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2,6-Pyridinedimethanol

    • Product Name 2,6-Pyridinedimethanol
    • Alias 2,6-Pyridinedimethanol
    • Einecs 226-046-5
    • 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

    353385

    Cas Number 1194-47-4
    Molecular Formula C7H9NO2
    Molecular Weight 139.15 g/mol
    Appearance White to off-white crystalline solid
    Melting Point 125-129°C
    Boiling Point 344°C at 760 mmHg
    Density 1.219 g/cm³
    Solubility In Water Slightly soluble
    Synonyms 2,6-Bis(hydroxymethyl)pyridine
    Purity >98% (commonly available)
    Smiles C1=CC(=NC(=C1)CO)CO
    Inchi InChI=1S/C7H9NO2/c9-4-6-2-1-3-7(5-10)8-6/h1-3,9-10H,4-5H2

    As an accredited 2,6-Pyridinedimethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2,6-Pyridinedimethanol is packaged in a 100-gram amber glass bottle with a secure screw cap for light-sensitive chemicals.
    Shipping 2,6-Pyridinedimethanol is typically shipped in tightly sealed containers, protected from moisture and light. It should be packed according to chemical safety regulations, labeled appropriately, and transported in compliance with local and international guidelines. Ensure temperature control as needed and handle with care to prevent leaks or spills during transit.
    Storage 2,6-Pyridinedimethanol should be stored in a tightly sealed container in a cool, dry, well-ventilated area, away from incompatible substances such as oxidizing agents. Keep the chemical away from sources of ignition and direct sunlight. Store at room temperature and ensure containers are clearly labeled to prevent accidental misuse. Avoid moisture exposure, and always follow local regulations for chemical storage and safety.
    Application of 2,6-Pyridinedimethanol

    Applications of 2,6-Pyridinedimethanol in Industrial Manufacturing

    2,6-Pyridinedimethanol finds precise and vital uses across specific industrial manufacturing channels, contributing unique chemical attributes as a diol monomer or intermediate. Our vertically integrated supply and technical teams support global customers in achieving compliance and performance benchmarks in every downstream sector described below.

    1. Polyester Resin Production for Electronic Encapsulation

    Advanced polyester resins in the electronics industry rely on 2,6-pyridinedimethanol as a specialty diol to enhance dielectric properties and dimensional stability. Its regular inclusion during resin synthesis modifies polymer chain flexibility, thermal resistance, and cross-link density, delivering products that maintain encapsulation integrity in demanding circuit and sensor environments. Electronics formulators regulate input strictly according to insulation, creep resistance, and operational temperature requirements mandated in safety standards for embedded electrical assemblies.

    Industry compliance standards

    • IEC 61249-2-7 for base materials used in electrical and electronic insulation
    • UL 94 for flammability of plastic materials
    • RoHS Directive (2011/65/EU) for hazardous substances in electronics
    • ISO 9001-certified manufacturing processes

    Typical usage ratio

    • Pyridinedimethanol: 3–12 wt% of total diol content depending on target glass transition temperature and viscosity profile

    Downstream process integration

    • Directly charged with other diols (e.g., ethylene glycol, neopentyl glycol) and dicarboxylic acids in melt polycondensation reactors prior to catalyst addition

    Final product types

    • Potting compounds for sensors, relay modules, microchips
    • Electronic adhesive insulators
    • Printed circuit board (PCB) conformal coatings

    2. Polymer Modifier for Polyurethane Systems

    The unique molecular structure of this diol introduces rigidity and enhances flame resistance in polyurethane formulations. Polyol producers utilize it to tailor the molecular architecture of foams, elastomers, and adhesives where aromatic backbone benefits are required—particularly in settings where mechanical retention and regulatory compliance on VOC content present concurrent challenges. Formulators adjust the diol mixing based on the physical testing results and the required certification for each construction or transportation application.

