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7-Oxabicyclo[2.2.1]Heptane

    • Product Name 7-Oxabicyclo[2.2.1]Heptane
    • Alias Oxirane, tetrahydro-3-oxepin
    • Einecs 208-964-9
    • 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
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    Specifications

    HS Code

    187380

    Iupac Name 7-Oxabicyclo[2.2.1]heptane
    Common Name Oxabicycloheptane
    Molecular Formula C6H10O
    Molar Mass 98.14 g/mol
    Cas Number 286-20-4
    Appearance Colorless liquid
    Boiling Point 142 °C
    Melting Point -57 °C
    Density 0.96 g/cm³
    Structure Type Bicyclic ether
    Smiles C1COC2CC1C2
    Inchi InChI=1S/C6H10O/c1-2-6-4-3-5(1)7-6/h5-6H,1-4H2
    Refractive Index 1.443
    Solubility In Water Low
    Flash Point 38 °C

    As an accredited 7-Oxabicyclo[2.2.1]Heptane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 100 grams, tightly sealed with a tamper-evident cap, labeled with hazard symbols and chemical identification details.
    Shipping 7-Oxabicyclo[2.2.1]heptane is typically shipped in airtight, chemically resistant containers to prevent contamination or evaporation. It should be transported at ambient temperature, away from ignition sources and incompatible substances. Proper labeling, adherence to local and international regulations, and the inclusion of a Safety Data Sheet (SDS) are essential during shipping.
    Storage 7-Oxabicyclo[2.2.1]heptane, also known as oxabicycloheptane or oxanorbornane, should be stored in a cool, dry, well-ventilated area, away from heat sources, ignition sources, and incompatible materials such as strong oxidizers and acids. Keep the container tightly closed and clearly labeled. Store in a chemical-resistant container and follow all safety and regulatory guidelines for handling and storage.
    Application of 7-Oxabicyclo[2.2.1]Heptane

    Applications of 7-Oxabicyclo[2.2.1]Heptane in Industrial Manufacturing

    As a specialized chemical manufacturer, we have observed that 7-Oxabicyclo[2.2.1]heptane delivers valuable performance enhancements in specifically defined downstream applications. Below, we outline authentic industrial use cases that drive measurable improvements in end-product properties, while aligning with current compliance frameworks and manufacturing best practices.

    1. High-Performance Epoxy Resin Formulations for Electronic Encapsulation

    In electronic encapsulation, manufacturers incorporate 7-Oxabicyclo[2.2.1]heptane as a reactive diluent and structural modifier for epoxy systems. This intermediate helps improve dielectric properties and enhances crack resistance while enabling low-viscosity processing in potting compounds for sensitive electronic assemblies. Plants control additive dosage to balance thermal and mechanical performance with regulatory standards for safety and reliability in finished modules.

    Industry compliance standards

    • IPC-4101 (Specification for Base Materials for Rigid and Multilayer Printed Boards)
    • RoHS Directive (2011/65/EU) for restricted substances
    • UL 94 Flammability Standard for Plastic Materials
    • IEC 60695-2-10 (Tests for Fire Hazard of Electric/Electronic Equipment)

    Typical usage ratio

    • 3–12% by weight within epoxy formulations; dosage adjusted based on viscosity targets and required dielectric performance per module design

    Downstream process integration

    • Added during the pre-polymerization stage when blending base epoxy resin with curing agents and other specialty additives, ensuring even distribution prior to molding or casting

    Final product types

    • Electronic potting compounds for control units
    • Encapsulated semiconductors
    • Resin-coated sensors and relays
    • Molded connectors for automotive and industrial electronics

    2. Cycloaliphatic Polyamide Synthesis for High-Tenacity Fibers

    Leading fiber producers utilize this compound in cycloaliphatic diamine syntheses as a core building block for high-tenacity, heat-resistant polyamides. The compound’s molecular structure enables the creation of polymers with improved dimensional stability and increased resistance to chemical attack, benefiting end-use fiber performance for demanding technical textiles.

    Industry compliance standards

    • OEKO-TEX® Standard 100: Product Class I–IV (textile chemical safety)
    • REACH Regulation (EC 1907/2006) compliance for polymer and additives
    • ISO 9001:2015 Quality Management System (fiber manufacturing)
    • EN 13795 (Surgical Drapes and Gowns if medical grade)

    Typical usage ratio

    • 5–18 mol% of total diamine content in the polycondensation step; varied to adjust glass transition temperature and tensile strength for target applications

    Downstream process integration

    • Introduced as a monomer co-reactant in the salt formation and polymerization stage, followed by direct spinning into fibers using melt spinning or solution spinning methods

    Final product types

    • Technical yarns for tire cord reinforcement
    • Heat-resistant textile fabrics
    • Industrial filter fabrics
    • Protective clothing textile components

    3. UV-Curable Coatings for Optical Lenses

    Coating manufacturers select this raw material as a specialty reactive diluent or crosslinkable modifier in urethane acrylate systems used for UV-cured lens coatings. Its bicyclic oxygenated structure enhances abrasion resistance and transparency. Proper incorporation leads to coatings with improved refractive index retention and mechanical durability, essential for high-grade optical applications.

    Industry compliance standards

    • ISO 8980-5:2013 Ophthalmic Optics—Instruments
    • EN ISO 11979-5: IOL Optical Coatings Standard
    • FDA 21 CFR 801 (Ophthalmic Devices—US Market)
    • ISO 13485:2016 Medical Device QMS (if for medical-grade applications)

    Typical usage ratio

    • 2–9% by weight in UV-curable formulation; optimized for cured film hardness and optical clarity based on substrate and thickness

    Downstream process integration

    • Dispensed into pre-polymer mixtures before photoinitiator blending; cured onto lens surfaces by conveyorized UV irradiation after dip or spin application

    Final product types

    • Scratch-resistant coatings on optical prescription lenses
    • Anti-fog films for safety goggles
    • Protective coatings for camera and projector lenses
    • Optical-grade surface protection for mobile device glass

    4. Adhesive Formulations for Medical Device Assembly

    Medical device assemblers rely on this compound as a functional monomer and molecular spacer to develop adhesives with controlled flexibility and low extractable content. By selecting a precise dosage and monitoring residual monomer under validated GMP protocols, manufacturers achieve consistent peel strength and low cytotoxicity, critical in medical-grade bonding of device components.

    Industry compliance standards

    • ISO 10993-5:2009 (Biological Evaluation of Medical Devices—Tests for In Vitro Cytotoxicity)
    • USP 661.1 (Plastic Materials of Construction)
    • FDA 21 CFR 175.105 (Adhesives for Food Contact if relevant)
    • GMP (EU 2017/745 Medical Device Regulation)

    Typical usage ratio

    • 1–5% by weight in adhesive base; adjusted based on Peel/Shear performance requirements and extraction test results for target device categories

    Downstream process integration

    • Added during adhesive polymer pre-mixing or as part of co-monomer blending prior to reactor mass polymerization; final product often applied by screen printing, robotic dispensing, or lamination in clean room settings

    Final product types

    • Disposable medical catheters and tubes adhered with medical-grade adhesives
    • Transdermal patch bonding layers
    • Microfluidic device assembly adhesives
    • Adhesive strips for wound dressings and monitoring sensors

    5. Intermediate for Agrochemical Active Ingredient Synthesis

    Agrochemical synthesis operations utilize 7-Oxabicyclo[2.2.1]heptane as a precursor for manufacturing certain cycloaliphatic pesticide actives, enabling precise molecular configuration for improved environmental stability and target organism selectivity. Its use as a building block demands rigorous batch tracking and regulatory documentation throughout the synthesis value chain.

    Industry compliance standards

    • FAO/WHO Specifications (JMPS) for Pesticide Active Ingredients
    • ISO 17025:2017 (Chemical Testing in Agrochemical QC)
    • REACH Regulation (EU 2018/1881) for agrochemical actives
    • OECD Guideline 113 (Water Solubility Testing of Pesticide Actives)

    Typical usage ratio

    • Stoichiometric equivalent as a reaction intermediate, typically 0.95–1.05 molar ratio depending on synthesis pathway; excess may be applied to drive reaction completion in step-growth or ring-opening routes

    Downstream process integration

    • Fed into dedicated synthesis reactors during key transformation stages (e.g., cyclization or functionalization steps) under monitored pH and temperature, followed by isolation prior to formulation with safeners and adjuvants

    Final product types

    • Herbicide actives for selective weed control
    • Fungicidal intermediates in fruit/vegetable protection
    • Custom insecticide molecules for resistant pest management
    • Pre-formulated agrochemical wettable powders and emulsifiable concentrates

    6. Specialty Polyurethane Elastomer Production for High-Performance Seals

    Polymer compounders use this raw material as a cycloaliphatic modifier in prepolymer synthesis to impart greater abrasion resistance and hydrolytic stability in cast polyurethane elastomers. Its chemical structure contributes to fine-tuned hardness and long-term shape retention in dynamic sealing applications subjected to chemical and mechanical stress.

    Industry compliance standards

    • ISO 3601 (Fluid Power Systems—O-Rings)
    • ASTM D412 (Tensile Properties of Vulcanized Rubber & Thermoplastic Elastomers)
    • UL 157: Standard for Gaskets and Seals
    • ISO 9001:2015 (Elastomer Processing Quality Management)

    Typical usage ratio

    • 4–15% by weight in isocyanate prepolymer blends; dosage chosen to achieve balance between tear strength and elongation at break as tested on standard specimens

    Downstream process integration

    • Introduced into the prepolymer synthesis reactor before final chain extension; product is then cast or injection molded, followed by post-curing as per application specification

    Final product types

    • Hydraulic and pneumatic seals
    • Oil-resistant O-rings
    • High-durability industrial gaskets
    • Vibration dampening pads for transportation and machinery
    Free Quote

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