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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 | 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. |
Applications of 1-Aminoanthracene in Industrial Manufacturing1-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 ProductionMajor 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
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2. Pharmaceutical Intermediate SynthesisAPI 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
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3. Organic Semiconductor Material FabricationManufacturers 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
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4. Analytical Reagent and Chromatography Marker PreparationLaboratory 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
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5. Specialty Chemical Synthesis for Sensor and Detector SystemsSensor 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
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Email: admin@sinochem-nanjing.com
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