosphere to maintain product integrity.
    • Integrated with proprietary purification and crystallization protocols.
    • Passed to subsequent alkylation or halogenation stages before final API coupling.

    Final product types

    • CNS drug intermediates
    • Experimental neuroprotective APIs
    • Generic drug scaffolds
    • Small molecule research compounds for CNS projects

    4. Fine Chemical Synthesis of Advanced Dye Intermediates

    Colorant and dye manufacturers use this ketone in high-purity conditions to develop intermediates that impart improved stability and fastness in specialty dyes for plastics, textiles, and automotive coatings. Complexation reactions, including Friedel–Crafts acylation and subsequent cyclization, depend on precisely formulated raw material to secure consistent chromatographic profiles in finished pigments.

    Industry compliance standards

    • Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers (ETAD) guidelines
    • OEKO-TEX® Standard 100 (Textile and Leather Ecology Certification)
    • ISO 9001:2015 (Quality Management Systems)
    • REACH Annex XVII (Restriction of Hazardous Chemical Substances)

    Typical usage ratio

    • Conventional formulations utilize 3%–8% of total reactant input, altered according to required pigment density and solubility.

    Downstream process integration

    • Introduced after primary arylation step; combined with oxidizers for chromophore generation.
    • Transferred through series of filtration, milling, and spray drying units.
    • Quality control includes colorimetric and solubility testing at each stage.
    • Supplied as a solid or concentrated dispersion for further end-use compounding.

    Final product types

    • Synthetic fiber dyes
    • Engineering plastics pigments
    • Industrial inkjet colorants
    • Automotive and textile pigment concentrates
    Free Quote

    Competitive 5-Methoxy-3,4-Dihydro-2H-Naphthalen-1-One 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.

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    Certification & Compliance
    More Introduction

    5-Methoxy-3,4-Dihydro-2H-Naphthalen-1-One: A Chemist’s Perspective

    Introducing Our Process and the Value Behind 5-Methoxy-3,4-Dihydro-2H-Naphthalen-1-One

    In our factory, producing 5-Methoxy-3,4-Dihydro-2H-Naphthalen-1-One isn’t just about precise reactions, controlled environments, and ticking boxes for quality. It’s about understanding why clients trust a reputable chemical manufacturer’s methods and consistency, and what drives those demands. Walking through our operations, you see how thoughtful selection of raw materials leads to a more reliable product. Every batch reflects the importance of purity, traceability, and yield. In the end, it’s experience in synthesis, and in what matters to our customers, that makes the difference.

    The Anatomy of 5-Methoxy-3,4-Dihydro-2H-Naphthalen-1-One: From Molecule to Value

    What sets 5-Methoxy-3,4-Dihydro-2H-Naphthalen-1-One apart isn’t its complex name or structure alone; it’s the pathway by which it is developed and the impact it brings downstream. The compound itself presents a methoxy group at the 5-position on the dihydronaphthalenone skeleton—a setup that influences both reactivity and versatility for downstream transformations. As someone who has worked on these syntheses from the ground up, the difference between a compound that completes a reaction 95% and one that lags at 85% isn’t just a statistic; it means weeks back in the lab, recalculating, reordering, and troubleshooting. For our clients in advanced material manufacturing, fragrance development, and fine chemicals, these percentages reflect real-world advantages.

    Specifications That Shape Outcomes: Purity, Appearance, and Stability

    Working with chemicals daily, you begin to appreciate that specifications matter. Our typical batches reach a purity of 98% or above, and every step—hydrogenation, crystallization, and isolation—affects that. When crystallinity is off, it’s not just a cosmetic issue. Poor crystallinity can trip up automated dosing equipment or interfere with downstream blending processes. Moisture content and by-product traces directly affect reaction outcomes in client labs. We never treat these things as minor; a “minor” off-spec can ruin an entire formulation on the user’s end.

    We offer 5-Methoxy-3,4-Dihydro-2H-Naphthalen-1-One as a pale solid, typically a fine powder or sometimes small granules, depending on process variables. That solid form makes it much easier to weigh and incorporate into reaction setups, compared to gums or sticky oils that can tie up process lines.

