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3,4,5-Trifluorobenzaldehyde

    • Product Name 3,4,5-Trifluorobenzaldehyde
    • Alias 3,4,5-Trifluorobenzal
    • Einecs 702-168-8
    • 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

    893444

    Cas Number 55271-55-7
    Molecular Formula C7H3F3O
    Molecular Weight 160.09 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 75-77 °C at 10 mmHg
    Density 1.382 g/cm3 at 25 °C
    Refractive Index 1.5250 at 20 °C
    Purity Typically ≥ 98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles C1=CC(=C(C=C1F)F)C=O
    Flash Point 92 °C

    As an accredited 3,4,5-Trifluorobenzaldehyde 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 3,4,5-Trifluorobenzaldehyde, with tamper-evident cap and hazard labeling for laboratory use.
    Shipping 3,4,5-Trifluorobenzaldehyde is shipped in tightly sealed containers to prevent leaks and exposure. It should be labeled clearly according to hazardous material regulations, transported in a cool, well-ventilated space, and handled with care to avoid breakage. Appropriate documentation, including safety data sheets, must accompany all shipments.
    Storage 3,4,5-Trifluorobenzaldehyde should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, heat, and sources of ignition. Keep it separate from incompatible substances such as strong oxidizing agents. Proper labeling and secondary containment are recommended. Use appropriate personal protective equipment when handling this chemical.
    Application of 3,4,5-Trifluorobenzaldehyde

    Applications of 3,4,5-Trifluorobenzaldehyde in Industrial Manufacturing

    3,4,5-Trifluorobenzaldehyde serves as a critical intermediate in several specialty downstream segments, especially within pharmaceuticals, agrochemicals, fine chemical synthesis, and advanced materials. Detailed below are its principal applications, manufacturing roles, and market-driven performance requirements.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) Synthesis

    Our 3,4,5-Trifluorobenzaldehyde plays a key role in API synthesis for various fluorinated pharmaceuticals. End users employ this material as a precursor in the manufacturing of kinase inhibitors, anti-inflammatory agents, and central nervous system actives. Precise molecular incorporation of the trifluoromethyl group ensures specific bioactivity and metabolic stability. Stringent control over purity and trace metal content forms part of standard QC before downstream formylation or condensation processes. Partnering pharmaceutical customers integrate this compound in scalable routes such as Wittig, Grignard, or reductive amination pathways, supporting batch and continuous flow production technology.

    Industry compliance standards

    • ICH Q7 guidelines for API manufacture
    • GMP Part II bulk pharmaceutical standards
    • USP, Ph. Eur. monograph controls (impurity profile reference)
    • FDA 21 CFR compliance for intermediates

    Typical usage ratio

    • Feedstock levels in target molecule synthesis: 0.8–1.4 molar equivalents relative to target core; ratio adjusted based on API structural route

    Downstream process integration

    • Starts as core aldehyde in the alkylation, acylation, or ring closure stage
    • Input for reductive amination or condensation with primary amines
    • Feeds into multistep process including separation and crystallization
    • Direct transfer to hydrogenation or oxidation reactors

    Final product types

    • Kinase inhibitor drug substances
    • Trifluoromethylated analgesics and antipyretics
    • Neuroactive pharmaceutical intermediates
    • Custom fluorinated heterocycle APIs

    2. Agrochemical Synthesis (Herbicide and Fungicide Intermediates)

    Agricultural chemical manufacturers use 3,4,5-Trifluorobenzaldehyde as a building block for selected pyrimidinyl and pyrazole-based herbicides and fungicides. Its trifluorinated aromatic ring modulates physicochemical properties, crucial for agrochemicals requiring high field persistence and specific systemic transport. Our supply supports industrial-scale acylation and heterocycle formation, enabling reproducible yields and controlling byproducts under large-volume conditions. Downstream R&D teams directly link this intermediate with evaluated field trial data tied to finished agrochemical shelf-life and mode of action.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for agrochemical intermediate production
    • FAO specification for technical grade raw materials
    • REACH registration dossier (EC No. 225-673-7)
    • ISO 9001:2015 in plant traceability and batch release

    Typical usage ratio

    • Intermediate addition: 1.0–1.3 eq per target active-site precursor; slight excess used to drive coupling reactions

    Downstream process integration

    • Integrated in condensation with aminopyridines or hydrazines to generate active agrochemical cores
    • Input for Claisen-Schmidt condensation or hydrazone formation
    • Used in batch reactors before downstream halogenation and formulation
    • Direct transfer to formulation lines for wettable powders or ECs

    Final product types

    • Trifluorinated herbicide actives (e.g., ALS inhibitors)
    • Fungicidal heterocycles (pyrimidine or triazole groups)
    • Selective post-emergence herbicide intermediates
    • Seed-treatment active ingredient precursors

    3. Liquid Crystal Intermediate for Advanced Display Materials

    Manufacturers in the electronics sector employ 3,4,5-Trifluorobenzaldehyde as a core aromatic segment in synthesizing specialty liquid crystal esters and ethers. The trifluoromethyl group placement imparts unique dielectric and birefringence properties essential for TFT-LCD and OLED panels. High-purity lots reduce ionic contaminants, which affect the lifespan and contrast level of screen components. Downstream integration involves precision esterification and etherification reactions, with process control supported by real-time FTIR and GC analysis to maintain electronic-grade consistency for display production.

    Industry compliance standards

    • IEC 61249-2-51 standard for material purity (electronics)
    • JEITA standards for materials in flat panel display industry
    • RoHS Directive 2011/65/EU (lead/mercury-cadmium free)
    • ISO 14001 for environmental management during manufacture

    Typical usage ratio

    • Monomer feed: 0.5–1.0 eq to diol or phenol modifier, tailored by target viscosity and mesogenic behavior

    Downstream process integration

    • Feeds to esterification with aliphatic or aromatic diols
    • Participates in etherification reactions for mesogen core extension
    • Inflow to distillation and vacuum stripping for purification
    • Supplied to formulation units for LC mixtures prior to cell loading

    Final product types

    • Liquid crystal mixtures for TFT-LCD panels
    • OLED matrix intermediates
    • Advanced display phase retarders
    • Anisotropic conductive films (ACFs)

    4. Fine Chemical Synthesis for Specialty Polymer Additives

    Producers of specialty polymers deploy 3,4,5-Trifluorobenzaldehyde as a performance-modifier precursor within high-stability flavor barrier films and engineering thermoplastics. The compound enters manufacturing to introduce fluorinated aromatic structures, impacting polymer crystallinity, solvent resistance, and surface energy properties. Customers’ technical centers request our material for collaboration on additive systems incorporated in multilayer packaging films and wire insulation. Downstream pathways involve direct polycondensation, compatible with both melt and solution processing.

    Industry compliance standards

    • FDA 21 CFR 177.1630 for packaging film contact
    • UL 94 recognition for flame retardant polymer compounds
    • ISO 10993 for indirect medical device plastics
    • REACH Art. 33 declaration where applicable

    Typical usage ratio

    • Copolymer incorporation: 0.3–2.0 wt% depending on barrier and dielectric performance targets

    Downstream process integration

    • Input for direct copolymerization during condensation polymer formation
    • Pre-blended in monomer feed prior to melt extruder
    • Additive introduced during reactive extrusion for functionalization
    • Blended in solution casting lines for multilayer film production

    Final product types

    • High-barrier food packaging films
    • Wire and cable insulation with reduced permeability
    • Flame-retardant thermoplastic parts
    • Functionalized engineering resins for automotive and electronics
    Free Quote

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