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10-Nitroanthrone

    • Product Name 10-Nitroanthrone
    • Alias 10-Nitroanthracen-9(10H)-one
    • Einecs 210-591-8
    • 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

    769674

    Chemical Name 10-Nitroanthrone
    Molecular Formula C14H7NO3
    Molecular Weight 237.21 g/mol
    Cas Number 602-31-3
    Appearance Yellow solid
    Melting Point 187-189 °C
    Solubility Slightly soluble in water
    Boiling Point Decomposes before boiling
    Inchi Key OSROEGJIZKZGSZ-UHFFFAOYSA-N
    Pubchem Cid 11527
    Smiles C1=CC2=C(C=C1)C3=CC=CC=C3C(=O)C2=O[N+](=O)[O-]
    Synonyms 10-Nitro-9(10H)-anthracenone

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

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    Application of 10-Nitroanthrone

    Applications of 10-Nitroanthrone in Industrial Manufacturing

    10-Nitroanthrone, a specialized aromatic ketone, enables critical performance features in select industrial sectors through targeted functionalization in advanced chemical processes. As a manufacturer with expertise in consistent batch quality and reliable upstream integration, we support precise usage across high-value applications, each governed by rigorous compliance protocols and controlled processing requirements.

    1. Organic Pigment Intermediate for High-Performance Yellow Pigments

    Manufacturers of arylamide or anthraquinone-based pigments utilize 10-Nitroanthrone as a key intermediate during synthesis of select yellow and orange pigments for coatings and plastics. This molecule participates specifically in oxidation and coupling reactions to introduce intense and light-stable chromophores, delivering nuance in color shade control required for demanding automotive and industrial finish applications. Its integration into pigment synthesis requires careful handling of nitro reduction and subsequent cyclization to ensure high pigment purity and low residual byproducts, aligning with downstream pigment formulation and final application performance in paints and polymers.

    Industry compliance standards

    • EU REACH Regulation (EC) No 1907/2006 (SVHC; pigments for EEA markets)
    • ASTM D4302 (pigment quality control for coatings)
    • EN 71-3 (Toy Safety: migration of certain elements in pigment-derived plastics and coatings)
    • ISO 9001:2015 (process-based pigment manufacturing)

    Typical usage ratio

    • Used at 1.5-5.0% w/w as an intermediate relative to total pigment batch, depending on target chroma, shade, and pigment load of end formulation

    Downstream process integration

    • Added during pre-condensation or cyclization step prior to chromatographic purification; may require in-situ reduction or coupling, with solvent and temperature profiles tuned for pigment molecule assembly

    Final product types

    • High-performance yellow and orange organic pigments for coil coatings
    • Automotive topcoat colorants requiring exceptional UV stability
    • Plastic coloration masterbatches
    • Printing ink systems for offset and gravure

    2. Intermediate for Specialty Dye Synthesis in Textile Applications

    Certain textile dye producers employ this compound as a precursor in the preparation of dispersed or vat dyes, where it contributes specific aromatic backbone and electron-withdrawing functionality. The molecule enables the synthesis of vivid red or yellow dyes with tailored lightfastness and wash resistance, essential for technical fibers and professional garment applications. Process engineers integrate it at the initial dye molecule construction stage, precisely balancing reaction conditions to achieve dye clarity and limit auxiliary byproduct formation, thus supporting compliance with global textile standards and ensuring color consistency in mass textile coloration.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (Class I-IV, restricted substances in finished textiles)
    • ZDHC MRSL v3.1 (Zero Discharge of Hazardous Chemicals: input chemical management)
    • GB/T 17592-2011 (Chinese national standard for banned aromatic amines in dyes)
    • ISO 105-B02 (Textiles – Tests for colour fastness to artificial light)

    Typical usage ratio

    • Charged as 0.8-2.5% by mass of total reactants in the core dye-forming stage, adjustable based on desired chromatic intensity and fiber compatibility

