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2,4-Diphenyl-5,6,7,8-Tetrahydrochromenylium Trifluoromethanesulphonate

    • Product Name 2,4-Diphenyl-5,6,7,8-Tetrahydrochromenylium Trifluoromethanesulphonate
    • Alias 7-(Trifluoromethanesulfonyl)-2,4-diphenyl-5,6,7,8-tetrahydro-4H-chromen-4-ylium
    • Einecs 684-470-8
    • 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

    579999

    Iupac Name 2,4-diphenyl-5,6,7,8-tetrahydrochromenylium trifluoromethanesulfonate
    Molecular Formula C22H19O+ · CF3SO3−
    Molar Mass 456.46 g/mol
    Appearance Solid, often crystalline
    Solubility Soluble in polar organic solvents
    Melting Point Varies, typically 120-180°C
    Counter Ion Trifluoromethanesulfonate (triflate)
    Functional Groups Chromenylium, phenyl rings, tetrahydro moiety
    Cation 2,4-diphenyl-5,6,7,8-tetrahydrochromenylium
    Color Usually reddish or deep orange
    Stability Sensitive to light and moisture
    Storage Conditions Store in a cool, dry place away from light
    Applications Used in organic synthesis and photophysical studies

    As an accredited 2,4-Diphenyl-5,6,7,8-Tetrahydrochromenylium Trifluoromethanesulphonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 1-gram amber glass vial sealed with a black screw cap, labeled with chemical name, hazard warnings, and lot number, in protective packaging.
    Shipping 2,4-Diphenyl-5,6,7,8-Tetrahydrochromenylium Trifluoromethanesulphonate is shipped in tightly sealed containers compatible with chemicals, protected from moisture and light. Transportation follows relevant hazardous material regulations, including clear labeling and documentation. Packaging ensures stability and containment to prevent leaks or contamination during transit. Refrigeration or temperature control may be used if required by product specifications.
    Storage 2,4-Diphenyl-5,6,7,8-Tetrahydrochromenylium Trifluoromethanesulphonate should be stored in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers. Store at room temperature or as recommended by the manufacturer. Ensure proper labeling and implement standard safety protocols for handling organic salts.
    Application of 2,4-Diphenyl-5,6,7,8-Tetrahydrochromenylium Trifluoromethanesulphonate

    Applications of 2,4-Diphenyl-5,6,7,8-Tetrahydrochromenylium Trifluoromethanesulphonate in Industrial Manufacturing

    2,4-Diphenyl-5,6,7,8-Tetrahydrochromenylium Trifluoromethanesulphonate serves as a high-performance specialty intermediate across several industrial fields. Below, we outline proven downstream applications in distinct manufacturing sectors, each reflecting unique industry requirements related to compliance, formulation, processing, and final products.

    1. Fine Chemical Synthesis for Photoinitiators

    This compound acts as a key building block in advanced photoinitiator synthesis, where its chromenylium core supports efficient light absorption and radical generation for UV-curable formulations used in inks and coatings. Manufacturers integrate this intermediate in a multi-step organic synthesis, tailoring it for cured systems with specific absorption wavelengths critical to end-user requirements in graphic arts and electronics. Quality assurance mandates strict monitoring of purity and reactivity at every stage.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • REACH (EC 1907/2006) Compliance for Chemical Safety
    • RoHS Directive (2011/65/EU) for electronics applications
    • OECD Guidelines for Testing of Chemicals

    Typical usage ratio

    • Ranges from 5% to 15% by molar equivalence in photoinitiator synthesis; adjustment depends on desired photoreactivity and absorption maximum.

    Downstream process integration

    • Used during intermediate condensation steps forming diaryl chromenylium photoreactive units prior to final functionalization and purification.

    Final product types

    • UV-curing photoinitiators
    • Photoresist additives for semiconductor manufacturing
    • Digital and offset printing inks
    • High-performance coatings for automotive electronics

    2. Active Pharmaceutical Intermediate in Antineoplastic Agent Synthesis

    The material functions as a structurally defined intermediate during the synthesis of certain chromene-based anticancer agents. Its stable trifluoromethanesulphonate counter-ion ensures solubility and reactivity throughout controlled GMP manufacturing environments. Downstream pharmaceutical companies source this intermediate according to precise quality control specifications, as dictated by regulatory bodies and international pharmacopoeias, to enable consistent small-molecule drug production for oncology pipelines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice
    • United States Pharmacopeia (USP) General Chapters on APIs
    • European Pharmacopoeia (Ph. Eur.) monographs
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • Introduced at stoichiometric quantities (1:1 molar ratio) in key coupling stages, with excess typically ranging from 2% to 5% based on yield optimization trials.

