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1-Aminoanthracene

    • Product Name 1-Aminoanthracene
    • Alias 1-amino-anthracene
    • Einecs 204-080-0
    • 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

    427791

    Cas Number 613-89-8
    Molecular Formula C14H11N
    Molecular Weight 193.25 g/mol
    Appearance Yellow to orange crystalline powder
    Melting Point 105-108°C
    Boiling Point 415.7°C at 760 mmHg
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.18 g/cm³
    Synonyms Anthracen-1-amine, 1-Anthrylamine
    Pubchem Cid 12094

    As an accredited 1-Aminoanthracene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1-Aminoanthracene is packaged in a sealed amber glass bottle, labeled clearly, containing 25 grams of pale yellow crystalline solid.
    Shipping 1-Aminoanthracene is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Transport follows regulations for hazardous chemicals, ensuring labeling for toxic and potentially flammable materials. Appropriate documentation, including safety data sheets, accompanies each shipment to ensure safe handling and emergency response during transit.
    Storage 1-Aminoanthracene should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, well-ventilated area. Keep the storage area away from incompatible substances such as strong oxidizers and acids. Ensure appropriate chemical labeling and restrict access to authorized personnel. Store at room temperature, and follow all applicable safety guidelines and storage regulations for hazardous organic chemicals.
    Application of 1-Aminoanthracene

    Applications of 1-Aminoanthracene in Industrial Manufacturing

    1-Aminoanthracene enables specialized downstream processes in modern chemicals. As a direct manufacturer, we support advanced industries by supplying high-purity raw materials that meet precise composition and compliance requirements in regulated applications. Below are key industrial fields using 1-Aminoanthracene, describing unique application details for each.

    1. Fluorescent Dye and Tracer Production

    Major dye manufacturers use 1-Aminoanthracene as an essential aromatic amine intermediate in the synthesis of anthracene-based fluorescent dyes and markers. The amino group enables regioselective coupling during dye molecule construction, facilitating high photostability and quantum yield demanded in biomedical tracers, analytical reagents, and security inks. Producers must control substitution patterns strictly to meet end-use fluorescence thresholds and spectral properties.

    Industry compliance standards

    • REACH (EC No 1907/2006) registration for imported aromatic amines.
    • ISO 9001:2015 for quality management in dye and pigment production.
    • OSHA 1910.1200 for chemical hazard communication in handling and downstream preparation.
    • DIN EN 71-7 for safety of toys (tracer applications for children's toys and marking).

    Typical usage ratio

    • Generally 5–25% by weight of total dye intermediate charge, depending on desired emission wavelength. Adjust usage to fine-tune color intensity and stability in multistep syntheses.

    Downstream process integration

    • Incorporated in the initial diazotization or condensation stage for chromophore core formation.
    • Introduced prior to final sulfonation/acylation to install functional groups for water solubility or substrate affinity.
    • Purification via column chromatography to remove isomers and residual starting materials.
    • Quality control via HPLC and spectrofluorometry before formulating tracer concentrates.

    Final product types

    • Biomedical fluorescent tracers and immunofluorescent reagents.
    • Security marker inks for document protection.
    • Analytical stains for forensic applications.
    • Fluorescent pigments for plastic and textile manufacturing.

    2. Pharmaceutical Intermediate Synthesis

    API manufacturers employ 1-Aminoanthracene as a targeted intermediate when constructing polycyclic aromatic frameworks for drug candidates, anti-tumor agents, and photosensitizing compounds. The unique nitrogen position allows for controlled derivatization, enabling synthesis pathways that require minimal purification steps and high batch-to-batch reproducibility. Production lots must achieve consistent purity and trace impurity profiles suitable for regulated environments.

    Industry compliance standards

    • Good Manufacturing Practice (GMP) guidelines per ICH Q7 for API intermediates.
    • USP and Ph. Eur. reference monographs for intermediates in registered routes.
    • 21 CFR Part 211 (FDA) compliance for records and process validation when used in U.S. supply chains.
    • EMA quality requirements for starting materials (Directive 2001/83/EC).

    Typical usage ratio

    • Ranges from 12–35% molar equivalent in stepwise synthesis; calculated based on stoichiometry of coupling or cyclization reaction. Ratio varies with end molecule pattern and yield optimization strategy.

    Downstream process integration

    • Introduced during cycloaddition or Buchwald–Hartwig amination stages for ring system extension.
    • Stage-wise isolation and compound tracing using NMR and LC/MS for batch traceability.
    • Inline removal of byproduct amines and unreacted starting material.
    • Transferred to API finishing or converted to advanced building blocks for late-stage functionalization.

