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HS Code |
818586 |
| Cas Number | 103-74-2 |
| Molecular Formula | C7H9NO |
| Molecular Weight | 123.15 g/mol |
| Iupac Name | 2-(2-hydroxyethyl)pyridine |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 229-231°C |
| Melting Point | -10°C |
| Density | 1.083 g/cm³ at 25°C |
| Solubility In Water | Miscible |
| Refractive Index | 1.523 |
| Flash Point | 108°C |
| Synonyms | 2-(2-Pyridyl)ethanol |
| Odor | Characteristic, pyridine-like |
| Pka | 5.52 (for pyridine nitrogen) |
| Storage Temperature | Store at room temperature |
As an accredited 2-(2-Hydroxyethyl)Pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 mL of 2-(2-Hydroxyethyl)Pyridine, tightly sealed with a screw cap and tamper-evident label. |
| Shipping | 2-(2-Hydroxyethyl)pyridine is typically shipped in tightly sealed containers made of glass or HDPE to prevent leaks and contamination. It should be transported according to standard chemical safety regulations, ideally with cushioning materials, clearly labeled packaging, and proper documentation. Avoid exposure to heat, moisture, and incompatible substances during transit. |
| Storage | Store 2-(2-Hydroxyethyl)pyridine in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as oxidizers and strong acids. Keep away from moisture and ignition sources. Clearly label the storage container, and ensure access is limited to trained personnel. Use secondary containment to prevent accidental leaks or spills. |
Applications of 2-(2-Hydroxyethyl)Pyridine in Industrial ManufacturingOur direct production of 2-(2-Hydroxyethyl)Pyridine supports a range of highly specialized industrial sectors. As a functional pyridine derivative, it proves essential as a performance additive, intermediate, and catalyst component in precisely controlled chemical processes. Below we detail verified application scenarios, each with relevant regulatory considerations, industry-accepted formulation guidance, integration into customer production workflows, and final output forms. 1. Intermediate for Anti-Corrosion Additives in Metalworking FluidsMultiple producers of heavy-duty metalworking fluids use this compound as a key intermediate in high-performance anti-corrosion packages. Its polar functional groups provide complexation with ferrous and non-ferrous ions, interrupting electrochemical corrosion pathways in water-based and semi-synthetic fluid systems. Selection and calibration of this pyridine derivative depend on base oil formulation, expected pH, and metal alloy exposure during operation. Industry compliance standards
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2. Chelating Agent Component in Electroless Nickel Plating BathsIn electroless nickel plating, maintaining stable metal ion concentration and preventing uncontrolled precipitation require selective chelating agents. This pyridine-based compound is incorporated in high-end plating bath formulations to control nickel(II) ion activity, modifying deposit texture and phosphorus level. Chemical engineers select the additive concentration based on desired plating rate, bath turnover, and substrate material properties. Industry compliance standards
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3. Precursor in Synthesis of Pyridine-Based Pharmaceutical IntermediatesPharmaceutical API manufacturers utilize this molecule as a structural building block in synthesizing active intermediates, especially in anti-infective and central nervous system drug candidates. Medicinal chemistry routes rely on its bidentate coordination capacity and substitutable hydroxyl group for subsequent function group formation, enabled by strong nucleophilicity and controlled substitution reactions. Industry compliance standards
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4. Catalyst Promoter in Polymerization of Vinyl CompoundsProducers of specialized functional polymers employ this pyridine alcohol as a catalyst promoter and ligand for metal-based initiators, especially within vinyl chloride and acrylate polymerizations. Its chelating nature modifies the electron density around transition metal catalysts, boosting initiation rates, modulating molecular weight distribution, and influencing chain termination dynamics. Levels depend on monomer-to-initiator ratio and target polymer grade. Industry compliance standards
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5. Synthetic Intermediate for Agrochemical Active IngredientsMajor agrochemical formulators source this molecule for the synthesis of heterocyclic building blocks in systemic fungicides and seed treatment agents. Its hydroxyethyl side chain allows for selective substitution, supporting multi-step synthesis of bioactive molecules effective against a range of fungal pathogens. Agricultural chemists base usage on desired crop spectrum and formulation stability requirements. Industry compliance standards
Typical usage ratio
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