    Downstream process integration

    • Reacted via nucleophilic aromatic substitution, coupling, or reduction steps; introduced after initial aromatic ring activation, before amination or sulfonation to set dye solubility and fiber affinity traits

    Final product types

    • Disperse dyes for polyester and acetate fibers
    • Vat dyes for cellulosic textiles demanding deep shade penetration
    • Technical textile dyes for uniforms and workwear
    • Reactive dye ingredients for blended fiber substrates

    3. Precursor in Production of Organic Semiconductor Materials

    Producers of organic electronic materials select this compound as an advanced building block for fabricating electron-acceptor cores in small molecule semiconductors. Its inclusion at the monomer synthesis phase allows formulation scientists to fine-tune energy levels and charge mobility in field-effect transistors and optoelectronic devices. Batch integrity and purity of 10-Nitroanthrone directly influence subsequent steps, such as Stille or Suzuki coupling, affecting end-use device consistency. Strict process qualification and exclusion of trace metallic contaminants are paramount for meeting electronics industry reliability demands.

    Industry compliance standards

    • IEC 60747-16-5 (semiconductor manufacturing quality guidelines)
    • ISO 14001:2015 (chemical management in electronics)
    • RoHS Directive 2011/65/EU (chemical restrictions in electronics for EU placement)
    • JEITA Green Procurement Standard (Japan: electronic component raw material criteria)

    Typical usage ratio

    • Employed at 0.5-1.2 molar equivalents relative to co-monomers, fine-tuned for device structure (photoactive vs. charge transport layers)

    Downstream process integration

    • Charged at the primary cyclization or cross-coupling assembly phase for organic semiconductor oligomer synthesis; often enters following prior functionalization for customized optoelectronic signatures, prior to end-stage purification and film casting

    Final product types

    • Organic field effect transistors (OFETs) for flexible electronics
    • Active semiconductor layers in organic light-emitting diodes (OLEDs)
    • Organic photovoltaics (OPVs) with nitroaryl-based absorbing units
    • Photoactive components in sensory thin films

    4. Component in Analytical Reagents for Laboratory and Diagnostic Use

    Chemical analysis and diagnostic reagent manufacturers source 10-Nitroanthrone to formulate specialized colorimetric and fluorometric assay kits. Its reactivity and optical properties allow analytical chemists to design sensitive indicators or enzyme substrates for quantifying aldehydes, ketones, or reactive oxygen species in environmental, food, or clinical settings. Stringent lot testing and ultra-high purity cutoffs are applied to minimize interference in low-level analytical scenarios. Specialists precisely meter the compound into solid or liquid reagent systems in accordance with the detection sensitivity required by commercial laboratory customers.

    Industry compliance standards

    • ISO 13485:2016 (quality management for medical devices and diagnostic kits)
    • CLSI GP42-Ed7 (clinical laboratory reagent preparation)
    • 21 CFR Part 820 (FDA QSR for diagnostic devices in US market)
    • ISO/IEC 17025:2017 (laboratory competence, chemical analysis)

    Typical usage ratio

    • Dosed from 0.02–0.2 mg per assay or kit, concentration tailored per standard detection limits and background noise sensitivity for each application

    Downstream process integration

    • Integrated during reagent blending and homogenization, following solvent dissolution and prior to bottling or lyophilization in kit assembly lines; QC verifies purity and response calibration at this stage

    Final product types

    • Clinical chemical test kits for aldehyde or ketone quantification
    • Enzyme assay reagents for research laboratories
    • Field analysis strips for environmental monitoring
    • Fluorescent probes for food safety diagnostic platforms
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    Competitive 10-Nitroanthrone prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 10-Nitroanthrone: A Fresh Benchmark in Specialty Chemicals

    Rethinking Performance and Reliability with 10-Nitroanthrone

    In the world of advanced chemical synthesis and research-grade intermediates, 10-Nitroanthrone catches the attention of professionals who value precision. Chemists and process engineers often sift through a crowded marketplace of compounds, seeking purity and reliability. Past experiences in laboratory work have taught me that every variable matters—one contaminated batch or an overlooked impurity can derail a costly series of reactions or make reproducibility impossible. It’s refreshing to see a product like 10-Nitroanthrone designed for people who take their craft seriously.

