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6-Hydroxy-2,3-Dihydrobenzo[B]Furan-3-One

    • Product Name 6-Hydroxy-2,3-Dihydrobenzo[B]Furan-3-One
    • Alias 6-Hydroxy-3,4-dihydro-1-benzofuran-3-one
    • Einecs 629-451-2
    • 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

    172228

    Iupac Name 6-Hydroxy-2,3-dihydro-1-benzofuran-3-one
    Molecular Formula C8H6O3
    Molecular Weight 150.13 g/mol
    Cas Number 4874-97-7
    Appearance White to off-white solid
    Melting Point 170-174°C
    Solubility Slightly soluble in water; soluble in organic solvents like ethanol
    Smiles C1C(=O)OC2=C1C=CC(=C2)O
    Inchi InChI=1S/C8H6O3/c9-6-3-1-2-5-7(6)8(10)4-11-5/h1-3,9H,4H2

    As an accredited 6-Hydroxy-2,3-Dihydrobenzo[B]Furan-3-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 10 grams of 6-Hydroxy-2,3-Dihydrobenzo[B]Furan-3-One, tightly sealed, with clear chemical labeling.
    Shipping 6-Hydroxy-2,3-Dihydrobenzo[B]Furan-3-One is shipped in a tightly sealed container, protected from light and moisture. The package is labeled according to chemical safety regulations, ensuring safe handling during transit. It is dispatched via certified carriers, compliant with local and international regulations for chemical transport. Expedited and temperature-controlled options are available if required.
    Storage **6-Hydroxy-2,3-Dihydrobenzo[b]furan-3-one** should be stored in a tightly sealed container, protected from light and moisture. Keep the chemical in a cool, dry, and well-ventilated area, preferably at room temperature or lower. Avoid sources of ignition and incompatible substances like strong oxidizers. Proper labeling and secure storage are essential to ensure safety and maintain chemical stability.
    Application of 6-Hydroxy-2,3-Dihydrobenzo[B]Furan-3-One

    Applications of 6-Hydroxy-2,3-Dihydrobenzo[B]Furan-3-One in Industrial Manufacturing

    6-Hydroxy-2,3-dihydrobenzo[b]furan-3-one supports multiple specialized industrial sectors with its unique aromatic and lactone structure. Through direct participation in synthesis and formulation steps, it serves as a crucial intermediate in downstream applications for advanced material fabrication and fine chemicals production.

    1. Pharmaceutical Intermediate for CNS Drug Synthesis

    Many pharmaceutical manufacturers apply this compound as a core intermediate in central nervous system (CNS) active molecules. Its furanone scaffold forms the basis for antidepressant, anticonvulsant, and anxiolytic candidate APIs. The compound enables regioselective ring transformations and controlled functionalization steps. Downstream manufacturers integrate it directly into process route for high-purity synthesis, with stringent quality controls at each step, to yield safe and reproducible final formulations.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (EP)
    • USP-NF General Chapter <787> Residual Solvents
    • 21 CFR Part 211: US cGMP for Finished Pharmaceuticals

    Typical usage ratio

    • 5–12% as an intermediate, adjusted by molecular pathway yield requirements and API batch scale

    Downstream process integration

    • Enter synthesis step after initial condensation; undergoes selective functionalization and ring closure in multistage batch reactors
    • Intermediates monitored by HPLC for structure confirmation; transferred to subsequent coupling or alkylation stages

    Final product types

    • Generic and branded CNS drug substances (API)
    • Intermediates for neuroprotective compounds
    • Small molecule development candidates for clinical trials
    • Precursor APIs for finished dosage forms (tablets, capsules)

    2. Aroma and Flavor Ingredient Synthesis

    The lactone structure of this building block enables synthesis of aroma compounds for food and beverage applications. Manufacturers employ it to create nature-identical flavor compounds by lactonization and selective reduction. It plays a specific role in constructing notes for caramel, nut, and roasted flavors found in finished beverages and confectionery. Regulatory and sensory validations govern downstream use.

