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2-Hydroxy-9-Fluorenone

    • Product Name 2-Hydroxy-9-Fluorenone
    • Alias 2-Hydroxyfluoren-9-one
    • Einecs 207-476-4
    • 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
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    Specifications

    HS Code

    258821

    Name 2-Hydroxy-9-Fluorenone
    Cas Number 2587-90-8
    Molecular Formula C13H8O2
    Molecular Weight 196.20 g/mol
    Appearance Yellow crystalline powder
    Melting Point 178-182 °C
    Boiling Point No data available
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Synonyms 2-Hydroxyfluoren-9-one
    Density 1.33 g/cm³ (estimated)
    Ec Number 219-966-2

    As an accredited 2-Hydroxy-9-Fluorenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical 2-Hydroxy-9-Fluorenone is packaged in a 25g amber glass bottle, sealed, with hazard and identification labeling.
    Shipping 2-Hydroxy-9-Fluorenone is typically shipped in tightly sealed containers to prevent moisture and light exposure. It should be transported at ambient temperature, following standard chemical safety regulations. Proper labeling and documentation are required, and handling should minimize inhalation and skin contact. Shipping complies with all relevant hazardous material guidelines.
    Storage 2-Hydroxy-9-Fluorenone should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from direct sunlight and sources of ignition. Store separately from strong oxidizing agents and acids. Use appropriate chemical storage cabinets, avoid excessive heat, and ensure labelling is clear. Always follow standard laboratory safety and chemical storage guidelines to prevent contamination or degradation.
    Application of 2-Hydroxy-9-Fluorenone

    Applications of 2-Hydroxy-9-Fluorenone in Industrial Manufacturing

    2-Hydroxy-9-Fluorenone serves as a specialty intermediate in multiple high-value industrial sectors. Our production experience ensures refined quality for each scenario, supporting advanced synthesis protocols and critical performance benchmarks worldwide.

    1. Pharmaceuticals: Synthesis of Active Pharmaceutical Ingredients (APIs)

    API manufacturers use this compound as a key building block in the synthesis of several fluorenone-based drug molecules, especially those targeting central nervous system indications. Its hydroxyl functionality enables site-specific functionalization under controlled conditions. Production batches incorporate tight solvent handling and phase separation, meeting narrow impurity specifications. We supply material for integration into regulated GMP lines for innovative and generic drug development projects.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidelines
    • European Pharmacopoeia 11.0 (fluorenone derivatives section)
    • USP 44 (for relevant intermediates)
    • FDA 21 CFR Part 210/211 for API manufacturing

    Typical usage ratio

    • 5–20% molar basis as a key intermediate, based on reaction stoichiometry and selected API synthesis pathway.
    • Adjustment depends on target molecule and downstream route optimization.

    Downstream process integration

    • Charged into hydrogenation or acylation steps following primary condensation reactions.
    • Frequently used in protected form, then deprotected for subsequent transformations.
    • Supports multi-stage synthesis towards final API core structures.

    Final product types

    • Antidepressants (e.g., fluorenone derivatives)
    • Experimental CNS agents under development
    • Pharmaceutical intermediates for small molecule drugs

    2. Electronics: Organic Photovoltaic Materials and OLED Emitters

    In advanced materials sectors, device manufacturers incorporate this molecule as a crucial building unit for synthesizing dendrimer and polymer matrices. Its unique photochemical properties allow controlled bandgap engineering, improving charge transport in active electronic layers. Process engineers use it in scalable solution-phase reactions to achieve high purity and stable performance in large-area device fabrication.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for electronic components
    • IEC 61249-2-21 standards for base materials in PCBs
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EU)
    • UL 94 for flammability rating of finished plastic parts

    Typical usage ratio

    • 2–10% weight basis in organic small molecule or polymer blends, depending on emitter or transport layer design.
    • Blend ratios adjusted based on device type: OLED, OPV, or organic FET.

    Downstream process integration

    • Introduced during solution casting or ink formulation for spin-coating or inkjet printing processes.
    • Integrated into step-growth polymerizations or post-polymerization functionalization reactions.

    Final product types

    • Organic light emitting diodes (OLED displays)
    • Organic photovoltaic (OPV) panels
    • Organic semiconductor thin films

    3. Dyes and Pigments: Fluorescent Dye Synthesis

    Specialty dye manufacturers utilize this intermediate as a precursor in the creation of xanthene and acridine-based fluorescent dyes. Its structural rigidity and hydroxyl group facilitate electrophilic aromatic substitution, producing high-performance colorants for research staining, coatings, and security printing. The process involves multi-step condensation and oxidative reactions under monitored temperature and pH profiles, supporting durable and photostable end products.

