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9(10H)-Acridone

    • Product Name 9(10H)-Acridone
    • Einecs 201-594-2
    • 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
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    Specifications

    HS Code

    851762

    Iupac Name 9H-Acridin-9-one
    Molecular Formula C13H9NO
    Molar Mass 195.22 g/mol
    Cas Number 578-95-0
    Appearance Yellow solid
    Melting Point 352-354 °C
    Solubility In Water Slightly soluble
    Density 1.32 g/cm³
    Smiles O=C1C2=CC=CC=C2NC3=CC=CC=C13
    Pubchem Cid 70298
    Inchi InChI=1S/C13H9NO/c15-13-10-5-3-1-2-8(10)12-9-6-4-7-11(12)14-13/h1-7,14H

    As an accredited 9(10H)-Acridone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g of 9(10H)-Acridone is packaged in a sealed amber glass bottle with a tamper-evident cap and clear labeling.
    Shipping 9(10H)-Acridone is shipped in tightly sealed containers to prevent contamination and moisture ingress. It should be packaged according to chemical safety standards, labeled appropriately, and transported under conditions protecting it from extreme temperatures and physical damage. Ensure compliance with local, national, and international regulations for chemical transportation.
    Storage 9(10H)-Acridone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. It should be kept away from light and moisture. Ensure appropriate labeling and follow all chemical safety protocols, including the use of gloves and eye protection during handling.
    Application of 9(10H)-Acridone

    Applications of 9(10H)-Acridone in Industrial Manufacturing

    As a direct manufacturer of 9(10H)-Acridone, we support specialized downstream users in select industrial settings where its aromatic heterocyclic structure provides essential functional performance. This section outlines the primary industrial application scenarios where our material demonstrates established value based on its chemical compatibility, regulatory acceptance, and manufacturing practicality. For each scenario, we detail compliance benchmarks, technical integration points, proportioning guidelines, and resultant downstream product types.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) Synthesis

    In advanced pharmaceutical synthesis, acridone scaffolds serve as critical intermediates for API production, particularly in the development of anti-malarial, anti-cancer, and anti-viral drug molecules. Specialist pharmaceutical processors use 9(10H)-Acridone in multi-step organic syntheses where the controlled introduction of acridone residues underpins target compound efficacy and regulatory acceptability. Our clients leverage its stability in high-yield, scalable batch productions compliant with leading global medical standards.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) Guidelines for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (current Good Manufacturing Practice for Finished Pharmaceuticals)
    • EU EudraLex Volume 4 GMP Guidelines
    • Pharmacopoeias: USP, EP, JP (where intermediate use is declared)

    Typical usage ratio

    • 0.5–2.5 mole equivalents relative to target API precursor, determined by specific route requirements and scale; batch sheet ratios adjusted for synthesis step conversion rates

    Downstream process integration

    • Charged at intermediate coupling or cyclization step in multi-stage batch reactors, generally after initial halogenation or condensation reactions; purity supported by in-process HPLC verification

    Final product types

    • Anti-malarial agents such as amodiaquine derivatives
    • DNA-targeted anti-cancer agents (acridone-based alkaloids)
    • Antiviral intermediates for research and preclinical candidates

    2. High-Performance Pigment Synthesis in Specialty Coatings

    Chemical processors employ 9(10H)-Acridone as a precursor in the synthesis of high-performance anthraquinone-derived pigments. These pigments deliver enhanced chromatic stability and heat resistance in advanced coating systems, such as those required for industrial machinery, automotive parts, and architectural materials. Our material supports pigmentary chromophores through nucleophilic addition steps, ensuring consistent tone and resistance to environmental degradation according to end-user acceptance specifications.

