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4,4',4''-Trihydroxytriphenylmethane

    • Product Name 4,4',4''-Trihydroxytriphenylmethane
    • Alias Aurine
    • Einecs 210-322-0
    • 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
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    Specifications

    HS Code

    412959

    Chemical Name 4,4',4''-Trihydroxytriphenylmethane
    Molecular Formula C19H16O3
    Molecular Weight 292.33 g/mol
    Appearance white to off-white solid
    Melting Point 280-284 °C
    Solubility sparingly soluble in water, soluble in organic solvents
    Cas Number 631-10-1
    Structure Type Aromatic hydrocarbon with three hydroxy groups
    Synonyms Tris(4-hydroxyphenyl)methane
    Smiles C1=CC(=CC=C1)C(C2=CC=C(C=C2)O)(C3=CC=C(C=C3)O)O
    Inchi InChI=1S/C19H16O3/c20-16-9-3-13(4-10-16)19(21,17-11-5-14(6-12-17)22)18-7-1-2-8-15(18)21/h1-12,20-22H
    Pubchem Cid 15932
    Pka Approximately 10 (for phenolic groups)

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

    Packing & Storage
    Packing The 100g package is a sealed amber glass bottle labeled "4,4',4''-Trihydroxytriphenylmethane," featuring hazard symbols and handling instructions.
    Shipping **4,4',4''-Trihydroxytriphenylmethane** is shipped in tightly sealed containers, protected from moisture and light. It is labeled in accordance with chemical safety regulations. The shipment complies with relevant transportation guidelines for non-hazardous laboratory chemicals. Appropriate documentation is included to ensure safe handling during transit and upon delivery to the end user.
    Storage 4,4',4''-Trihydroxytriphenylmethane should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture, heat sources, and direct sunlight. Keep it separate from incompatible materials such as strong oxidizers. Properly label the container and ensure storage in accordance with local regulatory guidelines. Use personal protective equipment when handling the chemical.
    Application of 4,4',4''-Trihydroxytriphenylmethane

    Applications of 4,4',4''-Trihydroxytriphenylmethane in Industrial Manufacturing

    4,4',4''-Trihydroxytriphenylmethane serves as a specialty intermediate in several industrial sectors. Its structure offers unique hydroxyl functionality, supporting both color development and polymer network formation. Below, we outline actual industrial uses, including compliance obligations, industrial-scale dosing, process routes, and end product examples.

    1. Dye Intermediates for Triarylmethane Colorants

    Manufacturers in the dyes sector use 4,4',4''-Trihydroxytriphenylmethane as a core building block in producing triarylmethane-based dyes. Its three phenolic positions facilitate selective sulfonation, nitration or alkylation, enabling fine-tuning of hue and fastness. Plants incorporate the intermediate at the condensation stage with selected aromatic compounds to synthesize colorants for textiles, paper, and ink. Quality control focuses on isomer purity, trace metals, and reaction completion to prevent unwanted by-products. Production lines validate compliance for export to regulated markets, with tight oversight over raw material origins and process records.

    Industry compliance standards

    • DIN EN ISO 9001:2015 for dyes manufacturing QC system
    • REACH (EC) No 1907/2006 registration for Europe
    • ZDHC MRSL conformance for textile dyehouses
    • Oeko-Tex Standard 100 Annex 4 limit testing for dye residues

    Typical usage ratio

    • 10%–35% based on mole ratio in condensation reactions; adjusted per target chromophore specificity and required tinctorial strength

    Downstream process integration

    • Feeds directly into dye synthesis kettle at the intermediate coupling/condensation stage
    • Monitored in inline HPLC to ensure complete incorporation and minimal carryover

    Final product types

    • Basic Blue 9 (Methylene Blue) derivatives
    • Brilliant Green dyes
    • Textile direct and acid dyes
    • Inkjet printing dyes for industrial use

    2. Photographic Chemical Synthesis

    In the photographic industry, 4,4',4''-Trihydroxytriphenylmethane functions in the synthesis of color-forming couplers and developer intermediates. Its reactive hydroxyl sites enable attachment of sensitizing groups, facilitating accurate color development during film processing. Industrial users dose the material precisely to regulate the color balance and stability of silver halide emulsions. Highly controlled batch management ensures traceability and lot consistency, given the material’s effect on image quality.