    Industry compliance standards

    • EN 71-3 Safety of Toys: Migration of certain elements for inks and pigments
    • Eco Passport by OEKO-TEX® for textile dyes
    • ISO 9001:2015 for pigment batch production QC
    • REACH Annex XVII restrictions for specific aromatic compounds

    Typical usage ratio

    • 5–25% weight of dye precursor mix, optimally tuned for color intensity and solvent compatibility.
    • Higher ratios used in specialized high-brightness applications.

    Downstream process integration

    • Added at the initial condensation stage for ring formation steps.
    • Functionalized further with sulfonic acid or amine groups for enhanced solubility or binding.
    • In-process crystallization and purification before blending with other dye components.

    Final product types

    • Fluorescent textile dyes
    • Microscopy and bioimaging stains
    • Security inks for anti-counterfeiting

    4. Agrochemical Intermediates: Synthesis of Plant Protection Actives

    Agrochemical companies employ this compound in the controlled synthesis of certain fluorenone-derived herbicides and fungicides. Its presence ensures targeted mode-of-action molecules, which integrate into multi-step formulation lines. Process engineers apply precise feed rates and solvent control to minimize byproducts, enabling stability and biological efficacy of the finished active ingredient. Production operates under strict health, safety, and environmental controls for the protection of downstream handlers and application environments.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 for agrochemical manufacturing
    • European Regulation (EC) No 1107/2009 for registration of plant protection products
    • EPA 40 CFR Part 158 (USA) for pesticide active ingredients

    Typical usage ratio

    • 3–12% molar feedstock in synthesis of selective actives, varying by end-use crop and compound complexity.
    • Adjusted based on required final purity and bioactivity levels.

    Downstream process integration

    • Charged at the cyclization or functionalization phase of batch reactors.
    • Quickly isolated and reformulated for combination with carriers or adjuvants.

    Final product types

    • Fluorenone-based herbicides
    • Fungicidal active concentrates
    • Crop protection premixes

    5. Analytical Reagents: Chromatography and Luminescence Markers

    Producers of analytical reagents select this material for the preparation of specialty markers used in HPLC, capillary electrophoresis, and photometric assays. Its stable fluorescence emission and strong UV absorption provide sharp detection windows, even in demanding analytical matrices. Integration requires high-purity isolation and rigorous impurity profiling, ensuring reliable quantitation in pharmaceutical and environmental labs worldwide.

    Industry compliance standards

    • ISO 17034 for reference material producers
    • ISO/IEC 17025 for analytical laboratory quality
    • GLP (Good Laboratory Practice) OECD Guidelines
    • USP Analytical Reagent Standards

    Typical usage ratio

    • 0.1–2% weight, dependent on required sensitivity and instrument configuration.
    • Lower dosages used for trace markers, higher for preparative detection tags.

    Downstream process integration

    • Dissolved in solvent systems or conjugated with reporting ligands for direct assay development.
    • Covalently linked during final derivatization in analytical kits.

    Final product types

    • Fluorescent labeling reagents
    • Calibration standards for chromatography
    • Luminescent detection kits
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    Certification & Compliance
    More Introduction

    2-Hydroxy-9-Fluorenone: Behind the Scenes in Chemical Manufacturing

    A Day in the Factory: How We Approach 2-Hydroxy-9-Fluorenone

    Our story with 2-Hydroxy-9-Fluorenone traces back to the push for higher standards in organic synthesis. Over the years, we noticed more laboratories and advanced materials research teams searching for a consistent source of this particular fluorenone derivative. Many applications use it as an intermediate, especially when a project calls for oxidation detection, photophysical studies, or the pursuit of new molecules built on polycyclic frameworks.

    Production starts from fluorenone itself with targeted hydroxylation reactions. We learned early to watch our conditions closely—solvent purity, pH, temperature—all play crucial roles in influencing not only yield but also downstream use of the product. Our chemists have shared more than a few stories about failed runs in the early years due to old stock solvents or hasty reagent selection. Over time, we built a quality control process that tracks every batch from initial charge to the end material packed away in sealed amber glass.

    Typical output reaches purity grades above 98%, measured not only by HPLC but also by NMR. Most of our regular clients request yellow crystalline powder, which works best for their solution-phase experiments. A few opt instead for smaller crystalline plates, especially when setting up spectroscopic calibration. For bulk projects or scale-up, we accommodate gram to multi-kilo orders, packaged under dry nitrogen to reduce any risk of unwanted side reactions.

