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1-[3,5-Bis(Trifluoromethyl)Phenyl]Ethan-1-ol

    • Product Name 1-[3,5-Bis(Trifluoromethyl)Phenyl]Ethan-1-ol
    • Alias 3,5-Bis(trifluoromethyl)phenylethanol
    • Einecs 251-806-6
    • 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

    506981

    Iupac Name 1-[3,5-Bis(trifluoromethyl)phenyl]ethan-1-ol
    Molecular Formula C10H8F6O
    Molar Mass 258.16 g/mol
    Cas Number 67515-17-9
    Appearance White to off-white solid
    Melting Point 54-57 °C
    Density 1.42 g/cm³ (approximate)
    Smiles CC(O)C1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1
    Inchi InChI=1S/C10H8F6O/c1-6(17)7-2-8(10(12,13)14)4-9(3-7)11(15,16)18/h2-4,6,17H,1H3

    As an accredited 1-[3,5-Bis(Trifluoromethyl)Phenyl]Ethan-1-ol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a 25-gram amber glass bottle with a tamper-evident cap, labeled with safety and identification information.
    Shipping 1-[3,5-Bis(Trifluoromethyl)Phenyl]Ethan-1-ol is shipped in tightly sealed, chemically resistant containers to prevent leakage and contamination. It is transported under ambient conditions, protected from moisture and direct sunlight. Proper labeling, including hazard information, is provided, and handling follows standard chemical safety and regulatory guidelines for safe and compliant delivery.
    Storage Store **1-[3,5-Bis(Trifluoromethyl)phenyl]ethan-1-ol** in a cool, dry, and well-ventilated area away from direct sunlight, sources of ignition, and incompatible substances such as strong oxidizers. Keep the container tightly closed and use proper labeling. Avoid storing above room temperature. Use only in a chemical fume hood and wear appropriate personal protective equipment when handling.
    Application of 1-[3,5-Bis(Trifluoromethyl)Phenyl]Ethan-1-ol

    Applications of 1-[3,5-Bis(Trifluoromethyl)Phenyl]Ethan-1-ol in Industrial Manufacturing

    1-[3,5-Bis(Trifluoromethyl)Phenyl]Ethan-1-ol is a specialty fluorinated alcohol widely used across pharmaceutical, agrochemical, liquid crystal, and advanced polymer synthesis sectors. Our direct process integration and raw material traceability ensure practical application for downstream manufacturers. The following sections detail genuine industry uses, compliance protocols, and integration methods.

    1. Pharmaceutical Intermediate for Active Ingredient Synthesis

    Pharmaceutical manufacturers employ this raw material as a building block in the synthesis of novel fluorinated drug candidates, particularly in small molecule API and investigational new drug development. Substitution with bis(trifluoromethyl) groups brings metabolic stability and modulates pharmacokinetic properties. It enters multi-step reaction sequences, frequently in Friedel–Crafts acylation, and serves as a precursor to chiral secondary alcohols needed for selective therapeutic agents.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP/NF and EP monograph conformity for process reagents; absence of residual solvents based on ICH Q3C
    • Pharmaceutical grade processing requires ISO 9001 and ISO 14001 site accreditation
    • Documentation according to DMF (Drug Master File) protocols for regulated markets

    Typical usage ratio

    • Used at 0.1–5% molar ratio relative to primary reactant, depending on target molecular scaffold and scale
    • Adjustment based on stoichiometric yield optimization and downstream chiral purity targets

    Downstream process integration

    • Introduced inline in the early alkylation stage or as a resolving agent in late-stage synthesis steps
    • Employed under inert atmosphere with controlled temperature protocols (0°C–30°C) to minimize side reactions
    • Handovers to purification units for crystallization before API isolation

    Final product types

    • Patent-protected small molecule APIs with fluorinated functionalities
    • Clinical trial bulk intermediates for oncology, CNS, and anti-infective therapies
    • Precursor for advanced antidiabetic and antiviral compound synthesis