    Consistency Through Process Control

    The foundation for reliability sits in production discipline and deep know-how. Over the years we’ve optimized the hydrogenation step, which demands stability and selectivity—just one hour too long or too short impacts final purity. We monitor temperature by the minute to avoid over-reduction. Downstream, the methoxylation step rewards precise timing. Even small ambiguities in time and pressure can skew product output, impacting both cost and downstream yield.

    Every batch undergoes spectral confirmation—NMR, GC-MS, and sometimes HPLC. This may sound routine, but our lab technicians know that every extra minute running checks saves days, or even weeks, spent resolving customer complaints or replacing suspect shipments. It’s an investment in trust.

    Applications: More Than an Intermediate

    Clients use our 5-Methoxy-3,4-Dihydro-2H-Naphthalen-1-One as a building block toward many goals. In fragrances, the methoxy functional group provides both a distinct aromatic boost and flexibility in formulating new profiles. Having spent time walking plant floors in both chemical and perfume manufacturing, I know how a single off-note causes entire runs to get scrapped. The consistency in this intermediate makes blending and scaling much more predictable, which matters greatly where economics are tight.

    Pharmaceutical research draws on the molecule’s core structure for several synthetic pathways. The partial hydrogenation inherent in its backbone offers specific reactivity compared to its related naphthalenone cousins. Process chemists repeatedly tell us they appreciate the balance between reactivity and shelf stability—this isn’t a compound that “ages” or discolors quickly due to ambient conditions, because we’re strict about moisture control and storage atmospheres from the first step onward.

    Polymer and material science sectors occasionally call for this molecule when exploring new polymers or cross-linking reagents. Its stable aromatic system and functional handle make it attractive for experimentation, especially where conventional naphthalenones prove too rigid. We’ve supplied it in volumes that range from small pilot runs to full process-scale bags for that very reason.

    Differences From Other Ketone Intermediates

    Having spent decades synthesizing and handling a range of naphthalenone derivatives, the contrast becomes clear to anyone who works at bench scale or manages a process line. 5-Methoxy-3,4-Dihydro-2H-Naphthalen-1-One isn’t just another dihydronaphthalenone. The methoxy substitution at the 5-position alters both solubility and chemical reactivity. For some synthesis steps, the methoxy group acts as a directional activator, improving yields where unsubstituted analogues tend toward lower selectivity or incomplete conversion. We’ve seen downstream synthetic steps accelerate, or even simplify, when clients switch from a general naphthalenone intermediate to this variant.

    The physical form matters too. Some related products produce sticky, partially crystalline masses that make both weighing and dissolution frustrating, as any technician with a clogged beaker can confirm. Our material’s fine powder form handles well, flows consistently, and dissolves more readily in common solvents. These properties come from attention during form isolation—agitation speed, precipitation temperature, and solvent blend during crystallization.

    Safety handling profiles differ as well. The methoxy group reduces volatility and odor compared to lower-molecular-weight alkoxyketones. Our routine tests confirm that the dusting tendency remains very low, minimizing operator exposure. This has allowed us to streamline plant procedures and reduce waste, with less need for extensive local exhaust systems.

    Quality: Not a Checkmark, a Daily Practice

    Talk to anyone on our technical team and you’ll hear stories about discovering where shortcuts affect quality. Extra drying time can reduce trace water that, left unchecked, turns the best intermediate into trouble when used in sensitive syntheses. The quality process starts right at material intake: raw methoxyphenols often carry low-level impurities invisible in specs but visible in a NMR spectrum on final product. We reject these supplies, even if the price is right, to preserve the final product’s integrity.

    Each batch’s certificate comes from real measurement, not standard assumptions. Assay, melting point, moisture, ash content—these numbers reflect sample checks from every run, not handwaving. Customers notice differences between lots less frequently as a direct result. Most reporting involves not just compliance to known regulatory expectations, but a recognition that these materials often turn up downstream in human-contact products or regulated sectors.

    Supply Chain: Stability in a World That Demands It

    Having ridden the roller coaster of raw material shortages and price volatility for years, we know the difference between a backed-up batch and a cancelled production run. We’ve developed parallel sourcing relationships for our critical precursors; if one supplier drops the ball on quality, delivery, or price, we have another route ready to keep batches on schedule. We maintain buffer stocks of both starting material and final compound, and we’re transparent about our lead times. This reduces bottleneck anxiety for our clients; they know upfront if a delayed feedstock might affect delivery.

