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4'-Trifluoromethyl-Biphenyl-3-Carboxylic Acid

    • Product Name 4'-Trifluoromethyl-Biphenyl-3-Carboxylic Acid
    • Alias 4'-(Trifluoromethyl)-[1,1'-biphenyl]-3-carboxylic acid
    • Einecs 629-675-5
    • 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

    884775

    Product Name 4'-Trifluoromethyl-Biphenyl-3-Carboxylic Acid
    Cas Number 886498-84-6
    Molecular Formula C14H9F3O2
    Molecular Weight 266.22
    Appearance White to off-white solid
    Purity Typically ≥98%
    Melting Point 160-164°C
    Solubility Slightly soluble in water, soluble in organic solvents (e.g., DMSO, ethanol)
    Smiles C1=CC=C(C=C1)C2=CC(=CC=C2C(=O)O)C(F)(F)F
    Inchi InChI=1S/C14H9F3O2/c15-14(16,17)11-6-2-4-9(7-11)10-5-1-3-8-12(10)13(18)19/h1-8H,(H,18,19)
    Storage Temperature Room temperature, protected from light and moisture
    Synonyms 3-Carboxy-4'-trifluoromethylbiphenyl
    Hazard Class Non-hazardous for transport

    As an accredited 4'-Trifluoromethyl-Biphenyl-3-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 5-gram quantity comes in a sealed amber glass bottle, labeled with chemical name, formula, hazard symbols, and storage instructions.
    Shipping 4'-Trifluoromethyl-Biphenyl-3-Carboxylic Acid is shipped in tightly sealed containers, protected from moisture and light. It is transported under standard conditions at ambient temperature, labeled in accordance with chemical safety regulations. Handling and shipping comply with current hazardous material guidelines to ensure safe delivery and prevent contamination or degradation during transit.
    Storage 4'-Trifluoromethyl-Biphenyl-3-Carboxylic Acid should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, typically at room temperature (15–25°C). Avoid exposure to heat, strong acids, and bases. Ensure proper labeling and store separately from incompatible materials to maintain chemical stability and safety.
    Application of 4'-Trifluoromethyl-Biphenyl-3-Carboxylic Acid

    Applications of 4'-Trifluoromethyl-Biphenyl-3-Carboxylic Acid in Industrial Manufacturing

    4'-Trifluoromethyl-Biphenyl-3-Carboxylic Acid is an advanced intermediate valued for its unique trifluoromethyl and biphenyl structure, supporting demanding synthesis in high-performance downstream sectors. As a direct manufacturer, we focus on serving industries where this building block enables precise molecular functionality, strict compliance, and proven efficiency at scale.

    1. Pharmaceutical API Synthesis

    This compound functions as a key intermediate in the synthesis of medicinal agents, particularly in designing specific kinase inhibitors and specialty anti-inflammatory molecules. It allows chemists to introduce a stable trifluoromethyl group in late-stage synthesis, critical for enhancing pharmacokinetic profiles and metabolic stability in regulated pharmaceutical pipelines.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA cGMP)
    • European Pharmacopoeia (EP) and United States Pharmacopeia (USP) when relevant to end APIs
    • Chinese Pharmacopeia (ChP) for domestic formulations

    Typical usage ratio

    • 0.5–1.5 molar equivalents relative to target API; adjusted based on stoichiometry in stepwise synthesis and the efficiency of final coupling reactions

    Downstream process integration

    • Added at the late-stage building block introduction or coupling stage during multi-step organic synthesis of pharmaceutical intermediates
    • Submitted to purification, crystallization, and conversion steps before final API formation

    Final product types

    • Branded and generic kinase inhibitor APIs
    • Specialty anti-inflammatory APIs
    • Small molecule cancer therapy precursors
    • Complex custom research compounds for clinical development batches

    2. Liquid Crystal Monomer Preparation

    With its rigid biphenyl backbone and electronegative trifluoromethyl group, this compound is essential for synthesizing structural monomers tailored for high-contrast and highly stable liquid crystal display (LCD) mixtures, where sharp melting points and chemical stability underpin downstream device quality and yield.