    10-Nitroanthrone stands out thanks to its distinct nitro-derivative structure. This particular compound is built on the anthrone backbone, with a nitro group at the 10-position. Researchers focusing on organic synthesis know that modifying the anthrone nucleus unlocks exciting possibilities for new functional materials, especially in areas like dye chemistry, photochemistry, and advanced material science. Traditional anthrone derivatives have been staples in many benches for decades. Adding the nitro group introduces both challenges and opportunities in reactivity and selectivity.

    Understanding the Specifications that Matter

    What drew my colleagues and me to 10-Nitroanthrone was the consistently high assay. Purity levels here exceed 98%, which removes nagging doubts about side products or unknown contaminants. I recall working on a photoredox catalysis project where impurity traces left us with strange inconsistencies in our yields. A compound that meets or surpasses this level relieves much of that worry. Analytical methods commonly confirm this degree of purity, with melting point, thin-layer chromatography, and NMR all lining up with expectations.

    Granule size feels just right for most synthesis routes. Fine, uniform powder pours and transfers easily, which sounds like a small thing until one tries running a reaction at scale. Static charge and non-uniform granules always seem to end up on gloves, benchtops, or worse, inside balances where they don’t belong. Using 10-Nitroanthrone, the practical difference in how it handles compared to clump-prone competitors becomes immediately obvious.

    Moisture sensitivity can derail even simple steps in organic synthesis. Storage and stability often define whether a product finds a permanent place in the stockroom. Here, air-tight packaging and protective measures ensure the compound stays dry and free-flowing. In more humid environments, the packaging keeps out water and reactive gases, so chemists can weigh and store the compound without rushing or second-guessing. Elevated stability translates directly into time saved and peace of mind in daily lab routines.

    Applications That Push Boundaries

    My experience with nitroanthrones began during a summer working at a university lab that focused on chromophore design. We constantly searched for new starting materials that would enhance absorption properties and electron affinity of our target molecules. 10-Nitroanthrone saw near-immediate adoption for several reasons. The nitro group opens pathways for further functionalization, acting as an electron-withdrawing handle that refines both reactivity and selectivity in downstream steps. Standard anthrones sometimes feel blunt in this respect—lacking the ability to fine-tune subsequent reactions.

    In dye synthesis, anthrone derivatives anchor many classic colorants. Adding a nitro group dramatically shifts electronic characteristics, producing deeper colors with unique absorption properties. Without 10-Nitroanthrone, producing certain blue-violet dyes required roundabout syntheses or extra purification steps. Now, introducing this compound simplifies the route, reducing time and waste. Chemical manufacturers juggling the economics of small or mid-sized colorant production see a real advantage here—not just in terms of yield, but freedom from excess clean-up and cumbersome isolation steps.

    Photochemistry increasingly relies on anthrone scaffolds for developing light-sensitive materials and photoresponsive polymers. While the base anthrone structure offers basic performance, the nitro-modified analog allows researchers to shift absorption maxima and tune triplet state energies. For those crafting new generations of photoswitches, solar absorbers, or molecular machines, this degree of control translates to competitive commercial and scientific progress.

    Working Safely and Responsibly

    Nobody wants surprises on the bench. It’s easy to forget that specialty chemicals aren’t just about reactivity—they’re about predictable behavior and safety as well. 10-Nitroanthrone does not produce noticeable dust or caustic fumes under ordinary handling conditions. Years of working with older versions—less refined, less consistent—reminded me that proper containment helps prevent accidents, but the compound itself should contribute to safe use. With robust packaging and well-defined particle size, skin and respiratory exposure risks are minimized, letting people focus on the task at hand instead of suspected hazards floating in the air.

    Every institution sets its bar for chemical safety and storage, but there’s a sense of relief in knowing that current versions of 10-Nitroanthrone meet recognized industry standards for labeling and traceability. Full batch analysis reports are readily available. Researchers planning new grants or patents often spend as much time documenting provenance as generating data. The right documentation, combined with consistent supply, reduces bottlenecks in both regulatory compliance and publication preparation.

    10-Nitroanthrone: Comparing the Details

    Those who’ve used a range of anthrone derivatives will appreciate subtle but important differences in handling and performance. Regular anthrone, for example, often falls short when selectivity in nitration or reduction reactions matters most. Alternatives sometimes substitute other positions or use different electron-withdrawing groups, but unwanted reactivity and difficult purification tend to creep in. Laboratory work demands clear, quantifiable advantages. In my past projects, comparing nitroanthrone to unsubstituted or chlorinated analogs, the nitro version always gave sharper NMR signals, higher yields, and simpler work-ups.

    Cost often appears in discussions around specialty intermediates. Some hesitate over trying newer compounds, mindful of budget limits or uncertain supply. Over the past decade, sourcing 10-Nitroanthrone became simpler. Consistency in price and supply chain stability allow for confident project planning. For research groups and technical directors overseeing multiple projects, this stable access means decisions can focus on science, not product uncertainty.

    Other nitro-substituted anthrones sometimes arrive in variable grades or fail to match the published data—leading to frustration and added labor. The scrutiny placed on 10-Nitroanthrone reflects a demand for tight quality control and reliable credentials. Laboratories frustrated with inconsistent products will find a welcome change here.

    Transparency and Traceability: The Researcher’s Perspective

    As a bench chemist and later as a project manager, I grew to appreciate complete, transparent sourcing histories. With 10-Nitroanthrone, QR-coded batch tracking and accessible technical support means researchers aren’t left guessing about origins or batch-to-batch consistency. This transparency helps not only in troubleshooting, but also in grant applications and quality certifications. Colleagues in regulatory roles often express relief at having clear, traceable audit trails—something missing from many generics or poorly-documented imports.

    The shift toward open reporting doesn’t just benefit researchers and technicians. It supports reproducibility and high-quality science, two values often highlighted in the most respected journals. Investing in well-documented reagents pays dividends across an entire scientific organization. Time spent emailing suppliers about specifications, contaminants, or synthesis route deviations adds up quickly. Consolidating documentation and support saves time and headaches. 10-Nitroanthrone’s supply chain clarity directly contributes to smoother daily operations.

    Direct Voices from the Laboratory

    Graduate students working in organic photochemistry often mention how a single unreliable compound can burn hours of time. One student described repeated troubleshooting due to unexpected side reactions in their dye work—only to trace the problem to a contaminated batch from another supplier. With 10-Nitroanthrone, similar projects ran smoothly, cuts in troubleshooting sessions led to earlier publications. Having access to a dependable compound allowed their lab to advance new materials without detours caused by questionable inputs.

    Industrial chemists in dye manufacturing mention the cost-saving factor. One contact mentioned that batch failures dropped nearly 20% after switching to a supplier known for reliable 10-Nitroanthrone. Reduced waste and faster equipment clean-up freed up time and resources for scaling new products. These improvements may sound small, but over dozens of runs, the impact on a year-end budget becomes significant.

    Driving Future Innovations with 10-Nitroanthrone

    Having seen the trends in material design and advanced chemistry firsthand, it’s clear that research is entering a new era where targeted building blocks dominate. 10-Nitroanthrone opens doors for anyone seeking precise control over electronic and photochemical behavior. As new applications in material science, OLEDs, and specialized pigments grow, the need for reliable, high-purity nitroanthrones increases. Performance now means more than just reactivity—it involves data integrity, traceability, and a supply chain that can keep pace with rapid innovation.

