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3'-Trifluoromethylbiphenyl-3-Carbaldehyde

    • Product Name 3'-Trifluoromethylbiphenyl-3-Carbaldehyde
    • Alias 3-(Trifluoromethyl)-[1,1'-biphenyl]-3-carbaldehyde
    • Einecs 631-852-5
    • 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

    192141

    Product Name 3'-Trifluoromethylbiphenyl-3-Carbaldehyde
    Molecular Formula C14H9F3O
    Molecular Weight 250.22 g/mol
    Cas Number 145358-96-7
    Appearance White to off-white solid
    Melting Point 86-89°C
    Solubility Soluble in organic solvents (e.g., dichloromethane, ethanol)
    Purity Typically ≥98%
    Smiles C1=CC(=CC=C1C2=CC=CC(=C2)C(F)(F)F)C=O
    Inchi Key KDOVZEXMCIQPOB-UHFFFAOYSA-N

    As an accredited 3'-Trifluoromethylbiphenyl-3-Carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 1-gram quantity of 3'-Trifluoromethylbiphenyl-3-Carbaldehyde is supplied in a tightly sealed amber glass vial with hazard labeling.
    Shipping 3'-Trifluoromethylbiphenyl-3-carbaldehyde is shipped in tightly sealed containers, protected from light and moisture. Packaging complies with international chemical transport regulations. It is dispatched with proper labeling and documentation, ensuring safe and secure transit. Temperature-sensitive: store and ship at ambient conditions unless specified otherwise. Handle and unpack using appropriate protective equipment.
    Storage 3'-Trifluoromethylbiphenyl-3-carbaldehyde should be stored in a tightly sealed container under a dry, inert atmosphere, such as nitrogen or argon, to prevent moisture absorption and degradation. Keep it in a cool, well-ventilated area, away from direct sunlight, sources of ignition, and incompatible materials such as strong oxidizers. Always store at recommended temperature, typically room temperature or as specified by the supplier.
    Application of 3'-Trifluoromethylbiphenyl-3-Carbaldehyde

    Applications of 3'-Trifluoromethylbiphenyl-3-Carbaldehyde in Industrial Manufacturing

    3'-Trifluoromethylbiphenyl-3-carbaldehyde acts as a precision building block and functional additive across advanced manufacturing sectors. The following application scenarios derive from ongoing collaborations with active ingredient formulators and specialty chemical producers. As the original manufacturer, we maintain strict adherence to quality, compliance, and technical specifications throughout production and customer supply.

    1. Pharmaceutical Intermediates for Anti-inflammatory and Oncology APIs

    API manufacturers employ this compound as a core intermediate for synthesizing select anti-inflammatory and anti-cancer drug molecules. Its trifluoromethyl and biphenyl functional motif supports key ring-building and functionalization steps via palladium-catalyzed cross-coupling and subsequent formyl chemistry. The aldehyde enters the active compound synthesis route in gram to kilogram scale, tailored to route optimization and regulatory validation. Customers rely on consistent impurity profile control and trace residual solvent management throughout cGMP operations.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US FDA cGMP for finished pharmaceuticals)
    • EU EudraLex Vol. 4 Annex 13 (EU GMP for APIs and Intermediates)
    • ICH Q3A Impurities in New Drug Substances

    Typical usage ratio

    • 5-20% molar input versus main pharmaceutical scaffolds depending on synthetic route and targeted yield optimization

    Downstream process integration

    • Enters Suzuki or Buchwald-Hartwig couplings as aromatic substrate
    • Serves as electrophile in Knoevenagel or aldol reaction steps

    Final product types

    • Small molecule APIs for clinical and commercial pharmaceutical products (e.g. kinase inhibitors, COX-2 modulators)
    • Advanced pharma intermediates supplied under DMF or CEP registration

    2. Liquid Crystal Materials for Electronic Displays

    Specialty chemical companies formulate this compound into advanced liquid crystal mixtures for high-performance TFT-LCD and OLED panel production. The fluorinated biphenyl structure imparts essential dielectric anisotropy and thermal stability, influencing switching voltages and cell response time. The aldehyde functionality allows downstream derivatization with precise homologs to match panel manufacturer specifications. The product supports annual contracts with strict supply chain traceability and technical data validation required for electronics customers.

    Industry compliance standards

    • IEC 62899-201 Electronic Displays – Performance Testing and Quality Requirements
    • ISO 9001:2015 Quality Management Systems (for electronic material supply chains)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in Electrical and Electronic Equipment)

    Typical usage ratio

    • 3-10% mass fraction in multi-component liquid crystal blends; ratio adjusted based on targeted birefringence and driving voltage

    Downstream process integration

    • Blended during masterbatch preparation with other liquid crystal monomers and additives
    • Subjected to fine filtration and QC under inert nitrogen prior to panel cell assembly

    Final product types

    • TFT-LCD and OLED display panels for smartphones, tablets, technical monitors
    • Specialty display films for automotive and industrial instrumentation

    3. Agrochemical Synthesis: Aryl Aldehyde Building Block for Fungicides

    Crop protection chemical companies incorporate this specialty aldehyde during the multi-step synthesis of aryl-heterocycle-based fungicidal active ingredients. The molecule's electronic properties enable formation of enaminone and hydrazone intermediates relevant to current patented classes of fungicide products. Downstream partners require assurance of low trace moisture and robust analytical batch records for REACH and pesticide registration dossiers. Reactions scale from pilot to full commercial volume based on seasonal demand, with close coordination on technical process changes.

    Industry compliance standards

    • ISO 17025 Analytical Laboratory Accreditation
    • EU Regulation (EC) No 1107/2009 (Pesticide registration in the EU)
    • US EPA 40 CFR Part 158 (Data requirements for pesticide registration)
    • REACH Regulation (EC) No 1907/2006 (for non-active substances in EU)

    Typical usage ratio

    • 2-8% molar feed to key condensation or cyclization steps; actual ratio determined by desired yield and impurity profile

    Downstream process integration

    • Direct addition to batch reactors with strong base or nucleophilic reagents
    • Undergoes isolation, chromatography, or in situ transformation prior to formulation

    Final product types

    • Systemic fungicide AI pre-concentrates and technical-grade intermediates
    • Final formulation fungicide products for crops and seed treatments meeting local registration

    4. Organic Electronic Material Synthesis: OLED and Advanced Polymer Precursors

    Manufacturers of organic semiconductors utilize this aldehyde derivative as an early-stage precursor in OLED emitter and charge transport layer development. The trifluoromethyl-biphenyl scaffold lends high electron affinity and supports formation of heterocyclic core units required in next-generation organic electronics. The aldehyde group’s reactivity allows customization through lienar chain extension or condensation with electron-rich diamines. Production batches meet high-purity requirements (≥99.5%) and documentation for downstream electronic material qualification.

    Industry compliance standards

    • JEDEC JESD24-2 (Quality and Reliability in OLED Materials)
    • ISO 14001:2015 (Environmental management systems in chemical manufacturing)
    • Sony Green Partner Program (for electroluminescent material suppliers)

    Typical usage ratio

    • 1-5% molar fraction in target monomer streams depending on specific emitter or polymer backbone synthesis

    Downstream process integration

    • Condensation with aromatic diamines to yield polyarylene or heterocyclic materials
    • Participates in Grignard or Friedel-Crafts-type reactions in batch or flow reactors

    Final product types

    • Organic emitters and charge transport molecules for OLED displays and lighting panels
    • Specialty polymers for printable electronics and sensors
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