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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 | 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. |
Applications of 4,4',4''-Trihydroxytriphenylmethane in Industrial Manufacturing4,4',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 ColorantsManufacturers 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
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2. Photographic Chemical SynthesisIn 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
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3. Polymer Crosslinker and Resin ModifierResin 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
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4. Color Base in Ballpoint and Marking Ink ProductionInk 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
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5. Analytical Reagent FormulationsThe 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
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