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4-Bromo-4'-N-Heptylbiphenyl

    • Product Name 4-Bromo-4'-N-Heptylbiphenyl
    • Alias 4-Bromo-4'-heptyl-1,1'-biphenyl
    • Einecs 607-096-6
    • 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

    803275

    Cas Number 842111-74-4
    Molecular Formula C19H23Br
    Molecular Weight 331.29
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Insoluble in water; soluble in organic solvents
    Chemical Class Biphenyl derivative
    Smiles CCCCCCCNC1=CC=C(C=C1)C2=CC=C(Br)C=C2
    Storage Temperature Room temperature, in a dry place
    Synonyms 4-Bromo-4'-heptylaminobiphenyl

    As an accredited 4-Bromo-4'-N-Heptylbiphenyl factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 10 grams of 4-Bromo-4'-N-Heptylbiphenyl, tightly sealed, labeled with hazard warnings and batch information.
    Shipping 4-Bromo-4'-N-Heptylbiphenyl is shipped in tightly sealed containers, protected from light, moisture, and physical damage. The packaging complies with relevant chemical safety regulations. During transit, it is handled as a hazardous material, with appropriate labeling and documentation provided to ensure safe and legal transportation in accordance with local and international shipping guidelines.
    Storage 4-Bromo-4'-N-Heptylbiphenyl should be stored in a tightly sealed container, protected from light, moisture, and sources of ignition. Store in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Proper chemical storage cabinets or designated flammable storage areas are recommended to ensure safety and to maintain the compound’s stability.
    Application of 4-Bromo-4'-N-Heptylbiphenyl

    Applications of 4-Bromo-4'-N-Heptylbiphenyl in Industrial Manufacturing

    As a direct manufacturer of 4-Bromo-4'-N-Heptylbiphenyl, we supply this specialty intermediate to advanced material industries requiring precise performance and structural features. The following are real downstream application sectors relying on this compound as a key building block, with actual process, compliance, and formulation details from the manufacturing field.

    1. Liquid Crystal Material Synthesis for Display Technologies

    Display panel producers use this compound as a primary intermediate during the synthesis of specific liquid crystal (LC) mixtures employed in automotive, consumer, and signage TFT-LCD screens. The extended alkyl side chain and brominated biphenyl core enhance phase behavior, thermal stability, and electro-optical threshold characteristics needed for modern mid- and high-retardation LC blends. The compound integrates during the formation of biphenyl ester and Schiff base LC mixtures, allowing manufacturers to tailor switching speeds and alignment properties.

    Industry compliance standards

    • RoHS Directive (EU 2011/65/EU, latest amendments)
    • IEC 61249-2-21 (Halogen-free materials for electronic assemblies)
    • REACH Regulation (EC 1907/2006) for SVHC content
    • ISO 9001-certified production for LC mixture precursors

    Typical usage ratio

    • 0.5%–12% by total LC blend mass, fine-tuned by end-use pixel response and viscosity control; precise ratio depends on integration with homologous biphenyls and ester functional group concentration.

    Downstream process integration

    • Direct use in Grignard or Ullmann-type coupling to assemble larger mesogenic units for LC mixture formulation
    • Batch or continuous stirred-tank blending with other liquid crystal intermediates, followed by ultra-fine filtration and isotropic point matching

    Final product types

    • TFT-LCD display panel liquid crystal blends
    • Passive-matrix LCDs for industrial controls
    • Advanced automotive instrument cluster displays
    • High-contrast e-paper and signage modules

    2. Organic Semiconductor Precursor in OLED and OTFT Manufacturing

    Within the optoelectronics segment, downstream fabrication of organic semiconducting layers for organic light-emitting diodes (OLEDs) and organic thin-film transistors (OTFTs) deploys this compound as a pivotal precursor. The molecule’s heptyl side chain supports film-forming attributes and ensures compatibility with various hole-transport or electron-transport architectures. During Suzuki or Stille cross-coupling polymerizations, it anchors the biphenyl scaffold, promoting charge mobility and threshold voltage tuning while maintaining strict impurity thresholds demanded by device reliability and color purity standards.

    Industry compliance standards

    • JEITA (Japan Electronics and Information Technology Industries Association) color purity and reliability guidelines
    • IEC 62341 standards for OLED performance and safety
    • IPC-4101B specifications for organic electronic materials purity
    • ISO 14001 for environmental management in device material production

    Typical usage ratio

    • 5–30 mol% relative to the overall conjugated polymer chain-forming monomer mixture; usage level defined through device layer architecture and required emission/transport properties.

    Downstream process integration

    • Entrained into Suzuki or Stille coupling reactors with arylboronic acids or stannanes to produce polymerized semiconductor films
    • Film casting or inkjet coating substrates with the resultant pre-polymer mixture, followed by controlled annealing

    Final product types

    • OLED emitting and transport layers
    • Organic field-effect transistor channel films
    • Flexible display drivers
    • Wearable optoelectronic circuit components

    3. Intermediary in High-Performance Liquid Chromatography (HPLC) Column Packing Production

    Column packing specialists use 4-Bromo-4'-N-Heptylbiphenyl as a surface modifying agent during the preparation of reversed-phase HPLC stationary phases. It functionalizes silica or polymer beads via covalent bonding, leveraging its hydrophobic tail and aromatic moiety to impart customized partition properties. This intermediate determines the selectivity and peak symmetry in analytical separation of pharmaceuticals, biochemicals, and toxicological samples, complying with strict batch documentation for traceability.

    Industry compliance standards

    • USP <621> Chromatography standard for analytical media validation
    • ISO 17025 for laboratory quality management in column manufacturing
    • FDA 21 CFR Part 211 for process traceability in pharmaceutical supply
    • REACH registration for raw material use in analytical applications

    Typical usage ratio

    • 2–7% by mass relative to functionalized support, adjusted based on required stationary phase hydrophobicity and test chromatogram retention times.

    Downstream process integration

    • Biphenyl incorporation via silanization or direct coupling with porous silica or polystyrene-divinylbenzene beads under controlled moisture and temperature conditions
    • Packing slurry preparation and column filling, followed by performance validation (theoretical plate count, asymmetry factor testing)

    Final product types

    • Analytical HPLC columns for pharmaceuticals
    • Bioanalytical and proteomic separation columns
    • Custom chromatography cartridges for food safety labs
    • Environmental pollutant testing columns

    4. Building Block for Specialty Aromatic Polymers

    Polymer processing companies incorporate the molecule as an end-capping or main chain component in the precision synthesis of aromatic polymers for high-temperature and chemical-resistant applications. The compound’s bromine functional group promotes controlled copolymerization with phthalic anhydride or bisphenol-A derivatives, contributing to enhanced mechanical strength and surface durability. It integrates during melt polycondensation or solution polymerization steps, enabling the production of advanced molding pellets and specialty coatings.

    Industry compliance standards

    • ASTM D5336 for aromatic thermoplastic resin properties
    • UL 94 vertical burning test for flame retardant polymers
    • ISO 7822 for chemical resistance in plastic components
    • Restriction of Halogen Compounds (per customer or end-use requirements)

    Typical usage ratio

    • 3–10% of total monomer feed, based on target molecular weight, end-group saturation, and final product mechanical profile.

    Downstream process integration

    • Batched into preheating or in-situ catalysis units during melt polycondensation or controlled solution-feed reactors
    • Post-polymerization blending, extrusion, and pelletizing for molding compound preparation

    Final product types

    • High-temperature polymer engineering pellets
    • Corrosion-resistant circuit board coatings
    • Specialty automotive under-the-hood plastic parts
    • Advanced electronic encapsulant materials
    Free Quote

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