    Industry compliance standards

    • ISO 5466:2010 (Photographic-grade chemicals)
    • Harmonized Tariff Schedule (HTS) 3707
    • RoHS (as processed impurity control, Europe)
    • REACH SVHC screening

    Typical usage ratio

    • 2%–7% based on total developer or coupler formulation; exact value tailored to emulsion reactivity and target color density

    Downstream process integration

    • Added during synthesis of color couplers via controlled nucleophilic/electrophilic substitution reactions
    • Monitored by spectrophotometry for endpoint analysis

    Final product types

    • Photographic color developers (CD dyes)
    • Silver halide film couplers
    • Photo paper color emulsions
    • Analog photographic printing materials

    3. Polymer Crosslinker and Resin Modifier

    Resin producers incorporate this material as a multifunctional crosslinking agent or structural modifier in phenolic and epoxy resins. Its trihydroxy structure promotes formation of dense, thermoset networks, improving mechanical strength, heat resistance, and chemical durability. The precise addition rate depends on desired crosslink density and target product properties, with special focus on batch uniformity and residual monomers. Quality control validates the full reaction of hydroxyl sites and absence of unreacted phenols.

    Industry compliance standards

    • ASTM D1655 for resin composition
    • UL 94 (flammability standards for polymers)
    • ISO 14001 (environmental management in plants)
    • RoHS/REACH (residual monomer and impurity controls)

    Typical usage ratio

    • 0.2%–1.2% by weight of total resin batch, depending on resin type and application method

    Downstream process integration

    • Blended into masterbatch before thermal cure or casting
    • Post-added in two-pack epoxies for property adjustment

    Final product types

    • Circuit board laminates
    • High-durability cast phenolic resins
    • Coil and motor insulation coatings
    • Adhesive and potting compounds

    4. Color Base in Ballpoint and Marking Ink Production

    Ink manufacturers use this triphenylmethane derivative as a core color base in high-performance marking, stamp pad, and ballpoint inks. Its molecular structure provides vivid shades and strong lightfastness after appropriate sulfonation and coupling steps. The ingredient enters formulation as a pre-purified intermediate, where in-line blending and dispersion directly impact ultimate print clarity and ink viscosity. Regulatory checks ensure safety and migration limits, especially for stationery used in sensitive or educational environments.

    Industry compliance standards

    • EU Toy Safety Directive 2009/48/EC for ink components
    • EN 71-3 for chemical migration in writing inks
    • ISO 12757-1:2017 (requirements for ballpoint inks)
    • BS 5665 for felt tip and marker ink

    Typical usage ratio

    • 8%–18% w/w in ink concentrates; final ink adjusted for color strength and regulatory limits

    Downstream process integration

    • Dispersed into aqueous or glycol-based base stocks at coloring step
    • Filtered before canning and ink cartridge filling

    Final product types

    • Ballpoint pen refills
    • Permanent marking inks
    • Stamp pad colors
    • Whiteboard and dry erase markers

    5. Analytical Reagent Formulations

    The laboratory chemicals sector uses this raw material to synthesize specific colorimetric and complexometric analysis reagents. After hydroxyl functionalization, analysts use small batch methods to prepare indicators for detecting trace metals or biological species. Rigorous purity requirements apply, including metal trace residue testing, controlled pH response, and background absorbance checks. Only pharma or lab-qualified grades qualify for indicator production.

    Industry compliance standards

    • ACS Reagent Chemicals specifications
    • ISO 17025 (testing and calibration laboratories requirements)
    • Ph. Eur. (European Pharmacopoeia) for analytical reagents
    • USP General Chapter <851>

    Typical usage ratio

    • 0.1%–5% in indicator stock solution, based on target analyte sensitivity and detection wavelength

    Downstream process integration

    • Synthesized and purified prior to formulation into analytical test kits
    • Packaged under inert atmosphere to prevent oxidation/degradation

    Final product types

    • Colorimetric iron and copper detection reagents
    • Acid-base indicator powders
    • Titration endpoint indicators for process labs
    • Standardized lab test kits
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