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1-Bromo-3-Ethylbenzene

    • Product Name 1-Bromo-3-Ethylbenzene
    • Alias m-Bromoethylbenzene
    • Einecs 210-177-9
    • 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
    VTB
    Specifications

    HS Code

    174053

    Iupac Name 1-Bromo-3-ethylbenzene
    Molecular Formula C8H9Br
    Molar Mass 185.06 g/mol
    Cas Number 585-89-5
    Appearance Colorless to pale yellow liquid
    Density 1.320 g/cm³
    Boiling Point 215-217 °C
    Melting Point -18 °C
    Flash Point 86 °C (closed cup)
    Refractive Index 1.545
    Solubility In Water Insoluble
    Main Uses Organic synthesis intermediate

    As an accredited 1-Bromo-3-Ethylbenzene 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 mL, with secure screw cap, labeled "1-Bromo-3-Ethylbenzene, CAS 585-88-6", warning and hazard symbols.
    Shipping 1-Bromo-3-Ethylbenzene is shipped in tightly sealed containers, stored upright in a cool, dry, and well-ventilated area. It should be handled as a flammable and potentially harmful chemical. Transport must comply with relevant regulations, including labeling and documentation for hazardous substances. Avoid exposure to heat, sources of ignition, and incompatible materials.
    Storage **1-Bromo-3-ethylbenzene** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep it isolated from incompatible substances such as strong oxidizers. Ensure proper labeling and access for authorized personnel only. Store at room temperature, or as specified by the manufacturer’s safety data sheet.
    Application of 1-Bromo-3-Ethylbenzene

    Applications of 1-Bromo-3-Ethylbenzene in Industrial Manufacturing

    As a direct manufacturer, we ensure reliable quality and consistent supply of 1-Bromo-3-Ethylbenzene for core sectors in the chemical industry. Its brominated aromatic structure plays a crucial role in multiple advanced synthesis processes. Below, we outline several specialized industrial applications, covering standards, usage ratios, integration methods, and main end products.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)

    1-Bromo-3-Ethylbenzene forms a key building block in the multi-step synthesis of certain APIs, especially within antihypertensive and anti-inflammatory drug production chains. Reacting via selective bromination and subsequent coupling transforms the intermediate into complex molecules for medicinal chemistry pipelines. The material’s purity and controlled halogenation minimize byproduct formation and align with stringent GMP practices. Close collaboration with downstream formulators ensures reliable input consistency for regulated bulk API manufacture.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 Current Good Manufacturing Practice (cGMP) for Finished Pharmaceuticals
    • European Pharmacopoeia (Ph. Eur.) requirements for intermediates
    • US FDA guidelines on process validation and impurity control

    Typical usage ratio

    • Mixing ratios generally in the range of 0.08–0.16 mol per mol of target API
    • Adjusted according to specific process steps and reaction scale

    Downstream process integration

    • Introduced in the halogenation or Friedel–Crafts alkylation stage within multi-step syntheses
    • Reaction proceeds under nitrogen with metal catalysts or strong Lewis acids
    • Process includes rigorous in-process control sampling for residual bromide and purity analysis
    • Intermediate then funneled into main API crystallization or condensation stages

    Final product types

    • Bulk antihypertensive drug APIs (e.g., certain sartans or analogues)
    • Non-steroidal anti-inflammatory drug (NSAID) precursors
    • Specialty pharmaceutical building blocks for contract manufacturing
    • Intermediates for custom synthesis projects

    2. Agrochemical Intermediate—Herbicide Synthesis

    The material serves as a fundamental precursor for developing selective herbicides. Via controlled nucleophilic aromatic substitution or Grignard reactions, it gives rise to ethyl-substituted aniline or phenoxy derivatives. Its high reactivity enables precise functionalization to match desired herbicidal activity. Our clients benefit from certified batches meeting the trace impurity limits required for crop protection compounds.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Plant Protection Products
    • OECD Guidelines for the Testing of Chemicals
    • ISO 9001:2015 for process traceability
    • REACH Registration dossier requirements for agrochemicals in the EU

    Typical usage ratio

    • Reactant ratios: 0.1–0.15 mol per mol of target herbicide intermediate
    • Fine-tuned based on reaction yield analysis and byproduct minimization

    Downstream process integration

    • Charged into alkylation reactors with controlled temperature and solvent systems
    • After completion, the reaction mass undergoes phase separation and purification
    • Subsequent molecule derivatization to generate target active ingredient
    • Batch documentation includes bromine balance checks and final QC clearance