    As a medium-scale producer, we’ve seen how larger conglomerates sometimes lose touch with the needs of custom order volumes or specialized logistics. Our flexibility means ordering as little as a few kilograms up to multi-ton consignments is supported by the same production and analytical oversight. Palletizing, packaging, and labeling are handled onsite, and requests for special drum sizes or moisture-barrier liners draw from what we’ve already established for more demanding regulated industries.

    Environmental Responsibility in Practice

    The shift toward greener chemistry is real, not a slogan, in our plant. Solvent recovery sits at the heart of our cost management, but it also trims down waste outputs. Hydrogenation steps once prone to overuse of pressure and high temperatures now run at optimized loads, extending catalyst life and cutting down both energy use and by-product formation. Rather than landfill chemical waste, we contract with recyclers who close the loop on our spent drums and solvents. Effluent controls exceed local regulatory expectations, because we prefer to avoid surprises at the next inspection, not to chase paperwork after the fact.

    We constantly look for changes—enzymatic routes for some steps, lower-toxicity extractives, and better in-plant monitoring—to cut down not just emissions but also personnel exposure. Employee suggestions from the shop floor occasionally lead to process adjustments, and we reward them. Protecting our people and our neighbors isn’t about compliance alone, but about maintaining respect for the broader community.

    Risk Management and Handling Considerations

    Those who produce and handle chemicals daily take stock not only of product abilities but also of handling needs and built-in safety. 5-Methoxy-3,4-Dihydro-2H-Naphthalen-1-One offers lower dust risk, manageable flammability, and less pronounced odor, which makes operations safer and more pleasant for operators downstream. Our on-site safety protocols teach workers to recognize hazards, and this knowledge travels with our product through the supply chain.

    Packaging reflects what we’ve learned over years of field returns and customer feedback. Double-bagging in lined drums, desiccant packs, and tamper-evidence seals now come as standard, based on real-world lessons—container failures, moisture incursions, or contamination from bulk shipments can interrupt entire chains of production. We train our team and our logistics providers to spot these risks before the product ever leaves our plant.

    Challenges and Our Response to Industry Concerns

    Three challenges keep recurring in discussions with downstream users: reliability of supply, batch consistency, and ongoing technical support. We’ve listened to complaints about last-minute changes in specification, tolerance drifts between lots, and rare but real contamination episodes suffered with less attentive firms. Our approach rests on making each run traceable, with full documentation, retained samples, and open communication with client technical teams. Every process issue gets logged, reviewed, and—if repeatable—reworked in the operating procedure.

    Quality troubleshooting is never treated as a one-way street; we’ve flown in samples, provided MSDS before orders, and tracked down root causes in partnership with clients. We see ourselves as accountable for more than just the delivery. That responsibility doesn’t end at the plant gate.

    R&D and Continuous Improvement

    Research doesn’t stop once a molecule meets contract specs the first time. Our R&D team revisits ongoing runs, studying where we can refine step yields, lower by-product rates, or improve robustness. Sometimes it means sourcing a new grade of starting material, or tweaking catalyst reused lifecycles. Other times it’s a full rework of an isolation method to move away from graded solvents toward recyclable, lower-impact alternatives.

    Feedback from our partners has shaped product development, just as much as innovations from inside the lab. For one customer, we found lowering particle size enhanced solubility and improved downstream automation. For another, tighter moisture tolerances reduced side-reactions in their own manufacturing. These tweaks result from genuine two-way dialogue and a willingness to run trials, not just ship a brochure.

    Final Reflections From the Manufacturing Floor

    Over years of making and supplying 5-Methoxy-3,4-Dihydro-2H-Naphthalen-1-One, we’ve seen its growing role in specialty synthesis, and the way production discipline drives both efficiency and satisfaction for our partners. We retain skilled chemists, invest in equipment, and uphold transparency—not as slogans, but because doing so reflects the realities of our craft and the character of our team.

    Every kilogram shipped stands for more than just a line on an invoice. This product brings together the lessons, effort, and honesty of a team that stands behind what it delivers. For those who demand reliability, performance, and real technical partnership, we continue to commit our experience and resources to making 5-Methoxy-3,4-Dihydro-2H-Naphthalen-1-One an asset in the evolving landscape of chemical manufacturing.