    Industry compliance standards

    • EN 71-3 Safety of Toys: Migration of Certain Elements (for pigments in coatings)
    • ISO 787-24 General Methods of Test for Pigments and Extenders – Determination of Resistance to Heat
    • Global Automotive OEM paint standards (e.g., Chrysler PF-4202, Ford WSS-M2P-37-B1 for pigment use)
    • REACH Regulation 1907/2006 (Registration, Evaluation, Authorisation and Restriction of Chemicals)

    Typical usage ratio

    • 5–15% w/w relative to total pigment precursor input; actual incorporation adjusted for shade target, dispersion grade, and resin compatibility

    Downstream process integration

    • Introduced during pigment synthesis prior to final coupling or laking phase, with intermediate filtration and grind checks; pigment then dispersed in resin and solvent blends before shipping for formulation

    Final product types

    • High-durability industrial coatings (powder coatings, metal protective topcoats)
    • Color-stable automotive paints
    • Architectural and façade specialty paints requiring UV stability

    3. Fluorescent Dye Manufacturing for Analytical and Imaging Applications

    9(10H)-Acridone serves as a key intermediate in the synthesis of acridone-based fluorescent dyes utilized in biotechnological and environmental monitoring fields. Downstream dye manufacturers rely on its photophysical stability and functionalizable positions to achieve high-quantum-yield fluorophores, which support signal enhancement in HPLC, fluorescence microscopy, and flow cytometry. Careful process inclusion achieves purity standards essential for analytical consistency in regulated laboratories.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems (for specialty chemical synthesis)
    • Chemical purity guidelines per ACS Reagent Grade, where relevant
    • OECD Good Laboratory Practice (GLP) Principles for chemicals in laboratory use
    • Restriction of Hazardous Substances (RoHS) Directive for electronic and imaging component dyes

    Typical usage ratio

    • 1–8% w/w of final dye mass, modulated by desired emission wavelength and concentration yield; adjusted per downstream derivatization or functional group installation

    Downstream process integration

    • Introduced at primary condensation step with subsequent alkylation or sulfonation reactions; intermediates subject to column purification and spectral verification prior to packaging

    Final product types

    • Fluorescent tagging dyes for cell imaging reagents
    • Reference standards for chromatographic calibration
    • Signal amplifiers in immunoassay kits

    4. Photo-Active Materials for Organic Semiconductors

    Manufacturers of organic electronic materials incorporate 9(10H)-Acridone derivatives as core building blocks in the assembly of organic semiconductors and photoactive thin films. Its planar aromatic backbone and electron-transport attributes facilitate the construction of charge-transport layers in optoelectronic devices. Integration into advanced material syntheses requires tight process controls to support high-purity layers necessary for device yield and long-term electrical stability.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (for electronic materials)
    • ISO 14001 Environmental Management System (for sustainable electronics manufacturing)
    • JEITA: Technical Standard for Organic TFT Manufacturing
    • IEC 62607 Nanomanufacturing Standard for Organic Electronic Devices

    Typical usage ratio

    • 0.2–3% by mass within semiconductor layer; level adapted based on polymer matrix compatibility and layer deposition method (spin-coating, inkjet printing, or vapor deposition)

    Downstream process integration

    • Introduced during organic material precursor blending before thin film casting or vapor-deposition; in-line film thickness monitoring and electrical property QC inform batch adjustments

    Final product types

    • Organic thin-film transistors (OTFTs)
    • Organic light-emitting diode (OLED) components
    • Integrated photodetector layers for low-power sensor devices

    5. Corrosion-Resistant Resin Additives in Engineering Plastics

    Specialty engineering plastics producers use acridone-based intermediates during the formulation of corrosion-resistant resins, particularly for molding parts exposed to aggressive chemical environments. The integration of this heterocyclic backbone provides improved oxidative stability to the polymeric chain, supporting downstream requirements for durability and color retention in precision-molded technical parts for process equipment and transportation infrastructure.

    Industry compliance standards

    • ASTM D2565 Practice for Xenon-Arc Exposure of Plastics for Outdoor Applications
    • ISO 11357 Plastics — Differential Scanning Calorimetry (for polymer stability)
    • UL 94 Standard for Safety of Flammability of Plastic Materials
    • Regulation (EU) No 10/2011 on plastic materials for contact with foodstuff (for food-grade plastics)

    Typical usage ratio

    • 0.3–1.2% w/w of total polymer resin matrix; precise dosage determined by resin type, end-use stress profile, and compatibility with reinforcing agents

    Downstream process integration

    • Added at feed hopper or compounding extruder phase prior to polymerization or molding; in-line compounding controls monitor dispersion and thermal profile

    Final product types

    • Injection-molded technical parts for pumps and valve housings
    • Corrosion-resistant sheets and panels for process industry installations
    • Protective housings for transportation and electrical infrastructure
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    Certification & Compliance
    More Introduction

    Understanding 9(10H)-Acridone from the Perspective of a Chemical Manufacturer

    The Nature and Background of 9(10H)-Acridone

    Working in the core of chemical synthesis and production, people in this field encounter dozens of compounds every day, each with its own set of challenges and history. Among heterocyclic compounds, 9(10H)-Acridone keeps surfacing as one that stimulates ongoing scientific curiosity. Chemists have known acridone and its structural kin for several generations. Over decades, we've seen this molecule go from a laboratory curiosity into a recognized key substance for research and industrial innovation.

