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HS Code |
352881 |
| Product Name | 5-Bromo-3-Pyridinecarboxaldehyde |
| Cas Number | 21901-55-1 |
| Molecular Formula | C6H4BrNO |
| Molecular Weight | 186.01 g/mol |
| Appearance | Light yellow to brown solid |
| Melting Point | 67-69 °C |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents such as DMSO, ethanol |
| Smiles | C1=CC(=CN=C1C=O)Br |
| Inchi | InChI=1S/C6H4BrNO/c7-6-2-1-5(4-9)8-3-6/h1-4H |
| Storage Temperature | Store at 2-8°C |
As an accredited 5-Bromo-3-Pyridinecarboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 5-Bromo-3-Pyridinecarboxaldehyde is packaged in a 25g amber glass bottle with a secure, tamper-evident screw cap. |
| Shipping | 5-Bromo-3-pyridinecarboxaldehyde is shipped in sealed, chemical-resistant containers to prevent moisture and contamination. Packages comply with relevant regulations for hazardous substances and are clearly labeled. During transport, temperature and handling are controlled to ensure product stability and safety. Material Safety Data Sheets (MSDS) accompany shipments for proper handling and response. |
| Storage | 5-Bromo-3-pyridinecarboxaldehyde should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Keep it at room temperature or as specified on the supplier label. Avoid moisture and sources of ignition. Use secondary containment to prevent accidental release or contamination. |
Applications of 5-Bromo-3-Pyridinecarboxaldehyde in Industrial ManufacturingWe focus on real downstream integrations of 5-Bromo-3-Pyridinecarboxaldehyde, enabling reliable and consistent supply chains for key sectors. The following application scenarios demonstrate its use in synthesis-based industries where targeted intermediates and advanced building blocks are essential to finished product performance and regulatory conformity. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisPharmaceutical manufacturers source 5-Bromo-3-Pyridinecarboxaldehyde for its pyridine-based heterocycle, directly utilizing it as a core intermediate in multi-step API synthesis. The aldehyde group allows for precise condensation or reductive amination steps, supporting various small-molecule drug projects, including kinase inhibitors and neuroactive agents. Users select this material due to reaction specificity, high chemical stability, and traceability, aligning with batch-to-batch control requirements for regulated substances. Industry compliance standards
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2. Agrochemical Intermediate for Herbicide SynthesisAgrochemical formulators turn to 5-Bromo-3-Pyridinecarboxaldehyde for constructing pyridine-based heterocycles central to active herbicidal ingredients. Its controlled reactivity under standard condensation and halogen-metal exchange routes enables the generation of lead candidates for broad-spectrum weed management. Continuous plant operation standards demand robust quality traceability and lot certification throughout all synthesis and downstream derivatization stages. Industry compliance standards
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3. Fine Chemical Synthesis of Specialty DyesManufacturers in the dyes sector employ 5-Bromo-3-Pyridinecarboxaldehyde for the synthesis of tailored pyridine-based chromophores. The electrophilic site facilitates regioselective condensation reactions with amines and hydrazines, forming highly specific dye precursors with precisely tuned absorption spectra for electronic and display applications. The focus on product purity and spectral quality drives adherence to advanced QC protocols. Industry compliance standards
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4. Electronic Chemicals for OLED and Display Material IntermediatesProducers of advanced electronic and optoelectronic materials leverage 5-Bromo-3-Pyridinecarboxaldehyde as a key functionalized aromatic building block in the development of organic light-emitting diode (OLED) intermediates and electron-transport materials. The well-defined bromoaldehyde functionality permits precision coupling and cross-coupling reactions essential for synthesizing electron-rich and electron-deficient subunits in complex molecular architectures. Each step demands highest purity and minimal metal content to avoid electrical property interference in final applications. Industry compliance standards
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