Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

1-[1,1'-Biphenyl]-4-Yl-1-Pentanone

    • Product Name 1-[1,1'-Biphenyl]-4-Yl-1-Pentanone
    • Alias 4-Benzoyl-1-phenylpentane
    • Einecs 249-714-9
    • 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

    595154

    Product Name 1-[1,1'-Biphenyl]-4-Yl-1-Pentanone
    Molecular Formula C17H18O
    Molecular Weight 238.33 g/mol
    Cas Number 5449-42-3
    Appearance White to off-white solid
    Boiling Point 384.6 °C at 760 mmHg
    Melting Point 55-59 °C
    Density 1.06 g/cm³
    Flash Point 175.6 °C
    Solubility Insoluble in water, soluble in organic solvents
    Purity Typically ≥98% (varies by supplier)
    Synonyms 4-Benzoyl-n-pentylbenzene
    Smiles CCCCC(=O)C1=CC=C(C=C1)C2=CC=CC=C2
    Storage Temperature Room temperature, keep container tightly closed
    Refractive Index 1.563

    As an accredited 1-[1,1'-Biphenyl]-4-Yl-1-Pentanone 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 25 grams of 1-[1,1'-Biphenyl]-4-Yl-1-Pentanone, sealed, labeled with hazard and safety information.
    Shipping 1-[1,1'-Biphenyl]-4-Yl-1-Pentanone is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is handled per chemical safety regulations, often classified as non-hazardous but should be accompanied by a Safety Data Sheet (SDS). Temperature control may be necessary to maintain product stability during transit.
    Storage 1-[1,1'-Biphenyl]-4-yl-1-pentanone should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light. Store at room temperature, and ensure proper labeling to prevent accidental exposure or misuse. Use secondary containment to avoid spills or leaks.
    Application of 1-[1,1'-Biphenyl]-4-Yl-1-Pentanone

    Applications of 1-[1,1'-Biphenyl]-4-Yl-1-Pentanone in Industrial Manufacturing

    As a high-purity manufacturer, we supply 1-[1,1'-Biphenyl]-4-Yl-1-Pentanone to critical downstream sectors that require reliability, lot-to-lot consistency, and compliance with stringent regulatory and application-specific standards. The following sections present detailed industrial application scenarios based on established use, process integration knowledge, and actual practices by chemical and materials producers who specify this compound.

    1. High-Performance Liquid Crystal Intermediate Synthesis

    Electronic material companies use 1-[1,1’-Biphenyl]-4-Yl-1-Pentanone as an essential intermediate in the production of specialized liquid crystal components for display technologies. The compound provides the rigid biphenyl core structure necessary for advanced mesogenic compounds used in high-resolution LC displays. Production protocols require thorough qualification testing for purity, residue solvent, and trace metal content, following international display industry qualification norms for critical intermediates.

    Industry compliance standards

    • IEC 61290 series (Liquid Crystal display materials quality)
    • ISO 9001:2015 (Manufacturing quality management systems)
    • REACH Annex XVII (SVHC restrictions for electronic chemical components in Europe)
    • RoHS 2011/65/EU (Restriction of hazardous substances in electronics)

    Typical usage ratio

    • Normally formulated at 10–35 mol% as a building block in multi-component mesogen mixtures; exact proportion depends on desired viscosity, birefringence, and thermal range of the liquid crystal blend.

    Downstream process integration

    • Charged during the initial mesogen precursor synthesis (Suzuki, Heck, or Friedel-Crafts coupling). Reacts directly with halogenated phenyl intermediates in closed inert-reactor systems, followed by distillation or recrystallization for purity control before formulation into display-grade mixtures.

    Final product types

    • Twisted nematic (TN) and in-plane switching (IPS) liquid crystal panels
    • Advanced OLED and LCD display units
    • Alignment materials for high-specification display manufacturing

    2. Pharmaceutical Intermediate for Biphenyl-Structured Drug Synthesis

    Several pharmaceutical process plants rely on this compound as a key intermediate in the synthesis routes of biphenyl-based APIs and specialty generics. The distinct aromatic structure serves as a precursor for final APIs where specific chain length and steric properties are needed to optimize biological binding activity. Formulators must control residual solvent and impurity profiles in accordance with regulatory submissions for the intended finished drug products.

    Industry compliance standards

    • Good Manufacturing Practice (EU GMP, US FDA 21 CFR 210/211)
    • ICH Q3A/B (Impurities guidelines for pharmaceuticals)
    • USP/NF, Ph. Eur., JP monographs for final API materials
    • DMF/CEP filing requirements for regulated markets

    Typical usage ratio

    • Usually 1 eq. (molar equivalent) as a building block or acylation reagent per synthetic batch, with input range of 0.5–2.5 mol depending on the targeted API and synthesis scale. Adjustments arise from yield optimization and impurity management in process development.