    In our experience as a direct manufacturer, not a middleman, acridone reveals both its reliability and complexity through daily production. Its molecular formula, C13H9NO, and signature tricyclic skeleton underscore its hybrid aromatic-aliphatic character. Working with this substance on the manufacturing floor, our teams find that the seemingly simple yellow crystal holds impressive resilience during extended handling and storage. The chemical’s aromatic core and integrated carbonyl group confer steady thermal properties and resistance to ordinary humidity during transit or long-term warehousing.

    Offering Detailed Product and Model Selection

    Our approach to acridone production centers around offering both standard and custom-purity options to meet research and industrial requirements. The default reference for 9(10H)-Acridone is the compound with CAS number 578-59-4. This is the principal model users reference across industry and academic laboratories. By direct synthesis, the purity landscape ranges primarily between 98% to over 99%, using purification sequences such as recrystallization, vacuum drying, and chromatography. We have found that while trace impurities rarely pose functional issues in R&D applications, pharmaceutical and analytical clients often request higher specificity and documentation, which our in-house analytical team provides through NMR, HPLC, and mass spectrometry validation.

    Packaging logic around 9(10H)-Acridone balances stability, moisture resistance, and logistical safety. Over the years, we switched from basic glass containers to more robust amber glass bottles with polytetrafluoroethylene-lined caps for research-scale orders. On the plant scale, we ship the material in lined steel or high-density polyethylene drums, always sealed and inerted to minimize oxidative or photolytic degradation. Our field experience confirms that this coating strategy nearly eliminates risk of cross-contamination during bulk processing.

    Recognizing the Range of Acridone Applications

    Any manufacturer tracking chemical trends notices the growing attention acridone receives in research, particularly as a building block in pharmaceuticals, agrochemicals, and dyes. We have responded to increased demand from synthetic chemists designing anticancer agents, given that acridone serves as a core for scaffold-hopping and bioactive molecule synthesis. Several years ago, a notable client team used our product in a multi-step sequence to generate potent PARP inhibitors; in post-project review, they observed that our crystalline batch maintained purity throughout their 16-step synthesis—underscoring functional benefits far beyond crude mass yield.

    Beyond research-use, process chemists come to us seeking acridone as an intermediate for xanthene dyes and, in a few cases, as a fluorescence probe. Its UV-absorbance edge and robust emission signature make it a reporter group for sequence-verified DNA labeling or as a base for high-sensitivity HPLC detection. Throughout recent years, we noticed surprising versatility in customer feedback, with the acridone core popping up in pigment design, photoinitiators, and even as a participant in organic battery prototypes. The common denominator: chemists value its stability and compatibility with a wide range of reagents and solvents.

    Comparison of 9(10H)-Acridone with Related Structures

    Part of a manufacturer’s job is to help customers select the right molecule, cutting through catalog clutter. Over dozens of technical discussions, users compare acridone to anthracene, carbazole, and acridine. Not all researchers have the time for a detailed exploration of which backbone works best, so real-world commentary matters.

    Carbazole has a similar tricyclic arrangement but swaps a carbonyl for nitrogen in the central ring. This may look like a nuance, but it changes reactivity: carbazole resists nucleophilic addition and suits electronics or polymer applications rather than pharmaceutical use. Acridine also lines up as an aromatic tricycle, yet without the ketone of acridone, it lacks the same hydrogen-bonding profile and redox-behavior sought by medicinal chemists.

    Acridone’s N-H proton and the adjacent carbonyl alter both hydrogen-bonding and electronic properties. We’ve watched medicinal chemists tailor these functionalities when preparing derivatives active at varied biological targets—a flexibility that isn’t present in close cousins. Feedback from a client screening kinase inhibitors consistently points to acridone’s improved solubility in various polar organic media over anthracene- or acridine-scaffolds, which tend to precipitate or degrade.