    Final product types

    • Precursor for experimental anti-cancer and anti-viral APIs.
    • Model compound for phototherapy drug research.
    • Photosensitizers for medical imaging agents.
    • Probes and reference standards for regulatory method validation.

    3. Organic Semiconductor Material Fabrication

    Manufacturers specializing in organic electronics use 1-Aminoanthracene to create extended π-conjugated systems for light-emitting diodes (OLEDs), thin-film transistors, and photoconductors. The amine functionality enables efficient coupling onto electrode surfaces and controls charge transport properties. Rigid quality systems ensure that the starting material does not introduce electronic traps or reduce device stability in multilayer assemblies.

    Industry compliance standards

    • IEC 62321 for hazardous substance restrictions in electronic materials.
    • RoHS 2011/65/EU compliance for restricted substances in final electronic components.
    • ISO 14001:2015 for environmental control during functional material manufacturing.
    • Internal QC protocols for electronic grade purity.

    Typical usage ratio

    • 3–8% of total monomer charge when making emitting or charge-transport layers; dosage defined by photophysical property targets and film uniformity requirements.

    Downstream process integration

    • Undergoes Suzuki coupling or C–N bond formation during conjugated polymer synthesis.
    • Purified via sublimation or recrystallization to minimize dopant levels and metal impurities.
    • Solution-cast or vapor-deposited during device manufacturing for high-purity layer formation.
    • Real-time spectroscopic monitoring to ensure consistency with device fabrication protocols.

    Final product types

    • OLED emitter layers for display and lighting.
    • Organic photoconductors for imaging systems.
    • Thin-film field-effect transistors (OFETs).
    • Photovoltaic active layers for solar cell applications.

    4. Analytical Reagent and Chromatography Marker Preparation

    Laboratory reagent producers and instrument calibration suppliers use 1-Aminoanthracene as a molecular marker and derivatization agent in chromatographic analysis, fluorescence detection systems, and trace chemical identification. Its specific emission profile enables sensitive detection in complex matrices, supporting standardization and traceability in routine and advanced QA/QC assays for various industries.

    Industry compliance standards

    • ISO/IEC 17025 for testing and calibration laboratory accreditation.
    • USP <1225> for analytical method validation, traceability, and system suitability.
    • EPA TSCA Inventory Status (for analytical chemical supply in the U.S.).
    • GLP (OECD series 1) for use in regulatory laboratory environments.

    Typical usage ratio

    • Used at 0.01–0.1 mg/mL concentration for marker or derivatizing agent depending on detection threshold required by the analytical protocol.

    Downstream process integration

    • Dissolved in certified organic solvents for creation of calibration standards.
    • Added post-column as a derivatization marker for HPLC or capillary electrophoresis.
    • Quality-checked using reference spectra for emission comparison.
    • Bottled and labeled under ISO-compliant reagent labelling systems for traceability.

    Final product types

    • HPLC or GC calibration markers for analytical instrument manufacturers.
    • Fluorescence reference standards for laboratory QA programs.
    • Derivatization agents for trace organics detection.
    • Certified reference materials for regulatory agencies and contract labs.

    5. Specialty Chemical Synthesis for Sensor and Detector Systems

    Sensor manufacturers and advanced detector system producers select 1-Aminoanthracene as an integral precursor for producing aromatic amine derivatives with strong and selective sensor signal transduction properties. Its high-purity grade supports the fabrication of reproducible chemical sensor films for detection of volatile organic compounds, environmental toxins, and security threats. Blending and functionalization protocols require precise control over impurity content to avoid false signal generation.

    Industry compliance standards

    • ISO 13485:2016 for manufacturing of chemical components used in medical or bio-sensors.
    • RoHS and REACH compliance when integrated in sensor modules for consumer or industrial products.
    • EN 45545-2 for hazardous material use in railway and infrastructure sensor systems.
    • Customer-specific COA and batch traceability requirements.

    Typical usage ratio

    • Applied at 2–10% loading in sensor film or resin composites depending on detector sensitivity and selectivity range.

    Downstream process integration

    • Integrated during solution mixing or polymerization to functionalize sensor substrate surface.
    • Pre-treated for residual moisture and organic acid removal via vacuum drying.
    • Sensor batch formulation monitored for signal drift and chemical background interference using standardized QC protocols.
    • Packaged in controlled environment to maintain shelf life and operational reliability.

    Final product types

    • Vapor and gas detector films for industrial safety systems.
    • Surface-enhanced fluorescence sensors for homeland security.
    • Integrated environmental monitoring chips.
    • Selective room air quality probes in HVAC systems.
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