    Final product types

    • Pre-emergent and post-emergent herbicide technical concentrates
    • Processed herbicide formulations (liquid, granular, suspension concentrate)
    • Plant growth regulation intermediates
    • Weed control actives for custom crop protection blends

    3. Custom Synthesis of Liquid Crystal Monomers

    Specialty electronics manufacturers use this aromatic bromide as a molecular core to synthesize advanced liquid crystal monomers. The high selectivity in cross-coupling reactions, such as Suzuki or Stille procedures, yields rigid rod-like biphenyl or terphenyl structures essential for high-performance display panels. Stable input specifications facilitate scale-up and reproducibility in downstream electronic applications.

    Industry compliance standards

    • IEC 61249-2-21 for materials in the electronics industry
    • RoHS Directive 2011/65/EU on restricted substances in electronics
    • ISO 14001 Environmental Management for electronic material manufacturing
    • Internal client-specific purity protocols for telecom and TFT manufacturing

    Typical usage ratio

    • Employ at 0.2–0.25 mol per mol of aryl halide coupling partner
    • Adjusted to optimize yield and minimize excess byproduct formation

    Downstream process integration

    • Introduced during Suzuki, Heck, or Stille cross-coupling stages with palladium-based catalysts
    • Reaction vessels maintained under inert atmosphere with carefully controlled temperature
    • Downstream purification by column chromatography or crystallization
    • Material transferred to monomer formulation and blend tanks post-purification

    Final product types

    • Mono-, di-, and oligomeric liquid crystal agents for LCD and OLED panels
    • Polymerizable liquid crystal monomers for advanced flexible display films
    • Specialty aromatic intermediates for organic photovoltaic and sensor devices
    • Smart window and tunable optical films

    4. Fine Chemical Intermediate for Dye and Pigment Synthesis

    Downstream pigment and dye makers employ this intermediate in elaborating key chromophores for specialty colorants. Electrophilic substitution followed by further functionalization gives high-purity aromatic compounds suitable for textile and specialty ink applications. Close process control minimizes color drift and off-shade risk, critical for automotive and industrial uses.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006—dye and pigment registration
    • ISO 9001 Quality Management for chemical processing
    • Oeko-Tex Standard 100 class II (for textiles and garments)
    • Customer-specific banned substances lists (e.g., automotive OEMs)

    Typical usage ratio

    • Adopt ratios of 0.05–0.12 mol per mol of target dye precursor
    • Modify based on required chromophore chain length and batch scale

    Downstream process integration

    • Dosed into aromatic substitution reactions with controlled acid or alkaline catalysis
    • Undergoes subsequent sulfonation, nitration, or amination depending on chromophore
    • Purified by phase separation and solvent extraction
    • Transferred to blending and granulation or spray-drying as per final use

    Final product types

    • Azo and anthraquinone class dyes for textile, leather, and paper industries
    • Special effect pigments for plastics and automotive coatings
    • Heat-stable colorants for masterbatch and engineering resins
    • Specialty printing inks for packaging and electronics

    5. Intermediate for Performance Polymers

    Chemical processors use this aromatic bromide as a functional group source when preparing performance polymers through controlled polycondensation or chain-growth techniques. Bromine atoms enable subsequent substitution or crosslinking, enhancing polymer properties such as thermal resistance or mechanical strength. Strict QC ensures no contaminants hamper polymerization reactions, allowing precise control over the final material profile demanded by automotive, aerospace, and construction applications.

    Industry compliance standards

    • ASTM D638 and ISO 527—mechanical testing of polymer materials
    • ISO 9001 Quality Management for polymer manufacturing
    • UL 94 Flammability for flame-retardant polymer applications
    • TSCA Inventory listing for polymerizable intermediates (US)

    Typical usage ratio

    • Usage range: 1–5% w/w relative to total monomer feed in copolymerization
    • Varies according to polymer backbone structure and target performance attributes

    Downstream process integration

    • Metered into automated batch or continuous polymerization reactors
    • Initiation under specific temperature and pressure profiles for consistent chain length
    • Subsequent blending with reinforcing fillers or flame retardants
    • Final granulation, pelletizing, or compounding ready for converters

    Final product types

    • High-temperature aramid or polyimide engineering plastics
    • Flame-retardant thermoplastic and thermoset blends
    • Adhesive resins for electronic subassemblies
    • Precursor blocks for advanced hybrid polymers
    Free Quote

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