    Industry compliance standards

    • IEC 61747 for liquid crystal devices
    • ISO 9001 and ISO 14001 certified quality management systems
    • RoHS Directive 2011/65/EU for restriction of hazardous substances
    • Internal LCD manufacturer specification sheets (ex: Sharp, LG Display procurement guidelines)

    Typical usage ratio

    • 2–12% w/w of total monomer blend, regulated by phase sequence and desired birefringence of target nematic or smectic LC mixtures

    Downstream process integration

    • Reacted with alkyloxybenzenes, cyanobiphenyls, and other functionalized core structures during monomer synthesis
    • Post-synthetic purification and blending into custom LC mixtures during upstream compounding for cell filling

    Final product types

    • High-performance nematic LC mixtures for thin-film transistor (TFT) panels
    • Advanced monochrome and color STN panel ingredients
    • Specialty optical films
    • Finished LCD module prepolymer blends

    3. Agrochemical Intermediate Manufacturing

    This material serves as a trusted backbone in synthesizing advanced agrochemical actives, specifically herbicide and insecticide molecules requiring fluoroaromatic scaffolds for metabolic resistance and increased selectivity. Its use enables the stepwise construction of actives designed to pass modern environmental and residue standards.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius MRL listings for crop protection chemicals
    • ISO 9001 certified manufacturing
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (Europe)
    • China Pesticide Registration (ICAMA)

    Typical usage ratio

    • 0.8–1.2 molar equivalents per agrochemical target molecule; determined via stoichiometry of final coupling or substitution reactions

    Downstream process integration

    • Incorporated at key aryl-coupling or electrophilic aromatic substitution stages in multi-step synthesis of pesticide actives
    • Further processed to yield crude actives, then refined for technical concentrate formulation

    Final product types

    • Active ingredients for new-generation herbicides
    • Advanced insecticidal scaffolds
    • Research intermediates for agricultural chemical discovery
    • Technical concentrates for further formulation

    4. Advanced Polymer Additive Compounding

    The compound’s fluorinated biphenyl structure enables it to function as a specialty modifier in high-performance polymer synthesis and compounding. It influences thermal stability, dielectric properties, and chemical resistance, which are critical in engineering plastics and specialty coatings for electronics and automotive sectors.

    Industry compliance standards

    • UL 94 for flame retardancy in plastics
    • IEC 60216 for thermal endurance of insulation materials
    • ISO 14001 for environmental management during compounding
    • RoHS Directive 2011/65/EU for electronic component applications

    Typical usage ratio

    • 0.2–2.1% by polymer resin weight, optimized for required property modification without phase separation or impact on mechanical properties; adjusted after batch trials

    Downstream process integration

    • Premixed with monomer streams or added during reactive extrusion to dispersive compounding lines
    • Dispersed into polymer matrices before molding, film formation, or extrusion of high-performance materials

    Final product types

    • High-frequency printed circuit board (PCB) substrates
    • Specialty insulation films for flexible devices
    • Automotive interior polymers
    • Electronics-grade coating resins

    5. Specialty Dye and Pigment Intermediate Production

    Its strong electron-withdrawing trifluoromethyl group and biphenyl ring make this compound attractive as an intermediate for synthesizing organic pigments and dyes with superior photostability, solvent resistance, and precise color properties. Manufacturers employ it to introduce desired functional motifs in high-value pigment molecules.

    Industry compliance standards

    • EN 71-3 (Safety of Toy Colorants, Europe, for applicable pigment types)
    • REACH Annex XVII restrictions for pigments and dyes
    • ISO 1248 for pigment quality assessment
    • OEKO-TEX Standard 100 (when targeting textile end-use)

    Typical usage ratio

    • 0.6–2.4 molar equivalents in condensation or acylation step, based on targeted chromophore structure and final pigment load requirements

    Downstream process integration

    • Engaged at the core structure-building stage in dye manufacturing, especially for diketopyrrolopyrrole (DPP), perylene, or azo pigment synthesis
    • Subsequently worked into final finishing, milling, and dispersion processes

    Final product types

    • High-performance organic pigments for automotive paints
    • Specialty dyes for technical textiles
    • Electronic display colorants
    • Industrial-grade solvent-resistant inks
    Free Quote

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