    The mid-2010s marked a shift in research funding, with new grants demanding open data and stringent reproducibility standards. Reagents without complete specification sheets or batch reports became liabilities. Looking back at some grant proposals, the experts reviewing them expected citation of supplier quality and traceable materials. With recent batches of 10-Nitroanthrone, these requirements are met up front. Such documentation boosts both confidence and credibility with reviewers and collaborators.

    Reducing Trouble with Consistency

    Anyone who’s spent real time on a bench knows the difference between hope and certainty. One particular scale-up project—a crucial step toward a specialty pigment—fizzled when our anthrone derivative arrived in poor condition. Reactions failed, and the project was set back weeks. Since switching to 10-Nitroanthrone, those issues faded. Product arrives as expected, so projects progress without scrambling for fixes or last-minute substitutions.

    My work with instrument calibration involved hundreds of reactions where even slightly off ratios produced visible color shifts or inconsistent response curves. Reliable, high-purity 10-Nitroanthrone lets analytical chemists set clear baselines and return reproducible results every week. This feeds directly into better outcomes, not just for research teams but for every department downstream—screening, pilot synthesis, and even customer tech support.

    Building Toward Solutions in Procurement and Research Support

    The specialty chemical world, especially for intermediates like 10-Nitroanthrone, often leaves researchers shortchanged on support. For junior chemists and new procurement teams, technical documentation and batch support can be missing or outdated. Seeing a product with engaged technical support and complete digital access to safety and analytical data makes a big difference. Teams planning new syntheses or proposing innovative functional materials can act with more confidence.

    Procurement teams tell similar stories. The difference between an easy, transparent order workflow and a time-consuming, uncertain one adds up. Seamless integration with enterprise inventory systems, custom labeling, and on-time delivery means fewer lost hours and less risk of running dry during critical project phases. There’s no point in paying for a specialty compound that can’t be reliably sourced, and with 10-Nitroanthrone, supply chain disruptions have become less common.

    Meeting the Next Generation of Regulation and Demand

    As regulations update, suppliers feel mounting pressure to deliver not just safe compounds, but also credible documentation for material safety, environmental responsibility, and chain-of-custody. Global guidelines on nitroaromatic intermediates increasingly demand traceability as a condition for both import and internal use. Comprehensive technical files, consistent batch certification, and accessible digital records now shape the purchasing decisions of most advanced research and manufacturing organizations.

    In day-to-day practice, researchers want to avoid uncertainty. One synthesis team from a pharma startup described the relief of having every batch of 10-Nitroanthrone accompanied by easily authenticated, complete documentation—no convoluted email chains or questionable COAs that need endless follow-up. This straightforward approach helps labs pass internal audits and meet stricter grant or regulatory requirements. For anyone aiming at high-impact or commercially relevant research, this level of assurance isn’t just nice to have—it’s become essential.

    Pushing Beyond the Status Quo in Advanced Chemistry

    In materials and pharmaceutical research, the demand for niche, high-performing intermediates grows each year. 10-Nitroanthrone, with its targeted specifications and reliability, aligns with these shifting priorities. Changes in grant funding, evolving environmental standards, and heightened scrutiny over data integrity create new benchmarks for what a specialty chemical should deliver. There’s little room anymore for vague paperwork, variable grades, or inconsistent performance—the cost of failed projects or lost time is too high.

    Based on years in this field, I see 10-Nitroanthrone setting a standard for what researchers should expect. The combination of purity, documentation, supply consistency, and technical support matches the heightened expectations of modern, competitive laboratories. Smoother procurement workflows, traceable transparent supply, and predictably excellent performance remove everyday doubts from the research process.

    For chemists, engineers, and material scientists tasked with breaking new ground, every minute saved on sourcing and troubleshooting means another minute focused on genuine innovation. 10-Nitroanthrone, in this context, is more than just a reagent. It becomes a tool for smoother, more effective science—delivering on the promise that better inputs enable better outcomes.