    Downstream process integration

    • Introduced during the central coupling or condensation stage; most often used in Friedel-Crafts acylation with functional aromatic amines or esters, followed by downstream purification (chromatography or crystallization) tailored for pharmaceutical-grade quality.

    Final product types

    • Biphenyl carboxylate anti-inflammatory APIs
    • Intermediates for antihypertensive agents and CNS-active drugs
    • Contract-manufactured APIs for branded and generic pharmaceuticals

    3. Advanced Polymer Modifier Production

    Polymer compounders and specialty resin manufacturers use 1-[1,1’-Biphenyl]-4-Yl-1-Pentanone as a functional additive to impart rigidity, thermal stability, and improved processability in high-performance engineering polymers. The compound integrates into copolymer backbones via melt mixing or reactive extrusion, enabling processors to fine-tune mechanical and dielectric properties to meet stringent specifications for technical molded parts and insulation layers.

    Industry compliance standards

    • UL 94 (Flame retardancy classification for plastics)
    • ISO 11357 (Polymer thermal analysis)
    • Restriction of REACH SVHC monomer content
    • ISO 14001:2015 (Environmental management for chemical processing)

    Typical usage ratio

    • Standard addition is 1.5–6 wt% in polycarbonate or liquid-crystal polymer matrices; levels adjusted based on mechanical target (tensile modulus, heat distortion), intrinsic viscosity, and compatibility testing.

    Downstream process integration

    • Dosed at the pellet extrusion or compounding stage, typically in twin-screw extruders. Can also react into copolymer chains via solution polymerization or reactive blending with maleic anhydride-functional polymers, prior to granulation or direct injection molding.

    Final product types

    • Glass fiber reinforced engineering plastics for electronic housings
    • Dielectric films for automotive and electronic applications
    • Injection-molded structural components

    4. UV-Curable Coating Raw Material

    Industrial coatings manufacturers employ this biphenyl ketone as a specialty UV-reactive precursor for formulating high-durability surface coatings used in electronics and precision device packaging. Its aromatic skeleton enhances UV absorbance and crosslink density, providing scratch and chemical resistance required in protective film applications. Compliance and purity levels must adhere to sector-specific performance and environmental mandates.

    Industry compliance standards

    • ISO 12944 (Protective paint and coating systems)
    • EN 71-3 (Chemical safety for coatings on toys and electronics)
    • REACH Annex XIV (Authorisation list for coating raw materials)
    • IEC 62321 (RoHS test method for electronic coatings)

    Typical usage ratio

    • Integrated at 0.8–3.5 wt% as a photoreactive monomer or crosslinker in UV formulation blends; dosage tailored to required film hardness and optical properties.

    Downstream process integration

    • Blended into oligomer/resin base before batch mixing and UV photoinitiator addition. Dispensed by automated proportioning, then coated (spin, spray, or curtain) prior to in-line UV irradiation and thermal post-curing for end-use performance optimization.

    Final product types

    • Protective films for smartphone and display touch panels
    • Microelectronic device encapsulation layers
    • Wear-resistant coatings for high-reliability electronics

    5. Organic Photovoltaic (OPV) Material Precursor

    Manufacturers in the renewable energy sector select this raw material as a high-performance scaffold for low band-gap, donor-acceptor type conjugated polymers used in next-generation OPV devices. Its structural motif promotes π-conjugation and electron mobility critical for energy conversion efficiency. Handling and QC procedures must consider environmental traceability and batch reproducibility to conform to green chemistry policies and device certification programs.

    Industry compliance standards

    • IEC 61215 (Photovoltaic module performance qualification)
    • EN 50583 (Photovoltaics in buildings—environmental safety)
    • ISO 14040 (Life cycle assessment for photovoltaics)
    • REACH environmental and safety data for photovoltaic precursors

    Typical usage ratio

    • Usually specified at 5–20 mol% as a linker in donor backbone polymer synthesis; modified according to target absorption profile, charge carrier mobility, and final device layer thickness.

    Downstream process integration

    • Enters the synthetic process at the aromatic coupling or condensation stage during donor-acceptor polymer building, followed by solution blending and deposition via slot-die coating or spin-coating onto flexible substrates in cleanroom conditions.

    Final product types

    • Organic photovoltaic modules for building-integrated PV
    • Semi-transparent and flexible solar panels
    • Thin-film energy generation devices for portable electronics
    Free Quote

    Competitive 1-[1,1'-Biphenyl]-4-Yl-1-Pentanone prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance