Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing sales6@sinochem-nanjing.com
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Epibromohydrin

    • Product Name Epibromohydrin
    • Alias Bromomethyloxirane
    • Einecs 203-654-0
    • 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
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    Specifications

    HS Code

    519545

    Cas Number 106-96-7
    Molecular Formula C3H5BrO
    Molar Mass 136.98 g/mol
    Iupac Name 2-Bromomethyloxirane
    Boiling Point 99-101°C
    Melting Point -56°C
    Density 1.527 g/cm3 at 20°C
    Appearance Colorless to pale yellow liquid
    Flash Point 18°C (closed cup)
    Solubility In Water Slightly soluble
    Refractive Index 1.461 at 20°C
    Vapor Pressure 19 mmHg at 20°C

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

    Packing & Storage
    Packing Epibromohydrin is supplied in a 500 mL amber glass bottle with a tightly sealed cap, labeled with hazard and handling instructions.
    Shipping Epibromohydrin should be shipped in tightly sealed containers, protected from light, heat, and moisture. It is a hazardous chemical and must be handled according to local, national, and international transport regulations (such as DOT, IATA, IMDG). Proper labeling, use of compatible packaging, and necessary documentation are essential for safe shipment.
    Storage Epibromohydrin should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong acids, bases, and oxidizers. Store under an inert atmosphere if possible. Keep away from ignition sources, as it is flammable. Ensure proper labeling and access only to trained personnel.
    Application of Epibromohydrin

    Applications of Epibromohydrin in Industrial Manufacturing

    As a direct manufacturer of Epibromohydrin, we support diverse industrial clients by supplying consistent quality for complex downstream synthesis. Epibromohydrin enters well-defined application pipelines, serving specific chemical transformations and end-use formulations across high-value manufacturing sectors.

    1. Epoxy Resin Modifier for Specialty Coatings

    Epibromohydrin is widely used as a functional monomer and reactive diluent in the modification of epoxy resin systems for high-performance coatings. Industrial resin producers incorporate this raw material to enhance chemical resistance, thermal durability, and flame-retardant properties in specialty coatings. During compounding, producers adjust addition levels based on formulation solids and performance targets. The use of Epibromohydrin requires careful handling to meet environmental and worker safety codes, as well as to achieve targeted mechanical and electrical properties for advanced coatings.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • OSHA Hazard Communication Standard 29 CFR 1910.1200
    • RoHS Directive 2011/65/EU for electronics coatings
    • ISO 9001:2015 Quality Management for process control

    Typical usage ratio

    • 3–10% by weight of resin solids, adjusted for viscosity and cure rate
    • Higher loading (up to 15%) for increased reactivity in two-component systems
    • Lower bounds for compliance coatings or thin-film applications

    Downstream process integration

    • Dosed into the pre-polymerization kettle during epoxy backbone synthesis
    • Reacted under controlled temperature and pH to limit side reactions
    • In-line QC for color, bromine index, and residual monomer
    • Subsequent curing with amine or anhydride hardeners

    Final product types

    • Anticorrosive coatings for pipelines and tanks
    • Protective electrical component coatings
    • Fire retardant decorative paints
    • Industrial-grade flooring compounds

    2. Intermediary for Pharmaceutical Synthesis

    Epibromohydrin serves as a reactive intermediate in the synthesis of active pharmaceutical ingredients, where its functionality provides a path to complex heterocyclic compounds and chiral auxiliaries. Process chemists exploit its bifunctional nature in multi-stage syntheses of APIs, such as anti-infectives and central nervous system drugs. Process validation and GMP documentation must accompany any batch for pharmaceutical conversion, and residuals require strict control.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) and European Pharmacopoeia (EP) monographs relevant to product
    • 21 CFR Parts 210 and 211 (US FDA cGMP regulations)
    • ICH M7 guideline on control of genotoxic impurities

    Typical usage ratio

    • Stoichiometric use based on target molecule, typically 0.8–1.2 equivalents per step
    • Adjusted for yield optimization in scale-up synthesis
    • Tighter range for regulated drug intermediates, max 1.05 equivalents

    Downstream process integration

    • Charged into closed reaction vessels for nucleophilic substitution or ring closure
    • Integrated with base or phase-transfer catalyst systems
    • Residuals monitored by GC-MS according to DMF specifications
    • Process chemistry includes work-up, purification, and API isolation steps