    Downstream process integration

    • Charged into active intermediate steps after base-ring construction, followed by functionalization and purification processes compatible with GMP pharmaceutical synthesis.

    Final product types

    • Benzopyran-based antineoplastic API precursors
    • Small molecule oncology drugs
    • Research-grade reference standards
    • Bulk intermediates for clinical API scale-up

    3. Dye and Pigment Synthesis for High-End Textiles

    Chemical manufacturers use this compound as a chromenylium cation precursor in the controlled synthesis of vivid, stable cationic dyes used in luxury fabrics, leather, and technical textiles. Strict colorfastness and toxicity regulations apply, especially where final goods contact human skin. Process engineers fine-tune reactions incorporating the compound to enhance brightness and environmental resistance of finished colorants, ultimately boosting performance in downstream dyehouses and textile finishing lines.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile chemicals
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • ISO 105:2010 for colorfastness testing
    • Global Organic Textile Standard (GOTS) Section 2.4 (dye inputs)

    Typical usage ratio

    • Employed at 3% to 7% relative to total chromenylium base mass, based on the targeted tint strength and dye bath yield curves.

    Downstream process integration

    • Introduced following primary chromenylium skeleton formation, then coupled with specific aromatic substituents; handled under inert conditions to prevent premature oxidation before isolation and purification of the dye salt.

    Final product types

    • Cationic textile dyes for polyester, acrylic, and blends
    • High-brightness pigment concentrates for luxury fabrics
    • Water-soluble digital textile inks
    • Specialty leather colorants

    4. Specialty Electronic Materials: Organic Semiconductors

    In organic electronic material manufacturing, this compound supplies a crucial electron-rich core for organic semiconductor synthesis. Makers of OLED and OFET devices adopt it during custom organic synthesis workflows where purity, crystallography, and molecular design affect the performance and processing of thin-film electronics. The input material’s reactivity and compatibility with anionic triflate-based processes ensure that device makers achieve reproducible and reliable charge transport properties in finished layers.

    Industry compliance standards

    • IEC 62341 – OLED panel manufacturing standards
    • JEITA technical standards for organic field-effect transistors
    • ISO 14644 for cleanroom manufacturing
    • REACH (EC 1907/2006) compliance for workplace safety and supply chain disclosure

    Typical usage ratio

    • 1% to 5% by weight in precursor formulations, precisely adjusted per molecular stacking requirements and electrical testing results on pilot film runs.

    Downstream process integration

    • Fed into oligomer or polymer coupling steps after initial chromenylium functionalization, followed by film casting and vacuum deposition for device active layers.

    Final product types

    • OLED emitter molecules
    • Organic semiconductors for printable electronics
    • Active-layer materials for OFETs
    • Flexible electronic substrate coatings

    5. Analytical Reagents in Fluorescent Probes Manufacturing

    The material finds use as a luminous precursor for producing highly specific fluorescent probes and dyes for biological analysis. Analytical reagent companies, under ISO and specialized quality frameworks, incorporate the compound during advanced organic synthesis protocols, engineering targeted emission and absorption spectra for laboratory and clinical diagnostic kits. Downstream processes rely on the stability conferred by the triflate anion throughout storage and use.

    Industry compliance standards

    • ISO 13485:2016 for medical device manufacturing (diagnostic reagents)
    • EU In Vitro Diagnostic Regulation (IVDR 2017/746)
    • GLP (Good Laboratory Practice) for analytical testing
    • Standard Methods for the Examination of Water and Wastewater (fluorescence probes)

    Typical usage ratio

    • Applied at 1 mg/mL to 10 mg/mL in conjugation reactions, with adjustments per dye loading capacity and target quantum efficiency.

    Downstream process integration

    • Appears in early-stage organic synthesis of fluorophore conjugates, followed by linker attachment and purification prior to formulation with stabilizers for diagnostic applications.

    Final product types

    • Fluorescent markers for flow cytometry
    • Molecular probes for biological imaging
    • Clinical diagnostic reagents
    • Research kits for cell analysis
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