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Tetrahydro-2-Furanmethanol

    • Product Name Tetrahydro-2-Furanmethanol
    • Alias tetrahydro-2-furylmethanol
    • Einecs 214-010-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales6@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    238041

    Chemicalname Tetrahydro-2-Furanmethanol
    Molecularformula C5H10O2
    Molecularweight 102.13 g/mol
    Casnumber 2681-07-0
    Appearance Colorless liquid
    Boilingpoint 171-173 °C
    Meltingpoint -51 °C
    Density 1.074 g/mL at 25 °C
    Refractiveindex 1.445
    Solubilityinwater Miscible
    Flashpoint 69 °C
    Synonyms 2-(Hydroxymethyl)tetrahydrofuran

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

    Packing & Storage
    Packing 500g of Tetrahydro-2-Furanmethanol supplied in an amber glass bottle, tightly sealed with a tamper-evident screw cap for protection.
    Shipping Tetrahydro-2-Furanmethanol should be shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. Use appropriate labels indicating it is a chemical substance. Follow relevant hazardous material transport regulations, including proper cushioning and secure packaging to prevent leaks or spills during transit. Store in a cool, dry, and well-ventilated area.
    Storage Tetrahydro-2-Furanmethanol should be stored in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep the container tightly closed and protected from moisture. Store away from strong oxidizing agents, acids, and bases. Use only approved containers and ensure proper labeling. Follow all local regulations for safe chemical storage.
    Application of Tetrahydro-2-Furanmethanol

    Applications of Tetrahydro-2-Furanmethanol in Industrial Manufacturing

    As the original producer of Tetrahydro-2-Furanmethanol, we partner with downstream manufacturers who require consistent performance and compliance in their specialty chemical formulations. Our material integrates into stringent B2B workflows across a spectrum of mature, quality-regulated applications. Below we detail key industrial sectors utilizing our product, outlining specific regulatory compliance, dosage guidelines, manufacturing integration points, and the nature of downstream finished goods.

    1. Pharmaceutical API Synthesis

    Tetrahydro-2-Furanmethanol acts as a critical intermediate in processes for synthesizing select heterocyclic pharmaceutical APIs, specifically within routes requiring the introduction of protected primary alcohol functionalities. Its stability under mild reaction conditions and suitability for scale-up support the continual demand from fine chemical and GMP API producers, particularly for antihypertensive and central nervous system medications. Our consistent production quality ensures traceability from material delivery to drug substance batch release, and supports streamlined validation during regulatory audits.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (Finished Pharmaceuticals)
    • Ph. Eur., USP, JP monographs (when applicable to end-product)
    • REACH registration for chemical intermediates

    Typical usage ratio

    • 5–20 mol% in target step; adjusted according to substrate reactivity and desired yield; detailed ratio determined by process chemist for route optimization

    Downstream process integration

    • Charged as a nucleophilic agent or building block after initial alkylation stage in multi-step reaction sequences; incorporated before deprotection or further functionalization; in continuous or batch reactors with reaction monitoring for impurity control

    Final product types

    • Small-molecule APIs (e.g., CNS-active piperidine derivatives, antiarrhythmic agents, select β-lactam analogues)
    • Advanced pharmaceutical intermediates for hospital-use injectables

    2. Agrochemical Active Ingredient Production

    In crop protection chemical manufacture, our material serves as a molecular intermediate for specific pyran and furan-based fungicides and insecticides. Its structure enables functionalization during coupling and cyclization stages, ensuring the final active complies with selectivity and stability requirements. Agrochemical formulators value our strict adherence to impurity profiling demanded by international pesticide registrations, which streamlines approval in multi-jurisdictional markets.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • US EPA FIFRA Compliance
    • EU Regulation (EC) No 1107/2009 (approvals for PPPs)
    • ISO 9001:2015 Quality Management (for traceability and reproducibility)

    Typical usage ratio

    • 2–10 wt% as an intermediate; concentration is tailored based on molecule complexity and downstream conversion efficiency