    2. Liquid Crystal Monomer Synthesis for Display Technology

    Downstream display technology corporations utilize this compound as an intermediate during the manufacture of high-performance fluorinated liquid crystal monomers, which confer enhanced dielectric anisotropy and thermal stability. Specialized fluorination allows finished liquid crystals to meet strict response time and alignment standards for LCD and OLED panels.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) restriction for hazardous substances in electronic components
    • IEC 62321 for determination of certain substances in electrotechnical products
    • ISO 9001:2015 Quality Management System certification for raw material traceability
    • JIS standards for Japanese display industry acceptance

    Typical usage ratio

    • Integrated at 1–8% by weight relative to total monomer mix in custom liquid crystal production
    • Ratio determined by performance specs on viscosity, clearing point, and birefringence requirements

    Downstream process integration

    • Supplied as a processed intermediate directly into condensation, esterification, or etherification stages for monomer backbone formation
    • Final functionalization occurs in batch reactors with controlled solvent systems
    • Finished monomers undergo filtration and QC before mixing into liquid crystal master batches

    Final product types

    • Advanced nematic and ferroelectric liquid crystal mixtures for TFT-LCD / OLED displays
    • Premium-grade liquid crystal cells for automotive and industrial displays
    • Materials for high-resolution e-paper and optical shutter panels

    3. Agrochemical Synthesis for Fluorinated Herbicide and Pesticide Actives

    Major agrochemical producers leverage the material in the development of novel fluorinated phenyl-based herbicides and crop protection products. The compound’s electron-withdrawing groups improve environmental stability and bioavailability, making it attractive for next-generation actives with reduced environmental impact and improved efficacy against resistant weeds.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 registration for agricultural chemicals
    • EPA 40 CFR Part 158 – Data requirements for pesticide registration in the United States
    • OECD Guidelines for the Testing of Chemicals for environmental fate and residue analysis
    • ISO 9001 process control for batch-to-batch consistency

    Typical usage ratio

    • Used at 0.5–7% molar equivalent depending on the final target molecule’s structure and the synthesis stage
    • Ratio tailored by LC/MS monitoring to achieve desired activity spectrum

    Downstream process integration

    • Fed into early-stage etherification or coupling reactions with pyridine or phenoxy cores
    • Purified via liquid-liquid extraction or flash chromatography prior to finishing reactions
    • Incurs additional screening for absence of regulated impurities (e.g., PFOS/PFOA contaminants)

    Final product types

    • New-generation fluorinated herbicides for resistant grass and broadleaf control
    • Insecticidal compounds optimized for controlled-release formulations
    • Crop protection co-formulant building blocks

    4. Monomer for High-Performance Fluorinated Polymers

    Polymer manufacturers apply this specialty alcohol in the creation of non-stick, chemically resistant, and high-dielectric fluorinated polymers. Its incorporation raises the polymer’s glass transition temperature and hydrophobicity. It is primarily employed for performance coatings, specialty films, and electrical insulation requiring exceptional weathering and solvent resistance.

    Industry compliance standards

    • ASTM D6287 – Standard Practice for Cutting, Mixing, and Molding of Thermoplastic Polymers
    • UL 94 Flammability Testing for Plastics used in devices and appliances
    • ISO 14001 Environmental Management System for emission control
    • EN 60243 for electrical insulating materials (high-voltage insulating films)

    Typical usage ratio

    • Typically dosed at 2–12 parts per hundred resin (phr) dependent on polymer backbone and targeted end-use performance
    • Tailored by melt index and final dielectric constant specifications

    Downstream process integration

    • Mixed directly into co-polymerization reactors during melt or solution phase polymer synthesis
    • Reacts with isocyanates, acrylates, or vinyl ethers under controlled conditions
    • Ensured dispersion checked with FTIR and DSC analysis post-reaction

    Final product types

    • Fluorinated polyurethane coatings for industrial anti-corrosion applications
    • High-dielectric films for electronic substrates
    • Hydrophobic membranes for filtration and medical use
    • Specialty non-stick coating compounds for cookware or food processing lines
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