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2-(2-Hydroxyethyl)Pyridine

    • Product Name 2-(2-Hydroxyethyl)Pyridine
    • Alias 2-(2-Pyridyl)ethanol
    • Einecs 219-276-5
    • 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

    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 & Storage
    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.
    Application of 2-(2-Hydroxyethyl)Pyridine

    Applications of 2-(2-Hydroxyethyl)Pyridine in Industrial Manufacturing

    Our 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 Fluids

    Multiple 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

    • ASTM D4627 (Corrosion Inhibitors in Water-Extendable Metalworking Fluids)
    • REACH Registration for Use in Lubricants and Formulated Fluids
    • OSHA 29 CFR 1910.1200 for workplace safety in chemical mixing
    • ISO 6743–13 (Classification of Lubricants, Industrial Oils, and Related Products)

    Typical usage ratio

    • High-activity fluids: 0.2 – 0.4% w/w, adjusted based on total inhibitor system
    • General-purpose fluids: 0.05 – 0.15% w/w; higher use for harsher environments

    Downstream process integration

    • Formulators add the ingredient during the mixing of aqueous phase inhibitors at ambient temperature prior to emulsion formation or blending into concentrate, followed by QC sampling for corrosion testing.

    Final product types

    • Semi-synthetic cutting fluids
    • Full synthetic metalworking coolants
    • Corrosion-protective storage fluids for machinery and parts

    2. Chelating Agent Component in Electroless Nickel Plating Baths

    In 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

    • ISO 4527 (Electroless Nickel-Phosphorus Coatings – Specifications and Test Methods)
    • RoHS Directive 2011/65/EU (Restriction on use of hazardous substances)
    • EU REACH Regulation EC No 1907/2006 (Substances of Very High Concern reporting)
    • US EPA 40 CFR Part 433 (Metal Finishing Point Source Category)

    Typical usage ratio

    • Standard nickel plating: 0.1 – 0.35 g/L, varying based on bath life cycle and desired deposition uniformity
    • Special alloys (bright finish): 0.2 – 0.4 g/L as required by deposit profile

    Downstream process integration

    • Technicians introduce the additive directly into the prepared bath after temperature stabilization, monitoring metal ion analysis and redox potential to maintain consistent deposit quality during continuous plating.

    Final product types

    • Wear-resistant nickel-plated connectors
    • High-precision printed circuit boards
    • Corrosion-resistant fittings for automotive and aerospace use

    3. Precursor in Synthesis of Pyridine-Based Pharmaceutical Intermediates

    Pharmaceutical 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

    • Current Good Manufacturing Practice (cGMP), as defined by 21 CFR Parts 210 and 211
    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. standards for related substance limits and impurities
    • Drug Master File (DMF) registration as per US FDA requirements

    Typical usage ratio

    • Synthetic routes: input ratio depends on final API molecule; typical batch conversion ranges from 1.1 to 2.2 molar equivalents per targeted pyridyl intermediate

    Downstream process integration

    • Pharmaceutical QC and process chemists charge the material to glass-lined or stainless steel reactors, initiating nucleophilic substitution or functionalization steps under inert atmospheres with in-process HPLC monitoring for selectivity and purity.

    Final product types

    • Pyridine-derivative drug intermediates
    • API precursors for anti-tuberculosis medications
    • Building blocks for cognition-enhancing drugs under clinical development

    4. Catalyst Promoter in Polymerization of Vinyl Compounds

    Producers 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

    • ISO 9001:2015 (Quality Management Systems in polymer manufacturing)
    • EN 71-3 (Safety of Toys: Migration of certain chemical elements, where food contact is relevant)
    • EU Regulation (EC) No 1935/2004 (Materials and articles intended to come into contact with food, as applicable)
    • REACH registration for use in polymer additives and intermediates

    Typical usage ratio

    • Polyvinyl chloride and derivatives: 0.02 – 0.1 mol% relative to total monomer batch size; process control chemists modulate dosage based on initiator type and reaction profile

    Downstream process integration

    • Polymerization engineers introduce the additive at catalyst charging phase, immediately prior to monomer addition, or during pre-polymerization staging. In large-scale continuous reactors, automated feed systems maintain precise dosages linked with polymer analytical feedback.

    Final product types

    • High-performance PVC resins for wire and cable insulation
    • Acrylic polymers for specialty coatings
    • Impact-modified engineering plastics used in automotive and electronics production

    5. Synthetic Intermediate for Agrochemical Active Ingredients

    Major 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

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) technical material standards
    • EU Regulation (EC) No 1107/2009 (concerning the placing of plant protection products on the market)
    • ISO 17025 laboratory accreditation for agrochemical analysis and batch release
    • China ICAMA pesticide registration for local use compliance

    Typical usage ratio

    • Initial pyridine precursor step: 1.1–1.5 equivalents per synthetic sequence
    • Final formulation: typically <0.1% w/w of finished product, post-synthesis residue control

    Downstream process integration

    • Process chemists introduce the compound in first-stage condensation reactions, then isolate targeted heterocycles through distillation, crystallization, or chromatographic purification before formulation into concentrated active or SC/EC dispersions.

    Final product types

    • Systemic fungicide technical concentrates
    • Ready-to-use seed treatment solutions
    • Multi-mode crop protection blends
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