    Final product types

    • Antiviral drug intermediates
    • Beta-adrenergic blocking agents
    • Central nervous system stimulants
    • Intermediate building blocks for custom synthesis

    3. Synthesis of Ion Exchange Membranes and Polymers

    Major membrane and polymer manufacturers use Epibromohydrin as a precursor for the production of ion exchange resins and specialty polymers, particularly those requiring crosslinked ether-bromide structures. The raw material is grafted or copolymerized to achieve targeted ion selectivity and mechanical properties for use in energy storage, industrial separations, and water purification. All manufacturing steps must demonstrate compliance with regional chemical safety and polymer processing regulations.

    Industry compliance standards

    • ISO 14001 Environmental Management for chemical operations
    • EU Regulation (EU) 2019/1021 on Persistent Organic Pollutants (POP) for membrane disposal
    • ASTM D2187 for ion exchange resin performance
    • China RoHS for electronics-related polymers

    Typical usage ratio

    • 10–25% by mass in graft copolymer recipes
    • 5–12 mol% in crosslinking for thermoset membranes
    • Varies with targeted ion-exchange capacity and resin bead size

    Downstream process integration

    • Polymerized through solution or suspension techniques
    • Introduced directly in functional monomer charge
    • Followed by quaternization or sulfonation stages
    • End-of-line QC for exchange capacity and mechanical strength

    Final product types

    • Cation and anion exchange resins
    • Proton exchange membranes for fuel cells
    • Industrial wastewater treatment cartridges
    • High-capacity ion selective filters

    4. Production of Agrochemical Intermediates

    Agrochemical manufacturers select Epibromohydrin to build halogenated intermediates crucial to crop protection agent synthesis. Its bifunctionality enables precise ring-opening, chain extension, and hybridization reactions as part of multi-step technical grade active ingredient production. Plant operators control input ratios and monitor conversion due to regulatory limits on residuals and byproduct hazards. Full traceability and product stewardship practices are mandatory in this sector.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 17025 Laboratory Management for contaminant testing
    • China GB 2763 Maximum Residue Limit standards
    • EPA 40 CFR Part 170: Worker Protection Standard (US)

    Typical usage ratio

    • 0.8–1.3 equivalents per target intermediate, process-defined
    • Lower ratios (0.8–0.95 equiv.) to reduce unreacted material in high volume synthesis
    • Higher usage for certain isomeric compounds built by multi-stage alkylation

    Downstream process integration

    • Reacts in closed reactors during halogenation or etherification steps
    • Added after solvent charging and catalyst seeding
    • Conversion monitored by HPLC and GC during process validation
    • Product isolation and purification by fractional distillation or crystallization

    Final product types

    • Pesticide intermediates
    • Herbicide building blocks
    • Fungicide precursor molecules
    • Formulated technical agrochemical concentrate components

    5. Fine Chemical Synthesis for Fragrance and Flavors Industry

    Manufacturers of high-purity fragrance ingredients utilize Epibromohydrin as an alkylating agent in the synthesis of select aroma compounds. Its controlled reactivity supports the production of cyclic ethers and specialty lactones for perfumery and flavorings. Process managers address volatility and byproduct minimization through continuous or batchwise additions under closed systems. Compliance focuses on purity, trace impurity thresholds, and food-contact suitability.

    Industry compliance standards

    • IFRA Standards for fragrance compound safety
    • FDA 21 CFR Part 172 (Food Additives Permitted for Direct Addition to Food)
    • ISO 22000 Food Safety Management for process facilities
    • EU Regulation (EC) No 1334/2008 on flavorings and certain food ingredients

    Typical usage ratio

    • 0.5–2.0 equivalents in controlled batch alkylation
    • Higher ratios for polyfunctional flavor ingredients
    • Tightly monitored to avoid off-odor byproducts

    Downstream process integration

    • Added to precursor alcohols or acids under reflux with phase transfer catalysis
    • Monitoring via GC-FID for completion and side product minimization
    • Final purification by short-path distillation and liquid chromatography
    • End product’s residual solvents checked per IFRA/FEMA requirements

    Final product types

    • Musk and macrocyclic fragrances
    • Cyclic ether flavor ingredients
    • Lactone-based perfumery components
    • Specialty aroma derivatives for beverages and toiletries
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