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HS Code |
805881 |
| Iupac Name | benzo[c]cinnoline |
| Molecular Formula | C12H8N2 |
| Molar Mass | 180.21 g/mol |
| Cas Number | 86-28-4 |
| Appearance | yellow solid |
| Melting Point | 177-179 °C |
| Solubility In Water | Insoluble |
| Structure Type | Polycyclic aromatic compound |
| Smiles | c1ccc2c(c1)nc3ccccc3n2 |
| Inchi | InChI=1S/C12H8N2/c1-2-4-10-8-13-12-9-6-5-7-11(9)14-12(10)3/h1-8H |
| Pubchem Cid | 70522 |
| Synonyms | 2,3-phenanthroline |
As an accredited Benzo[C]Cinnoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Benzo[C]Cinnoline, 25g: Supplied in a clear, tightly sealed amber glass bottle with hazard labels, chemical name, and lot information. |
| Shipping | Benzo[C]cinnoline is shipped in tightly sealed containers, protected from light and moisture. It is packaged according to safety regulations for hazardous chemicals, with clear labeling and documentation. Handling and transportation follow relevant chemical shipping guidelines to ensure safe delivery, compliance with legal standards, and to prevent contamination or environmental release. |
| Storage | Benzo[C]cinnoline should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Ensure the storage area is free from moisture and sources of ignition. Appropriate personal protective equipment should be worn when handling the chemical to prevent exposure and contamination. |
Applications of Benzo[C]Cinnoline in Industrial ManufacturingBenzo[C]Cinnoline serves as a specialized intermediate supporting distinct downstream manufacturing workflows where its unique heterocyclic structure is advantageous. Our production controls and supply chain allow consistent delivery to high-standard industrial clients integrating this raw material into regulated value-added product platforms. The following application scenarios illustrate established end-use sectors adopting Benzo[C]Cinnoline as a core synthetic node, each governed by sector-specific compliance benchmarks and production protocols. 1. Advanced Organic Semiconductor ManufactureLeading materials science enterprises utilize this compound during the fine chemical synthesis of n-type organic semiconductor layers for thin‐film devices, leveraging its stable heterocyclic motif to enhance electron mobility. Organic transistor and OLED producers rely on the material’s specific conjugation for achieving finely tuned charge transport layers. Integration follows stringent electronics purity specifications, with close control of impurity profiles and batch-to-batch consistency essential for maintaining material performance and device yield. Industry compliance standards
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2. Pharmaceutical Research and Development—Antitumor Agent SynthesisMedicinal chemistry and preclinical R&D laboratories deploy Benzo[C]Cinnoline as a targeted building block when synthesizing novel antineoplastic small molecules, taking advantage of its fused ring system for rapid lead generation in oncological compound libraries. Regulatory expectations for research-grade material supply demand detailed impurity tracking and documentation throughout catalytic coupling, isolation, and purification stages. Each research project may re-optimize input ratios to maximize derivative yields or minimize byproduct formation, guided by iterative SAR studies. Industry compliance standards
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3. High-Performance Dye and Pigment SynthesisIndustrial pigment manufacturers employ Benzo[C]Cinnoline during the development of high-stability azo and heterocyclic dyes, where its rigid framework imparts photostability and resistance to thermal fading. End-use compliance concerns center on colorant migration and toxicological safety for regulated industrial coatings and specialty inks—demands requiring traceability and batch analytics from precursor through final dispersion or encapsulation. Optimization of addition ratio follows target absorbance and application substrate parameters. Industry compliance standards
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4. Specialty Corrosion Inhibitor FormulationCorrosion inhibitor formulators working in high-temperature or acidic process environments integrate Benzo[C]Cinnoline as a nitrogen-based chelating agent, exploiting its electronic properties to form tenacious passivation layers on ferrous or copper alloys. Its addition complements other passivators requiring compatibility with process fluids and minimal side-product drift, critical when targeting compliance with regulated water and petrochemical systems. Industry compliance standards
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5. Electronics Wet Chemical Process AidsProducers of microelectronic wet etching and cleaning formulations employ Benzo[C]Cinnoline to stabilize process baths and modulate redox potential in photolithography and pattern transfer workflows, demanding low residual metal contamination and trace analysis suitability. The compound’s persistently conjugated system enables controlled chelation of unwanted metallic traces, supporting consistent wafer surface quality. Any formulation must withstand continuous monitoring for byproduct generation and persistent purity under process cycling. Industry compliance standards
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Competitive Benzo[C]Cinnoline prices that fit your budget—flexible terms and customized quotes for every order.
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