    Industry compliance standards

    • FAO/WHO JECFA Food Additives Specifications
    • 21 CFR Part 172: Food Additives Permitted for Direct Addition
    • FEMA GRAS (Flavor and Extract Manufacturers Association)
    • ISO 22000: Food Safety Management Systems

    Typical usage ratio

    • 0.1–1.5% in aroma synthesis routes; final flavoring levels regulated below 20 ppm in finished food depending on application and local limits

    Downstream process integration

    • Added at condensation or reduction stage in batch synthesis to yield lactone-based aroma chemicals
    • Treated with controlled heat to promote desired isomerization for flavor profile development

    Final product types

    • Cream, nut, and butter-type flavors for bakery and confectionery
    • Caramel and roasted flavorings for beverages
    • Encapsulated aroma preparations for processed foods
    • Regulatory-submitted food additive compounds

    3. Agrochemical Synthesis Intermediate

    This compound acts as a structural intermediate for producing selective herbicide actives and growth regulators. Agrochemical formulators introduce the lactone moiety to provide controlled degradability and targeted biological activity. Firms employ it during heterocycle assembly and subsequent derivatization, supporting synthesis of modern, low-residue actives for crop protection.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • ISO 9001: Quality Management Systems
    • Regulation (EC) No 1107/2009: Placing of plant protection products on the market
    • China Institute for the Control of Agrochemicals, Ministry of Agriculture (ICAMA) registration rules

    Typical usage ratio

    • 3–8% in intermediate synthesis for selective herbicide or plant growth regulator APIs; ratio chosen per downstream compound structure

    Downstream process integration

    • Processed via alkylation and esterification in plant reactors to form active intermediates
    • Blends with other building blocks during fine purification and formulation into final crop protection solutions

    Final product types

    • Plant growth regulators
    • Selective herbicides for cereal and oilseed crops
    • Custom pesticide intermediates provided to formulation partners
    • Degradable field application actives

    4. Functional Polymer Additive Production

    In advanced polymer manufacturing, this chemical serves as a monomeric modifier for specialty resins and engineering plastics. When introduced into polycondensation or co-polymerization steps, it imparts thermal resistance and specific color or aroma properties. Producers manage its addition by precise process control to ensure final properties and regulatory compliance for consumer or industrial use.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 (Registration, Evaluation, Authorisation and Restriction of Chemicals)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 9001: Quality Management for Chemical Manufacturing
    • UL 94: Flammability Standard for Plastics Materials

    Typical usage ratio

    • 0.5–6% by weight as a functional additive depending on polymer type and required technical properties

    Downstream process integration

    • Metered into polycondensation reactors with main monomers at the start of reaction
    • Homogenized into pre-polymer melt; conversion tracked by IR and GPC analytical tools

    Final product types

    • Specialty engineering plastics for automotive and electronics
    • Color-modified or aroma-infused resins
    • Masterbatch additives for films and fibers
    • Consumer goods requiring specific olfactory or appearance features

    5. Fine Chemical Intermediate for Dye and Pigment Synthesis

    Colorant producers employ this compound as a furanone-based building block for manufacturing specialty dyes and pigments. Its ring system allows for targeted substitution and coupling to aromatic amine or azo systems. The material enters controlled reaction stages during synthesis of stable, high-performance pigments for coatings, inks, and plastics, facilitating custom color development based on downstream customer requirements.

    Industry compliance standards

    • EN 71-3: Safety of toys – Migration of certain elements (for colorants used in toys and children’s products)
    • ASTM D4236: Labeling of art materials for chronic health hazards
    • ISO 16128: Guidelines on technical definitions and criteria for natural and organic cosmetic ingredients and products (for dyes used in cosmetics)
    • REACH registered substances

    Typical usage ratio

    • 1–7% in dye or pigment precursor synthesis, tailored per chromophore pathway and color intensity targets

    Downstream process integration

    • Added during initial aromatic ring assembly or condensation stages, followed by subsequent halogenation or azo coupling
    • Pigment finished by filtration and controlled particle size reduction

    Final product types

    • High-stability pigments for automotive paints
    • Specialty inks for high-speed industrial printers
    • Cosmetic-grade colorants for personal care
    • Plastic color masterbatches for molded parts
    Free Quote

    Competitive 6-Hydroxy-2,3-Dihydrobenzo[B]Furan-3-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

    6-Hydroxy-2,3-Dihydrobenzo[B]Furan-3-One: An Insider’s View from the Shop Floor

    Real Chemistry Behind the Label

    In a sea of bench reagents and off-the-shelf intermediates, 6-Hydroxy-2,3-Dihydrobenzo[B]Furan-3-One stands out on any production line for reasons you don’t find on the label. Our team has been turning out this compound for years, watching each batch go from carefully weighed starting material to the final powdered or crystalline product, always following strict process control. This chemistry can look routine from a lab notebook, yet demands the kind of vigilance and understanding only gained on the job.