    Model and Specifications

    The standard model follows a structural formula of C13H8O2. We produce batches in both analytical and technical grades, always documenting physical constants, spectral data, and impurity profiles. Melting point checks fall in the range of 168-172°C, and IR as well as UV absorption patterns are confirmed against reference spectra for every run. Water content, residual solvents, and trace metals get analyzed before anything leaves the plant.

    Some colleagues in the field ask about scale. Our continuous-flow reactor setup runs up to 10 kilograms in a single charge, but we also handle small, highly purified orders down to 5 grams with the same tracking method as the larger lots. As the end user, you can request detailed COA with every shipment—reflecting not just minimum legal requirements, but also test results from our independent QA lab. Sometimes researchers need these details for their own validation or regulatory filing.

    Applications of 2-Hydroxy-9-Fluorenone

    We have seen 2-Hydroxy-9-Fluorenone open new possibilities for both traditional and emerging fields. In the dye and pigment sector, researchers use it for tuning fluorescence in compounds designed to sense specific ions, for example, copper or zinc, within biological systems. Several pharmaceutical projects build on this intermediate to modify core polycyclic skeletons. In semiconductor R&D, we watched engineers test this molecule for organic electronic materials, especially in the search for new charge-transport layers.

    Analytical labs depend on its strong UV-visible absorption, making it a reference standard for calibrating instruments. Our industrial partners often mention its use as a photochemical sensitizer, where small changes in purity or moisture content can affect results. We know from feedback that batch consistency matters. A project aiming at reproducible results needs reliable supply. We worked with several clients to tweak crystal size and water content for better solubility in non-polar solvents, making sure the product fits the quirks of each process or experiment.

    University groups studying polycyclic aromatic hydrocarbon derivatives use 2-Hydroxy-9-Fluorenone as a benchmarking material. In some cases, they're interested in the reactivity of the hydroxy group for further derivatization—halogenation, alkylation, or coupling reactions. We field technical questions about protecting group strategies and provide trial samples to support new synthetic steps. Real-world feedback from small-scale academic projects has helped us fine-tune our purification steps, sometimes substituting glass columns or adopting greener solvents.

    Comparing 2-Hydroxy-9-Fluorenone with Other Products

    Compared to standard 9-fluorenone, the hydroxy-substituted version stands out for increased reactivity in electrophilic substitution and complexing capability. We observed during test synthesis that substitution on the fluorenone core influences both solubility and photophysical traits. Colleagues working in organometallic catalysis have reported much higher ligand affinity with the 2-hydroxy form due to the extra electron donor. This feeds directly into performance in catalytic cycles and photoredox applications.

    Sometimes customers evaluate 2-hydroxy against 4-hydroxy-9-fluorenone or 2,7-dihydroxy versions, both of which are available but require different synthetic steps. The 2-position substitution shifts the absorption maxima and modifies hydrogen-bonding patterns, which can be critical in designing fluorescent sensors or photoinitiators. Over the years, we encountered confusion caused by inconsistent labeling from less reliable suppliers, and so we started offering full spectral data to clarify distinctions between the isomers.

    We do not use harsh oxidants in our process, which means less environmental impact and reduced risk of trace contamination. Competing manufacturers sometimes chase cheaper routes at the expense of batch-to-batch variability. Our team understands firsthand how tiny differences in impurity levels surface in downstream experiments. We have rejected entire runs because of detectable by-products that could not be removed by recrystallization alone. Time spent refining techniques has improved not only our own standards, but also those of collaborators relying on us for reproducibility.

    Typical fluorenone derivatives are available from many sources worldwide, but meeting the demands of high-purity custom synthesis requires a closer connection with customers and their research aims. We host regular meetings with R&D teams from multiple industries to gather feedback. After switching to a new purification step tailored for water-sensitive applications, several groups confirmed improved performance in their own studies using our 2-Hydroxy-9-Fluorenone as a starting point.

    Quality Assurance: Lessons Learned

    Experience taught us that batch consistency doesn't come from automated systems alone. Human oversight, especially from chemists who understand the molecule at a structural level, still catches unexpected problems—solvent exchange errors, trace impurities from glassware, or even subtle variations in crystal shape. We document failures alongside successes. In our production floor diary, you find notes from the night shift flagging off-color batches, or maintenance logs about a pressurized filter clogging mid-cycle.

    We test each lot not just for the headline purity, but also for key secondary characteristics: moisture level, residual solvent profile, trace metal analysis, and stability under ordinary storage. Some users require solid-state NMR to ensure the product will behave correctly when packed into device prototypes. Our scale-up teams work closely with client process chemists to provide trial samples, run pilot lots, and share data openly if there are any anomalies. Through this process, we built trust and reduced rework both in our facility and at the client’s bench.