    Industry compliance standards

    • LVD (Low Voltage Directive) 2014/35/EU for construction materials
    • REACH Regulation (EC 1907/2006) Annex XVII for chemical safety
    • EN 45545-2 for fire safety in railway vehicle applications
    • ASTM D3574 for flexible cellular materials

    Typical usage ratio

    • 1.5–7 mol% replacement of conventional diols in polyol blends, adjusted according to target compression set and dimensional stability

    Downstream process integration

    • Blended with polyether or polyester polyols during the prepolymer preparation stage prior to reaction with isocyanates

    Final product types

    • Low VOC insulation foams for buildings and transport
    • High-resilience polyurethane elastomers for automotive bushings
    • Reactive hot-melt polyurethane adhesives

    3. Intermediate for Synthesis of UV-Curable Coating Monomers

    Monomer manufacturers employ 2,6-pyridinedimethanol to design specialty acrylate and methacrylate monomers with intrinsic aromaticity and hydroxyl-bearing sites. These intermediates support rapid photopolymerization kinetics while imparting resistance to yellowing during prolonged UV exposure. When integrated into high-performance coatings, the material contributes to compliance benchmarks for migration, weatherability, and surface hardness in electronics, optical lenses, and specialty plastic products.

    Industry compliance standards

    • ISO 10993 series for biocompatibility of materials used in medical devices
    • EN 71-3 for chemical safety in toy coatings
    • REACH Art. 33 for information on substances of very high concern (SVHCs)
    • ISO 178 for thermoset plastic mechanical testing

    Typical usage ratio

    • 5–16 mol% of total monomer feed; proportion calibrated for desired crosslink density and UV curing speed

    Downstream process integration

    • Reacted with (meth)acrylic acid under controlled esterification followed by purification and functionalization to obtain UV-reactive monomers

    Final product types

    • Scratch-resistant optical coatings
    • LED display surface varnishes
    • Medical device overcoats

    4. Component in Specialty Polycarbonate Resin Synthesis

    Producers of engineering plastics introduce this raw material during the preparation of polycarbonate resins where improved flame retardancy and high glass transition temperature are necessary. Its incorporation impacts the copolymer backbone, thereby reducing optical birefringence and stress cracking in molded products. The level of incorporation varies with the end-use mechanical and thermal profile mandated in automotive, electrical housing, and advanced consumer applications due to applicable global standards for material reliability and human safety.

    Industry compliance standards

    • UL 746C for polymeric materials used in electrical equipment
    • ISO 7391-1 for testing methods for polycarbonates
    • EN 71-12 for safety of toys (organic chemicals)
    • ISO/TS 16949 for automotive regulatory requirements

    Typical usage ratio

    • 2–8 mol% within bisphenol-based copolymer streams, controlled through melt-phase or interfacial synthesis by the end user

    Downstream process integration

    • Used as a reactive monomer within the phosgenation or transesterification process during polycarbonate chain assembly

    Final product types

    • Flame-retardant polycarbonate sheets for electronics
    • Molded optical discs
    • Automotive under-the-hood connectors and housings

    5. Building Block for Agrochemical Actives Synthesis

    Agrochemical manufacturers utilize 2,6-pyridinedimethanol within multi-step syntheses to create pyridyl-based compounds with targeted bioactivity. The controlled addition of this diol provides molecular scaffolds for plant growth regulators and advanced crop protection agents. Downstream processors must operate within strict stewardship and residue requirements set by international regulatory bodies, maintaining batch specifications for both yield and trace impurity levels in fields where food safety and regulatory reviews demand robust analytical monitoring.

    Industry compliance standards

    • FAO Specifications for Plant Protection Products
    • ISO 17025-certified laboratory testing
    • OECD Guidelines for the Testing of Chemicals (Section 5: Pesticides)
    • EU Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market

    Typical usage ratio

    • 2–6 mol% as a molecular fragment within active ingredient synthesis pathways; loading depends on target molecule structure and downstream purification constraints

    Downstream process integration

    • Supplied to reaction steps alongside halogenated intermediates and coupling agents to form heterocyclic agrochemical cores, followed by isolation and formulation

    Final product types

    • Pyridine-based herbicides
    • Plant growth regulators
    • Crop disease resistance agents
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