    From our experience, synthetic routes using acridone often progress more cleanly, avoiding some of the harsh conditions acridine reductions sometimes require. The carbonyl group tolerates mild base or acid, and subsequent functionalization on the aromatic rings becomes accessible by standard coupling or halogenation techniques. This trait simplifies downstream steps and reduces the risk of unwanted side reactions—a key factor as process efficiency and cost control grow more crucial in scale-ups.

    Challenges and Solutions in Manufacturing

    Production realities shape every decision. Acridone molecules don’t appear overnight; they evolve from batchwise oxidations and cyclizations. Sourcing reliable feedstock, such as 2-nitrobenzaldehyde and aniline derivatives, forms the first of many gates. Over time, our crew noticed that choosing the right solvent and temperature range at the initial cyclization leads to higher batch yields and purities. Several years ago, a supplier switch led to a week of batch stoppages and quality variation—a hard-learned lesson to avoid unvetted intermediates.

    Controlling reaction temperatures below 120°C circumvents unwanted side products and tars. Several rounds of pilot runs taught us that using copper-based catalysts at this stage consistently leads to a cleaner conversion, while strictly monitoring dissolved oxygen content. At scale, we now catch impurities faster with in-line IR sensors, slashing off-grade output by half versus traditional sampling.

    Solvent recovery and waste management make up another slice of daily work. Our experienced engineering team installed closed-loop solvent stripping and condensation lines, reclaiming over 85% of DMF and toluene used in the main cyclization route. Not only does this cut costs, it meets stricter environmental expectations and makes our site audits smoother. The few grams of acrylamide-type unwanted byproducts produced in each cycle travel directly to our waste treatment partners, never mixing with finished material.

    Managing storage and packaging creates everyday wins and challenges. Acridone’s inherent stability means batches don’t require refrigeration, which helps keep overheads lower, yet dust control must stay tight. Anyone who has handled fine acridone crystals knows their tendency to cling to static-prone surfaces; bulk transfer teams use antistatic containers and precise scoop procedures to minimize product loss.

    Customer Needs and Application Feedback

    Customers shape much of how product quality and production processes evolve over time. The first years in direct sales taught us that consistency, not just purity, wins repeat business in the pharmaceutical sector. For advanced intermediates or active pharmaceutical ingredient (API) candidates, chemists and procurement managers want a batch history they can trace through several months. Instead of shifting synthesis conditions batch to batch, we fix our production parameters, then formally track each lot through digital and physical sample retains.

    Occasionally, synthetic chemists request fine-tuning on particle size, seeking smoother dissolution for rapid chemical reactions. With these researchers, we modify drying and milling steps, blending batches under monitored humidity until specifications line up. This precision raises yield in their subsequent steps and nudges forward their program timelines—feedback confirms that even minor manufacturing adjustments, when executed at scale, can ripple through to affect overall project success.

    Materials researchers exploring novel applications—such as organic solar absorbers or high-performance composites—bring new requirements. Sometimes, they require even longer-term stability data under varied humidity and light. Our quality group now logs accelerated weathering and photostability results for each production campaign, so downstream users can match these metrics to their planned uses. Conversations with our technical support team often spark iterative improvement projects, prompted by real-world lab feedback.

    Safety and Handling in Daily Operations

    Worker safety remains part of every day in the factory. Acridone itself doesn’t vaporize under standard conditions, so inhalation risks rank low versus some low-boiling solvents. However, the extra handling needed for large drying beds during final steps does increase skin and particulate exposure. The shop floor team wears fitted respirators and sleeves to avoid dermatitis and keeps handling in well-ventilated rooms. These measures, repeatedly tested during safety drills, have kept incident levels low and earned high scores in site safety audits year after year.

    As with other powdered aromatic derivatives, fine acridone can become airborne if mishandled. Factory improvements focused on dust-control engineering—HEPA-filtered enclosures, spot vacuum extraction, and regular equipment cleaning. These steps aren’t just regulatory box-ticking, they ensure staff keeps healthy and production areas run efficiently, with lower cleanup downtime. Consistent health monitoring and ongoing job training go hand-in-hand with these equipment upgrades.