    Our typical offering comes at a purity level that exceeds 98%, which we continuously verify using in-house HPLC and NMR, not just with a glance at a printout but with a genuine understanding of spectral quirks and batch history. Spec sheets can summarize, but the proof sits in the hands-on checks—sharply defined melting ranges, consistent crystal morphology, and smooth handling behavior, right down to the finest grain.

    Form and Function: Why This Molecule Matters to Industry

    For developers chasing the next active pharmaceutical ingredient or fragrance, the furanone scaffold has always been a key building block. The hydroxy group at position six adds that critical functional handle for further modification, such as coupling reactions or reduction steps. In cosmetic chemistry, where small changes in aroma or reactivity matter, this intermediate has become a favorite base. The stability profile lets our partners store and utilize it without noticing loss in yield, even after months on the shelf.

    Compared to pure benzo[b]furan or other substituted furanones, adding a hydroxy group creates a polar handle that changes everything from crystallinity to solubility. For chemists aiming to introduce new reactivity, this feature opens routes to esters, ethers, or other derivatives. Through our own scaled syntheses and by feedback from long-term clients in agriculture and specialty chemicals, we’ve seen this flexibility turn a tricky project into a successful process route.

    Quality Control Isn’t Guesswork

    In specialty chemical manufacturing, shortcuts lead nowhere. Too much unreacted starting material or side product—even a minor impurity—will surface in stability studies fast, so our own process includes triple-phase filtration and precisely controlled reaction conditions. The temperature curves and batch records tell a story not always obvious to someone reading only an MSDS.

    After years of process re-optimization, we saw how trace metals and solvent residues affected crystallization. Early on, we ran into problems with batch-to-batch color changes and stubborn particulate formation. Dialing in the right solvent, purification system, and drying protocol took effort, but the results speak for themselves: strong batch reproducibility, predictable melting points, and the sort of stability data that lets customers ramp up production smoothly.

    Real-Life Usage: Lessons Learned with Every Batch

    Labs and plant R&D teams reach out to us for practical support, not just off-the-shelf material. We’ve observed this molecule deployed in reactions forming fused aromatic rings, as a precursor for bioactive esters, and in flavor ingredient syntheses where pinpoint purity means success or failure. One major client, for instance, used our product as a starting point for a new class of UV-absorbing agents; small tweaks to the hydroxy position let them create a series of unique, IP-protected materials.

    Not every attempt goes smoothly. In client pilot runs, minor contaminants blocked downstream purification steps. Working closely with their chemists, we identified trace sulfur residues from raw material supply as the culprit. By changing suppliers and adjusting our cleaning protocol, we were able to meet their critical threshold, prevent fouling, and help them avoid costly downtime.

    What Sets Our Approach Apart

    The technical side is only part of the equation. Consistent packaging—glass bottles for research labs, lined drums for scale-ups—prevents contamination and moisture ingress. Shipment at the right warehouse temperature during hot months helps the product hold up under transit stress, especially for our long-haul partners. We field regular questions from formulators about batch consistency and have no problem sharing not just certificates, but recent analytical run details when asked. That transparency didn't arise because of regulation; it grew out of failure analysis and real conversations with technical staff facing their own project deadlines.

    We’ve also seen trends in market pricing linked to raw material volatility. Furan derivatives rely on particular aromatic feedstocks, which remain vulnerable to global supply chain swings. By investing in advance forecasting and bringing in secondary suppliers, disruptions haven’t reached our production floor the way they have at some smaller shops. During global logistics crunches, the ability to continue uninterrupted deliveries helped our partners keep their own projects on time.

    Differences from Other Benzofuranone Compounds

    It’s tempting to assume all substituted benzofuranones work interchangeably in a synthesis. Having run multiple kilo-lot syntheses for similar compounds, we know far better. Once, a partner swapped in 5-Hydroxy-2,3-dihydrobenzo[b]furan-3-one, speculating the change would alter downstream reactivity only slightly. Instead, yield plummeted from 90% to below 50%. The position of the hydroxyl group does more than add polarity—it shapes hydrogen bonding, ring activation, and even the crystalline lattice.

