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2,3',4,4',6-Pentahydroxybenzophenone

    • Product Name 2,3',4,4',6-Pentahydroxybenzophenone
    • Einecs 210-142-0
    • 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
    VTB
    Specifications

    HS Code

    133910

    Chemical Name 2,3',4,4',6-Pentahydroxybenzophenone
    Molecular Formula C13H10O6
    Molecular Weight 262.22 g/mol
    Cas Number 490-62-0
    Appearance yellow solid
    Melting Point 254-256°C
    Solubility In Water slightly soluble
    Synonyms 2,3',4,4',6-Pentahydroxy diphenyl ketone
    Structure Type benzophenone derivative

    As an accredited 2,3',4,4',6-Pentahydroxybenzophenone 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 secure screw cap, labeled with product details and safety information.
    Shipping 2,3',4,4',6-Pentahydroxybenzophenone is shipped in tightly sealed, chemically-resistant containers to prevent moisture and contamination. It is packed following relevant chemical safety regulations, including labeling with hazard symbols if applicable. The packaging ensures secure transport under ambient conditions, with supplementary documentation provided for handling and storage guidelines.
    Storage 2,3',4,4',6-Pentahydroxybenzophenone should be stored in a cool, dry, and well-ventilated area, away from sources of heat and ignition. Keep the container tightly closed and protected from light to prevent degradation. Store away from incompatible substances such as strong oxidizers and bases. Use clearly labeled and chemically resistant containers to avoid contamination or accidental reactions.
    Application of 2,3',4,4',6-Pentahydroxybenzophenone

    Applications of 2,3',4,4',6-Pentahydroxybenzophenone in Industrial Manufacturing

    2,3',4,4',6-Pentahydroxybenzophenone serves as a specialty chemical intermediate in several high-value industrial sectors. Our direct manufacturing expertise supports clients with consistent quality for stringent downstream use. The following application scenarios represent established downstream integrations, where this raw material delivers precise functional and regulatory performance according to industry-specific requirements.

    1. UV Absorber for Industrial Coatings

    Many clients in the coatings sector incorporate this pentahydroxybenzophenone structure to produce advanced UV absorbers, essential for transparent wood finishes, automotive topcoats, and industrial plastics. The molecule’s abundant phenolic groups provide stable absorption in the 300–400 nm UV range, directly protecting polymers and colorants from photodegradation over sustained outdoor exposure. It fits into final additive packages formulated for compliance with color stability and gloss retention mandates in Europe, North America, and East Asia.

    Industry compliance standards

    • EN ISO 11341 (Artificial Weathering of Coatings)
    • Automotive OEM performance requirements (e.g., GMW14797)
    • GB/T 1766 (China paint and varnish ageing specification)
    • RoHS Directive 2011/65/EU limiting hazardous substances

    Typical usage ratio

    • 0.3%–2.0% w/w of total resin solids, adjusted for UV exposure class and substrate thickness

    Downstream process integration

    • Dispersed into solventborne or waterborne binder pre-mix stage before pigment grinding
    • Co-dissolved or melt-compounded with polymer in masterbatch production for clear plastics
    • Final UV absorber dosage verified by HPLC in finished additive blend QC

    Final product types

    • Clear automotive topcoats and OEM refinish paints
    • Architectural varnishes and transparent wood sealants
    • Polycarbonate or acrylic sheets for outdoor signage and glazing
    • Industrial protective clear coats for factory equipment

    2. Intermediate for Pharmaceutical Synthesis (API Precursor)

    This raw material functions as a selective intermediate in the multistep synthesis of flavone and xanthone derivatives, recognized for their bioactivity in investigational pharmaceuticals. Medicinal chemistry groups employ it in controlled condensation and cyclization steps, exploiting the pentahydroxy substitution pattern to produce advanced intermediates for further functionalization—especially where ortho-para directing effects are required for regioselectivity. All API manufacturing with this molecule proceeds under strict compliance and traceability systems, with batch release contingent on validated impurity profiles.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for active pharmaceutical ingredients (APIs)
    • U.S. FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • European Pharmacopoeia Monograph 5.2.8 – Impurities in starting materials
    • China Pharmacopoeia (ChP) – for locally registered APIs

    Typical usage ratio

    • Applied as a limiting reagent; 1.0–1.2 molar equivalents relative to core condensation partner, exact input based on reaction efficiency and desired yield

    Downstream process integration

    • Charged into heated batch reactor with acid catalyst for cyclization reactions
    • Purified by recrystallization or chromatographic isolation prior to onward coupling
    • In-process checks for residual solvents and trace heavy metals in API synthesis flow

    Final product types

    • Xanthone analogs for oncology small molecule pipelines
    • Flavone derivatives with documented antioxidant activity
    • Pharmaceutical intermediates registered for further API functionalization

    3. Photoinitiator Manufacturing for UV-Curing Systems

    Downstream producers of photoinitiators for UV-curing inks and adhesives value this pentahydroxybenzophenone as a core building block, leveraging its electron-rich aromatic structure to create substitutions that yield high-activity initiators. Chemical processing groups use the compound as a precursor for benzophenone-based Type II photoinitiators, ensuring rapid polymer matrix crosslinking and minimal migration in finished UV-cured products. This supports compliance with specialized regulations on residual migration for packaging and labeling substrates.

    Industry compliance standards

    • Swiss Ordinance on Materials and Articles in Contact with Food (817.023.21)
    • EU Regulation (EC) No 1935/2004 on food contact materials
    • ISO 9001:2015 for production and QC systems
    • Japanese Positive List System for food packaging inks

    Typical usage ratio

    • 2%–8% as a core reactant in synthesis batch, tailored to target photoinitiator functionality and substitution profile

    Downstream process integration

    • Reacted in alkylation or acylation steps before photoinitiator core formation
    • Isolated by liquid-liquid extraction after condensation and neutralization
    • Final photoinitiator grade controlled for UV absorbance and purity

    Final product types

    • UV-curable flexographic and offset printing inks
    • UV-setting adhesives for electronics assembly
    • Photo-cured coatings for flexible packaging and labels

    4. Natural-Analog Antioxidant Additive for Polymer Stabilization

    Polymer manufacturers integrate this pentahydroxybenzophenone as a specialty antioxidant additive to retard oxidative chain scission during extrusion and long-term service, especially in polyolefin and polyester fibers. Its phenolic groups disrupt radical propagation, extending the mechanical and optical life of polyolefin-based products under heat and sunlight. Downstream compounding lines introduce it in precise ratios to balance thermal stability, mechanical integrity, and compliance with migration restrictions for consumer safety.

    Industry compliance standards

    • U.S. FDA 21 CFR 177 (Polymers in contact with food, sections .1520 and .1630)
    • EU Regulation (EU) No 10/2011 (Plastics intended to come into contact with food)
    • OEKO-TEX Standard 100 for textile components
    • REACH Regulation (EC) No 1907/2006—Substance Registration

    Typical usage ratio

    • 0.05%–0.5% by wt in masterbatch formulation or final resin, with dosage refined by migration risk assessment and fiber denier

    Downstream process integration

    • Blended directly with base polymer resins during melt mixing at compounding plant
    • Quality control by DSC and SEC to monitor stabilization against chain breakdown
    • Pre-tested for non-interference with pigment or flame retardant performance

    Final product types

    • Outdoor polyolefin fibers (e.g., turf, rope, sacking)
    • Food-grade polypropylene sheets and injection parts
    • High-clarity PET bottles for beverage or detergent packaging
    • Technical films for agricultural covering
    Free Quote

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