    Quality Control Practices

    Not every batch turns out perfect, and as a manufacturer, it pays to acknowledge and address process variability. Our laboratory team implements batch sampling at each critical point: post-cyclization, post-purification, and prior to packaging. Routine analytical checks go beyond simple melting point or TLC; we use ultraviolet-visible (UV-Vis) spectroscopy to confirm aromatic core integrity, and high-performance liquid chromatography for purity diagnostics. These tests, combined with decade-long experience, help us catch off-spec batches long before material reaches the customer.

    Where off-specification occurs, root cause analysis becomes immediate. A spike in UV absorption outside expected maxima, for example, signals over-cyclization or side-chain formation. At scale, our team reviews instrument logs, solvent batch histories, and operator notes to trace the issue back. Over time, this has improved our response speed and reduced recurring problems line-to-line. We openly share selected testing data with customers, building trust and avoiding disputes about purity or consistency before orders even ship.

    Environmental and Regulatory Considerations

    Manufacturing chemical intermediates today brings a changing set of environmental compliance hurdles. Several years back, we shifted to closed solvent management to reduce emissions and improved waste documentation to match updated regional standards. Each plant inspection and third-party audit sharpened our process reporting; the upshot is lower risk both for us and downstream users in regulated spaces, such as pharma or food-related research.

    We also track developments in chemical hazard classification. 9(10H)-Acridone, while not classed as highly hazardous, earns close monitoring in line with ongoing regulatory updates. Our EHS team maintains routines to anticipate future restrictions and works directly with advocacy groups, lending practical feedback on how regulatory frameworks affect large-scale chemistry. Several times, our firsthand reports motivated clearer substance categorization and safer labeling guidelines among users.

    Customers working on large-scale or export projects often inquire about compliance for national and regional imports. Having seen firsthand how unclear documentation can upset shipping schedules, we prioritize timely certifications and standardized labeling. Most shipments move with full transport declarations and local certificates as needed for faster customs clearance.

    Continuous Improvement and Looking Forward

    Making acridone year after year instills deep knowledge about both the molecule and the people and systems used to make it. Each customer inquiry starts as a technical request, but often opens the door to dialogue about process improvements, alternate grades, or custom synthesis. Over time, these conversations sparked investments in better lab automation, higher capacity reactors, and expanded technical support.

    Watching trends in academic and technical literature, our production chemists stay aware of fresh synthetic pathways. Several partners sponsor collaborations with university teams to pilot-test greener routes or broaden acridone’s substitution patterns. In these experiments, early access to high-purity material often accelerates discovery—sometimes a subtle tweak in one of our upstream steps lets research groups publish faster or scale new active molecules days earlier.

    On the customer side, larger research consortia and contract manufacturers push for greater batch transparency, more customizable documentation, and deeper engagement with process details. Our teams now host quarterly customer workshops and technical briefings, sharing interim findings and feeding back lessons learned from external users. Over years of direct customer discussions, transparent communication and predictable outcomes upstage any theoretical catalog advantage. Repeat orders and long relationships follow not just from product reliability, but from an open-door mentality to manufacturing questions, concerns, and evolving applications.

    As new fields demand smarter materials—organic semiconductors, adaptive sensors, or next-generation dye lasers—real-world insights from the factory floor prove their worth. Chemists still need a stable, reliable, and well-documented supply of 9(10H)-Acridone. Through measured investments in plant reliability and honest reporting of product strengths and limits, we remain committed to supporting both traditional and unexpected users of this venerable molecule.

    Final Thoughts from the Plant Floor

    Working with acridone means blending tradition and continual change. It’s been a mainstay in chemical labs and plants for generations, but each season brings a new application, a new compliance threshold, or a new customer challenge. Feedback loops between operators, chemists, and clients improve the process, refine logistics, and ensure that even long-standing products like 9(10H)-Acridone continue evolving to meet the highest expectations.

    Open lines of communication remain central. Customers trust real-world experience to cut through theoretical or catalog hype. By centering our operations on consistency, practical safety, and transparency, we strive to make 9(10H)-Acridone a dependable choice—whether used in a university test tube or a pilot-scale demonstration plant. This approach, built from decades of firsthand production, allows both science and business to advance hand-in-hand.