    Downstream process integration

    • Fed into cyclization or condensation units; typically prior to heterocycle ring closure or halogenation steps during technical-grade active synthesis

    Final product types

    • Furan- or pyran-based fungicide actives (e.g., carboxamide fungicides)
    • Novel insecticides with heterocyclic cores

    3. Polymer and Resin Modifier Manufacturing

    Specialty polymer producers utilize our compound as a chain terminator or crosslinking agent in high-performance polyurethane and epoxy resin systems. Its hydroxymethyl group enables targeted molecular weight control and improved backbone flexibility. Applications focus on advanced coatings, adhesives, and composite matrices where controlled hydroxyl functionality is mandatory for finished material specifications. Our analytical support allows producers to model downstream aging and curing accurately.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management for specialty polymers)
    • ASTM D1655 (for application in aerospace coatings)
    • REACH Annex IV, V (for substances in manufactured articles)
    • SOCMA ChemStewards (Responsible distribution for specialty chemicals)

    Typical usage ratio

    • 0.5–3 phr (parts per hundred resin) as a modifier; dosing varies depending on targeted glass transition temperature and mechanical properties; adjusted after batch viscosity and FTIR analysis

    Downstream process integration

    • Added during prepolymer stage or late-chain extension in batch reactors; introduced before final curing to modify polymer backbone; often metered in with catalyst systems

    Final product types

    • High-durability industrial coatings
    • Epoxy adhesives for electronics assembly
    • Polyurethane foams with tailored cell structure

    4. Solvent and Processing Aid for Fine Chemicals

    Certain fine chemical syntheses benefit from the solubilizing and slightly reactive properties of this material in etherification and reduction operations. Its unique molecular structure facilitates selective solubility during intermediate purification and imparts reactivity for conversion into more complex alcohols. Downstream processors value the precise volatility and compatibility with both acid and base-catalyzed systems. Usage requires control of moisture and trace metals for batch reproducibility.

    Industry compliance standards

    • ISO 14001 (Environmental Management for chemical processing)
    • Responsible Care Certification
    • REACH and TSCA inventory compliance for transportation and formulation
    • OECD guidelines for organic solvents, if used in lab or pilot plant scale

    Typical usage ratio

    • Variable: 1–15% v/v as a co-solvent or processing aid; proportion determined by solubility of reactants and desired partition coefficient; adjusted based on reaction scale and waste handling constraints

    Downstream process integration

    • Introduced at crystallization or separation phases during intermediate refinement; employed to moderate polarity in reaction media; sometimes utilized in azeotropic distillation or as a carryover solvent for downstream extraction

    Final product types

    • Purified heterocyclic intermediates
    • Specialty alcohols and ethers used in performance materials
    • Chiral auxiliaries for advanced organic synthesis

    5. Fragrance Ingredient Precursor

    Fragrance house intermediates requiring a controlled aliphatic alcohol building block integrate our product in the early synthetic stages for musk and floral notes. Its contribution to ring-opening reactions fosters the creation of stable, safe aroma compounds compliant with international fragrance safety standards. Downstream aroma chemical producers emphasize batch traceability and allergen monitoring.

    Industry compliance standards

    • IFRA Standards and Guidelines
    • EU Cosmetics Regulation (EC) No 1223/2009
    • ISO 22716 (Good Manufacturing Practices for Cosmetics)
    • REACH Annex XVII (Restriction of certain fragrance compounds)

    Typical usage ratio

    • 3–8 mol% in condensation or ring-opening; adjusted based on desired fragrance compound concentration and stability testing results

    Downstream process integration

    • Charged during precursor assembly for muscone or cyclopentadecanolide derivatives; enters once core macrocycle is established and isomerization step is complete; validated by GC-MS aroma profile comparison

    Final product types

    • Macrocyclic musk aroma chemicals
    • Synthetic jasmine, muguet (lily of the valley) and floral base substances
    • Ready-to-blend fragrance intermediates for personal care
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