    Sustainability and Environmental Commitment

    Both industry partners and regulatory agencies now ask tough questions about sourcing, processing, and effluent management. We made the decision to use more base-metal catalysts and greener solvents after local water authority audits, and we publish an annual report on by-product disposal. Using milder conditions for hydroxylation has lowered our process energy requirements and cut down emissions. Any leftover solvents from washing and extraction go to in-house recovery and are reused in non-critical cleaning steps, reducing both waste and hazard exposure for our staff.

    Those who have come for a plant tour see how we monitor waste streams at every stage. Teams meet each week to review recent lab data, discuss cooling water usage, and track our carbon footprint. Several clients from the electronics sector express appreciation for supporting their drive to meet environmental targets—not just a paper promise, but in the deliveries that show up at their doors every month.

    Client Support Beyond the Sale

    Our involvement doesn't end after a shipment leaves the loading dock. We field technical support calls and do real troubleshooting—analyzing product behavior in foreign media, advising on storage protocols, and walking customers through root cause investigations if unexpected results turn up. An R&D chemist once called after finding unexpected degradation, and with our data archives, we helped reconstruct the timeline and identified a storage humidity issue.

    New teams sometimes reach out while they are designing an experiment, not just during a purchase. We offer guidance on solubility parameters or handling recommendations that often go far beyond a simple product sheet. Some clients ask us to modify particle size or tweak water content for specific downstream chemistry. Our approach favors honest conversation—if a request stretches what the molecule can safely provide, we’ll share our perspective and discuss alternatives or modifications.

    International partners often face differences in import regulations or storage needs due to climate conditions. We developed custom packaging over time, based on client feedback and field returns. Several times, a project depended on every material arriving ready-to-use, so we engineered composite liners and selected new moisture barrier films to preserve product quality across long transit and varied climates.

    Research Collaborations and Innovation

    We maintain regular dialogue with university groups working at the frontiers of organic chemistry. Supporting innovative uses of 2-Hydroxy-9-Fluorenone often means supplying more than just a reference-grade compound: it involves providing technical data, troubleshooting unexpected results, and exploring synthetic pathways that might extend the molecule’s range of applications. Several academic partners have asked us to participate in joint development projects, ranging from new dye molecules for solar cells to targeted industrial sensors.

    With the rise of computational chemistry, some investigators request digital spectral libraries, so their automated systems can match experimental data. We supply full characterization datasets—NMR, IR, MS—to support these efforts and open up discovery. Knowing our products end up in published research inspires us to keep high standards and invest in the best available technology for analysis and synthesis. Feedback from researchers often translates directly into new process controls or material improvements that benefit the wider chemical community.

    Challenges in Meeting Market Demands

    Supply chain interruptions—raw material fluctuations, logistics issues, or regulatory changes—can impact availability. Our policy: maintain a healthy inventory buffer and not pass sudden cost increases down the line without justification. We build relationships with trusted upstream suppliers and run periodic checks on incoming raw materials. On a few occasions, we worked alongside partner suppliers to trace minor contaminants in base fluorenone, tracking the cause to changes in their storage protocols.

    We have faced shortages in key reagents during times of global supply disruption. In such cases, we re-examine older synthesis routes or look for alternative suppliers who meet transparency standards. Experience from lean years has taught us the value of contingency planning—mapping not just direct suppliers, but also second- and third-tier sources to avoid single points of failure.

    Future Directions: More Than Just Intermediates

    Markets are shifting fast, and we see a real trend toward integrating chemical intermediates directly into systems for testing or device fabrication. In our labs, we are now looking at custom formulations, blend-ready batches, and special grades designed to plug right into emerging processes for printed electronics, specialty sensors, or next-generation materials. Clients want a partner who not only pushes for higher purity and consistency, but who understands the shifting needs of synthesis and applications at the interface of chemistry and engineering.

    Some new projects challenge our team to think bigger—for example, developing scaled versions of 2-Hydroxy-9-Fluorenone compatible with continuous-flow manufacturing or biocompatible sensor technologies. Researchers push us to support advanced analytics, longer shelf life, and detailed impurity fingerprinting. We are adapting both our plant and our support team as expectations rise.

    We remain committed to open, honest feedback, real-world technical support, and continual improvement. Demand for performance materials and research chemicals will only grow. As manufacturers with hands-on experience, we believe the only way to deliver on that promise is through rigorous quality, transparent processes, and partnerships built on trust—not just transactions.