    Other manufacturers sometimes offer mixtures of positional isomers, claiming comparable utility. From our own pilot trials, mixed-material sources often cause unplanned side reactions, separation headaches, and irreproducible yields. Markets selling cheaper “furanone” intermediates with relaxed specifications rarely meet the needs of teams aiming for robust, IP-clear development. Our process emphasizes separation of isomers in both intermediate and finished product, not out of bureaucratic necessity but following hard-earned lessons in process optimization and scale-up headaches.

    Consistent Support over the Product Lifecycle

    Many chemical suppliers vanish once a batch reaches the loading dock. Years of fielding technical questions taught us that real technical partnership matters. Post-sale, we help troubleshoot scale-up snags—what to do if a process unexpectedly emulsifies, or if solid loads start to rise as seasons change. Rapid response, not just a generic answer, comes from knowing how the compound behaves under different process conditions.

    In another instance, a customer’s glassware showed etching after several months. Their protocol involved trace base, and our application support flagged the hydroxy group’s potential for slow side reactions under alkaline conditions. This exchange led to minor yet effective tweaks in their downstream process, saving them from switching to a more expensive protective-group intermediate.

    Sustainable Choices: Waste Management and Scale-Up

    Environmental compliance and circular economy goals now play a bigger role in commercial procurement than ever before. Our work with 6-Hydroxy-2,3-Dihydrobenzo[b]furan-3-one includes recycling spent solvents and reducing mother liquor discharge. As waste disposal costs spike worldwide, more clients request detailed breakdowns of our own emission and residue profiles. Our team provides this data because we’ve found waste minimization isn’t just good citizenship—it keeps long-term production costs in check. Regulating reactions to cut down on non-target impurities and recapturing by-products means less cleanup, both for us and for our customers.

    We’ve seen, more than once, that chemical innovation goes hand in hand with responsible handling. Several downstream clients have worked with us to trial their own on-site solvent recycling. The technical outcome? Lower raw material demand and reduced risk of accidental environmental discharge—a win for both manufacturer and user.

    Continuous Learning and Adaptive Process Improvement

    It pays to stay vigilant. Every batch run uncovers lessons, whether it’s a yield drop traced back to seasonal humidity or a melting point shift hinting at micro-impurities. Open process logs and regular operator training keep quality high, not just after a complaint but before there is one. By collecting and reviewing both in-process and end-product data, we’ve adjusted protocols to increase throughput, cut cycle times, and improve product flow without compromising chemical characteristics.

    Visits from client quality assurance teams don’t just check a box—they bring useful feedback about downstream compatibility, packaging issues, and missed analytical parameters. We act on this information because it keeps our process robust and market-focused.

    Looking Ahead: Meeting Demands for Innovation

    The market for furan derivatives continually presents new challenges. Clients push for higher purity, modified physical forms, even micronized grades to meet formulation challenges. By staying hands-on in the process and maintaining open channels with R&D teams, we anticipate requests instead of merely reacting. Already we’re exploring more energy-efficient synthetic steps, swapping out high-impact reagents without sacrificing throughput.

    We have also joined collaborations on greener solvent systems and automated reaction monitoring, providing test batches to support next-gen green chemistry projects. Our history handling similar aromatic intermediates equips us to scale up these trials when demand moves from kilograms to tonnage.

    Closing Thoughts from the Production Floor

    To outside eyes, 6-Hydroxy-2,3-Dihydrobenzo[B]furan-3-one might feel like just another catalog item. To those working day in and day out with this compound, its character shows in more than numbers: in the way it crystallizes after a slow overnight cool, the aroma wafting from a solidifying batch, the feedback loop between analytical data and hands-on operator observation. Every kilogram reflects investments in process fine-tuning, honest conversations with users, and lessons learned through trial, error, and collaboration.

    As the needs of formulators, researchers, and manufacturers evolve, so too will our approach. Our experience spans well beyond datasheets, rooted in the realities of the shop floor, the practicalities of scale-up, and the give-and-take between process constraints and customer demands. The future will bring new challenges in sustainable chemistry, complex syntheses, and value-added modification. We’ll face them with the same core values—transparency, technical excellence, and real-world experience.